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65 results for “species status assessment”
FIGURES 9 in Revision of the Australian Oenochroma vinaria Guenée, 1858 species-complex (Lepidoptera: Geometridae, Oenochrominae): DNA barcoding reveals cryptic diversity and assesses status of type specimen without dissection
FIGURES 9. Male genitalia. Oenochroma vinaria, Tasmania (genitalia from slide TMAG F4720; aedeagus from gen.prp. ZSM G 13969) (photo CY/AH). Scale bars 2 mm.
FIGURE 19 in Revision of the Australian Oenochroma vinaria Guenée, 1858 species-complex (Lepidoptera: Geometridae, Oenochrominae): DNA barcoding reveals cryptic diversity and assesses status of type specimen without dissection
FIGURE 19. Oenochroma barcodificata sp. nov. mature larva on Grevillea sp. Scale bar 10 mm (photo CY)
FIGURES 13–18 in Revision of the Australian Oenochroma vinaria Guenée, 1858 species-complex (Lepidoptera: Geometridae, Oenochrominae): DNA barcoding reveals cryptic diversity and assesses status of type specimen without dissection
FIGURES 13–18. Egg of Oenochroma barcodificata. sp. nov. 13: anterior pole, scale bar 300 micrometers. 14: micropylar area, scale bar 200 micrometers. 15: whole egg, scale bar 1 mm. 16: aeropyles, scale bar 35 micrometers. 17: chorion on middle top of egg, scale bar 50 micrometers. 18: lateral chorion, scale bar 500 Μm. (photos CY).
FIGURES 10, 11. Female genitalia. 10 in Revision of the Australian Oenochroma vinaria Guenée, 1858 species-complex (Lepidoptera: Geometridae, Oenochrominae): DNA barcoding reveals cryptic diversity and assesses status of type specimen without dissection
FIGURES 10, 11. Female genitalia. 10: Oenochroma barcodificata sp. nov., Tasmania (paratype, DNA barcode LOTSA125-06/06-TASA-00125) (photo CY). 11: Oenochroma vinaria, South Australia (gen. prp. ZSM G 13864) (photo AH). Scale bars 2 mm.
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003). in Muridae
Deccan region, Madras, India. Genus Vandeleuria is masculine, so widely used specific name oleracea has been changed for gender agreement. Vandeleuria oleraceusis possibly a composite of species. Polytypic, but subspecific taxonomy requires reassessment. Distribution. Widespread in S Asia (India, Nepal, Bhutan, Bangladesh, and Sri Lan-ka), S China (W & S Yunnan), and mainland SE Asia N of the Isthmus of Kra. Descriptive notes. Head-body 68 mm, tail 105 mm, ear 13 mm, hindfoot 17 mm; weight 10 g. The Indomalayan Long-tailed Climbing Mouse is small, with flat nail on outer finger and outertoe; tail is slender, brown, twice as long as head-body length, and lacks distal tuft. Dorsal pelageis silky and salmon in color; venter is white, with fulvous hues. Habitat. Tall cane and tangled vines in primary and secondary forest such as bamboo forest, moist deciduous forest, temperate forests, montane wet zone, and disturbed secondary forests, and perhaps agricultural areas at elevations of 150-1500 m. Food and Feeding. Indomalayan [Long-tailed Climbing Mice eat fruits, buds, and flowers. Breeding. Litters of the Indomalayan Long-tailed Climbing Mouse have 3-6 young. Activity patterns. Indomalayan Long-tailed Climbing Mice are arboreal and nocturnal, although one individual was caught duringthe day. Movements, Home range and Social organization. Indomalayan Long-tailed Climbing Mice build nests in tall bushes or cane to rear their young. Status and Conservation. Classified as Least Concern on The IUCN Red Last (as V. olacea). The Indomalayan Long-tailed Climbing Mouse occurs in several habitats and a wide distribution that includes national parks. Further taxonomical studies are required to assess conservation status ofthis potentially diverse species complex. Bibliography. Corbet & Hill (1992), Dang Huy Huynh et al. (1994), Ellerman (1941), Marshall (1977b), Musser & Carleton (2005), Osgood (1932), Phillips (1980), Wang Yingxiang (2003).
FIGURE 5 in A botanical expedition in Eastern Alborz (Iran): rare plant species and assessing their conservation status
FIGURE 5. Distribution map of rare or threatened-endemic species of EasternAlborz. Alcea semnanica (black triangle), Allium barsczewskii (gray triangle) Allium brachyodon (white triangle), Asperula glomerata subsp. filiformis (black star), Asperula gorganica (gray star), Gnaphalium supinum (white star), Leontodon stenocalathius (black square), Leutea glaucopruinosa and Eriocycla ghafooriana (both gray square), Leutea translucens (white square), Linaria orientalis (black polygon), Linaria shahroudensis (gray polygon), Potentilla ghazniensis (white polygon), Tulipa ulophylla (black ellipse), Veronica bungei (gray ellipse) and Veronica longipedicellata (white ellipse). Retrieved from Global Mapper v.22.1.1.
FIGURE 2 in A botanical expedition in Eastern Alborz (Iran): rare plant species and assessing their conservation status
FIGURE 2. Habit of selected threatened-endemic species of Eastern Alborz, A: Myopordon hyrcanum; B: Astragalus megalocystis; C: Astragalus anacamptus; D: Astragalus plagiophacos; E: Cousinia joharchii; F: Jurinea sharifiana.
FIGURE 4 in A botanical expedition in Eastern Alborz (Iran): rare plant species and assessing their conservation status
FIGURE 4. Distribution map of rare or threatened-endemic species of Eastern Alborz. Astragalus nubicola (black triangle), Astragalus olangensis (gray triangle), Astragalus rubrolineatus (white triangle), Cousinia decumbens (black square), Cousinia joharchii (gray square), Corydalis chionophila subsp. firouzii (white square), Crepis frigida (black ellipse), Crepis papposissima (gray ellipse), Echinops shahrudensis (white ellipse), Jurinea sharifiana (black polygon), Oxytropis kordkoyensis (gray polygon), Oxytropis shahvaria (white polygon), Atraphaxis radkanensis (black star), Eritrichium gracillimum (gray star) and Saxifraga koelzii (white star). Retrieved from Global Mapper v.22.1.1.
FIGURE 3 in A botanical expedition in Eastern Alborz (Iran): rare plant species and assessing their conservation status
FIGURE 3. Distribution map and new localities of rare or threatened-endemic species of Eastern Alborz (Damghan-Shahrud). Jurinea boreoiranica (black triangle), Myopordon hyrcanum (gray triangle), Drymocallis damghanensis (black square), Lindelofia stylosa (gray square), Dracocephalum ghahremanii (black star), Silene aminiradii (gray star), Silene orientoalborzensis (gray ellipse), Astragalus anacamptus (black ellipse), Astragalus plagiophacos (black polygon) and Astragalus megalocystis (gray polygon). Retrieved from Global Mapper v.22.1.1.
Data from: Assessing the in situ fertilization status of two marine copepod species, Temora longicornis and Eurytemora herdmani; how common are unfertilized eggs in nature?
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Data from: Improving species distribution models for stream networks by incorporating spatial autocorrelation in multi-sourced datasets: An assessment of Idaho giant salamander status and future risk
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Data from: Assessing current genetic status of the Hainan gibbon using historical and demographic baselines: implications for conservation management of species of extreme rarity
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Supplementary material 1 from: Hawkes PG (2020) A new species in the Tetramorium solidum-group (Hymenoptera, Formicidae, Myrmicinae) from the Richtersveld National Park, South Africa, with an assessment of threats and conservation status. ZooKeys 965: 55-71. https://doi.org/10.3897/zookeys.965.52735
File S1
Figure 2 from: Hawkes PG (2020) A new species in the Tetramorium solidum-group (Hymenoptera, Formicidae, Myrmicinae) from the Richtersveld National Park, South Africa, with an assessment of threats and conservation status. ZooKeys 965: 55-71. https://doi.org/10.3897/zookeys.965.52735
Figure 2 Dorsal view of mesosoma and petiole segments ATetramorium nama sp. nov. holotype worker, CASENT0818990 BT. grandinode, CASENT0818846. (Photos by Peter Hawkes, from www.AntWeb.org)
Figure 1 from: Hawkes PG (2020) A new species in the Tetramorium solidum-group (Hymenoptera, Formicidae, Myrmicinae) from the Richtersveld National Park, South Africa, with an assessment of threats and conservation status. ZooKeys 965: 55-71. https://doi.org/10.3897/zookeys.965.52735
Figure 1 Tetramorium nama sp. nov. A–C holotype worker, CASENT0818990: A full-face view B lateral view C dorsal view D map of Africa (inset, with South Africa shaded dark grey) and detail of South Africa (main image), showing known distribution of Tetramorium nama sp. nov. (black dot), with a white outline indicating the Richtersveld National Park. (Photos by Bradley Reynolds, from www.AntWeb.org)
Figure 3 from: Hawkes PG (2020) A new species in the Tetramorium solidum-group (Hymenoptera, Formicidae, Myrmicinae) from the Richtersveld National Park, South Africa, with an assessment of threats and conservation status. ZooKeys 965: 55-71. https://doi.org/10.3897/zookeys.965.52735
Figure 3 A riverine fringe habitat in which Tetramorium nama sp. nov. was collected, showing living vegetation dominated by Euclea pseudebenus as well as numerous cut Prosopis glandulosa (freshly cut and piles of dry branches) B alluvial terrace gravel and C alluvial fan habitats (in which T. pogonion and T. rufescens were collected) between the river and the rocky mountains to the southwest: the alluvial fan lies between the gravel terrace and the mountains.
FIGURE 12 in Revision of the Australian Oenochroma vinaria Guenée, 1858 species-complex (Lepidoptera: Geometridae, Oenochrominae): DNA barcoding reveals cryptic diversity and assesses status of type specimen without dissection
FIGURE 12. Egg of Oenochroma barcodificata. sp. nov. freshly laid egg, scale bar 1 mm. (photo CY)
Conservation status assessment of banana crop wild relatives using species distribution modelling
<p><strong>Aim: </strong>Crop wild relatives (CWR) are an essential source of genetic material for the improvement of certain traits in related crop species. Despite their importance, increasing public, scientific and political support, large gaps exist in the amount of genetic material collected and conserved of many CWR. Here, we construct a dataset on the distribution of wild banana species (Musa spp.) and assess their risk and conservation status. We deal with the questions (1) what areas are potentially suitable for wild banana species (2) how much of the wild banana diversity is currently at risk or insufficiently conserved ex- and in-situ.</p> <p><span><strong>Location: </strong>Native distribution area of wild banana species, ranging from the northeastern states of India to northeastern Australia.</span></p> <p><span><strong>Methods:</strong> We assessed the potential environmental range of wild species using a species distribution modelling approach with MaxEnt. Extinction risk was evaluated following IUCN criterion B and the <i>ex- </i>and <i>in-situ</i> conservation status was assessed using an indicator for biodiversity and sustainable development targets.</span></p> <p><span><strong>Results:</strong> We found that 11 out of 59 assessed species can be considered as vulnerable and nine as endangered. Highest species richness was found along the border of south China and northern Vietnam, in the northeastern states of India and on the Malayan peninsula. Our distribution modelling approach indicates that the northern Indo-Burmese region has the highest environmental suitability for most wild banana species and that lowland rainforests in general are highly suitable for bananas. Assessment of <i>in</i>- and <i>ex-situ</i> conservation status indicates that 56 out of 59 assessed species are currently insufficiently conserved <i>ex-situ</i> and that 49 are of high priority for further conservation. Additional <i>in-situ</i> conservation is of high priority for six species and of medium priority for 40 species.</span></p> <p><span><strong>Main Conclusions:</strong> To date, little of the banana CWR are sufficiently conserved both <i>in- </i>and <i>ex-situ</i>.</span></p>
Figure 8 in The Simulium vernum group (Diptera: Simuliidae) in Europe: multiple character sets for assessing species status
Figure 8. Neighbour-joining analysis of the Kimura twoparameter (K2P) distances of mitochondrial 16S sequences from Simulium crenobium (Knoz, 1961), Simulium juxtacrenobium Bass & Brockhouse, 1990, and Simulium vernum s.s. Macquart, 1826 in relation to Simulium costatum Friederichs, 1920 and Simulium silvestre (Rubtsov, 1956); AU, Austria; EN, England; FN, Finland; SW, Sweden; samples of S. silvestre are from Canada (Mn, Manitoba) and Wyoming (USA).
Figure 6 in The Simulium vernum group (Diptera: Simuliidae) in Europe: multiple character sets for assessing species status
Figure 6. The IIL chromosome arm of Simulium juxtacrenobium Bass & Brockhouse, 1990 (male larva from Finland, site 5), showing IIL-1ju inversion; Pb, parabalbiani marker; sections 56–59 are omitted.
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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)
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DANDI Archive for NWB datasets
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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.