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103 results for “Shepherding”
Shepherd's burial NB1K1B12
Krasnodar Territory, Timashevsky District. Necropolis Brick-1. Mound No. 1. Burial №12. Chronology: Bronze Age. Краснодарский край, Тимашевский район. Некрополь Кирпичный-1. Курган №1. Захоронение №12. Хронология: эпоха бронзы. Region Krasnodar, Bezirk Timashevsky. Necropolis Brick-1. Hügel Nr. 1. Begräbnis №12. Chronologie: Bronzezeit. Source: Objaverse 1.0 / Sketchfab
On following pages: 4. Northern Bottlenose Whale (Hyperoodon ampullatus); 5. Southern Bottlenose Whale (Hyperoodon planifrons); 6. Shepherd's Beaked Whale (Tasmacetus shepherd). in Ziphiidae
On following pages: 4. Northern Bottlenose Whale (Hyperoodon ampullatus); 5. Southern Bottlenose Whale (Hyperoodon planifrons); 6. Shepherd's Beaked Whale (Tasmacetus shepherd).
Data from: Genetic evidence for prevalence of alloparental care in a socially monogamous biparental cichlid fish, Perissodus microlepis, from Lake Tanganyika supports the "selfish shepherd effect" hypothesis
Alloparental care – care for unrelated young – is rare in animals, and its ecological or evolutionary advantages or, alternative maladaptive nature, remain unclear. We investigate alloparental care in the socially monogamous cichlid fish Perissodus microlepis from Lake Tanganyika that exhibits bi-parental care. In a genetic parentage analysis, we discovered a surprisingly high percentage of alloparental care represented by brood mixing, extra-pair paternity and extra-pair maternity in all broods that we investigated. The percentage of nondescendant juveniles of other parents, i.e., brood mixing, ranged from 5% to 57% (mean = 28%). The distribution of genetic parentage also suggests that this socially monogamous species has, in fact, polygamous mating system. The prevalence of genetically mixed broods can be best explained by two, not mutually exclusive hypotheses on farming-out and fostering behaviors. In the majority of broods, the sizes of the parents' own (descendant) offspring were significantly larger than those of the adopted (nondescendant) juveniles, supporting the 'selfish shepherd effect' hypothesis, i.e., that foster parents preferentially accept unrelated "smaller or not larger" young since this would tend to lower the predation risks for their own larger offspring. There was also a tendency for larger parents particularly mothers, more so than smaller parents, to care predominantly for their own offspring. Larger parents might be better at defending against cuckoldry and having foreign young dumped into their broods through farming-out behavior. This result might argue for maladaptive effects of allopatric care for the foster parents that only larger and possibly more experienced pairs can guard against. It needs to be determined why, apparently, the ability to recognize one's own young has not evolved in this species.
Good Shepherd: Back to Reality Series
ClinicalTrials.gov study NCT02710019. IPD Sharing: NO. Countries: 1. Publications: 1.
Data from: Gene flow between wolf and shepherd dog populations in Georgia (Caucasus)
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Data from: Genomic signature of successful colonization of Eurasia by the allopolyploid shepherd’s purse (Capsella bursa-pastoris)
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Data from: The shepherds' tale: a genome-wide study across 9 dog breeds implicates two loci in the regulation of fructosamine serum concentration in Belgian shepherds
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Data from: Directed dispersal by rotational shepherding supports landscape genetic connectivity in a calcareous grassland plant
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Data from: Genetic evidence for prevalence of alloparental care in a socially monogamous biparental cichlid fish, Perissodus microlepis, from Lake Tanganyika supports the "selfish shepherd effect" hypothesis
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Data from: Shift in ecological strategy helps marginal populations of shepherd's purse (Capsella bursa-pastoris) to overcome a high genetic load
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SuperDARN grid files used to create the Thomas and Shepherd [2018] statistical convection model
<p>Daily Northern Hemisphere SuperDARN grid files in DataMap format for the years 2010-2016 (inclusive) used to create the <em>Thomas and Shepherd</em> [2018] statistical convection model. Grid files were processed using a modified copy of v4.2 of the Radar Software Toolkit (RST) where the average slant range associated with each grid vector is stored in the 'pwr.median' field.</p> <p>References:</p> <ul> <li>Thomas, E. G., and S. G. Shepherd (2018), Statistical patterns of ionospheric convection derived from mid-latitude, high-latitude, and polar SuperDARN HF radar observations, J. Geophys. Res. Space Physics, 123, 3196-3216, doi:10.1002/2018JA025280.</li> <li>SuperDARN Data Analysis Working Group. Participating members: Thomas, E. G., P. V. Ponomarenko, D. D. Billett, E. C. Bland, A. G. Burrell, K. Kotyk, A. S. Reimer, M. Schmidt, S. G. Shepherd, K. T. Sterne, and M.-T. Walach, (2018), SuperDARN Radar Software Tookit (RST) v4.2, Zenodo, doi:10.5281/zenodo.1403226.</li> </ul>
Figure 5 from: Shepherd B, Phelps TAY, Pinheiro HT, Rocha CR, Rocha LA (2020) Two new species of Plectranthias (Teleostei, Serranidae, Anthiadinae) from mesophotic coral ecosystems in the tropical Central Pacific. ZooKeys 941: 145-161. https://doi.org/10.3897/zookeys.941.50243
Figure 5 Living specimens of APlectranthias hinano sp. nov. at Steinhart Aquarium, California Academy of Sciences BPlectranthias cf. bennetti photographed at a depth of 120 m at Maloelap Atoll, Republic of the Marshall Islands, and CPlectranthias bennetti photographed in an aquarium. Photographs by T Wong (A), LA Rocha (B), and YK Tea (C).
Figure 1 from: Shepherd B, Phelps TAY, Pinheiro HT, Rocha CR, Rocha LA (2020) Two new species of Plectranthias (Teleostei, Serranidae, Anthiadinae) from mesophotic coral ecosystems in the tropical Central Pacific. ZooKeys 941: 145-161. https://doi.org/10.3897/zookeys.941.50243
Figure 1 Plectranthias polygonius sp. nov. holotype A shortly after death B preserved C radiograph, and paratype D shortly after death E preserved F radiograph. Photographs by LA Rocha (A), A Gaisiner (B, E), J Fong (C, F), and T Sinclair-Taylor (D).
Figure 2 from: Shepherd B, Phelps TAY, Pinheiro HT, Rocha CR, Rocha LA (2020) Two new species of Plectranthias (Teleostei, Serranidae, Anthiadinae) from mesophotic coral ecosystems in the tropical Central Pacific. ZooKeys 941: 145-161. https://doi.org/10.3897/zookeys.941.50243
Figure 2 Plectranthias polygonius sp. nov. at Erikub Atoll, Republic of the Marshall Islands, at a depth of 120 m (A), aquarium photos of P. inermis (B), and P. altipinnatus (C). Photographs by LA Rocha (A) and YK Tea (B, C).
Figure 4 from: Shepherd B, Phelps TAY, Pinheiro HT, Rocha CR, Rocha LA (2020) Two new species of Plectranthias (Teleostei, Serranidae, Anthiadinae) from mesophotic coral ecosystems in the tropical Central Pacific. ZooKeys 941: 145-161. https://doi.org/10.3897/zookeys.941.50243
Figure 4 Plectranthias hinano sp. nov. holotype A shortly after death B preserved specimen C radiograph. Photographs by LA Rocha (A), A Gaisiner (B), and J Fong (C).
Figure 3 from: Shepherd B, Phelps TAY, Pinheiro HT, Rocha CR, Rocha LA (2020) Two new species of Plectranthias (Teleostei, Serranidae, Anthiadinae) from mesophotic coral ecosystems in the tropical Central Pacific. ZooKeys 941: 145-161. https://doi.org/10.3897/zookeys.941.50243
Figure 3 Habitat of Plectranthias polygonius sp. nov. and Plectranthias hinano sp. nov. in A Tahiti, French Polynesia, depth of approximately 100 m, and B Erikub Atoll, Republic of the Marshall Islands, depth of approximately 120 m. Photographs by LA Rocha.
Supplementary material 1 from: Salvador RB, Brook FJ, Shepherd LD, Kennedy M (2020) Molecular phylogenetic analysis of Punctoidea (Gastropoda, Stylommatophora). Zoosystematics and Evolution 96(2): 397-410. https://doi.org/10.3897/zse.96.53660
Species identification and stylommatophoran phylogeny
Figure 1 from: Salvador RB, Brook FJ, Shepherd LD, Kennedy M (2020) Molecular phylogenetic analysis of Punctoidea (Gastropoda, Stylommatophora). Zoosystematics and Evolution 96(2): 397-410. https://doi.org/10.3897/zse.96.53660
Figure 1 Bayesian tree for the "Punctoidea", rooted by the Hygrophila. Numbers shown on nodes are BI posterior probabilities (0 to 1) followed by ML bootstrap values (0 to 100%). Scale bar is substitutions per site.
Supplementary material 8 from: Shepherd KA, Lepschi BJ, Johnson EA, Gardner AG, Sessa EB, S. Jabaily R (2020) The concluding chapter: recircumscription of Goodenia (Goodeniaceae) to include four allied genera with an updated infrageneric classification. PhytoKeys 152: 27-104. https://doi.org/10.3897/phytokeys.152.49604
Goodenia Clade A cpDNA (trnL-F, matK) alignment
Supplementary material 11 from: Shepherd KA, Lepschi BJ, Johnson EA, Gardner AG, Sessa EB, S. Jabaily R (2020) The concluding chapter: recircumscription of Goodenia (Goodeniaceae) to include four allied genera with an updated infrageneric classification. PhytoKeys 152: 27-104. https://doi.org/10.3897/phytokeys.152.49604
Goodenia Clade B nrITS alignment
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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