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558 results for “dry forest”
FIGURE 8 in Three new endemic species of Epictia Gray, 1845 (Serpentes: Leptotyphlopidae) from the dry forest of northwestern Peru
FIGURE 8. Type localities of Epictia septemlineata sp. nov. (Red star), Epictia vanwallachi sp. nov. (Green star), Epictia antoniogarciai sp. nov. (Yellow star) and locality of paratypes of Epictia antoniogarciai sp. nov. (Yellow dot) in the Northern Peruvian Andes.
FIGURE 4 in Three new endemic species of Epictia Gray, 1845 (Serpentes: Leptotyphlopidae) from the dry forest of northwestern Peru
FIGURE 4. Holotype of Epictia vanwallachi sp. nov. (CORBIDI 14682). Dorsal view in life (A); Detail of dorsal aspect of head and tail in life (B); Detail of ventral aspect of tail in preservative (C).
FIGURE 2 in Three new endemic species of Epictia Gray, 1845 (Serpentes: Leptotyphlopidae) from the dry forest of northwestern Peru
FIGURE 2. Lateral (A), dorsal (B) and ventral (C) views of head of Holotype of Epictia septemlineata sp. nov. (CORBIDI 14683); Lateral (D), dorsal (E) and ventral (F) views of head of Holotype of Epictia vanwallachi sp. nov. (CORBIDI 14682); Lateral (G), dorsal (H) and ventral (I) views of head of Paratype of Epictia antoniogarciai sp. nov. (ZFMK 90934).
FIGURE 7 in Three new endemic species of Epictia Gray, 1845 (Serpentes: Leptotyphlopidae) from the dry forest of northwestern Peru
FIGURE 7. Habitat and localities of Epictia antoniogarciai sp. nov. Track in the type locality (A); and vicinities of Zapatalgo, Utcubamba Province, Amazonas Region, Peru (B), where the paratypes were collected.
FIGURE 8 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 8. Male holotype of Ameiva concolor (UMMZ 59192): dorsal (A), lateral (B) and ventral (C) views of head, ventral view of cloacal region and right thigh with femoral pores (D).
FIGURE 3 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 3. Maximum clade credibility tree (A) of the Ameiva ameiva-bifrontata-group inferred with BEAST using 866 bp of mitochondrial DNA (concatenated 12S and 16S rRNA). Values above branches are posterior probabilities, outgroup (Holcosus festivus) not shown. Map (B) showing the distribution of A. nodam sp. nov. (red triangles), A. aggerecusans sp. nov (orange squares) and A. concolor (green dots). The stars mark the type localities of A. nodam sp. nov (red), A. aggerecusans sp. nov (orange) and A. concolor (green). The following abbreviations for the locality names are used: LAB = La Balza; PER = Perico; BEL = Bellavista; JGA = Jaén/Gotas de Agua; BAC = Bagua Chica; PUC = Pucará; CUE = Cumba; PUW = Puerto Malleta; ZAP = Zapatalgo; CHA = Chacanto; BAL = Balsas; PPY = Paipoy; CAL = Calemar; VIJ = Vijus; CGL = Chagual; PIA = Pías.
FIGURE 2 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 2. Male holotype of Ameiva nodam sp. nov (CORBIDI 1870) from Bellavista, Cajamarca, Peru in dorsal (A) and ventral (B) view; adult female paratype from Bellavista, Cajamarca, Peru (C); and juvenile paratype (ZFMK 88736) from Bagua Chica, Amazonas, Peru (D). Please note: the depression on the back of the holotype is a bone fracture, which was accidentally caused when the animal was captured.
FIGURE 11 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 11. Principle component analysis plots (PCA-env) representing niche separation of Ameiva aggerecusans and A. concolor (A), A. aggerecusans and A. nodam (B) and A. concolor and A. nodam (C) along the first two axes of the PCA. The solid contour line describes 100% and the dashed line 50% of the available environmental space (background). The density of the occurrences of the species by cell is depicted by the gray shadings. The correlation circles explain the contribution of all 19 climatic variables (BIO1–BIO19, see Appendix II for a more detailed explanation of the variables) on the two PC axes and contains the percentage of variation explained by each axe.
FIGURE 6 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 6. Male holotype of Ameiva aggerecusans sp. nov. (ZFMK 85024) from Balsas, Amazonas, Peru (A); adult female (ZFMK 90861) from Zapatalgo, Amazonas, Peru with dorsal stripe (B); adult male (ZFMK 85010) from Balsas, Amazonas, Peru with a dark, fringed dorsolateral stripe (C); and juvenile (ZFMK 90859) from Balsas, Amazonas, Peru (D); close-up of front leg coloration of ZFMK 85024 (E).
FIGURE 9 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 9. Male holotype of Ameiva concolor (UMMZ 59192) from Paipoy, Cajamarca, Peru (A), photograph by G. Schneider; adult female (ZFMK 91788) from Pías, La Libertad, Peru (B).
FIGURE 5 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 5. Male holotype of Ameiva aggerecusans sp. nov. (ZFMK 85024): dorsal (A), lateral (B) and ventral (C) views of head, ventral aspect of left foot (D), ventral aspect of left hand (E), ventral view of cloacal region and right thigh with femoral pores (F).
FIGURE 1 in Two new endemic species of Ameiva (Squamata: Teiidae) from the dry forest of northwestern Peru and additional information on Ameiva concolor Ruthven, 1924
FIGURE 1. Male holotype of Ameiva nodam sp. nov. (CORBIDI 1870): dorsal (A), lateral (B) and ventral (C) views of head, ventral aspect of left foot (D), ventral aspect of left hand (E), ventral view of cloacal region and right thigh with femoral pores (F).
FIGURES 15–16 in The first schizomid from a dry forest in South America (Arachnida: Schizomida)
FIGURES 15–16. Habitat Where the holotype of S. algodoal sp. nov. Was found. 15 vieW of Within the restinga forest; 16 detail of the microhabitat: dry leaves on the ground covered by thin layer of dune sand bloWn in by the Wind.
FIGURES 9–10 in The first schizomid from a dry forest in South America (Arachnida: Schizomida)
FIGURES 9–10. Surazomus algodoal sp. nov., male holotype, flagellum. 9 dorsal vieW; 10 lateral vieW.
FIGURES 11–13 in The first schizomid from a dry forest in South America (Arachnida: Schizomida)
FIGURES 11–13. Surazomus algodoal sp. nov., male holotype, flagellum. 11 dorsal vieW; 12 ventral vieW; 13 lateral vieW.
FIGURES 1–4 in The first schizomid from a dry forest in South America (Arachnida: Schizomida)
FIGURES 1–4. Surazomus algodoal sp. nov., male holotype. 1 dorsal vieW; 2 prosoma, dorsal vieW; 3 right palp, retrolateral vieW; 4 abdomen, ventral vieW.
FIGURES 5–7 in The first schizomid from a dry forest in South America (Arachnida: Schizomida)
FIGURES 5–7. Surazomus algodoal sp. nov., male holotype. 5 prosoma, dorsal vieW; 6 left leg I, retrolateral vieW; 7 right palp, retrolateral vieW.
Fig. 1 in The Cerambycid Fauna Of The Tropical Dry Forest Of ''El Aguacero,'' Chiapas, México (Coleoptera: Cerambycidae)
Fig. 1. Number of species and individuals of Cerambycidae collected monthly in ''El Aguacero,'' Chiapas, México. Diamonds, number of species obtained during the year of regular sampling; circles, number of species obtained during the year of regular sampling and miscellaneous collections; squares, number of individuals obtained during the year of regular sampling.
Fig. 2 in The Cerambycid Fauna Of The Tropical Dry Forest Of ''El Aguacero,'' Chiapas, México (Coleoptera: Cerambycidae)
Fig. 2. Observed and estimated richness of the cerambycid fauna of ''El Aguacero,'' Chiapas, México. Squares, richness observed; diamonds richness estimated using ICE. The values used were only the data obtained during the year of regular sampling.
Coastal dry tropical forests in Florida and the Caribbean in peril: A review
<p>Coastal dry tropical forests (CDTFs) are important yet vulnerable ecosystems. In this paper, we highlight the special conservation issues facing CDTFs by focusing on one variant of the type, those that occupy limestone substrate in the northeastern Caribbean. Our analysis draws largely from the coastal terrestrial broadleaf forests of the northern Bahamas, the Florida Keys, and southwestern Puerto Rico. Based on surveys of storm surges recorded during major hurricanes during the last 50 years, we define CDTFs as coastal terrestrial broadleaf forests on ground surfaces elevated up to 5 m above sea level and occurring within 5 km of the coast. These forests are not only threatened by land-use change from urbanization but also climate-driven sea level rise (SLR) and hurricanes, which have degraded them and reduced their extent. CDTFs are distinguished from other dry tropical forests by the occasional influence of marine water incursion during periodic storms, requiring species common to these forests to have some level of salt tolerance despite experiencing well-drained, freshwater conditions during most of their life span. With precipitation being the sole freshwater source for most coastal dry tropical forests, SLR and the resulting salinization in the rooting zone subject these forests to increasingly stressful conditions. Hence, even a modest rise in sea level can push numerous imperiled and endangered species and coastal terrestrial broadleaf communities to the edge of their tolerance, causing a decline in extent or their complete disappearance. Outside of protected areas, rapid urbanization has fragmented these forests and reduced their extent, which in turn has modified the interaction between rising seas and forest function. This work emphasizes the need for refined risk assessments to be completed and for conservation measures to be enforced so that resources can be directed appropriately to prevent further loss of coastal dry tropical forests.</p>
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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
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.