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1,473 results for “Geographic distribution”
FIGURE 4 in Revisiting the circumscription of Chusquea anelythra (Poaceae-Bambusoideae- Bambuseae): lectotypification, redescription, geographic distribution, and conservation status
FIGURE 4. Geographic distribution of Chusquea anelythra in Brazil. Brazilian states: BA (Bahia), ES (Espírito Santo), MG (Minas Gerais), RJ (Rio de Janeiro).
FIGURE 3. Chusquea anelythra. A in Revisiting the circumscription of Chusquea anelythra (Poaceae-Bambusoideae- Bambuseae): lectotypification, redescription, geographic distribution, and conservation status
FIGURE 3. Chusquea anelythra. A. Habitat in Parque Estadual da Serra do Brigadeiro, state of Minas Gerais. B. Scandent habit. C. Flowering branches. D. Detail of the synflorescence, showing the spikelets. E. White waxy band below the node. F. Culm leaf. G‒H. Nodal region. G. Bud complement. H. Central and subsidiary branches. I‒K. Foliage leaves. I‒J. Branches, showing blades and sheath indument in detail. K. Detail of the pseudopetiole, outer ligule, sheath summit extension indument, and a tuft of trichomes at the base of blade. L. Infravaginal branching. (Photos: A‒F by E.M. Pianissola; G‒H and K‒L by L.G. Clark; and I‒J by A.P. Silva)
FIGURE 1 in Revisiting the circumscription of Chusquea anelythra (Poaceae-Bambusoideae- Bambuseae): lectotypification, redescription, geographic distribution, and conservation status
FIGURE 1. Photograph of the lectotype of Chusquea anelythra (Sellow s.n., K - H.965.88-7). Photo by I.L.C. Oliveira.
FIGURE 2 in Revisiting the circumscription of Chusquea anelythra (Poaceae-Bambusoideae- Bambuseae): lectotypification, redescription, geographic distribution, and conservation status
FIGURE 2. Chusquea anelythra (A, C–F) and C. aff. anelythra (B) morphological characters. A. Subsidiary branch bearing a mature synflorescence with subtending bracts and a foliage leaf complement. B. Bud complement with two rows of subsidiary branches (cropped) just developing. C. Culm leaf showing the girdle, infravaginal branching, and the fused base of the sheath. D. Ligular region of a foliage leaf. E. Immature synflorescence. F. Spikelet. [A and F based on Sellow s.n. US 1021552; B based on Clark et al. 673; C–D based on Sarahyba et al. 1057; and E based on Glaziou 17453; the acronym GH refers to Graham Hagan (illustrator)].
FIGURES 52–55 in A review of the Cetoniinae (Coleoptera: Scarabaeidae) from Argentina and adjacent countries: systematics and geographic distributions
FIGURES 52–55. Male parameres: 52, Gymnetis chalcipes (Buenos Aires: Florencio Varela); 53, Gymnetis litigiosa (La Rioja: Los Molinos); 54, Gymnetis hepatica (paratype, Santiago del Estero: Sachayoj); 55, Gymnetis undata.
Subspecies and Distribution. M.a.auriculusBR.H.Baker&Stains,1955-EsideofSierraMadreOrientalfromNuevoLeonintoTamaulipasandVeracruz(Mexico). M. a. apache Hoffmeister & Krutzsch, 1955 — from the mountains of SE Arizona and SW New Mexico (USA) S to Jalisco (Mexico); also in N Coahuila (Mexico). There is a record from Guatemala, but geographic discontinuity and absence of new records in almost 40 years indicates need for taxonomic revision ofthis specimen. in Vespertilionidae
Subspecies and Distribution. M.a.auriculusBR.H.Baker&Stains,1955-EsideofSierraMadreOrientalfromNuevoLeonintoTamaulipasandVeracruz(Mexico). M. a. apache Hoffmeister & Krutzsch, 1955 — from the mountains of SE Arizona and SW New Mexico (USA) S to Jalisco (Mexico); also in N Coahuila (Mexico). There is a record from Guatemala, but geographic discontinuity and absence of new records in almost 40 years indicates need for taxonomic revision ofthis specimen.
Data from: Do genetic drift and gene flow affect the geographic distribution of female plants in gynodioecious Lobelia siphilitica?
<p>Variation in population sex ratio is particularly pronounced in gynodioecious angiosperms. Extremely high female frequencies in gynodioecious populations cannot be readily explained by selective forces alone. To assess the contributions of drift and gene flow to extreme sex-ratio variation, we documented sex ratio and population size in 92 populations of <em>Lobelia siphilitica</em> across its range and genotyped plants using plastid and nuclear genetic markers. Similarity in spatial patterns of genetic and demographic variables may suggest that drift and/or gene flow have contributed to population sex-ratio variation in <em>L. siphilitica</em>. We found strong spatial structuring of extremely high female frequencies: populations with >50% female plants are restricted to the south–central portion of the range. However, we did not detect any spatial structuring in population size nor metrics of genetic diversity, suggesting that extreme variation in female frequency is not strongly affected by drift or gene flow. Extreme sex-ratio variation is frequently observed in gynodioecious plants, but its causes are difficult to identify. Further investigation into mechanisms that create or maintain spatial structure of sex ratios in gynodioecious species will provide much needed insight.</p>
Distribution. Known from two localities in SW Ecuador (El Oro Province); more recently, it has been recorded in the Pacific coast of Colombia (Choco and Valle del Cauca departments), and NW Peru (Tumbes Department). Known distribution is changing as existing specimens from NW South America (listed as S. Lilium parvidens) are reidentified as this species; new geographic and ecological information is being gathered in the process, and it could be locally common at some specific habitats. in Phyllostomidae
Distribution. Known from two localities in SW Ecuador (El Oro Province); more recently, it has been recorded in the Pacific coast of Colombia (Choco and Valle del Cauca departments), and NW Peru (Tumbes Department). Known distribution is changing as existing specimens from NW South America (listed as S. Lilium parvidens) are reidentified as this species; new geographic and ecological information is being gathered in the process, and it could be locally common at some specific habitats.
FIGURE 3 in Geographical and ecological distribution of native bamboo species in San Luis Potosí, Mexico
FIGURE 3. Ordination of the attributes, based on the botanical collection of native bamboo species in the Huasteca Potosina.
FIGURE 2 in Geographical and ecological distribution of native bamboo species in San Luis Potosí, Mexico
FIGURE 2. Dendrogram of the sub-basins of the Huasteca Potosina classified according to the Jaccard Similarity Index by the presence of native bamboo species.
FIGURE 18 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 18. Syntype sheets of Artemisia tangutica var. tomentosa. B. Inset a: portion of a leaf, adaxially viscid-pubescent; inset b: capitula, phyllaries abaxially sparsely pubescent.
FIGURE 17 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 17. Artemisia tainingensis in the wild (China, Sichuan, Dawu County, the type locality). A. Habitat and habit. B. Rhizome and roots. C. Portions of stem (left: distal portion; right: proximal portion). D. Leaves. E. Adaxial side of leaf. F. Abaxial side of leaf. G. Portion of synflorescence. H. Capitula. I. Phyllaries (abaxial side). J. Receptacle. K. Marginal female florets. L. Disk florets.
FIGURE 15 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 15. Specimens of Artemisia somae. S.T. Chiu et al. 3371 (HAST, PE) from Nantou County in Taiwan, China.
FIGURE 11 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 11. Specimens of Artemisia neosinensis (= A. sinensis) misidentified as A. moorcroftiana (A), A. tainingensis (B). A, B. Qinghai-Xizang Exped. 12142 (PE) from Yanyuan County in Sichuan.
FIGURE 14 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 14. Lectotype (A), isolectotype (B), and remaining syntype (C, D) sheets of Artemisia strongylocephala var. sinensis f. virgata. A, B. H. Handel-Mazzetti 3104 (E, WU) from Ninglang County in Yunnan, belonging to A. neosinensis. C. G. Mussot 205 (P) from Kangding County in Sichuan, belonging to A. tangutica var. tomentosa. D. J.A. Soulié 640 (P) from Kangding County in Sichuan, belonging to A. tangutica var. tomentosa.
FIGURE 12 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 12. Specimens of Artemisia neosinensis (= A. sinensis) misidentified as A. tangutica (A), A. kanashiroi (B), A. mattfeldii (C) and A. smithii (D). A. H. Sun & Z.G. Qian 696 (KUN) from Dêqên in Yunnan. B. Gucheng Exped. 530702353 (IMDY) from Yulong County (= Lijiang County) in Yunnan (the type locality of A. neosinensis). C. T.C. Kao 1297 (PEM) from Yulong County in Yunnan (the type locality of A. neosinensis). D. South-to-North Water Diversion Exped. 6325 (PE) from Yulong County in Yunnan (the type locality of A. neosinensis).
FIGURE 10 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 10. Specimens of Artemisia neosinensis (= A. sinensis) misidentified as A. mongolica (A), A. roxburghiana (B), A. imponens (C) and A. divaricata (D). A–C. Qinghai-Xizang Exped. 6011 (CDBI, KUN, PE) from Daocheng County in Sichuan. D. Anonymous 28262 (CDBI) from Litang County in Sichuan.
FIGURE 9 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 9. Specimens of Artemisia neosinensis (= A. sinensis) misidentified as A. moorcroftiana (A, B), A. campbellii (C) and A. orientalihengduangensis (D). A–D. Sichuan Veget. Exped. 2446 (CDBI, KUN) from Daocheng County in Sichuan.
FIGURE 7 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 7. Specimens of Artemisia verlotiorum (A), A. qinlingensis (B), A. lactiflora var. incisa (C) and A. imponens (D) misidentified as A. sinensis (= A. neosinensis). A. T.H. Hsiung & T.L. Chow 92692 (HIB) from Nanchuan County in Chongqing. B. Yellow River Exped. 5950 (KUN) from Yuzhong County in Gansu. C. Z. Zheng 91-46 (KUN) from Zhuxi County in Hubei. D. X.N. Tang et al. 878 (CDBI) from Jiuzhaigou County in Sichuan.
FIGURE 8 in Clarification of morphological characters and geographical distribution of Artemisia neosinensis (Asteraceae, Anthemideae), a strikingly misunderstood species from China
FIGURE 8. Specimens of Artemisia tangutica var. tangutica (A), A. tridactyla (B), A. zayuensis var. zayuensis (C) and A. robusta (D) misidentified as A. sinensis (= A. neosinensis). A. Y.H. Wu et al. 49363 (HNWP) from Huangyuan County in Qinghai. B. X.C. Chen et al. 2988 (HNWP) from Baima County in Qinghai. C. T.T. Yu 20281 (PE) from Gongshan County in Yunnan; inset: portion of a leaf, adaxially viscid-pubescent. D. K.M. Feng 8372 (PE) from Gongshan County in Yunnan.
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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.