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.
605
datasets available to search
ShareScore release 0.9.0
Dataset results
605 results for “conservation implication”
The location of solar farms within England's ecological landscape: implications for biodiversity conservation
<p>Data associated to the article entitled 'The location of solar farms within England's ecological landscape: implications for biodiversity conservation'. </p> <p> </p>
Data from: Species delimitation in endangered groundwater salamanders: implications for aquifer management and biodiversity conservation
Groundwater-dependent species are among the least-known components of global biodiversity, as well as some of the most vulnerable because of rapid groundwater depletion at regional and global scales. The karstic Edwards–Trinity aquifer system of west-central Texas is one of the most species-rich groundwater systems in the world, represented by dozens of endemic groundwater-obligate species with narrow, naturally fragmented distributions. Here, we examine how geomorphological and hydrogeological processes have driven population divergence and speciation in a radiation of salamanders (Eurycea) endemic to the Edwards–Trinity system using phylogenetic and population genetic analysis of genome-wide DNA sequence data. Results revealed complex patterns of isolation and reconnection driven by surface and subsurface hydrology, resulting in both adaptive and non-adaptive population divergence and speciation. Our results uncover new cryptic species diversity and refine the borders of several threatened and endangered species. The U.S. Endangered Species Act has been used to bring state regulation to unrestricted groundwater withdrawals in the Edwards (Balcones Fault Zone) Aquifer, where listed species are found. However, the Trinity and Edwards–Trinity (Plateau) aquifers harbor additional species with similarly small ranges that currently receive no protection from regulatory programs designed to prevent groundwater depletion. Based on regional climate models that predict increased air temperature, together with hydrologic models that project decreased springflow, we conclude that Edwards–Trinity salamanders and other co-distributed groundwater-dependent organisms are highly vulnerable to extinction within the next century.
Data from: Species delimitation in endangered groundwater salamanders: implications for aquifer management and biodiversity conservation
Open the record for dataset details and reuse information.
Fig. 1 in Is the Egyptian fruit-bat Rousettus aegyptiacus a pest in Israel? An analysis of the bat's diet and implications for its conservation
Fig. 1. Monthly mean number of droppings (with standard error bars) of Rousettus aegyptiacus in Nachash and Rakefet caves during 1994 and 1995. Samples collected from three 1 m2 sheets during 48 h each month.
Fig. 7 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 7 (opposite page). Kalloconus canariensis sp. nov. A–B. Holotype (dorsal and ventral views), 89.0 mm (MNCN 15.05/200091H). C. Paratype 1, 85.3 mm (MNCN 15.05/200091P). D. Paratype 5, 76.3 mm (MNCN 15.05/200092). E. Paratype 3, 92.1 mm (MNCN 15.05/200093). F. Paratype 2, 132.0 mm (MNCN 15.05/200094). G. Paratype 4, 93.9 mm (MNCN 15.05/200092). H. Paratype 6, 47.4 mm (MNCN 5.05.200091P). I. Paratype 7, 43.3 mm (MNCN 15.05/200095). J–K. Radular tooth. K. K. canariensis sp. nov., paratype 1. K. K. pulcher ([Lightfoot], 1786), Joal Fadiouth, Senegal (MJT), SL = 96.7 mm. Scale bars = 10 mm unless otherwise indicated
Fig. 8 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 8. Plot of maximum diameter (MD, mm) versus shell length (SL, mm) for K. canariensis sp. nov. (Ɨ) and K. pulcher ([Lightfoot], 1786) (-). The lectotype of K. siamensis (Hwass in Bruguiére, 1792) (A) is also shown.
Fig. 6 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 6 (opposite page). A. Conus navarroi navarroi Rolán, 1986, holotype, 16 mm (MNCN 15.05/1008). B. Africonus angeluquei Tenorio, Abalde & Zardoya, 2018 (= perrineae Cossignani & Fiadeiro, 2018), holotype, 30.0 mm (MNCN 15.05/78710). C. Conus raulsilvai Rolán, Monteiro & Fernandes, 1998, holotype, 19.7 mm (MNCN 15.05/27230). D. Conus regonae Rolán & Trovão, 1990, holotype, 32.7 mm (MNCN 15.05/1092). E. Conus roeckeli Rolán, 1980, holotype, 13.2 mm (MNCN 15.05/1049). F. Africonus salletae Cossignani, 2014, holotype, 15.5 mm (MMM). G. Africonus santaluziensis Cossignani & Fiadeiro, 2015, paratype, 28.1 mm (Paul Kersten coll.). H. Africonus santanaensis Afonso & Tenorio, 2014, holotype, 17.1 mm (MNCN 15.05/60118). I. Conus saragasae Rolán, 1986, holotype, 21.8 mm (MNCN 15.05/1009). J. Africonus verdensis (Trovão, 1979), 22.5 mm (MNCN 15.05/78864). K. Conus vulcanus Tenorio & Afonso, 2004, holotype, 25.2 mm (MNCN 15.05/46652). L. Chelyconus ermineus (Born, 1778), 54.3 mm (MNCN 15.05/80014). M. Genuanoconus genuanus (Linnaeus, 1758), 50.2 mm (MNCN 15.05/78547). N. Kalloconus ateralbus (Kiener, 1850), 40.1 mm (MNCN 15.05/79649). O. Kalloconus byssinus (Röding, 1798), 56.4 mm (MNCN 15.05/90429). Scale bars = 10 mm.
Fig. 2 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 2. Phylogenetic relationships of West African cones and species delimitation. A time tree (relaxed molecular clock) was reconstructed following methods and calibrations in Abalde et al. (2017a). Dates are in million years. Bold names indicate new mitogenomes. A red line indicates the threshold (uncorrected p distance of 0.2%, based on the divergences between Africonus verdensis (Trovão, 1979) and its sister group and Varioconus guanche (Lauer, 1993) and its sister group) for species delimitation.
Fig. 10 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 10 (opposite page). A. Conus ambiguus Reeve, 1844, neotype, 39.3 mm (NBC). B. Conus bellocqae van Rossum, 1996, paratype, 60 mm (F. Gubbioli coll., Marbella, Spain). C. Monteiroconus tabidus (Reeve, 1844), 33.6 mm (MNCN 15.05/78864). D. Conus belairensis Pin & Leung Tack in Pin, 1989, holotype, 36.7 mm (MNHN IM-2000-32668). E. Varioconus bruguieresi (Kiener, 1846) comb. nov., 32.1 mm (MNCN 15.05/78497). F. Varioconus cloveri (Walls, 1978) comb. nov., 23.2 mm (MNCN 15.05/78457). G. Varioconus echinophilus (Petuch, 1975b) comb. nov., 22.0. mm (MNCN 15.05/90430). H. Conus franciscanus Hwass in Bruguière, 1792, lectotype, 56.6 mm (MHNG-MOLL-52625). I. Varioconus franciscanus (Hwass in Bruguière, 1792) comb. nov., 53.6 mm (MNCN 15.05/78491). J. Varioconus franciscanus f. hybridus (Kiener, 1847), 40.0 mm (MNCN 15.05/78427). K. Conus guanche Lauer, 1993, holotype, 34.0 mm (MNHN IM-2000-2553). L. Conus guinaicus Hwass in Bruguière, 1792, lectotype, 43.0 mm (MHNG-MOLL-52638). M. Varioconus guinaicus (Hwass in Bruguière, 1792) comb. nov., 50.2 mm (MNCN 15.05/78443). N. Lautoconus wolof Petuch & Berschauer, 2018, holotype, 21.1 mm (MNHN IM-2000-34015). O. Conus pineaui Pin & Leung Tack in Pin, 1989, holotype, 28.7 mm (MNHN IM-2000-2528). P. Conus dorotheae Monnier & Limpalaër, 2010, holotype, 26.8 mm (MNHN IM-2009-8702). Scale bars = 10 mm.
Fig. 4 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 4 (opposite page). A. Conus felitae Rolán, 1990, holotype, 12.7 mm (MNCN 15.05/1099). B. Africonus fernandesi (Tenorio, Afonso & Rolán, 2008), 14.5 mm (MNCN 15.05/78598). C. Africonus freitasi Tenorio, Afonso, Rolán, Pires, Vasconcelos, Abalde & Zardoya, 2018, holotype, 13.7 mm (MNCN 15.05/200008) D. Conus verdensis furnae Rolán, 1990, holotype, 21.1 mm (MNCN 15.05/1097). E. Africonus fuscoflavus (Röckel, Rolán & Monteiro, 1980), 22.3 mm (MNCN 15.05/80407). F. Conus damottai galeao Rolán, 1990, holotype, 21.3 mm (MNCN 15.05/1093). G. Africonus gonsaloi Afonso & Tenorio, 2014, holotype, 19.3 mm (MNCN 15.05/60119). H. Africonus grahami (Röckel, Cosel & Burnay, 1980), 24.0 mm (MNCN 15.05/78549). I. Conus infinitus Rolán, 1990, holotype, 20.8 mm (MNCN, 15.05/1095). J. Conus isabelarum Tenorio & Afonso, 2004, holotype, 22.8 mm (MNCN 15.05/46654). K. Conus josephinae Rolán, 1980, holotype, 25.8 mm (MNCN 15.05/1050). L. Africonus kersteni (Tenorio, Afonso & Rolán, 2008), holotype, 20.8 mm (MNCN 15.05/47051). M. Africonus longilineus (Röckel, Rolán & Monteiro, 1980), 21.7 mm (MNCN 15.05/79738). N. Africonus lugubris (Reeve, 1849), 14.5 mm (MNCN 15.05/90431). O. Africonus maioensis (Trovão, Rolán & Félix-Alves, 1990), 29.5 mm (MNCN 15.05/78689). P. Africonus miruchae (Röckel, Rolán & Monteiro, 1980), 12.9 mm (MNCN 15.05/79789). Scale bars = 10 mm.
Fig. 3 in New acoustic and molecular data shed light on the poorly known Amazonian frog Adenomera simonstuarti (Leptodactylidae): implications for distribution and conservation
Fig. 3. Preserved male of nominal Adenomera simonstuarti (Angulo & Icochea, 2010) (= genetic lineage 3): call voucher INPA-H 40967 (SVL = 23.4 mm) from the upper Juruá River, in Tarauacá, Brazilian state of Acre. This specimen corresponds to a call voucher (see Fig. 5). A−B. Body in dorsal and ventral views, not to scale. C−D. Detail of the ventral surface of right foot and hand, respectively. Note the nearly solid, dark-colored stripe along the underside of the forearm. Photographs by J. Magnusson. Scale bar = 5 mm.
Figure 1 in Helminth fauna of the invasive American red-eared slider Trachemys scripta in eastern Spain: potential implications for the conservation of native terrapins
Figure 1. Sampling localities of the American red-eared slider, Trachemys scripta in eastern Spain. (A) Protected wetland 'Marjal de Peñíscola'; (B) 'Cabanes-Torreblanca' Natural Park; (C) Protected Landscape 'Desembocadura del Mijares'; (D) Protected wetland 'Marjal de Gandía'; (E) Site of Community Importance 'Marjal de La Safor'.
Supporting data: Grain-dependent responses of mammalian diversity to land-use and the implications for conservation set-aside
<p>Camera trap and live trap datasets underlying the analyses in an <em>Ecological Applications </em>paper (http://onlinelibrary.wiley.com/doi/10.1890/15-1363/abstract), provided in .csv format. Each row consists of a single trap night at a given location, with species in different columns. Old-growth forest, logged forest and oil palm plantation locations have the prefixes "Old", "Log" and "Palm", respectively. Values in each cell are the number of independent captures, as defined in the paper. </p>
Fig. 5 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 5. Nonlinear multidimensional scaling of bird survey data pooled by point-transect. Vectors represent correlations between the ordination and habitat variables. Vectors and Pearson correlation coefficients are plotted for habitat variables with an r2> 0.200 for axis 1.
Fig. 4 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 4. Plots of (A) species and (B) individual rates (from Fig. 1) versus number of species listed by www.birdlife.org (Table 1) per habitat type.
Fig. 1 in Bird Diversity Differs Between Industrial Tree Plantations On Borneo: Implications For Conservation Planning
Fig. 1. Map of forest occurrence in Borneo in 2005 (WWF-Malaysia, 2005) showing the localities of the Sarawak Planted Forest Project and Sabah Softwoods plantation.
Fig. 3 in The vascular plant diversity of Burkina Faso (West Africa) - a quantitative analysis and implications for conservation
Fig. 3. – Origin of introduced plant species in Burkina Faso. The majority of introduced species originates in the Americas.
Fig. 6 in The vascular plant diversity of Burkina Faso (West Africa) - a quantitative analysis and implications for conservation
Fig. 6. – Province species richness in relation to province characteristics. Species richness per province is shown dependent on 4 factors.
Fig. 1 in The vascular plant diversity of Burkina Faso (West Africa) - a quantitative analysis and implications for conservation
Fig. 1. – The provinces of Burkina Faso and their assignment to the phytogeographic zones used in this study. The classification of provinces to the PGZs is modified after WHITE (1983) and GUINKO (1984a). [1: Les Balé; 2: Bam; 3: Banwa; 4: Bazègua. 5: Bougouriba; 6: Boulgou; 7: Boulkiemdé; 8: Ganzourgou; 9: Gnagna; 10: Gourma; 11: Houet; 12: Ioba; 13: Kadiogo; 14: Kénédougou; 15: Comoé; 16: Komandjari; 17: Kompienga; 18: Kossi; 19: Koulpélogo; 20: Kouritenga; 21: Kourwéogo; 22: Léraba; 23: Loroum; 24: Mouhoun; 25: Nahouri; 26: Namentenga; 27: Nayala; 28: Oubritenga; 29: Oudalan; 30: Passoré; 31: Sanguié; 32: Sanmatenga; 33: Séno; 34: Sissili; 35: Soum; 36: Sourou; 37: Tapoa; 38: Tuy; 39: Yagha; 40: Yatenga; 41: Ziro; 42: Zondoma; 43: Zoundwéogo; 44: Poni; 45: Noumbiel]
Genetic diversity of wild and cultivated Coffea canephora in northeastern DR Congo and the implications for conservation - Additional Data
<p>List of wild and cultivated <em>Coffea canephora </em>accessions from northeastern Democratic Republic of the Congo included in Vanden Abeele et al. 2021 - American Journal of Botany, and the corresponding alleles for each of the 18 microsatellite markers (0 indicates missing alleles).</p>
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.