Showing papers by "Jonathan B. Losos published in 1990"

Ecomorphology, Performance Capability, and Scaling of West Indian Anolis Lizards: An Evolutionary Analysis

Abstract: Studies of ecomorphology–the relationship among species between morphology and ecology–contain two implicit and rarely tested hypotheses: (1) that morphological differences among species result in differences in performance capability at ecologically relevant tasks, which, in turn, produce differences in behavior and ecology; and (2) that morphology, performance capability, ecology and behavior have evolved synchronously. I tested these hypotheses using the Anolis lizards of Jamaica and Puerto Rico. I measured morphological and performance variables on recently caught lizards. Movement, display rate and microhabitat measurements were made on lizards observed in the field. Body size explained most of the variation in morphology and performance ability, but was not correlated with the ecological or behavioral variables. When the effect of body size is removed from the morphological and performance variables, the ecomorphological hypotheses were confirmed. Species that were similar morphologically were also ...

The evolution of form and function: morphology and locomotor performance in west indian anolis lizards.

Abstract: I tested biomechanical predictions that morphological proportions (snout-vent length, forelimb length, hindlimb length, tail length, and mass) and maximal sprinting and jumping ability have evolved concordantly among 15 species of Anolis lizards from Jamaica and Puerto Rico. Based on a phylogenetic hypothesis for these species, the ancestor reconstruction and contrast approaches were used to test hypotheses that variables coevolved. Evolutionary change in all morphological and performance variables scales positively with evolution of body size (represented by snout-vent length); size evolution accounts for greater than 50% of the variance in sprinting and jumping evolution. With the effect of the evolution of body size removed, increases in hindlimb length are associated with increases in sprinting and jumping capability. When further variables are removed, evolution in forelimb and tail length exhibits a negative relationship with evolution of both performance measures. The success of the biomechanical predictions indicates that the assumption that evolution in other variables (e.g., muscle mass and composition) did not affect performance evolution is probably correct; evolution of the morphological variables accounts for approximately 80% of the evolutionary change in performance ability. In this case, however, such assumptions are clade-specific; extrapolation to taxa outside the clade is thus unwarranted. The results have implications concerning ecomorphological evolution. The observed relationship between forelimb and tail length and ecology probably is a spurious result of the correlation between these variables and hindlimb length. Further, because the evolution of jumping and sprinting ability are closely linked, the ability to adapt to certain microhabitats may be limited.

A phylogenetic analysis of character displacement in caribbean anolis lizards

Abstract: Twenty-seven islands in the Lesser Antilles contain either one or two species of Anolis lizards. On nine of the ten two-species islands, the species differ substantially in size; 16 of the 17 one-species islands harbor an intermediate-sized species. Two processes could produce such a pattern: size adjustment (or character displacement), in which similar-sized species evolve in different directions in sympatry; and size assortment, in which only different-sized species can successfully colonize the same island together. Previous analyses implicitly have assumed that size is evolutionarily plastic and determined solely by recent ecological conditions, and consequently have tested the hypothesis that character displacement has occurred on each of the ten two-species islands. Other studies have focused only on size assortment. By analyzing such patterns in a phylogenetic context, I explicitly consider historical effects and can distinguish between size adjustment and size assortment. Using a minimum evolution algorithm, I assess evidence for size adjustment by partitioning changes in size along branches of the phylogenetic tree. Size evolution appears rare (a minimum of 4-7 instances of substantial size evolution). In the northern (but not the southern) Lesser Antilles, size change was significantly greater when a descendant taxon occurred on a two-species island and its hypothetical ancestor occurred on a one-species island, thus supporting the size adjustment hypothesis, though size adjustment might have occurred only once. The relative rarity of size evolution suggests that size assortment might be responsible for nonrandom patterns. In both the northern and southern Lesser Antilles, a null model of no size assortment is convincingly rejected. Closely related taxa, however, are usually similar in size, and hybridization between species has been reported. Consequently, similar-sized species might not coexist because they interbreed and coalesce into one gene pool. A null model that only allows species from different "clades" to co-occur is rejected for the northern Lesser Antilles, but is ambiguous with regard to the southern Lesser Antilles. Thus, competitive exclusion is probably responsible for the pattern of size assortment in the northern Lesser Antilles; both competitive exclusion and interbreeding of closely related species of similar size might be responsible for the patterns evident in the southern Lesser Antilles.

Water and Energy Turnover in a Small Monitor Lizard, Varanus-Acanthurus

Abstract: The field metabolic rates and water influxes of Varanus acanthurus were determined by means of doubly-labelled water during late spring. The mean metabolic rate was 0.101 +/- 0.032 mL CO2 g-1 h-1, which was equivalent to an energy expenditure of 63 kJ kg-1 day-1 and a fresh food consumption rate of 13.2 g kg-1 day-1. The mean rate of water influx was 15.9 +/- 6.8 mL kg-1 day-1 and it is suggested that up to 30% of water influxes are via pulmo-cutaneous exchange and drinking. It is considered that V. acanthurus is a secretive 'sit and wait' predator and that this accounts for the lower than predicted water influx and metabolic rates of this species.

A phylogenetic analysis of character displacement in

Abstract: Twenty-seven islands in the Lesser Antilles contain either one or two species of Anolis lizards. On nine of the ten two-species islands, the species differ substantially in size; 16 of the 17 one-species islands harbor an intermediate-sized species. Two processes could produce such a pattern: size adjustment (or character displacement), in which similar-sized species evolve in different directions in sympatry; and size assortment, in which only different-sized species can successfully colonize the same island together. Previous analyses implicitly have assumed that size is evolutionarily plastic and determined solely by recent ecological conditions, and consequently have tested the hypothesis that character displacement has occurred on each of the ten two-species islands. Other studies have focused only on size assortment. By analyzing such patterns in a phylogenetic context, I explicitly consider historical effects and can distinguish between size adjustment and size assortment. Using a minimum evolution algo- rithm, I assess evidence for size adjustment by partitioning changes in size along branches of the phylogenetic tree. Size evolution appears rare (a minimum of 4-7 instances of substantial size evolution). In the northern (but not the southern) Lesser Antilles, size change was significantly greater when a descendant taxon occurred on a two-species island and its hypothetical ancestor occurred on a one-species island, thus supporting the size adjustment hypothesis, though size adjustment might have occurred only once. The relative rarity of size evolution suggests that size assortment might be responsible for non-random patterns. In both the northern and southern Lesser Antilles, a null model of no size assortment is convincingly rejected. Closely related taxa, however, are usually similar in size, and hybridization between species has been reported. Con- sequently, similar-sized species might not coexist because they interbreed and coalesce into one gene pool. A null model that only allows species from different "clades" to co-occur is rejected for the northern Lesser Antilles, but is ambiguous with regard to the southern Lesser Antilles. Thus, competitive exclusion is probably responsible for the pattern of size assortment in the northern Lesser Antilles; both competitive exclusion and interbreeding of closely related species of similar size might be responsible for the patterns evident in the southern Lesser Antilles.