https://journal.asu.ru/biol/issue/feedActa Biologica Sibirica2025-12-31T10:57:26+07:00Alex Matsyuraamatsyura@gmail.comOpen Journal Systems<div class="additional_content"> <p><strong>ISSN 2412-1908 (Online)</strong></p> <p align="justify">We should like to inform our readers and authors that since January 1st, 2022 we are moving from Pensoft Publishers back to Altai State University portal. We extend our deep and sincere gratitude to the Pensoft team and L. Penev personally for productive and valuable cooperation. </p> <p>Please refer to <a href="http://abs.pensoft.net">http://abs.pensoft.net</a> for journal articles within 2020-2021.</p> <div id="content"> <div id="journalDescription"> <div id="additionalHomeContent"> <p align="justify"><em><strong>Acta Biologica Sibirica</strong></em> publishes original, previously unpublished articles on the following fields: Faunistics, Floristics, Biogeography, Biological systematics, Nature conservation and protected areas, Reviews of published articles and monographs on the above topics, Memorial articles. Preference is given to articles in English. There are no restrictions on the article volume and number of articles in the issue. In the fields of faunistics and floristics, we accept articles of two types: floral and faunal lists on any region of the world (areas, regions, countries, mountain ranges, national parks), and faunal and floral discoveries (finding new species for the regions, additions to previously published inventories…). We also accept articles on methodology of faunal and floral studies. 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We will publish one rolling volume consisting of a single issue per calendar year from 2020. All the articles will be continuously paginated and the universal digital object identifier (DOI) should be used for citations.</p> </div> </div> </div> </div> </div>https://journal.asu.ru/biol/article/view/16761Technogenic effects on scots pine generative organs: a cross-country study2025-03-13T10:15:28+07:00Gulmira Assylbekovazhumabekovab@ppu.edu.kzBibigul Zhumabekovazhumabekovab@ppu.edu.kzMikhail Klimenkozhumabekovab@ppu.edu.kzMulk Khan Shujaulzhumabekovab@ppu.edu.kzKarlygash Aubakirovazhumabekovab@ppu.edu.kz<p>This article presents the results of a study assessing the state of morphological changes in the male generative organs of Scots pine (<em>Pinus sylvestris </em>L.) in Kazakhstan and Poland. The purpose of this study is to assess the transformation of pine pollen under different environmental conditions. Research and pollen sampling were carried out in 2023 in different environmental conditions and in different geographical areas: Astana (Kazakhstan), Bayanaul State National Natural Park (BSNNP) (Kazakhstan) and Poznan (Poland). For cytological analysis, microsporophylls were selected from the middle part of the microstrobilus, the material was stained with 1% Lugol's pharmaceutical solution, the preparations were studied on a Nikon eclipse E 200 microscope with a magnification of 10x15x40. The results of the analysis showed that the maximum number of disturbances in pine pollen was detected in samples from Poznan - 63%. In the Bayanaul Natural Park and in Astana, pine has fewer anomalies in pollen - 57% and 55%. The most common types of anomalies found in Scots pine pollen in the study areas are: deformed (26.3%), pollen with impaired shell formation (19%) and degraded (7.4%). Under conditions of technogenic pollution in coniferous trees (<em>Pinus sylvestris </em>L.), a higher level of abnormality of pollen grains was revealed than in relatively clean conditions, and a wide spectrum (sterile, deformed and small pollen grains with disturbances (without air sacs, with one and three air bags).</p>2025-01-15T00:00:00+07:00Copyright (c) 2025 https://journal.asu.ru/biol/article/view/16772Uranium phytoremediation by Helianthus annuus L. and Amaranthus caudatus L. plants2025-03-23T20:16:15+07:00Majid Mahdiehm-mahdiyeh@araku.ac.irMohammedreza Sangim-mahdiyeh@araku.ac.irSaeid Hamidim-mahdiyeh@araku.ac.irSeyed M. Talebiseyedmehdi_talebi@yahoo.comAlex V. Matsyuraamatsyura@gmail.com<p>Uranium contamination presents significant challenges to biological systems due to its chemical toxicity and radiological impacts. Rhizofiltration emerges as a cost-effective strategy for environmental remediation of uranium. This study aimed to compare the uranium uptake capabilities of two plant species, <em>Helianthus annuus </em>L. (sunflower) and <em>Amaranthus caudatus </em>L. (purple amaranth), in a hydroponic system. The plants were cultivated in nutrient solutions supplemented with 0.5 mM or 1 mM UO₂(NO₃)₂.6H₂O without phosphate. After 14 days of growth, we assessed uranium uptake. Our findings revealed that <em>H. annuus </em>effectively removed over 95% of the initial uranium concentration from the solution, while <em>A. caudatus </em>exhibited a removal efficiency of approximately 65–80%. In both species, uranium accumulation and transport to the upper, harvestable parts were limited. The highest uranium concentration was observed in the roots of <em>H. annuus </em>(37,050.8 ± 3,547 mg kg-1 DW), whereas <em>A. caudatus </em>roots had a noticeably lower concentration (14,944.68 ± 3,278 mg kg-1 DW). Interestingly, <em>A. caudatus </em>demonstrated greater uranium accumulation in its shoots compared to <em>H. annuus</em>. Overall, while <em>H. annuus </em>demonstrates superior potential for uranium rhizofiltration, <em>A. caudatus </em>emerges as a promising candidate as a hyperaccumulator for uranium.</p>2025-01-17T00:00:00+07:00Copyright (c) 2025 Majid Mahdieh, Mohammadreza Sangi, Saeid Hamidi, Seyed M. Talebi, Alex V. Matsyurahttps://journal.asu.ru/biol/article/view/16775The effect of micro-plastics on the growth and development of Eisenia fetida (Savingy, 1826) in vermiculture2025-03-23T20:18:22+07:00Andrey S. Babenkoandrey.babenko.56@mail.ruAlexander V. Kurovskijandrey.babenko.56@mail.ru<p>The effect of different concentrations of e-waste plastic (acrylonitrilebutadiene styrene) in vermiculture on the growth and development of the compost earthworm <em>E. fetida </em>was studied. It was shown that at low concentrations of microplastics (1%) in vermiculture, earthworms practically do not reduce their growth and development indicators, while with an increase in the plastic concentration to 5–10%, the number of cocoons and juveniles decreases, and the growth of earthworm biomass slows down. Avoidance of the substrate and death of worms are not observed even with a relatively high (10%) proportion of plastic in the composted mixture.</p>2025-01-18T00:00:00+07:00Copyright (c) 2025 Andrey S. Babenko, Alexander V. Kurovskijhttps://journal.asu.ru/biol/article/view/16836New records of Lepidoptera on the South of the West Siberian Plain: report on 2024 field season2025-04-14T09:29:07+07:00Svyatoslav V. Knyazevkonungomsk@yandex.ruVadim I. Ivoninkonungomsk@yandex.ru<p>Fourteen species of Sesiidae Pieridae, Lycaenidae, Satyridae, Geometridae, Arctiidae, Erebidae and Noctuidae are reported from the territory of Omsk and Novosibirsk Regions of Russia. <em>Chamaesphecia crassicornis </em>Bartel, 1912 is new to Asian part of Russia, <em>Synanthedon altaica </em>O. Gorbunov, 2018 and <em>Gonospileia munita </em>(Hübner, 1813) are new to the Russian Part of the West Siberian Plain. Five species are reported from the territory of Omsk Region for the first time. Nine species are new to the fauna of Novosibirsk Region. The first record of <em>Triphysa nervosa </em>Motschulsky, 1866 on the South of the West Siberian Plain provided.</p>2025-01-19T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazev, Vadim V. Ivoninhttps://journal.asu.ru/biol/article/view/16867Nuclear DNA content in some Chondrilla taxa (Asteraceae) of European Russia and Western Kazakhstan2025-04-14T09:29:07+07:00Alena S. Parkhomenkokashinas2@yandex.ruMikhail V. Skaptsovkashinas2@yandex.ruAnna O. Kondratievakashinas2@yandex.ruSaveliy F. Efimenkokashinas2@yandex.ruAleksandr S. Kashinkashinas2@yandex.ru<p>The aim of study was to evaluate the nuclear DNA content in samples of <em>Chondrilla </em>taxa from European Russia and Western Kazakhstan using flow cytometry approach. The analysis was performed in 30 populations of 8 taxa from the genus (<em>C. brevirostris</em>, <em>C. laticoronata</em>, <em>C. juncea</em>, <em>C. latifolia</em>, <em>C. graminea</em>, <em>C. canescens</em>, <em>C. ambigua</em>, and <em>C. pauciflora</em>). It was revealed that <em>C. juncea</em>, <em>C. graminea</em>, <em>C. canescens </em>and <em>C. latifolia </em>have the smallest monoploid genome size (1Cx) (1.078–1.098 pg), <em>C. laticoronata </em>and <em>C. brevirostris </em>have the intermediate values (1.190–1.203 pg), and <em>C. pauciflora </em>and <em>C. ambigua </em>have the largest (1.309–1.449 pg), i.e. the DNA content consistently increases by approximately 10% between these groups of taxa. The obtained results confirm the opinion that <em>C. juncea</em>, <em>C. graminea</em>, <em>C. latifolia </em>and <em>C. canescens </em>are synonymous with the priority name <em>C. juncea</em>. <em>C. ambigua </em>is the only one diploid species among the studied taxa. <em>C. pauciflora </em>is most likely its triploid cytotype. The position of <em>C. laticoronata </em>and <em>C. brevirostris </em>DNA contents between the <em>C. juncea </em>subspecies group, and the group including <em>C. pauciflora </em>and <em>C. ambigua </em>can be explained by distant hybridization that took place in the past, when <em>C. ambigua </em>or <em>C. pauciflora </em>acted as a maternal parent, and two species from the subgenus <em>Chondrilla</em>, different for each combination, acted as a paternal ones. The obtained results indicate that within the studied range the DNA content in <em>Chondrilla </em>at the interpopulation level changes regularly along the latitudinal gradient. From the south to about 50 °N, the genome size increases. From 50 °N to the north, the nuclear DNA content decreases.</p>2025-02-03T00:00:00+07:00Copyright (c) 2025 Alena S. Parkhomenko, Mikhail V. Skaptsov, Anna O. Kondratieva, Saveliy F. Efimenko, Aleksandr S. Kashinhttps://journal.asu.ru/biol/article/view/16868Results of the entomological expedition of Altai State University to Pamir in 2023: Nolidae, Erebidae sensu stricto and Noctuidae (Lepidoptera)2025-04-14T09:29:07+07:00Alexey Y. Matovnoctua2006@yandex.ruBalázs Benedeknoctua2006@yandex.ruBalázs Tóthnoctua2006@yandex.ruVyacheslav V. Doroshkinnoctua2006@yandex.ruRoman V. Yakovlevyakovlev_asu@mail.ru<p>We present the faunal list of Nolidae, Erebidae sensu stricto and Noctuidae (Lepidoptera) of Mountain-Badakhshan Autonomous Region of the Republic of Tajikistan, including 184 species. Two species: <em>Hadena chrysocyanea </em>Boursin, 1961 and <em>Chilodes distracta </em>(Eversmann, 1848) (Noctuidae: Noctuinae) are reported for Tajikistan for the first time.</p>2025-02-03T00:00:00+07:00Copyright (c) 2025 Alexey Y. Matov, Balázs Benedek, Balázs Tóth, Vyacheslav V. Doroshkin, Roman V. Yakovlevhttps://journal.asu.ru/biol/article/view/16876Composition of fatty acids, essential oils and morphological characteristics of some medial plants growing in permafrost ecosystems2025-04-14T09:29:07+07:00Vasiliy V. Nokhsorovvv.nokhsorov@mail.ruFedor F. Protopopovprotopopov_fedor@mail.ru<p>Using chromatographic (TLC, GC-FID), spectrophotometric methods (3D fluorescence spectroscopy), and scanning electron microscopy (SEM), the composition and content of fatty acids (FA), essential oils (EO) and morphological features were investigated in five plant species (<em>Alnus alnobetula</em> subsp. fruticosa (Rupr.) Raus, <em>Equisetum arvense</em> L., <em>Tanacetum vulgare</em> L., <em>Thymus serpyllum</em> L. subsp. <em>mongolicus</em> Ronniger, <em>Juniperus sibirica</em> Burgsd.) from different taxonomic groups (angiosperms, gymnosperms, and cryptogams) growing in the conditions of cryolithozone of Yakutia. Differences in the magnitude and variability of FA composition in the studied species were revealed. The main components of total lipids were found to be polyunsaturated fatty acids (PUFA) of the acid families omega-3 (n-3) and omega-6 (n-6), such as linoleic [18:2(n-6)], (LA) and alpha-linolenic [18:3(n-3)], (ALA), the content of which reached up to 47.4% of the sum of FA. Comparative analysis of the component composition of the components of EO of essential oils revealed that two species were characterized by a high content from polyphenolic compounds of <em>T. serpyllum</em> and <em>J. sibirica</em>, compared to other species studied. When plants were examined using SEM, morphological features such as the presence of well-formed trichomes, megasporophylls, and microphylls were identified. The identification of features such as high PUFA content in total lipids, polyphenolic components in essential oils, and well-formed trichomes, megasporophylls, and microphylls contribute to the survival and subsequent vegetation of perennial plants in cold climate permafrost ecosystems.</p>2025-02-07T00:00:00+07:00Copyright (c) 2025 Vasiliy V. Nokhsorov, Fedor F. Protopopovhttps://journal.asu.ru/biol/article/view/16877Annotated list of vascular plants of Zarafshan National Natural Park (Uzbekistan)2025-04-14T09:29:07+07:00Flora Kabulovaflorakabulova0@gmail.comShuhrat Valievflorakabulova0@gmail.comNoila Jumakulovaflorakabulova0@gmail.comShoxira Atayevaflorakabulova0@gmail.com<p>The article provides an annotated list of vascular plants growing since the beginning of the formation of the Zarafshan State Reserve in 1975 and then in 2018 transferred to another category of protected area – Zarafshan National Natural Park. The list includes 416 plant species belonging to 229 genera and 61 families. One of the serious problems of our time is the degradation of ecosystems, the reduction of biological diversity and the irreparable loss of the gene pool of the plant world. Therefore, protection of the natural environment, accounting and rational use of biological resources is the basis for the development of any state.</p>2025-02-08T00:00:00+07:00Copyright (c) 2025 Flora Kabulova, Shuhrat Valiev, Noila Jumakulova, Shoxira Atayevahttps://journal.asu.ru/biol/article/view/16895Differences in individual behavior and trophic niche of the red wood ant Formica aquilonia from urban and natural habitats: a case study in Novosibirsk region (West Siberia, Russia)2025-04-14T09:29:07+07:00Ivan K. Iakovlevivaniakovlev@gmail.comAleksei A. Maslovivaniakovlev@gmail.com<p>Behavior plays a key role in the ability of animals to adapt to human-induced environmental change, although the consistency of these behavioral changes and their links to ecological niche are less clear. In this study, we examined the effects of habitat type and season on behavioral variation, trophic isotopic niche, and their relationships in the ant Formica aquilonia, a keystone species of forest communities in North Eurasia, collected from an urban forest park and a natural forest in spring and autumn. We found that exploratory activity was lower in urban than in natural forest ants. Aggression scores towards competitors (<em>Lasius fuliginosus, L. niger</em>) were similar in both habitats, but urban ants interacted longer with <em>L. niger.</em> Individual ant responses were positively correlated as an aggression-boldness syndrome (more aggressive individuals are more exploratory) in the natural habitat, but not in the urban environment, where the association between aggression and exploration was negative in autumn and decoupled in spring. The trophic niche of the ants differed between the habitats, expressed by lower δ15N and δ13C values in urban ants. It indicates that ants in the urban park fed at a lower trophic level and presumably consumed less tree-related resources than in the natural forest. Exploratory activity was positively correlated with δ13C value, suggesting a possible link between personality traits and ant diet. Our results on ants support findings on human-induced behavioral changes in vertebrates and highlight the need for further studies on the adaptation of wood ants to life in urban environments.</p>2025-02-09T00:00:00+07:00Copyright (c) 2025 Ivan K. Iakovlev, Aleksei A. Maslovhttps://journal.asu.ru/biol/article/view/16914Lepidoptera of South Ossetia (Northern Transcaucasia). Part VI. Family Geometridae Leach, 18152025-04-14T09:29:07+07:00Artem E. Naydenovnaydenov.24@mail.ruAleksandr N. Streltzovnaydenov.24@mail.ruPetr Ya. Ustjuzhaninnaydenov.24@mail.ruRoman V. Yakovlevnaydenov.24@mail.ru<p>Here we provide the faunal list of 121 species from five subfamily of geometrid moths collected in South Ossetia. A total of 120 species are being reported for the first time in this territory.</p>2025-02-17T00:00:00+07:00Copyright (c) 2025 Artem E. Naydenov, Aleksandr N. Streltzov, Petr Ya. Ustjuzhanin, Roman V. Yakovlevhttps://journal.asu.ru/biol/article/view/16941An annotated checklist of ladybeetle species (Coleoptera, Coccinellidae) of Ferghana Valley (Uzbekistan)2025-04-14T09:29:07+07:00Saodat T. Gafurovasaodat.0312.84@mail.ruBakhtiyor R. Kholmatovsaodat.0312.84@mail.ruGulnara S. Mirzaevasaodat.0312.84@mail.ru<p>The article presents the results of a study on the fauna of lady beetles (Coleoptera, Coccinellidae) based on our observations in the Fergana Valley during the spring, summer, and autumn seasons as well as the winter season from 2022 to 2024. Thirty-five species of lady beetles, belonging to 5 subfamilies (Scymninae, Chilocorinae, Ortaliinae, Coccinellinae, and Hyperaspidinae), 9 tribes, and 19 genera, were found along the valley. Noteworthy species identified in the Fergana Valley during the research include<em> Novius yemenensis</em> (Raimundo & Fürsch, 2006), <em>Platynaspidius saundersi</em> (Crotch, 1874), <em>Brachiacontha ursine</em> (Chevrolat in Dejean, 1837), <em>Scymnus marinus</em> (Mulsant, 1850). The species<em> Calvia muiri</em> (Timberlake, 1943) and <em>Clitostethus arcuatus</em> (Rossi, 1794) were recorded for the first time in the fauna of Uzbekistan and 23 species were recorded for the first time in the Fergana Valley.</p>2025-02-26T00:00:00+07:00Copyright (c) 2025 Saodat T. Gafurova, Bakhtiyor R. Kholmatov, Gulnara S. Mirzaevahttps://journal.asu.ru/biol/article/view/16951On the morphology and systematics of Bembecia jakuta (Herz, 1903) (Lepidoptera, Sesiidae)2025-04-27T13:02:11+07:00Oleg G. Gorbunovgorbunov.oleg@mail.ru<p>The description and illustrations of <em>Bembecia jakuta</em> (Herz, 1903) are presented herein. To stabilize the species epithet, clarify the taxonomic status, and define the type locality of this under-researched species of clearwing moths (Lepidoptera, Sesiidae) within the Palearctic region, a neotype is designated. A comprehensive analysis of the external morphology, along with the examination of the male genitalia, indicates that this species is closely related to <em>B. aktashica</em> O. Gorbunov, 2018; however, it exhibits distinct differences in the coloration of certain body parts and the configuration of the transparent areas of the forewing. Furthermore, these two species display minor variations in the structure of the male genitalia. The female, host plants, and biological characteristics of the larvae remain unidentified.</p>2025-03-02T00:00:00+07:00Copyright (c) 2025 Oleg G. Gorbunovhttps://journal.asu.ru/biol/article/view/16957First records of two Triplax species (Coleoptera, Erotylidae) from Kazakhstan. Report 22025-04-14T09:29:07+07:00Izbasar I. Temreshevtemreshev76@mail.ru<p>Pleasing fungus beetles (Erotylidae) <em>Triplax rufipes </em>(Fabricius, 1787) and <em>Triplax scutellaris </em>Charpentier, 1825 is firstly recorded from Kazakhstan. A new key to known species of the genus <em>Triplax </em>from Kazakhstan is given. The finds of <em>T. rufipes </em>from North Kazakhstan are currently new record for this species for Kazakhstan and Central Asia. Mealy oyster <em>Ossicaulis lignatilis </em>(Pers.) Redhead & Ginns mushroom were first recorded from Kazakhstan for <em>T. rufipes </em>and <em>T. scutellaris</em>.</p>2025-03-06T00:00:00+07:00Copyright (c) 2025 Izbasar I. Temreshevhttps://journal.asu.ru/biol/article/view/16975Review of rare bird species in the North Kazakhstan: update and additions to the regional avifauna list2025-04-14T09:29:07+07:00Ivan A. Zubanzuban_ia@mail.ruAlexey Y. Timoshenkozuban_ia@mail.ruPavel S. Dmitriyevzuban_ia@mail.ruSergey N. Gashevzuban_ia@mail.ruMikhail N. Kalashnikovzuban_ia@mail.ruBakhytzhan M. Suindykovzuban_ia@mail.ruVladislav S. Lunyovzuban_ia@mail.ruStanislav V. Shnelzuban_ia@mail.ru<p>The study details long-term observations conducted in the North Kazakhstan region from 2016 to 2024, focusing on bird species that were either previously unrecorded or rarely encountered. The research clarified data on the occurrence and seasonal activity of specific species by analyzing unpublished observations and recent publications. A notable outcome was the addition of six new species to the regional avifauna list, enhancing our understanding of local bird diversity. These findings underscore the dynamic nature of bird populations and the potential impacts of ecological and climatic changes. Key factors contributing to the registration of new species include climate change and habitat transformation. The results highlight the importance of ongoing biodiversity monitoring in light of global changes.</p>2025-03-11T00:00:00+07:00Copyright (c) 2025 Ivan A. Zuban, Alexey Y. Timoshenko, Pavel S. Dmitriyev, Sergey N. Gashev, Mikhail N. Kalashnikov, Bakhytzhan M. Suindykov, Vladislav S. Lunyov, Stanislav V. Shnelhttps://journal.asu.ru/biol/article/view/16971Triodia laetus (Staudinger, 1877) – new species of ghost moths (Lepidoptera, Hepialidae) for the fauna of Russia, Armenia and Azerbaijan2025-04-27T13:16:00+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ru<p>A poorly-known Hepialidae species Triodia laetus (Staudinger, 1877) is reported from the territory of Russia, Armenia, and Azerbaijan for the first time. The new locations proved its wide distribution in the Caucasus and Transcaucasia. Type specimens, materials from museum and private collections, as well as photographic observations on iNaturalist were studied. A description of the external characteristics of the male and female is given, as well as a description and images of the genitals. The distinctive features are compared with the closely related species Triodia sylvina (Linnaeus, 1761).</p>2025-03-12T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazevhttps://journal.asu.ru/biol/article/view/16980A new species of the genus Bembecia Hübner, 1819 (Lepidoptera, Sesiidae) from Omsk Region of Russia (West Siberia)2025-04-26T11:55:46+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ru<p>A new species, Bembecia lavrovi Knyazev, sp. n. from Omsk Region of Russia in West Siberia, is described based on a series of 80 specimens. A detailed description of the external characteristics of the male and female, as well as the structure of the male genitalia, is provided. The new species is close to Bembecia sareptana (Bartel, 1912) and Bembecia aktashica O. Gorbunov 2018 but is distinguished by its large size, more contrasting and bright coloring, details of the wing pattern and the structure of the genitals.</p> <p> </p>2025-03-13T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazevhttps://journal.asu.ru/biol/article/view/17026First record of Sphenoptera (Chilostetha) egena Mannerheim, 1852 (Coleoptera: Buprestidae) from Kazakhstan with notes on its bionomics and distribution2025-04-14T09:29:07+07:00Aizhan M. Tleppaevaatleppaeva@mail.ru<p>During the fieldwork conducted between 2021 and 2023 in the territory adjacent to the Tarbagatai Natural Park, a new species of jewel beetle (Coleoptera, Buprestidae), Sphenoptera (Chilostetha) egena Mannerheim, 1852, was discovered, marking a noteworthy addition to the fauna of Kazakhstan. Specimens of this species were collected in June from arid shrub-steppe slopes in the western part of the Tarbagatai Range, specifically near the village of Taskesken in the Karakol River floodplain. Prior to this discovery, Sphenoptera egena had only been reported from regions in Russia (Western and Eastern Siberia) and Mongolia. This paper presents a concise diagnostic overview of the genus Sphenoptera Dejean, 1833, along with a brief description of the species. Using ArcGIS PRO 3.1.1, we created a distribution map and modeled the favorable habitat conditions for Sphenoptera egena. Additionally, we provide a description of the background vegetation in the species' collection site. Photographs of the jewel beetle were captured using a Canon Kiss X4 camera with a Canon 60 mm Macro USM lens, illustrating the collection site of S. egena. Furthermore, other species, such as Agrilus sericans Kiesenwetter, 1857, and Meliboeus morawitzi (Semenov, 1905), were concurrently identified in the fauna of these steppe slopes. The identification of Sphenoptera egena not only enriches the inventory of jewel beetles in Kazakhstan, which currently includes over 200 species and subspecies across five subfamilies, twelve tribes, and twenty-eight genera, but also extends the known distribution range of this species.</p>2025-03-17T00:00:00+07:00Copyright (c) 2025 Aizhan M. Tleppaevahttps://journal.asu.ru/biol/article/view/17022Age structure and growth of the black-ocellated racerunner (Eremias nigrocellata, Reptilia, Lacertidae) in the loess desert of Tajikistan2025-04-14T09:29:07+07:00Artem A. Kidovkidov_a@mail.ruVladimir O. Erashkinkidov_a@mail.ruRoman A. Ivolgakidov_a@mail.ruTatyana E. Kondratovakidov_a@mail.ruAndrey A. Ivanovkidov_a@mail.ru<p>The paper presents the results of age and growth studying of the black-ocellated racerunner (Eremias nigrocellata) by skeletochronology. 23 adult individuals (14 females and 9 males) collected on the border of Shaartuz and Nosiri-Khusrav districts in Khatlon region of Tajikistan were studied. All animals, on the section of tubular bones had a birth (hatching) line appearing shortly after the lizards hatching. Females were 1–7 years old (average 3.64 years), and males 1–5 years old (average 3.11 years). In the group of studied animals, the majority of individuals were 2–4 years old (65.2%). The largest number of females were aged three and four years (21.4% each). The male group was dominated by individuals aged four (33.3%), three and two years (22.2% each). Females and males did not differ in size from each other. The body length of the studied females was 55.25–65.61 mm (average 60.28), and males 58.42–63.32 mm (average 60.11). The calculated maximum body length (SVLmax) of females (61.33 mm) did not differ from the length of males (61.57 mm). The growth coefficient (k) of females (0.99) was higher than males (0.87). The annual survival score (S) in females (0.74) was similar to males (0.70). The life expectancy of individuals who survived one wintering (ESP) was 4.35 years for females and 3.88 years for males.</p>2025-03-19T00:00:00+07:00Copyright (c) 2025 Artem A. Kidov, Vladimir O. Erashkin, Roman A. Ivolga, Tatyana E. Kondratova, Andrey A. Ivanovhttps://journal.asu.ru/biol/article/view/17025List of fungus gnats (Diptera: Bolitophilidae, Diadocidiidae, Ditomyiidae, Keroplatidae and Mycetophilidae) of the Republic of Mordovia (Russia)2025-04-14T09:29:07+07:00Mikhail N. Esinruchin.alexander@gmail.comDmitriy I. Gavryushinruchin.alexander@gmail.comAlexander B. Ruchinruchin.alexander@gmail.com<p>The annotated checklist includes 309 species from the families Bolitophilidae, Diadocidiidae, Ditomyiidae, Keroplatidae, and Mycetophilidae. In addition to the previous records, 242 species have been recorded for the fauna of the Republic of Mordovia for the first time. Among these are species new to Russia (Orfelia boreoalpina, Mycetophila rudis, Neoclastobasis draskovitsae, Novakia scatopsiformis) and a species new to the Palearctic (Sciophila emarginata). The collection sites are described. For the first time, 242 species are recorded for the fauna of the Republic of Mordovia. Over the course of the study, 275 species were noted in the Mordovia Nature Reserve, 91 species in National Park "Smolny", and 47 species in other locations within the region. Data on trapping methods for the collected fungus gnats are provided. Comparative data on species abundance in neighboring regions are also discussed.</p>2025-03-19T00:00:00+07:00Copyright (c) 2025 Mikhail N. Esin, Dmitriy I. Gavryushin, Alexander B. Ruchinhttps://journal.asu.ru/biol/article/view/17027Key factors of avian diversity and sustainability in the forest-steppe lakes of Western Siberia2025-04-14T09:29:07+07:00Maria Yu. Ivanovanatalya.v.sorokina@gmail.comSergey N. Gashevs.n.gashev@utmn.ruPolina E. Pokazanevap.e.pokazaneva@utmn.ruStepan L. Boldyrevboldyrev.stepan@yandex.ruAlexander O. Ivanovfalcon_bf@mail.ruIliya P. Klimshinklimshin-ilya@mail.ruNadezhda V. Ganzherlin.v.ganzherli@utmn.ruAlena Yu. Levykhaljurlev@mail.ruNatalya V. Sorokinanatalya.v.sorokina@gmail.com<p>The article examines the relationship between various parameters of 25 forest–steppe lakes in Western Siberia and the biological diversity of bird communities, based on bird censuses conducted from 2002 to 2023. It focuses on factors such as the lakes' physical characteristics, climate zone peculiarities, salinity levels, lake area, and the extent of overgrowth. A total of 180 bird species typical of the Western Siberia forest–steppe zone were recorded. The study found a statistically significant differentiation in bird communities across subzones, with the mean total bird abundance in the middle forest–steppe being 2.5 times greater than that in the northern forest–steppe. Correlation analysis revealed a significant inverse relationship between lake salinity levels and both species number and total bird abundance, as well as the species diversity and resilient sustainability indices of water bird communities. Conversely, a significant direct influence of salinity on the resistant sustainability index was observed. Additionally, a statistically significant, albeit weak, positive correlation was found between total bird abundance and the degree of lake overgrowth by aquatic and semi-aquatic vegetation. However, no clear correlation was established between the area of the lakes and the examined properties of bird communities.</p>2025-03-21T00:00:00+07:00Copyright (c) 2025 Maria Yu. Ivanova, Sergey N. Gashev, Polina E. Pokazaneva, Stepan L. Boldyrev, Alexander O. Ivanov, Ilia P. Klimshin, Nadezhda V. Ganzherli, Alena Yu. Levykh, Natalya V. Sorokinahttps://journal.asu.ru/biol/article/view/17051Myriapoda (Diplopoda, Chilopoda) of the Southern Cultures Park (Krasnodar Province, Southern Russia): unappreciated biodiversity2025-04-27T13:29:04+07:00Aleksandr P. Evsyukovaevsukov@mail.ruRoman V. Zuevaevsukov@mail.ruYurii V. Dyachkovaevsukov@mail.ruYuri A. Chumachenkoaevsukov@mail.ruIuliia P. Chebotarevaaevsukov@mail.ruIgor V. Popovaevsukov@mail.ruIgor Y. Zabiyakaaevsukov@mail.ru<p>The biodiversity of botanical gardens and arboreta is typically assessed by vegetation, birds, and insects such as beetles and butterflies. At the same time, most of the invertebrate animals live in litter and soil, while remaining hidden and poorly studied. Here we present the results of studies of two classes of myriapods in Southern Cultures Park, Adler, Krasnodar Province, Russia. During 2021, the diversity and abundance of myriapods were assessed by quantitative data obtained using pitfall traps. From these traps, 20 species of diplopods and 14 species of chilopods were recorded. Alpha diversity of myriapods was significantly higher (p=0.043) in the spring-summer season in comparison to summer-fall. Beta diversity also significantly differed (p≤0.031) between these seasons. The abundance of Brachyiulus lusitanus (p=0.018), Polydesmus mediterraneus (p=0.047), Julus colchicus (p=0.020), and Cylindroiulus placidus (p=0.047) was significantly higher in the spring season, while in the summer season, the abundance of Anthroleucosomatidae Gen. sp.1 (p=0.047) was significantly dominant. Also, from 2018 to 2024, using hand collection from litter, 2 additional species of diplopods and 7 species of chilopods were recorded. Species of myriapods that were not previously recorded in Russia and introduced species were identified and illustrated.</p>2025-03-25T00:00:00+07:00Copyright (c) 2025 Aleksandr P. Evsyukov, Roman V. Zuev, Yurii V. Dyachkov, Yuri A. Chumachenko, Iuliia P. Chebotareva, Igor V. Popov, Igor Y. Zabiyakahttps://journal.asu.ru/biol/article/view/17181Genetic diversity of microsymbionts from legumes Oxytropis putoranica M. Ivanova, Oxytropis mertensiana Turcz., Astragalus norvegicus Grauer, Astragalus tugarinovii Basil. growing on the Putorana Plateau in Arctic Russia2025-04-14T09:29:06+07:00Irina G. Kuznetsovaig.kuznetsova@arriam.ruAnna L. Sazanovaig.kuznetsova@arriam.ruDenis S. Karlovig.kuznetsova@arriam.ruPolina V. Guroig.kuznetsova@arriam.ruIrina A. Alekhinaig.kuznetsova@arriam.ruNina Yu. Tikhomirovaig.kuznetsova@arriam.ruEdgar A. Seksteig.kuznetsova@arriam.ruOleg S. Yuzikhinig.kuznetsova@arriam.ruIgor N. Pospelovig.kuznetsova@arriam.ruElena B. Pospelovaig.kuznetsova@arriam.ruAndrey A. Belimovig.kuznetsova@arriam.ruVera I. Safronovaig.kuznetsova@arriam.ru<p>There is a significant potential for the introduction of legumes into the Arctic regions of Russia. The ability of legumes to form a nitrogen-fixing symbiosis with nodule bacteria is one of their most important characteristics. The article studies the genetic diversity of the 24 bacterial strains isolated from root nodules from wild populations of legumes Oxytropis putoranica M. Ivanova, O. mertensiana Turcz., Astragalus norvegicus Grauer, and A. tugarinovii Basil. collected on the Putorana Plateau (Krasnoyarsk region, Arctic Russia). The microbial strains were isolated using yeast broth made with a standard method using YMA mannitol. Genomic DNA was isolated from pure cultures and the primary identification of the strains was carried out by PCR followed by sequencing of the 16S rRNA marker gene fragment. To clarify the identity of the species, ITS sequencing of the region was performed. The isolates were assigned to six genera and to five families of the order Hyphomicrobiales: Pararhizobium and Neorhizobium (family Rhizobiaceae), Phyllobacterium (Phyllobacteraceae), Microvirga (Methylobacteriaceae), Bosea (Boseaceae) and Tardiphaga (Bradyrhizobiaceae). Isolates from O. putoranica nodules were identified as Neorhizobium galegae, Bosea sp., Bosea vaviloviae, and Tardiphaga robiniae. The isolated nodules of O. mertensiana were identified as Pararhizobium herbae, Tardiphaga robiniae, Microvirga ossetica, and Microvirga sp. Microsymbionts of A. norvegicus were assigned to Bosea psychrotolerans and to Pararhizobium herbae and Tardiphaga robiniae species, while isolates from A. tugarinovii were identified as Phyllobacterium zundukense, Bosea sp., and Tardiphaga robiniae. Symbiotic the nodA gene was detected in strains P. herbae P14/2-4 and P20/1-1, P. zundukense P17/1-7 and P17/3-2, while the nodC gene was not detected in any of the strains. The sterile test tube experiment confirmed the inability of strains P. herbae P14/2-4 and P20/1-1 to form nodules in host plants O. mertensiana and A. norvegicus, as well as in other wild arctic (A. tugarinovii, O. putoranica) and forage legumes (Trifolium repens, Vicia cracca, and Lathyrus pratensis). The results obtained expand the understanding of the taxonomic status and biodiversity of local microsymbionts of wild legumes that grow on the Putorana Plateau. The study of the symbiotic efficiency of Arctic rhizobia will allow us to identify the most promising strains for the development of effective biofertilizers for the cultivation of forage and pasture legumes under the extreme soil and climatic conditions of the Russian Arctic. In turn, the creation of highly adapted legume-rhizobial systems based on valuable genetic resources of Arctic rhizobia strains will expand the range of legume species promising for use in the creation of multi-component agrophytocenoses necessary for the sustainable development of animal husbandry in Arctic regions of Russia.</p>2025-04-02T00:00:00+07:00Copyright (c) 2025 Irina G. Kuznetsova, Anna L. Sazanova, Denis S. Karlov, Polina V. Guro, Irina A. Alekhina, Nina Yu. Tikhomirova, Edgar A. Sekste, Oleg S. Yuzikhin, Igor N. Pospelov, Elena B. Pospelova, Andrey A. Belimov, Vera I. Safronovahttps://journal.asu.ru/biol/article/view/17184Anthropogenic origin of island entomofaunas: a case study of Diptera and Odonata2025-04-14T09:29:06+07:00Nikita E. Vikhrevnikita6510@yandex.ru<p>Several examples of modern entomofaunas (particularly orders Diptera and Odonata) of remote islands, and to a lesser degree, recently colonised continents were considered. The author presents taxonomic, biogeographical, logical, and molecular-genetic arguments to support the idea that the modern composition of these entomofaunas can be effectively explained by the anthropogenic invasion that has occurred within the last 3000 years. The author estimates that rare undoubted cases of natural colonisation do occur on islands once every one to three million years. It is assumed that preanthropogenic entomofaunas were poorer, but much more endemic. If so, entomologists should consider this when proposing taxonomic hypotheses. Molecular genetic methods can verify the author's conceptual idea.</p>2025-04-03T00:00:00+07:00Copyright (c) 2025 Nikita E. Vikhrevhttps://journal.asu.ru/biol/article/view/17185First record of the genus Combocerus Bedel, 1868 (Coleoptera, Erotylidae) for the fauna of Kazakhstan2025-04-14T09:29:06+07:00Izbasar I. Temreshevtemreshev76@mail.ru<p>Pleasing fungus beetle Combocerus Bedel, 1868 with species C. glaber (Schaller, 1783) of the family Erotylidae is firstly recorded from Kazakhstan. The finds of C. glaber from Akmola Oblast of North Kazakhstan are currently the easthmost localities for this species and first record for Central Asia. Beetles found under the bark of dead Salix alba L., on the fungi – wood mushroom Agaricus silvicola (Vittad.) Peck, 1872, scaly sawgill Neolentinus lepideus (Fr.) Redhead & Ginns, 1985 and violet-toothed polypore Trichaptum biforme (Fr.) Ryvarden, 1972, which is new data on the biology of this species. Now there are eight genera and twenty one species of the Erotylidae in Kazakhstan.</p>2025-04-05T00:00:00+07:00Copyright (c) 2025 Izbasar I. Temreshevhttps://journal.asu.ru/biol/article/view/17187Biochemical and antioxidant characteristics of the soil strain Chlorococcum oleofaciens (Chlorophyceae, Chlorophyta) grown in light, dark and bicarbonate conditions2025-04-14T09:29:06+07:00Aleksandr V. Yakoviichukalex.yakov1991@gmail.comAngelica V. Kochubeyalex.yakov1991@gmail.comIrina A. Maltsevaalex.yakov1991@gmail.comAlex V. Matsyuraamatsyura@gmail.comSvetlana V. Cherkashinaalex.yakov1991@gmail.comEkaterina A. Lysovaalex.yakov1991@gmail.com<p>This study aimed to examine the biochemical and antioxidant characteristics of a soil strain of Chlorococcum oleofaciens CAMU MZ–Ch4 (Chlorophyceae, Chlorophyta) when cultured in light, darkness, and a combination of light-bicarbonate and dark-bicarbonate in an acute 96-hour experiment. The study established that cultivation in the dark is accompanied by an increase in the antioxidant status of Chlorococcum oleofaciens CAMU MZ–Ch4 strain cells, which is associated with the accumulation of low-molecular antioxidants and the activation of antioxidant enzymes. Culturing in the dark also causes the accumulation of chlorophyll a, ascorbic acid, astaxanthin, and lipids. But biomass productivity and concentration decreased. Introducing NaHCO3 into the medium inhibits the biosynthesis and accumulation of α-tocopherol, ascorbic acid, phenolic compounds, and chlorophylls both under illuminated and in the dark. The intensity of lipid peroxidation decreases and the activity of antioxidant enzymes increases under light and in the dark conditions with NaHCO3 in the medium.</p>2025-04-05T00:00:00+07:00Copyright (c) 2025 Aleksandr V. Yakoviichuk, Angelica V. Kochubey, Irina A. Maltseva, Alex V. Matsyura, Svetlana V. Cherkashina, Ekaterina A. Lysovahttps://journal.asu.ru/biol/article/view/17193Geographic gradients in a functional trait: variation of body size and size diversity in ground beetle Poecilus cupreus (Linnaeus, 1758) (Coleoptera, Carabidae)2025-04-14T09:29:06+07:00Raisa A. Sukhodolskayasl_luzyanin@mail.ruSergey L. Luzyaninsl_luzyanin@mail.ruTeodora M. Teofilovasl_luzyanin@mail.ruVladimir Landgrafsl_luzyanin@mail.ruNadezhda L. Ukhovasl_luzyanin@mail.ruTamara A. Avtaevasl_luzyanin@mail.ruKirill Yu. Maksimovichsl_luzyanin@mail.ruAndrey D. Belosludcevsl_luzyanin@mail.ruRoman P. Gorbunovsl_luzyanin@mail.ru<p>The aim of this study was to test the character of body size variation and its diversity in the widespread ground beetle Poecilus cupreus in geographical gradients. Beetles were sampled in 14 regions of Europe and the Asia, and sampling territories differed by 17° in latitude and 121° in longitude. We measured six linear traits in each captured beetle and formed a data set that included 6745 individuals. In the latitudinal gradient, three of the six traits studied decreased their values (direct trends), and the variability curve of four of the six features studied is hump-shaped with a maximum value in the middle latitudes (polynomial trends). In the longitudinal gradient, three traits decreased their values (direct trends), and the variability of three ones had the form of a concave curve with minimum values in the middle longitudes. The variability coefficients of the features themselves behave differently. Their value increased in the latitudinal gradient and decreased in the longitudinal gradient (direct trends). Polynomial trends show a hump-shaped curve – the greatest variability of feature values is observed in the middle latitudes and middle longitudes. We worked according to a single methodology and our analysis is intraspecific, so we insist that such eco-geographic and morphometric studies be conducted in the same way.</p>2025-04-06T00:00:00+07:00Copyright (c) 2025 Raisa A. Sukhodolskaya, Sergey L. Luzyanin, Teodora M. Teofilova, Vladimír Langraf, Nadezhda L. Ukhova, Tamara A. Avtaeva, Kirill Yu. Maksimovich, Andrey D. Belosludcev, Roman P. Gorbunovhttps://journal.asu.ru/biol/article/view/17211The grasshopper Eremippus simplex (Eversmann) (Orthoptera, Acrididae) in South Siberia: Rediscovery of a rare species2025-04-14T09:29:06+07:00Michael G. Sergeevmgs@fen.nsu.ruOlesya G. Buleaumgs@fen.nsu.ruMarya N. Kim-Kashmenskayamgs@fen.nsu.ruVladimir V. Molodtsovmgs@fen.nsu.ruOxana V. Yefremovamgs@fen.nsu.ru<p>The general distribution of the grasshopper Eremippus simplex (Eversmann, 1859) is described. Its taxonomic position and ecological peculiarities are characterized. It is one of the most widespread representatives of the genus and is the only species crossing the 52nd parallel in the north direction. The species is associated with dry steppes, semi-deserts and northern deserts and prefers habitats with dominance of different low sagebrushes (Artemisia spp.) and salinized soils. In the southern parts of Siberia and in the south-eastern parts of European Russia, its populations were and are very rare and insular. The MaxEnt models generated for the contemporary period and for 2021–2040 and 2041–2060 according the Shared Socioeconomic Pathway 3-7.0 and the global climate model CNRM- ESM2-1 provide an opportunity to evaluate the suitability of conditions for the species and show that, in the future, the general character of its distribution may change quite slightly, but its populations may become more prosperous in the future.</p> <p> </p>2025-04-09T00:00:00+07:00Copyright (c) 2025 Michael G. Sergeev, Olesya G. Buleu, Marya N. Kim-Kashmenskaya, Vladimir V. Molodtsov, Oxana V. Yefremovahttps://journal.asu.ru/biol/article/view/17326Trophic structure and soil depth stratification as ecological drivers of taxonomic and species diversity in the nematode community in Central Asian peach orchards2025-05-07T09:41:54+07:00Dilnoza M. Nurmatovanarzullayevsardorbek1990@gmail.comSardorbek B. Narzullayevnarzullayevsardorbek1990@gmail.comOchil Mavlyanovnarzullayevsardorbek1990@gmail.comNaimitdin Khakimovnarzullayevsardorbek1990@gmail.comAbdurashid R. Jabborovnarzullayevsardorbek1990@gmail.comKomil S. Boltayevnarzullayevsardorbek1990@gmail.comUktam N. Mirzaevnarzullayevsardorbek1990@gmail.comAbbos A. Ashrapovnarzullayevsardorbek1990@gmail.comShahlo S. Tursnunovanarzullayevsardorbek1990@gmail.comShakhboz Khujamovnarzullayevsardorbek1990@gmail.com<p>The formation of nematode communities and their drivers remain poorly understood in arid agroecosystems, particularly in Central Asia’s intensive orchards. We investigated nematode fauna in peach orchards of Uzbekistan’s Zarafshan Valley (2023–2024), where low-organic soils (0.9–1.3% OM) and monoculture practices create unique ecological constraints. From 180 samples (149 nematode-positive), we identified 61 species across 38 genera, including <em>Butlerius butleri </em>Goodey, 1929 (Rhabditida) as a new country record. The study revealed clear patterns in how nematodes distribute themselves across different habitats within peach orchards. Root systems showed a strong preference for endoparasitic nematodes like <em>Meloidogyne </em>and <em>Pratylenchus</em>, which were found to be 9.2 times more likely to occur in roots compared to soil. Meanwhile, the soil layers hosted the majority (85.7%) of bacterivorous nematodes, though their populations decreased significantly with depth – diversity indices dropped from 3.88 in the top 0–15 cm layer to 3.81 in the 15–30 cm layer. Interestingly, while the types of nematode species remained quite similar between soil layers (with a 92% similarity index), their actual numbers varied considerably, suggesting that environmental conditions primarily affect population sizes rather than species presence. Several key environmental factors emerged as important drivers of these distribution patterns. Organic matter content stood out as the strongest predictor, accounting for 51% of the variation in nematode diversity, followed closely by soil bulk density at 43%. Soil chemistry also played a significant role, with pH and nutrient levels (N, P, K) showing moderate to strong correlations (0.58–0.64) with nematode abundance. Some nematode groups displayed remarkable adaptability – omnivorous species like <em>Eudorylaimus </em>showed no particular depth preference, maintaining consistent populations throughout the soil profile. These findings provide important ecological insights about soil communities in agricultural systems. The feeding habits of nematodes explained about 18% of how communities were structured, revealing how agricultural practices create different nematode communities compared to natural ecosystems. One of the most striking observations was that changes in soil depth affected nematode numbers 2.3 times more strongly than they affected which species were present. This suggests that farming practices likely influence nematode communities more by changing population sizes than by eliminating particular species, with soil quality parameters like organic matter and compaction being particularly important factors shaping these communities.</p>2025-04-10T00:00:00+07:00Copyright (c) 2025 Dilnoza M. Nurmatova, Sardorbek B. Narzullayev, Ochil Mavlyanov, Najmitdin Khakimov, Abdurashid R. Jabborov, Komil S. Boltayev, Uktam N. Mirzaev, Abbos A. Ashrapov, Shahlo Sh. Tursunova, Shakhboz Khujamovhttps://journal.asu.ru/biol/article/view/17223Water mites (Acariformes, Hydrachnidia) of the Sob River basin (Polar Urals)2025-04-15T20:46:28+07:00Vitaly A. Stolbovvitusstgu@mail.ruSergey D. Sheykinvitusstgu@mail.ruSergey S. Tupitsynvitusstgu@mail.ru<p>Water mites were investigated in water bodies of the Sob River basin, which flows in the central part of the Polar Urals, in the region of the Arctic Circle. The upper and middle courses of the River Sob, its tributaries in the mountainous and plain regions, as well as lakes and floodplain ponds were studied. In total, 35 species from 8 families were identified from 12 waterbodies, 24 species were found in rivers and 12 species in lakes. It was found that the fauna of water mites in the rivers was very rich and diverse. Lebertiidae, Sperchontidae and Hygrobatidae dominated in terms of species number and abundance. The fauna of the mountain rivers was poorer than that of the plain rivers. <em>Feltria minuta</em> and <em>Sperchon glandulosus</em> dominated in different sites of the upper course of the Sob River and its mountain tributaries. The highest number of mites and the greatest diversity of species were found in the middle reaches of the Sob River and its tributaries in the plain area. Species of the genera <em>Atractides</em> and <em>Lebertia</em> dominated in these rivers. The number of mites was low in lakes and they were represented by a small number of species. In stagnant waters, <em>Lebertia litoralis</em> and species of the genus <em>Piona</em> predominated in abundance and occurrence. The fauna of water mites in the River Sob basin is similar to other parts of the Urals, especially in the Nether-Polar Ural water bodies. In comparison with the southern regions of the Urals, the species composition of water mites in the Polar Urals is poorer. Some genera and families that are numerous in the Central and Northern Urals are absent. In the same time species of northern and eastern origin such as <em>Sperchonopsis minutiporus</em> and <em>Sperchon laurenticus</em> are present.</p>2025-04-11T00:00:00+07:00Copyright (c) 2025 Vitaly A. Stolbov, Sergey D. Sheykin, Sergey S. Tupitsynhttps://journal.asu.ru/biol/article/view/17230New and poorly known species of Berlandina Dalmas, 1922 (Araneae: Gnaphosidae) from Uzbekistan2025-04-27T13:11:27+07:00Feruz A. Shodmonova.fomichov@mail.ruAlexander A. Fomicheva.fomichov@mail.ru<p>Three new species of the gnaphosid spider genus <em>Berlandina </em>Dalmas, 1922 are described from Uzbeki- stan based on males: <em>B. izzatullaevi </em>sp. n. (Samarkand Region), <em>B. jabborovi </em>sp. n. and <em>B. khalimovi </em>sp. n. (both from Surxondaryo Region). The poorly-illustrated species, <em>B. plumalis </em>(O. Pickard-Cambridge, 1872), is redescribed based on newly collected specimens from Uzbekistan. All studied species are assigned to their respective species-groups. Detailed (re)descriptions, digital photographs and a distribution map are provided.</p>2025-04-14T00:00:00+07:00Copyright (c) 2025 Feruz A. Shodmonov, Alexander A. Fomichevhttps://journal.asu.ru/biol/article/view/17237New records of Macroheterocera (Insecta, Lepidoptera) from the southernmost part of the Khabarovsk Krai (Russian Far East)2025-12-02T08:46:46+07:00Evgeny S. Koshkinekos@inbox.ru<p>Fourteen species of Lepidoptera from the families Limacodidae, Uraniidae, Notodontidae, Erebidae, Nolidae, and Noctuidae are reported from the Bikin District (Khabarovsk Krai, Russia). Among these, <em>Rhamnosa angulata </em>Fixsen, 1887 (Limacodidae), <em>Dysaethria illotata </em>(Christoph, 1880) (Uraniidae), <em>Hypena narratalis </em>Walker, 1858, and <em>Hypersypnoides astrigera </em>(Butler, 1885) (Erebidae) represent first records for Khabarovsk Krai. New occurrences of <em>Miltochrista pallida </em>(Bremer, 1864) and <em>Stigmatophora flava </em>(Bremer & Gray, 1852) (Erebidae) confirm their presence in the region. Additionally, rare East Asian species – <em>Mimopydna pallida </em>(Butler, 1877) (Notodontidae), <em>Stigmatophora leacrita </em>(Swinhoe, 1894) (Erebidae), <em>Gelastocera eminentissima </em>Bryk, 1948 (Nolidae), <em>Imosca coreana </em>(Matsumura, 1926), <em>Orthosia satoi </em>Sugi, 1960, <em>O. ryrholmi </em>G. Ronkay, L. Ronkay, Gyulai & Hacker, 2010, and <em>Perigrapha extincta </em>Kononenko, 1989 (Noctuidae) – were documented, significantly expanding knowledge of their Far Eastern distributions. The boreal species <em>Brachionycha sajana </em>Draudt, 1934 (Noctuidae) was recorded at its southernmost known range limit.</p>2025-04-16T00:00:00+07:00Copyright (c) 2025 Evgeny S. Koshkinhttps://journal.asu.ru/biol/article/view/17265De novo transcriptome assembly of the Baikal stone sculpin Paracottus knerii (Dybowski, 1874) from the Angara River as the first transcriptomic resource for Lake Baikal Cottidae2025-12-02T08:46:46+07:00Vasiliy Pomazkina.n.gurkov@gmail.comPolina Drozdovaa.n.gurkov@gmail.comEkaterina Borvinskayaa.n.gurkov@gmail.comElizaveta Indosovaa.n.gurkov@gmail.comMaxim Timofeyeva.n.gurkov@gmail.comAnton Gurkova.n.gurkov@gmail.com<p>Lake Baikal is the largest freshwater reservoir inhabited by a number of endemic species flocks belonging to different taxa. However, genomic resources for these groups of endemics are still relatively scarce, limiting understanding of the molecular mechanisms behind their physiology. One of these species flocks are Baikal sculpins of the family Cottidae. Here, we present the first transcriptome assembly for this group using stone sculpin <em>Paracottus knerii </em>(Dybowsky, 1874) as a model. The transcriptome was obtained from the whole body of a <em>P. knerii </em>fry and contains a diverse array of immunity-related transcripts, paving the way for studies investigating the immune response of Lake Baikal sculpins.</p>2025-04-17T00:00:00+07:00Copyright (c) 2025 Vasiliy Pomazkin, Polina Drozdova, Ekaterina Borvinskaya, Elizaveta Indosova, Maxim Timofeyev, Anton Gurkovhttps://journal.asu.ru/biol/article/view/17262New regional records of vascular plants from Kyrgyzstan2025-12-02T08:46:46+07:00Alexey P. Sereginbotanik.seregin@gmail.comDmitry F. Lyskovbotanik.seregin@gmail.comDmitry A. Germanbotanik.seregin@gmail.com<p>We present and discuss noteworthy floristic records obtained during the Moscow University summer expedition to Kyrgyzstan in 2016. Three taxa are reported as new for Kyrgyzstan: a native species (<em>Utricularia australis </em>R. Br.), an established alien (<em>Artemisia verlotiorum </em>Lamotte), and a nothospecies of local origin (<em>Arctium </em>× <em>ambiguum </em>(Čelak.) Nyman). Additionally, we document 31 species (26 native and 5 alien – <em>Anthemis ruthenica </em>M. Bieb., <em>Atriplex oblongifolia </em>Waldst. et Kit., <em>Chenopodium vulvaria </em>L., <em>Lepidotheca suaveolens </em>(Pursh) Nutt., and <em>Medicago sativa </em>L. s. l.) as new records for one of the seven floristic regions defined in the standard national checklist. These include 12 new records for Western Tian Shan, six for the Alay Valley, six for Inner Tian Shan, four for Fergana, three for the Ysyk-Köl Depression, and two for Northern Kyrgyzstan. Furthermore, we provide supplementary records for 12 species previously overlooked in the national checklist, supported by historical references and newly collected specimens.</p>2025-04-23T00:00:00+07:00Copyright (c) 2025 Alexey P. Seregin, Dmitry F. Lyskov, Dmitry A. Germanhttps://journal.asu.ru/biol/article/view/17264A new species of the Genus Triodia Hübner, [1820] from Turkmenistan (Lepidoptera, Hepialidae)2025-12-02T08:46:46+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ru<p>A new species, <em>Triodia turkmenica </em>Knyazev, sp.n. from Turkmenistan, is described. A detailed description of the external characteristics of the male and female, as well as the structure of the genitalia, is provided. The new species is closely related to <em>Triodia laetus </em>(Staudinger, 1877) but is distinguished by its smaller size, lighter and more mottled coloring. There is also an external similarity with <em>Triodia amasinus </em>(Herrich-Schäffer, [1852]) from which the new species differs well in the structure of the genitals. The female of the new species is similar to the female of <em>Triodia sylvina </em>(Linnaeus, 1761), but differs well from it in a strongly segmented wing pattern.</p>2025-04-24T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazevhttps://journal.asu.ru/biol/article/view/17272Materials on the Lepidoptera of Uzbekistan. Part I. Family Geometridae Leach, 18152025-12-02T08:46:46+07:00Artem E. Naydenovnaydenov.24@mail.ruIlya A. Makhovnaydenov.24@mail.ruVladimir G. Mironovnaydenov.24@mail.ruMukhammadtuychi R. Rakhimovnaydenov.24@mail.ruFazlitdin Z. Khalimovnaydenov.24@mail.ruRoman V. Yakovlevnaydenov.24@mail.ru<p>The article provides a list of seventy-four collected species of geometrid moths from the territory of Uzbekistan based on the results of four expeditions in 2022–2024 in Andizhan, Namangan, Fergana, Tashkent, Jizzakh, Samarkand, Bukhara, Qashqadaryo and Surxondaryo regions. Twenty-three species recorded for the first time for the fauna of the country are indicated and illustrated.</p>2025-04-26T00:00:00+07:00Copyright (c) 2025 Artem E. Naydenov, Ilya A. Makhov, Vladimir G. Mironov, Mukhammadtuychi R. Rahimov, Fazlitdin Z. Khalimov, Roman V. Yakovlevhttps://journal.asu.ru/biol/article/view/17283Colonization of reclaimed post-mining habitats by Myriapoda (Diplopoda, Chilopoda) in southwestern Siberia, Russia2025-12-02T08:46:46+07:00Sergey L. Luzyaninsl_luzyanin@mail.ruPavel S. Nefedievsl_luzyanin@mail.ruGyulli Sh. Farzalievasl_luzyanin@mail.ru<p>Post-mining landscapes undergo profound ecological transformations, yet the recovery of soil fauna remains poorly understood. This study examines the colonization patterns of myriapods (Diplopoda and Chilopoda) on reclaimed coal mining dumps in southwestern Siberia (Kemerovo Oblast, Russia) across different successional stages. From 2014 to 2017, we sampled two coal mining sites, comparing dumps of varying recovery ages with undisturbed control habitats. Results reveal stark contrasts between the two myriapod groups: Diplopoda exhibited low abundance and species richness, colonizing only at later successional stages, influenced by soil pH, organic carbon, and vegetation cover. In contrast, Chilopoda rapidly colonized young dumps, with pioneer species like <em>Lamyctes africanus </em>dominating early successional stages. Statistical modeling identified soil moisture (HTC), nitrogen content, and pH as key drivers of myriapod distribution. These findings highlight the slow recovery of millipede communities compared to centipedes, which act as early colonizers shaping trophic networks. The study underscores the need for targeted reclamation strategies that enhance soil conditions and vegetation to facilitate soil fauna restoration. Understanding these successional dynamics can improve biodiversity recovery in post-mining ecosystems.</p>2025-04-30T00:00:00+07:00Copyright (c) 2025 Sergey L. Luzyanin, Pavel S. Nefediev, Gyulli Sh. Farzalievahttps://journal.asu.ru/biol/article/view/17318Taxonomic review of the Plebejus christophi (Staudinger, 1874) species group from Central Asia with the descriptions of new taxa (Lepidoptera, Lycaenidae)2025-12-02T08:46:46+07:00Sergey V. Churkinserghelios16@gmail.comAnatoly V. Krupitskyserghelios16@gmail.com<p>The review includes the comparative analyses of <em>Plebejus christophi </em>(Staudinger, 1874), <em>P. argivus </em>(Staudinger, 1886), <em>P. argivus noah </em>(Herz, 1900), comb. nova et stat. novus, and P<em>. roxane </em>(Grum- Grshimailo, 1887). Three new taxa are described: <em>P. karinae </em>sp. nova (NW Kazakhstan, Atyrau reg., NW Kulsary town), <em>P. paveli </em>sp. nova (E Kazakhstan, south of Lake Zaisan, Zhagalbaily Mts.) and <em>P. argivus kazakh </em>ssp. nova (Kazakhstan, Transili Alatau Mts., northern foothills). The distinctions of the genitalia are discussed in details. Some notes about <em>P. bergi </em>Kuznetzov, 1908 are added, including designation of the neotype.</p>2025-05-05T00:00:00+07:00Copyright (c) 2025 Sergei V. Churkin, Anatoly V. Krupitskyhttps://journal.asu.ru/biol/article/view/17327First record of Euzophera alpherakyella Ragonot, 1887 (Lepidoptera: Pyralidae: Phycitinae) from Uzbekistan2025-12-02T08:46:46+07:00Malikjon R. Shermatovmalikjonshermatov@gmail.comMuminjon M. Mukhammedovmalikjonshermatov@gmail.comOygulkhon I. Kayumovamalikjonshermatov@gmail.comElyor A. Botirovmalikjonshermatov@gmail.comGulnara S. Mirzaevamalikjonshermatov@gmail.comSardorbek Q. Kimyonazarovmalikjonshermatov@gmail.com<p>This study presents the first confirmed record of <em>Euzophera alpherakyella </em>Ragonot, 1887 (Lepidoptera: Pyralidae: Phycitinae: Phycitini) from Uzbekistan. The species was identified based on two specimens collected from the Chimgan foothills in the southern part of the Fergana Valley. In addition to a detailed morphological description of adult moths, diagnostic images of the male and female genitalia are provided to support the identification of the species.</p> <p> </p>2025-05-08T00:00:00+07:00Copyright (c) 2025 Malikjon R. Shermatov, Muminjon M. Mukhammedov, Oygulkhon I. Kayumova, Elyor A. Botirov, Gulnara S. Mirzaeva, Sardorbek Q. Kimyonazarovhttps://journal.asu.ru/biol/article/view/17328Diversity of entomopathogenic micromycetes associated with orchard pest species Cydia pomonella (Lepidoptera: Tortricidae) and Caliroa cerasi (Hymenoptera: Tenthredinidae)2025-12-02T08:46:46+07:00Nygora Y. Zukhritdinovan.ahmedova67@mail.ruZukhra Y. Akhmedovan.ahmedova67@mail.ruSardorbek Q. Kymionazarovn.ahmedova67@mail.ruKumri X. Allaberdiyevan.ahmedova67@mail.ru<p>This study reports the first isolation and characterization of entomopathogenic micromycetes from naturally deceased specimens of two key orchard pests in Uzbekistan: the codling moth <em>Cydia pomonella </em>(Linnaeus, 1758) and the cherry slug sawfly <em>Caliroa cerasi </em>(Linnaeus, 1758). Comparative analysis revealed distinct fungal communities associated with each species, with <em>C. cerasi </em>harboring 15 species of micromycetes and <em>C. pomonella </em>hosting 14 species. Dominant genera included <em>Aspergillus</em>, <em>Penicillium</em>, <em>Fusarium</em>, <em>Alternaria</em>, <em>Cladosporium</em>, <em>Metarhizium</em>, and <em>Mucor</em>. The widespread occurrence of these entomopathogenic fungi suggests their dual ecological role as both indicators of potential phytopathogens affecting fruit trees and as natural antagonists of pest insects. These findings provide a foundation for developing targeted biological control strategies against orchard pests while offering insights into plant-pathogen-insect interactions in agroecosystems. The results highlight the potential of native fungal isolates for sustainable pest management in Uzbek orchards.</p>2025-05-08T00:00:00+07:00Copyright (c) 2025 Nigora Y. Zukhritdinova, Zukhra Y. Akhmedova, Sardorbek Q. Kimyonazarov, Kumri X. Allaberdiyevahttps://journal.asu.ru/biol/article/view/17364Morphology of the preimaginal stages of Carcinopyga lichenigera C. Felder & R. Felder, 1874 (Lepidoptera: Erebidae: Arctiinae)2025-12-02T08:46:46+07:00Vitaly M. Spitsynspitsyn.v.m.91993@yandex.ruSergey I. Evdoshenkospitsyn.v.m.91993@yandex.ruRafaqat Masroorspitsyn.v.m.91993@yandex.ruSundar Tiwarispitsyn.v.m.91993@yandex.ruElizaveta A. Spitsynaspitsyn.v.m.91993@yandex.ru<p>In this paper, we describe the preimaginal stages of <em>Carcinopyga lichenigera </em>C. Felder & R. Felder distributed in the mountain regions of eastern Afghanistan, northern Pakistan, and northwestern India (Ladakh; Jammu and Kashmir). Additionally, we illustrate adults of both sexes as well as their genitalia. Illustrations of female genitalia are provided for the first time.</p>2025-05-24T00:00:00+07:00Copyright (c) 2025 Vitaly M. Spitsyn, Sergey I. Evdoschenko, Rafaqat Masroor, Sundar Tiwari, Elizaveta A. Spitsynahttps://journal.asu.ru/biol/article/view/17400Planktonic crustaceans of the Balkhash-Alakol lake system (South-Eastern Kazakhstan)2025-12-02T08:46:46+07:00Akerke Kenzheyevaakerke.kenzheyeva@zool.kzElena G. Krupaakerke.kenzheyeva@zool.kz<p>Planktonic crustaceans are the basis of the food supply for animals with higher trophic levels and determine the fish productivity of any water body. Large Cladocera play a significant role in the natural purification of the water column. Some Copepods are intermediate hosts of parasites, including those that are dangerous to humans. Given the key role of planktonic invertebrates, their research is essential for effective management of aquatic ecosystems. The Balkhash-Alakol system includes five main lakes (Balkhash, Alakol, Koshkarkol, Sasykkol, and Zhalanashkol), with a pronounced gradient of water mineralization. The study of planktonic crustaceans in the lakes of the Balkhash-Alakol system was carried out between 2002 and 2007. Previous studies addressed zooplankton; however, planktonic crustaceans were not studied separately, making this research necessary. The samples and the processing of the zooplankton samples were performed using standard methods. During the study, 74 planktonic crustaceans were recorded, with the highest species richness in the East Balkhash and Alakol lakes (48–47 species) and the lowest values in Zhalanashkol (9 species). According to the results of the cluster analysis, the species composition of planktonic crustaceans in the lakes surveyed was characterized by a low level of similarity. Ecologically, euryhaline forms predominated throughout. The abundance of planktonic crustaceans ranged from 31,836 to 105,860 individuals/m³. The dominant species included <em>Diaphanosoma lacustris</em>, <em>Mesocyclops leuckarti</em>, <em>Thermocyclops crassus</em>, <em>Arctodiaptomus salinus</em>, and <em>Ceriodaphnia reticulata</em>. The results obtained expand our understanding of the formation of the structure of plankton communities under the influence of external factors.</p>2025-06-01T00:00:00+07:00Copyright (c) 2025 Аkerke Kenzheyeva, Elena G. Krupahttps://journal.asu.ru/biol/article/view/17407Spatial ecology and population trends of the scavengers (Aves: Falconiformes) in Azerbaijan2025-12-02T08:46:46+07:00Arzu F. Mammadovyarasa65@mail.ruTahir A. Karimovyarasa65@mail.ruAlex V. Matsyuraamatsyura@gmail.comDashgin Sh. Ganbarovyarasa65@mail.ru<p>Avian scavengers in Azerbaijan, including the Griffon Vulture (<em>Gyps fulvus</em>), Black Vulture (<em>Aegypius monachus</em>), Egyptian Vulture (<em>Neophron percnopterus</em>), and Bearded Vulture (<em>Gypaetus barbatus</em>), are experiencing significant population declines, with a 15.3% reduction in breeding pairs documented between 2012 and 2024. This study presents the first comprehensive assessment of their nesting ecology, population trends, and anthropogenic threats across Azerbaijan’s three major mountain regions: the Greater Caucasus, Lesser Caucasus, and Talysh Mountains. Systematic surveys of 33 nesting sites revealed distinct spatial and elevational segregation, with 60.6% of nests located in the Lesser Caucasus, 36.3% in the Greater Caucasus, and 3.0% in the Talysh Mountains. Species exhibited pronounced stratification by elevation: Bearded Vultures nested exclusively above 2000 m, Griffon and Egyptian Vultures occupied mid-elevation zones (500–1800 m), and Black Vultures were restricted to lowland forests (<500 m). The primary drivers of decline were linked to anthropogenic factors, including a 28.5% reduction in livestock populations, which diminished carrion availability, and a 15.7% expansion of agricultural lands, which reduced foraging habitats. Direct threats such as nest destruction, poaching, and incidental capture for commercial use further exacerbated declines, particularly for Black Vultures in the Talysh Mountains, where only a single breeding cluster remains. Breakpoint analysis identified critical years of accelerated decline: 2018 for Griffon Vultures and 2015 for Black Vultures, coinciding with regional reductions in wild ungulate populations and increased human disturbance. Comparative analysis with global datasets revealed parallels to declines observed in Mediterranean and South Asian vulture populations, though Azerbaijan’s unique socioecological context, including post-Soviet land-use changes and its role as a migratory corridor, demands tailored conservation strategies. We propose urgent interventions, including supplemental feeding programs, habitat protection in the Lesser Caucasus, and mitigation of power line collisions, informed by successful case studies from Europe. These findings underscore Azerbaijan’s importance as a critical stronghold for vulture conservation in the Caucasus and highlight the need for transboundary cooperation to safeguard these keystone scavengers.</p>2025-06-05T00:00:00+07:00Copyright (c) 2025 Arzu F. Mammadov, Tahir A. Karimov, Alex V. Matsyura, Dashgin Sh. Ganbarovhttps://journal.asu.ru/biol/article/view/17406A new invasive species Proagopertha lucidula (Faldermann, 1835) (Coleoptera, Scarabaeidae, Rutelinae) for Kazakhstan2025-12-02T08:46:46+07:00Izbasar I. Temreshevtemreshev76@mail.ru<p>Shining leaf chafer<em> Proagopertha lucidula</em> (Faldermann, 1835) is firstly found in Kazakhstan. Records in South-East Kazakhstan (Almaty and Zhetysu oblast) are the westernmost for this species. This species causes damage in the fruit orchards of the Almaty and Zhetysu oblast.</p>2025-06-05T00:00:00+07:00Copyright (c) 2025 Izbasar I. Temreshevhttps://journal.asu.ru/biol/article/view/17439Modern distribution and nesting ecology of White storks (Ciconia ciconia L.) in Nakhchivan Autonomous Republic, Azerbaijan2025-12-02T08:46:46+07:00Arzu F. Mammadovyarasa65@mail.ruElchin H. Sultanovyarasa65@mail.ruAlex V. Matsyuraamatsyura@gmail.comVefa F. Mammadovayarasa65@mail.ru<p>The white stork (<em>Ciconia ciconia</em>) has increasingly adapted to nesting on artificial structures, yet the drivers of nest-site selection and reproductive success in human-dominated landscapes remain poorly understood. Here, we integrate spatial ecology and habitat modeling to assess nesting patterns of white storks in Azerbaijan, where populations rely heavily on utility poles. We surveyed 51 poles (87 nests) along a 35-km transect, recording nest distribution, chick productivity, and environmental variables. Our key findings reveal strong preference for metal poles (68% of nests; χ² = 9.3, p = 0.002), which sup- ported 13% higher chick survival than concrete poles (85% vs. 72%; HR = 2.1, p = 0.02), spatial clustering at 0.5–2 km scales (Ripley’s K, p < 0.01), with two high-density hotspots (>9 nests/km²) linked to floodplain and agricultural habitats, altitude-driven productivity: higher elevations (≥900 m) had fewer but more productive nests (PCA: PC1 = 58% variance). We also considered critical movement corridors between colonies, avoiding urban areas and steep slopes (least-cost path analysis). Habitat suitability models (AUC = 0.82) identified water proximity and altitude as key predictors of nesting. Our results demonstrate how human infrastructure shapes stork nesting ecology, with metal poles acting as critical refuges. We recommend prioritizing metal pole maintenance in high-suitability zones and protecting foraging corridors to sustain populations. This study provides a template for conserving synanthropic birds in rapidly developing regions.</p>2025-06-11T00:00:00+07:00Copyright (c) 2025 Arzu F. Mammadov, Elchin H. Sultanov, Alex V. Matsyura, Vefa F. Mammadovahttps://journal.asu.ru/biol/article/view/17454Dining in the wild: Unraveling wild Asian elephant (Elephas maximus) feeding behaviour and dietary dynamics in Jaldapara National Park, West Bengal, India2025-12-02T08:46:46+07:00Subrata Sahakarpradip@gmail.comManjil Guptakarpradip@gmail.comSurovi Roykarpradip@gmail.comRachita Sahakarpradip@gmail.comSergey N. Kirpotinkirp@mail.tsu.ruAndrey S. Babenkokarpradip@gmail.comIrina I. Volkovakarpradip@gmail.comAldynay O. Khovalygkarpradip@gmail.comPradip Kumar Karkarpradip@gmail.com<p>Megaherbivores like the Wild Asian elephant (<em>Elephas maximus</em>) are keystone species, playing a pivotal role in ecosystem dynamics. However, their survival is increasingly threatened by habitat loss and resource constraints due to their extensive spatial and nutritional needs. This study investigates the dietary preferences and feeding behaviours of elephants inhabiting the riverine floodplains of North Bengal, particularly Jaldapara National Park. Using a combination of direct observations, feeding sign analysis along elephant routes, and microhistological faecal analysis, we identified 41 plant species in their diet. Dietary composition revealed a preference for tree species (34.16%), followed by grasses (21.95%), mosses (17.07%), herbs (17.07%), shrubs (4.87%), and climbers (4.87%). The prominence of trees highlights their importance as a critical food resource, while the high diversity of Poaceae emphasizes the significance of grasslands in elephant habitats. A diurnal feeding pattern was observed, with heightened activity during the latter times of the day. These findings underscore the importance of conserving heterogeneous landscapes comprising forests and grasslands to support the dietary requirements of elephants. Additionally, the study provides insights into the ecological adaptations of Asian elephants and highlights the necessity of effective habitat management to ensure the availability of critical food resources throughout the year. The results offer valuable guidance for mitigating human-elephant conflicts and advancing conservation strategies for this ecologically vital yet endangered species</p>2025-06-16T00:00:00+07:00Copyright (c) 2025 Subrata Saha, Manjil Gupta, Rachita Saha, Surovi Roy, Sergey N. Kirpotin, Andrey S. Babenko, Irina I. Volkova, Aldynay O. Khovalyg, Pradip Kumar Karhttps://journal.asu.ru/biol/article/view/17703A new species of Dasydorylas Skevington, 2001 (Diptera: Pipunculidae) from the Colombian Andes, and an updated key to males of the Neotropical species2025-12-02T08:46:46+07:00Yardany Ramos-Pastranaya.ramos@udla.edu.coEric Córdoba-Suarezya.ramos@udla.edu.coMarta Wolffya.ramos@udla.edu.co<p>Dasydorylas Skevington, 2001 has a cosmopolitan distribution. A new species of Dasydorylas is described from Colombian Andes, namely Dasydorylas spinifera sp. n. (type locality: Páramo Santa Inés, Antioquia). Illustrations of the new species, dichotomous key to males of all Neotropical species and distribution map of the Colombian species is presented.</p>2025-07-29T00:00:00+07:00Copyright (c) 2025 Yardany Ramos-Pastrana, Eric Córdoba-Suarez, Marta Wolffhttps://journal.asu.ru/biol/article/view/17708New data on the morphology of pollen of Pulsatilla Mill. (Ranunculaceae)2025-12-02T08:46:46+07:00Vladimir F. Zaykovvz1703@mail.ruAlexander P. Shalimovvz1703@mail.ruAlexey V. Vaganovvz1703@mail.ruTatiana A. Sinitsynavz1703@mail.ruSergey G. Kudrinvz1703@mail.ruAlexey A. Kechaykinvz1703@mail.ruKseniya K. Ryabovavz1703@mail.ruSergey Yu. Pankratovvz1703@mail.ruAlexander A. Batkinvz1703@mail.ruAlexander I. Shmakovvz1703@mail.ru<p>The genus <em>Pulsatilla </em>Mill. represents a taxonomically complex group, with its systematic classification having undergone numerous revisions. Pollen grain morphology plays a crucial role in the intrageneric taxonomy of <em>Pulsatilla</em>; however, it remains unexamined for several species within the genus. This study presents the results of a comprehensive palynological analysis of 18 <em>Pulsatilla </em>species, including nine species investigated for the first time. The majority of species exhibited a 3-colpate aperture, including <em>P. astragalifolia</em>, <em>P. bungeana</em>, <em>P. ajanensis</em>, <em>P. cernua</em>, <em>P. ambigua</em>, <em>P. taurica</em>, <em>P. kryloviana</em>, <em>P. herba-somnii</em>, <em>P. turczaninovii</em>, <em>P. multifida</em>, and <em>P. archarensis</em>. A pantocolpate aperture was characteristic of <em>P. herbertii </em>and <em>P. neobungeana</em>, while <em>P. campanella</em>, <em>P. andina</em>, and <em>P. neobungeana </em>displayed a pantoporate aperture. The exine sculpture of all examined pasqueflowers was consistently microspinate, with predominantly smooth surfaces, except for occasional tuberculate textures. Pollen grain shapes varied from elongated ellipsoidal to spheroidal forms.</p>2025-07-31T00:00:00+07:00Copyright (c) 2025 Vladimir F. Zaikov, Alexander P. Shalimov, Alexey V. Vaganov, Tatiana A. Sinitsyna, Sergey G. Kudrin, Alexey A. Kechaykin, Kseniya K. Ryabova, Sergey Yu. Pankratov, Alexander А. Batkin, Alexander I. Shmakovhttps://journal.asu.ru/biol/article/view/17716First teratological case of Pseudomyrmex termitarius (Smith, 1855) (Hymenoptera: Formicidae: Pseudomyrmecinae)2025-12-02T08:46:46+07:00Yennifer Andrea Carreño-Guevaray.carreno@udla.edu.coLeonardo Malagón-Aldanay.carreno@udla.edu.coJean Gamboay.carreno@udla.edu.co<p>A case of abnormalities in segmentation (symphysomery) on the metasoma in a worker ant of the species <em>Pseudomyrmex termitarius </em>(Smith, 1855) is described for the first time from Colombia. In the abnormal metasoma, the petiole and postpetiole are fused, and the number of segments of the opisthogaster is reduced. For taxonomic studies, these kinds of abnormalities can generate confusion when identifying individuals at the genus and species levels. For an individual, an anatomical abnormality might affect its biology and interaction with other individuals inside its social insect colony.</p>2025-08-05T00:00:00+07:00Copyright (c) 2025 https://creativecommons.org/licenses/by/4.0/https://journal.asu.ru/biol/article/view/17717First registration and description of the breeding biology of the Great cormorant Phalacrocorax carbo (Linnaeus, 1758) in the Fergana Valley of Uzbekistan2025-12-02T08:46:45+07:00Sanjarbek S. Umarovsanjarbek5671@gmail.comRoman D. Kashkarovsanjarbek5671@gmail.com<p>This study provides information on the discovery and preliminary ecological assessment of a new nest colony of the Great cormorant <em>Phalacrocorax carbo </em>(Linnaeus, 1758) in the Uzbek part of the Fergana Valley. Field studies conducted during the 2024 breeding season revealed the presence of nest colonies on two islands along the Syr Darya River. However, due to the existence of a border regime, the main work was carried out on the same island. In the study area, nests were found on 54 trees. Nests are mainly located in the poplar tree (<em>Populus pruinosa </em>Schrenk). Conducting monitoring using direct observations and camera traps, we recorded the nest occupancy, morphometric indicators of eggs, and the growth dynamics of chicks. The results show that the morphometric characteristics of great cormorant eggs can vary significantly depending on regional and ecological conditions. The chicks’ weight increased rapidly from the moment they hatched until they flew away, although some deaths were also observed. Spatial analysis showed the expansion of colonies and the accumulation of nests, which indicates the successful settlement of the species in the region. These results provide important initial data on the ecology of the reproduction of the Great cormorant in Central Asia, emphasize the species' adaptability to local habitats, and indicate the need for continuous observations to develop conservation measures.</p>2025-08-05T00:00:00+07:00Copyright (c) 2025 Sanjarbek S. Umarov, Roman D. Kashkarovhttps://journal.asu.ru/biol/article/view/17722Differential expression of the multiplicated silicon transporter genes at different stages of morphogenesis of daughter frustule of the freshwater diatom Ulnaria acus2025-12-02T08:46:45+07:00Artem M. Marchenkovmarchenkov.am@gmail.comYulia R. Zakharovamarchenkov.am@gmail.comDarya P. Petrovamarchenkov.am@gmail.com<p>Diatoms are known for their unique ability to form species-specific silicon exoskeletons (shells) richly decorated with various ornaments, outgrowths, and holes. The absorption of silicic acid from the environment by cells is a critical step in this process. It is known that silicic acid is transported into diatom cells by silicic acid transport proteins (SIT). However, the mechanism and regulation of the work of proteins of this family currently remain insufficiently studied. In the present study, we attempted to determine the stages of daughter valve morphogenesis in the pennate freshwater diatom <em>Ulnaria acus </em>and to assess the expression level of <em>sit-m </em>genes encoding multiplexed silicon transporters. The experiment showed that simultaneously with the formation of the main axial element of the daughter valves (sternum) and first-order branching (virga), the level of <em>sit-tri </em>gene expression increases. While, during the formation of second-order branching (vimin) and areoles, an increase in the level of <em>sit-td </em>gene expression was noted, with a simultaneous decrease in <em>sit-tri</em>. Based on the data obtained, it can be assumed that after duplication of <em>sit </em>genes in the diatom genome, with the formation of multiplexed structures, their subfunctionalization occurs at different stages of daughter valve morphogenesis.</p>2025-08-07T00:00:00+07:00Copyright (c) Artem M. Marchenkov, Yulia R. Zakharova, Darya P. Petrovahttps://journal.asu.ru/biol/article/view/17726The Emerald ash borer Agrilus planipennis Fairmaire (Coleoptera: Buprestidae) invaded Belarus2025-12-02T08:46:45+07:00Vyacheslav B. Zviagintsevnkirichenko@yahoo.comNatalia I. Kirichenkonkirichenko@yahoo.comMaxim I. Cherniknkirichenko@yahoo.comLidia G. Serayankirichenko@yahoo.comYuri N. Baranchikovnkirichenko@yahoo.com<p>The emerald ash borer, <em>Agrilus planipennis </em>Fairmaire, 1888 (Coleoptera: Buprestidae), is a harmful East Asian insect pest damaging ash trees <em>Fraxinus </em>spp. Over the past three decades, it has invaded European part of Russia and Ukraine, causing widespread mortality of ash trees in both urban and natural ecosystems. Here, we report first occurrence of this devastating pest in Belarus, specifically in the city of Gomel. During reconnaissance survey performed in the late June 2025, a total of 46 ash trees, including 39 <em>Fraxinus pennsylvanica </em>and 7 <em>F. excelsior </em>trees, displayed characteristic symptoms of infestation: canopy dieback, epicormic sprouting, and distinct D-shaped exit holes in the bark. A single larva of the IV instar was found within a typical gallery beneath the bark, and 13 adult beetles mating and feeding on the foliage of both ash species were recorded. Given the proximity of infested regions in neighboring countries – specifically Bryansk (243 km away from Gomel) and Smolensk (270 km) in Russia, as well as Kiev (220 km) in Ukraine – it is suspected that the buprestid was accidentally introduced from some of these localities rather than expanding its range by itself. Urgent research is required to delineate the extent of its spread within Belarus. Moreover, decisive actions must be taken promptly to suppress current infestation foci and prevent further distribution of this highly aggressive alien pest.</p>2025-08-07T00:00:00+07:00Copyright (c) 2025 Vyacheslav B. Zviagintsev, Natalia I. Kirichenko, Maxim I. Chernik, Lidia G. Seraya, Yuri N. Baranchikovhttps://journal.asu.ru/biol/article/view/17727The native parasitoids exploiting the invasive leafminer Coptodisca lucifluella (Lepidoptera: Heliozelidae) in Southern Russia and Abkhazia2025-12-02T08:46:45+07:00Oksana V. Koshelevankirichenko@yahoo.comElena N. Zhuravlevankirichenko@yahoo.comNatalia N. Karpunnkirichenko@yahoo.comNatalia I. Kirichenkonkirichenko@yahoo.com<p>The leafmining moth <em>Coptodisca lucifluella </em>(Lepidoptera: Heliozelidae) is the North American species, which recently invaded Europe. Here, we provide first data on the parasitoid assemblage associated with this leafminer in Southern Russia and Abkhazia. In 2024, altogether 28 parasitoid specimens were reared from the late-instar larvae and pupae of <em>C. lucifluella </em>and identified to seven parasitic wasp species. Among them, six species were from Eulophidae: <em>Pnigalio soemius </em>(Walker), <em>Cirrospilus variegatus </em>(Masi), <em>C. viticola </em>(Rondani), <em>Chrysocharis pentheus </em>(Walker), <em>Closterocerus </em>sp. (presumably new species to science), <em>Minotetrastichus frontalis </em>(Nees) and one from Eupelmidae: presumably <em>Eupelmus kiefferi </em>De Stefani. All these parasitoids are native to the studied area and have been documented on <em>C. lucifluella </em>for the first time. In Russia and Abkhazia, the parasitism rates reached 13% and 31%, respectively. Four species contributed the most to the leafminer mortality: <em>M. frontalis </em>(11 out of 13%) in Sochi (Russia), <em>C. pentheus </em>(12 out of 31%), <em>C. viticola </em>(8%), and <em>C. variegatus </em>(8%) in Gagra (Abkhazia). For the recorded parasitoids, the distribution and hosts are mentioned, and the original photographs of parasitoid adults are provided. Additionally, an exhaustive checklist of parasitoids associated with <em>C. lucifluella </em>in its modern range was compiled, accounting 32 species. Altogether, our findings suggest that during the invasion, <em>C. lucifluella </em>escaped from its aborigine enemies but became a target for the parasitoids naturally present in Southern Russia and Abkhazia.</p>2025-08-09T00:00:00+07:00Copyright (c) 2025 Oksana V. Kosheleva, Elena N. Zhuravleva, Natalia N. Karpun, Natalia I. Kirichenko https://journal.asu.ru/biol/article/view/17731Carbon stock in grass cover of forests with different severity of stem pest-related stand weakening in the southern taiga zone of Western Siberia2025-12-02T08:46:45+07:00Nina V. Klimovaninmilk@yandex.ruArtem N. Nikiforovninmilk@yandex.ruAnastasia E. Zelentsovaninmilk@yandex.ru<p>The paper addresses the study of dark coniferous forests of the southern taiga, which were analyzed with regard to severity of stand weakening caused by stem pests, up to stand death. To assess the carbon stock of grass cover, the mass fraction of carbon in grass species and the aboveground mass of grass were measured. The carbon stock of grass cover was shown to vary during the change in its main microgroups caused by stand weakening. The carbon content in grass species abundant in different grass microgroups exhibits a narrow range of variation of 33.4–44.7 %, with an average of 41.1±0.9 %. The amount of carbon stored in the grass cover of dark coniferous forests in uplands ranges from 16.2 to 32.9 gC/m2. It was revealed that in weakened stands, the grass cover stores 2–5 fold more carbon due to an increase in grass biomass. Considering that most of the grass carbon released to the atmosphere within a year, the efficiency of carbon sink in forest areas with dead stands becomes lower, despite an increase in grass mass, compared to forest areas where the stands are not damaged by stem pests.</p>2025-08-11T00:00:00+07:00Copyright (c) 2025 Nina V. Klimova, Artem N. Nikiforov, Anastasia E. Zelentsovahttps://journal.asu.ru/biol/article/view/17743The records of Dolichovespula pacifica (Birula, 1930) (Hymenoptera: Vespidae) and the northern limits of its range in European North of Russia2025-12-02T08:46:45+07:00Grigory S. Potapovgrigorij-potapov@yandex.ruGalina V. Bovykinagrigorij-potapov@yandex.ruNatalia A. Zubriigrigorij-potapov@yandex.ruVitaly M. Spitsyngrigorij-potapov@yandex.ruYulia S. Kolosovagrigorij-potapov@yandex.ruAlexander V. Kondakovgrigorij-potapov@yandex.ru<p>In this study, we present new records of <em>Dolichovespula pacifica </em>(Birula, 1930) in Northern European Russia. The range of <em>D. pacifica </em>in the studied region extends up to transitional zone between taiga and low-shrub tundra. The northernmost records of this species in Northern European Russia are located in the northern part of Murmansk Region and the south of Nenets Autonomous District. Among the island territories of Northern European Russia, <em>D. pacifica </em>has been recorded only in the Solovetsky Archipelago.</p>2025-08-15T00:00:00+07:00Copyright (c) 2025 Grigory S. Potapov, Galina V. Bovykina, Natalia A. Zubrii, Vitaly M. Spitsyn, Yulia S. Kolosova, Alexander V. Kondakovhttps://journal.asu.ru/biol/article/view/17750Development of biota within the Seliverstov Glacier deglaciation zone after the Little Ice Age maximum (Mongun-Taiga mountain range, Southeastern Altai)2025-12-02T08:46:45+07:00Dmitry A. Ganyushkinxoxoxanas123@gmail.comEkaterina S. Derkachxoxoxanas123@gmail.comAndrei I. Pyakxoxoxanas123@gmail.comAndrei S. Babenkoxoxoxanas123@gmail.comYuri N. Kurochkinxoxoxanas123@gmail.comAldynay O. Khovalygxoxoxanas123@gmail.comBuyan A. Adygbayxoxoxanas123@gmail.comSayana D. Mongushxoxoxanas123@gmail.comMaria I. Dongakxoxoxanas123@gmail.comSergey O. Ondarxoxoxanas123@gmail.comBogdan A. Mikhaleikoxoxoxanas123@gmail.comPradip Kumar Karxoxoxanas123@gmail.comSergey N. Kirpotinxoxoxanas123@gmail.com<p>Recognized as part of the so-called Third Pole, the highlands of the Tuvan Altai represent the most arid part of the Russian Altai with a sharply continental climate, despite these features being a large glaciation node. Deglaciation caused by global climate change creates conditions for the initiation of postglacial vegetation successions. However, if the newest dynamics of glaciers of the high mountain massif of Mongun-Taiga, located at the junction of the mountain structures of the south-east of the Russian Altai and the mountain systems of the Sayan and Mongolian Altai, is well studied from a glaciological point of view, the issues of postglacial successions of biota in this region remain practically unstudied. This article is an attempt to give the first characteristics of the biota in the deglaciation zones of the Seliverstov Glacier in relation to deglaciation zones of different ages and typologies.</p>2025-08-18T00:00:00+07:00Copyright (c) 2025 Dmitry A. Ganyushkin, Ekaterina S. Derkach, Andrei I. Pyak, Andrei S. Babenko, Yuri N. Kurochkin, Aldynay O. Khovalyg, Buyan A. Adygbay, Sayana D. Mongush, Maria I. Dongak, Sergey O. Ondar, Bogdan A. Mikhaleiko, Pradip Kumar Kar, Sergey N. Kirpotinhttps://journal.asu.ru/biol/article/view/17886A new record of the genus Calymma Hübner, 1823 (Lepidoptera: Erebidae) from Uzbekistan2025-12-02T08:46:45+07:00Malikjon R. Shermatovmirzayeva.gulnora@mail.ruGulnara S. Mirzaevamirzayeva.gulnora@mail.ruIslomjon I. Zokirovmirzayeva.gulnora@mail.ruMuminjon M. Mukhammedovmirzayeva.gulnora@mail.ruElyor A. Botirovmirzayeva.gulnora@mail.ruSardorbek Q. Kimyonazarovmirzayeva.gulnora@mail.ruOygulkhon I. Kayumovamirzayeva.gulnora@mail.ruBekzod D. Abdikakhorovmirzayeva.gulnora@mail.ru<p>This study was conducted in the Fergana Valley, located in eastern Uzbekistan, during the 2023–2024 period. The genus <em>Calymma </em>Hübner, 1823 and the species <em>Calymma communimacula </em>(Denis & Schiffermüller, 1775) are reported for the first time from Uzbekistan. Several adult specimens were collected using light traps from Chimgan, the Kuvasay foothills, and the city of Fergana in the Fergana Valley, Uzbekistan. The species was identified based on external morphology. We provide a detailed description of the collected specimens and document diagnostic characters with photographs of the male and female genitalia. The discovery of <em>C. communimacula </em>in Uzbekistan represents the second known location of the species in Central Asia and confirms its presence in the region. This finding contributes new data to the Lepidoptera fauna of Central Asia and highlights the importance of continued entomological surveys in the region.</p>2025-09-18T00:00:00+07:00Copyright (c) 2025 Malikjon R. Shermatov, Gulnara S. Mirzaeva, Islomjon I. Zokirov, Muminjon M. Mukhammedov, Elyor A. Botirov, Sardorbek Q. Kimyonazarov, Oygulkhon I. Kayumova, Bekzod D. Abdikakhorovhttps://journal.asu.ru/biol/article/view/17887Influence of tributaries on the species richness of silica-scaled chrysophytes in the Angara River (Russia, Eastern Siberia)2025-12-02T08:46:45+07:00Anna Y. Bessudovaadfir71@yandex.ruAlena D. Firsovaadfir71@yandex.ruYuri P. Galachyantsadfir71@yandex.ruDarya P. Petrovaadfir71@yandex.ruMaria A. Nalimovaadfir71@yandex.ruMaria V. Sakirkoadfir71@yandex.ruYelena V. Likhoshwayadfir71@yandex.ru<p>The escalating impact of climate change requires comprehensive monitoring of aquatic microeukaryotic communities. Specifically, it is essential to study their successional dynamics under natural thermal fluctuations and identify organisms particularly sensitive to these changes. During the hydrological spring (early June), the watercourses of the Angara region differ in the intensity of water warming and can serve as promising model systems for studying such variations. Chrysophytes, which form siliceous scaled shells, serve as indicators of water temperature changes. In this study, we analyzed the influence of the main tributaries in the upper reaches of the Angara River–Irkut, Kuda, Kitoy, Belaya, and Ida–on the species richness of silica-scaled chrysophytes in the river channel, which is mainly affected by the cold, oligotrophic waters of Lake Baikal. During research performed in June 2024, a total of 57 silica-scaled chrysophytes species were identified in the study area using scanning and transmission electron microscopy. Among these, 11 species are potentially new to science, while one rare species <em>Paraphysomonas capreolata </em>and the form <em>Synura petersenii </em>f. <em>columnata </em>were recorded for the first time in Russian water bodies. The analysis demonstrated a positive correlation between the species diversity of silica-scaled chrysophytes and both water temperature and silicon concentration, alongside a negative correlation with pH levels. Statistical analysis of silica-scaled chrysophytes occurrence revealed two main profile groups: those from the main channel of the Angara River and those from its tributaries. Thus, it was determined that tributaries considerably increase the species richness of silica-scaled chrysophytes communities in the large river system, thereby increasing the overall stability of the aquatic ecosystem. This research is important for understanding the underlying mechanisms of the formation of biodiversity in freshwater ecosystems.</p>2025-09-19T00:00:00+07:00Copyright (c) 2025 Anna Y. Bessudova, Alena D. Firsova, Yuri P. Galachyants, Darya P. Petrova, Maria A. Nalimova, Maria V. Sakirko, Yelena V. Likhoshwayhttps://journal.asu.ru/biol/article/view/17896Fauna of Curculionoidea (Coleoptera) of the Republic of Mordovia2025-12-02T08:46:45+07:00Leonid V. Egorovruchin.alexander@gmail.comSergei V. Dedyukhinruchin.alexander@gmail.comAlexander B. Ruchinruchin.alexander@gmail.comMikhail N. Esinruchin.alexander@gmail.comSergei V. Lukiyanovruchin.alexander@gmail.comEvgeniy A. Lobachevruchin.alexander@gmail.comGennadiy B. Semishinruchin.alexander@gmail.comIrina G. Esinaruchin.alexander@gmail.com<p>The known fauna of the Republic of Mordovia comprises 506 species of Curculionoidea from six families: Anthribidae (8), Attelabidae (15), Brentidae (81), Cimberididae (1), Curculionidae (400), and Nemonychidae (1). The checklist includes 36 species newly recorded for the region. For each species, the number of plots and specimens is provided. The article also discusses the zoogeographical structure of the regional Curculionoidea fauna, demonstrating its complex nature. Against the background of the predominance of widespread species with Trans-Palaearctic and Western-Central Palaearctic ranges, a significant portion of the fauna is represented by the Western Palaearctic complex (96 species, 19%), along with smaller assemblages of species characterized by predominantly Central Palaearctic (14 species) and Central-Eastern Palaearctic distributions (16 species), as well as eight amphipalaearctic forms. In terms of zonal affiliation, nearly half of the fauna consists of polyzonal species. The Subboreal and Southern Boreal-Subboreal complexes are also strongly represented (together comprising 44%), with a smaller group of boreal forms (35 species; 7%).</p>2025-09-21T00:00:00+07:00Copyright (c) 2025 Leonid V. Egorov, Sergei V. Dedyukhin, Alexander B. Ruchin, Mikhail N. Esin, Sergei V. Lukiyanov, Evgeniy A. Lobachev, Gennadiy B. Semishin, Irina G. Esinahttps://journal.asu.ru/biol/article/view/17921Helminth fauna of the Asian badger (Meles leucurus Hodgson, 1847) in the Southern Aral Sea region2025-12-02T08:46:45+07:00Abat S. Berdibaevsh-erkinjon@mail.ruErkinjon B. Shakarboevsh-erkinjon@mail.ruSardorbek N. Turgunovsh-erkinjon@mail.ruShinbergen R. Bekbaulievsh-erkinjon@mail.ruOybek A. Abduganiyevsh-erkinjon@mail.ruZiroatkhon S. Abduqodirovash-erkinjon@mail.ru<p>Between 2017 and 2025, helminthological investigations were conducted on 32 wild badgers (<em>Meles leucurus</em>) across four natural geographic regions of Karakalpakstan. As a result, helminth infections were detected in 17 individuals, accounting for 53.1%. In total, 20 species of helminths were identified in the examined badgers, belonging to three phylum, four classes, nine orders, sixteen families, and eighteen genera. These included four species of cestodes, one species of trematode, three species of acanthocephalans, and twelve species of nematodes. Among the 20 helminth species, fifteen species were classified as helminths with indirect lifestyle and five species as helminths with direct lifestyle. The highest prevalence of infection was recorded for <em>Toxocara canis </em>(34.3%), followed by <em>Toxocara mystax </em>(25.0%). In terms of the intensity range, <em>T. canis </em>showed the highest range, with two to 77 specimens per host, while <em>T. mystax </em>ranged from three to 35 specimens. The intensity range of other helminth species varied between one and 33 specimens.</p> <p> </p>2025-09-24T00:00:00+07:00Copyright (c) 2025 Abat S. Berdibaev, Erkinjon B. Shakarboev, Sardorbek N. Turgunov, Shinbergen R. Bekbauliev, Oybek A. Abduganiyev, Ziroatkhon S. Abduqodirovahttps://journal.asu.ru/biol/article/view/17993Lepidoptera fauna of Kunashir Island (Russia): Update 20252025-12-02T08:46:45+07:00Vitaly M. Spitsynspitsyn.v.m.91993@yandex.ruEugeny S. Koshkinspitsyn.v.m.91993@yandex.ruAlexander E. Kostyuninspitsyn.v.m.91993@yandex.ruVitaly G. Bezborodovspitsyn.v.m.91993@yandex.ruElizaveta A. Spitsynaspitsyn.v.m.91993@yandex.ru<p>In the present study, the twenty-eight Lepidoptera species are recorded from Kunashir Island for the first time (one of them, <em>Chibidokuga hypenodes </em>Inoue, 1979, is also new record to the fauna of Russia). Additionally, the occurrences of <em>Eurydoxa advena </em>Filipjev, 1930, <em>Stigmatophora leacrita </em>(Swinhoe, 1894) and <em>Zanclognatha obliqua </em>Staudinger, 1892 on the Kuril Islands are confirmed.</p>2025-10-09T00:00:00+07:00Copyright (c) 2025 Vitaly M. Spitsyn, Evgeny S. Koshkin, Alexander E. Kostyunin, Vitaly G. Bezborodov, Elizaveta A. Spitsynahttps://journal.asu.ru/biol/article/view/18039Methods of microplastic separation from soil and soil arthropods: a systematic review2025-12-02T08:46:45+07:00Brer Al-Kinaniaevsukov@mail.ruAleksandr P. Evsyukovaevsukov@mail.ru<p>Microplastics – small plastic particles ≤ 5 mm – have quietly invaded soils, threatening the delicate balance of ecosystems and soil organisms. This review dives into the toolbox scientists use to detect and extract these hidden pollutants from soil and soil-dwelling organisms. We explore methods such as floating plastics in salty solutions, breaking down organic matter with hydrogen peroxide or enzymes, and using high-tech imaging like infrared spectroscopy. While some techniques, like sodium iodide separation, recover over 95% of microplastics, their high cost and complexity remain hurdles. Gentler approaches, such as enzyme-based digestion, protect fragile organisms but take longer. Despite advances, the field struggles with inconsistent methods and the near-invisible challenge of nanoplastics. Innovations like atomic force microscopy hint at future breakthroughs, but unifying global standards and blending old and new techniques will be key to turning the tide. This work calls for teamwork across disciplines to sharpen our tools, safeguard soils, and stem the silent spread of microplastic pollution.</p>2025-10-14T00:00:00+07:00Copyright (c) 2025 Brer Al-Kinani, Aleksandr P. Evsyukovhttps://journal.asu.ru/biol/article/view/18045Distribution patterns of the common predatory bush-cricket Saga pedo (Pallas, 1771) (Orthoptera, Tettigoniidae) in the Asian part of its range: Real rarity or mysterious commonness2025-12-02T08:46:45+07:00Ekaterina S. Shibkovamgsergeev@aol.comVladimir V. Molodtsovmsergeev@aol.comMuratbek K. Childebaevmsergeev@aol.comOxana V. Yefremovamsergeev@aol.comMichael G. Sergeevmsergeev@aol.com<p>The distribution patterns of the common predatory bush-cricket <em>Saga pedo </em>(Pallas, 1771) across the Asian part of its geographic range are revealed. It is the most widespread member of the genus and is the only species crossing the 55th parallel in the north direction. Preferable habitats of <em>S. pedo </em>are more or less uniform across its range, it favors variable steppe or steppe-like habitats covering by relatively dense grass vegetation with presence of forbs and especially shrubs. In the western parts of its range, the species is commonly distributed across regions with the subtropical Mediterranean and the temperate southern broadleaf forests, and its populations are mainly associated with local open landscapes. In the central and eastern parts, its distribution is different, because it is usually found over the forest-steppe, steppe and semi-desert life zones and also in the mountains of Middle Asia. The MaxEnt models produced for the contemporary period and for 2021-2040 and 2041-2060 according the Shared Socioeconomic Pathway 3-7.0 and the global climate model CNRM-ESM2-1 provide an opportunity to estimate the suitability of conditions for the species and demonstrate that, in the future, the general character of its distribution may change very significantly, especially in the southern half of the West Siberian Plain. The conservation status of <em>S. pedo </em>is discussed for the Asian part of its range as well.</p>2025-10-18T00:00:00+07:00Copyright (c) 2025 Ekaterina S. Shibkova, Vladimir V. Molodtsov, Muratbek K. Childebaev, Oxana V. Yefremova, Michael G. Sergeevhttps://journal.asu.ru/biol/article/view/18067New and interesting records of early spring and late autumn Heterocera species (Insecta, Lepidoptera) in Altai Republic (Russia, South Siberia)2025-12-02T08:46:45+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ruVadim V. Ivoninkonungomsk@yandex.ru<p>Twenty two species from the families of Chimabachidae, Ethmiidae, Crambidae, Geometridae, Lasiocampidae, Lemoniidae, Sphingidae, Erebidae and Noctuidae are reported from Altai Republic of Russia. Seven species are new to the Russian Altai among them <em>Dasystoma salicella </em>(Hübner, 1796), <em>Ethmia aurifluella </em>(Hübner, 1810), <em>Ethmia discrepitella </em>(Rebel, 1901), <em>Agriphila deliella </em>(Hübner, 1813), <em>Rheumaptera neocervinalis </em>(Inoue, 1982), <em>Lemonia dumi </em>(Linnaeus, 1761), <em>Hyles churkini </em>(Saldaitis et Ivinskis, 2006). New data on 15 rare and local species provided.</p>2025-10-19T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazev, Vadim V. Ivoninhttps://journal.asu.ru/biol/article/view/18106Recent observation of seasonal variability of plankton in Maloe More Strait (Lake Baikal)2025-12-02T08:46:45+07:00Nina A. Bondarenkoshevn@lin.irk.ruNatalia G. Shevelevashevn@lin.irk.ruOlga G. Pen'kovashevn@lin.irk.ru<p>In this paper, we describe the structure and quantitative characteristics of phyto- and zooplankton from Maloe More Strait of Lake Baikal studied in June-October, 2024. Maloe More is a popular rec- reational zone facing higher anthropogenic stress. In summer, phytoplankton in the littoral area of the strait showed continuous biomass maximum, starting from July until late August during cyanobacterial blooms. Two smaller maxima were observed in the strait pelagic zone, the first by the end of spring vegetation of phytoplankton, and second during excessive cyanobacterial growth in August. Elevated water temperatures resulted in prolonged cyanobacterial vegetation with a change of dominants. Restructuring of food resources and temperature fluctuations entailed transformations in the zooplankton structure. In June, the pelagic plankton was dominated by <em>Epischura</em>, a Baikal endemic. As the water temperature rose, the dominant position was occupied by <em>Cyclops kolensis</em>, the population of which was represented by mature specimens and nauplii. In summer, <em>Cladocera </em>reached its abundance peak in the nearshore. The highest number of rotifers was documented during maximal rise of nanoplanktonic flagellate concentrations in autumn.</p>2025-10-23T00:00:00+07:00Copyright (c) 2025 Nina A. Bondarenko, Natalia G. Sheveleva, Olga G. Pen’kovahttps://journal.asu.ru/biol/article/view/18107Phytocenotic characteristics of the vegetation cover of avalanche paths in Central Altai2025-12-02T08:46:45+07:00Petr A. Kosachevpakosachev@mail.ruNikolay I. Bykovpakosachev@mail.ruMadina E. Kulushpaevapakosachev@mail.ruNatalia V. Ovcharovapakosachev@mail.ru<p>The article presents the characteristics of plant cenoses in the studied avalanche paths of Central Altai (Aigulaksky, Kuraisky, Listvyaga, North Chuisky Ridges). They were analyzed using the Juss 7.0 software package and divided into 2 main groups: forest and shrub-herbaceous. The forest group includes 8 cenoses with 130 plant species; shrub-herbaceous one includes 16 communities with 205 species. Forest cenoses divided into 2 groups, and shrub-herbaceous – into 3 groups, classified on the basis of diagnostic species, characteristics of tree, shrub and herb layers, as well as the coenoflora core. All the groups of communities, both forest and shrub-herbaceous, according to the geobotanical zoning of G.N. Ogureeva (1980), correspond to two geobotanical districts and regions of Central Altai highland- taiga-forest-steppe province: 1) Kholzunsko-Korgonsky highland-taiga district and Verkhnekatunsky highland-taiga-forest-steppe region (Listvyaga Ridge); 2) Chuisko-Argutsky nival-highland-taiga-forest-steppe district and Chuisko-Argutsky taiga-forest-steppe region (Aigulaksky, Kuraisky, North Chuisky Ridges). Considering the shrub-herbaceous vegetation of the studied avalanche paths of Central Altai, it is possible to assume their annual avalanche activity. In some avalanche paths, the type of avalanche, the time of a catastrophic avalanche, and the approximate last year of a powerful avalanche were estimated.</p>2025-10-24T00:00:00+07:00Copyright (c) 2025 Petr A. Kosachev, Nikolay I. Bykov, Madina E. Kulushpaeva, Natalia V. Ovcharovahttps://journal.asu.ru/biol/article/view/18110A new Cteipolia Staudinger, 1896 species from Russian Altai (Lepidoptera, Noctuidae)2025-12-02T08:46:45+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ruVadim V. Ivoninkonungomsk@yandex.ru<p>A new species, <em>Cteipolia altaica </em>Knyazev et Ivonin, <strong>sp.n. </strong>from Altai Republic (Russia, Siberia), is described. New species is morphologically similar to <em>C. murina </em>(Ménétriés, 1848), <em>C. isotima </em>Püngeler, 1914 and <em>C. amissa </em>Gordeeva, Gordeev, G. Ronkay, L. Ronkay, 2023, but it differs in some external features, as well as in the structure of the genitals. The article presents an images of type specimens, the genital preparations of both sexes, diagnosis and the distributional map of <em>Cteipolia </em>species in Russia and Kazakhstan.</p>2025-10-25T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazev, Vadim V. Ivoninhttps://journal.asu.ru/biol/article/view/18112Spatial patterns of breeding colonies of Great Cormorant (Phalacrocorax carbo) and Palas’s Gull (Larus ichthyaetus) on Kitay Island in the Central Sivash lagoon system2025-12-02T08:46:45+07:00Alex V. Matsyuraamatsyura@gmail.comValery D. Siokhinamatsyura@gmail.com<p>This study analyzes the spatial distribution patterns of breeding colonies of Great Cormorants (<em>Phalacrocorax carbo</em>) and Palas’s Gull (<em>Larus ichthyaetus</em>) on Kitay Island in the Central Sivash lagoon system. Using spatial point pattern analyses, we quantified clustering and dispersion at multiple spatial scales. Our results reveal a marked contrast in nesting strategies: Great Cormorant nests exhibited strong, statistically significant clustering (mean Nearest Neighbor Distance, NND = 0.23 m; Moran's I = 0.34, p = 0.02) and significant positive spatial autocorrelation, consistent with colonial breeding. In contrast, Palas’s Gull nests were significantly more dispersed (mean NND = 0.67 m) and showed no significant spatial autocorrelation, reflecting territorial nesting behavior. Cross-species analysis indicated moderate spatial segregation, evidenced by a negative correlation of nest densities (r = -0.56) and Ripley's cross K-function, suggesting niche partitioning that facilitates coexistence. These findings quantitatively highlight distinct nesting ecologies and emphasize the critical importance of integrating spatial ecology into conservation planning for colonial waterbirds in saline lagoon islands. The study provides new quantitative baselines crucial for effective monitoring and habitat management in the Azov-Black Sea region.</p>2025-10-26T00:00:00+07:00Copyright (c) 2025 Alex V. Matsyura, Valery D. Siokhinhttps://journal.asu.ru/biol/article/view/18160Effect of environmental temperature on fecundity of Rutilus rutilus (L.) (Cypriniformes, Cyprinidae) in different types of water bodies in southern Western Siberia2025-12-02T08:46:45+07:00Elena A. Interesovainteresovaea@yandex.ruOksana A. Zavgorodniaiainteresovaea@yandex.ruElizaveta A. Vyalkovainteresovaea@yandex.ruVladislav A. Shatalininteresovaea@yandex.ruMichael A. Dorogininteresovaea@yandex.ruEgor M. Mityaevinteresovaea@yandex.ruMaria V. Seleznevainteresovaea@yandex.ru<p>The data on individual absolute and relative fecundity, and gonadosomatic index of roach <em>Rutilus rutilus </em>(L.) from different types of water bodies in southern Western Siberia: Lake Chany, the Novosibirsk Reservoir, and the Middle Ob are presented. The reproductive capacity of <em>R. rutilus </em>is vary widely and increase with age and size of female species. The roach from Lake Chany exhibit higher reproductive capacity compared to the Novosibirsk Reservoir and the Middle Ob. Furthermore, same-age roach specimens from Lake Chany and the Middle Ob have significant interannual differences in the reproductive indicators. The individual absolute fecundity of roach is statistically significantly related to water temperature at onset of oocytes trophoplasmic growth in the previous year, which occurs in mid-June in Lake Chany and mid-July in the Middle Ob.</p> <p> </p>2025-10-31T00:00:00+07:00Copyright (c) 2025 Elena A. Interesova, Oksana A. Zavgorodniaia, Elizaveta A. Vyalkova, Vladislav A. Shatalin, Michael A. Dorogin, Egor M. Mityaev, Maria V. Seleznevahttps://journal.asu.ru/biol/article/view/18161Description of the female of Dasypolia maria Volynkin 2012 (Lepidoptera: Noctuidae) with the notes on the distribution of the genus in the Altai Republic (Russia, South Siberia)2025-12-02T08:46:45+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ruVadim V. Ivoninkonungomsk@yandex.ru<p>The unknown female of <em>Dasypolia maria </em>Volynkin 2012 is described and diagnosed. Adults of male and female are illustrated as well as genitals of both sexes. Distribution map of <em>D. maria </em>is given. Additional data on the distribution of other species of the genus <em>Dasypolia </em>Guenée, 1852 in Russian Altai is provided.</p>2025-11-01T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazev, Vadim V. Ivoninhttps://journal.asu.ru/biol/article/view/18173Confirming the presence of the invasive moth Ypsolopha chazariella (Lepidoptera: Ypsolophidae) in Siberia: insights into the species biology and molecular genetics2025-12-02T08:46:45+07:00Natalia I. Kirichenkonkirichenko@yahoo.comNikita S. Babichevnkirichenko@yahoo.comMaria A. Ryazanovankirichenko@yahoo.comStanislav Gombocnkirichenko@yahoo.comYuri N. Baranchikov<p><em>Ypsolopha chazariella </em>(Mann, 1866) (Lepidoptera: Ypsolophidae) is a European moth species known to feed on Tatar maple (<em>Acer tataricum L.</em>), a tree species naturally present in Europe. In 2009–2023, characteristic damage provisionally attributed to <em>Y. chazariella </em>was documented in botanical gardens in Novosibirsk, Krasnoyarsk (Russia, Siberia), suggesting the occurrence of a new pest. In 2024, significant damage was observed in an arboretum in Krasnoyarsk (Eastern Siberia) on the introduced <em>A. tataricum </em>and East Asian <em>Acer ginnala </em>Maxim. Two adult specimens of <em>Y. chazariella </em>were reared from larvae collected on both maple hosts and identified using genital morphology. Seven DNA barcodes (mitochondrial COI gene fragments) obtained for the specimens from Krasnoyarsk (6 specimens) and Novosibirsk (1) analyzed together with available DNA barcodes from Belarus and Finland showed low intraspecific divergence (0.7%). Among six haplotypes detected, two of them were formed solely by the Siberian specimens connected with the haplotypes recorded in Europe through two mutation steps. Genetic distance analyses revealed clear differentiation from closely related species (<em>Y. dorsimaculella</em>, <em>Y. arizonella</em>, and <em>Y. rubrella</em>) in the Barcode of Life Database (BOLD), with pairwise minimal distances between <em>Y. chazariella </em>and above-mentioned species ranging from 10.6% to 12.9%. A brief species essay was compiled, providing a note on the species biology, molecular genetics, present species range, and impact in ornamental plantings. Photographic documentation includes characteristic feeding damage and images of adult moths, along with detailed illustrations of male and female genitalia.</p>2025-11-07T00:00:00+07:00Copyright (c) 2025 Natalia I. Kirichenko, Nikita S. Babichev, Maria A. Ryazanova, Stanislav Gomboc, Yuri N. Baranchikovhttps://journal.asu.ru/biol/article/view/18175Floristic composition and ecological-biological characteristics of avalanche path vegetation of Central Altai2025-12-02T08:46:45+07:00Petr A. Kosachevpakosachev@mail.ruNikolay I. Bykovpakosachev@mail.ruTatiana I. Grokhlinapakosachev@mail.ruNatalia V. Ovcharovapakosachev@mail.ru<p>The article analyzes the floristic composition, ecological groups in relation to soil moisture and substrate, and life forms in the phytocenoses of avalanche paths in Central Altai. It was found that the species composition of the plant communities of the avalanche paths of Central Altai differs significantly. The floristic similarity of the communities, estimated by the index of biotal dispersion (IBD), is weak in all parts of avalanche paths and reaches the highest value (14.2 %) for undisturbed forest communities (Z), and the lowest (9.3%) – in sites X, the central parts of avalanche paths. Data on the higher biodiversity of the central parts of avalanche paths (X) compared to the surrounding forest communities have been confirmed. It was found that family Gentianaceae and genus <em>Gentiana </em>indicate the central parts of avalanche paths, where avalanches occur most frequently. Shrub species of genera <em>Salix </em>and <em>Betula </em>and <em>Lonicera altaica </em>are characteristic of the avalanche path vegetation, have a high abundance, indicate frequent avalanching and can be indicators of avalanche ecotopes. At the same time, species of genus <em>Betula </em>(<em>B. humilis</em>, <em>B. rotundifolia</em>) and <em>Lonicera altaica </em>have high projective cover at level of the B track, while <em>Salix glauca </em>has high projective cover at level of the C track. Using the EcoScaleWin program, geobotanical descriptions on the ecological scales of D.N. Tsyganov were processed to assess the ecological conditions of ecotopes in avalanche paths of Central Altai. In turn, we used the obtained values of ecological scales to identify the dependencies between factors and their influence on the ecotopes using the principal component analysis (PCA). According to the analysis, in the central areas in avalanche paths located on the northwestern slopes, vegetation is influenced to a greater extent by 4 factors: high soil moisture, their nitrogen richness, salt richness, and lower soil acidity. However, in sites X (the central trough) there are more ecotopes, the soils of which are rich in nitrogen and salts, in sites Y (intermediate sections) soil moisture plays an important role. Ecotopes with high shading are typical for forest communities (sites Z). The sites of the avalanche paths studied are located in the forest belt, which is emphasized by the predominance of mesophytes and a high percentage of short-rhizome and long-rhizome herbs in the avalanche paths of Central Altai. Besides, in the central areas of the paths in avalanching sites, there is a high proportion of plants living on waterlogged soils, including cold and moist soils (hygrophytes, hygropsychrophytes, mesohygrophytes, psychrophytes, and mesopsychrophytes), i.e. these ecological groups are indicators of avalanche paths and point out frequent avalanches. On the eastern and southeastern (less often northwestern but then on rocky substrates) slopes in sites X and Y, species of dry and rocky habitats appear in the avalanche paths – xerophytes and petrophytes, many of which are tap-rooted herbs. In the spectrum of life forms of the avalanche paths of Central Altai, in addition to the predominant short-rhizome, long-rhizome and tap-rooted herbs, there is a large proportion of shrubs and brush-rooted herbs in the central parts, indicating frequent avalanches. In open areas, shrubs are abundant in herbaceous-shrubby communities, they are dominant and edificators. In general, short-rhizome, tap-rooted, and brush-rooted herbs (as well as brush-rooted tuber-forming and bulbous), which dominate in shrub-herbaceous cenoses of the avalanche paths, are confined to habitats with poor soil aeration in the X and Y sites; in forest communities (site Z), long-rhizome and loose-bush (also creeping herbs) are characteristic of sufficiently moist and loose soils.</p>2025-11-10T00:00:00+07:00Copyright (c) 2025 Petr A. Kosachev, Nikolay I. Bykov, Tatiana I. Grokhlina, Natalia V. Ovcharovahttps://journal.asu.ru/biol/article/view/18197The first record of the greater noctule bat, Nyctalus lasiopterus (Schreber, 1780) (Chiroptera, Vespertilionidae), in the Republic of Mordovia (European Russia)2025-12-02T08:46:45+07:00Nadezhda Yu. Kirillovaparasitolog@yandex.ruAlexander A. Kirillovparasitolog@yandex.ruAlexander B. Ruchinparasitolog@yandex.ru<p>As part of a systematic five-year (2021–2025) mist-netting survey of bats in the Mordovia State Nature Reserve, we documented the first confirmed presence of the greater noctule bat, <em>Nyctalus lasiopterus</em>, in the Republic of Mordovia. This species is listed as Vulnerable on the IUCN Red List. From a total of 2560 captured bats representing 11 species, ten individuals of <em>N. lasiopterus </em>were recorded at two distinct locations in July 2025. The capture of both young-of-the-year and an adult post-lactating female suggests the potential presence of a maternity colony in the region. This finding significantly updates the regional chiropterofauna, confirms the northeastern expansion of this rare species’ range, and underscores the critical importance of the reserve’s broadleaf forests for its conservation. We recommend the inclusion of <em>N. lasiopterus </em>in the official faunal list of Mordovia.</p>2025-11-15T00:00:00+07:00Copyright (c) 2025 Nadezhda Yu. Kirillova, Аlexander А. Kirillov, Аlexander B. Ruchinhttps://journal.asu.ru/biol/article/view/18198To the Lepidoptera fauna of Evenk District (Russia, East Siberia)2025-12-02T08:46:45+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ruVeronika G. Nikonovakonungomsk@yandex.ru<p>The article contains a list of 47 species of Lepidoptera from the Thyrididae, Crambidae, Tortricidae, Hesperiidae, Papilionidae, Pieridae, Lycaenidae, Nymphalidae (including Satyrinae), Geometridae, Erebidae families from the territory of Evenkia. 18 species are new to the North Yenisei Region in Catalog of Lepidoptera of Russia, among them <em>Thyris fenestrella </em>(Scopoli, 1763), <em>Chrysoteuchia culmella </em>(Linnaeus, 1758), <em>Crambus lathoniellus </em>(Zincken, 1817), <em>Epiblema simploniana </em>(Duponchel, 1835), <em>Grapholita compositella </em>(Fabricius, 1775), <em>Euphydryas intermedia </em>(Ménétriés, 1859), <em>Mellicta britomartis </em>Assmann, 1847, <em>Lomaspilis marginata </em>(Linnaeus, 1758), <em>Chiasmia clathrata </em>(Linnaeus, 1758), <em>Jodis putata </em>(Linnaeus, 1758), <em>Xanthorhoe deflorata </em>(Erschoff, 1877), <em>Xanthorhoe designata </em>(Hufnagel, 1767), <em>Mesoleuca albicillata </em>(Linnaeus, 1758), <em>Idaea pallidata </em>([Denis & Schiffermüller], 1775), <em>Scopula immorata </em>(Linnaeus, 1758), <em>Polypogon tentacularia </em>(Linnaeus, 1758), <em>Phytometra viridata </em>(Clerck, 1759), <em>Callistege mi </em>(Clerck, 1759).</p> <p> </p>2025-11-15T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazev, Veronika G. Nikonovahttps://journal.asu.ru/biol/article/view/18199First record of Denticollis borealis (Paykull, 1800) (Coleoptera, Elateridae) from Kazakhstan2025-12-02T08:46:45+07:00Izbasar I. Temreshevtemreshev76@mail.ru<p><em>Denticollis borealis </em>(Paykull, 1800) (Coleoptera: Elateridae) is recorded for the first time in Kazakhstan. Species was found in bracket fungus and under bark, in galleries of larvae of <em>Upis ceramboides </em>(Linnaeus, 1758) and <em>Sinodendron cylindricum </em>(Linnaeus, 1758). It is possible that the larvae of <em>D. borealis </em>are predators of the species of beetles in whose galleries it was found. A key to the known species of the genus <em>Denticollis </em>from Kazakhstan is also given.</p>2025-11-16T00:00:00+07:00Copyright (c) 2025 Izbasar I. Temreshevhttps://journal.asu.ru/biol/article/view/18219Taxonomic status and phylogenetic relationships of the desert monitor Varanus griseus caspius (Squamata: Varanidae) from the territory of Uzbekistan2025-12-02T08:46:45+07:00Abdurakhim E. Kuchboevabdurakhimkuchboev@gmail.comOybek O. Amirovabdurakhimkuchboev@gmail.comAzamat A. Yuldoshxonovabdurakhimkuchboev@gmail.comRuziboy K. Shapaotovabdurakhimkuchboev@gmail.comBaxodir A. Raxmatullayevabdurakhimkuchboev@gmail.comTimur V. Abduraupovabdurakhimkuchboev@gmail.com<p>This study investigates the phylogenetic position and genetic diversity of <em>Varanus griseus caspius</em>, a widely distributed yet understudied subspecies of monitor lizard in Central Asia, with a focus on samples collected from Uzbekistan. Using DNA barcoding based on the mitochondrial cytochrome oxidase subunit I (COI) gene, molecular phylogenetic analyses were conducted via Maximum Likelihood (ML) and Bayesian Inference (BI) approaches. In addition, genetic distance and Disparity Index analyses were employed to assess evolutionary relationships among <em>Varanus </em>species. The <em>V. g. caspius </em>specimens formed a highly supported clade with <em>V. griseus </em>sequences in GenBank, indicating a close genetic affinity and confirming its subspecies status. Genetic distance values and substitution pattern similarities further revealed minimal divergence between <em>V. g. caspius </em>and other <em>V. griseus </em>lineages, suggesting recent common ancestry and ongoing gene flow. In contrast, significantly greater divergence was observed between <em>V. g. caspius </em>and other <em>Varanus </em>species. These findings clarify the phylogenetic placement of <em>V. g. caspius </em>within the <em>V. griseus </em>complex and provide essential baseline data for future taxonomic and conservation efforts.</p>2025-11-20T00:00:00+07:00Copyright (c) 2025 Abdurakhim E. Kuchboev, Oybek O. Amirov, Azamat A. Yuldoshxonov, Ruziboy K. Shapaotov, Baxodir A. Raxmatullayev, Timur V. Abduraupovhttps://journal.asu.ru/biol/article/view/18220Adsorption of different types of microplastic particles by macrophytes of Lake Baikal2025-12-02T08:46:45+07:00Artem T. Guliguevkarnauhovdmitrii@gmail.comAnastasia A. Solodkovakarnauhovdmitrii@gmail.comIvan D. Kodatenkokarnauhovdmitrii@gmail.comDarya S. Kondratievakarnauhovdmitrii@gmail.comSofya A. Biritskayakarnauhovdmitrii@gmail.comArina V. Lavnikovakarnauhovdmitrii@gmail.comYana K. Ermolayevakarnauhovdmitrii@gmail.comAnna N. Solomkakarnauhovdmitrii@gmail.comNatalya A. Kulbachnayakarnauhovdmitrii@gmail.comAnastasia B. Olimovakarnauhovdmitrii@gmail.comVasily S. Vishnyakovkarnauhovdmitrii@gmail.comRenat V. Adelshinkarnauhovdmitrii@gmail.comDmitry Yu. Karnaukhovkarnauhovdmitrii@gmail.com<p>Submerged macrophytes are capable of adsorbing microplastic particles on their surface. This can affect the vital activity of plants and associated aquatic communities. At present, no studies have been conducted on the distribution and concentration of microplastics on the macrophytes of Lake Baikal. In this study, the possibility of adsorption of different types of microplastic particles by representatives of different groups of macrophytes from Lake Baikal was investigated under experimental conditions. The study showed that all three studied macrophyte species (<em>Myriophyllum spicatum</em>, <em>Draparnaldioides baicalensis </em>and <em>Stuckenia </em>sp.) are able to adsorb microplastic particles on their surface. From 2.9 to 50.7% of fibers and from 42.8 to 95.1% of fragments from the prepared sample were adsorbed on macrophytes. Part of the adsorbed plastic (not exceeding 10% of the total amount) remains on the sample even after interaction with the hypersaline solution. At the same time, for <em>D. baicalensis</em>, a higher percentage of plastic particles remaining on the sample is noted, which is associated with the presence of a mucous sheath on the surface of the plant. The methodology used in this study can be effectively applied to assess the possibility of microplastic particle adsorption by macrophytes both in laboratory studies and for studies of the level of contamination of macrophytes with microplastic particles in natural conditions.</p>2025-11-20T00:00:00+07:00Copyright (c) 2025 Artem T. Guliguev, Anastasia A. Solodkova, Ivan D. Kodatenko, Darya S. Kondratieva, Sofya A. Biritskaya, Arina V. Lavnikova, Yana K. Ermolaeva, Anna N. Solomka, Natalya A. Kulbachnaya, Anastasia B. Olimova, Vasily S. Vishnyakov, Renat V. Adelshin, Dmitry Yu. Karnaukhovhttps://journal.asu.ru/biol/article/view/18263Ecological and biological features of Polygala sibirica from the southern part of Western Siberia2025-12-02T08:46:44+07:00Alexey S. Prokopyevrareplants@list.ruTatiana N. Kataevarareplants@list.ruMikhail S. Yamburovrareplants@list.ruElena Yu. Machkinisrareplants@list.ruElena S. Prokopyevarareplants@list.ruAlexandra S. Mudarisovarareplants@list.ru<p>The paper reports data on the distribution and status of coenopopulations of the rare and valuable medicinal plant <em>P. sibirica </em>from the southern part of Western Siberia. The study investigated the phytocoenotic confinement, demographic characteristics of coenopopulations, seasonal patterns of growth, morphology, and reproductive biology. In mountainous areas, the species permanently inhabits rocky mountain steppes. In the plain of Western Siberia, its localities are fragmentary. <em>P. sibirica </em>coenopopulations are characterized by low density, ranging from 1.83 to 4.57 ind./m<sup>2</sup>. The ontogenetic structure of coenopopulations shows a predominance of generative individuals (53.6–76.9%). The ontogenetic spectrum of coenopopulations is characterized as incomplete, unimodal (CP 1–3, CP 5, CP 7–9) or bimodal (CP 4 and CP 6), with a predominance of generative individuals and a low proportion of old age groups. The analysis of the morphological characteristics of <em>P. sibirica </em>indicates that the largest plants with long, branched shoots and large leaves and inflorescences are found at the range boundary. Coenopopulations differ significantly in LMA, leaf chlorophyll content and nitrogen status values. It is shown that vegetation indices CCI, CRI1, VREI1 and ZMI can be used to assess the physiological status of plants under different ecological and coenotic conditions. <em>P. sibirica </em>reproduces exclusively by seed. Most flowers develop into mature fruits (FFR = 77.1–93.5%). Real seed productivity varies considerably, ranging from 10.8 to 77.8 seeds per shoot. Most of the studied coenopopulations exhibit the above-average level of reproductive potential (Cp = 65.2–77.9%). Under anthropogenic pressure, <em>P. sibirica </em>coenopopulations retain self-sustaining ability and can survive for extended periods within the range.</p>2025-11-26T00:00:00+07:00Copyright (c) 2025 Alexey S. Prokopyev, Tatjana N. Kataeva, Mikhail S. Yamburov, Elena Yu. Machkinis, Elena S. Prokopyeva, Alexandra S. Mudarisovahttps://journal.asu.ru/biol/article/view/18264Current state of spring phytoplankton of the Bratsk and Ust-Ilimsk reservoirs of the Angara Cascade2025-12-12T14:48:59+07:00Alena D. Firsovaannabessudova@mail.ruYuri P. Galachyantsannabessudova@mail.ruAnna Y. Bessudovaannabessudova@mail.ruVasilisa V. Buzevich (Buvaeva)annabessudova@mail.ruValentina K. Shirshovaannabessudova@mail.ruArtyom M. Marchenkovannabessudova@mail.ruAndrey I. Tanichevannabessudova@mail.ruSvetlana S. Vorobyovaannabessudova@mail.ruYelena V. Likhoshwayannabessudova@mail.ru<p>Continental reservoirs are sources of fresh water, but they are currently experiencing increasing anthropogenic stress. Reservoirs are among the most important water bodies for the needs of the populaion, and they require regular monitoring. However, some of these reservoirs have not been monitored for decades. The aim of this study was to assess the species richness, structure and density of spring phytoplankton of the Bratsk and Ust-Ilimsk reservoirs in the modern period. As a result of studies of these reservoirs, 62 taxa of planktonic algae were identified in phytoplankton in the spring season of 2024, of which diatoms and chrysophytes predominated in species richness. The dominant complex included the diatoms <em>Aulacoseira islandica</em>, <em>Nitzschia graciliformis</em>, <em>Asterionella formosa</em>, <em>Fragilaria radians</em>, and <em>Stephanodiscus minutulus</em>, the proportion of which in the total abundance and biomass varied between stations and reservoirs. The most significant predictors of phytoplankton community structure were nitrate and phosphate; conductivity, transparency and temperature were also important. Maximum values of total abundance and total biomass of phytoplankton were observed in the Bratsk Reservoir – 1119 thousand cells/L and 579 mg/m3, in the Ust-Ilimsk – 577 thousand cells/L and 274 mg/m3 respectively. These values do not exceed the indicators of previous years of observaions. The values of phytoplankton biomass characterize the studied areas of the Bratsk and Ust-Ilimsk reservoirs in June 2024 as oligotrophic.</p>2025-11-27T00:00:00+07:00Copyright (c) 2025 Alena D. Firsova, Yuri P. Galachyants, Anna Y. Bessudova, Vasilisa V. Buzevich (Buvaeva), Valentina K. Shirshova, Artyom M. Marchenkov, Andrey I. Tanichev, Svetlana S. Vorobyova, Yelena V. Likhoshwayhttps://journal.asu.ru/biol/article/view/18316The tribe Lychnideae A. Br., 1843 (Caryophyllaceae Juss., 1789) in the flora of Southern Siberia: opportunities and prospects for utilization2025-12-03T13:17:40+07:00Aleksandr S. Revushkinda46611@gmail.comDaria I. Kazantsevada46611@gmail.com<p>This study investigates the biodiversity and biochemical potential of the tribe Lychnideae (Caryophyllaceae) within the unique and extreme environments of Southern Siberia. The research is motivated by the premise that the region's specific climatic stressors drive the synthesis of unique secondary metabolites, such as ecdysteroids and phenolic compounds, with prospective pharmacological applications. Through integrated field studies (2017–2023), herbarium specimen analysis, and a systematic literature review, we evaluated the species composition, distribution, and phytochemical profiles of the local Lychnideae flora. Applying a standardized resource assessment algorithm, we categorized the 44 documented species. Results indicate that 19 species (43.2%) possess significant bioprospecting potential, meriting further investigation for sustainable use via wild harvest or controlled cultivation. Concurrently, five species (11.4%) were identified as threatened, underscoring an urgent need for dedicated conservation measures. This work highlights the critical dual mandate in phytochemical research: the sustainable utilization of promising plant resources for drug discovery and the imperative conservation of biodiversity to ensure the resilience and continuity of these natural pharmacopeias.</p>2025-12-04T00:00:00+07:00Copyright (c) 2025 Aleksandr S. Revushkin, Daria I. Kazantsevahttps://journal.asu.ru/biol/article/view/18369Ecological and geographical study of Lasius platythorax Seifert, 1991 in the Asian part of Russia2025-12-15T18:44:33+07:00Larisa S. Levchenkoxoxoxanas123@gmail.comBogdan A. Mikhaleikoxoxoxanas123@gmail.comAndrey S. Babenkoxoxoxanas123@gmail.comSergey N. Kirpotinxoxoxanas123@gmail.com<p>The present study aims to identify a potential shift in the distribution of <em>Lasius platythorax </em>Seifert, 1991, in the context of future climate change using ecological and geographic modeling methods. Climate models from the WorldClim database were used for the years 1970–2000, 2061–2080, and 2081–2100. Three out of four modeled scenarios predict a decrease in available <em>L. platythorax </em>habitat by 2100. One scenario predicts an increase in available habitat, where atmospheric temperature increases by a maximum of 4.4 degrees Celsius by 2100. This result is thought to be due to a decrease in limiting factors associated with increased air temperature. During the study, an updated map of known <em>L. platythorax </em>distribution was also created.</p>2025-12-13T00:00:00+07:00Copyright (c) 2025 Larisa S. Levchenko, Bogdan A. Mikhaleiko, Andrei S. Babenko, Sergey N. Kirpotinhttps://journal.asu.ru/biol/article/view/18371Population recovery and demographically constrained growth of Bezoar goat (Capra aegagrus) and Asian mouflon (Ovis gmelinii) in the Leopard Range of Nakhchivan, Azerbaijan2025-12-15T09:36:54+07:00Elmar Babaevelmar.b@mail.ruIsmail Mammadovelmar.b@mail.ruParviz Fatullayevelmar.b@mail.ruElshad Askerovelmar.b@mail.ruKonul Akhmedovaelmar.b@mail.ruDashgin Ganbarovelmar.b@mail.ruSamir Gyliyevelmar.b@mail.ru<p>The population status of the bezoar goat (<em>Capra aegagrus</em>) and the Asian mouflon (<em>Ovis gmelinii</em>), the primary prey of the Persian leopard (<em>Panthera pardus</em>), was assessed within the leopard's range in the southeastern part of the Nakhchivan Autonomous Republic of Azerbaijan. Surveys conducted from 2021 to 2022 using the transect method revealed a positive population trend for both ungulate species compared to previous censuses. Estimated densities of bezoar goats varied from 5.4 to 16.6 individuals/km² across different study sites, while mouflon densities ranged from 1.2 to 5.4 individuals/km². The total populations were estimated at approximately 2,000–2,200 bezoar goats and 800–1,000 mouflons across Nakhchivan. However, the sex-age structure of both species was characterized by a relatively low proportion of juveniles and yearlings, suggesting slow population growth. This demographic pattern is likely influenced by forage availability rather than poaching, which has been virtually eliminated since a complete hunting ban was instituted in 2001. The recovery of these prey populations is a critical factor for the conservation of the leopard in this region.</p>2025-12-14T00:00:00+07:00Copyright (c) 2025 Elmar Babaev, Ismail Mammadov, Parviz Fatullayev, Elshad Askerov, Konul Akhmedova, Dashgin Ganbarov, Samir Guliyevhttps://journal.asu.ru/biol/article/view/18373Towards the knowledge of the fauna of clearwing moths (Lepidoptera, Sesiidae) of Nakhchivan Autonomous Republic, Azerbaijan2025-12-16T16:21:21+07:00Oleg G. Gorbunovgorbunov.oleg@mail.ruNataly Snegovayagorbunov.oleg@mail.ruNazar A. Shapovalgorbunov.oleg@mail.ruIsmayil B.-O. Mammadovgorbunov.oleg@mail.ruRoman V. Yakovlevgorbunov.oleg@mail.ru<p>A small collection of five clearwing moths (Lepidoptera, Sesiidae) collected using artificial sex attractants in the vicinity of Ordubad, Nikhchivan Autonomous Republic, Azerbaijan, is presented and illustrated. Four species, viz. <em>Paranthrene tabaniformis </em>(Rottemburg, 1775), <em>Conopia amasina </em>(Staudinger, 1856), <em>Synanthedon myopaeformis </em>(Borkhausen, 1789), and <em>Chamaesphecia turbida </em>Le Cerf, 1937, are recorded for the fauna of the region for the first time. <em>Synanthedon armeniaca </em>O. Gorbunov, 1991, is restored from synonyms of <em>S. myopaeformis </em>(Borkhausen, 1789). The important role of artificial sex attractants in studies of the faunal composition of Sesiidae is noted.</p>2025-12-14T00:00:00+07:00Copyright (c) 2025 Oleg G. Gorbunov, Nataly Snegovaya, Nazar A. Shapoval, Ismayil B.-O. Mammadov, Roman V. Yakovlevhttps://journal.asu.ru/biol/article/view/18374Diversity and ecological drivers of lichens on Kunashir Island (Kuril Islands, Russian Far East)2025-12-19T09:45:30+07:00Anna S. Zuevalukinbrat@mail.ruSergey V. Chesnokovlukinbrat@mail.ruLiudmila A. Konorevalukinbrat@mail.ruIlya A. Prokopievlukinbrat@mail.ru<p>The purpose of this study is to examine the diversity of lichens in different communities of Kunashir Island and to identify factors influencing their distribution on the island. In total, we identified 172 species of lichens and related fungi. <em>Ochrolechia lijiangensis</em> and <em>Pertusaria plittiana</em> are new to Russia. <em>Amandinea pelidna</em>, <em>Bacidina brandii,</em> and <em>Lecanora caesiosora</em> are new for the Russian Far East. Thirteen species are reported for the first time for the Sakhalin Region. Six species are new for the Kuril Islands and 37 are new for Kunashir Island. Most of the identified lichens are corticolous species. The richest in the number of lichen species are <em>Abies sachalinensis</em>, <em>Betula ermanii</em>, <em>Quercus crispula</em>, <em>Picea ajanensis</em>, <em>Acer mayrii</em>, <em>Alnus hirsuta,</em> and <em>Salix udensis</em> (25–40 species). It is shown that at the landscape level the only significant factor for the species composition of lichens is the community type, while at the substrate level, the coniferous or deciduous nature of the substrate and the acidity of the bark have an impact.</p>2025-12-15T00:00:00+07:00Copyright (c) 2025 Anna S. Zueva, Sergey V. Chesnokov, Liudmila A. Konoreva, Ilya A. Prokopievhttps://journal.asu.ru/biol/article/view/18379Checklist of marine algal floras from Paramushir and Shumshu (Northern Kuril Islands)2025-12-20T14:23:43+07:00Nina G. Klochkovaninakl@mail.ruTatyana A. Klochkovaninakl@mail.ru<p>This study provides the most comprehensive checklist of marine macroalgae to date for Paramushir and Shumshu Islands (Northern Kuril Islands), based on recent field collections and a critical review of historical records. The resulting flora comprises 192 species (33 Chlorophyta, 115 Rhodophyta, 44 Phaeophyceae), extending the known flora of Paramushir by 17 species and that of Shumshu by 37 species. A standout finding is the discovery of <em>Alaria marginata</em>, which represents a first record for the entire Russian Far Eastern seas. Furthermore, we report a dense population of <em>Feditia simuschirensis </em>near Paramushir, indicating this kelp is not endemic to Simushir Island and necessitating a revision of its biogeographic status. In total, 17 species are newly reported for the Northern Kuril Islands, significantly enhancing the understanding of North Pacific phytogeography.</p>2025-12-17T00:00:00+07:00Copyright (c) 2025 Nina G. Klochkova, Tatyana A. Klochkovahttps://journal.asu.ru/biol/article/view/18431Scolopendromorph centipedes on the Karst Plateau: A survey from Bat Dai Son Nature Reserve, northern Vietnam2025-12-20T14:09:57+07:00Le X. Sonlesonenv86@gmail.comDo T. Thinhlesonenv86@gmail.comNguyen H. Thuclesonenv86@gmail.comTran T.T. Binhlesonenv86@gmail.comNguyen D. Anhlesonenv86@gmail.com<p>The species diversity of scolopendromorph centipedes in the Bat Dai Son Nature Reserve, located on the southwestern edge of the Dong Van Karst Plateau in northern Vietnam, is documented based on freshly collected specimens. A total of 27 specimens were examined resulting in six species belonging to four genera and three families, namely <em>Cryptops </em>(<em>Cryptops</em>) <em>tahitianus</em>, <em>Otostigmus aculeatus</em>, <em>Otostigmus voprosus</em>, <em>Scolopendra cataracta</em>, <em>Scolopendra dawydoffi</em>, and <em>Scolopocryptops spinicaudus</em>. This study provides information on examined specimens, illustrative photographs, and a discussion of the species’ geographic distributions. An identification key is also presented to the scolopendromorph centipedes in Bat Dai Son Nature Reserve. The findings contribute to the understanding of myriapod diversity in northern Vietnam and highlight the faunal distinctiveness of transitional karst highlands within the Dong Van Plateau system.</p>2025-12-19T00:00:00+07:00Copyright (c) 2025 Le X. Son, Do T. Thinh, Nguyen H. Thuc, Tran T.T. Binh, Nguyen D. Anhhttps://journal.asu.ru/biol/article/view/18440Arising and development of the population of Matteuccia struthiopteris (L.) Tod. in the University Grove of Tomsk University2025-12-27T15:37:20+07:00Irina I. Gureyevagureyeva@yandex.ruDmitry S. Feoktistovgureyeva@yandex.ruAlexander A. Kuznetsovgureyeva@yandex.ruRoman S. Romanetsgureyeva@yandex.ruAleksandr S. Revushkingureyeva@yandex.ru<p><em>Matteuccia struthiopteris </em>(L.) Tod. – Ostrich fern (Onocleaceae) is a circumboreal species widely distributed in the temperate zone of the northern hemisphere. We present the results of observations on the formation of <em>M. struthiopteris </em>population on a man-made lawn situated in the University Grove (Tomsk, Russia). The formation of the plant community on the new lawn occurred naturally, and sporophytes of the fern appeared naturally. During the observation period (2009–2025), we observed two wave of colonization of the lawn by <em>M. struthiopteris</em>, both waves coincided with covering of the lawn surface with a fresh soil. The first filling of the lawn occurred during its construction in 2007. The soil used for the lawn construction was taken from a native area located 6.65 km the southwest of the University Grove. The first <em>M. struthiopteris </em>sporophytes were found in 2009 in significant numbers: 263 individuals of early stages of ontogenesis. A new wave of colonization by spores occurred after a severe damage to the lawn and disruption of the established plant community in 2020 and subsequent refilling of the lawn with the new soil in 2023. By 2025, 315 new sporophytes of the initial stages of ontogenesis were added to sporophytes that survived the disruption. Thus, both waves of colonization of the lawn by <em>M. struthiopteris </em>were associated with its filling with the new soil, which means that the spores were presented in this soil. Both time, two years passed between the moments when the lawn was covered with the new soil and sporophytes became visible. This time was required for the germination of spores, development of gametophytes, fertilization and formation of sporophytes. No fertile (spore-bearing) sporophytes appeared during the whole observation period (17 years). For detection of the source of spores, from which the first wave of colonization occurred and <em>M. struthiopteris </em>population on the lawn formed, we conducted a molecular-genetic analysis of total DNA using ISSR method. The proven genetic identity of sporophytes from the lawn population to sporophytes growing at the site, where the soil was taken for the lawn construction, indicates that the spores were introduced to the lawn with this soil and that green spores of <em>M. struthiopteris </em>are capable of the formation of the spore bank, albeit a short-lived one.</p>2025-12-20T00:00:00+07:00Copyright (c) 2025 Irina I. Gureyeva, Dmitry S. Feoktistov, Alexander A. Kuznetsov, Roman S. Romanetshttps://journal.asu.ru/biol/article/view/18453Fungal microbiome biodiversity in Larix sibirica Ledeb. needles under biotic and technogenic stress in the Arctic2025-12-20T13:59:15+07:00Ksenia A. Miroshnikovamixe96@mail.ruYulia A. Litovkamixe96@mail.ruAnton A. Timofeevmixe96@mail.ruIgor N. Pavlovmixe96@mail.ru<p>Biodiversity plays a crucial role in maintaining the stability of both ecosystems (biocenoses) and individual trees, as it enhances resistance to biotic and abiotic stressors. This study focuses on the phyllosphere fungal communities of <em>Larix sibirica </em>Ledeb. and their role in host resilience under combined stresses from the root pathogen <em>Porodaedalea niemelaei </em>M. Fisch. and technogenic pollution. Samples were collected from four groups of trees: infected with the root pathogenic fungus <em>P. niemelaei</em>, exposed only to technogenic pollution, subjected to both <em>P. niemelaei </em>infection and technogenic pollution, and control trees, which were neither infected nor affected by pollution. DNA was amplified, sequenced, and analyzed using Illumina sequencing technology, yielding 598,891 raw ITS sequences. Varying degrees of larch needle necrosis were observed across the groups, likely influenced by different microbial genera under specific environmental conditions. In samples infected with <em>P. niemelaei</em>, <em>Fusarium </em>and <em>Alternaria </em>dominated, whereas in the group exposed to both <em>P. niemelaei </em>and technogenic pollution, <em>Valsa </em>and <em>Cytospora </em>were the most represented. Notably, the latter group also exhibited a reduced number of unique taxa compared to others, though further studies are needed to confirm statistical significance. The dominant pathogenic genera detected – <em>Fusarium</em>, <em>Alternaria</em>, <em>Valsa</em>, and <em>Cytospora </em>– likely interact with other fungi such as <em>Exobasidium</em>, <em>Ophiognomonia</em>, <em>Sarocladium</em>, <em>Phomopsis</em>, and <em>Taphrina</em>, exacerbating damage and altering the microbiome, particularly under pollution-induced stress.</p>2025-12-20T00:00:00+07:00Copyright (c) 2025 Ksenia A. Miroshnikova, Yulia A. Litovka, Anton A. Timofeev, Igor N. Pavlovhttps://journal.asu.ru/biol/article/view/18475New and noteworthy records of Plants, Lichens and Insects in Altai Territory and Republic of Altai (Southern Siberia). II.2025-12-22T16:55:35+07:00Evgeny A. Davydovyakovlev_asu@mail.ruPetr Kozachevyakovlev_asu@mail.ruPavel Golyakovyakovlev_asu@mail.ruTimofei Zalutskyyakovlev_asu@mail.ruEgor Svirinyakovlev_asu@mail.ruOleg Kudrovyakovlev_asu@mail.ruPolina Pavlovayakovlev_asu@mail.ruAndrei Slepchenkoyakovlev_asu@mail.ruSvyatoslav Knyazevyakovlev_asu@mail.ruYulia Storozhenkoyakovlev_asu@mail.ruLidia Yakovchenkoyakovlev_asu@mail.ruRoman Yakovlevyakovlev_asu@mail.ru<p>This study reports new geographical occurrences for seven species of vascular plants (<em>Cyperus michelianus</em>, <em>Gymnocarpium continentale</em>, <em>Rhynchospora alba</em>, <em>Scheuchzeria palustris</em>, <em>Schoenoplectiella supina</em>, <em>Veronica </em>× <em>schmakovii</em>, and <em>V. </em>× <em>sessiliflora</em>), eight species of lichens (<em>Chaenotheca chlorella</em>, <em>Lathagrium dichotomum</em>, <em>Myrionora albidula</em>, <em>Scoliciosporum perpusillum</em>, <em>Physcia alnophila</em>, <em>P. tenella</em>, <em>Peltigera collina</em>, and <em>P. extenuata</em>), and nine species of Lepidoptera in the Altai Territory and the Republic of Altai. For each recorded species, localities and ecological preferences are detailed. Plants <em>Veronica </em>× <em>schmakovii</em>, <em>V</em>. × <em>sessiliflora</em>, and <em>Rhynchospora alba </em>are recorded for the first time in the Altai Territory; <em>Scheuchzeria palustris </em>and <em>Gymnocarpium continentale </em>for the second time. <em>Scheuchzeria palustris </em>and <em>Rhynchospora alba</em>, identified as rare fog-dependent plants, are recommended for inclusion in the Red Book of the Altai Territory. Lichen <em>Chaenotheca chlorella </em>is recorded as a new species for Southern Siberia; <em>Lathagrium dichotomum </em>is recorded for the first time in the Altai Territory; <em>Myrionora albidula</em>, <em>Scoliciosporum perpusillum</em>, <em>Physcia alnophila</em>, and <em>P. extenuata </em>are reported as new lichen species for the Salair Ridge; <em>Physcia tenella </em>and <em>Peltigera collina </em>are new records for the Salair botanical-geographical province within the Altai Territory. New faunistic records for Lepidoptera include first reports for the Altai Territory of the tortricids <em>Cydia medicaginis</em>, <em>Cochylis pallidana</em>, and <em>Aethes cnicana</em>; the chimabachid <em>Dasystoma salicella</em>; the erebids <em>Catocala helena</em>, <em>Catocala bella</em>, and <em>Hypena crassalis</em>; the noctuid <em>Conistra rubiginea</em>; and the lasiocampid <em>Dendrolimus pini</em>. Additionally, the cossid <em>Dyspessa salicicola </em>is reported as a new species for Western Siberia. The sphingids <em>Agrius convolvuli </em>and <em>Macroglossum stellatarum </em>are newly recorded for the Republic of Altai, with the latter's spring discovery suggesting the potential formation of a stable local population. The noctuid <em>Orthosia cerasi </em>is also reported for the first time in the Republic of Altai. Furthermore, this study contributes rare quantitative data on population dynamics, presenting an estimated population size for a newly documented locality of the lichen <em>Lathagrium dichotomum</em>. This information is crucial for conservation planning and assessing the status of this Red Data Book listed species.</p>2025-12-21T00:00:00+07:00Copyright (c) 2025 Evgeny A. Davydov, Petr Kosachev, Pavel Golyakov, Timofei Zalutsky, Egor Svirin, Oleg Kudrov, Polina Pavlova, Andrei Slepchenko, Svaytoslav Knyazev, Yulia Storozhenko, Lidia Yakovchenko, Roman Yakovlevhttps://journal.asu.ru/biol/article/view/18509Legacies of historical ploughing in the soils of secondary forests, Western Siberia2025-12-25T13:06:49+07:00Sergey V. Loikos.loyko@yandex.ruDarya M. Kuzminas.loyko@yandex.ruGeorgy I. Istigichevs.loyko@yandex.ruArtyom G. Lims.loyko@yandex.ruTatyana N. Belkinas.loyko@yandex.ruSergey P. Kulizhskys.loyko@yandex.ru<p>The abandonment of agricultural land, followed by afforestation, is a widespread global phenomenon. This process is not always well documented. Many ecosystems carry a post-agricultural legacy that is not always obvious, but which can be identified using a series of indicators. One way to identify these indicators is to examine arable soils, the existence of which can be confirmed using archival cartographic information. This study aims to identify morphological indicators of historical ploughing in the soils of secondary forests in southern Western Siberia. The study focused on Luvic Greyzemic Phaeozems that formed on the site of documented peasant arable land abandoned approximately 120–130 years ago. A comprehensive approach combining historical map analysis, field morphological description, laboratory soil analysis and radiocarbon dating of charcoal enabled land-use history to be reconstructed and long-term indicators of former soil ploughing to be identified. These indicators include: a smooth lower boundary of the Ap horizon, its uniform colouration, the presence of agrogenic microrelief (furrows and ridges), the absence of treefall pit-and-mound topography associated with windthrow, and a specific distribution of fine earth particles. The activity of soil fauna (e.g. moles, ants, insects and earthworms) has been shown to be a leading factor in the transformation and masking of these features during post-agrogenic succession. Despite a lengthy recovery period, the soils have not completely returned to a quasi-pristine state. This work provides a methodological foundation for identifying ancient arable lands within forest landscapes in Siberia.</p>2025-12-23T00:00:00+07:00Copyright (c) 2025 Sergey V. Loiko, Darya M. Kuzmina, Georgy I. Istigechev, Artyom G. Lim, Tatyana N. Belkina, Sergey P. Kulizhskyhttps://journal.asu.ru/biol/article/view/18536Biodiversity oases in the southern tundra: the role of shrub-herbaceous communities (Western Siberia)2025-12-25T22:00:18+07:00Nikita V. Shefervchifz@mail.ruIvan V. Kritskovvchifz@mail.ruGeorgy I. Istigechevvchifz@mail.ruSergey V. Loikovchifz@mail.ru<p>The southwestern Gydan Peninsula remains a significant data gap in understanding tundra ecosystem responses to climate change and shrub expansion. Detailed studies linking plant community composition to soil properties in this region are critically lacking. This study provides the integrated analysis of shrub-herbaceous communities and their underlying soils in this region. Based on comprehensive geobotanical and soil surveys at 52 sites, we identified four distinct community types using multivariate analysis. Our results reveal a clear hierarchy of environmental drivers. Primary vegetation patterns and the formation of biodiversity hotspots, including the discovery of several plant species new to the local flora, are predominantly shaped by landscape heterogeneity, such as the mosaic of slopes, valleys, and snow hollows. Soil properties, notably those related to texture, active layer dynamics, and hydromorphy, act as significant secondary filters, structuring communities along a key soil gradient. However, the overall correlation between soil and vegetation matrices was limited, indicating a substantial role for other unmeasured factors. We conclude that plant community assembly in the southern Gydan tundra is governed by an interplay where the geomorphic template sets the stage for diversity, while localized soil conditions fine-tune composition. These findings establish an essential baseline for monitoring and underscore that conserving landscape heterogeneity is crucial for the resilience of these rapidly changing Arctic ecosystems.</p>2025-12-24T00:00:00+07:00Copyright (c) 2025 Nikita V. Shefer , Ivan V. Kritskov , Georgyi I. Istigechev , Sergey V. Loikohttps://journal.asu.ru/biol/article/view/18480Dynamics and composition of breeding bird communities on Kitay Island, Central Sivash region2025-12-24T21:39:19+07:00Valery D. Siokhinamatsyura@gmail.comAlex V. Matsyura<p>The Central Sivash region, a unique ecosystem of saline lakes and reed-beds, hosts important colonial waterbird communities. This study analyzes long-term changes (1949–2024) in the breeding bird population on Kitay Island, one of the area’s key islands. Our results reveal a significant ecological restructuring, marked by a pronounced increase in Great Cormorants (<em>Phalacrocorax carbo</em>), which became the dominant species, and a concurrent decline in Yellow-legged Gulls (<em>Larus cachinnans</em>). Total nest numbers peaked in the late 20th century before declining to a lower, stable level. Community analyses identified three distinct succession phases: a gull/tern-dominated assemblage (1950–1980), a cormorant-dominated phase (1990–2010), and a more mixed and diverse recent community. These shifts are interpreted in the context of environmental drivers including habitat change, interspecific competition, predation pressure, and reduced human disturbance. This most recent phase is characterized by a slight reduction in species dominance and an increase in diversity, driven by the arrival of new species. These findings demonstrate profound community turnover and highlight the dynamic response of avian populations to environmental change, providing critical insights for the conservation management of this sensitive habitat.</p>2025-12-24T00:00:00+07:00Copyright (c) 2025 Valery D. Siokhin, Alex V. Matsyurahttps://journal.asu.ru/biol/article/view/18545Molecular characterization of Amitermes rhizophagus Belyaeva, 1974 (Blattodea: Isoptera), newly recorded from Uzbekistan2025-12-25T11:00:52+07:00Gulnara S. Mirzaevamirzayeva.gulnora@mail.ruBakhtiyor R. Kholmatovmirzayeva.gulnora@mail.ruKakhramon D. Rustamovmirzayeva.gulnora@mail.ruZumrad A. Ganievamirzayeva.gulnora@mail.ruVakhidjon N. Akhmedovmirzayeva.gulnora@mail.ruNatalia I. Lebedevamirzayeva.gulnora@mail.ruMukhabbat Kh. Khashimovamirzayeva.gulnora@mail.ruSobir K. Sobirovmirzayeva.gulnora@mail.ruOybek A. Amirovmirzayeva.gulnora@mail.ruKumri X. Allaberdiyevamirzayeva.gulnora@mail.ru<p>This study presents the first molecular confirmation of <em>Amitermes rhizophagus </em>Belyaeva, 1974 (Blattodea: Termitidae) from Uzbekistan. Specimens collected in the Kashkadarya Region were identified through combined morphological and molecular analyses. Ribosomal DNA (ITS) and mitochondrial DNA (COI) fragments were amplified, sequenced, and compared with reference sequences from GenBank. Phylogenetic analyses using the Maximum Likelihood method placed <em>A. rhizophagus </em>within a well-supported <em>Amitermes </em>clade (bootstrap = 98-100%), closely related to <em>A. deplanatus</em>, <em>A. conformis</em>, and <em>A. foreli</em>. Genetic distances were low within <em>Amitermes </em>(0.017-0.034) but high between genera (0.13-0.19), confirming clear evolutionary separation from <em>Drepanotermes </em>and <em>Microcerotermes</em>. These findings validate the taxonomic identity of <em>A. rhizophagus </em>and provide the first molecular evidence for its occurrence in Uzbekistan, enriching knowledge of Central Asian termite diversity and phylogeny.</p>2025-12-25T00:00:00+07:00Copyright (c) 2025 Gulnara S. Mirzaeva, Bakhtiyor R. Kholmatov, Kakhramon D. Rustamov, Zumrad A. Ganieva, Vakhidjon N. Akhmedov, Natalia I. Lebedeva, Mukhabbat Kh. Khashimova, Sobir K. Sabirov, Oybek A. Amirov, Kumri X. Allaberdiyevahttps://journal.asu.ru/biol/article/view/18566Distribution of Dirofilaria repens (Railliet et Henry, 1911) in Southern and Southeastern Russia2025-12-25T23:13:25+07:00Yuri O. Prilepskys.konyaev@yahoo.comSergey V. Konyaevs.konyaev@yahoo.com<p>The aim of the study was to investigate the current distribution of <em>Dirofilaria </em>repens in dogs from the Southern, Volga, and North Caucasian federal districts of European Russia. A total of 6,444 canine blood samples from 100 localities were screened using a species-specific real-time PCR assay. <em>D. repens </em>DNA was detected in 485 samples (7.52% prevalence), confirming the parasite's presence across a vast area. Positive cases were identified in the Republics of Bashkortostan, Mari El, Mordovia, Tatarstan, Chuvashia, Karachay-Cherkessia, Chechnya, Adygea, and the Crimean Peninsula, as well as in Perm, Stavropol, Krasnodar, Rostov, Volgograd, Astrakhan, Ulyanovsk, Samara, Penza, Nizhny Novgorod, and Kirov regions. The prevalence varied significantly among regions, ranging from 1.04% in Astrakhan region to 48.39% in the Republic of Mari El. While the lack of travel histories for sampled dogs means that some detected cases could be imported, the high prevalence observed in many cities provides robust evidence of autochthonous transmission. Our findings demonstrate that <em>D. repens </em>is now endemic across a much broader territory of European Russia than previously recognized, including lesser-known foci in the Volga Basin and the Western Urals, which has significant implications for veterinary and public health surveillance.</p>2025-12-25T00:00:00+07:00Copyright (c) 2025 Yury O. Prilepsky, Sergey V. Konyaevhttps://journal.asu.ru/biol/article/view/18543Fauna of Curculionoidea of the Khopersky State Nature Reserve (Russia)2025-12-28T17:16:47+07:00Sergei V. Dedyukhinded@udsu.ru<p>For the first time, a detailed inventory and zoogeographical characterization of the Curculionoidea fauna of the Khopersky State Nature Reserve have been conducted, along with an analysis of the landscape and habitat distribution of weevils. In total, 361 species of Curculionoidea belonging to 5 families have been recorded within the reserve. Of these, 169 species are reported from the Khopersky Reserve for the first time, and 76 of them are new to the fauna of the Voronezh Region, including several rare species. The main features of the zoogeographical structure of the fauna are a very high proportion of species belonging to the Western Palaearctic arealogical complex (100 species, almost 28%), as well as considerable species richness of the nemoral (66 species), Mediterranean (64 species), and, to a lesser extent, Scythian (steppe) (59 species) faunal complexes, with a minor participation of weevils of Kazakh–Turanian origin (9 species).</p>2025-12-25T00:00:00+07:00Copyright (c) 2025 Sergei V. Dedyukhinhttps://journal.asu.ru/biol/article/view/18627Factors influencing the fauna of pit lakes in the Cheremkhovo district (Irkutsk region, Russia)2025-12-28T20:44:44+07:00Dmitry Yu. Karnaukovkarnauhovdmitrii@gmail.comArina V. Lavnikovakarnauhovdmitrii@gmail.comYana K. Ermolayevakarnauhovdmitrii@gmail.comVeronika A. Belovakarnauhovdmitrii@gmail.comDiana G. Rechilekarnauhovdmitrii@gmail.comEkaterina R. Khadeevakarnauhovdmitrii@gmail.comYulia A. Zharovakarnauhovdmitrii@gmail.comDmitry I. Golubetskarnauhovdmitrii@gmail.comSofia A. Biritskayakarnauhovdmitrii@gmail.comElena V. Minchevakarnauhovdmitrii@gmail.comAleksandr B. Kupchinskykarnauhovdmitrii@gmail.com<p>Recently, the global scientific community has shown interest in studying pit lake ecosystems. This interest is driven by a number of factors, including the significant role of pit lakes in enhancing regional biodiversity and providing ecosystem services. The Irkutsk region contains a large number of pit lakes. This study compares aquatic organism groups and the hydrochemical and physicochemical parameters of two pit lakes in the Cheremkhovo district. Thus, using the example of two lakes, three stages of colonization of pit lakes by macrophytes and aquatic invertebrates can be identified. These stages differ in both the level of development and organization of macrophyte communities and aquatic invertebrate communities. The obtained data demonstrate that even under common geological and geographical conditions, the formation of hydrobiocenoses in pit lakes can occur according to different scenarios. The results of the study show that the presence of a forest on the site of a future pit lake contributes to stabilization, a reduction in acidity, and the formation of a fully functioning aquatic ecosystem within less than 40 years. At the same time, the nearby lake, around which vegetation is still sparse, has a low pH (3.05), and the most favorable conditions are created by thickets of moss (<em>Warnstorfia exannulata</em>).</p>2025-12-27T00:00:00+07:00Copyright (c) 2025 Dmitry Yu. Karnaukhov, Arina V. Lavnikova, Yana K. Ermolaeva, Veronika A. Belova, Diana G. Rechile, Ekaterina R. Khadeeva, Yuliya A. Zharova, Dmitry I. Golubets, Sofya A. Biritskaya, Elena V. Mincheva, Aleksandr B. Kupchinskyhttps://journal.asu.ru/biol/article/view/18640Seasonal changes in dehydrin composition in Picea obovata Ledeb. from the cryolithozone of Yakutia2025-12-28T20:32:13+07:00Tatiana D. Tatarinovat.tatarinova@gmail.comAnatoley G. Ponomarevt.tatarinova@gmail.comAleksandr A. Perkt.tatarinova@gmail.comIrina V. Vasilevat.tatarinova@gmail.com<p>This study presents the first analysis of the composition and seasonal dynamics of low-temperature-induced dehydrins in the shoots of Siberian spruce (<em>Picea obovata</em> Ledeb.) from the cryolithozone of Central Yakutia. Dehydrins were identified using antibodies specific to the conserved K-segment. Most major dehydrins (17–57 kDa) were present constitutively throughout the annual cycle. In contrast, low-molecular-weight dehydrins (13 and 15 kDa) were seasonal and inducible, disappearing in summer and reappearing during autumn cold acclimation. High levels of major dehydrins persisted through the winter, coinciding with ultra-low temperatures and maximum frost resistance. These dynamics and the substantial abundance of dehydrins are likely key to the unique extreme cold adaptation of <em>P. obovata</em> in the Yakutian cryolithozone.</p>2025-12-29T00:00:00+07:00Copyright (c) 2025 Tatiana D. Tatarinova, Anatoley G. Ponomarev, Aleksandr A. Perk, Irina V. Vasilevahttps://journal.asu.ru/biol/article/view/18639Drainage and pyrogenic influence alter the physicochemical properties and carbon storage of oligotrophic peatlands in Western Siberia2025-12-30T15:03:46+07:00Liliya G. Nikonovanikonovalilig@gmail.comArtem N. Nikiforovnikonovalilig@gmail.comRailya T. Kozhamberlievanikonovalilig@gmail.comEvgenia A. Golovatskayanikonovalilig@gmail.com<p>The study assesses the impact of drainage and pyrogenic exposure on the physical and chemical composition and properties of oligotrophic peat soils in the southern taiga of Western Siberia. These factors have been found to induce significant changes in phytocoenoses, resulting in soil degradation. Changes include alterations in vegetation cover, fluctuations in water table level, a decrease in acidity, increased peat ash content, total nitrogen content, and a reduction in the C/N ratio. Drainage and fires also lead to a change in the carbon sequestration potential of peatlands. In anthropogenically modified peatlands, carbon stocks in the 0 to 100 cm layer were 2.5 to 2.8 times higher than in undisturbed sites due to increased bulk density. These structural modifications in peat deposits indicate significant changes in their ecological function, particularly through altered carbon sequestration capacity, which may adversely affect regional carbon balance.</p>2025-12-28T00:00:00+07:00Copyright (c) 2025 Liliya G. Nikonova, Artem N. Nikiforov, Railya T. Kozhamberlieva, Evgenia A. Golovatskayahttps://journal.asu.ru/biol/article/view/18656Anatomical features of leaves of the Busch lily (Lilium buschianum G. Lodd.) in Western Siberia forest zone2025-12-30T15:50:08+07:00Tatiana N. Belaevasbg-flowers@yandex.ruSi Liusbg-flowers@yandex.ruAlina N. Butenkovasbg-flowers@yandex.ru<p>The Busch lily (<em>Lilium buschianum </em>G.Lodd.) is the least studied of the four species of lilies that grow in Siberia. In the Russian Federation, <em>L. buschianum </em>is listed in the Red Books of the Transbaikal Territory, Amur Region, Jewish Autonomous Region, and Khabarovsk Territory. The aim of this study was to investigate the anatomical features of <em>L. buschianum </em>leaf blades and compare them with those of other species in the genus growing in Siberia. The information obtained is necessary for developing effective introduction and reintroduction strategies aimed at preserving biodiversity and restoring species populations. The study revealed that the <em>L. buschianum </em>is characterized by the following anatomical features of the leaf blade: the cell walls of the epidermis are straight or wavy, dorsiventral leaves and stomata in the lower epidermis, the anomocytic stomatal apparatus, high density of cells in both the upper and lower epidermis, as well as stomata in the lower epidermis, large stomata (on average 78.3 µm long and 53.7 µm wide). The conducted study classifies <em>L. buschianum </em>as a heliophyte and mesophyte, but the plants also have a number of features that can be considered as an adaptation mechanism to arid environments. <em>L. buschianum </em>is a species with a fairly wide range of tolerance in relation to substrate moisture, which allows it to grow both in habitats with a well-balanced moisture supply and in conditions of moisture deficiency. The species is recommended for cultivation in stony gardens and open areas with good drainage.</p>2025-12-30T00:00:00+07:00Copyright (c) 2025 Tatiana N. Belaeva, Si Liu, Alina N. Butenkovahttps://journal.asu.ru/biol/article/view/18669Additions to the Lepidoptera fauna of Omsk and Novosibirsk Regions, Russia2025-12-31T10:57:26+07:00Svyatoslav A. Knyazevkonungomsk@yandex.ruVadim V. Ivoninkonungomsk@yandex.ru<p>The article provides a list of 23 species from the Chimabachidae, Pieridae, Nymphalidae, Geometridae, Notodontidae, Erebidae, Noctuidae families from Omsk and Novosibirsk Regions in West Siberia. Three species – <em>Pseudobaptria corydalaria </em>(Graeser, 1889), <em>Paragona cognata </em>(Staudinger, 1892), <em>Polia</em><em> malchani </em>(Draudt, 1934) are new to the South-West Siberian Region in Catalogue of Lepidoptera of Russia. Three species are new to the Omsk Region, among them <em>Pseudobaptria corydalaria </em>(Graeser, 1889), <em>Scopula incanata </em>(Linnaeus, 1758), <em>Egira conspicillaris </em>(Linnaeus, 1758); seven species are new to Novosibirsk Region, among them <em>Dasystoma salicella </em>(Hübner, 1796), <em>Apatura ilia </em>([Denis & Schiffermüller], 1775), <em>Stauropus fagi </em>(Linnaeus, 1758), <em>Catocala deducta </em>Eversmann, 1843, <em>Acronicta menyanthidis </em>(Esper, 1789), <em>Amphipyra pyramidea </em>(Linnaeus, 1758), <em>Euxoa nigrofusca </em>(Esper, [1788]).</p>2025-12-30T00:00:00+07:00Copyright (c) 2025 Svyatoslav A. Knyazev, Vadim V. Ivonin