Abstract:Life history and recruitment information of tropical trees in natural populations is scarce even for important commercial species. This study focused on a widely exploited Neotropical canopy species, Pachira quinata (Malvaceae), at the southernmost, wettest limit of its natural distribution, in the Colombian Amazonia. We studied phenological patterns, seed production and natural densities; assessed the importance of seed dispersal and density-dependent effects on recruitment, using field experiments. At this s… Show more
“…Clearing the forests in this site, for cardamom plantations, could have paved the way for more light thus enhancing seed germination. Similar observations have been made for a number of endemic species in tropical forests (Baskin & Baskin 1998;Ganesan 2001;Ganesan et al 2001;Castellanos & Stevenson 2011). There has been little anthropogenic interference in this region after declaring it as a biosphere reserve in 2005 (MoEF 2012).…”
Section: Figure 2 Population Structure Of E Venustus In Kanyakumarisupporting
“…Clearing the forests in this site, for cardamom plantations, could have paved the way for more light thus enhancing seed germination. Similar observations have been made for a number of endemic species in tropical forests (Baskin & Baskin 1998;Ganesan 2001;Ganesan et al 2001;Castellanos & Stevenson 2011). There has been little anthropogenic interference in this region after declaring it as a biosphere reserve in 2005 (MoEF 2012).…”
Section: Figure 2 Population Structure Of E Venustus In Kanyakumarisupporting
“…). Several Neotropical studies have experimentally shown reduced pathogen‐induced mortality of seeds dispersed to gaps as these fungal associations shifted from detrimental to neutral in drier, high‐light environments (Augspurger & Kelly , Augspurger , Wenny & Levey , Castellanos & Stevenson ).…”
Section: Processes Linking Dispersal To Plant Recruitmentmentioning
confidence: 99%
“…For plants relying on dispersal to particular microsites, such as light gaps, overharvesting of reproductive trees, disperser loss, or even alterations in disperser behavior can increase seed limitation and may decrease the probability of seeds reaching habitats necessary for recruitment (Brodie et al . , Castellanos & Stevenson , Tang et al . ).…”
Section: Consequences Of Disperser Loss In Human‐dominated Landscapesmentioning
confidence: 99%
“…). Overharvesting of a gap‐dependent, wind‐dispersed species, Pachira quinata , in the Colombian Amazon is hypothesized to have caused population declines due to the combination of seed limitation and specific habitat requirements (Castellanos & Stevenson ). Large‐seeded species tend to be most affected by declines in the frugivore community because the large frugivores are often the most affected by harvesting and habitat fragmentation (Stoner et al .…”
Section: Consequences Of Disperser Loss In Human‐dominated Landscapesmentioning
confidence: 99%
“…In a hurricane-impacted forest in Puerto Rico, the effect of conspecific seedling densities weakened with canopy openness (Comita et al 2009). Several Neotropical studies have experimentally shown reduced pathogen-induced mortality of seeds dispersed to gaps as these fungal associations shifted from detrimental to neutral in drier, high-light environments (Augspurger & Kelly 1984, Augspurger 1984, Wenny & Levey 1998, Castellanos & Stevenson 2011.…”
Section: The Effect Of a Seed's Neighborhood On Plantmentioning
Seed dispersal sets the stage for the suite of biotic and abiotic interactions that determine the fate of individual seeds. In this review, we first focus on how dispersal influences the ‘seedscape’, or the combination of abiotic and biotic factors that affect the probability of recruitment once a seed has reached its final location. We review recent papers that examine the effect of different dispersal vectors on (1) the quality of the habitat in which a seed lands; (2) the distance seeds are dispersed from the parent tree; and (3) the density and composition of plants within the neighborhood of a seed following deposition. Next, we explore methods used to scale these processes up to the level of populations. We highlight demographic models that integrate across multiple life history stages and predict the impact of dispersal in variable environments on population growth. We also review studies that analyze existing spatial patterns of trees within large forest plots and use various strategies to infer the processes that led to those patterns. We continue to scale up from populations to communities, and discuss approaches that have been taken to understand how dispersal may affect diversity and abundance in the community. We then turn to human disturbances and discuss the implications of frugivore defaunation for plant communities. We finish by highlighting several areas of research that are particularly promising for future directions of study.
Research Highlights: Seasonally flooded and terra firme forests are characteristic ecosystems of the Colombian Orinoco Basin and of great importance in the maintenance of regional biodiversity and ecosystem function. These forests have a unimodal precipitation regime that can cause a temporal effect on the seedling regeneration niche. This could partly explain the high diversity and coexistence of plant species in these forests, as well as the similarity in composition of seedlings and trees. Background and Objectives: Seedlings are a key factor in the assembly of plant communities. We evaluated the effect of flooding and rains on the dissimilarity and compositional affinity between trees and seedlings of seasonally flooded and terra firme forests. Materials and Methods: the tree community of these forests in San Martín (Meta, Colombia) was characterized and compared with their respective seedling communities before (June) and after (December) rain and flooding (during the rainy season). We evaluated plant species diversity and abundance (Shannon diversity and Pielou eveness index), as well as the compositional dissimilarities of each tree community with their corresponding seedling community sampled at the beginning and end of rains and flooding (Bray–Curtis dissimilarity). We also compared sampling site composition using a NMDS analysis. Results: We found that the terra firme forest had higher diversity compared to the flooded forest. Seedling density in the seasonally flooded forest decreased significantly after the flood but not in the terra firme forest at the end of the rainy season. The compositional dissimilarity between trees and seedlings in the seasonally inundated forest also decreased after the flood. However, this pattern was not evident in the terra firme forest. Conclusions: These results indicate that seasonal flooding generates a strong ecological filter that affects the realized niche of plants in these forests. Our results can contribute valuable information for the effective development of assisted restoration and conservation programs.
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