Correlations between Ontogenetic Change in Color Pattern and Antipredator Behavior in the Racer, Coluber constrictor

Ethology ◽  
2005 ◽  
Vol 111 (3) ◽  
pp. 287-300 ◽  
Author(s):  
Douglas A. Creer
2008 ◽  
Vol 6 (2) ◽  
pp. 169-174 ◽  
Author(s):  
Luiz G. G. Silveira ◽  
Francisco Langeani ◽  
Weferson J. da Graça ◽  
Carla S. Pavanelli ◽  
Paulo A. Buckup

Characidium xanthopterum is described from tributaries of the upper rio Paraná and upper rio Tocantins basins, in the Central Brazilian Plateau, Goiás State, Brazil. The new species is diagnosed among congeners by the absence of dark bars on the sides of the body in adult specimens, and by the deep yellow coloration in all fins. Ontogenetic change of color pattern is recorded for the first time for Characidium species. Specimens smaller than 32 mm SL possess dark bars on body. These bars disappear with growth between 32 and 35 mm SL, and are always absent in individuals larger than 35 mm SL.


Author(s):  
Anne E. Margurran

Predators are extremely effective agents of selection. After all, if an individual member of a prey species does not survive long enough to reproduce, it will have lost its chance (kin selection considerations apart) to bequeath its genes to future generations. It is not surprising, therefore, that many cases of population difference have been attributed to geographic variation in risk. These population differences can take a variety of forms and may, for example, involve modifications to morphology or to life-history traits. The correlation between armor and predation in the three-spined stickleback, Gasterosteus aculeatus, is one case that has been well documented (see Reimchen 1994 for a review and discussion), while another is the association between reproductive allotment and risk (Reznick and Endler 1982) and male color pattern and risk (Endler 1980) in the Trinidadian guppy, Poecilia reticulata. However, such adaptations can be futile if they are not accompanied by effective antipredator behavior. For instance, a cryptic color pattern confers no advantage if its holder chooses the “wrong” background or behaves in a conspicuous manner. Behavior is also flexible in a way that life histories or morphology may not be, and it allows moment-to-moment changes in response as risk increases or decreases. Because it is such an important weapon in the evolutionary arms race, antipredator behavior provides important insights into the causes and consequences of natural selection. Some of the best examples of geographically variable antipredator responses occur in populations of freshwater fish (see, e.g., Bell and Foster 1994). The predation regime of these populations is relatively easy to classify—at least in terms of the presence and absence of predatory species—and the distribution of key predators can explain much of the documented variation in antipredator behavior (see p. 140). Covariance in predation regime and antipredator responses is compelling evidence for natural selection. Moreover, because predation regimes can change (or be manipulated) over relatively short periods of time, there is an opportunity to record heritable changes in antipredator responses—in other words, to watch evolution in action.


1988 ◽  
Vol 62 (01) ◽  
pp. 83-87 ◽  
Author(s):  
Patricia H. Kelley ◽  
Charles T. Swann

The excellent preservation of the molluscan fauna from the Gosport Sand (Eocene) at Little Stave Creek, Alabama, has made it possible to describe the preserved color patterns of 15 species. In this study the functional significance of these color patterns is tested in the context of the current adaptationist controversy. The pigment of the color pattern is thought to be a result of metabolic waste disposal. Therefore, the presence of the pigment is functional, although the patterns formed by the pigment may or may not have been adaptive. In this investigation the criteria proposed by Seilacher (1972) for testing the functionality of color patterns were applied to the Gosport fauna and the results compared with life mode as interpreted from knowledge of extant relatives and functional morphology. Using Seilacher's criteria of little ontogenetic and intraspecific variability, the color patterns appear to have been functional. However, the functional morphology studies indicate an infaunal life mode which would preclude functional color patterns. Particular color patterns are instead interpreted to be the result of historical factors, such as multiple adaptive peaks or random fixation of alleles, or of architectural constraints including possibly pleiotropy or allometry. The low variability of color patterns, which was noted within species and genera, suggests that color patterns may also serve a useful taxonomic purpose.


2018 ◽  
Author(s):  
Juan Carlos Villaseñor-Derbez

Stomach contents were analyzed from 109 individuals. A total of 4 Genera and 14 Species were identified. Crustaceans accounted for %N=67.39% , %IRI= 86.37% of the total identified taxa and Teleosts %N=32.61% (%IRI = 13.63%). An ontogenetic change was observed in P. volitans diet.


2009 ◽  
Vol 7 (3) ◽  
pp. 371-376 ◽  
Author(s):  
Valdener Garutti ◽  
Francisco Langeani

Astyanax goyacensis Eigenmann, 1908 is redescribed based on the holotype and 25 topotypes. The species belongs to the A. bimaculatus species complex, sharing with those species a black, horizontally ovate, humeral spot (the most conspicuous feature of this complex), two diffuse vertical brown bars in the humeral area (the first through humeral spot and the second 2-3 scales behind), and black medium caudal-fin rays. Furthermore, A. goyacensis possesses a black stripe extending along midlateral body portion, more conspicuous in alcohol preserved specimens. These characteristics allow its inclusion in the putative "black lateral stripe" sub-group of A. bimaculatus species complex. From the species of this complex it differs by the black lateral stripe shape, pattern of chromatophores on the flank, coloration of the caudal fin, scales on the lateral line, branched rays on anal fin, eye diameter, and caudal peduncle depth. Comments about the color pattern in Astyanax bimaculatus species complex are added.


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