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Our model makes the unique and testable prediction that, when comparing species of reptiles with pattern 1A of TSD, those species that have ranges where the sex ratios tend to be female biased will also to have male-mediated dispersal, while those that persist where the sex ratios tend to be male biased will have female-mediated dispersal.
In mammals, males seem to have lower 2D:4D ratios than females (Manning et al. 1998, 2002; Putz et al. 2004), while in birds and reptiles, the pattern (when found) seems to be the opposite (Burley and Foster 2004; Rubolini et al. 2006; Navarro et al. 2007; Saino et al. 2007; Leoni et al. 2008; this study; but see Chang et al. 2006).
In this study, we tested whether legume or wheat fields differed in their effects on reptiles' movement patterns.
The pigmentation patterns on those Cretaceous marine reptiles followed a pattern called countershading, in which the animal's back is dark and the belly is lighter.
A simple plot of stratigraphic ranges of Mesozoic marine reptile groups reveals a pattern (Fig. 2).
Here we apply a landscape-level survey design to test how reptiles respond to patterns resulting from these three processes in the Brigalow Belt of eastern Australia, a region highly modified by recent agricultural expansion.
The skeletons of reptiles fit the general pattern of vertebrates.
We used a community framework based on dune geomorphology and wind-precipitation gradients to identify variables that explain patterns of reptile abundance.
Patterns resembling reptile skin and war paint emerge on Russell's flesh.
Further, it has been recognized that the prevalent pattern in reptiles with TSD is pattern Ib [40], which is the equivalent of pattern 1, found to be the only one actually present in fish.
Squamate reptiles show a different pattern, with little or no ontogenetic shift in heart rates from embryo to hatchling stages (e.g., the skink Bassiana duperreyi - [25]).
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