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.
247
datasets available to search
ShareScore release 0.9.0
Dataset results
247 results for “forest types”
FIGURE 3 in Type locality, distribution and conservation of the threatened catfish Taunayia bifasciata (Eigenmann & Norris 1900) (Siluriformes: Heptapteridae) in the Atlantic Forest streams of Southeastern Brazil
FIGURE 3. Geographic distribution of Taunayia bifasciata. Symbols: white star: type locality of T. bifasciata; blue circle: records in Tietê river basin; red diamonds: records in Paraíba do Sul river basin; purple square: records Itapanhaú River basin; orange pentagon: new record of T. bifasciata in Mambucaba river basin. White outline: Serra da Bocaina National Park; black lines: state limits.
FIGURE 4. A in Type locality, distribution and conservation of the threatened catfish Taunayia bifasciata (Eigenmann & Norris 1900) (Siluriformes: Heptapteridae) in the Atlantic Forest streams of Southeastern Brazil
FIGURE 4. A. Sampling site of Taunayia bifasciata (Eigenmann & Norris 1900) in the Mambucaba river basin at the Serra da Bocaina National Park, Rio de Janeiro State, Brazil. B. The Veados waterfall, which is just upstream the sampling site.
FIGURE 1 in Type locality, distribution and conservation of the threatened catfish Taunayia bifasciata (Eigenmann & Norris 1900) (Siluriformes: Heptapteridae) in the Atlantic Forest streams of Southeastern Brazil
FIGURE 1. Specimens of Taunayia bifasciata (Eigenmann & Norris 1900) in dorsal (tops), lateral (middles), and ventral (bottoms) views. Left is the holotype of Nannoglanis bifasciatus Eigenmann & Norris 1900 (CAS 75771), photo by David Catania; right is the specimen collected in the Mambucaba river basin, Serra da Bocaina National Park, Rio de Janeiro State, Brazil (UFRN 5592), photo by Lucas Medeiros. Scale bar: 10 mm.
Distribution. SE coastal Madagascar, currently known only from the area ofits type locality, the Manombo Special Reserve and Agnalazaha Forest. in Indriidae
Distribution. SE coastal Madagascar, currently known only from the area ofits type locality, the Manombo Special Reserve and Agnalazaha Forest.
Distribution. NE of DR Congo, and possibly restricted to this region; known from type locality, Ituri Forest, and Medje. Recently it has been reported from Okapi Wildlife Reserve and Masako Forest. in Soricidae
Distribution. NE of DR Congo, and possibly restricted to this region; known from type locality, Ituri Forest, and Medje. Recently it has been reported from Okapi Wildlife Reserve and Masako Forest.
Distribution. NE DR Congo; until 1990, recorded only from type locality and Masako Forest, near Kisangani. Since then, it has been recorded in various forests in vicinity of Kisangani. Also, found 2 km W of Epulu Forest and on Kungulu I. Its distribution still appears to be very limited. in Soricidae
Distribution. NE DR Congo; until 1990, recorded only from type locality and Masako Forest, near Kisangani. Since then, it has been recorded in various forests in vicinity of Kisangani. Also, found 2 km W of Epulu Forest and on Kungulu I. Its distribution still appears to be very limited.
Distribution. Uganda, along the N & NW shores of Lake Victoria, including Mabira Forest (most likely the type locality), Bujuko and Bukasa Forests, and along the E side of the Albertine Rift, especially in Kibale Forest National Park and the Bukoma area; it is also found in Sango Bay Forest and in Minziro Forest, NW Tanzania, both parts of the Minziro-Sango Bay Transboundary Site. in Cercopithecidae
Distribution. Uganda, along the N & NW shores of Lake Victoria, including Mabira Forest (most likely the type locality), Bujuko and Bukasa Forests, and along the E side of the Albertine Rift, especially in Kibale Forest National Park and the Bukoma area; it is also found in Sango Bay Forest and in Minziro Forest, NW Tanzania, both parts of the Minziro-Sango Bay Transboundary Site.
FIGURE. Landscapes and vegetation types at Quiçama National Park. A. Wooded savannah with Adansonia digitata. B. Mosaic of wooded savannah and thicket. C. Grassy savannah. D. Slope with thicket. E. Grassy savanna with Setaria welwitschi. F. Wooded savannah. G. Cuanza River shores with herbaceous vegetation. H. Herbaceous vegetation on the banks of the Cuanza River and slope with open forest. I. Coastal sands. J. Mangrove at the Cuanza River estuary, with Rhizophora racemosa. (Photographs by the authors). in An annotated checklist of the vascular flora of Quiçama National Park, Angola
FIGURE. Landscapes and vegetation types at Quiçama National Park. A. Wooded savannah with Adansonia digitata. B. Mosaic of wooded savannah and thicket. C. Grassy savannah. D. Slope with thicket. E. Grassy savanna with Setaria welwitschi. F. Wooded savannah. G. Cuanza River shores with herbaceous vegetation. H. Herbaceous vegetation on the banks of the Cuanza River and slope with open forest. I. Coastal sands. J. Mangrove at the Cuanza River estuary, with Rhizophora racemosa. (Photographs by the authors).
FIGURE. Multilocus phylogenetic tree inferred from Bayesian analysis based on the combined TEF1-α and ACT sequences. Bayesian posterior probabilities are indicated next to the nodes. The tree was rooted with Cladosporium herbarum CBS 121621. The species in this study are indicated in bold. Types of species are indicated after the culture collection number (T = ex-type, ex-epitype, ex-neotype, or reference strain). in Six new species of Cladosporium associated with decayed leaves of native bamboo (Bambusoideae) in a fragment of Brazilian Atlantic Forest
FIGURE. Multilocus phylogenetic tree inferred from Bayesian analysis based on the combined TEF1-α and ACT sequences. Bayesian posterior probabilities are indicated next to the nodes. The tree was rooted with Cladosporium herbarum CBS 121621. The species in this study are indicated in bold. Types of species are indicated after the culture collection number (T = ex-type, ex-epitype, ex-neotype, or reference strain).
FIGURE. (Continued) Multilocus phylogenetic tree inferred from Bayesian analysis based on the combined TEF1-α and ACT sequences. Bayesian posterior probabilities are indicated next to the nodes. The tree was rooted with Cladosporium herbarum CBS 121621. The species in this study are indicated in bold. Types of species are indicated after the culture collection number (T = ex-type, ex-epitype, exneotype, or reference strain). in Six new species of Cladosporium associated with decayed leaves of native bamboo (Bambusoideae) in a fragment of Brazilian Atlantic Forest
FIGURE. (Continued) Multilocus phylogenetic tree inferred from Bayesian analysis based on the combined TEF1-α and ACT sequences. Bayesian posterior probabilities are indicated next to the nodes. The tree was rooted with Cladosporium herbarum CBS 121621. The species in this study are indicated in bold. Types of species are indicated after the culture collection number (T = ex-type, ex-epitype, exneotype, or reference strain).
Species list, with traits, in four forest types
<p>Ecological strategy is the tactics employed by species in adapting to abiotic and biotic conditions. Ecological strategy spectrum is defined as the relative proportion of species in different ecological strategy types within a community. Determinants of ecological strategy spectrum of plant community explored by most previous studies are about abiotic factors. Yet, the roles of biotic factors in driving variations of ecological strategy spectra of forest communities across different geographic regions remains unknown. Here, we established 200 0.04-ha forest dynamics plots and measured three leaf functional traits of tree and shrub species in four forest vegetation types across four climatic zones. Based on Grime's CSR triangular framework and the StrateFy method, we categorized species into four ecological strategy groups (C-, S-, Int-, and R-groups) and related the ecological spectra of the forests to three species diversity indices (species richness, Shannon Wiener index, and stem density (stem abundance)). Linear-regression, redundancy analysis and variance partition analysis were utilized for assessing the roles of species diversity in regulating ecological strategy spectra of forest communities across different climatic zones. We found that the proportion of species in the C- and Int-groups increased, while that in the S-group decreased, with the increase of three indices of species diversity. Among the three species diversity indices, stem abundance played the most important role in driving variations in ecological strategy spectra of forests across different climatic zones. Our finding highlights the necessity of accounting for biotic factors, especially stem abundance, in modeling or predicting the geographical distributions of plant species with varied ecological adaptation strategies to future environmental changes.</p>
FIGURES 23–25 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 23–25. Types of Chrysomelidae deposited in NFIC. 23, Elytropachys sandalensis, Paratype. 24, Longitarsus taklechensis, Cotype. 25, Longitarsus cyanipennis, Paratype.
FIGURES 20–22 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 20–22. Types of Chrysomelidae deposited in NFIC. 20, Gynandrophthalma flaviventris, Cotype. 21, Trichotheca beesoni, Paratype. 22, Chaetocnema merguiensis, Paratype.
FIGURES 14–16 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 14–16. Types of Chrysomelidae deposited in NFIC. 14, Aspidolopha ornaticollis, Cotype. 15, Melixanthus coorgensis, Paratype. 16, Chlamys padmanabhai, Type.
FIGURES 17–19 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 17–19. Types of Chrysomelidae deposited in NFIC. 17, Chlamys travancorensis, Type. 18, Exema fulvitarsis, Cotype. 19, Exema salemensis, Paratype.
FIGURES 8–10 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 8–10. Types of Chrysomelidae deposited in NFIC. 8, Estigmena bicolor, Type. 9, Callispa almora, Cotype. 10, Downesia sasthi, Cotype.
FIGURES 11–13 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 11–13. Types of Chrysomelidae deposited in NFIC. 11, Platypria garthwaitei, Cotype. 12, Aetheomorpha coorgensis, Cotype. 13, Aspidolopha nigrocurvilinea, Cotype.
FIGURES 5–7 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 5–7. Types of Chrysomelidae deposited in NFIC. 5, Bruchus bilineatopygus, Cotype. 6, Bruchus gardneri, Cotype. 7, Bruchus maculatithorax, Cotype.
FIGURES 1–3 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 1–3. Types of Chrysomelidae deposited in NFIC. 1, Spermophagus atroapicalis, Cotype. 2, Spermophagus notatipennis, Cotype. 3, Spermophagus uniformis, Cotype.
FIGURES 26–28 in Type specimens of Chrysomelidae and Megalopodidae (Coleoptera) in the National Forest Insect Collection (NFIC), Forest Research Institute, Dehra Dun, India
FIGURES 26–28. Types of Chrysomelidae deposited in NFIC. 26, Podagrica apicefulva, Paratype. 27, Diorhabda trirakha, Paratype. 28, Sastra mamaya, Paratype.
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.