In southern Mexico, four native and one introduced species of Opiinae (Braconidae) attack larvae of Anastrepha spp. fruit flies. There is a substantial overlap in the hosts of the parasitoids, and every species has been collected from fruit flies attacked by at least one or two other species. The ovipositors of these braconids have a broad interspecific range of lengths, some are less than the length of the abdomen, and others, several times the length of the abdomen. The following three hypotheses are proposed to account for this variety of lengths: (1) Because of differences in the host stage attacked, there are differences in host vulnerability; i.e., mature host larvae feed at greater depths within fruit pulp and can be best reached with a longer ovipositor. There is an implication that competition among the wasp species has selected for foraging on different host stages and that this diversifying selection has resulted in different ovipositor lengths. (2) Although longer ovipositors increase host range and thus have competitive advantages, they may be heavy, awkward, and expensive to move around. If so, species with longer ovipositors might have to invest more in locomotion (reflected in wing size) and less in reproductive capacity (numbers of mature eggs held in the ovarial calyx). Balancing selection would then maintain both short ovipositor-small winged-high fecundity species and long ovipositor-large wing-low fecundity species. (3) Although there are niche overlaps among the species, each has a “core environment” determined by factors such as temperature, humidity, seasonality, and host diversity. Ovipositor lengths have evolved to met the requirements of these specialized environments, and are not due to interspecific competition mediated by ovipositor length; i.e., there has been no diversifying or balancing selection for differences in ovipositor length. Hypothesis number 1 fails because all the species attack similar host stages. Neither was there support for hypothesis number 2. There were no correlations between wing size, or potential fecundity, and ovipositor length. The lack of correlation between species-pairs niche overlaps and differences in species-pairs relative ovipositor length is most consistent with hypothesis number 3. That is, because species with similar ovipositors are neither more or less likely to co-occur in the same samples from various fruits and locations than species with different ovipositor lengths it may be that species interactions are unimportant in the evolution of ovipositor lengths. If so, the lack of a pattern of competition made easily recognizable by differences in ovipositor length could influence biological control tactics. For example, if it is difficult to predict the abilities of newly introduced species to integrate in the existing guild of natural enemies, it may be more prudent over the short term to concentrate on the conservation of the natural enemies already present rather than pursue the “classical” introductions of new species.
You have requested a machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Neither BioOne nor the owners and publishers of the content make, and they explicitly disclaim, any express or implied representations or warranties of any kind, including, without limitation, representations and warranties as to the functionality of the translation feature or the accuracy or completeness of the translations.
Translations are not retained in our system. Your use of this feature and the translations is subject to all use restrictions contained in the Terms and Conditions of Use of the BioOne website.
Vol. 94 • No. 6