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535 results for “Stripes”

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zenodo32/100

Fig. 3 in Skeletogenesis and sequence heterochrony in rodent evolution, with particular emphasis on the African striped mouse, Rhabdomys pumilio (Mammalia)

Fig. 3 Cleared and double-stained rodents prepared at the Paläontologisches Institut, Zürich. Left: Octodon degus. Right: Rhabdomys pumilio. Scale: 2 mm

opennotspecifiedMar 2010View details →
zenodo32/100

Fig. 4 in Skeletogenesis and sequence heterochrony in rodent evolution, with particular emphasis on the African striped mouse, Rhabdomys pumilio (Mammalia)

Fig. 4 Ossification of elements of the left hand (respective up- per row) and foot (lower row), in dorsal views, of Rhabdomys pumilio; black = ossified, grey = calcified. Number of specimens examined (N)= 1, except at stages a (N =16), f (6), g (2), n (9), y (4), and z (2)

opennotspecifiedMar 2010View details →
zenodo32/100

Fig. 1 in Skeletogenesis and sequence heterochrony in rodent evolution, with particular emphasis on the African striped mouse, Rhabdomys pumilio (Mammalia)

Fig. 1 Phylogenetic relationships among the species includ- ed in this study, reconstructed from Steppan et al. (2004), Bininda-Emonds et al. (2007), and Blanga-Kanfi et al. (2009)

opennotspecifiedMar 2010View details →
zenodo32/100

Fig. 2 A in Skeletogenesis and sequence heterochrony in rodent evolution, with particular emphasis on the African striped mouse, Rhabdomys pumilio (Mammalia)

Fig. 2 A sample of ontogenetic series prepared for this study at the Paläontologisches Institut und Museum, Zürich. a Cavia porcellus. b Rhabdomys pumilio. c Octodon degus. Scales: 2 mm

opennotspecifiedMar 2010View details →
zenodo32/100

FIGURE 9. Cultived woody bamboos. A–B. Bambusa vulgaris var. vittata, yellow culms with green stripes. B. Guadua angustifolia culms. C in Morphological keys to the genera and species of bamboos (Poaceae: Bambusoideae) of Mexico

FIGURE 9. Cultived woody bamboos. A–B. Bambusa vulgaris var. vittata, yellow culms with green stripes. B. Guadua angustifolia culms. C. Phyllostachys aurea, showing ventricose basal nodes.. D. Phyllostachys bambusoides, diffuse culms. E. Bambusa oldhamii, showing glaucous culms and culm leaves. Photos by E. Ruiz-Sanchez.

opennotspecifiedNov 2015View details →
zenodo32/100

Figure 3 in Striped hyena Hyaena hyaena (Linnaeus 1758): feeding ecology based on den prey remains in a pastoralist landscape, southern Kenya

Figure 3: General and detail view of the (a) Lenkobei basal block of rugged rock outcrops containing (b) many cavities and hideouts, with dispersed bones and scats (credit J.-Ph. Brugal).

opennotspecifiedMay 2024View details →
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Figure 2 in Striped hyena Hyaena hyaena (Linnaeus 1758): feeding ecology based on den prey remains in a pastoralist landscape, southern Kenya

Figure 2: Location of the Hill Den and panorama of the Shompole plains (white car: red arrow). Photo taken from the hilltop where den was located (credit J.-Ph. Brugal).

opennotspecifiedMay 2024View details →
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Figure 1 in Striped hyena Hyaena hyaena (Linnaeus 1758): feeding ecology based on den prey remains in a pastoralist landscape, southern Kenya

Figure 1: Study area and striped hyena dens location (Shompole conservancy). Map realized using Google Earth software. CAD J.-B. Fourvel.

opennotspecifiedMay 2024View details →
zenodo32/100

Figure 7 in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)

Figure 7: Adult roadkilled hyaenas in Batna (Algeria) during the study period on the national road 3: (A) January, (B) December 2018, (C) October 2020, (D) December 2020 (FCB reports).

opennotspecifiedMay 2024View details →
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Figure 6 in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)

Figure 6: Response curves plot generated by MaxEnt that show how each environmental variable affects the MaxEnt prediction: (A) shrubland, (B) slope, (C) built-up areas, (D) distance to roads.

opennotspecifiedMay 2024View details →
zenodo32/100

Figure 5 in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)

Figure 5: Jacknife test for the relative importance of environmental variables in the development of the MaxEnt model for the hyaena.

opennotspecifiedMay 2024View details →
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Figure 4 in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)

Figure 4: Habitat suitability for hyaena in Batna, Algeria. The model is based on occurrence records and seven environmental variables. Warmer colours represent the most suitable habitats. The probability of species occurrence ranges from 0 (unsuitable) to 1 (most suitable).

opennotspecifiedMay 2024View details →
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Figure 2 in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)

Figure 2: Direct sightings of the hyaena in Batna: (A) Natal den with four hyaenas (one adult and three sub-adults) observed in the central south part of Batna (photo: Tahar Mebarki); (B) Hyaena captured on camera trap in northern Batna (photo: Hakim Benmokhtar).

opennotspecifiedMay 2024View details →
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Figure 1 in Understanding habitat suitability and road mortality for the conservation of the striped hyaena (Hyaena hyaena) in Batna (East Algeria)

Figure 1: Map of the study area, showing the location of Batna in Algeria, and the limits of the Belezma National Park (BNP) (ALOS World 3D 30-m DEM. V3.2).

opennotspecifiedMay 2024View details →
dryad32/100

Genomic population structure of striped bass (Morone saxatilis) from the Gulf of St. Lawrence to Cape Fear River

<p>Striped Bass, Morone saxatilis (Walbaum, 1792), is an anadromous fish species that supports fisheries throughout North America and is native to the North American Atlantic Coast. Due to long coastal migrations that span multiple jurisdictions, a detailed understanding of population genomics is required to untangle demographic patterns, understand local adaptation, and characterize population movements. This study used 1256 single nucleotide polymorphism (SNP) loci to investigate genetic structure of 477 Striped Bass sampled from 15 locations spanning the North American Atlantic coast from the Gulf of St. Lawrence, Canada to the Cape Fear River, United States (US). We found striking differences in neutral divergence among Canadian sites, which were isolated from each other and US populations, compared with US populations that were much less isolated. Our SNP dataset was able to assign 99% of Striped Bass back to six reporting groups, a 39% improvement over previous genetic markers. Using this method, we found (1) evidence of admixture within Saint John River, indicating that migrants from the US and from Shubenacadie River occasionally spawn in the Saint John River; (2) Striped Bass collected in the Mira River, Cape Breton, Canada were found to be of both Miramichi River and US origin ; (3) juveniles in the newly restored Kennebec River population had small and nonsignificant differences from the Hudson River; and (4) tributaries within the Chesapeake Bay showed a mixture of homogeny and small differences among each other. This study introduces new hypotheses about the dynamic zoogeography of Striped Bass at its northern range and has important implications for the local and international management of this species.</p>

opencc-zeroApr 2020View details →
zenodo32/100

Figure 3 in Vocal communication in the striped field mouse, Apodemus agrarius, in dyadic encounters and intraspecific cage groups

Figure 3. Examples of the calls resembling clucks: (A) shorter and more rapidly modulated and (B) longer and slightly modulated.

opennotspecifiedFeb 2008View details →
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Figure 2 in Vocal communication in the striped field mouse, Apodemus agrarius, in dyadic encounters and intraspecific cage groups

Figure 2. Harsh calls produced by Apodemus agrarius at (A) threatening postures and (B) harsh calls (the second, third and fifth signals) alternated by calls, resembling clucks (the first and fourth signals).

opennotspecifiedFeb 2008View details →
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Figure 1 in Vocal communication in the striped field mouse, Apodemus agrarius, in dyadic encounters and intraspecific cage groups

Figure 1. Examples of the vocal sounds produced by Apodemus agrarius in response to (A) opponent approach and (B) during attacks and fights.

opennotspecifiedFeb 2008View details →
dryad32/100

Data for: A novel function of banded stripes to prevent cannibalism in snake-eating snakes

<p>Colour pattern are widespread in the animal kingdom and have various functions that play key roles in many ecological interactions. We present a novel function for the evolution of banded stripes in preventing cannibalism in snakes that feed on other snakes—ophiophagy. We first examined the phylogenetic relationship between ophiophagy and banded stripes by categorising pattern types and known diet of 3,568 snake species. We then conducted a series of behavioural predation experiments with California kingsnake (<i>Lampropeltis californiae</i>) morphs, with and without band stripes, and a non- ophiophagous prey species, the corn snake (<i>Elaphe guttata</i>). We found 75% of ophiophagous snakes had banded stripe patterns. Body pattern type and ophiophagy was highly conserved across snake phylogeny, and the evolution of ophiophagy was co-dependent with banded stripe patterns. Our behavioural experiments revealed banded stripes on both inter- and intraspecific prey subjects reduced the probability of predation attempts, and that kingsnakes took longer to strike prey with banded stripes. Overall, the evolution of ophiophagy in snakes appears to be facilitated by the evolution of banded stripe patterns and may help reduce cannibalism in ophiophagous species.</p>

opencc-zeroSep 2021View details →
dryad32/100

Data from: Hypoxia tolerance is unrelated to swimming metabolism of wild, juvenile striped bass (Morone saxatilis)

Open the record for dataset details and reuse information.

publicFeb 2020View details →

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Allen Brain Atlas

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International Brain Laboratory public data

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Last verified 2026-04-29Open record

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