Over the past decades, tropical forests have experienced both compositional and structural changes. In the Neotropics, researchers at multiple sites have observed significant increases in the abundance and biomass of lianas (i.e. woody vines) relative to trees. However, the role of dynamics at early life stages in contributing to increasing liana abundance remains unclear. We took advantage of a unique dataset on seedling dynamics over 16 years in ~20 000 1‐m2plots in a tropical forest in Panama to examine temporal and spatial trends in liana and tree seedling abundance. We found that the relative abundance of liana seedlings increased across the study period, from 0.18 in 2001 to 0.24 in 2017. However, increases in liana seedling relative abundance appear to have levelled off in more recent years. The observed increases in liana relative abundance appear to be the result of both higher survival and higher recruitment rates of liana seedlings compared to tree seedlings. Increasing liana abundance in the seedling layer was not explained by annual variation in dry season length, total rainfall or the proportion of area occupied by canopy gaps. In addition, liana seedlings did not exhibit a demographic advantage (i.e. higher recruitment or survival) over tree seedlings in dry habitats.
This content will become publicly available on July 18, 2024
Tropical forests are well known for their high woody plant diversity. Processes occurring at early life stages are thought to play a critical role in maintaining this high diversity and shaping the composition of tropical tree communities. To evaluate hypothesized mechanisms promoting tropical tree species coexistence and influencing composition, we initiated a census of woody seedlings and small saplings in the permanent 50 ha Forest Dynamics Plot (FDP) on Barro Colorado Island (BCI), Panama. Situated in old‐growth, lowland tropical moist forest, the BCI FDP was originally established in 1980 to monitor trees and shrubs ≥1 cm diameter at 1.3 m above ground (dbh) at ca. 5‐year intervals. However, critical data on the dynamics occurring at earlier life stages were initially lacking. Therefore, in 2001 we established a 1‐m2seedling plot in the center of every 5 × 5 m section of the BCI FDP. All freestanding woody individuals ≥20 cm tall and <1 cm dbh (hereafter referred to as seedlings) were tagged, mapped, measured, and identified to species in 19,313 1‐m2seedling plots. Because seedling dynamics are rapid, we censused these seedling plots every 1–2 years. Here, we present data from the 14 censuses of these seedling plots conducted between the initial census in 2001 to the most recent census, in 2018. This data set includes nearly 1 M observations of ~185,000 individuals of >400 tree, shrub, and liana species. These data will permit spatially‐explicit analyses of seedling distributions, recruitment, growth, and survival for hundreds of woody plant species. In addition, the data presented here can be linked to openly‐available, long‐term data on the dynamics of trees and shrubs ≥1 cm dbh in the BCI FDP, as well as existing data sets from the site on climate, canopy structure, phylogenetic relatedness, functional traits, soil nutrients, and topography. This data set can be freely used for non‐commercial purposes; we request that users of these data cite this data paper in all publications resulting from the use of this data set.
more » « less- NSF-PAR ID:
- 10441882
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Ecology
- Volume:
- 104
- Issue:
- 9
- ISSN:
- 0012-9658
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Synthesis. Our results reveal that seedling communities experienced important compositional changes in the past, but liana seedling relative abundance may have stabilized in recent years. Longer‐term monitoring is needed to determine whether tropical forests will continue to experience compositional changes that may alter forest structure and ecosystem function. -
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Abstract 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.
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Abstract Habitat fragmentation remains a major focus of research by ecologists decades after being put forward as a threat to the integrity of ecosystems. While studies have documented myriad biotic changes in fragmented landscapes, including the local extinction of species from fragments, the demographic mechanisms underlying these extinctions are rarely known. However, many of them—especially in lowland tropical forests—are thought to be driven by one of two mechanisms: (1) reduced recruitment in fragments resulting from changes in the diversity or abundance of pollinators and seed dispersers or (2) increased rates of individual mortality in fragments due to dramatically altered abiotic conditions, especially near fragment edges. Unfortunately, there have been few tests of these potential mechanisms due to the paucity of long‐term and comprehensive demographic data collected in both forest fragments and continuous forest sites. Here we report 11 years (1998–2009) of demographic data from populations of the Amazonian understory herb
Heliconia acuminata (LC Rich.) found at Brazil's Biological Dynamics of Forest Fragments Project (BDFFP). The data set comprises >66,000 plant× year records of 8586 plants, including 3464 seedlings established after the first census. Seven populations were in experimentally isolated fragments (one in each of four 1‐ha fragments and one in each of three 10‐ha fragments), with the remaining six populations in continuous forest. Each population was in a 50× 100 m permanent plot, with the distance between plots ranging from 500 m to 60 km. The plants in each plot were censused annually, at which time we recorded, identified, marked, and measured new seedlings, identified any previously marked plants that died, and recorded the size of surviving individuals. Each plot was also surveyed four to five times during the flowering season to identify reproductive plants and record the number of inflorescences each produced. These data have been used to investigate topics ranging from the way fragmentation‐related reductions in germination influence population dynamics to statistical methods for analyzing reproductive rates. This breadth of prior use reflects the value of these data to future researchers. In addition to analyses of plant responses to habitat fragmentation, these data can be used to address fundamental questions in plant demography and the evolutionary ecology of tropical plants and to develop and test demographic models and tools. Though we welcome opportunities to collaborate with interested users, there are no restrictions on the use of this data set. However, we do request that those using the data for teaching or research purposes inform us of how they are doing so and cite this paper and the data archive when appropriate. Any publication using the data must also include a BDFFP Technical Series Number in the Acknowledgments. Authors can request this series number upon the acceptance of their article by contacting the BDFFP's Scientific Coordinator or E. M. Bruna. -
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Abstract Questions How do spatial patterns of tree distribution and species co‐occurrence differ between primary and secondary tropical rain forests? What signatures of ecological processes might be discerned by comparing the spatial patterns of trees between primary and secondary forest plots?
Location Tropical rain forest vegetation, lowlands of Papua New Guinea.
Methods All trees over 5 cm DBH were surveyed in two non‐replicated 1‐ha plots situated in primary and secondary forest. Grid location, DBH, height and species identity were recorded for all surveyed trees. Analysis of the spatial pattern and the autocorrelation of tree sizes and identities were used to assess the structure of the forest found within the plots. Functions combining Ripley's K and the individual species–area relationship were applied to study the spatial distribution of trees and species diversity.
Results The spatial distribution of common species, and all stems collectively, was aggregated in the secondary forest plot but not different from random in the primary forest plot. Diameter and height were also strongly spatially auto‐correlated in the secondary forest plot but not in the primary forest plot. Conspecific aggregations were more common in the secondary forest plot. Finally, the secondary forest plot was characterized by the presence of diversity‐repelling species and lower diversity than the primary forest plot, where diversity‐accumulating species were present.
Conclusions We attribute the weaker autocorrelation of tree size in the primary forest to the development of size hierarchies throughout the course of stand aging. The conspecific aggregation and low local diversity within the secondary forest plot are likely caused by dispersal limitation during a brief period of establishment after disturbance. The higher local diversity of the primary forest can be explained by the reduction of species aggregation through increased mortality of conspecifics. This is caused by strong intraspecific competition, supporting the spatial segregation hypothesis (interspecific spatial segregation).
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