Neotropical fish-fruit interactions: eco-evolutionary dynamics and conservation.

Frugivorous fish play a prominent role in seed dispersal and reproductive dynamics of plant communities in riparian and floodplain habitats of tropical regions worldwide. In Neotropical wetlands, many plant species have fleshy fruits and synchronize their fruiting with the flood season, when fruit-eating fish forage in forest and savannahs for periods of up to 7 months. We conducted a comprehensive analysis to examine the evolutionary origin of fish-fruit interactions, describe fruit traits associated with seed dispersal and seed predation, and assess the influence of fish size on the effectiveness of seed dispersal by fish (ichthyochory).

Ecosystem services provided by bats.

Ecosystem services are the benefits obtained from the environment that increase human well-being. Economic valuation is conducted by measuring the human welfare gains or losses that result from changes in the provision of ecosystem services. Bats have long been postulated to play important roles in arthropod suppression, seed dispersal, and pollination; however, only recently have these ecosystem services begun to be thoroughly evaluated.

Exploring demographic, physical, and historical explanations for the genetic structure of two lineages of Greater Antillean bats.

Observed patterns of genetic structure result from the interactions of demographic, physical, and historical influences on gene flow. The particular strength of various factors in governing gene flow, however, may differ between species in biologically relevant ways. We investigated the role of demographic factors (population size and sex-biased dispersal) and physical features (geographic distance, island size and climatological winds) on patterns of genetic structure and gene flow for two lineages of Greater Antillean bats.

The evolution of bat pollination: a phylogenetic perspective.

Background: Most tropical and subtropical plants are biotically pollinated, and insects are the major pollinators. A small but ecologically and economically important group of plants classified in 28 orders, 67 families and about 528 species of angiosperms are pollinated by nectar-feeding bats. From a phylogenetic perspective this is a derived pollination mode involving a relatively large and energetically expensive pollinator.

Characterization of polymorphic microsatellite loci for two species of phyllostomid bats from the Greater Antilles (Erophylla sezekorni and Macrotus waterhousii).

We developed 12 polymorphic microsatellite loci for the buffy flower bat (Erophylla sezekorni) and 10 loci for Waterhouse's big-eared bat (Macrotus waterhousii). In E. sezekorni, we tested 65 individuals from three islands, Cuba, Exuma, and Abaco.

Genetic population structure and mobility of two nectar-feeding bats from Venezuelan deserts: inferences from mitochondrial DNA.

Glossophaga longirostris and Leptonycteris curasoae are nectar-feeding bats associated with arid zones in northern South America. Despite their close phylogenetic relationship, sympatric condition and niche similarities, morphological and ecological evidence suggest that these species differ in dispersal capabilities. Using mitochondrial DNA, we tested the hypothesis that these species exhibit different levels of population structure that are congruent with their particular movement capabilities.

The evolution of obligate pollination mutualisms: senita cactus and senita moth.

We report a new obligate pollination mutualism involving the senita cactus, Lophocereus schottii (Cactaceae, Pachyceereae), and the senita moth, Upiga virescens (Pyralidae, Glaphyriinae) in the Sonoran Desert and discuss the evolution of specialized pollination mutualisms. L. schottii is a night-blooming, self-incompatible columnar cactus.

Seasonal changes in the diets of migrant and non-migrant nectarivorous bats as revealed by carbon stable isotope analysis.

Three species of nectar-feeding bats migrate from tropical and subtropical Mexico into the Sonoran and Chihuahuan deserts during the spring and summer months. We examined geographic and seasonal changes in the diet of one migrant species, Leptonycteris curasoae, using carbon stable isotope techniques to determine the relative importance of C3 and CAM (Cactaceae, Agavaceae) plants in its diet. We also examined the diet of a non-migratory nectar-feeding bat, Glossophaga soricina, from southern Mexico using the same techniques.

On the analysis of phenological overlap.

We briefly review current methods for detecting nonrandom patterns in the temporal overlap of flowering and fruiting curves. We discuss the assumptions behind these methods and propose a new method of analysis using computer simulations to measure n-wise, rather than pairwise, temporal overlap. We quantify the extent to which observed n-wise overlap differs from minimum possible n-wise overlap and apply our method to several data sets to test the hypothesis that interspecific competition for animal visitors has produced flowering curves whose overlap is less than that expected by chance.

Parallel trends in the species diversity of west indian birds and bats.

In this paper I compare several biogeographic patterns of West Indian resident land birds and bats, including species-area and trophic diversity-area relationships, the number of islands inhabited per species and levels of endemism, trophic structure as compared with tropical mainland areas, and the degree of faunal simlarity between islands of similar sizes but different locations. In most respects, the bat and bird patterns are strikingly similar. Groups of birds that are conspicuously missing from the Antilles because of the absence of appropriate resources also have missing chiropteran counterparts.

Fecundity, fruiting pattern, and seed dispersal in Piper amalago (Piperaceae), a bat-dispersed tropical shrub.

This paper describes the nightly and seasonal production of ripe fruit by Piper amalago (Piperaceae), a patchily distributed, bat-dispersed forest shrub, at Parque Nacional Santa Rosa, Costa Rica. Phenological observations over several years indicate that individuals produce a low (usually 1-3) and variable number of ripe fruit each night for 3-4 wks in the early wet season (June and July). Observations of the disappearance rates of marked fruits and fruit manipulation experiments indicate that fruit removal probabilities are high (often nearly 1.