Despite the aseasonality of temperature and day length of many tropical regions, especially when compared with temperate latitudes, most tropical animals show fairly pronounced seasonal shifts in foraging, movement patterns and reproduction (Flecker & Feifarek 1994, Saul 1975, Wolda & Fisk 1981). Understanding reproductive seasonality in tropical avian communities involves distinguishing among complex interactions between weather, resource abundance, hormones, behaviour and other life-history traits (Wikelski et al. 2003). While there is a great deal of evidence that many tropical bird species breed seasonally (Hau 2001, Marchant 1959, Miller 1963, Snow & Snow 1964), we still understand little of the causes which drive observed patterns (Wikelski et al. 2003). Most studies which address the seasonality of reproduction in tropical birds have focused on locations with fairly extreme temporal changes in rainfall (Cruz & Andrews 1989, Lack 1950, Marchant 1959, Poulin et al. 1992, Voous 1950), and comparatively few have looked at relatively aseasonal low-latitude locations (Miller 1963, Moreau 1950). Similarly, though a few studies have pointed out slight variation in the within-species initiation of breeding based on microhabitat (Wikelski et al. 2003), we know very little about how micro-habitat choice for nesting may affect (or be affected by) breeding seasonality. In this study I describe the nesting cycle of the spotted barbtail (Premnoplex brunnescens), from the Ecuadorian Andes to better understand how reproduction may be seasonal when climatic cues are subtle or absent.

The directional orientation of pre- and post-reproductive migration was studied in the Brazilian red-bellied toad Melanophryniscus cambaraensis, a species that forms explosive-breeding aggregations at irregular intervals throughout the entire year. Migrating toads were captured by enclosing the breeding site in dual drift fences with inward- and outward-facing funnel traps. Data were collected over 5 mo and totalled 333 captures. The observed directional orientation was significantly different from expected under a uniform distribution for both pre- and post-reproductive migration, regardless of gender. Males and females did not differ significantly from each other in the orientation of entry or exit, and the directional orientation of pre-reproductive migration was not significantly different from post-reproductive migration. It is suggested that the observed directional bias may be due to a dirt road next to the breeding site that could restrict juvenile dispersal to the adjacent forest.

Because anuran species are highly dependent on environmental variables, we hypothesized that anuran species richness and the number of reproductive modes from different Brazilian localities vary according to climatic and altitudinal variables. Published data were compiled from 36 Brazilian localities and climatic and altitudinal data were extracted from an available database. A partial redundancy analysis (pRDA) showed that 23.5% of the data set's variation was explained by climatic and altitudinal data, while the remaining 76.5% remained unexplained. This analysis suggests that other factors not analysed herein may also be important for predicting anuran species richness and the number of reproductive modes in Brazil. Altitude and total annual rainfall were positively correlated with anuran species richness and the number of reproductive modes, and total annual rainfall was strongly associated with these two biotic variables in the triplot of pRDA. The positive association of total annual rainfall and the negative association of the concentration of annual rainfall were already expected based on physiological and reproductive requirements of anurans. On the other hand, temperature was not associated with richness or the number of reproductive modes.

At Lamto, little is known about animal community responses to habitat variability resulting from fires and the mosaic pattern of the vegetation in general and in particular about that of termites which play key roles in this ecosystem. With a standardized method, data were collected on termites from four habitats differing in their vegetation cover and fire-history: annually burned savanna, savanna woodland, forest island and gallery forest. A range of environmental variables was measured and correlated with species abundances. The number of termite species collected in the savanna woodland was very close to that found in the gallery forest while the forest island was the richest habitat. The species richness of the savanna woodland and forest island seemed partly due to their heterogeneous and transitional vegetation structures and variable food resources. With regard to the fire-history of habitats, Connell's intermediate disturbance hypothesis offers an explanation for differences in the patterns of habitat-specific species richness. Variation in species abundances was significantly correlated with only two environmental variables (soil pH and woody plant species richness). The pH appeared as the most influential factor for fungus-growers while tree invasion in the savanna strongly reduces the abundance of grass-feeding species (e.g. Trinervitermes geminatus). Although not significantly correlated with species abundances, soil carbon showed a positive correlation with the dominant soil-feeder Basidentitermes potens. As for wood-feeders, they were not strongly correlated with woody plant species richness; this fact might be linked to their use for other sources of nourishment. Overall, it appears that habitat variability in the Lamto reserve contributes to the maintenance of different subsets of the termite community.

Trees of the family Dipterocarpaceae dominate the emergent canopy of most lowland rain forests in Asia (Ashton et al. 1988). The family is, therefore, one of the most ecologically important in South-East Asia. Shorea curtisii Dyer ex King is the most common tree species in the hill dipterocarp forests of Peninsular Malaysia (Burgess 1975, Symington 2004), and is considered a key species for the dynamics of such forests. Currently, most Malaysian hill forests are selectively logged. Trees over 50 cm dbh are harvested, and any subsequent harvests depend on the remaining smaller trees. Such selective logging takes no account of seedling regeneration. Hence, subsequent timber harvests rely on trees derived from the seedlings that are already present and future seeds produced by the residual trees (Appanah & Mohd. Rasol 1994). Existing seedlings of S. curtisii in the forest, therefore, play a significant role in the dynamics of the hill forest. However, the conditions that constitute a suitable habitat for S. curtisii seedling establishment and survival remain unknown.

Riparian vegetation varies according to hydrogeomorphic processes operating across different scales over two didmensions: transversely (across-stream) and longitudinally (parallel to stream). We tested the hypothesis that vegetation patterns reveal the scale and direction of underlying processes. We correlated patterns of dominant woody vegetation with environmental variables at 28 sites located within four geomorphologically distinct regions along the length of the South Alligator River catchment of Kakadu National Park, northern Australia. Across the catchment there existed a strong transverse boundary between upland savanna vegetation and two zones of riparian vegetation: Melaleuca-spp.-dominated closed-forest vegetation along stream channels and mixed open-woodland vegetation adjacent to closed forest. We surmise that there is hierarchic constraint on smaller-scale catchment processes due to fire incursion into the riparian zone and access to water during the dry season. Within the closed-forest zone, vegetation did not vary transversely, but did longitudinally. Riparian woodlands also varied longitudinally, but in the upper reaches varied independently of stream variables. By contrast, in the lower reaches woodland was strongly correlated with stream variables. The observed pattern of weak transverse linkages in headwaters but strong linkages in lower reaches is analogous to models developed for in-stream patterns and processes, particularly the river continuum and flood-pulse concepts.

Wild populations of a small neotropical primate, Geoffroy's tamarin (Saguinus geoffroyi), were studied through 30-s instantaneous observational sampling to identify different canopy habitats used by this tamarin. Tree and shrub canopies were sampled in randomly selected plots and in nearby plots that tamarins were observed to use in the forests of Agua Clara, Panama (28 d, 59 100-m2 plots, 32.25 h of tamarin observations, 27 tamarins in total), and in the nearby forests of Barro Colorado Island (49 d, 29 100-m2 plots, 29.6 h of tamarin observations, 14 tamarins in total). Light penetration through the canopy, ambient temperature and humidity, presence of other primates, stem diameters, plant life-forms, distribution of woody flora, abundance of fleshy fruits and arthropods typically consumed by tamarins and abundance of thorny vegetation and biting arthropods in plots used by tamarins were compared with control plots. Habitats used by tamarins had significantly shorter distances between adjacent tree canopies and between canopies and the ground. There was a random distribution of large insects and fleshy fruits that tamarins are known to eat. Habitat selection by tamarins may not be influenced by spiny vegetation, but tamarins may avoid areas with abundant hooked thorns and blood-sucking arthropods. Mobility along runways in various tiers of a rain-forest canopy may be of primary importance, with local abundance of food being a secondary consideration in habitat selection by this small primate.

Carbon and nitrogen stable isotope ratios (δ13C and δ15N) have been used to study the structure of food webs. However, few studies have examined how a terrestrial food web can be depicted by this technique. We measured δ13C and δ15N in various consumers of four trophic groups (detritivores, herbivores, omnivores and predators), including vertebrates and invertebrates (14 orders, ≥24 families), as well as canopy and understorey leaves in a tropical rain forest in Malaysia. We found that δ13C and δ15N of the consumers differed significantly among the trophic groups. The predators had significantly higher δ13C than the herbivores, and were similar in δ13C to the detritivores, suggesting that most predators examined depend largely on below-ground food webs. δ15N was higher in predators than detritivores by about 3‰. The comparison of δ13C in plant materials and herbivores suggests that most herbivores are dependent on C fixed in the canopy layers. The vertebrates had significantly higher δ15N and δ13C than the invertebrates of the same trophic group, likely reflecting differences in the physiological processes and/or feeding habits. This study indicates that stable isotope techniques can help better understanding of the terrestrial food webs in terms of both trophic level and the linkage of above- and below-ground systems.

For birds, moulting is an energetically costly endeavour (Murphy & King 1991), the timing and location of which may be flexible and governed by local ecological factors (Pyle et al. 2009, Rohwer et al. 2005). Some species or individuals may pause during long-distance migration, or migrate specifically to moult (Greenberg et al. 1974, Pyle et al. 2009, Rohwer et al. 2005, 2008). This strategy may be most common when food abundance reaches a nadir at the end of the breeding period, promoting movement to areas where food is more plentiful and the energetic and nutritive demands of moult may be met more suitably (Rohwer et al. 2005). This pattern is exemplified by insectivorous songbirds breeding in temperate, western North America that pause on southward migration to moult amidst the food flush that occurs following heavy rains in the Mexican monsoon region (Pyle et al. 2009, Rohwer et al. 2005, 2009), or more rarely, migrate upslope after breeding to moult in more moist, productive areas at higher elevation (Butler et al. 2002, Greenberg et al. 1974, Rohwer et al. 2008, Steele & McCormick 1995). Such altitudinal migration may be much more common in the Neotropics where many species engage in seasonal shifts in elevation. Hypotheses proposed to explain this behaviour, however, have focused on links made between migration and a principally frugivorous or nectarivorous diet (Levey & Stiles 1992, Stiles 1985, 1988) and not on moult requirements or phenology. Fruit and nectar availability may vary seasonally over an elevational gradient, and birds may migrate in order to track peak abundances (Levey & Stiles 1992, Loiselle & Blake 1991). Hummingbirds may also track arthropod (particularly spider) abundance, but this possibility remains little explored (Cotton 2007, Stiles 1980).

Leaf blade physical and chemical characteristics, wood composition and anatomy, as well as long-term water-use efficiency and hydraulic characteristics of leaf-bearing terminal branches were assessed in tree species growing in contrasting forests of the Venezuelan Amazonas: mixed forest on oxisol soil and caatinga on podzol soil. Two upper-canopy tree species were selected in each forest, and three individuals per species were tagged for sampling. Leaf nitrogen isotopic signatures (δ15N) were negative and species-specific, which suggests that in species of both forest the N-cycle is closed, and that tree species can withdraw N from a variety of N-pools. Leaf construction costs, dry mass to leaf area ratio, thickness and sclerophylly index tended to increase in microhabitats with lower fertility and large water table fluctuations. The hydraulic characteristics and long-term water use are species-specific and related to the particular conditions of the habitat at the local scale. Ocotea aciphylla (mixed forest) with a combination of low δ13C and high hydraulic sufficiency may maintain high water loss without risk of xylem embolisms. By contrast, Micranda sprucei (slopes of the caatinga forest), had a combination of relatively high hydraulic sufficiency and the highest long-term water-use efficiency, which suggest that embolism risk would be avoided by water loss restriction. Assuming a warmer and drier climate in the future, the species with more conservative water transport and/or better stomatal control would be at lower risk of mortality.

Dioecious plants often exhibit male-biased sex ratios and sexual differences in life history traits such as plant size, growth rate and frequency of flowering, which arise from the different costs of reproduction for male and female plants. In tropical dioecious species sexual differences in reproductive costs have been demonstrated for several subcanopy species, but few canopy dioecious trees have been studied. We recorded the sexual expression of c. 2600 trees of Cecropia schreberiana and Dacryodes excelsa, two canopy dioecious species, during several censuses over 2 y in a 16-ha plot located in ‘subtropical wet forest’ in the Luquillo Mountains, Puerto Rico. There were similar numbers of male and female trees of C. schreberiana but D. excelsa had a female-biased population. Cecropia schreberiana showed no differences in male and female diameter distributions or growth rates, suggesting that reproductive maturation and longevity are similar for both sexes. This lack of differences in size and growth rate in C. schreberiana may result from mechanisms to compensate for the higher cost of reproduction in females, no resource limitation related to its pioneer life-history, or similar male and female reproductive costs. In contrast, D. excelsa males were larger than females, probably because males grow slightly faster than females. This sexual difference in D. excelsa may reflect a higher cost of reproduction in females than in males. Spatial segregation of males and females into different habitats is not common in tropical forest and neither C. schreberiana nor D. excelsa males and females exhibited significant spatial segregation. The contrasting results for these two canopy species reflect their different life history strategies in this hurricane-affected forest.

The distribution of epiphytes differs between branches within tree crowns as well as within habitats. Where the original forests have been lost, shade coffee plantations can be important refuges for epiphytes, but are not suitable for all species. To understand what affects habitat quality, we transplanted 1440 seedlings each of two orchids, one, Lycaste aromatica, restricted to forests, the other, Jacquiniella teretifolia, common on trees in coffee plantations and in forests. Seedling mortality and growth were compared between three forests, three young and three old coffee plantations to test for differences between habitats and to analyse which habitat features affect growth and mortality. In J. teretifolia there was no clear pattern of habitat effect on mortality (c. 0.08 mo−1), but the production of new shoots was higher in coffee plantations than in forests. In L. aromatica, growth rates as well as seedling mortality increased over time. During the last census growth rates in forests (1.8 mm mo−1) were significantly higher than in old (0.9 mm mo−1) and young (1.2 mm mo−1) coffee plantations, and seedling mortality was about four times higher in old (0.10 mo−1) and young (0.11 mo−1) coffee plantations than in forests (0.025 mo−1), which may explain the natural absence of L. aromatica from coffee plantations. Mortality in L. aromatica at individual sites was negatively correlated with bryophyte cover on branches (Pearson r = –0.75) and positively with lichen cover (r = 0.70) and canopy openness (r = 0.75). Branch cover with non-vascular epiphytes, whether directly responsible by improving the water supply to epiphytes or indicative of differences in microclimate, may be a useful indicator of suitable habitats for vascular epiphytes.

A honeydew-producing scale insect, Stigmacoccus garmilleri (Margarodidae), is associated with oak trees (Quercus spp.) in highland forests of Mexico. Although feeding by ants on scale-insect honeydew is more frequently documented in the literature, the honeydew produced by feeding instars of S. garmilleri is sufficient to provide nourishment for birds. This study elucidates bird use of honeydew in the tropical montane forests near Chiconquiaco, Veracruz, Mexico, and uncovers patterns in honeydew foraging. Over a 2-mo period, 40 trees harbouring scale insects, located in both forest and pasture areas, were intensely studied (160 h of bird-foraging observations along with quantitative measurements of honeydew production). Fifteen resident bird species and 18 migrant species were observed visiting observation trees. Approximately 72% of the resident bird species and 83% of the migrant bird species observed were recorded to forage on scale-insect honeydew. Audubon's warbler (Dendroica coronata auduboni) was the most active consumer and defender of the resource. Of 118 aggressive chases observed, only 9.65% occurred in forest observation trees, and 90.3% in pasture trees. Audubon's warbler demonstrated preferential defence and territorial patrolling of scale-insect honeydew in scattered pasture trees.

Thousands of plant species throughout tropical and temperate zones secrete extrafloral nectar (EFN) (see www.biosci.unl.edu/emeriti/keeler/extrafloral/worldlistfamilies.htm) to attract ants, whose presence leads to an indirect defence against herbivores (Chamberlain & Holland 2009, Heil 2008, Heil & McKey 2003, Rico-Gray & Oliveira 2007). Although termed ‘extrafloral’ because the nectar is not involved in pollination, EFN can also be secreted within the inflorescences (Bentley 1977, Holland et al. 2010, Martins 2009). Because ants tend to defend reliable food sources against all types of putative competitors, it has been hypothesized that the presence of extrafloral nectaries close to flowers may lead to competition among ants and pollinators, or even to direct ant–pollinator conflicts. Such antagonistic interactions would reduce the access of pollinators to flowers and, thereby, may cause significant ‘ecological costs’ of indirect, ant-mediated defences (Heil 2002).

Ants (Hymenoptera: Formicidae) are important predators of herbivorous insects on plants (Rosumek et al. 2009). Ant removal or absence may result in negative indirect effects on plants, as herbivore abundance and herbivory increase and plant growth and reproduction decline (Rosumek et al. 2009, Schmitz et al. 2000). Ant presence on plants often results from a mutualistic interaction. For example, strong highly coevolved ant–plant mutualisms are found on myrmecophytic plants that house ants in domatia (specialized nesting sites). Weaker mutualistic associations are found with myrmecophilic plants that only offer extra-floral nectaries (EFNs) or food bodies to attract ants, or on other plants hosting honeydew-producing hemipterans (indirect ant–plant interactions) that mediate ant abundance (Hölldobler & Wilson 1990). However, in most cases, plants and arboreal ants form more passive associations, where ants nest in the natural cavities of branches or bark, or construct carton nests on plant substrates (Hölldobler & Wilson 1990) and the only reward plants offer these ants is the use of their substrates. In these situations the indirect effect of ants on plants is merely by chance, a byproduct of ant presence (byproduct association).

We tested the hypothesis that species of a diverse leaf-litter ant community are separated by the temperature preferences of their broods along a thermal gradient. Therefore, temperature preferences of brood-tending workers from 41 ant species co-occurring in four types (alluvial, limestone, kerangas and dipterocarp forest) of primary rain forest in Sarawak, Malaysia were measured in an experimental set-up. Preferred temperatures of species ranged from 16.0 °C to 31.7 °C, with the median at 25.8 °C. The ten commonest species (n ≥ 4) showed significantly different temperature preferences. In particular, species of the genus Pheidole differed clearly in their preferences over a broad range of temperatures. Temperature preferences varied significantly among ant assemblages from different forest types and nest sites. Experimentally obtained temperature preferences of species correlated significantly with vegetation density in the plots inhabited by the respective species, but not with plot canopy cover. When we tested the temperature preferences of all ant species with null models for niche overlap, we found a significant niche separation only among the tested species from the kerangas. Our results suggest that nest temperature is an important ecological factor for leaf-litter ants in rain forests on Borneo, but other factors may override its influence during community assembly.

Previous studies in Sundaland (Borneo, Sumatra, Java and Peninsular Malaysia) have shown that termite assemblages in natural forests have a characteristic structure. These typical forest assemblages contain many soil-feeding species. However, this study investigated four natural forest sites in Borneo with depauperate termite assemblages, and compared their soils with soils from four other sites that have typical termite assemblages. In contrast to the typical assemblages, the four depauperate assemblages all have low species density (<35%), low relative abundance (<30%), a virtual absence of soil-feeders, significantly fewer wood-feeders, and a near-absence of species of Rhinotermitidae, Amitermes-group, Termes-group, Pericapritermes-group and Oriensubulitermes-group. The depauperate sites are on ultramafic-derived soils and have significantly higher concentrations of calcium, magnesium, nickel, chromium, cobalt, copper and zinc compared with the non-ultramafic soils at sites with typical assemblages. In addition, soil pH at the depauperate sites is significantly higher (>pH 5.4) compared with soils at the typical sites (which are all below pH 4.7). Possible mechanisms to explain the depauperate termite assemblages on ultramafic soils include metal toxicity, high pH disrupting gut physiology, and microbial interactions with metals.

In tropical climates, nest movements by mature ant colonies are probably widespread but the phenomenon of nest relocation is poorly described (McGlynn 2007, McGlynn et al. 2004, Smallwood 1982a). For species that nest in soil, the costs and risks associated with excavating and establishing new nests are consequential, and it is assumed that relocation occurs when the costs are offset by a more advantageous nest location (Avargues-Weber & Monnin 2009, Banschbach & Herbers 1999). Nest movements may occur to areas with greater availability of food resources or to a more favourable microclimate. Here we provide the first report of nest relocation in one of the most widespread and well described ant species in the Neotropics, Ectatomma ruidum (Roger), and we perform a manipulative experiment to test whether food availability or light environment influence nest movement.

Parrots represent a large biomass of canopy granivores in tropical forests, and may be effective pre-dispersal seed predators. We evaluated the importance of the lilac-crowned parrot (Amazona finschi) as a pre-dispersal seed predator of Astronium graveolens (Anacardiaceae) in tropical dry forest. Seeds were collected in fruit-traps beneath 22 trees to compare pre-dispersal seed predation by parrots and insects, and determine whether intensity of seed predation was related to fruit-crop size or the aggregation of fruiting conspecifics around focal trees. Ground-level exclosures were established to compare post-dispersal seed predation by vertebrates and insects. The lilac-crowned parrot predated 43% of seeds pre-dispersal, while insects predated only 1.3%. Intensity of pre-dispersal seed predation by parrots was significantly greater in high-fruiting 0.79-ha resource patches, and was not related to fruit abundance of the focal tree. Foraging parrots also discarded immature fruits below the tree, causing a total 56% pre-dispersal loss of seed production, which was greater than post-dispersal removal by vertebrates, mainly rodents (51%) or insects (36%). Our results show that parrots play an important role as pre-dispersal seed predators in tropical dry forests. The reduction of parrot populations in tropical forests may have consequences for seed predation, affecting recruitment patterns of canopy trees.