Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
152
datasets available to search
ShareScore release 0.7.1
Dataset results
152 results for “Peromyscus”
Fig. 3 in Peromyscus levipes (Rodentia: Cricetidae)
Fig. 3.—Geographic distribution of Peromyscus levipes. Subspecies are 1, P. l. ambiguus and 2, P. l. levipes. Map modified from Carleton (1989).
Fig. 1.—Adult male Peromyscus levipes from 7.9 in Peromyscus levipes (Rodentia: Cricetidae)
Fig. 1.—Adult male Peromyscus levipes from 7.9 km SW San Salvador el Seco (19°04933.60N and 97°41911.10W), Puebla, Mexico. Photograph by Noe´ Gonza´lez-Ruiz.
Figure 2. A in Mitochondrial Dna Sequence Data Indicate Evidence For Multiple Species Within Peromyscus Maniculatus
Figure 2. A) Phylogenetic tree generated using Bayesian (MrBayes; Huelsenbeck and Ronquist 2001), maximum likelihood (RAxML; Version 8.1.17, Stamatakis 2006), and parsimony methods (PAUP* v. 4.0a165, Swofford 2002) and DNA sequence data from the mitochondrial cytochrome-b gene. The topology depicted is from the Bayesian analysis. Clade probability values (≥ 0.95) for the Bayesian analysis are indicated by an asterisk (*) and are to the left of the first slash, bootstrap values for the maximum likelihood analysis are shown between the two slashes, and bootstrap values obtained from the parsimony analysis are to the right of the last slash. Line at bottom of figure depicts the nucleotide substitution rate per site per million years. B) Same phylogenetic tree as depicted in Figure 2A except unsupported nodes (C, G, and H) were collapsed.
Figure 4. Approximate distributions and associated divergence times for A in Mitochondrial Dna Sequence Data Indicate Evidence For Multiple Species Within Peromyscus Maniculatus
Figure 4. Approximate distributions and associated divergence times for A) Peromyscus maniculatus-like ancestor; B) P. melanotis-like ancestor; C) P. gambelii/keeni/sejugis/sp.-like ancestor; D) P. polionotus-like ancestor; E) P. sonoriensis-like ancestor; F) P. labecula and P. maniculatus - like ancestor; G) P. keeni/sp.-like ancestor; and H) P. keeni-like, P. gambelii-like, P. sejugis-like, and P. sp.-like ancestors. Divergence times were estimated from the BEAST analysis (Version 2.4, Bouckaert et al. 2014) of the mitochondrial cytochrome-b gene dataset (see Fig. 3). Shading schemes that correspond to species distributions are shown in the inset.
Figure 1 in Mitochondrial Dna Sequence Data Indicate Evidence For Multiple Species Within Peromyscus Maniculatus
Figure 1. Distribution of selected populations and species of the Peromyscus maniculatus species group from Canada, Mexico, and the United States. Shaded areas represent distributions of taxa (defined in figure insert) as originally defined by Hall (1981) and modified based on the results of this study. Closed circles represent collecting localities listed in the Appendix; note that multiple individuals may be represented by a single closed circle. White boxes with black stars indicate type localities for each taxon and triangles indicate localities where haplotypes representing P. sonoriensis were found to be in sympatry with samples of P. gambelii and P. labecula, respectively.
Figure 3 in Mitochondrial Dna Sequence Data Indicate Evidence For Multiple Species Within Peromyscus Maniculatus
Figure 3. Time-calibrated ultrametric tree obtained from the BEAST analysis (Version 2.4, Bouckaert et al. 2014) of the mitochondrial cytochrome-b gene dataset. Scale bars at nodes represent the 95% highest posterior densities and numbers associated to each node are the estimated divergence times in million years ago.
Figure 2 in Taxonomy And Phylogenetics Of The Peromyscus Maniculatus Species Group
Figure 2. Maximum parsimony tree derived from sequence variation (ND3/ND4/ND4L) for the northeastern, central and western samples of Peromyscus maniculatus and reference sequences for P. sejugis, P. gambelii, P. keeni, P. polionotus, P. melanotis, and P. leucopus. Numbers associated with the branches are maximum parsimony bootstrap values and Bayesian posterior probabilities. Locality and GenBank references are given in the Materials and Methods.
Peromyscus genome annotation
<p>Genome annotations and predicted proteins and transcripts for Peromyscus attwateri, nudipes, aztecus, melanophrys. </p>
Figure 3 in Intragonadal evaluation of sexual steroid hormones during three reproductive events in two species of Peromyscus (Rodentia: Cricetidae)
Figure 3. Fluctuations of each intraovarian [SSH] in the ∆4 pathway throughout three reproductive events in two species of Peromyscus. Mean concentrations of sexual steroid hormones, [SSH], were obtained from estrous cycle, pregnancy and lactation in free-living, adult females of P. melanotis (A) and P. difficilis (B). Symbology as in Fig. 2. Note that scales differ; complete ANOVA information is available in Table S2.
Figure 1 in Intragonadal evaluation of sexual steroid hormones during three reproductive events in two species of Peromyscus (Rodentia: Cricetidae)
Figure 1. Intraovarian contents of selected ∆ 4 pathway's SSH in two Peromyscus species. Sexual steroid hormones (SSH: progesterone, P4; androstenedione, A; testosterone, T; estradiol, E2) were obtained from free-living, adult females of P. melanotis (A) and P. difficilis (B), during a complete estrous cycle (CEC: proestrus to diestrus), and after ovulation (vertical arrows) followed by fecundation in a successful estrous cycle (SEC: proestrus, estrus + early gestation 1 and late gestation 2 + overall lactation); note that proestrus and estrus data from CEC are duplicated in SEC). The oogenetic and anabolic/ catabolic phases of the ovarian cycle are also depicted (see Table 1).
Fig. 2 in Parasite species co-occurrence patterns on Peromyscus: Joint species distribution modelling
Fig. 2. Results of variance partitioning for variation in ectoparasite prevalence explained by fixed and random effects for each ectoparasite species (columns). Explained variance presented for the constrained model for deer mice (n = 229 individuals). DM, deer mice; RBV, southern red-backed vole; WJM, woodland jumping mouse; PA, population abundance. Population abundance of small mammal species measured as captures per 100 trap nights. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Efficacy of a federally approved flea bait, orally administered to white-footed mice (Peromyscus leucopus), against blood feeding Ixodes scapularis larvae under simulated field conditions
Fig. 2. Representative images of Day 2 and Day 4 capsules observations. Nonengorging larvae attached to Treatment mouse at (A) Day 2 and (B) Day 4. Engorging larvae attached and actively feeding on Control mouse at (C) Day 2 and (D) Day 4. At Day 4, the majority of larvae fed to repletion and detached from the Control mice, while the majority died in situ on the Treatment mice. Green arrows indicate live larvae and red arrows indicate dead larvae. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Efficacy of a federally approved flea bait, orally administered to white-footed mice (Peromyscus leucopus), against blood feeding Ixodes scapularis larvae under simulated field conditions
Fig. 1. Capsule observations via microscopy. (A) Non-engorged (deceased) larvae, (B) engorging larvae, (C) fully engorged (replete) larvae nearing detachment.
Fig. 2 in Peromyscus boylii (Rodentia: Cricetidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of an adult male Peromyscus boylii boylii (Museum of Vertebrate Zoology [MVZ] 156578) from Hopland Field Station, Mendocino County, California (30u009N, 123u059W). Greatest length of skull is 27.3 mm. Photograph by Matina C. Kalcounis- Rueppell.
Fig. 3 in Peromyscus boylii (Rodentia: Cricetidae)
Fig. 3.—Geographic distribution of Peromyscus boylii. Subspecies are: 1, P. b. boylii; 2, P. b. glasselli; 3, P. b. rowleyi; 4, P. b. utahensis. Map redrawn from Carleton (1989) and Bradley and Schmidly (1999) with modifications from Hoffmeister (1986), Cockrum (1982), and Cockrum (1960) for Arizona; Stephens (1906), Jameson and Peeters (1988), and Grinnell (1933) for California; Armstrong (1972), Warren (1910), and Svoboda et al. (1988) for Colorado; Hall (1946) for Nevada; Bailey (1931) and Findley et al. (1975) for New Mexico; Caire et al. (1989) for Oklahoma; Verts and Carraway (1998) and Grinnell (1933) for Oregon; Davis and Schmidly (1994) and Schmidly (1977) for Texas; Durrant (1946), Barnes (1927), and Durrant (1952) for Utah; and Tiemann-Boege et al. (2000) for Mexico. The position of San Pedro Nolasco Island, Gulf of California, Sonora, Mexico (27u589N, 111u249W) is approximate.
Fig. 1 in Peromyscus boylii (Rodentia: Cricetidae)
Fig. 1.—An adult male Peromyscus boylii rowleyi from lower Robertson Creek at the Hastings Natural History Reserve, Monterey County, California (22.5 km southeast of Carmel Valley, 36u229N, 121u229W). Photograph by Matina C. Kalcounis-Rueppell, 27 July 2002.
Fig. 3 in Peromyscus perfulvus (Rodentia: Cricetidae)
Fig. 3.—Geographic distribution of Peromyscus perfulvus in Mexico. Subspecies are: 1, P. perfulvus chysopus; and 2, P. perfulvus perfulvus. Modified from Hall (1981) and Carleton (1989).
Fig. 4 in Peromyscus perfulvus (Rodentia: Cricetidae)
Fig. 4.—Peromyscus perfulvus in elevated vegetation, which is typical for the species. Photograph taken at the Chamela Biological Station, Jalisco, Mexico (19u299510N, 105u029390W, 106 m) by Cornelio Sa´nchez-Herna´ndez.
Fig. 2 in Peromyscus perfulvus (Rodentia: Cricetidae)
Fig. 2.—Dorsal, ventral, and lateral views of skull and lateral view of mandible of adult female Peromyscus perfulvus from 1.5 km sout h of P etembo, M ich oacan, Mexi co (19 u 06.9229 N, 101u29.9799W, 1,227 m; catalog no. 2749, M. L. Romero-Almaraz). Greatest length of skull is 30.45 mm. Photograph by Cornelio Sa´nchez-Herna´ndez.
Fig. 1 in Peromyscus perfulvus (Rodentia: Cricetidae)
Fig. 1.—Peromyscus perfulvus approaching nest located just inside entrance to the Tiamaro Mine, 4 km southeast of Lajas del Bosque, Michoacan, Mexico (19u139430N, 100u289390W, 1,010 m). Photograph by Cornelio Sa´nchez-Herna´ndez.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.