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34 results for “taiga”
Рис. 1. Карта района иссΛеΑований. 1 – граница зон раститеΛьности; 2 – граница поΑзон раститеΛьности; 3 – места сбора материаΛа; I – южная тайга; II – среΑняя тайга; III – северная тайга; IV – крайнесеверная тайга; V – ΛесотунΑра; VI – южная тунΑра; VII – северная тунΑра. Fig. 1. Map of the studied area. 1 – boundary of vegetation zones; 2 – boundary of vegetation subzones; 3 – collection points; I – southern taiga; II – middle taiga; III – northern taiga; IV – extremely northern taiga; V – forest tundra; VI – southern tundra; VII – northern tundra. in Fauna and landscape-zonal distribution of Orthoptera in the Komi Republic (Russia)
Рис. 1. Карта района иссΛеΑований. 1 – граница зон раститеΛьности; 2 – граница поΑзон раститеΛьности; 3 – места сбора материаΛа; I – южная тайга; II – среΑняя тайга; III – северная тайга; IV – крайнесеверная тайга; V – ΛесотунΑра; VI – южная тунΑра; VII – северная тунΑра. Fig. 1. Map of the studied area. 1 – boundary of vegetation zones; 2 – boundary of vegetation subzones; 3 – collection points; I – southern taiga; II – middle taiga; III – northern taiga; IV – extremely northern taiga; V – forest tundra; VI – southern tundra; VII – northern tundra.
Рис. 2. UPGMA-ΑенΑрограмма схоΑства виΑового состава (А) и фаунистическая структура (B) сообществ земΛероек в пяти ΛокаΛитетах Амурской обΛасти: ЗЗ — Зейский заповеΑник; НЗ — Норский заповеΑник; ХЗ — Хинганский заповеΑник; ЧФЗ — ХинганоАрхаринский заказник; НБС — территория зоны вΛияния Нижнебурейской ГЭС. ΔТФ — Αревнетаежная фауна; БФ — бореаΛьная фауна; НФ — немораΛьная фауна; Αр. — преΑставитеΛи Αругих фауногенетических группировок (пояснения в тексте) Fig. 2. UPGMA dendrogram of species composition similarity (A) and fauna structure (B) of shrew communities in five Amur region localities: ZZ — Zeya nature reserve; NZ — Norsky nature reserve; KhZ — Khingansky nature reserve; ChFZ — KhinganoArkharinsky nature reserve; NBS — the area influenced by the Nizhnebureyskaya hydroelectric power station. DTP — ancient taiga fauna; BF — boreal fauna; NF — nemoral fauna; others — representatives of other faunagenetic groups (explained in the text) in Shrew species composition and fauna structure in the Norsky reserve
Рис. 2. UPGMA-ΑенΑрограмма схоΑства виΑового состава (А) и фаунистическая структура (B) сообществ земΛероек в пяти ΛокаΛитетах Амурской обΛасти: ЗЗ — Зейский заповеΑник; НЗ — Норский заповеΑник; ХЗ — Хинганский заповеΑник; ЧФЗ — ХинганоАрхаринский заказник; НБС — территория зоны вΛияния Нижнебурейской ГЭС. ΔТФ — Αревнетаежная фауна; БФ — бореаΛьная фауна; НФ — немораΛьная фауна; Αр. — преΑставитеΛи Αругих фауногенетических группировок (пояснения в тексте) Fig. 2. UPGMA dendrogram of species composition similarity (A) and fauna structure (B) of shrew communities in five Amur region localities: ZZ — Zeya nature reserve; NZ — Norsky nature reserve; KhZ — Khingansky nature reserve; ChFZ — KhinganoArkharinsky nature reserve; NBS — the area influenced by the Nizhnebureyskaya hydroelectric power station. DTP — ancient taiga fauna; BF — boreal fauna; NF — nemoral fauna; others — representatives of other faunagenetic groups (explained in the text)
Figure 11 in True bugs (Hemiptera: Heteroptera) from the taiga zone of the mountainous Altai of Russia: the first records and new data on rare species
Figure 11. Habitat of Gampsocoris culicinus Seidenstücker at the environs of Lake Teletskoye, Altai Republic (Photo by V.A. Soboleva).
Figure 10 in True bugs (Hemiptera: Heteroptera) from the taiga zone of the mountainous Altai of Russia: the first records and new data on rare species
Figure 10. Habitat of Bryocoris pteridis (Fallén) in taiga at the environs of Lake Teletskoye, Altai Republic (Photo by N.V. Golub).
Figures 4–9 in True bugs (Hemiptera: Heteroptera) from the taiga zone of the mountainous Altai of Russia: the first records and new data on rare species
Figures 4–9. Adult specimens and paramere of Heteroptera. 4, 5. Nabis (Dolichonabis) americolimbatus (Carayon) (4 – dorsal view, 5 – paramere, arrow indicates lamellar carina at its base), 6. Xylocoris cursitans (Fallén), 7. Bryocoris pteridis (Fallén), 8. Phytocoris longipennis Flor, 9. Gampsocoris culicinus Seidenstücker (Photo by V.A. Soboleva).
Figure 3 in True bugs (Hemiptera: Heteroptera) from the taiga zone of the mountainous Altai of Russia: the first records and new data on rare species
Figure 3. One of habitats of Nabis (Dolichonabis) americolimbatus (Carayon) on the taiga edge near of Artybash village (Photo by E.V. Aksenenko).
Figure 2 in True bugs (Hemiptera: Heteroptera) from the taiga zone of the mountainous Altai of Russia: the first records and new data on rare species
Figure 2. Habitat of Pachycoleus pusillimus (J. Sahlberg, 1870) and Saldula orthochila (Fieber, 1859) in the environs of village Artybash, Altai Republic (Photo by V.A. Soboleva).
Figure 1 in True bugs (Hemiptera: Heteroptera) from the taiga zone of the mountainous Altai of Russia: the first records and new data on rare species
Figure 1. Taiga on the slopes of the Altai mountains at northern part of the Lake Teletskoye (Photo by V.A. Soboleva).
EGMP 2023 Offtake Assessment for Finland and NW Russia / Sweden, Denmark and Germany population of Taiga Bean Goose (former Central MU)
<p>Data and model files for the 2023 EGMP offtake assessment for Finland and NW Russia / Sweden, Denmark and Germany population of Taiga Bean Goose (former Central MU).</p> <p>https://gitlab.com/aewa-egmp/taiga-bean-goose/harvest-assessment-2023</p>
Database of experimental determinations of soil respiration in pine and spruce forests during the growing season of 2023 at the Lyalsky test site (middle taiga, northeast of the East European Plain)
<p>The data set includes the results of 342 measurements of CO2 emissions (SR, gС/m2/day) from the soil surface of coniferous ecosystems at the Lyalsky test site during the growing season (May-September) of 2023. The objects of the study were: pine forest (PS, Gleyic Folic Albic Podzol (Arenic)) and spruce forest (SM, Albic Retisols). The values of temperature (Ts, at a depth of 10 cm), moisture (Ms, in a layer of 0-5 cm) of the soil and air temperature (Ta) are also given.</p><p>The research was carried out by employees of the Institute of Biology of Komi Science Centre of the Ural Branch of the Russian Academy of Sciences as part of the most important innovative project of national importance "Development of a system for ground-based and remote monitoring of carbon pools and greenhouse gas fluxes in the territory of the Russian Federation, ensuring the creation of recording data systems on the fluxes of climate-active substances and the carbon budget in forests and other terrestrial ecological systems" (Registration number: 123030300031-6). </p>
Repeated measure plant community data after fire in boreal forest, Taiga Shield, Northwest Territories, Canada, 1998-2018
<p>10 transects were established in the years following fire in boreal forest stands on the Taiga Shield, Northwest Territories, Canada in 1998-1999. These were remeasured annually. Six transects were returned to on 2018 for another measurement. At each measurement, we recorded ground covers, species identities, and counted tree stems (seedlings).</p>
Data from: Translocation experiment of taiga bean geese Anser fabalis provides evidence for oblique social learning of moult migration
<p>While there is ample evidence supporting genetic control of migratory behaviour in short-lived passerines, long-lived social species have been assumed to rely solely on cultural inheritance of migratory routes. Evidence from experimental studies supporting this idea is scarce. We tested whether the moult migration in taiga bean geese <em>Anser fabalis </em>has an inherited component or whether the birds need oblique social learning (where knowledge on migration is transferred from any experienced individual to any naïve individual conspecific) to carry out this journey. In many waterfowl species, non-breeders and failed breeders migrate to remote places for wing moult while successful breeders stay at the breeding grounds and moult with their chicks. We translocated one-year-old taiga bean geese before their first moult migration to sites outside of the breeding range to examine whether they display innate moult migration behaviour without experienced conspecifics or not. The birds were equipped with GPS-transmitters and released in randomly assigned groups of two. Wild control one-year-old birds were released immediately after capture with other non-breeding geese, while a procedural control group consisting of older birds was held in captivity until released at the same time with the translocated one-year-old birds but in the place where they were captured. Most translocated birds found conspecifics and either joined locally moulting breeders or followed experienced birds to moulting sites in Russia. Two of the translocated birds did not find other bean geese and settled to moult together in SW Finland. The wild control birds moult-migrated as expected, while only one of the procedural control birds moult-migrated to Russia and the remaining three stayed with locally moulting breeders in Finland. Our results support the idea that moult migration in geese is culturally inherited, highlighting the importance of the non-relative, experienced adult individuals have in maintaining population-specific behaviours.</p>
Data from: Translocation experiment of taiga bean geese Anser fabalis provides evidence for oblique social learning of moult migration
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Repeated measure plant community data after fire in boreal forest, Taiga Shield, Northwest Territories, Canada, 1998-2018
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FIGURES 1–5 in A new species of Arctoseius Thor, 1930 (Acari: Ascidae) from taiga regions of the Palaearctic, with a key to Arctoseius species of Fennoscandia, NW Europe
FIGURES 1–5. Arctoseius ambiguus sp. nov., female. 1. tritosternum; 2. ambulacrum and tarsus II distally, ventral aspect; 3. gnathotectum; 4. peritrematal region; 5. idiosomal dorsum. Scales: 1–2 25 µm, 3–5 50 µm.
FIGURES 6–11 in A new species of Arctoseius Thor, 1930 (Acari: Ascidae) from taiga regions of the Palaearctic, with a key to Arctoseius species of Fennoscandia, NW Europe
FIGURES 6–11. Arctoseius ambiguus sp. nov., female. 6. acetabula II–IV and exopodal platelets; 7. subcapitulum; 8. idiosomal ventrum; 9. anal shield; 10. cheliceral digits, dorsal aspect; 11. chelicera without basal joint, paraxial aspect. Scales: 6–9 50 µm, 10–11 25 µm.
Fig. 11 in Zoogeographic relationships between true bugs (Heteroptera) in the fauna of relict forest-steppes of the middle taiga subzone of Yakutia and the steppes of southern East Siberia
Fig. 11. Dendrogram of the similarity of the steppe faunogenetic complexes of hemipterans in Yakutia, the Minusinsk basin, Cis-Baikalia and Transbaikalia according to the Chekanovsky-Sørensen coefficient (DICE). Рис. 11. Дендрограмма сходства степных фауногенетических комплексов полужесткокрылых Якутии, Минусинской котловины, ПрибайкальЯ и ЗабайкальЯ по коЭффициенту Чекановского-СЪеренсена (DICE).
Fig. 10 in Zoogeographic relationships between true bugs (Heteroptera) in the fauna of relict forest-steppes of the middle taiga subzone of Yakutia and the steppes of southern East Siberia
Fig. 10. True bugs of the steppe complex, found in relict forest-steppe phytocenoses of Central and North-East Yakutia. Foto by N.N. Vinokurov. Рис. 10. Полужесткокрылые степного комплекса реликтовых лесо-степных фитоценоЗов Центральной и Северо-Восточной Якутии. Pentatomomorpha: 10a — Enoplops sibiricus, 10b — Megalotomus ornaticeps, 10c — Rhopalus distinctus, 10d — Stictopleurus sericeus, 11e — Adomerus notatus, 10f — Irochrotus sibiricus, 10h — Sternodontus binodulus, 10i — Aelia frigida, 10j — Aelia sibirica, 10k — Carpocoris coreanus, 10l — Peribalus inclusus. Фото Н.Н. Винокурова.
Fig. 9 in Zoogeographic relationships between true bugs (Heteroptera) in the fauna of relict forest-steppes of the middle taiga subzone of Yakutia and the steppes of southern East Siberia
Fig. 9. True bugs of the steppe complex, found in relict forest-steppe phytocenoses of Central and North-East Yakutia. Foto by N.N. Vinokurov. Рис. 9. Полужесткокрылые степного комплекса реликтовых лесо-степных фитоценоЗов Центральной и Северо-Восточной Якутии. a–g — Cimicomorpha: 9a — Nabis nigrovittatus, 9b — Leptopterna albescens, 9c — Notostira sibirica, 9d — Macrotylus mundulus, 9e — Derephysia foliacea abbreviata, 9f — Lasiacantha haplophylli, 9g — Tingis bianchii; h–l — Pentatomomorpha: 9h — Neides propinquus, 9i — Lygaeosoma sibiricum, 9j — Geocoris mongolicus, 9k — Pionosomus monochrous, 9l — Crophius bermani. Фото Н.Н. Винокурова.
Fig. 8 in Zoogeographic relationships between true bugs (Heteroptera) in the fauna of relict forest-steppes of the middle taiga subzone of Yakutia and the steppes of southern East Siberia
Fig. 8. The relationship of chorological groups within the steppe complex of heteropteran in the middle taiga subzone of Yakutia. Рис. 8. СоотношениЯ хорологических групп степного комплекса полужесткокрылых среднетаежной подЗоны Якутии.
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