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opencc-by-4.0Sep 2019View details →

Fig. 1 in Response to enantiomers of (Z3Z9)-6,7-epoxy-octadecadiene, sex pheromone component of Ectropis obliqua Prout (Lepidoptera: Geometridae): electroantennagram test, field trapping, and in silico study

Fig. 1. Sex pheromone components of Ectropis obliqua Prout. (A) sex pheromone components; (B) enantiomers of Z3Z9-6,7-epo-18:Hy.

opencc-by-4.0Sep 2019View details →

Fig. 5. Modeled 3D in Response to enantiomers of (Z3Z9)-6,7-epoxy-octadecadiene, sex pheromone component of Ectropis obliqua Prout (Lepidoptera: Geometridae): electroantennagram test, field trapping, and in silico study

Fig. 5. Modeled 3D structure and validation of EoblPBP1. (A) Sequence alignment of EoblPBP1 and template 1DQE_A. α-helices are displayed as squiggles. Identical residues are highlighted in white letters with deep blue background. (B) Overall structure of the EoblPBP1. Three disulfide bonds are in red. N-terminus, C-terminus, and α-helices are labeled. Two potential key residues: Thr117 and Arg 121 are in orange. (C) Ramachandran plot of EoblPBP1.

opencc-by-4.0Apr 2022View details →

Fig. 1 in Do observed sex ratios in a turtle community in northern Indiana vary over 35 years (1979-2014)?

Fig. 1. Proportions of males for (A) Chelydra serpentina, (B) Chrysemys picta, (C) Graptemys geographica, (D) Sternotherus odoratus, and (E) Trachemys scripta elegans over the course of the 37-year study in Dewart Lake, Indiana, USA. Open circles indicate years when <10 individuals were captured, and closed circles indicate years when ≥ 10 individuals were captured. The vertical dashed lines indicate the transition from non-fyke net years to fyke net years, and the horizontal dashed lines represent a 1:1 sex ratio (i.e., 50% males).

Fig. 7 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 7. Ulna. Distribution of males (black dots) and females (white dots) of Chaetophractus villosus (Desmarest, 1804) in the plane determined by the first two relative warps (RW1 and RW2). Numbers indicate specimens. Deformation grids below the graph show shape changes linked to negative (left) and positive (right) scores in RW1. Grids on the right show deformations linked to negative (below) and positive (above) scores in RW2.

Fig. 6 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 6. Scatterplot for the ulna of Chaetophractus villosus (Desmarest, 1804), showing the distribution of the individuals in the plane formed by the two first principal components. The black outlines below the plot represent the shape variation associated to PC1, and those of the right show the changes associated to PC2 with respect to the consensus of the species (grey outlines).

Fig. 4 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 4. Humerus. Distribution of males (black dots) and females (white dots) of Chaetophractus villosus (Desmarest, 1804) in the plane determined by the first two relative warps (RW1 and RW2). Numbers indicate specimens. Deformation grids below the graph show shape changes linked to negative (left) and positive (right) scores in RW1. Grids on the right show deformations linked to negative (below) and positive (above) scores in RW2.

Fig. 3 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 3. Scatterplot for the humerus of Chaetophractus villosus (Desmarest, 1804), showing the distribution of the individuals in the plane formed by the two first principal components. The black outlines below the plot represent the shape variation associated to PC1, and those of the right show the changes associated to PC2 with respect to the consensus of the species (grey outlines).

Fig. 2 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 2. Canonical analysis for the humerus of males and females of Chaetophractus villosus (Desmarest, 1804). The bone outlines below the graph represent the tendencies to deformation in males and females (black dots and lines) with respect to the consensus of the species (grey dots and lines) along the axis.

Fig. 1 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 1. Landmarks digitised on the left appendicular bones of Chaetophractus villosus (Desmarest, 1804). Scapula in dorsal view; humerus in caudal view; ulna in lateral view.

Fig. 5 in A geometric morphometric study of sex differences in the scapula, humerus and ulna of Chaetophractus villosus (Xenarthra, Dasypodidae)

Fig. 5. Canonical analysis for the ulna of males and females of Chaetophractus villosus (Desmarest, 1804). The bone outlines below the graph represent extreme individuals (black dots and lines) with respect to the consensus of the species (grey dots and lines) along the axis.

opencc-by-4.0Dec 2016View details →

Fig. 1 in Sex differences on the feeding of the gobiid fish Bathygobius soporator in tide pools of Maiandeua Island, Pará, Brazil

Fig. 1. Non-Metric Multidimensional Scaling (NMDS) shows the variation in the diet of males and females Bathygobius soporator (Valenciennes, 1837) specimens and the formation of three main groups with different diets in the population of Maiandeua Island, Pará, Brazil.

Fig. 2 in Patterns of gastrointestinal parasite infections in bighorn sheep, Ovis canadensis, with respect to host sex and seasonality

Fig. 2. Seasonal differences in fecal egg counts in female (blue) and male (red) bighorn sheep. Point intervals display the mean count ±95% confidence intervals as predicted by generalised linear mixed effects models. Seasons are: Late gestation (Late gestation/early lactation between April to June); Lactation/summer (between July and October); Rut (November and December); Winter (Winter/early gestation from January to March). Parasites are a) Strongyle; b) Nematodirus; c) Marshallagia; d) Protostrongylus lungworm; e) Eimeria. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Patterns of gastrointestinal parasite infections in bighorn sheep, Ovis canadensis, with respect to host sex and seasonality

Fig. 1. Schematic of the reproductive biology and seasons of bighorn sheep. The blue circle represents the entire year, where the top is December, 3 o'clock March, 6 o'clock June, 10 o'clock October etc. The grey quarter circle represents the season Jan–March = Winter/early gestation; the dark green quarter circles represent the season from April–June = late gestation/early lactation; the light green line represents the season between July and October, which is also representing lactation/summer; and the brown line is representing November and December, or the rutting season. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 3 in Patterns of gastrointestinal parasite infections in bighorn sheep, Ovis canadensis, with respect to host sex and seasonality

Fig. 3. Differences in mean and standard error in strongyle counts between males that use the coursing or tending mating tactic. Point intervals display the mean count ±95% confidence intervals as predicted by the generalised linear mixed effects model.

opencc-by-4.0Jun 2023View details →

FIGURE 1 in Size and sex composition of three carcharhiniform sharks landed by a coastal artisanal fleet from the northeastern coast of Brazil

FIGURE 1 | Operational area of the artisanal fishing fleet based in the Mucuripe Embayment, Fortaleza, Ceará (delimited by dotted lines). Bathymetric curves and the municipalities' location on the Ceará coast are indicated as additional references to the limit of the fleet operation in the study area, highlighting the Ceará State.

opencc-by-4.0Jun 2023View details →

FIGURE 2 in Size and sex composition of three carcharhiniform sharks landed by a coastal artisanal fleet from the northeastern coast of Brazil

FIGURE 2 | Total length frequency for the (A) blacknose, Carcharhinus acronotus, (B) dusky smoothhound, Mustelus cf. canis, and (C) great hammerhead, Sphyrna mokarran, landed at the Mucuripe Embayment, Fortaleza, Ceará. White bars, female; black bars, male. The grey dashed line indicates maturation size for male (M), female (F) or for both sexes.

opencc-by-4.0Jun 2023View details →

FIGURE 3 in Size and sex composition of three carcharhiniform sharks landed by a coastal artisanal fleet from the northeastern coast of Brazil

FIGURE 3 | Total length frequency for the (A) blacknose, Carcharhinus acronotus, and (B) dusky smoothhound, Mustelus cf. canis, landed at the Mucuripe Embayment, Fortaleza, Ceará, over three periods. Black bars, May 1998 to April 1999; white bars, November 2006 to October 2008; grey bars, August 2015 to July 2016.

Black Soldier Fly detection, phenotyping and sex prediction dataset

BSF_Larvae for training the detection and segmentation model consists of 321 images with over 5000 larvae instances.  Single_Larvae_data consists of 1608 single larvae images for the measurement of body weight, length and width of the individual larva.  The Larvae size  excel sheet contains the size and sex data corresponding to the individual larva.  The Larvae sex classification dataset includes images cropped from the Single_Larvae_data for sex classification.

Early life adversity has sex-dependent effects on survival across the lifespan in rhesus macaques

Data for: Early life adversity has sex-dependent effects on survival across the lifespan in rhesus macaques Patterson, S.K., Andonov, E., Arre, A.M., Martinez, M.I., Negron-Del Valle, J.E., Petersen, R.M, Phillips, D., Rahman, A., Ruiz-Lambides, A., Villanueva, I., Lea, A.J., Snyder-Mackler, N., Brent, L.J., Higham, J.P. "Early life adversity has sex-dependent effects on survival across the lifespan in rhesus macaques." 2024. Philosophical Transactions B.