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52 results for “Pastoralism”

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zenodo32/100

Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae

Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).

opennotspecifiedNov 2017View details →
dryad32/100

Diurnal pastoralism does not reduce juvenile recruitment nor elevate allostatic load in spotted hyenas

<p>1. Anthropogenic activity can have substantial effects on wildlife. These effects may vary according to the characteristics of the activity and the species involved. While effects on behavior are well-studied, studies of effects on fitness and physiology are scarce, particularly for group-living species.</p> <p>2. We exploited a natural experimental setup to investigate the effect of diurnal pastoralism on juvenile recruitment and allostatic load in a population of free-ranging spotted hyenas in the Ngorongoro Crater, Tanzania, over a 24-year period.</p> <p>3. Pastoralism was restricted to the territories of two of the eight study clans, allowing us to compare juvenile recruitment in exposed and unexposed clans. We also compared fecal glucocorticoid metabolite concentrations (fGMC) – a biomarker of an organism's allostatic load – between exposed and unexposed clans using 975 fecal samples from 475 hyenas.</p> <p>4. We found no detectable difference in juvenile recruitment nor fGMC between the exposed and unexposed clans, indicating that the pastoralism had no substantial deleterious effect on the spotted hyenas. The lack of a deleterious effect likely stems from the combined effect of the predictable and undisruptive nature of the pastoralism, the socio-ecology of spotted hyenas, and the Ngorongoro Crater's consistently abundant prey.</p> <p>5. Our findings demonstrate that exposure to anthropogenic activity may be compatible with the persistence of certain group-living species, especially if the overlap between the species' critical behaviors and the activity is limited. Our study thereby provides new perspectives for ecologists, conservation biologists, and stakeholders who seek to assess human-wildlife conflicts and balance the needs of local human communities and wildlife.</p>

opencc-zeroSep 2022View details →
zenodo32/100

Flight of Rosy Straling (Pastor roseus Linnaeus, 1758) in District Harnai, Balochistan, Pakistan

<p>Flight of Rosy Straling (Pastor roseus Linnaeus, 1758) in District&nbsp;<br>Harnai, Balochistan, Pakistan</p>

opencc-by-4.0Sep 2024View details →
zenodo32/100

FIGURE 1. Herbarium specimen J.F.B. Pastore & H. Moreira 4067 in Heterophylly and post-fire flowering of Lippia horridula (Verbenaceae): a "phoenix" of Brazilian Cerrado

FIGURE 1. Herbarium specimen J.F.B. Pastore &amp; H. Moreira 4067 (CEN!) selected as epitype for Lippia horridula with presence of both vegetative and reproductive structures.

opennotspecifiedApr 2020View details →
dryad32/100

Data from: Computational research on mobile pastoralism using agent-based modeling and satellite imagery

Dryland pastoralism has long attracted considerable attention from researchers in diverse fields. However, rigorous formal study is made difficult by the high level of mobility of pastoralists as well as by the sizable spatio-temporal variability of their environment. This article presents a new computational approach for studying mobile pastoralism that overcomes these issues. Combining multi-temporal satellite images and agent-based modeling allows a comprehensive examination of pastoral resource access over a realistic dryland landscape with unpredictable ecological dynamics. The article demonstrates the analytical potential of this approach through its application to mobile pastoralism in northeast Nigeria. Employing more than 100 satellite images of the area, extensive simulations are conducted under a wide array of circumstances, including different land-use constraints. The simulation results reveal complex dependencies of pastoral resource access on these circumstances along with persistent patterns of seasonal land use observed at the macro level.

opencc-zeroDec 2015View details →
dryad32/100

Datasets associated with: Late Holocene spread of pastoralism coincides with endemic megafaunal extinction on Madagascar

<p><span>Recently expanded estimates for when humans arrived on Madagascar (up to ~10,000 years ago) highlight questions about the causes of the island's relatively late megafaunal extinctions (~2000-500 years ago). Introduced domesticated animals could have contributed to extinctions, but the arrival times and past diets of exotic animals are poorly known. To conduct the first explicit test of the potential for competition between introduced livestock and extinct endemic megafauna in southern and western Madagascar, we generated new radiocarbon and stable carbon and nitrogen isotope data from the bone collagen of introduced ungulates (zebu cattle, ovicaprids, and bushpigs, n=66) and endemic megafauna (pygmy hippopotamuses, giant tortoises, and elephant birds, n=68) and combined these data with existing data from endemic megafauna (n=282, including giant lemurs). Radiocarbon dates confirm that introduced and endemic herbivores briefly overlapped chronologically in this region between 1000 and 800 calibrated years before present (cal BP). Moreover, stable isotope data suggest that goats, tortoises, and hippos had broadly similar diets or exploited similar habitats. These data support the potential for both direct and indirect forms of competition between introduced and endemic herbivores. We argue that competition with introduced herbivores, mediated by opportunistic hunting by humans and exacerbated by environmental change, contributed to the late extinction of endemic megafauna on Madagascar.</span></p>

opencc-zeroJun 2021View details →
dryad32/100

Data from: Long-term persistence of wildlife populations in a pastoral area

<p>Facilitating coexistence between people and wildlife is a major conservation challenge in East Africa. Some conservation models aim to balance the needs of people and wildlife, but the effectiveness of these models is rarely assessed. Using a case-study approach, we assessed the ecological performance of a pastoral area in northern Tanzania (Manyara Ranch) and established a long-term wildlife population monitoring programme (carried out intermittently from 2003-2008 and regularly from 2011-2019) embedded in a distance sampling framework. By comparing density estimates of the road-transect based long-term monitoring to estimates derived from systematically distributed transects, we found that the bias associated with non-random placement of transects was non-significant. Overall, cattle, and sheep and goat reached the greatest densities and several wildlife species occurred at densities similar (zebra, wildebeest, waterbuck, Kirk's dik-dik) or possibly even greater (giraffe, eland, lesser kudu, Grant's gazelle, Thomson's gazelle) than in adjacent national parks in the same ecosystem. Generalized linear mixed models suggested that most wildlife species (8 out of 14) reached greatest densities during the dry season, that wildlife population densities either remained constant or increased over the 17-year period, that herbivorous livestock species remained constant, while domestic dog population decreased over time. Cross-species correlations did not provide evidence for interference competition between grazing or mixed livestock species and wildlife species but indicate possible negative relationships between domestic dog and warthog populations. Overall, wildlife and livestock populations in Manyara Ranch appear to coexist over the 17-year span. Most likely, this is facilitated by existing connectivity to adjacent protected areas, effective anti-poaching efforts, spatio-temporal grazing restrictions, favourable environmental conditions of the ranch and spatial heterogeneity of surface water and habitats. This long-term case study illustrates the potential of rangelands to simultaneously support wildlife conservation and human livelihood goals if livestock grazing is restricted in space, time and numbers.</p>

opencc-zeroJul 2021View details →
dryad32/100

Large carnivore conservation and traditional pastoralism: An economic analysis on the efficacy of bear-reindeer predation mitigation measures: Dataset for 2014–2016 corralling versus forest treatment analysis

<p>While wildlife and cultural preservation goals can be either complimentary or counteractive, the goals of large carnivore conservation and traditional pastoralist lifestyles are often at odds.  Livestock depredation can negatively impact the economies of livestock herders, while subsequent lethal removals contribute to local carnivore population declines. Here, we collaborated with two Sámi reindeer herding communities (2010–2016) situated in Sweden's boreal forest to evaluate the efficacy and economic feasibility of three brown bear predation mitigation measures: corralling pregnant reindeer during parturition, lethal bear management removals, and public bear-license hunting. Calving corrals increased survival for reindeer calves born to average-sized females by 7% to 15% and by 14% to 30% for calves born to small females. However, the realized cost of implementing calving corrals outweighed the financial gain for both our study areas (net losses ranged between €1,111 and €6,210 per calf saved from bear predation per year when using the updated 2021 calf value), as well as for almost every theoretical scenario we explored (net losses €234 and €13,995 per calf saved from bear predation). The exception was the theoretical scenario where small herding communities overlapped large bear populations, which crossed the breakeven efficacy bear/reindeer ratio of 13.5 bears/100 reindeer and had a potential net gain of €36 per saved calf. Similarly, the cost of lethal management removals of bears also outweighed the potential financial gain from saved calves, with net losses between €75 and €239 per calf. License hunting, where the hunters voluntarily incur the monetary costs of removing bears, is in most cases the only economically viable mitigation measure where the cost of mitigation did not outweigh the financial gain from increased reindeer survival. While the annual public license hunt was the most cost-effective mitigation measure, it may be less biologically effective, i.e., bear hunting occurs in the fall and reindeer parturition the following spring which leaves time for the empty niche of harvested bears to be filled by survivors. Economically and biologically effective predation mitigation measures are key for promoting coexistence, and we suggest that potential mitigation measures should be studied in collaboration with local people.</p>

opencc-zeroMay 2023View details →
dryad32/100

Data from: The effects of pastoral intensification on the feeding interactions of generalist predators in streams

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publicNov 2017View details →
dryad32/100

Datasets associated with: Late Holocene spread of pastoralism coincides with endemic megafaunal extinction on Madagascar

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publicJun 2021View details →
dryad32/100

Diurnal pastoralism does not reduce juvenile recruitment nor elevate allostatic load in spotted hyenas

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publicSep 2022View details →
dryad32/100

Data from: Carbon isotopes of C3 herbs correlate with temperature on removing the influence of precipitation across a temperature transect in the agro-pastoral ecotone of Northern China

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publicNov 2017View details →
dryad32/100

Large carnivore conservation and traditional pastoralism: An economic analysis on the efficacy of bear-reindeer predation mitigation measures: Dataset for 2014–2016 corralling versus forest treatment analysis

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publicMay 2023View details →
dryad32/100

Results of high-performance computing parameter sweeps associated with the Zimbabwe agro-pastoral management model

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publicAug 2020View details →
dryad32/100

Data from: Computational research on mobile pastoralism using agent-based modeling and satellite imagery

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publicApr 2016View details →
dryad32/100

Data from: Long-term persistence of wildlife populations in a pastoral area

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publicJul 2021View details →
zenodo28/100

Figure 2 from: Watanabe MTC, Mota NFO, Pastore M, Santos FMG, Zappi DC (2018) Completing the jigsaw: the first record of the female plant of Daphnopsis filipedunculata (Thymelaeaceae), an endemic species from the Brazilian Amazon. PhytoKeys 109: 93-101. https://doi.org/10.3897/phytokeys.109.28773

Figure 2 Daphnopsisfilipedunculata Nevling &amp; Barringer. A pistillate flowering branch B detail of inflorescence with pistillate flowers C immature fruit with persistent hypanthium D, E mature fruits. Photographs by Fernando M. Santos.

opencc-by-4.0Oct 2018View details →
zenodo28/100

Figure 1 from: Watanabe MTC, Mota NFO, Pastore M, Santos FMG, Zappi DC (2018) Completing the jigsaw: the first record of the female plant of Daphnopsis filipedunculata (Thymelaeaceae), an endemic species from the Brazilian Amazon. PhytoKeys 109: 93-101. https://doi.org/10.3897/phytokeys.109.28773

Figure 1 Daphnopsisfilipedunculata Nevling &amp; Barringer, male individual (A–D) and female individual (E–O). A staminate flowering branch B base of leaf blade C detail of inflorescence with staminate flowers D dissected staminate flower with two whorls of stamens and one pistillode E pistillate flowering branch F detail of inflorescence with three pistillate flowers (fresh material) G detail of inflorescence with five pistillate flowers (dry material) H pistillate flower (dry material) I pistillate flower (fresh material) J Pistil with disc K dissected pistil, longitudinal cut of the ovary showing pendulous ovule L details of the lobed disc in female flower M fruit N seed O embryo. Drawn by João Silveira (A−D modified from Mota and Giulietti 2016) (E, G−H, J−L, N−OWatanabe et al. 485, F, I, MSantos et al. 395 and 396).

opencc-by-4.0Oct 2018View details →
zenodo28/100

Figure 3 from: Watanabe MTC, Mota NFO, Pastore M, Santos FMG, Zappi DC (2018) Completing the jigsaw: the first record of the female plant of Daphnopsis filipedunculata (Thymelaeaceae), an endemic species from the Brazilian Amazon. PhytoKeys 109: 93-101. https://doi.org/10.3897/phytokeys.109.28773

Figure 3 Distribution of Daphnopsisfilipedunculata Nevling &amp; Barringer along the Serra dos Carajás.

opencc-by-4.0Oct 2018View details →
zenodo28/100

Figure 4 from: Watanabe MTC, Mota NFO, Pastore M, Santos FMG, Zappi DC (2018) Completing the jigsaw: the first record of the female plant of Daphnopsis filipedunculata (Thymelaeaceae), an endemic species from the Brazilian Amazon. PhytoKeys 109: 93-101. https://doi.org/10.3897/phytokeys.109.28773

Figure 4 Distribution of Daphnopsisfilipedunculata Nevling &amp; Barringer along the Serra dos Carajás with convex polygon and grids of 4 km2.

opencc-by-4.0Oct 2018View details →

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dandi-nwb
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Last verified 2026-04-30Open record

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.

ibl
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Last verified 2026-04-29Open record

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openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record