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.
759
datasets available to search
ShareScore release 0.9.0
Dataset results
759 results for “Crab spiders”
Figure 3 in Phenology and impact of abiotic factors with a temporal lag on the abundance of common crab spider, Xysticus cristatus (Clerck, 1757) (Araneae: Thomisidae) in the agroecosystems of Kashmir
Figure 3. Carapace width frequency distribution of the monthly catches of Xysticus cristatus from April to September 2019.
Figure 4 in Phenology and impact of abiotic factors with a temporal lag on the abundance of common crab spider, Xysticus cristatus (Clerck, 1757) (Araneae: Thomisidae) in the agroecosystems of Kashmir
Figure 4. Activity pattern in terms of number of females caught in pitfall traps and abdominal width from March to July 2019 during the reproductive period in females of Xysticus cristatus.
Figure 2 in Phenology and impact of abiotic factors with a temporal lag on the abundance of common crab spider, Xysticus cristatus (Clerck, 1757) (Araneae: Thomisidae) in the agroecosystems of Kashmir
Figure 2. Circular histograms illustrating the frequency of age structure established for the population of Xysticus cristatus in agroecosystems of Kashmir from March 2018 to February 2020. The angular mean or direction of the data is indicated by the grey line vector inside the circle. The 95% confidence interval is indicated by the transverse line in the sector outside the circle.
Figure 7. Libinia ferreirae Brito Capello, 1871 in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 7. Libinia ferreirae Brito Capello, 1871. Heatmap showing variation in the abundance in relation to bottom salinity (BS), along the sampling stations of Ubatumirim (UBM), Ubatuba (UBA) and Mar Virado (MV), São Paulo State littoral. N total – number of individuals, she – sheltered, exp – exposed.
Figure 4. T-S in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 4. T-S diagrams of the temporal variation in bottom-water temperature and salinity during the sampling period (January 1998 – December 1999) at Ubatumirim, Ubatuba and Mar Virado, São Paulo State, South eastern Brazilian coast. CW – Coastal Water, TW – Tropical Water, SACW – South Atlantic Central Water.
Figure 2 in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 2. Bottom and surface temperature variation per seasons, areas and stations in 1998 and 1999 in Ubatumirim Bay, Ubatuba Bay and Mar Virado Bay. (BT) Bottom temperature. (ST) Surface temperature.
Figure 6. Libinia ferreirae Brito Capello, 1871 in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 6. Libinia ferreirae Brito Capello, 1871. Heatmap showing variation in the abundance in relation to phi, along the sampling stations of Ubatumirim (UBM), Ubatuba (UBA) and Mar Virado (MV), São Paulo State littoral. N total – number of individuals, she – sheltered, exp – exposed.
Figure 3 in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 3. Bottom salinity variation per seasons, areas and stations in 1998 and 1999 in Ubatumirim Bay, Ubatuba Bay and Mar Virado Bay.
Figure 1 in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 1. Map of the Ubatuba region (North eastern coast of São Paulo State), Brazil, showing the three bays and their respective sampling stations (modified from Fransozo et al. 2013).
Figure 5 in The spatial and temporal abundance of the spider crab Libinia ferreirae Brito Capello, 1871 (Crustacea, Brachyura) considering different environmental factors
Figure 5. Proportions of grain-size classes, central tendency of bottom sediments (phi) and mean values of the organic matter content of the sediment (% OM) for each depth in Ubatumirim, Ubatuba and Mar Virado, São Paulo State littoral, South eastern Brazilian coast. (A) Class A (gravel, very coarse sand, coarse sand, and intermediate sand). (B) Class B (fine and very fine sand). (C) Class C (silt-clay).
Figure 4 in Morphology of camouflage by encrustation in the spider crabs Schizophrys dahlak and Hyastenus hilgendorfi (Decapoda: Brachyura: Majoidea: Epialtidae) from the Suez Canal, Egypt
Figure 4. Hyastenus hilgendorfi. (a) Clusters of spinules on orbital regions; (b) close-up of a cluster; (c) arrow indicates typical hooked seta on the exoskeleton; (d) annuli on the basal region of the setal shaft of hooked setae indicated by arrow; (e) arrow indicates hair-like setules of pappose setae, randomly distributed on the medial and distal portions of setal shaft; (f) arrow indicates tendri-pappose setae with thread-like setules randomly distributed on proximal and distal portions of setal shaft; (g) cuspidate setae on the exoskeleton; (h) air-dried wedged setae on exoskeleton; (i) critical-pointdried wedged setae.
Figure 3 in Morphology of camouflage by encrustation in the spider crabs Schizophrys dahlak and Hyastenus hilgendorfi (Decapoda: Brachyura: Majoidea: Epialtidae) from the Suez Canal, Egypt
Figure 3. dahlak. (a) Typical cuspidate setae on exoskeleton. (b–e) Antler setae: (b) arrow indicates miniature (short) antler setae with horn-like setal shaft; (c) four large denticles near the distal portion; (d) tall antler setae; (e) arrow indicates tiny denticles arranged in a single row. (f) Pappose setae on exoskeleton indicated by arrow. (g) Plumose setae found randomly on carapace. Setules (S in inset) situated in grooves indicated by arrow. (h) Composite setae on lateral margins of carapace. (i) Setules flanking one side of setal shaft (S in inset). (j) Multiserrate setae found on branchial and abdominal regions of exoskeleton.
Figure 2 in Morphology of camouflage by encrustation in the spider crabs Schizophrys dahlak and Hyastenus hilgendorfi (Decapoda: Brachyura: Majoidea: Epialtidae) from the Suez Canal, Egypt
Figure 2. Schizophrys dahlak. (a) Arrows point to surface protuberances among hooked setae. (b–d) Patterns of distribution of the three types of tubercles on S. dahlak integument. (b) Arrow points to single denticles found in rows; (c) paired denticles indicated by arrow; (d) single denticle facing a group of spinules. (e) Arrow indicates typical hooked setae on exoskeleton. (f) Lateral slit present on the proximal portion up to distal end indicated by arrow. Denticles (De) on inside of curve on the distal portion of setal shaft. (g) Simple setae on the branchial and abdominal regions of the exoskeleton. (h) Arrow points to slightly curved distal end of the longest simple setae.
Figure 1 in Morphology of camouflage by encrustation in the spider crabs Schizophrys dahlak and Hyastenus hilgendorfi (Decapoda: Brachyura: Majoidea: Epialtidae) from the Suez Canal, Egypt
Figure 1. (a) Hyastenus hilgendorfi, totally inconspicuous individual; (b) Schizophrys dahlak, carapace visible through epibiota; (c) heavily fouled rostrum of H. hilgendorfi (air-dried sample, treatment method after Szebeni and Hartnoll (2005); (d) carapace of H. hilgendorfi masked with ascidians indicated by arrows; (e) arrows point to cleaned regions of the same carapace as in (d); (f) carapace regions of S. dahlak.
Figure 5 in Morphology of camouflage by encrustation in the spider crabs Schizophrys dahlak and Hyastenus hilgendorfi (Decapoda: Brachyura: Majoidea: Epialtidae) from the Suez Canal, Egypt
Figure 5. Hyastenus hilgendorfi. (a) Box with arrow indicates cuspdenticulate setae on the merus of 3rd pereiopod; (b) denticles distributed along shaft; (c) arrows indicate aristate setae; (d) setal shaft aristate, drastically tapers from base to tip, terminal part pointed with an acute angle. Inset: prickle-like denticles; (e) air-dried ribbed setae on rostrum; (f) critical-point-dried ribbed setae; (g) arrow indicates wide grooves of ridged setae bordered by long, narrow ridges running across setal shaft. Inset: spiny needle-like denticles; (h) frilled spatulate setae on the abdomen; (i) setal shaft heavily frilled starting from medial portion towards tip. High density of tuskshaped denticles.
FIGURE 1. Angaeus comatulus. A in On the crab spider genus Angaeus Thorell, 1881 and its junior synonym Paraborboropactus Tang and Li, 2009 (Araneae: Thomisidae)
FIGURE 1. Angaeus comatulus. A juvenile syntype (MNHN 22168/1573), habitus (dorsal). B–E Angaeus lenticulosus female syntype (MNHN 22125/1573). B prosoma (dorsal); C epigynum (ventral); D opisthosoma (dorsal); E chelicerae (ventral). Angaeus pudicus. F male holotype (MCSN), habitus (dorsal).
FIGURE 4 in On the crab spider genus Angaeus Thorell, 1881 and its junior synonym Paraborboropactus Tang and Li, 2009 (Araneae: Thomisidae)
FIGURE 4. Angaeus rhombifer. Syntype of Stephanopis weyersi (MNHN 10869). A female habitus (dorsal); B epigynum (ventral); C eye region.
FIGURE 3 in On the crab spider genus Angaeus Thorell, 1881 and its junior synonym Paraborboropactus Tang and Li, 2009 (Araneae: Thomisidae)
FIGURE 3. Angaeus christae sp. nov. A female (RMNH 15917), habitus (dorsal); B male holotype (RMNH 15946), habitus (dorsal); E female (RMNH 15917), epigynum (ventral). Angaeus rhombifer. C female from Poring Hot Springs (RMNH 15927), habitus (dorsal); D epigynum (ventral).
FIGURE 73 in Phylogenetics and comparative morphology of crab spiders (Araneae: Dionycha, Thomisidae)
FIGURE 73. Scanning electron micrographs of Stiphropus lugubris, male (USNM). A–F male palp (A retrolateral, B, F ventral, C, E prolateral D dorsal); G prosoma, frontal view; H chelicerae, frontal view. Scale bars = 100 µm.
FIGURE 58 in Phylogenetics and comparative morphology of crab spiders (Araneae: Dionycha, Thomisidae)
FIGURE 58. Scanning electron micrographs of Mecaphesa asperata. A spinnerets; B ALS; C PMS; D PLS; E epigynum, ventral view; F opisthosoma detail, dorsal view. Scale bars = 10 µm (B–D), 100 µm (A, E, F).
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.