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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 13 in New records of Alvinocarididae (Crustacea: Decapoda: Caridea) from the southwestern Pacific hydrothermal vents, with descriptions of one new genus and three new species
Figure 13. Manuscaris acuminatus gen. et. sp. nov., holotype, male (carapace length 8.4 mm), CBM-ZC 11955. Left mouthparts. (A) Mandible, inner view; (B) maxillule, outer view (coxal endite missing); (C) maxilla, outer view; (D) first maxilliped, outer view; inset, endopod, inner view; (E) left second maxilliped, outer view. Scale bars: 1 mm for C–E; 0.5 m for A, B.
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 2 in Feeding ecology of the common sun skink, Eutropis multifasciata (Reptilia: Squamata: Scincidae), in the plains of central Vietnam
Figure 2. Expected prey-taxon accumulation curves from the data of (A) stomach contents and (B) food item counts consumed by Eutropis multifasciata in the plains of central Vietnam. Circles represent the expected mean values, and the graphs show the 95% confidence intervals for male (filled circles) and female (open circles) skinks.
Figure 3 in You are what you eat: native versus exotic Crotalaria species (Fabaceae) as host plants of the Ornate Bella Moth, Utetheisa ornatrix (Lepidoptera: Erebidae: Arctiinae)
Figure 3. Rates of development of Utetheisa ornatrix larvae on different species of native and exotic Crotalaria in Florida and effect of leaves versus beans in the diet (see text for details): (A) partial development of larvae on the native C. rotundifolia versus exotic C. lanceolata; (B, C) partial development of larvae on the native C. pumila versus exotic C. lanceolata; (D, E) development of larvae on the exotic C. spectabilis/retusa versus exotic C. lanceolata; (F) development of larvae on C. incana (native to U. ornatrix range in the Neotropics, but introduced to Florida) versus exotic C. lanceolata. (F – based on data from Sourakov and Locascio 2013).
Figure 4 in You are what you eat: native versus exotic Crotalaria species (Fabaceae) as host plants of the Ornate Bella Moth, Utetheisa ornatrix (Lepidoptera: Erebidae: Arctiinae)
Figure 4. Fore wing size of Utetheisa ornatrix raised on different species of native and exotic Crotalaria and effect of leaves versus beans in the diet (see text for details): (A) Fore wing size of
Figure 2 in You are what you eat: native versus exotic Crotalaria species (Fabaceae) as host plants of the Ornate Bella Moth, Utetheisa ornatrix (Lepidoptera: Erebidae: Arctiinae)
Figure 2. (A) Understorey of the Florida hammock habitat occupied with invasive exotic Crotalaria spectabilis; (B) a clearing in a secondary Florida habitat, overgrown with exotic Crotalaria pallida; (C, D) mature larvae of U. ornatrix prefer pods of C. spectabilis over leaves; (E) carpenter ants are attracted to the extrafloral nectaries of C. lanceolata; (F, G) larva of U. ornatrix on C. pumila and a pod destroyed by it; (H) mature larva of U. ornatrix inside a pod of C. incana; (I, J) pods of C. pallida are numerous and large and provide ample food and shelter for U. ornatrix; (K) empty pods of C. spectabilis in December with all of their seeds consumed by U. ornatrix larvae; (L) in December, C. retusa becomes the preferred hostplant of U. ornatrix in the C. spectabilis-dominated habitat, when the latter declines; similarly, C. pumila becomes preferred for oviposition in C. lanceolata-dominated habitat; (M) the seeds of C. retusa are well protected by thick walls of the pod; here, a third instar larva is unable to penetrate it; (N) onset of the ultimate instar; (O–Q) prepupa-to-pupa development of U. ornatrix.
Figure 5 in New records of Alvinocarididae (Crustacea: Decapoda: Caridea) from the southwestern Pacific hydrothermal vents, with descriptions of one new genus and three new species
Figure 5. Chorocaris parva sp. nov., paratype, male (carapace length 6.9 mm), CBM-ZC 11940. (A) Anterior part of carapace and cephalic appendages, dorsal view (setae on antennal scale omitted); (B) same, lateral view; (C) endopod of left first pleopod, dorsal view; (D) appendices interna and masculina of left second pleopod, mesial view. Scale bars: 1 mm for A, B; 0.5 mm for C, D.
Figure 8 in New records of Alvinocarididae (Crustacea: Decapoda: Caridea) from the southwestern Pacific hydrothermal vents, with descriptions of one new genus and three new species
Figure 8. Chorocaris variabilis sp. nov., holotype, female (carapace length 13.6 mm), CBM-ZC 11945. Left mouthparts. (A) Mandible, inner view; (B) maxillule, outer view; (C) maxilla, outer view (posterior lobe of scaphognathite broken off); (D) first maxilliped, outer view; (E) left second maxilliped, outer view; inset, epipod and podobranch, inner view. Scale bars: 1 mm.
Figure 4 in New species and records of the Neoserica (sensu stricto) group (Coleoptera: Scarabaeidae: Sericini)
Figure 4. Distribution of Neoserica (s. str.) fanjingshanica, N. (s. str.) grossepunctata, N. (s. str.) lucidifrons, N. (s. str.) phuphanensis, N. (s. str.) shibingensis and N. (s. str.) unicolor.
Figure 1 in You are what you eat: native versus exotic Crotalaria species (Fabaceae) as host plants of the Ornate Bella Moth, Utetheisa ornatrix (Lepidoptera: Erebidae: Arctiinae)
Figure 1. (A) In the wild population of U. ornatrix, adult moth landing on the flower of exotic Crotalaria retusa, Micanopy, Florida; (B) a typical size of a moth from a wild population at Cross Creek, Florida, resulting from larval feeding on C. rotundifolia leaves (top) and its offspring raised in the laboratory on beans of C. spectabilis (bottom) (fore wing length = 20 mm); (C) a single egg batch split in two (experimental and control groups) prior to hatching; (D) hostplant preference test using mature larvae of U. ornatrix inside a tray; (E) differences in pod size and seed volume in six Crotalaria species found in Florida; (F) difference in sprouting rate under similar conditions: native Crotalaria pumila shows much slower sprouting rate than introduced invasive Crotalaria species; (G) upland pine habitat on the University of Florida campus overtaken by thousands of exotic Crotalaria lanceolata plants with a sporadic native C. pumila in the midst (October 2014); (H) U. ornatrix eggs on C. lanceolata; (I) first instar larvae; (J) third instar larva.
Figure 22. Stenothoe valida Dana, 1852 in Minute but constant morphological differences within members of Stenothoidae: the Stenothoe gallensis group with four new members, keys to Stenothoe worldwide, a new species of Parametopa and Sudanea n. gen. (Crustacea: Amphipoda)
Figure 22. Stenothoe valida Dana, 1852, from Gulf of Guinea: Gn 2 female = second gnathopod of female, Gn 2ʹ partly enlarged; P 3, 4 = peraeopod 3, 4; Ep 3 = epimeral plate 3; Us = urosome; U 1, 2, 3 = uropods 1, 2, 3; T = telson.
Figure 8. Stenothoe andamanensis n in Minute but constant morphological differences within members of Stenothoidae: the Stenothoe gallensis group with four new members, keys to Stenothoe worldwide, a new species of Parametopa and Sudanea n. gen. (Crustacea: Amphipoda)
Figure 8. Stenothoe andamanensis n. sp., Andaman Islands: P 7 = peraeopod 7; U 1, 2, 3 male resp. female = uropods; T = telson.
Figure 14. Stenothoe himyara n in Minute but constant morphological differences within members of Stenothoidae: the Stenothoe gallensis group with four new members, keys to Stenothoe worldwide, a new species of Parametopa and Sudanea n. gen. (Crustacea: Amphipoda)
Figure 14. Stenothoe himyara n. sp., Red Sea. A 1, 2 = antennae; Mx 1, 2 = first and second maxillae; Md = mandible; Mxp = maxilliped; Gn 2 = second gnathopod female.
Figure 10 in Redefinition of Nipponbathynella based on the four new species from East Asia (Crustacea: Bathynellacea: Parabathynellidae)
Figure 10. Nipponbathynella donggangensis sp. nov. (♀: holotype). (A) Pleotelson, uropod and furcal rami (lateral); (B) uropod (inner lateral); (C) pleotelson and furcal rami (dorsal). Scale bars = 0.05 mm.
Figure 12 in Redefinition of Nipponbathynella based on the four new species from East Asia (Crustacea: Bathynellacea: Parabathynellidae)
Figure 12. Nipponbathynella wanjuensis sp. nov. (♂: holotype). (A) Maxilla (dorsal); (B) thoracopod I (frontal); (C) left thoracopod II (frontal); (D) ornaments of right thoracopod II (frontal); (E) thoracopod III (frontal). Scale bars = 0.05 mm.
Figure 28. Sudanea inopinata n. g. n in Minute but constant morphological differences within members of Stenothoidae: the Stenothoe gallensis group with four new members, keys to Stenothoe worldwide, a new species of Parametopa and Sudanea n. gen. (Crustacea: Amphipoda)
Figure 28. Sudanea inopinata n. g. n. sp. female, Red Sea: A 1, 2 = antennae; Hd = head; Mx 2 = second maxilla; Md, Md' = mandible of both sides; Mxp = maxilliped; Gn 1 = first gnathopod; Gn 2 = second gnathopod.
Figure 9 in Redefinition of Nipponbathynella based on the four new species from East Asia (Crustacea: Bathynellacea: Parabathynellidae)
Figure 9. Nipponbathynella donggangensis sp. nov. (♀: holotype. ♂: allotype). (A) Thoracopod VI ♀ (frontal); (B) thoracopod VII ♀ (frontal); (C) thoracopod VIII ♂ (lateral); (D) thoracopod VIII ♂ (ventral). Scale bars = 0.05 mm.
ScienceDex guides
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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.