Abstract:Geographic variation of phenotypic traits is common across species and is often associated with variation in environmental conditions. Here, we found larger bodies and larger size at maturity in a northward, lower latitude population of the crab Goniopsis cruentata, which inhabits a hotter, drier environment in comparison with a southward, higher latitude population. Furthermore, the juvenile male gonopods grow more relative to body size in the population characterized by maturation at a smaller size. In contr… Show more
“…A.3). The nitrogen demand of this species is due to its faster growth rate than that of U. cordatus (e.g., Pinheiro et al, 2005;Reis et al, 2015, Leite et al, 2014, De Lira et al, 2015. In animals, an investment in growth increases the nitrogen demand during foraging (Sterner and Elser, 2002).…”
“…A.3). The nitrogen demand of this species is due to its faster growth rate than that of U. cordatus (e.g., Pinheiro et al, 2005;Reis et al, 2015, Leite et al, 2014, De Lira et al, 2015. In animals, an investment in growth increases the nitrogen demand during foraging (Sterner and Elser, 2002).…”
“…However, diverging from the results found in this study, Reis et al (2015) presented results for Goniopsis cruentata in which juvenile specimens showed negative allometry and adults positive allometry for the weight/growth relationship. Individual allometries for different locations observed in these crabs indicate that geographic variation (factors such as temperature) may influence the body size determination of Brachyura such as G. cruentata because, according to Lira et al (2015), local conditions influence variations in their biological characteristics. Therefore, geographic variations may be associated with differences in body size, maturity and variation in reproductive characteristics, a behaviour that is present and well defined in other organisms (Olalla-Tárraga et al 2009).…”
Section: Linear Morphometrymentioning
confidence: 99%
“…structure (Botelho et al 2004), sexual maturity (Moura and Coelho 2004), reproduction and growth, morphological and physiological sexual maturation, reproductive period, fecundity and the influence of environmental factors on reproduction Fransozo 2003, 2005), reproductive aspects (Lira and Calado 2013), reproductive biology (Garcia and Silva 2006), growth (traditional morphometry) (Lira et al 2015) and mangrove environmental quality (Ferreira et al 2019). However, there is still a lack of studies exploring and describing the shape of G. cruentata and information stemming from it using the geometric morphometry technique.…”
The hypothesis of this study was that significant variations in the growth rates of Goniopsis cruentata are related to intersexual and age-related characteristics, particularly in areas identified as secondary sexual (pleon, carapace and chelipeds). From February 2019 to January 2020, a total of 713 individuals were captured, 378 males and 335 females, with a carapace width ranging from 0.42 to 6.59 cm. Males and females showed negative allometry (β0<1) for all linear morphometric relationships, with an ontogenetic difference (p=0.0001) for all comparisons. In geometric morphometry, the dorsal view showed a significant difference in sexual comparisons (p=0.0001), in which males were wider in the posterior region than females. Furthermore, there was a significant difference in the abdominal region between young and adult females (p=0.0001), with the young ones being triangular and the adults oval, a characteristic brachyuran behaviour. We observed morphological separation in cheliped shape in sexual comparison (F×M) and laterality (R×L) (p=0.0001), with no ontogenetic variations (A×J). Goniopsis cruentata showed a noteworthy ontogenetic and sexual dimorphism. In addition, the discovery of cheliped variation was recorded for arboreal species that do not show a high degree of heterochely. Understanding these ontogenetic variations is crucial for effective conservation strategies because it allows specific life stages and their corresponding needs to be identified.
whereas the role played by other factors, such as ecological variation, is less often studied (Langerhans et al., 2016). One reason for this bias in effort might be the typical assumption that male genitalia do not interact much with the surrounding environment-and therefore would not be expected to show much of an ecological signature. That is, male genitalia tend to be small or are usually hidden away (for a review, see
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