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Figure 5 in Grooming behaviors and fouling of the spider crab Libinia dubia (Decapoda: Epialtidae)
Figure 5. Mean frequency of grooming mechanism, with standard error bars, mechanisms in 30-min isolation observations (N=142; scrape/pick: z=1.16, p=0.246; flap/brush: z=2.18, p=0.029). Note: Similar letters indicate no statistical significance (p>0.05) and different letters indicate a statistical significance (p<0.05).
Figure 4 in Grooming behaviors and fouling of the spider crab Libinia dubia (Decapoda: Epialtidae)
Figure 4. Mean frequency of grooms, with standard error bars, by grooming appendages in 30-min isolation observations (N=142). A. Mean frequency of grooms for each of the grooming appendages, with genders combined (z=3.39, p<001). B. Mean frequency of grooms for each of the grooming appendages, with the genders separated; males groomed with their 3M more than P1 (z=3.23, p=0.001) whereas females groomed with the 3M and P1 appendages equally (z=1.40, p=0.140). 3M, third maxilliped; P1, pereiopod #1 (cheliped). Note: Similar letters indicate no statistical significance (p>0.05) and different letters indicate a statistical significance (p<0.05).
Figure 4 in Tracking of spatial changes in the structure of the zooplankton community according to multiple abiotic factors along a hypersaline lagoon
Figure 4. Temporal correlations between larvae of Cirripedia and Acartia tonsa (A) and between Acartia tonsa and temperature (B).
Figure 3 in Grooming behaviors and fouling of the spider crab Libinia dubia (Decapoda: Epialtidae)
Figure 3. Frequency of grooms, with standard error bars, per body region during 30-min isolation observations (N=142; N=89 males; N=53 females) for males and females. A. Mean frequency of grooms for males and females for body regions (males: H=248, p<0.001; females: H=101, p<0.001); x-axis organized by anterior body regions on the left to posterior body regions on the right. B. Grooming frequency of sensory and respiratory structures compared to body regions where decorations are attached for males and females (sensory/respiratory: N=568, df=540, t=- 2.67, p=0.008; decorating: N=568, df=523, t=-1.97, p=0.049). A1, first antennae; A2, second antennae; ABD, abdomen; AM, all maxillipeds; E, eye; G, gills; M, dorsal mid-carapace; LC, left P1 cheliped; M1, first maxilliped; M2, second maxilliped; 3M, third maxilliped; P (_), pereiopods 2–5 (walking legs); R, rostrum; RC, right P1 cheliped; RG, lateral ridge. Note: Sensory and respiratory body regions were A1, A2, E, G; decoration body regions were R, RG, M, P. Note: Similar letters indicate no statistical significance (p>0.05) and different letters indicate a statistical significance (p<0.05).
Figure 3. Lynceus grossipedia n in A new Northeast Asian Lynceus (Crustacea: Branchiopoda: Laevicaudata) with uniquely modified thoracopods and an evaluation of DNA barcoding for clam shrimp species identification
Figure 3. Lynceus grossipedia n. sp., female, stereo microscopy (allotype, NHMD-616085). A. Right lateral view, intact animal. B. Right lateral view, carapace valve removed. C. Ventral view, carapace valves slightly apart. D. Dorsal view. E. Head close-up (from B). F. Telson close-up (from B). G. Carapace, right valve interior.
Figure 6. Lynceus grossipedia n in A new Northeast Asian Lynceus (Crustacea: Branchiopoda: Laevicaudata) with uniquely modified thoracopods and an evaluation of DNA barcoding for clam shrimp species identification
Figure 6. Lynceus grossipedia n. sp., male, scanning electron microscopy of claspers (same specimen as on Figs. 4, 7; paratype, NHMD-616086). A. Right clasper, anterior view. B. Left clasper, posterior view. C. Movable finger (endopod), large palp (endite 5), and gripping area (part of palm, endite 3), left clasper, apical view. D. Movable finger with band of minute setae, gripping area with type 4 setae, left clasper. E. Small palp (endite 4) and large palp (endite 5), right clasper. F. Palm with scales (encircled area in B), lateral view, right clasper. G. Setation on movable finger (endopod). H. Setation on posterior side of gripping area. I. Magnification of scales on clasper palm.
Figure 1 in Grooming behaviors and fouling of the spider crab Libinia dubia (Decapoda: Epialtidae)
Figure 1. Relationship between grooming frequency and grooming time budget by carapace width (mm) for males and females in 30-min isolation observations (N=142). A. Mean grooming frequency by carapace width for males and females; no relationship between number of times individuals groomed and their body size (R2=0.003, y=.092x+10.3). B. Mean grooming time budget by carapace width for males and females; no relationship between time spent grooming and body size (R2=0.005, y=1.044x+48.2).
Figure 5. Alpheus brasileiro Anker, 2012. Logistic curve interpolation where 50 in Growth, age at sexual maturity, longevity and natural mortality of Alpheus brasileiro (Caridea: Alpheidae) from the south-eastern coast of Brazil
Figure 5. Alpheus brasileiro Anker, 2012. Logistic curve interpolation where 50% of females reach functional sexual maturity (CL50).
Figure 3. Alpheus brasileiro Anker, 2012 in Growth, age at sexual maturity, longevity and natural mortality of Alpheus brasileiro (Caridea: Alpheidae) from the south-eastern coast of Brazil
Figure 3. Alpheus brasileiro Anker, 2012. Size–frequency distribution of individuals both sexually immature (2.5 to 4.5 mm CL) and sexually mature (5.5 to 9.5 mm CL). Undifferentiated individuals (white bars), males (black bars) and females (dark grey bars). The values of morphological sexual maturity (4.9 and 4.7 mm CL for males and females respectively) are from the study of population structure and relative growth with the same population (Pescinelli et al., 2018a).
Figure 2. A in Growth, age at sexual maturity, longevity and natural mortality of Alpheus brasileiro (Caridea: Alpheidae) from the south-eastern coast of Brazil
Figure 2. A, Lateral view of an ovigerous female of Alpheus brasileiro Anker, 2012; B, sampling area at the intertidal zone of the estuary of Cananéia, São Paulo, south–eastern Brazil.
Figure 1 in Setogenesis and characterization of the new moult substages in the freshwater shrimp Palaemon argentinus (Nobili, 1901) (Caridea: Palaemonidae)
Figure 1. Posterior region of Palaemon argentinus. a, Circle indicates the observed region of the uropods (U) and setae (S) for determining the moult stages. b, Microphotography in intermoult. Abbreviations: s.m, setal matrix; s.n, setal node; s.b, setal base.
Figure 7 in Dynamics of a subtropical population of the purse crab Persephona punctata (Decapoda: Brachyura: Leucosiidae) in Southeastern Brazil
Figure 7. Persephona punctata (Linnaeus, 1758). Percentage of ovigerous females and their gonadal stages: rudimentary (RU); developing (ED) and developed (DE); and the number of juveniles captured monthly from July 2012 to June 2014, in Cananéia, São Paulo, Brazil.
Figure 1. Experimental units for feeding rates tests with terrestrial isopods and fecal pellets from different food sources. A in Coprophagy in detritivores: methodological design for feeding studies in terrestrial isopods (Crustacea, Isopoda, Oniscidea)
Figure 1. Experimental units for feeding rates tests with terrestrial isopods and fecal pellets from different food sources. A) Treatment access; coprophagy is allowed. B) Treatment removal; coprophagy and bacterial activity on feces are avoided. C) Treatment net; coprophagy is avoided and bacterial activity on feces allowed. D) Fecal pellet from carrot (left) and decomposing leaf (right) consumption.
Figure 1 in Growth, age at sexual maturity, longevity and natural mortality of Alpheus brasileiro (Caridea: Alpheidae) from the south-eastern coast of Brazil
Figure 1. Location of the study area, water represented by dark grey in the map of the intertidal estuarine zone of Cananéia, São Paulo, south–eastern Brazil. Adapted from Pescinelli et al. (2017a).
Figure 6 in Dynamics of a subtropical population of the purse crab Persephona punctata (Decapoda: Brachyura: Leucosiidae) in Southeastern Brazil
Figure 6. Persephona punctata (Linnaeus, 1758). Adjustment of the logistic equation indicating the carapace width (CW mm) at which 50% of males and females were mature, according to the analysis of gonadal development.
Figure 4 in Coprophagy in detritivores: methodological design for feeding studies in terrestrial isopods (Crustacea, Isopoda, Oniscidea)
Figure 4. Growth rate of isopods in three different treatments. A. Growth rate of Atlantoscia floridana. B. Growth rate of Balloniscus glaber and Armadillidium vulgare. The values are mean ± SE and the numbers on top indicate the sample number for each index.
Figure 3 in Tracking of spatial changes in the structure of the zooplankton community according to multiple abiotic factors along a hypersaline lagoon
Figure 3. Relationship between temperature, salinity, and pH and their effect on the abundance of Cirripedia larvae over the months.
Figure 2. Lynceus grossipedia n in A new Northeast Asian Lynceus (Crustacea: Branchiopoda: Laevicaudata) with uniquely modified thoracopods and an evaluation of DNA barcoding for clam shrimp species identification
Figure 2. Lynceus grossipedia n. sp., male, stereo microscopy (holotype, NHMD-615874). A. Left lateral view, intact animal. B. Left lateral view, carapace valve removed. C. Ventral view, carapace valves apart. D. Dorsal view, carapace valves slightly apart. E. Head close-up (from B). F. Left side thoracopods, showing enlarged muscular bases. G. Carapace, left valve interior.
Figure 5. Lynceus grossipedia n in A new Northeast Asian Lynceus (Crustacea: Branchiopoda: Laevicaudata) with uniquely modified thoracopods and an evaluation of DNA barcoding for clam shrimp species identification
Figure 5. Lynceus grossipedia n. sp., female, scanning electron microscopy (paratype, NHMD-616086). A. Left lateral view, carapace valve removed. B. Frontal setal fields. C. Left ventrolateral view. D. Left second antenna. E. Head, lateral view. F. Head, anterior view. G. Head, anteroventral view. H. Dorsal organ. I. Telson and lamina abdominalis, dorsolateral view. J. Egg-carrying exopods of thoracopods IX and X. K. Distal part of right first antenna. L. Serration of rostral distal margin, lateral view (gap at edge likely due to drying artifact). M. Left mandible, lateral view. N. Left mandible, dorsal view. O. Mandible close-up (from N).
Figure 5 in Tracking of spatial changes in the structure of the zooplankton community according to multiple abiotic factors along a hypersaline lagoon
Figure 5. Variation of zooplankton density in each collection station, variations in the index of Shannon-Weaver which measures the Diversity (H) and the Pielou's uniformity which measures the Equitability (J) over the sampled months.
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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.