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Figure 4 in Development of predictive models for determining fetal age-at-length in belugas (Delphinapterus leucas) and their application toward in situ and ex situ population management
Figure 4. Comparisons of regression curves of TL growth during the first (●) and second half (○) of gestation (top graph) and the early (●), mid (○) and late (▲) pregnancy (bottom graph). The slopes of the regression lines for first half of gestation (F = 63.31, P <0.0001, df1 = 1, df2 = 33) and for early (F = 50.05, P <0.0001, df1 = 1, df2 = 37) and mid pregnancy (F = 135.04, P <0.0001, df1 = 1, df2 = 32) were different than those for the second half of gestation and late pregnancy, respectively. Note that the animals double in length during late pregnancy (315–473 d).
Figure 3 in Development of predictive models for determining fetal age-at-length in belugas (Delphinapterus leucas) and their application toward in situ and ex situ population management
Figure 3. Individual growth rate data from three animals (Animal 1, 2, 3). Regression line slopes during the first two-thirds of pregnancy (top graph) were similar (F = 0.48, P = 0.62, df1 = 2, df2 =18), while regression slopes where different (F = 15.13, P = 0.03, df1 = 2, df2 =3) from the second half to term. Animal 1 (▲) did not have any TL data beyond the first half of gestation so TL length data were used from the farthest in gestation and then again at term. Note that while growth rates were similar during the first two-thirds of pregnancy, fetuses were already different in size when initially detected.
Figure 2 in Development of predictive models for determining fetal age-at-length in belugas (Delphinapterus leucas) and their application toward in situ and ex situ population management
Figure 2. Fetal growth curve comparison illustrating different growth rates resulting in wide range in estimated gestation length as compared to known gestation length determined in this study. Data from Heide-Jørgensen and Teilmann (1994; dotted line) predicts a gestation length of 310 d for a 150 cm calf and similar to our study used a 2nd order polynomial regression to describe their data. Kleinenberg et al. ([1964] 1969: dashed line) developed a curve of the average monthly embryo/fetal growth. They did not provide the curve, only the predicted age at TL, which we then used to fit to a growth curve, which predicts 150 cm calf as 338 d.
Figure 1 in Development of predictive models for determining fetal age-at-length in belugas (Delphinapterus leucas) and their application toward in situ and ex situ population management
Figure 1. Ultrasonographic images of beluga fetuses. All images have yellow caliper lines used to measure dimensions. Biparietal diameter (A, B) at two different stages of gestation show the ovoid shaped skull and echo produced from falx (arrows) located midline between the parietal bones (arrowheads). The thoracic diameter (C) as measured between the yellow caliper marks (arrowheads) on the lateral side of the fetal thorax (d1 = 6.66 cm) at the level of the heart (white arrow) and thoracic circumference (c = 24.04 cm) determined by using the elliptical measurement caliper function to include the dorsal to ventral diameter (d2 = 8.67 cm). The total length of a fetus (D) which is bent in utero, thus requiring the addition of two separate measurements (arrowheads), 1) 8.38 cm from the cranial most aspect of the skull to mid abdomen and 2) 6.91 cm from mid abdomen to distal most portion of the peduncle for a total length of 15.29 cm.
Fig. 9 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 9. Population fluctuation of Thrips tabaci in the onion crops at Axochiapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (180 degree days) occurred to support 1 life cycle of T. tabaci from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 6 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 6. Population fluctuation of Frankliniella occidentalis related with tomato crops at Tlayacapan and Atlatlahucan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 2 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 2. Population fluctuation of Frankliniella occidentalis in the cucumber crops at Tlayacapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 7 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 7. Population fluctuation of Frankliniella occidentalis in the tomatillo crops at Tlayacapan, Morelos, and Tepeojuma, Puebla, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 4 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 4. Population fluctuation of Frankliniella occidentalis in the zucchini crops at Tlayacapan, Tepalcingo and Atlatlahucan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st red vertical arrow and between consecutive red arrows.
Fig. 5 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 5. Population fluctuation of Frankliniella occidentalis in the pepper crops at Izucar de Matamoros and Tepeojuma, Puebla, and Tlayacapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 1 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 1. Population fluctuation of Frankliniella occidentalis in the cucumber crops at Atlatlahucan and Tepalcingo, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 10 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico
Fig. 10. Population fluctuation of Thrips tabaci in the onion crops at Tilapa and Tepeojuma, Puebla, Mexico, 2010–2011. Sufficient thermal units (180 degree days) occurred to support 1 life cycle of T. tabaci from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.
Fig. 1 in Great variability in the infection rate of 'Candidatus Liberibacter asiaticus' in field populations of Diaphorina citri (Hemiptera: Liviidae) in Florida
Fig. 1. Percent infection rates of Diaphorina citri with 'Candidatus' Liberibacter asiaticus in groves across central and southern Florida as determined from 48 independent adult psyllids per site.
Fig. 1. A in Monitoring coffee berry borer, Hypothenemus hampei (Coleoptera: Curculionidae), populations with alcoholbaited funnel traps in coffee farms in Colombia
Fig. 1. A red funnel trap used to capture CBB (Hypothenemus hampei) (A) and the methanol–ethanol lure (3: 1 ratio) enclosed in a semi-permeable membrane (B). CBB were collected in a plastic container containing 200 mL of soapy water. Photo Alex. E. Bustillo.
Fig. 2 in Monitoring coffee berry borer, Hypothenemus hampei (Coleoptera: Curculionidae), populations with alcoholbaited funnel traps in coffee farms in Colombia
Fig. 2. Number of CBB (Hypothenemus hampei) captured per trap per month (mean ± SEM) and corresponding berry infestation (%) on large coffee farms (≥ 20 ha) in Risaralda, Caldas, Colombia (A), and on small coffee farms (≤ 3 ha) in Viterbo, Caldas, Colombia (B) in 2003-2004. Note differences in axis scales.
Figure 1 in The population structure of Mesobuthus gibbosus (Scorpiones: Buthidae) on Koufonisi Island (central Aegean Archipelago, Greece)
Figure 1: The geographic position of Koufonisi (red dot) in Greece and the location of the study site at Pori bay (in red).
FIGURE 10 in Morphology and Systematics of Kalophrynus interlineatus-pleurostigma Populations (Anura: Microhylidae: Kalophryninae) and a Taxonomy of the Genus Kalophrynus Tschudi, Asian Sticky Frogs
FIGURE 10. Images of neotype of Kalophrynus pleurostigma (USNM 36645, female, 34.5 mm SVL) in (A) dorsal, (B) lateral, and (C) ventral views [photographer, J.A. Poindexter].
Fig. 2 in A review of Sciurus Group studies on the red squirrel (Sciurus vulgaris): presence, population density and colour phases in Lombardy (Italy)
Fig. 2 - Fur colour polymorphism in Sciurus vulgaris. Collection of the Museum of Natural History of Milan MSNM. (Photo by Carlo Biancardi).
Fig. 1 - A in A review of Sciurus Group studies on the red squirrel (Sciurus vulgaris): presence, population density and colour phases in Lombardy (Italy)
Fig. 1 - A moment of the fieldwork in Luinese. From the left: Gianni Schiroli, Andrea Viganò, Luigi Cagnolaro e Laura Rinetti. (Photo by Carlo Biancardi).
Fig. 4 in A review of Sciurus Group studies on the red squirrel (Sciurus vulgaris): presence, population density and colour phases in Lombardy (Italy)
Fig. 4 - Observations of red and dark phases per altitudinal range. The dark phase became prevalent, with respect to the mean colour phase ratio, above 800 m a.s.l.
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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.