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Fig. 4 in Feeding and reproductive ecology of Cichla piquiti Kullander & Ferreira, 2006 within its native range, Lajeado reservoir, rio Tocantins basin
Fig. 4. Reproductive activity of Cichla piquiti, measured as the percentage of individuals in different reproductive phases within periods. Numbers above bars indicate sample size.
Fig. 2 in Feeding and reproductive ecology of Cichla piquiti Kullander & Ferreira, 2006 within its native range, Lajeado reservoir, rio Tocantins basin
Fig. 2. Nonmetric multidimensional scaling (NMDS) applied to investigate variation in the diet of Cichla piquiti according to periods, sex (m = males; f = females) and maturity (I = immature; A = adult).
Fig. 1 in Feeding and reproductive ecology of Cichla piquiti Kullander & Ferreira, 2006 within its native range, Lajeado reservoir, rio Tocantins basin
Fig. 1. Resource accumulation curves controlled by the number of stomachs of Cichla piquiti analyzed, considering all fish (a), sexes (b), maturity (c) and season (d). Sample size was reduced to 67 stomachs because this analysis considered only resources identified at some independent level, removing unidentified or combined items.
Figure 5 in Red deer on the move: home range size and mobility in Bulgaria
Figure 5. Comparison between male and female red deer mobility. Boxes – the interquartile range (25-75 percentiles); middle line in boxes – median values; diamonds – average values; whiskers – minimum and maximum values within the 95.0% confidence level; circles – outliers; the perimeter outside boxes shows the probability density of the of the 12 hours step-length displacement in males and females.
Figure 3 in Red deer on the move: home range size and mobility in Bulgaria
Figure 3. Comparison of the core and total area in males and females. Boxes – the interquartile range (25-75 percentiles); middle line in boxes – median values; diamonds – average values; whiskers – minimum and maximum values within the 95.0% confidence level; circles – outliers; circles with plus sign - "Far outside" outliers, points more than 3 times above the interquartile range.
Figure 1. Study area and 100 in Red deer on the move: home range size and mobility in Bulgaria
Figure 1. Study area and 100 % minimum convex polygons from the locations of the GPS-collared red deer
Figure 1 in Temperature variation in nests of Paleosuchus palpebrosus (Crocodylia: Alligatoridae) near the southern edge of the species´ range, Brazil
Figure 1. Egg-chamber temperature (upper filled circles), air temperature in the shade near the nest (triangle), and rainfall (lower filled circles). Nest 1 was from the ESSA in 2008; Nest 2 from the Serra do Urucum in 2010; Nest 3 from the Serra do Urucum in 2010; and Nest 4 from the Serra do Urucum in 2011.
Fig. 1 in The effects of short-term climate change on the range of species: the case of the expanding European dwarf mantis Ameles spallanzania in northern Italy (Mantodea: Amelidae)
Fig. 1 – Distribution of Ameles spallanzania in Italy across a, past period and b, current period. Confirmed data refer to already known presence cells in the previous time interval.
Fig. 2 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 2. Cloth wrapping used to cage beech trunk section in 2012 at Gulelebi Forest in Georgia where one part of the scale cohort survival study was conducted.
Fig. 6 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 6. Comparative cumulative day-degrees for Tianeti in the country of Georgia (cum DD GEO) and Windsor, Massachusetts, USA (cum DD MA), each in the years in which phenological observations on beech scale were made at the 2 locations.
Fig. 5 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 5. Phenology of life stages of beech scale in Massachusetts (USA) (Notchview Reservation, property of Trustees of Reservations, Windsor, 2013), showing univoltine cycle, with settled crawlers being the overwintering stage.
Fig. 4 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 4. Phenology of life stages of beech scale in Georgia (Gulelebi Forest, Tianeti District, 2011), showing bivoltine cycle, with adult females being the overwintering stage.
Fig. 3 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 3. (a) Example of trunk cages made from small Petri dishes (with an open bottom) that were used to isolate scale patches in Massachusetts. (b) Patches of beech scale initiated by delimiting groups (<50) of newly settled crawlers with top patch (defined by black circle marked on bark) lef uncaged, whereas lower patch was caged (caged removed here) from Oct 2011 to Oct 2012 (1 scale generation) at which time scales were a mixture of adults and crawlers of the next generation; done on American beech at Notchview Reservation (property of Trustees of Reservations), Windsor, Massachusetts, USA. Note the greater number of large white woolly dots (adults of the test generation) in the bottom circle, suggesting significant mortality due to factors, like generalist predators, that were excluded by the cages.
Fig. 1 in Comparative phenology and cohort survival of beech scale (Hemiptera: Eriococcidae) in part of its native range (Caucasus Mountains, Georgia) and in an invaded area (Massachusetts, USA)
Fig. 1. Sites in Georgia where studies were conducted. Site 1 (Gulelebi Forest) was used in 2011 for the phenology observations, and sites 2 (Gombori) and 3 (Lagodekhi) were used for the cohort survival experiment in 2012.
Fig. 1 in Field host range of Apanteles opuntiarum (Hymenoptera: Braconidae) in Argentina, a potential biocontrol agent of Cactoblastis cactorum (Lepidoptera: Pyralidae) in North America
Fig. 1. Distribution of Apanteles opuntiarum (circles) and Apanteles alexanderi (triangles) that emerged from species of Pyralidae collected in Argentina, Aug 2007–Mar 2014.
Figures 12–17. Fractipes tayrona, genitalia. 12 in A new species and significant range extension for the genus Fractipes Bechynĕ (Coleoptera: Chrysomelidae: Eumolpinae: Eumolpini)
Figures 12–17. Fractipes tayrona, genitalia. 12) Lateral view of median lobe and partially everted endophallus. 13) En-face view of median lobe. 14) Apical sclerite. 15) En-face view of endophallus at endophallic lateral digits. 16) Spermatheca. 17) Ovipositor.
Figures 1–4. Fractipes tayrona. 1 in A new species and significant range extension for the genus Fractipes Bechynĕ (Coleoptera: Chrysomelidae: Eumolpinae: Eumolpini)
Figures 1–4. Fractipes tayrona. 1) Holotype male, dorsal habitus. 2) Allotype female, dorsal habitus. 3) Head of male. 4) Underside of male showing femoral spur, and terminal abdominal segments plus pygidium.
Figure 1 in The first record of the jumping bristletail Pedetontus gershneri Allen, 1995 (Microcoryphia: Machilidae) from Alabama, USA significantly extends its known range
Figure 1. Map showing the known distribution of Pedetontus gershneri Allen 1995. Square represents the previous distribution records from the type locality of Magazine Mountain, Arkansas. Star represents the new record reported here from Bankhead National Forest, Alabama.
Figures 5–11 in A new species and significant range extension for the genus Fractipes Bechynĕ (Coleoptera: Chrysomelidae: Eumolpinae: Eumolpini)
Figures 5–11. Structures of Fractipes. 5) Male hind leg of F. tayrona. 6) Male sterna V–VIII of F. tayrona with tip of pygidium above. 7) Female sternum VII of F. tayrona. 8) Male hind leg of F. secundus. 9) Male hind leg of F. rhabdopteroides (Figures 8 and 9 are from Bechynĕ and Springlová de Bechynĕ [1961]; captions are reversed in the original figure). 10) Holotype and labels of F. secundus. 11) Holotype and labels of F. rhabdopteroides.
Figure 4 in The burmese trout Raiamas guttatus (Day, 1870) (Cypriniformes: Cyprinidae) in South Sumatra revealed its southernmost record of its distributional range
Figure 4. Head pattern of R. guttatus showing large mouth and jaw extending backwards far behind eye (Photo: Muhammad Iqbal).
ScienceDex guides
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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.