Abstract:Extrapolation of local abundance-environment relationships to broader scales provides species distribution models used for conservation planning. We investigated the importance of environmental heterogeneity and geographic distance on pteridophyte species spatial distribution on 38 plots of 250 x 2.5 m distributed over 90 km 2 in Central Amazon. Inclusion of canopy openness in our models increased the capacity of predicting community composition even under the narrow range of canopy openness found in our plots… Show more
“…The Brazilian acronym for LTER is PELD; hence the name for the method, RAPELD. there were no light measurements in the plots, but they are now being done at some of the sites (Zuquim et al 2009). All of these measures are summarized as the mean of the 6 sub-samples per plot.…”
“…The Brazilian acronym for LTER is PELD; hence the name for the method, RAPELD. there were no light measurements in the plots, but they are now being done at some of the sites (Zuquim et al 2009). All of these measures are summarized as the mean of the 6 sub-samples per plot.…”
“…Recent findings point out the important role of the environment component in structuring plant communities and how it can vary according to the scale evaluated, underlying geology and topography. The environmental determinism over plants distribution has thus received increasing attention and is considered essential towards the evaluation and comprehension of species coexistence models (Svenning et al 2004, Karst et al 2005, Jones et al 2008, Zuquim et al 2009, Li et al 2011. Therefore, it is reasonable to think that the ferns and lycophytes community differentiation pattern that we found may have emerged from environment variation related to the slope topographic orientation.…”
Section: Species Compositionmentioning
confidence: 99%
“…Some studies argue that topographic patterns are site-specific and slope effects seem to be a bad surrogate for the prediction of community structure because it is probably a synergistic response of the community to variable factors (Vormisto et al 2004, Zuquim et al 2009). We agree with this viewpoint, but slope topographic orientation may influence factors that are knowingly more important than others to a specific biological group.…”
Section: Species Compositionmentioning
confidence: 99%
“…Ranging from local to regional scales, several studies have shown that plant species composition and abundances answer to some common environmental variables such as topography (Vormisto et al 2004), soil characteristics (Jones et al 2006, Tuomisto et al 2003, length of the dry period and moisture availability (Engelbrecht et al 2005). Although there is considerable debate as to what degree floristic distributional patterns depend on environmental factors relative to other processes (Hubbell 2001, Dalling et al 2002, Wyatt and Silman 2004, findings appear to show that the major role is played by environmental factors (Karst et al 2005, Jones et al 2006, 2008, Zuquim et al 2009). …”
Section: Introductionmentioning
confidence: 99%
“…Not only do they have high richness and endemism levels (Tryon and Tryon 1982), but they are known to have had a large part of its floristic variation consistently predicted by environmental variation. Among the array of environmental factors, topographic and edaphic factors appear to be noticeably important at different scales (Karst et al 2005, Jones et al 2006, 2008, Zuquim et al 2009). It is thus reasonable to think that ferns exposed to the geomorphologic heterogeneity along the Atlantic Forest would be influenced by environmental variation.…”
A community of Ferns and Lycophytes was investigated by comparing the occurrence of species on different slopes of a paleoisland in Southeastern Brazil. Our goal was to evaluate the hypothesis that slopes with different geographic orientations determine a differentiation of Atlantic Forest ferns and lycophytes community. We recorded these plants at slopes turned towards the continent and at slopes turned towards the open sea. Analysis consisted of a preliminary assessment on fern beta diversity, a Non Metric Multidimensional Scaling (NMDS) and a Student t-test to confirm if sites sampling units ordination was different at each axis. We further used the Pearson coefficient to relate fern species to the differentiation pattern and again Student's t-test to determine if richness, plant cover and abundance varied between the two sites. There was a relatively low number of shared species between the two sites and ferns and lycophytes community variation was confirmed. Some species were detected as indicators of the community variation but we were unable to detect richness, plant cover or abundance differences. Despite the evidence of this variation between the slopes, further works are needed to evaluate which processes are contributing to determine this pattern.
Tropical forests have been rapidly deforested and degradation worldwide has outpaced biodiversity field sampling. No study to date has assessed the effects of insular habitats induced by hydroelectric dams on Amazonian understory plants. Fern community responses to anthropogenic effects on tropical forest islands can be revealed at a faster pace by using simple and cheap, yet informative, protocols that could be applied by non‐specialists.
This study seeks to both understand the drivers of fern and lycophytes assemblages on forest islands and investigate the relative costs and effectiveness of a simplified sampling protocol that can be applied by non‐specialists.
Fern species were sampled by a non‐specialist who photographed all ferns and lycophytes within seventeen 0.25‐ha plots on 10 forest islands at the lake of Balbina Hydroelectric dam, central Amazonia. Sampling was carried out opportunistically during a field expedition planned to conduct tree inventories. As predictors, we used locally measured or GIS‐derived descriptors of plot and landscape conditions. We used multivariate and linear models to further assess the influence of predictors on patterns of species richness and composition of ferns assemblages.
A total of 286 photographed individual ferns or lycophytes represented at least 23 species and 14 genera. The average number of taxa per plot was 6.1 in the islands and 14.3 in the mainland. The species pool found on islands was a nested subset of the mainland fern community. Species richness was positively related to island size and negatively related to isolation and fire severity. Area, isolation and fire severity also significantly explained variation in community composition.
The relative cost of the picture‐based fern protocol applied was very modest (only 4% of the total expedition budget), even compared to the typically low cost of alternative field campaigns.
We conclude that fern community structure in this forest archipelago was primarily driven by island size, isolation and fire disturbance. Moreover, we show that a simple sampling protocol carried out by a non‐specialist can lead to inexpensive and highly reliable ecological data. This opens an avenue for crowdsourcing ecological fern data collections using a citizen science approach.
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