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FIGURE 4 in How many valid Pleurosicya (Teleostei: Gobiidae) species are known from the Red Sea?

FIGURE 4. Lateral and upper view of cephalic sensory pore system of Pleurosicya mossambica. From Goren (1984).

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FIGURE 1 in How many valid Pleurosicya (Teleostei: Gobiidae) species are known from the Red Sea?

FIGURE 1. Maximum likelihood estimate of the phylogenetic relationships of Pleurosicya based on the mitochondrial gene cytochrome c oxidase subunit I (COI). Numbers near the branches indicate bootstrap values of SH-aLRT support (%)/ ultrafast bootstrap support (%) based on 1000 replicates. Specimens of Pleurosicya mossambica from the Red Sea and the Western Indian Ocean are colored in red and blue, respectively; asterisk denotes mislabeled sequences. Further information for this dataset is provided in Table 1.

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FIGURE 2. Pleurosicya bilobata. A in How many valid Pleurosicya (Teleostei: Gobiidae) species are known from the Red Sea?

FIGURE 2. Pleurosicya bilobata. A: Dahab, Egypt, Red Sea; B: Dahab, Egypt, Red Sea. Photos by T. Malkerova (A), C. von Mach (B).

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Oxygen-induced chromophore degradation in the photoswitchable red fluorescent protein rsCherry

Source data for figure 1, figure 3a, and supplementary figure 1.

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Future climate change accelerates the invasive rhythm of alien marine species: new insights into the invasive potential of the world's aquaculture species red drum Sciaenops ocellatus

This article accompanies the article "Integrating species distribution modeling, stable isotope and transcriptomic analysis provides insights into eco-position competition for alien red drum Sciaenops ocellatus". The file contains supplementary material to the article.

FIG. 2 in Maternal Body Size and Condition Predict Measures of Reproductive Success and Future Reproductive Allocation in Territorial Eastern Red-Backed Salamanders

FIG. 2. The regression of number of surviving offspring (at 185 d posthatching) on (A) maternal body size (SVL in mm) and (B) maternal condition (residuals of the regression of maternal mass, mm, on maternal body size, SVL in mm).

FIG. 3 in Maternal Body Size and Condition Predict Measures of Reproductive Success and Future Reproductive Allocation in Territorial Eastern Red-Backed Salamanders

FIG. 3. The body size of siblings that did and did not survive to 185 d after hatching. Each point represents the mean SVL of siblings from a single female that did or did not survive. The diagonal line represents the hypothetical situation in which the body size of siblings that did and did not survive are equal.

FIG. 1 in Maternal Body Size and Condition Predict Measures of Reproductive Success and Future Reproductive Allocation in Territorial Eastern Red-Backed Salamanders

FIG. 1. The regression of (A) clutch size (number of eggs) and of (B) mean juvenile size (measured as mean snout–vent length, SVL, in mm per clutch) on maternal body size (SVL in mm).

FIG. 4 in Maternal Body Size and Condition Predict Measures of Reproductive Success and Future Reproductive Allocation in Territorial Eastern Red-Backed Salamanders

FIG. 4. The regression of number of developing oocytes (visible through the body wall) produced by females on (A) maternal body size (SVL in mm) and (B) maternal condition (residuals of the regression of maternal mass, mm, on maternal body size, SVL in mm).

FIG. 7 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 7. Kaplan-Meier survival plots of (a) avian attacks and (b) mammalian attacks on striped and unstriped clay models (n = 40 each) that were checked weekly over 3 wk. (a) Unstriped models of P. cinereus were significantly more likely to not be attacked by birds (solid line, n = 38) than striped models (dashed line, n = 31) (Z = 5.04, P = 0.0248). (b) There was no difference in models' ''survival'' from mammalian attacks based on color (striped: n = 31; unstriped: n = 30; Z = 0.07, P = 0.787).

FIG. 6 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 6. The cumulative model weights for encounter probability (p) in Spring 2013, 2014, 2015 showed equivocal support for both age and color morph (a X c) affecting encounter probability in the spring seasons; the null model (.) had similar weights. In Fall 2013 and 2014, the model including both age and color morph (a X c) was more heavily weighted than the other models in each year.

FIG. 4 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 4. Color morph frequencies varied based on age but not adult sex. Juveniles of P. cinereus (SVL <28 mm) had a significantly higher frequency (mean ± SE) of striped individuals than adults (SVL> 35 mm; X2 = 3.177, P = 0.049, n = 356). Adult males and females of Plethodon cinereus (SVL> 1 35 mm) did not differ in frequencies of striped and unstriped color morphs (X2 = 0.90, P = 0.210, n = 286).

FIG. 3 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 3. Examples of clay model replicates of adult striped (top) and unstriped (bottom) Plethodon cinereus.

FIG. 2 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 2. Map of the location of the study site (Nanticoke River Wildlife Management Area, Wicomico County, Maryland, USA) in Eastern North America.

FIG. 1 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 1. Examples of striped (left) and unstriped (right) Plethodon cinereus. The striped individual pictured here has a previously autotomized tail, which, while originally striped (see Moore and Ouellet, 2014; Fig. 1), grew back without a red stripe (Petranka, 1998).

FIG. 5 in Differential Survival and the Effects of Predation on a Color Polymorphic Species, the Red-Backed Salamander (Plethodon cinereus)

FIG. 5. The cumulative model weights for survival (ψ) in Spring 2013, 2014, 2015 showed that both age and color morph (a X c) affected survival probability in the spring seasons. In Fall 2013 and 2014, the null model (.) was more heavily weighted than models including age or color.

FIGURE 12 in Hidden in plain sight: two new species of decapod crustaceans (Palaemonidae and Porcellanidae) discovered in the Red Sea on a university campus in Saudi Arabia

FIGURE 12. Enosteoides melissa (Miyake, 1942), male (cl 10.0 mm, cw 9.5 mm) from Pouébo, New Caledonia, MNHN-IU- 2018-1015, porcelain crab in life, dorsal; specimen collected from burrow of Alpheus rapax Fabricius, 1798. Photograph: A. Anker.

FIGURE 11 in Hidden in plain sight: two new species of decapod crustaceans (Palaemonidae and Porcellanidae) discovered in the Red Sea on a university campus in Saudi Arabia

FIGURE 11. Enosteoides habibi sp. nov., paratype, female (cl 6.2 mm, cw 6.2 mm) from Thuwal, Saudi Arabia (specimen lost, see text); A, porcelain crab in life, dorsal; B, same, ventral. Photographs: A. Anker.

FIGURE 10 in Hidden in plain sight: two new species of decapod crustaceans (Palaemonidae and Porcellanidae) discovered in the Red Sea on a university campus in Saudi Arabia

FIGURE 10. Enosteoides habibi sp. nov., paratype, male (cl 5.5 mm, cw 5.2 mm) from Thuwal, Saudi Arabia (specimen lost, see text); A, porcelain crab in life, frontal; B, same, dorsal; C, same, ventral. Photographs: A. Anker.

FIGURE 9 in Hidden in plain sight: two new species of decapod crustaceans (Palaemonidae and Porcellanidae) discovered in the Red Sea on a university campus in Saudi Arabia

FIGURE 9. Enosteoides habibi sp. nov., holotype, male (cl 8.1 mm, cw 7.5 mm) from Thuwal, Saudi Arabia, FLMNH UF 71320; A, porcelain crab in life, dorsal (left first and second pereiopods missing); B, same, frontal region, anterodorsal. Photographs: A. Anker.