Cross-taxon congruence in tree,bird and bat species distributions at a moderate spatial scale across four tropical forest types in the Philippines

Indicator species groups are often used as surrogates for overall biodiversity in conservation planning because inventories of multiple taxa are rare, especially in the tropics where most biodiversity is found. At coarse spatial scales most studies show congruence in the distribution of species richness and of endemic and threatened species of different species groups. At finer spatial scale levels however, cross-taxon congruence patterns are much more ambiguous. In this study we investigated cross-taxon patterns in the distribution of species richness of trees, birds and bats across four tropical forest types in a ca. 100 × 35 km area in the Northern Sierra Madre region of Luzon Island, Philippines. A non-parametric species richness estimator (Chao1) was used to compensate for differential sample sizes, sample strategies and completeness of species richness assessments. We found positive but weak congruence in the distribution of all and endemic tree and bird and tree and bat species richness across the four forest types; strong positive congruence in the distribution of all and endemic bat and bird species richness and low or negative congruence in the distribution of globally threatened species between trees, birds and bats. We also found weak cross-taxon congruence in the complementarity of pairs of forest types in species richness between trees and birds and birds and bats but strong congruence in complementarity of forest pairs between trees and bats. This study provides further evidence that congruence in the distribution of different species groups is often ambiguous at fine to moderate spatial scales. Low or ambiguous cross-taxon congruence complicates the use of indicator species and species groups as a surrogate for biodiversity in general for local systematic conservation planning.     

Species-area curves, diversity indices, and species abundance distributions: a multifractal analysis

Although fractals have been applied in ecology for some time, multifractals have, in contrast, received little attention. In this article, we apply multifractals to the species-area relationship and species abundance distributions. We highlight two results: first, species abundance distributions collected at different spatial scales may collapse into a single curve after appropriate renormalization, and second, the power-law form of the species-area relationship and the Shannon, Simpson, and Berger-Parker diversity indices belong to a family of equations relating the species number, species abundance, and area through the moments of the species abundance-probability density function. Explicit formulas for these diversity indices, as a function of area, are derived. Methods to obtain the multifractal spectra from a data set are discussed, and an example is shown with data on tree and shrub species collected in a 50-ha plot on Barro Colorado Island, Panama. Finally, we discuss the implications of the multifractal formalism to the relationship between species range and abundance and the relation between the shape of the species abundance distribution and area.     

Dependence of broad-scale geographical variation in fleshy-fruited plant species richness on disperser bird species richness

Aim We analysed the interdependence of avian frugivore‐ and fruited plant‐species richness at the scale of major river basins across Europe, taking into account several environmental factors along different spatial gradients. Location Continental Europe and the British Isles. Methods We focused on wintering birds and autumn/winter fruiting plants, and used major river basins as geographical units and Structural Equation Modelling as the principal analytical tool. Results The statistical influence of disperser species richness on fleshy‐fruited plant species richness is roughly double that of the reverse. Broad‐scale variation in frugivore richness is more dependent on environmental factors than on fruited plant richness. However, the influence of disperser richness on plant richness is four times higher than the influence of environmental factors. Environmental influences on both birds and plants are greater than purely spatial influences. Main conclusions Our results are interpreted as indicating that biotic dispersal of fruits strongly affects broad‐scale geographical trends of fleshy‐fruited plant species richness, whereas richness of fruited plants moderately affects frugivore richness.     

Large-scale spatial variation in palm fruit abundance across a tropical moist forest estimated from high-resolution aerial photographs

Fruit abundance is a critical factor in ecological studies of tropical forest animals and plants, but difficult to measure at large spatial scales. We tried to estimate spatial variation in fruit abundance on a relatively large spatial scale using low altitude, high‐resolution aerial photography. We measured fruit production for all 555 individuals of the arborescent palm Astrocaryum standleyanum across 25 ha of mapped tropical moist forest on Barro Colorado Island, Panama, by visually counting fruits from the ground. Simultaneously, we used high‐resolution aerial photographs to map sun‐exposed crowns of the palm across the same area, which were then linked to ground‐mapped stems. First, we verified that the fruit crop size of individual trees was positively associated with both crown presence on aerial photos and crown area visible on aerial photos. Then, we determined how well spatial variation in Astrocaryum fruit density across the study area was predicted by spatial densities of photo‐detected crowns and crown area compared to spatial densities of ground‐mapped stems and stem diameters. We found a positive association of fruit crop size with crown visibility on aerial photographs. Although representing just one third of all individuals in the study area, photo‐detected crowns represented 57% of all fruits produced. The spatial pattern of photo‐detected crowns was strongly correlated with the spatial pattern of fruit abundance based on direct fruit counts, and correctly showed the areas with the highest and lowest fruit abundances. The spatial density of photo‐detected crowns predicted spatial variation in fruit abundance equally well as did the spatial density of ground‐mapped stems. Photo‐detected crown area did not yield a better prediction. Our study indicates that remote sensing of crowns can be a reliable and cost‐effective method for estimating spatial variation in fruit abundance across large areas for highly distinctive canopy species. Our study is also among the few to provide empirical evidence for a positive relationship between crown exposure of forest trees and fruit production.     

Mapping Tropical Forest Trees Using High‐Resolution Aerial Digital Photographs

The spatial arrangement of tree species is a key aspect of community ecology. Because tree species in tropical forests occur at low densities, it is logistically challenging to measure distributions across large areas. In this study, we evaluated the potential use of canopy tree crown maps, derived from high‐resolution aerial digital photographs, as a relatively simple method for measuring large‐scale tree distributions. At Barro Colorado Island, Panama, we used high‐resolution aerial digital photographs (~0.129 m/pixel) to identify tree species and map crown distributions of four target tree species. We determined crown mapping accuracy by comparing aerial and ground‐mapped distributions and tested whether the spatial characteristics of the crown maps reflect those of the ground‐mapped trees. Nearly a quarter (22%) of the common canopy species had sufficiently distinctive crowns to be good candidates for reliable mapping. The errors of commission (crowns misidentified as a target species) were relatively low, but the errors of omission (missed canopy trees of the target species) were high. Only 40 percent of canopy individuals were mapped on the air photographs. Despite failing to accurately predict exact abundances of canopy trees, crown distributions accurately reproduced the clumping patterns and spatial autocorrelation features of three of four tree species and predicted areas of high and low abundance. We discuss a range of ecological and forest management applications for which this method can be useful.     

Richness and composition of plants and birds on land‐bridge islands: effects of island attributes and differential responses of species groups

Aim To test relationships between the richness and composition of vascular plants and birds and attributes of habitat fragments using a model land‐bridge island system, and to investigate whether the effects of fragmentation differ depending on species natural history traits. Location Thousand Island Lake, China. Methods We compiled presence/absence data of vascular plant and bird species through exhaustive surveys of 41 islands. Plant species were assigned to two categories: shade‐intolerant and shade‐tolerant species; bird species were assigned to three categories: edge, interior, and generalist species. We analysed the relationships between island attributes (area, isolation, elevation, shape complexity, and perimeter to area ratio) and species richness using generalized linear models (GLMs). We also investigated patterns of composition in relation to island attributes using ordination (redundancy analysis). Results We found that island area explained a high degree of variation in the species richness of all species groups. The slope of the species–area relationship (z) was 0.16 for all plant species and 0.11 for all bird species. The lowest z‐value was for generalist birds (0.04). The species richness of the three plant species groups was associated with island area per se, while that of all, generalist, and interior birds was explained mainly by elevation, and that of edge bird species was associated primarily with island shape. Patterns of species composition were most strongly related to elevation, island shape complexity, and perimeter to area ratio rather than to island area per se. Species richness had no significant relationship with isolation, but species composition did. We also found differential responses among the species groups to changes in island attributes. Main conclusions Within the Thousand Island Lake system, the effects of fragmentation on both bird and plant species appear to be scale‐dependent and taxon‐specific. The number of plant species occurring on an island is strongly correlated with island area, and the richness of birds and the species composition of plants and birds are associated with variables related to habitat heterogeneity. We conclude that the effects of fragmentation on species diversity and composition depend not only on the degree of habitat loss but also on the specific patterns of habitat fragmentation.     

Spatial scaling of extinction rates: Theory and data reveal nonlinearity and a major upscaling and downscaling challenge

Aim

Biodiversity loss is a key component of biodiversity change and can impact ecosystem services. However, estimation of the loss has focused mostly on per‐species extinction rates measured over a limited number of spatial scales, with little theory linking small‐scale extirpations to global extinctions. Here, we provide such a link by introducing the relationship between area and the number of extinctions (number of extinctions–area relationship; NxAR) and between area and the proportion of extinct species (proportion of extinctions–area relationship; PxAR). Unlike static patterns, such as the species–area relationship, NxAR and PxAR represent spatial scaling of a dynamic process. We show theoretical and empirical forms of these relationships and we discuss their role in perception and estimation of the current extinction crisis.

Location

U.S.A., Europe, Czech Republic and Barro Colorado Island (Panama).

Time period

1500–2009.

Major taxa studied

Vascular plants, birds, butterflies and trees.

Methods

We derived the expected forms of NxAR and PxAR from several theoretical frameworks, including the theory of island biogeography, neutral models and species–area relationships. We constructed NxAR and PxAR from five empirical datasets collected over a range of spatial and temporal scales.

Results

Although increasing PxAR is theoretically possible, empirical data generally support a decreasing PxAR; the proportion of extinct species decreases with area. In contrast, both theory and data revealed complex relationships between numbers of extinctions and area (NxAR), including nonlinear, unimodal and U‐shaped relationships, depending on region, taxon and temporal scale.

Main conclusions

The wealth of forms of NxAR and PxAR explains why biodiversity change appears scale dependent. Furthermore, the complex scale dependence of NxAR and PxAR means that global extinctions indicate little about local extirpations, and vice versa. Hence, effort should be made to understand and report extinction rates as a scale‐dependent problem. In this effort, estimation of scaling relationships such as NxAR and PxAR should be central.     

The epiphyte vegetation of Annona glabra on Barro Colorado Island, Panama

Aim Information on the community composition, structure, and dynamics of epiphyte vegetation is scarce. A survey of the epiphytes occurring on all individuals of one particular host tree species in a well-studied neotropical research site allowed us a comparison of the epiphyte flora of this tree with the local epiphyte flora, the analysis of spatial distribution patterns and the use of these patterns as indications for changes in time. In the future, our results can be used as a baseline data-set for the direct observation of the long-term dynamics in epiphyte communities. Location The study was conducted on Barro Colorado Island (BCI), Panama. Methods We recorded all individuals of the vascular epiphytes growing on Annona glabra L., a flood-tolerant, multiple-stemmed tree, which is restricted to the shoreline of BCI. Data on tree biometrics, epiphyte species, and epiphyte abundances were collected for more than 1200 trees. Results In total, we encountered almost 15,000 epiphytic individuals in sixty-eight species, corresponding to more than one third of the entire epiphyte flora of Barro Colorado Island. The component species differed strongly in abundance: the four most important species accounted for >75% of all individuals. In most cases, the same four species were also the first to colonize a tree (=phorophyte). Colonization patterns indicated no replacement of early colonizers by late arrivals. Species richness and epiphyte abundances showed a positive correlation with the size and the density of the host trees. All species showed a highly clumped distribution and the physiognomy of epiphyte communities of individual trees was dominated either by one or several of the four most common species or by a set of frequently co-occurring tank bromeliads. Other species were dominant only in exceptional cases. Most species were always rare. A distance effect on community composition was mostly confined to a local scale with an increased similarity in the species assemblage of stems of a tree v. neighbouring trees. Main conclusions The epiphytes on a single small phorophyte species may encompass a surprisingly large proportion of the local epiphyte flora. The observations that most tree crowns are inhabited by a single or only very few species, and that all epiphyte species show highly clumped distributions suggest a predominance of very local dispersal within a tree crown, which is only infrequently interrupted by successful long-distance dispersal between crowns.     

Geometric constraints and spatial pattern of species richness: critique of range-based null models

Abstract. Does the shape of a biogeographical region influence its spatial patterns of species richness? A complete answer must include careful distinction between the distribution of a species, which is a complex geometric object, and the range of a species, which is relatively simple, especially when reduced to one dimension. We consider range‐based models of species richness, in particular range overlap counts in one dimension, for which we give a unified mathematical treatment via the joint probability P(m,l) of midpoints and lengths of ranges. We discuss a number of difficulties, in practice and in principle, using range‐based models, and show that the so‐called mid‐domain effect, a proposed null model for the effect of geometric constraint, is qualitatively a property of all biologically realistic models based on range overlap counts. As such, range‐based models provide little insight into understanding or explaining biogeographical patterns in species richness. We characterize the quantitative null model for range overlap counts in one dimension, for which we give a simple and direct field test based on P(m,l). We apply this test to a large clade in a complete bioregion (the Proteaceae of the Cape Floristic Region): geometric constraint does not explain the spatial pattern in this case. We show that any geometric constraint on species richness, including range overlap counts, must act via edge effects. Thus, to understand biogeographical patterns, an understanding of the effects and consequences of edges is fundamental.     

Scale dependence of effective specialization: its analysis and implications for estimates of global insect species richness

Estimates of global insect species richness are sometimes based on effective specialization, a calculation used to estimate the number of insect species that is restricted to a particular tree species. Yet it is not clear how effective specialization is influenced by spatial scale or characteristics of the insect community itself (e.g. species richness). We investigated scale dependence and community predictors of effective specialization using 15,907 beetles (583 species) collected by insecticide fogging from the crowns of 96 trees (including 32 Quercus trees) located in Ohio and Indiana. Trees were distributed across 24 forest stands (∼1 ha) nested within six sites (∼10–100 km²) and two ecoregions (> 1000 km²). Using paired-sample randomization tests, we found that effective specialization ( f _k ) exhibited negative scale-dependence in early (May–June 2000) and late (August–September 2000) sampling periods. Our average effective specialization ( F ) values — those that are comparable to Erwin's (1982) estimates — ranged from 19% to 97%, and increased as spatial scale decreased. We also found that beetle species richness and the number of shared beetle species across host trees were significant and consistent negative predictors of F . This shows that increases in spatial scale, species richness, and the number of trees (and/or tree species) all coincide with decreases in effective specialization. Collectively, our results indicate that estimates of global insect species richness based on effective specialization at a single spatial scale are overestimating the magnitude of global insect species richness. We propose that scale dependence should be promoted to a central concept in the research program on global estimates of species richness.     

Estimating demographic models for the range dynamics of plant species

Aims To better understand how demographic processes shape the range dynamics of woody plants (in this case, Proteaceae), we introduce a likelihood framework for fitting process‐based models of range dynamics to spatial abundance data. Location The fire‐prone Fynbos biome (Cape Floristic Region, South Africa). Methods Our process‐based models have a spatially explicit demographic submodel (describing dispersal, reproduction, mortality and local extinction) as well as an observation submodel (describing imperfect detection of individuals), and are constrained by species‐specific predictions of habitat distribution models and process‐based models for seed dispersal by wind. Free model parameters were varied to find parameter sets with the highest likelihood. After testing this approach with simulated data, we applied it to eight Proteaceae species that differ in breeding system (monoecy versus dioecy) and adult fire survival. We assess the importance of Allee effects and negative density dependence for range dynamics, by using the Akaike information criterion to select between alternative models fitted for the same species. Results The best model for all dioecious study species included Allee effects, whereas this was true for only one of four monoecious species. As expected, sprouters (in which adults survive fire) were estimated to have lower rates of reproduction and catastrophic population extinction than related non‐sprouters. Overcompensatory population dynamics seem important for three of four non‐sprouters. We also found good quantitative agreement between independent data and most estimates of reproduction, carrying capacity and extinction probability. Main conclusions This study shows that process‐based models can quantitatively describe how large‐scale abundance distributions arise from the movement and interaction of individuals. It stresses links between the life history, demography and range dynamics of Proteaceae: dioecious species seem more susceptible to Allee effects which reduce migration ability and increase local extinction risk, and sprouters seem to have high persistence of established populations, but their low reproduction limits habitat colonization and migration.     

Plants on small islands revisited: the effects of spatial scale and habitat quality on the species–area relationship

Understanding how species diversity is related to sampling area and spatial scale is central to ecology and biogeography. Small islands and small sampling units support fewer species than larger ones. However, the factors influencing species richness may not be consistent across scales. Richness at local scales is primarily affected by small‐scale environmental factors, stochasticity and the richness at the island scale. Richness at whole‐island scale, however, is usually strongly related to island area, isolation and habitat diversity. Despite these contrasting drivers at local and island scales, island species–area relationships (SARs) are often constructed based on richness sampled at the local scale. Whether local scale samples adequately predict richness at the island scale and how local scale samples influence the island SAR remains poorly understood. We investigated the effects of different sampling scales on the SAR of trees on 60 small islands in the Raja Ampat archipelago (Indonesia) using standardised transects and a hierarchically nested sampling design. We compared species richness at different grain sizes ranging from single (sub)transects to whole islands and tested whether the shape of the SAR changed with sampling scale. We then determined the importance of island area, isolation, shape and habitat quality at each scale on species richness. We found strong support for scale dependency of the SAR. The SAR changed from exponential shape at local sampling scales to sigmoidal shape at the island scale indicating variation of species richness independent of area for small islands and hence the presence of a small‐island effect. Island area was the most important variable explaining species richness at all scales, but habitat quality was also important at local scales. We conclude that the SAR and drivers of species richness are influenced by sampling scale, and that the sampling design for assessing the island SARs therefore requires careful consideration.     

Spatial scaling of species abundance distributions

Species abundance distributions are an essential tool in describing the biodiversity of ecological communities. We now know that their shape changes as a function of the size of area sampled. Here we analyze the scaling properties of species abundance distributions by using the moments of the logarithmically transformed number of individuals. We find that the moments as a function of area size are well fitted by power laws and we use this pattern to estimate the species abundance distribution for areas larger than those sampled. To reconstruct the species abundance distribution from its moments, we use discrete Tchebichef polynomials. We exemplify the method with data on tree and shrub species from a 50 ha plot of tropical rain forest on Barro Colorado Island, Panama. We test the method within the 50 ha plot, and then we extrapolate the species abundance distribution for areas up to 5 km². Our results project that for areas above 50 ha the species abundance distributions have a bimodal shape with a local maximum occurring for the singleton classes and that this maximum increases with sampled area size.     

Beneath the veil: plant growth form influences the strength of species richness–productivity relationships in forests

Aim Species richness has been observed to increase with productivity at large spatial scales, though the strength of this relationship varies among functional groups. In forests, canopy trees shade understorey plants, and for this reason we hypothesize that species richness of canopy trees will depend on macroclimate, while species richness of shorter growth forms will additionally be affected by shading from the canopy. In this study we test for differences in species richness–productivity relationships (SRPRs) among growth forms (canopy trees, shrubs, herbaceous species) in small forest plots. Location We analysed 231 plots ranging from 34.0° to 48.3° N latitude and from 75.0° to 124.2° W longitude in the United States. Methods We analysed data collected by the USDA Forest Inventory and Analysis program for plant species richness partitioned into different growth forms, in small plots. We used actual evapotranspiration as a macroclimatic estimate of regional productivity and calculated the area of light‐blocking tissue in the immediate area surrounding plots for an estimate of the intensity of local shading. We estimated and compared SRPRs for different partitions of the species richness dataset using generalized linear models and we incorporated the possible indirect effects of shading using a structural equation model. Results Canopy tree species richness increased strongly with regional productivity, while local shading primarily explained the variation in herbaceous plant richness. Shrub species richness was related to both regional productivity and local shading. Main conclusions The relationship between total forest plant species richness and productivity at large scales belies strong effects of local interactions. Counter to the pattern for overall richness, we found that understorey herbaceous plant species richness does not respond to regional productivity gradients, and instead is strongly influenced by canopy density, while shrub species richness is under multivariate control.     

Mating systems of two Bombacaceous trees of a neotropical moist forest

Summary A multilocus mixed mating model was used to analyze the mating systems of two tropical canopy trees in the Bombacaceae that differ in successional status and overall abundance. One population of each species was studied on Barro Colorado Island, Republic of Panama. Population outcrossing estimates of 0.57 and 0.35 from two years indicate a mixed-mating system with intermediate outcrossing levels for the gap-specialist Cavanillesia platanifolia, a relatively rare component of the island flora. Population and individual outcrossing estimates were associated with flowering tree density or degree of spatial isolation. Trees within clusters of flowering individuals have a higher degree of outcrossing than isolated trees. Annual estimates of individual tree outcrossing rates varied greatly as a function of flowering in its nearest neighbors. In contrast to C. platanifolia, Quararibea asterolepis was completely outcrossed and may be self incompatible. Maternal trees of both species had significantly heterogeneous pollen pools indicating non-random outcrossing. Apomixis by sporophytic agamospermy was rejected in C. platanifolia as contributing to the apparent selfing rate.     

Moving beyond abundance distributions: neutral theory and spatial patterns in a tropical forest

Assessing the relative importance of different processes that determine the spatial distribution of species and the dynamics in highly diverse plant communities remains a challenging question in ecology. Previous modelling approaches often focused on single aggregated forest diversity patterns that convey limited information on the underlying dynamic processes. Here, we use recent advances in inference for stochastic simulation models to evaluate the ability of a spatially explicit and spatially continuous neutral model to quantitatively predict six spatial and non-spatial patterns observed at the 50 ha tropical forest plot on Barro Colorado Island, Panama. The patterns capture different aspects of forest dynamics and biodiversity structure, such as annual mortality rate, species richness, species abundance distribution, beta-diversity and the species–area relationship (SAR). The model correctly predicted each pattern independently and up to five patterns simultaneously. However, the model was unable to match the SAR and beta-diversity simultaneously. Our study moves previous theory towards a dynamic spatial theory of biodiversity and demonstrates the value of spatial data to identify ecological processes. This opens up new avenues to evaluate the consequences of additional process for community assembly and dynamics.     

Assessing the vulnerability of species richness to anthropogenic climate change in a biodiversity hotspot

Aim To compare theoretical approaches towards estimating risks of plant species loss to anthropogenic climate change impacts in a biodiversity hotspot, and to develop a practical method to detect signs of climate change impacts on natural populations. Location The Fynbos biome of South Africa, within the Cape Floristic Kingdom. Methods Bioclimatic modelling was used to identify environmental limits for vegetation at both biome and species scale. For the biome as a whole, and for 330 species of the endemic family Proteaceae, tolerance limits were determined for five temperature and water availability‐related parameters assumed critical for plant survival. Climate scenarios for 2050 generated by the general circulation models HadCM2 and CSM were interpolated for the region. Geographic Information Systems‐based methods were used to map current and future modelled ranges of the biome and 330 selected species. In the biome‐based approach, predictions of biome areal loss were overlayed with species richness data for the family Proteaceae to estimate extinction risk. In the species‐based approach, predictions of range dislocation (no overlap between current range and future projected range) were used as an indicator of extinction risk. A method of identifying local populations imminently threatened by climate change‐induced mortality is also described. Results A loss of Fynbos biome area of between 51% and 65% is projected by 2050 (depending on the climate scenario used), and roughly 10% of the endemic Proteaceae have ranges restricted to the area lost. Species range projections suggest that a third could suffer complete range dislocation by 2050, and only 5% could retain more than two thirds of their range. Projected changes to individual species ranges could be sufficient to detect climate change impacts within ten years. Main conclusions The biome‐level approach appears to underestimate the risk of species diversity loss from climate change impacts in the Fynbos Biome because many narrow range endemics suffer range dislocation throughout the biome, and not only in areas identified as biome contractions. We suggest that targeted vulnerable species could be monitored both for early warning signs of climate change and as empirical tests of predictions.     

Common spatial patterns of trees in various tropical forests: Small trees are associated with increased diversity at small spatial scales

Tropical forests are notable for their high species diversity, even on small spatial scales, and right‐skewed species and size abundance distributions. The role of individual species as drivers of the spatial organization of diversity in these forests has been explained by several hypotheses and processes, for example, stochastic dilution, negative density dependence, or gap dynamics. These processes leave a signature in spatial distribution of small trees, particularly in the vicinity of large trees, likely having stronger effects on their neighbors. We are exploring species diversity patterns within the framework of various diversity‐generating hypotheses using individual species–area relationships. We used the data from three tropical forest plots (Wanang—Papua New Guinea, Barro Colorado Island—Panama, and Sinharaja—Sri Lanka) and included also the saplings (DBH ≥ 1 cm). Resulting cross‐size patterns of species richness and evenness reflect the dynamics of saplings affected by the distribution of large trees. When all individuals with DBH ≥1 cm are included, ~50% of all tree species from the 25‐ or 50‐ha plot can be found within 35 m radius of an individual tree. For all trees, 72%–78% of species were identified as species richness accumulators, having more species present in their surroundings than expected by null models. This pattern was driven by small trees as the analysis of DBH >10 cm trees showed much lower proportion of accumulators, 14%–65% of species identified as richness repellers and had low richness of surrounding small trees. Only 11%–26% of species had lower species evenness than was expected by null models. High proportions of species richness accumulators were probably due to gap dynamics and support Janzen–Connell hypothesis driven by competition or top‐down control by pathogens and herbivores. Observed species diversity patterns show the importance of including small tree size classes in analyses of the spatial organization of diversity.     

Liana Abundance,Diversity, and Distribution on Barro Colorado Island,Panama

Lianas are a key component of tropical forests; however, most surveys are too small to accurately quantify liana community composition, diversity, abundance, and spatial distribution – critical components for measuring the contribution of lianas to forest processes. In 2007, we tagged, mapped, measured the diameter, and identified all lianas ≥1 cm rooted in a 50-ha plot on Barro Colorado Island, Panama (BCI). We calculated liana density, basal area, and species richness for both independently rooted lianas and all rooted liana stems (genets plus clones). We compared spatial aggregation patterns of liana and tree species, and among liana species that varied in the amount of clonal reproduction. We also tested whether liana and tree densities have increased on BCI compared to surveys conducted 30-years earlier. This study represents the most comprehensive spatially contiguous sampling of lianas ever conducted and, over the 50 ha area, we found 67,447 rooted liana stems comprising 162 species. Rooted lianas composed nearly 25% of the woody stems (trees and lianas), 35% of woody species richness, and 3% of woody basal area. Lianas were spatially aggregated within the 50-ha plot and the liana species with the highest proportion of clonal stems more spatially aggregated than the least clonal species, possibly indicating clonal stem recruitment following canopy disturbance. Over the past 30 years, liana density increased by 75% for stems ≥1 cm diameter and nearly 140% for stems ≥5 cm diameter, while tree density on BCI decreased 11.5%; a finding consistent with other neotropical forests. Our data confirm that lianas contribute substantially to tropical forest stem density and diversity, they have highly clumped distributions that appear to be driven by clonal stem recruitment into treefall gaps, and they are increasing relative to trees, thus indicating that lianas will play a greater role in the future dynamics of BCI and other neotropical forests.