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3,145 results for “Well Being”
Distribution. Ryukyu Is (Amami-Oshima, Tokunoshima, Okinoerabujima, Okinawajima, Kumejima, Ishigakijima, and Iriomotejima). There is a record of one individual captured on Jeju I (South Korea) regarded as a vagrant as well as an old record from Kii Peninsula (Honshu), but it now to be extinct there. in Miniopteridae
Distribution. Ryukyu Is (Amami-Oshima, Tokunoshima, Okinoerabujima, Okinawajima, Kumejima, Ishigakijima, and Iriomotejima). There is a record of one individual captured on Jeju I (South Korea) regarded as a vagrant as well as an old record from Kii Peninsula (Honshu), but it now to be extinct there.
Integrative taxonomic analysis to reveal the species status of Bombus flavidus, combining COI and nuclear sequencing, wing morphometrics and secretions used for mate attraction as well as patterns of color polymorphism
<p>Bumble bees, due to their morphological monotony and color diversity, have presented difficulties with species delimitation. Recent bumble bee declines have made it ever more imperative to resolve the status of species to address conservation concerns. Some of the taxa found to be most threatened are the often-rare socially parasitic bumble bees, which have additional trophic requirements. Among the socially parasitic bumble bees,<i> Bombus flavidus</i> Eversmann has contentious species status. While multiple separate species allied with <i>Bombus flavidus</i> have been suggested, until recently, recognition of two species, a Nearctic <i>Bombus fernaldae</i> (Franklin) and Palearctic <i>B. flavidus,</i> was favoured. Limited genetic data, however, suggested that even these could be a single widespread species, <i>B. flavidus</i>. We addressed the species status of this lineage using an integrative taxonomic approach, combining <i>COI</i> and nuclear sequencing, wing morphometrics and secretions used for mate attraction. We also explore patterns of color polymorphism that have previously confounded taxonomy in this lineage. Our results support the conspecific status of <i>Bombus fernaldae</i> and <i>Bombus flavidus,</i> however, sampling specimens from across the range of these two taxa revealed a distinct population within this broader species confined to eastern North America. This makes the distribution of the social parasite <i>B. flavidus</i> the broadest of any bumble bee, broader than the known distribution of any non-parasitic bumble bee species. Analysis of color phenotypes revealed that color polymorphisms are retained across the range of the species, but may be influenced by local mimicry complexes. Following these results, <i>Bombus flavidus</i> Eversmann, 1852<i> </i>is synonymized with <i>Bombus fernaldae </i>(Franklin, 1911) <b>syn. nov.</b> and a subspecific status, <i>Bombus flavidus </i><i>appalachiensis</i> <b>ssp. nov.</b>, is assigned to the distinct lineage ranging from the Appalachians to the eastern boreal regions of the United States and far southeastern Canada.</p>
A Machine Learning-Based Method for Classifying Well Test Responses in Naturally Fractured Reservoirs
<p>Complete dataset (raw data), processing codes (MATLAB v2020b) and numerical simulation model (Petrel v2017, ECLIPSE) for clustering of pressure derivatives in Naturally Fractured Reservoirs</p> <p> </p> <p> </p>
How well does molecular simulation reproduce environment-specific conformations of the intrinsically disordered peptides PLP, TP2 and ONEG?
<p>Simulation trajectory dataset to accompany publication:</p> <p>Reid, L.M., Guzzetti, I., Svensson, T., Carlsson, A-C., Su, W., Leek, T., von Sydow, L., Czechtizky, W., Miljak, M., Verma, C., De Maria, L., Essex, J.W., Chem. Sci., 2022, DOI: 10.1039/d1sc03496k</p> <p> </p>
Data from: Emerging wild virus of native grass bioenergy feedstock is well established in the Midwestern USA and associated with premature stand senescence
<p>This dataset includes values for the prevalence of switchgrass mosaic virus (Genus Marafivirus, Family Tymoviridae) detected with molecular diagnostics (RT-PCR) in individual Panicum virgatum (switchgrass) plants and in Graminella leafhoppers that feed on them. Surveys were conducted in 15 sites in August 2012. Stands surveyed had been established for some time and represent a range of landscape contexts. Measures of stand height and percent senescence were also collected. Land cover composition surrounding each site was calculated from the USDA-NASS Cropland Data Layer and estimates of drought impact were derived from the US Drought Monitor.</p>
Supplementary materials to "Brakenhoff et al., Application of time series analysis to estimate drawdown from multiple well fields."
<p>This repository contains the supplementary material that allow to reproduce all the results from the study submitted to Frontiers journal.</p> <p> </p>
Distribution. Papua New Guinea lowlands, although it is likely present on Papua Province side of New Guinea as well. in Vespertilionidae
Distribution. Papua New Guinea lowlands, although it is likely present on Papua Province side of New Guinea as well.
Distribution. Congo Basin in C Africa (S Cameroon, S Central African Republic, DR Congo, Equatorial Guinea, Gabon, and Republic of the Congo). Distribution of this recently recognized speciesis still not well known and the range map is only speculative. in Elephantidae
Distribution. Congo Basin in C Africa (S Cameroon, S Central African Republic, DR Congo, Equatorial Guinea, Gabon, and Republic of the Congo). Distribution of this recently recognized speciesis still not well known and the range map is only speculative.
Viral metagenomics reveals persistent as well as dietary acquired viruses in Antarctic fur seals
<p>Antarctic fur seal virome</p>
Subspecies and Distribution. A.p.pusillusSchreber,1775—coastalSAfrica,fromAngolatoAlgoaBayinSouthAfrica. A. p. doriferus Wood Jones, 1925 — coastal SE Australia, including Kangaroo I, through Victoria and New South Wales, as well as Tasmania and the Bass Strait. in Otariidae
Subspecies and Distribution. A.p.pusillusSchreber,1775—coastalSAfrica,fromAngolatoAlgoaBayinSouthAfrica. A. p. doriferus Wood Jones, 1925 — coastal SE Australia, including Kangaroo I, through Victoria and New South Wales, as well as Tasmania and the Bass Strait.
Distribution. Bahamas, only known from the type locality in East Plana Cay. Introduced into Little Wax Cay in 1973 and on Warderick Wells Cay in 1981, also in Bahamas. in Echimyidae
Distribution. Bahamas, only known from the type locality in East Plana Cay. Introduced into Little Wax Cay in 1973 and on Warderick Wells Cay in 1981, also in Bahamas.
Subspecies and Distribution. C.o.olivaceusSchomburgk,1848—mightberestrictedtotheVenezuelanAmazonBasinfromtheupperRioOrinoco,andthroughouttheOrinocosavannaabovethemouthoftheRioMeta,asfarNandWastheSierradePerijaandtheVenezuelanC.o.dela C.o. (C.o. Range), to the left bank of the Rio Essequibo in W Guyana, in forests of the Guiana Shield; distributional limits separating the two subspecies are not well known. C. o. castaneus 1. Geoffroy Saint-Hilaire, 1851 — Guianas (possibly from the Rio Essequibo in Guyana E through Suriname and French Guiana) and N Brazil, where its distributional limits are not well known but are possibly marked by the rios Negro and Branco and Catrimani (right bank affluent of the Rio Branco) in the W, the Rio Amazonas in the S, and the Atlantic coast in the E, and it also occurs on Caviana and Mexiana Is in the estuary of the Rio Amazonas. Small numbers introduced as pets are now feral on Margarita I off the Venezuelan coast. in Cebidae
Subspecies and Distribution. C.o.olivaceusSchomburgk,1848—mightberestrictedtotheVenezuelanAmazonBasinfromtheupperRioOrinoco,andthroughouttheOrinocosavannaabovethemouthoftheRioMeta,asfarNandWastheSierradePerijaandtheVenezuelanC.o.dela C.o. (C.o. Range), to the left bank of the Rio Essequibo in W Guyana, in forests of the Guiana Shield; distributional limits separating the two subspecies are not well known. C. o. castaneus 1. Geoffroy Saint-Hilaire, 1851 — Guianas (possibly from the Rio Essequibo in Guyana E through Suriname and French Guiana) and N Brazil, where its distributional limits are not well known but are possibly marked by the rios Negro and Branco and Catrimani (right bank affluent of the Rio Branco) in the W, the Rio Amazonas in the S, and the Atlantic coast in the E, and it also occurs on Caviana and Mexiana Is in the estuary of the Rio Amazonas. Small numbers introduced as pets are now feral on Margarita I off the Venezuelan coast.
Subspecies and Distribution. S.s.sciureusLinnaeus,1758—GuianasandNBrazil,NoftheAmazonRiverfromtheriosNegroandDemini(AmazonasState),Etotherivermouth,andSoftheAmazonRiverbetweentheRioXingu-Iriri(ParaState)EtotheRioPindaré(MaranhaoState),extendingStoc.6°SalongtheupperreachesoftheRioXingu. S. s. collins: Osgood, 1916 — N Brazil, Marajo I in the estuary of the Amazon River (Para State), but further studies are needed to identify the extent of its occurrence, which may well be much larger; the identity of the squirrel monkeys on other islands in the Amazon estuary (Gurupa, Caviana, and Mexiana) has yet to be ascertained. in Cebidae
Subspecies and Distribution. S.s.sciureusLinnaeus,1758—GuianasandNBrazil,NoftheAmazonRiverfromtheriosNegroandDemini(AmazonasState),Etotherivermouth,andSoftheAmazonRiverbetweentheRioXingu-Iriri(ParaState)EtotheRioPindaré(MaranhaoState),extendingStoc.6°SalongtheupperreachesoftheRioXingu. S. s. collins: Osgood, 1916 — N Brazil, Marajo I in the estuary of the Amazon River (Para State), but further studies are needed to identify the extent of its occurrence, which may well be much larger; the identity of the squirrel monkeys on other islands in the Amazon estuary (Gurupa, Caviana, and Mexiana) has yet to be ascertained.
Distribution. NW Madagascar, confined to the Lokobe region on Nosy Be. This may or may not be the species that occurred on the island of Nosy Komba as well, but in any case sportive lemurs have not been observed there for several years; in 2007, D. Zinner and coworkers found that some specimens from the mainland had identical mtDNA to that of the type specimen of the Nosy Be Sportive Lemur. in Lepilemuridae
Distribution. NW Madagascar, confined to the Lokobe region on Nosy Be. This may or may not be the species that occurred on the island of Nosy Komba as well, but in any case sportive lemurs have not been observed there for several years; in 2007, D. Zinner and coworkers found that some specimens from the mainland had identical mtDNA to that of the type specimen of the Nosy Be Sportive Lemur.
Distribution. CW Madagascar, known from the type locality, Andramasay, two larger forest fragments N and E of Andramasay, as well as Tsingy de Bemaraha National Park and the adjacent Strict Nature Reserve; it probably occurs throughout the entire area between the Tsiribihina River in the S and the Manambolo Riverin the N, although more research is needed to confirm the limits of its distribution. in Lepilemuridae
Distribution. CW Madagascar, known from the type locality, Andramasay, two larger forest fragments N and E of Andramasay, as well as Tsingy de Bemaraha National Park and the adjacent Strict Nature Reserve; it probably occurs throughout the entire area between the Tsiribihina River in the S and the Manambolo Riverin the N, although more research is needed to confirm the limits of its distribution.
Subspecies and Distribution. E.r.roumanicusBarrett-Hamilton,1900—C&EEurope(EofalinefromOderRivertoNAdriaticSea). E.r.bolkayiV.Martino,1930—Montenegroandadjacentcountries. E.r.drozdovskiiV.Martino&E.Martino,1933—Macedonia,EuropeanTurkey,andadjacentcountries. E.r.nesiotesBate,1906—CreteandIonianandAegeanIs,Greece. E. r. pallidus Ognev, 1928 — SW Russia S to N Caucasus and E to W Siberia. Distributions of most subspecies are not well known. in Erinaceidae
Subspecies and Distribution. E.r.roumanicusBarrett-Hamilton,1900—C&EEurope(EofalinefromOderRivertoNAdriaticSea). E.r.bolkayiV.Martino,1930—Montenegroandadjacentcountries. E.r.drozdovskiiV.Martino&E.Martino,1933—Macedonia,EuropeanTurkey,andadjacentcountries. E.r.nesiotesBate,1906—CreteandIonianandAegeanIs,Greece. E. r. pallidus Ognev, 1928 — SW Russia S to N Caucasus and E to W Siberia. Distributions of most subspecies are not well known.
Distribution. Japan, mainly E Honshu and adjacent islands, as well as isolated populations in W Japan, including W Honshu (Hiwa Town, Kyoto City, and Kii Peninsula), Shikoku (Mt Ishizuchi, Mt Tsurugi, and Mt Ohtaki), and Shodoshima I; W limit of distribution on E Honshu is located across Ishikawa, Gifu, Nagano, and Shizuoka prefectures, where SmallJapanese Mole shows parapatric or mixed distribution with the Large Japanese Mole (M. wogura), a species distributed in W Japan. In Echigo Plain, Niigata Prefecture, the Small Japanese Mole is parapatric with the Echigo Mole (M. etigo). in Talpidae
Distribution. Japan, mainly E Honshu and adjacent islands, as well as isolated populations in W Japan, including W Honshu (Hiwa Town, Kyoto City, and Kii Peninsula), Shikoku (Mt Ishizuchi, Mt Tsurugi, and Mt Ohtaki), and Shodoshima I; W limit of distribution on E Honshu is located across Ishikawa, Gifu, Nagano, and Shizuoka prefectures, where SmallJapanese Mole shows parapatric or mixed distribution with the Large Japanese Mole (M. wogura), a species distributed in W Japan. In Echigo Plain, Niigata Prefecture, the Small Japanese Mole is parapatric with the Echigo Mole (M. etigo).
Data for "Mixed impacts of protected areas and a cash crop boom on human well-being in north-eastern Madagascar"
<p>Dataset (1), codebook (2), explanation of responses (3), and interview protocol (4) for journal article "Mixed impacts of protected areas and a cash crop boom on human well-being in north-eastern Madagascar"<em> People and Nature</em>. DOI: 10.1002/pan3.10377</p> <p>Please note the following.</p> <p>The following variables have been removed from the dataset to guarantee respondents’ anonymity:</p> <p> </p> <p>1.a.2 - Place (place of origin if not born in the village)</p> <p>1.d.1b – Function (function in the village if the respondent has one)</p> <p> </p> <p>The following variable have been removed from the dataset given the few responses collected:</p> <p>4.c – Place_in_forest (places in the forest important to the respondent)</p>
Distribution. NE & E Australia on E Queensland (including Moa, Prince of Wales, Hinchinbrook, Magnetic, Hummock Hill, and Fraser Is) and NE New South Wales, as well as some tentative records from NE, S & SE New Guinea. in Pteropodidae
Distribution. NE & E Australia on E Queensland (including Moa, Prince of Wales, Hinchinbrook, Magnetic, Hummock Hill, and Fraser Is) and NE New South Wales, as well as some tentative records from NE, S & SE New Guinea.
Less-well-developed crustal flow in the central Tibetan Plateau revealed by receiver function and surface wave joint inversion
<p>A crustal flow model has been previously used to explain the crustal extension of the Tibetan Plateau. However, the existence of massive crustal flow in the central plateau is still controversial. We conducted a joint inversion of receiver functions and surface wave dispersions from the 2-D broadband seismic array SANDWICH deployed in the central plateau. The crustal S-wave velocity structure with high vertical resolution shows a low-velocity layer (LVL) in the middle-lower crust beneath most stations. The S-wave velocity of this LVL is mostly within 3.0-3.4 km/s, reflecting a melt volume percentage (MVP) ≤ 7%, except at two stations. Our study suggests that there is not a high enough melt volume in central Tibet to develop crustal flow, which requires an MVP ≥ 7% to decrease rock strength. The formation of extensional structures in the central plateau may contribute to ductile deformation in the middle-lower crust but not crustal flow.</p>
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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.