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306 results for “central Chile”
FIGURES 2–16. 2–7. Coronium petalos n in Description of a new Coronium s. l. (Gastropoda: Muricidae: Trophoninae) from south-central Chile and a brief survey of the genus Coronium Simone, 1996
FIGURES 2–16. 2–7. Coronium petalos n. sp. 2–4. Chile, 37°56.79' S, 74°01.25' W, 608 m, 64.4 mm, holotype MNHNCL-6746. 5–7. Same locality, 45.8 mm, paratype MNHNCL-6747. 8–11. Coronium cf. C. wilhelmense (Ramírez- Bohme, 1981). 8–10. Uruguay, 36°30' S, 53°41 W, 280–300 m, 35 mm, coll. RH. 11. Off Uruguay, crab traps, 300– 500m, 27.3 mm, coll. RH. 12–16. Coronium coronatum (Penna-Neme and Leme, 1978). 12–14. Southeast Brazil, 21°32' S, 40°09' W, 295–300 m, 26.7 mm, coll. RH. 15–16. Brazil, Rio de Janeiro State, off Cabo de São Tomé, 22°34'S, 40°29'W, 213m, sta.ix., holotype MZUSP 18994. Photo courtesy L.R.L. Simone.
FIGURE 2 in Genetic and morphological evidence for a new cryptic species of Ectinogonia (Coleoptera: Buprestidae) from central Chile
FIGURE 2. Distribution, environment and habitat of Ectinogonia cryptica Anguita-Salinas & Zuñiga-Reinoso n. sp. A) Map with the records of E. cryptica.; (B) environment in the locality of Las Comadres; (C) adult of E. cryptica on Colettia sp.
FIGURE 1 in Genetic and morphological evidence for a new cryptic species of Ectinogonia (Coleoptera: Buprestidae) from central Chile
FIGURE 1. Schematic abstract of the results of this study. A) Dorsal view of a paratype specimen of Ectinogonia cryptica Anguita-Salinas & Zuñiga-Reinoso sp. n., from Las Trancas, Ñuble province, bar length 10mm; B) E. crytica aedeagus, dorsal view, bar length 1mm. C) Not rooted NJ tree of the Ectinogonia sequences studied. The numbers over the nodes correspond to bootstrap value expressed in scale 0 to 1.
FIGURE 3 in Deep Divergences within Liolaemus nigroviridis (Squamata, Liolaemidae) Lineages Associated with Sky Islands in Central Chile
FIGURE 3. Mitochondrial gene tree with diversification times (expressed in millions years) above the branches. Gray bars on the nodes represent 95% highest prior density estimates (range in brackets) for the molecular rate. The bar represents the number of substitutions per site.
FIGURE 2 in Deep Divergences within Liolaemus nigroviridis (Squamata, Liolaemidae) Lineages Associated with Sky Islands in Central Chile
FIGURE 2. Unrooted network of L. nigroviridis using cytochrome b sequences with haplotypes depicted according to sampled localities. Size of circles represents the number of individuals per haplotype. Black dots represent mutational steps between haplotypes, and empty circles represent unknown/unsampled haplotypes.
FIGURE 1 in Deep Divergences within Liolaemus nigroviridis (Squamata, Liolaemidae) Lineages Associated with Sky Islands in Central Chile
FIGURE 1. Three-dimensional geographic visualization of the maximum likelihood phylogenetic tree using mitochondrial cytochrome b sequences for L. nigroviridis. Numbers indicate bootstrap values obtained with maximum likelihood (left) and posterior probabilities (right). Each terminal corresponds to sampled localities in the Andes and Coastal Mountains.
Aríbalo de Chile central
Aríbalo de Chile central Source: Objaverse 1.0 / Sketchfab
Supplementary material 1 from: Walter HE, Cádiz-Véliz A, Meriño BM, Villalobos-Barrantes HM, Guerrero PC (2024) Taxonomic dissection based on molecular evidence of the Eriosyce curvispina complex (Cactaceae): identifying nine endemic species from Central Chile. PhytoKeys 237: 117-139. https://doi.org/10.3897/phytokeys.237.107403
New accessions of taxa used in the phylogenetic analyses, including their laboratory code, population locality, and GenBank numbers
Distribution. Llamas are found at 3800-5000 m above sea level in the Central Andes, from C Peru to W Bolivia and N Argentina. Llama distribution reached its apex during the expansion of the Inca Empire (1470-1532 ap), when pack trains were used to carry supplies for the royal armies to S Colombia and C Chile. Although originally indigenous and endemic to South America, Llamas have now been exported to countries around the world as a companion animal, featured in livestock shows, used for trekking and backpacking, cottage industry and home use ofits wool, and in North America increasingly utilized as a guard animal for protecting sheep and goats from canid predators. in Camelidae
Distribution. Llamas are found at 3800-5000 m above sea level in the Central Andes, from C Peru to W Bolivia and N Argentina. Llama distribution reached its apex during the expansion of the Inca Empire (1470-1532 ap), when pack trains were used to carry supplies for the royal armies to S Colombia and C Chile. Although originally indigenous and endemic to South America, Llamas have now been exported to countries around the world as a companion animal, featured in livestock shows, used for trekking and backpacking, cottage industry and home use ofits wool, and in North America increasingly utilized as a guard animal for protecting sheep and goats from canid predators.
FIGURE 6. Eligmodontia dunaris MNHN 1546 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 6. Eligmodontia dunaris MNHN 1546 (holotype): dorsal (A), ventral (B) and lateral (C) views of skull. Occlusal view of upper (F) and lower molars (I) of paratype LCM 3377. Similar views of E. puerulus LCM 1993 (D and G) and E. hirtipes LCM 1748 (E and H) are included for comparisons.
FIGURE 4. Phylogenetic tree for 56 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 4. Phylogenetic tree for 56 Eligmodontia sequences and two outgroups resulting from the maximum-likelihood analysis of 1140 bp of the cytochrome b gene. Model of sequence evolution was HKY+G+I. Numbers above branches show the percentage values from 500 bootstrap iterations, and Bayesian posterior probabilities (>50 values).
FIGURE 3 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 3. Correspondence of G-band patterns between diploid chromosomes from Eligmodontia sp. 2N = 50 (left pair within each trio, large numbers below, male LCM 3374 from Playa Los Choros) and a representative haploid set from Eligmodontia hirtipes 2N = 50 (right, small numbers below, from male LCM 1283).
FIGURE 2 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 2. Chromosomes of Eligmodontia sp. ordered according size, 2N = 50 (male LCM 3374 from Playa Los Choros). From bone marrow spreads stained with standard Giemsa.
FIGURE 1 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 1. Map of southern South America showing localities for previously (numbered) and presently studied Eligmodontia specimens (modified from Mares et al. 2008). Below species names are modal diploid chromosome numbers/FN. New northcentral Chile Eligmodontia sites are marked with an X. Map of the infertile Atacama Desert in dark gray (from Latorre 2002).
FIGURE 5 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 5. Morphological multivariate relationships of Eligmodontia individuals from north-Central Chile and Argentina, and southern Peru. Projections of scores into Principal Component axes I and II were extracted from correlations of four body and eight skull measurements.
FIGURE 7 in A small, new gerbil-mouse Eligmodontia (Rodentia: Cricetidae) from dunes at the coasts and deserts of north-central Chile: molecular, chromosomic, and morphological analyses
FIGURE 7. (A) Eligmodontia dunaris MNHN 1547, paratype (Photo A. Spotorno). (B) Habitat at Playa Los Choros dunes, type locality (Photo C. Zuleta); intensive trapping at the plain belt (top, below sea border) failed to capture any Eligmodontia. (C) Eligmodontia dunaris captured and released alive at Caldera, Atacama, showing bipedal posture (Photo E. Valenzuela by permission).
Figure 6 in Integrative taxonomy reveals a new genus from Central Chile and suggests a systematic rearrangement in Stenochiinae (Coleoptera: Tenebrionidae)
Figure 6. Morphological features of the male of Nestorinus yanettae. A, dorsal view. B, details of pronotum. C, interstice of the elytra. D, aedeagus in dorsal, ventral and lateral view, respectively. Abbreviations: a, parameral alae; b, basal lamina; ls, lateral style.
Figure 7 in Integrative taxonomy reveals a new genus from Central Chile and suggests a systematic rearrangement in Stenochiinae (Coleoptera: Tenebrionidae)
Figure 7. Morphological features of the female of Nestorinus yanettae. A, dorsal view. B, ventral view of female genitalia. Abbreviations: c1b, baculus of coxite 1; c2–c4, coxites; pb, baculus of paraproct. C, spermatheca.
Figure 8 in Integrative taxonomy reveals a new genus from Central Chile and suggests a systematic rearrangement in Stenochiinae (Coleoptera: Tenebrionidae)
Figure 8. Morphological features of the mature larva of Nestorinus yanettae. A, lateral view of mature larva. Abbreviations: as, abdominal spiracle; ms, mesothoracic spiracle. B, last abdominal segments in dorsal and lateral view. Abbreviations: p, processes; u, urogomphi. C, posterior view, showing details of urogomphi.
Figure 5 in Integrative taxonomy reveals a new genus from Central Chile and suggests a systematic rearrangement in Stenochiinae (Coleoptera: Tenebrionidae)
Figure 5. Morphological features of mature larva of Nestorinus roitmani. A, lateral view of mature larva. Abbreviations: as, abdominal spiracle; ms, mesothoracic spiracle. B, details of the head. C, details of mouthparts and prothoracic legs. D, last abdominal segments in dorsal and lateral views. Abbreviations: p, processes; u, urogomphi. E, posterior view, showing details of urogomphi.
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Allen Brain Atlas
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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.