Coordinated hunting behaviors of mixed-species groups of piscivores and associated species at Isla del Coco National Park (Eastern Tropical Pacific)
Artículo académico
Studies of mixed-species groups of animals can reveal emergent complexities of collective behaviors. In this study we collected data on mixed-species hunting groups composed primarily of piscivorous fishes (species composition, abundance, behavioral interactions) and used both multivariate and network analyses to quantify pair-wise and guild level behavioral relationships. Our results indicate that such collective behaviors exhibit consistent patterns of associations (33 species with 282 pair-wise links within the observed network) with 10 dominant species accounting for 60% of pair-wise interactions. Species richness within groups varied (mean = 2.4, range 2-6 species) as did group size (mean = 8.1 individuals, range 2-80). Mixed-species groups, in general, were composed of species representing morphologically diverse forms that appeared to enhance access to shelter sites and implement diverse strategies for prey capture. It is noteworthy that the composition of groups did not reflect the relative abundances of their component species within the overall community of fishes, suggesting that group membership was an elective choice. The identification of these patterns, assuming they are persistent features of these communities, can be used as a foundation for studies to assess dynamics of mixed-species relationships, rates of predator success based on group membership, demographic consequences, and responses to variations in habitat attributes and associated prey resources. Such information could be used to interpret the nature of multispecies interactions within predator communities and potentially aid in conservation and management.
The pathogenesis of skeletal muscle necrosis induced by crude Bothrops asper venom and isolated myotoxic phospholipase was studied using light and electron microscopy. White mice were injected intramuscularly with a dose of 2.5 μg/g and tissue samples were taken at 30 min and 1, 3, 6, 12, 24, and 48 hr. Toxin-injected muscle showed localized wedgeshaped lesions (“delta lesions”) by 30 min, which included disrupted plasma membranes. At 1 and 3 hr the predominant type of necrotic cell contained clumped myofibrils in which individual myofilaments were indistinguishable. At later time periods there was a relaxation and redistribution of myofilaments resulting in a more homogeneous and hyaline appearance of necrotic cells. Some mitochondria were swollen and had flocculent densities, and most of them were disrupted, having only one membrane and vesiculated cristae. The basal lamina was intact at all time intervals. Phagocytosis of muscle cell debris started at 3 hr and was prominent by 24–48 hr. In crude venom-injected muscle many cells showed pathologic features identical to those observed after myotoxin injection. Crude venom also induced hemorrhage which was evident 30 min after injection, reaching its highest level by 12 hr. At 3, 6, and 12 hr some cells were undergoing different pathologic changes which appeared to be due to ischemia. Although these cells were irreversibly damaged, as indicated by ruptured plasma membrane, their myofibrillar structure was better preserved than that of toxin-affected cells. The Z line was absent, but A, I, H, and M bands were intact. As a result of Z line loss, sarcomeres were disoriented. It is proposed that the myotoxin induces myonecrosis by first altering the integrity of the plasma membrane, thereby increasing the permeability to calcium, other ions, and molecules which leads to death of the cell. Crude venom affects muscle cells in two ways: by direct action of myotoxin(s) and by ischemia due to hemorrhage.
