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.
59
datasets available to search
ShareScore release 0.7.1
Dataset results
59 results for “recent forests”
Fig. 4 in Ancient divergence and recent population expansion in a leaf frog endemic to the southern Brazilian Atlantic forest
Fig. 4 Extended Bayesian Skyline plots of Phyllomedusa distincta groups: a Northern group and b Southern group. Dashed line represents the median population size (multiply by thousand and by generation time of 1 year) and the lightly shaded gray the 95 % HPD. The accumulation of green lines represents the full posterior distribution. The y-axis is in logarithmic scale
Tropical Forest Monitoring: Challenges and Recent Progress in Research
<p>Data accompanying: </p> <p><em>Remote Sens.</em> <strong>2021</strong>, <em>13</em>(12), 2252; <a href="https://doi.org/10.3390/rs13122252">https://doi.org/10.3390/rs13122252</a></p>
Recent changes in mountain birch forest structure and understory vegetation depend on the seasonal timing of reindeer grazing
Open the record for dataset details and reuse information.
Data from: Yet another empty forest: considering the conservation value of a recently established tropical nature reserve
Open the record for dataset details and reuse information.
Data from: Molecular and iridescent feather reflectance data reveal recent genetic diversification and phenotypic differentiation in a cloud forest hummingbird
Open the record for dataset details and reuse information.
Data from: Of niche differentiation, dispersal ability and historical legacies: what drives woody community assembly in recent Mediterranean forests?
Open the record for dataset details and reuse information.
Recent population differentiation in the habitat specialist Glossy Antshrike (Aves: Thamnophilidae) across Amazonian seasonally flooded forests: Complete matrix
Open the record for dataset details and reuse information.
Recent population differentiation in the habitat specialist Glossy Antshrike (Aves: Thamnophilidae) across Amazonian seasonally flooded forests: Final SNPs dataset
Open the record for dataset details and reuse information.
Figure 1 from: Silva M, Suárez-Villota E, Di-Nizo C, Neves C (2013) First cytogenetic information for Drymoreomys albimaculatus (Rodentia, Cricetidae), a recently described genus from Brazilian Atlantic Forest. ZooKeys 303: 65-76. https://doi.org/10.3897/zookeys.303.4873
Figure 1 - Cytogenetic analyses in Drymoreomys albimaculatus from Santa Virgínia, state of São Paulo, Brazil. A Karyotype of male (2n=62, FN=62), after conventional staining. Inset: sex chromosomes of a female B CBG-banding of a male C GTG-banding of a male D Fluorescent in situ hybridization using telomeric PNA probe over male mitotic plates. Bar scale = 10 μm.
Figure 2 from: Silva M, Suárez-Villota E, Di-Nizo C, Neves C (2013) First cytogenetic information for Drymoreomys albimaculatus (Rodentia, Cricetidae), a recently described genus from Brazilian Atlantic Forest. ZooKeys 303: 65-76. https://doi.org/10.3897/zookeys.303.4873
Figure 2 - Maximum likelihood tree of combined molecular datasets [cytochrome b (Cyt b), interphotoreceptor retinoid binding protein (IRBP)] using Santa Virgínia specimens (UFES2271, UFES2272). Bootstrap nodal support indices and Bayesian posterior probabilities are shown above the branches, respectively. Outgroups include Peromyscus maniculatus (Neotominae); Nyctomys sumichrasti (Tylomyinae), Delomys sublineatus (Sigmodontinae), Thomasomys baeops (Sigmodontinae), and Wiedomys pyrrhorhinos (Sigmodontinae). Available diploid numbers (2n) of clade D are indicated (for details see Table 1), although the lowest diploid number (Nectomys palmipes, 2n= 16, Barros et al. 1992) does not appear in the figure.
Supplementary material 1 from: Cocos D, Klapwijk MJ, Schroeder M (2023) Tree species preference and impact on native species community by the bark beetle Ips amitinus in a recently invaded region. In: Jactel H, Orazio C, Robinet C, Douma JC, Santini A, Battisti A, Branco M, Seehausen L, Kenis M (Eds) Conceptual and technical innovations to better manage invasions of alien pests and pathogens in forests. NeoBiota 84: 349-367. https://doi.org/10.3897/neobiota.84.86586
Ips amitinus description, table S1
Recent bark beetle outbreaks influence wildfire severity in mixed-conifer forests of the Sierra Nevada, California, USA
Open the record for dataset details and reuse information.
Data from: Influence of land use and climate on recent forest expansion: a case study in the Eurosiberian-Mediterranean limit of northwest Spain
Open the record for dataset details and reuse information.
Distribution. Endemic to Chile, with a disjunct distribution in the forests of Chiloé Island, and on the mainland coastal mountains in Nahuelbuta National Park. Evidence of a new population was foud recently at Punta Chan Chan, N of Valdivia. in Canidae
Distribution. Endemic to Chile, with a disjunct distribution in the forests of Chiloé Island, and on the mainland coastal mountains in Nahuelbuta National Park. Evidence of a new population was foud recently at Punta Chan Chan, N of Valdivia.
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence. in Tragulidae
Subspecies and Distribution. H.a.aquaticusOgilby,1841—WAfricafromGuineaandSierraLeonetoGhana. H.a.bates:Lydekker,1906—Nigeria,Cameroon,andpresumablyneighboringcountries. H. a. cottoni Lydekker, 1906 — Republic of the Congo, DR Congo, and presumably Uganda. The Water Chevrotain reportedly has a disjunct distribution, occurring in coastal forests from West Africa and in the rainforests of Central Africa from Nigeria to DR Congo, marginally entering Uganda. It has been listed for the following countries in Central Africa: Angola (Cabinda), Cameroon, Central African Republic, DR Congo, Equatorial Guinea, Gabon, Nigeria, Republic of the Congo, and Uganda (Semliki Valley). A record from Angola's Lunda Norte Province, near the Cassai River,is the southernmost record of the species. The species' status in some countries remains unclear. It is apparently absent from the Republic of Benin and Togo (but the speciesis listed as probable in the Ot Basin in Togo); its supposed occurrence in Guinea Bissau and Senegal remains unsupported by evidence. The species was listed for Sierra Leone, although its presence had been called into question. Photographic evidence seems to clarify that the species occurs in Sierra Leone. In 1850, a specimen was recorded from Gambia, but the present status of the species is unclear. Local people report the species from the Boké Préfecture in NW Guinea, which might be the northernmost area from which the species has been recently reported. Extensive field and market surveys there and in the southern Guinea savanna belt did notfind evidence for the species' presence.
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S). in Atelidae
Subspecies and Distribution. A. g. guariba Humboldt, 1812 — Brazilian Atlantic Forest from the Rio Sao Francisco (although the Rio Paraguacu is the northernmost known locality) to the Rio Doce; however, based on his studies of morphology and pelage color patterns Gregorin in 2006 indicated that it extends from the Rio Paraguacu in Bahia State, S along the coast across the lower Rio Jequitinhonha extending inland somewhat into Minas Gerais State, S through the Rio Doce valley as far the Rio Paraiba do Sul Basin in Rio de Janeiro. A. g. clamitans Cabrera, 1940 — Brazilian Atlantic Forest S of Rio Doce (but Gregorin has recently identified howlers of the upper Rio Doce, Rio Matip6 and Caratinga, and the middle and upper Rio Jequitinhonha as marking the N limits of this subspecies) through the S of Espirito Santo to Rio de Janeiro, Sao Paulo, Parana, Santa Catarina, and Rio Grande do Sulstates (S limit is Rio Camaqua Basin in Rio Grande do Sul, 31° 10" S, where the Atlantic Forest gives way to the Pampas grasslands), and inland in the forested E of Minas Gerais ("Zona da Mata") and the Brazilian Highlands; also in NE Argentina (E of the Mts in Misiones Province to ¢.28° S).
FIGURE 10. A–B. Recently deceased female holotype V0641 in Contributions to the knowledge of Ceroys (Miroceroys) Piza, 1936 (Phasmatodea Heteronemiidae): two new mossy stick insects from the Atlantic Forest of Brazil
FIGURE 10. A–B. Recently deceased female holotype V0641 of Ceroys (Miroceroys) indicattii sp. nov., from Petrópolis, Rio de Janeiro, Brazil. A. Habitus in dorsal view. B. Body in dorsal, lateral and ventral view. Scale bar: 5 mm.
Fig. 2 in Ancient divergence and recent population expansion in a leaf frog endemic to the southern Brazilian Atlantic forest
Fig. 2 Possible demographic models of the diversification of Phyllomedusa distincta in the southern Brazilian Atlantic forest used in the approximate Bayesian computation analysis. Model parameters: θ= 4 Neμ of ancestral (A), Northern (N), and Southern (S) groups (see text for details); m =2 Nm with arrow indicating direction of migration (IMa2
Fig. 1 in Ancient divergence and recent population expansion in a leaf frog endemic to the southern Brazilian Atlantic forest
Fig. 1 Geographic distribution of Phyllomedusa distincta in the Southern Brazilian Atlantic forest (a) and mitochondrial haplotype genealogy derived from ND2 sequences (b). Sampling localities and haplotype numbers are indicated (see Table 1). The circle area of each haplotype is proportional to its frequency. Mutations are edges. Percentages indicate pairwise distance between haplogroups. Brazilian states: SP São Paulo, PR Paraná, SC Santa Catarina, RS Rio Grande do Sul
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.