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19,293 results for “western”
Figure 14. Metapenaeus dalli Post larvae I in Larval development of the western school prawn Metapenaeus dalli Racek, 1957 (Crustacea: Decapoda: Penaeidae) reared in the laboratory
Figure 14. Metapenaeus dalli Post larvae I (a) lateral view; (b) first antenna; (c) second antenna; (d) mandible; (e) first maxilla; (f) second maxilla; (g) first maxilliped; (h) second maxilliped; (i) third maxilliped; (j) third pereiopod; (k) fifth pereiopod; (l) pleopods; (m) telson and uropods. Scale bars: a–c, g–m = 0.1 mm; d–f = 0.05 mm.
Figure 7. Metapenaeus dalli Nauplius VI in Larval development of the western school prawn Metapenaeus dalli Racek, 1957 (Crustacea: Decapoda: Penaeidae) reared in the laboratory
Figure 7. Metapenaeus dalli Nauplius VI (a) ventral view; (b) first antenna; (c) second antenna; (d) mandible. Scale bar = 0.1 mm.
Figure 3 in Morphology, natural history and molecular identification of tadpoles of three endemic frog species of Nyctibatrachus Boulenger, 1882 (Anura: Nyctibatrachidae) from Central Western Ghats, India
Figure 3. Tadpole of N. jog, BNHS 5900. (a) Dorsal view; (b) ventral view; (c) lateral view; (d) mouth part (not to scale).
Figure 11 in Environmental influences on movements and distribution of a wild horse (Equus caballus) population in western Nevada, USA: a 25-year study
Figure 11. Relationships of human presence, horse key summer range (KSR) use, and lion numbers in the Montgomery Pass Wild Horse Territory (MPWHT). Human presence (May– September) is presented as per cent of its highest year. Horse KSR use is presented as per cent of the total population using the KSR. Adult lion numbers are presented as the percentage of the maximum single-year lion number.
Figure 6 in Environmental influences on movements and distribution of a wild horse (Equus caballus) population in western Nevada, USA: a 25-year study
Figure 6. Montgomery Pass Wild Horse Territory (MPWHT) horse use of non-key summer range (KSR) areas. Use outside the MPWHT primarily includes areas east of Basalt and west of Adobe Valley.
Figure 5. Changes from 1987 in Environmental influences on movements and distribution of a wild horse (Equus caballus) population in western Nevada, USA: a 25-year study
Figure 5. Changes from 1987 to 2007 in patterns of the geographic distribution of wild horses in the Montgomery Pass Wild Horse Territory (MPWHT). The central, lightly shaded area is the key summer range (KSR). The black mark within it is the highest elevation in the Territory (elevation decreases 360 degrees around it throughout). Dark shaded areas indicate regular horse use and represent> 90% of the population. Many wild horse populations in the intermountain west accommodate to seasonal conditions, spending winter at lower elevations and summer at higher elevations. The pattern across years in the MPWHT changed from summer horse concentration in the KSR to decreasing return to KSR from winter range. In addition to establishment of decreased KSR use and increased year-round use of historical winter-range areas, expansion of the geographic use areas occurred in the latter, including seasonal use beyond MPWHT map boundaries.
Figure 8 in Environmental influences on movements and distribution of a wild horse (Equus caballus) population in western Nevada, USA: a 25-year study
Figure 8. The relationship of key summer range (KSR) horse use and carrying capacity in the context of the Montgomery Pass Wild Horse Territory (MPWHT) horse population. As KSR horse numbers decreased, use outside the KSR increased. Total population range use is presented as a percentage of KSR carrying capacity. As total population increased across years, it remained <80% of carrying capacity for KSR alone, suggesting that considerable population growth can continue without reaching carrying capacity.
Figure 4 in Environmental influences on movements and distribution of a wild horse (Equus caballus) population in western Nevada, USA: a 25-year study
Figure 4. Relationship of mountain lions and foal survival in the Montgomery Pass Wild Horse Territory (MPWHT). Data are based on annual assessment between May and September. The majority of predation occurred in the key summer range (KSR). Adult lion numbers and foal survival in the MPWHT: foal survival is presented as the ratio of currentyear yearlings to previous-year foals expressed as a percentage, lion numbers are for individual lions documented by telemetry, track and/or sighting. The majority of lions were recorded in the KSR.
Figure 3 in Environmental influences on movements and distribution of a wild horse (Equus caballus) population in western Nevada, USA: a 25-year study
Figure 3. Annual total number of horses in the Montgomery Pass wild horse population. Numbers represent reliable estimate for all range areas (not complete enumeration).
Figure 1 in The hermit crab Sympagurus dimorphus (Anomura: Parapaguridae) at the edge of its range in the south-western Atlantic Ocean: population and morphometry features
Figure 1. Sympagurus dimorphus. Densities (number of individuals/100 m2) in the sampling areas from 2002 through 2006. Left column shows presence/absence data including all sampling sites, and right column shows densities on a relative scale.
Figure 3 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 3. Seasonal changes in sea ice concentration, surface chl. a (from satellite) and total mass flux (a), and daylight hours (b) at St. NAPt from October 2010 to September 2012.
Figure 8 in Seasonal changes in the population structure of dominant planktonic copepods collected using a sediment trap moored in the western Arctic Ocean
Figure 8. Seasonal changes in sea ice concentration, daylight hours, chl. a, and total mass flux from January to December (upper panel). The ecological characteristics of the five dominant copepods (lower panel). The open and solid bars indicate the high abundance and reproductive periods for each species, respectively.
Figure 1 in Winter-active wolf spiders (Araneae: Lycosidae) in thermal habitats from western Romania
Figure 1. Map of the surveyed localities with thermal habitats in western Romania (1, Moneasa; 2, Ciocaia; 3, Roşiori; 4, Roşiori/Tămăşeu; 5, Săcuieni I; 6, Săcuieni II; 7, Curtici; 8, Socodor; 9, Chiribiş; 10, Chişlaz; 11, Livada de Bihor; 12, Mădăras; 13, Răbăgani; 14, Sânnicolau de Munte; 15, Tărian; 16, Acâş; 17, Beltiug; 18, Mihăieni; 19, Chiraleu; 20, Oradea; 21, Săcuieni III; 22, Tămăşeu; AR = Arad county, BH = Bihor county, SM = Satu Mare county).
Figure 4 in Description of Ghatiana, a new genus of freshwater crab, with two new species and a new species of Gubernatoriana (Crustacea: Decapoda: Brachyura: Gecarcinucidae) from the Western Ghat Mountains, India
Figure 4. Ghatiana hyacintha sp. nov., holotype male (ZSI, WRC-C.1130). (A) Dorsal view; (B) frontal view; (C) ventral view. Scale bars: 10 mm.
Drone aerial imagery of macroalgae growing in a small embayment at the western end of the Nuussuaq Peninsula in Northwest Greenland
<p>Aerial images of a small embayment at the western tip of the Nuussuaq Peninsula (NW Greenland) were acquired on 10 August 2019 using a DJI Phantom 3 Standard quadcopter drone. The imagery was acquired during the Vaigat Iceberg-Microbial Oil Degradation and Archaeological Heritage Investiga- tion (VIMOA) research cruise. Overlapping images were acquired during two consecutive flights using the 'interval' setting with a period of 5 seconds in the DJI Go app. The drone was flown manually. This drone survey was carried out with two primary objectives in mind: 1) Identify and quantify the macroalgae growing on the coast; 2) Identify any archaeological and cultural heritage sites that may be present. Images were processed using Agisoft PhotoScan Pro (v1.4.4; Linux Ubuntu). Images were aligned using the script CARMA_PhotoScan_Align.py (see this script for settings). After image alignment, the bounding box was visually inspected and the sparse point cloud was thinned using thresholds for the reconstruction uncertainty, projection accuracy, and reprojection error (gradual selection). The remaining tie points in the sparse cloud were then used to build the dense cloud. The settings used for this step can be found in the script CARMA_PhotoScan_GS_DC_v2.py. Next, the dense point cloud was used to generate a digital elevation model (DEM) and, subsequently, an orthomosaic. The Agisoft PhotoScan processing report is also included.</p>
Figs 198–207 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 198–207. Tituboea lefevrei (Pic, 1894): 198 – male (Algeria, 6.6 mm); 199 – head of male; 200 – female (Algeria, 6.5 mm); 201 – head of female; 202 – holotype of Melitonoma lefevrei (female, 5.5 mm); 203 – labels. 204–207 – syntype of Antipa arabica var. palaestina Pic, 1929, male, 6.2 mm: 204 – habitus; 205 – habitus in lateral view; 206 – head; 207 – labels.
Figs 214–222 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 214–222. Tituboea saadensis (Pic, 1894). 214–216 – Syntype of Melitonoma saadensis (female, 4.7 mm): 214 – habitus; 215 – head; 216 – labels. 217–219 – Holotype of Melitonoma saadensis var. sefrensisPic, 1897 (male, 4.2 mm): 217 – habitus; 218 – head; 219 – labels. 220–222 – Possible paratype of Antipa reymondi Kocher, 1956 (male, 5.5 mm): 220 – habitus; 221 – head; 222 – labels.
Figs 165–172. 165–168 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 165–172. 165–168 – Tituboea chobauti (Pic, 1896): 165 – habitus of male (Algeria, 6.1 mm); 166 – habitus of female (Morocco, 5.8 mm); 167 – head of male; 168 – head of female. 169–172 – Tituboea cingulata (Lefèvre, 1883) (syntype, male, 6.7 mm): 169 – habitus; 170 – habitus in lateral view; 171– head; 172 – labels.
Figs 103–111. 103–107 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 103–111. 103–107 – Coptocephala sefrensis Pic, 1897: 103 – habitus of male (6.4 mm); 104 – head of male; 105 – habitus of male (holotype, 5.4 mm); 106 – head of male (holotype); 107 – labels of holotype. 108–111 – Labidostomis centrisculpta Pic, 1920 (syntype of L. alaiensis Pic, 1920, male, 9.9 mm): 108 – habitus; 109 – head; 110 – head in lateral view; 111 – labels.
Figs 46–50 in Identity of species-group taxa of the Western Palaearctic Clytrini (Coleoptera: Chrysomelidae) described by Maurice Pic and Louis Kocher
Figs 46–50. Tituboealefevrei (Pic, 1894): 46 – aedeagus (dorsal and lateral views, from Algeria); 47 – aedeagus (dorsal and lateral views, from Israel); 48 – spermatheca (from Algeria), 49 – spermatheca (from Jordan); 50 – right male protarsus. Scale bars: 1 mm for Fig. 50, 0.5 mm for Figs 46–47, 0.25 mm for Figs 48–49.
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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.