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575 results for “taxonomic changes”
FIGURE 4 in Taxonomic changes resulting from a review of the types of Australian Anoplognathini (Coleoptera: Scarabaeidae: Rutelinae) housed in Swedish natural history collections
FIGURE 4. Male paralectotypes (A–F), and female lectotype (G) of Rutela latreillei Schönherr & Gyllenhal, 1817. A, F–G, Dorsal habitus; B, ventral habitus; C, frontal view; D, aedeagus, frontal view; E, aedeagus, lateral view.
FIGURE 3 in Taxonomic changes resulting from a review of the types of Australian Anoplognathini (Coleoptera: Scarabaeidae: Rutelinae) housed in Swedish natural history collections
FIGURE 3. Lectotype females of Rutela olivieri Schönherr & Dalman, 1817 (A–D), Rutela lacunosa Thunberg, 1822 (E–H), and Rutela porosus Dalman, 1817 (I–L). A, E, I, Dorsal habitus; B, F, J, ventral habitus; C, G, K, lateral habitus; D, H, L, frontal view.
FIGURE 1 in Taxonomic changes resulting from a review of the types of Australian Anoplognathini (Coleoptera: Scarabaeidae: Rutelinae) housed in Swedish natural history collections
FIGURE 1. Lectotype females of Anoplognathus brunnipennis (Gyllenhal, 1817) (A–D) and Rutela chloropyga Thunberg, 1822 (E–H). A, E, Dorsal habitus; B, F, ventral habitus; C, G, lateral habitus; D, H, frontal view.
FIGURE 2 in Taxonomic changes resulting from a review of the types of Australian Anoplognathini (Coleoptera: Scarabaeidae: Rutelinae) housed in Swedish natural history collections
FIGURE 2. Lectotype male (A–D) and paralectotype females (E–P) of Anoplognathus flavipennis Boisduval, 1835 [photographs courtesy of MNHN]. A, E, I, M, Dorsal habitus; B, F, J, N, ventral habitus; C, G, K, O, caudal view; D, H, L, P, labels.
Data from: Effects of land-use change on functional and taxonomic diversity of Neotropical bats
Human land-use changes are particularly extensive in tropical regions, representing one of the greatest threats to terrestrial biodiversity and a key research topic in conservation. However, studies considering the effects of different types of anthropogenic disturbance on the functional dimension of biodiversity in human-modified landscapes are rare. Here, we obtained data through an extensive review of peer-reviewed articles and compared 30 Neotropical bat assemblages in well-preserved primary forest and four different human-disturbed habitats in terms of their functional and taxonomic diversity. We found that disturbed habitats that are structurally less similar to primary forest (pasture, cropland and early-stage secondary forest) were characterized by a lower functional and taxonomic diversity, as well as community level-functional uniqueness. These habitats generally retained fewer species that perform different ecological functions compared to higher-quality landscape matrices, such as agroforestry. According to functional trait composition, different bat ensembles respond differently to landscape change, negatively affecting mainly gleaning insectivorous bats in pasture, narrow-range species in cropland, and heavier animalivorous bats in secondary forest. Although our results highlight the importance of higher-quality matrix habitats to support elevated functional and taxonomic bat diversity, the conservation of bat species that perform different ecological functions in the mosaic of human-modified habitats also depends on the irreplaceable conservation value of well-preserved primary forests. Our study based on a pooled analysis of individual studies provides novel insights into the effects of different human-modified habitats on Neotropical bat assemblages.
Data from: Community-wide changes in inter-taxonomic temporal co-occurrence resulting from phenological shifts
Global climate change is known to affect the assembly of ecological communities by altering species' spatial distribution patterns, but little is known about how climate change may affect community assembly by changing species' temporal co-occurrence patterns, which is highly likely given the widely observed phenological shifts associated with climate change. Here we analyzed a 29-year phenological data set comprising community-level information on the timing and span of temporal occurrence in 11 seasonally occurring animal taxon groups from 329 local meteorological observatories across China. We show that widespread shifts in phenology have resulted in community-wide changes in the temporal overlap between taxa that are dominated by extensions, and that these changes are largely due to taxa's altered span of temporal occurrence rather than the degree of synchrony in phenological shifts. Importantly, our findings also suggest that climate change may have led to less phenological mismatch than generally presumed, and that the context under which to discuss the ecological consequences of phenological shifts should be expanded beyond asynchronous shifts.
FIGURE 21 in Taxonomic changes in the emerald moths (Lepidoptera: Geometridae, Geometrinae) of East Asia, with notes on the systematics and phylogeny of Hemitheini
FIGURE 21. Putative phylogeny of the selected genera of Hemitheini. Numbers right of internodes correspond to numbers of apomorphies in Table 1. Position of Aoshakuna Matsumura indicated by bold.
FIGURE 20 in Taxonomic changes in the emerald moths (Lepidoptera: Geometridae, Geometrinae) of East Asia, with notes on the systematics and phylogeny of Hemitheini
FIGURE 20. Distribution of Aoshakuna lucia lucia Thierry-Mieg; (squares) and Aoshakuna lucia ussurica ssp. n. (rings) in Russia and Korea: black symbol – type locality, and white symbols – other collection sites.
FIGURES 6–11 in Taxonomic changes in the emerald moths (Lepidoptera: Geometridae, Geometrinae) of East Asia, with notes on the systematics and phylogeny of Hemitheini
FIGURES 6–11. Aoshakuna lucia Thierry-Mieg, adults. 6–7, Aoshakuna lucia lucia Thierry-Mieg: 6, male; 7, female. 8–11, Aoshakuna lucia ussurica ssp. n.: 8, male; 9, female; 10, head; 11, wing venation.
FIGURES 18–19. Aoshakuna, female genitalia. 18 in Taxonomic changes in the emerald moths (Lepidoptera: Geometridae, Geometrinae) of East Asia, with notes on the systematics and phylogeny of Hemitheini
FIGURES 18–19. Aoshakuna, female genitalia. 18, Aoshakuna lucia lucia Thierry-Mieg; 19, Aoshakuna lucia ussurica ssp. n.
FIGURES 1–5. Jodis orientalis Wehrli. 1 in Taxonomic changes in the emerald moths (Lepidoptera: Geometridae, Geometrinae) of East Asia, with notes on the systematics and phylogeny of Hemitheini
FIGURES 1–5. Jodis orientalis Wehrli. 1, male, syntype; 2, labels on syntype; 3, male genitalia, aedeagus removed; 4, aedeagus; 5, eighth abdominal sternite.
FIGURES 12–17 in Taxonomic changes in the emerald moths (Lepidoptera: Geometridae, Geometrinae) of East Asia, with notes on the systematics and phylogeny of Hemitheini
FIGURES 12–17. Aoshakuna lucia Thierry-Mieg, male genitalia. 12–14, Aoshakuna lucia lucia Thierry-Mieg; 15–17, Aoshakuna lucia ussurica ssp. n. 12, 15, genitalia, aedeagus removed; 13, 16, aedeagus; 14, 17, eighth abdominal sternite.
FIGURES 1–12. Figs. 1–3 in Taxonomic changes and an updated catalogue for the Palaearctic Sericini (Coleoptera: Scarabaeidae: Melolonthinae)
FIGURES 1–12. Figs. 1–3: Maladera lignicolor (Fairmaire) (holotype of Serica tenebrosa Frey: Kuatun [China]); Figs. 4–5: M. verticalis (Fairmaire) (lectotype: "Pekin"[China]); Figs. 6–8: Eumaladera opaciventris (Moser) (syntype: "Seoul Korea / Autoserica opaciventris Type ♂ Mos."); Figs. 9–12: Eumaladera subrugata (Moser) (syntype: "Peking Exp. Stötzner / Autoserica subrugata Type Mos."). Figs. 1, 6, 9: aedeagus, left side lateral view; Figs. 3, 8, 12: aedeagus, right side lateral view; Figs. 2, 4, 7, 10: parameres, dorsal view; Figs. 5, 11: parameres, ventral view. Scale bar = 0.5 mm.
FIGURE 1. Majority consensus tree produced from 70 in The position of the Leptoscelini and other taxonomic changes within the family Coreidae (Hemiptera: Heteroptera)
FIGURE 1. Majority consensus tree produced from 70 equally parsimonious trees during analysis of leptosceline (underlined) and anisosceline genera. Numbers on branches = percentage of trees in which the branch occurs.
FIGURE 20 in The Neotropical genus Titanochrysa (Neuroptera, Chrysopidae): larval descriptions, biological notes, a new species, and taxonomic changes
FIGURE 20. Chrysopa nigripalpis, Lectotype, Museum of Comparative Zoology. A Habitus, dorsal; B. Wings.
FIGURE 18 in The Neotropical genus Titanochrysa (Neuroptera, Chrysopidae): larval descriptions, biological notes, a new species, and taxonomic changes
FIGURE 18. Chrysopa circumfusa, Lectotype, Humboldt-Universität zu Berlin. Upper, Forewing; Lower, Hindwing. Scale applies to both images.
FIGURE 17 in The Neotropical genus Titanochrysa (Neuroptera, Chrysopidae): larval descriptions, biological notes, a new species, and taxonomic changes
FIGURE 17. Chrysopa circumfusa, Lectotype, Humboldt-Universität zu Berlin. Head. A. Frontal; B. Dorsal; C. Lateral; D. Ventrolateral. Scale applies to all images.
FIGURE 19 in The Neotropical genus Titanochrysa (Neuroptera, Chrysopidae): larval descriptions, biological notes, a new species, and taxonomic changes
FIGURE 19. Chrysopa nigripalpis, Lectotype, Museum of Comparative Zoology. A. Head and thorax, dorsal; B. Head and prothorax, dorsal; C. Head, ventral; D. Head, prothorax, lateral.
FIGURE 15 in The Neotropical genus Titanochrysa (Neuroptera, Chrysopidae): larval descriptions, biological notes, a new species, and taxonomic changes
FIGURE 15. Female abdominal and genital characteristics: comparison between (A) Chrysopa annotaria, Lectotype, Museum of Comparative Zoology and (B) Ceraeochrysa pseudovaricosa Allotype, California Academy of Sciences. 1. Abdominal segments 6 to terminus, lateral; B. Spermathecal complex, lateral; C. Subgenitale, ventral. Abbreviations: inv, spermathecal invagination; sg, subgenitale (exterior face); sgb, heavily sclerotized structure with membranous attachment to spermathecal velum and subgenitale, probably the base of the subgenitale; sp, spermatheca; sp.d., spermathecal duct; S7, seventh sternite; T8, eighth tergite. The scales in column A also apply to column B.
FIGURE 11 in The Neotropical genus Titanochrysa (Neuroptera, Chrysopidae): larval descriptions, biological notes, a new species, and taxonomic changes
FIGURE 11. Titanochrysa simpliciala, Holotype, Entomological Collection, University of Minnesota. Male genitalia—gonarcal complex. A. Ventrolateral; B. Ventral; C. Dorsolateral (Note gonapsis.); D. Dorsal; E. Gonapsis, lateral [Note scalloped edge on dorsal margin of distal lobe (right)]. Abbreviations: beak, mediuncal beak; g.a., gonarcal arm; gon, gonarcus; gps, gonapsis; gsa, gonosaccus; gse, gonosetae; lobe, mediuncal lobe; mu, mediuncus; rod, mediuncal rod; s.s., short setae.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.