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50 results for “Forest Structure and Composition”

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dryad32/100

Data from: Massive structural redundancies in species composition patterns of floodplain forest moths

Terrestrial arthropod communities usually consist of very large species numbers. Data from experiments or long time-series would be required to ascertain the functional significance of individual species. Both are largely unavailable for species-rich natural communities. Recognising structural redundancies in species composition allows for an alternative approach to address how strong functional redundancy might be in natural assemblages, if structural and functional redundancies are related to each other. Determining structural redundancies is a regular topic in aquatic ecology, but has rarely been applied to terrestrial communities. We explored the extent of structural redundancy in species-rich terrestrial insect assemblages and whether structural redundancies are contingent to species abundances or functional group affiliations. We used the BVSTEP algorithm to determine structural redundancies in a large data set of moth species (32 181 individuals; 448 species) that had been sampled with light-traps in three different floodplain forests in eastern Austria. We partitioned the moth species into 12 functional types based on larval host-plant affiliations to test if moth species included in reduced subsets represent functional groups in the same proportions as they occur in the entire fauna. We observed far more massive structural redundancies in moth assemblages than previously found in aquatic communities. Subsets containing only 8–15 species (1.8–3.3% of all recorded species) were still highly representative for the overall data. Subsets selected by the BVSTEP procedure performed better than equally small subsets that were defined solely by species abundances or by functional group affiliations. Effective 'surrogate' subsets contained only 6–9 of the 12 functional moth types. High abundance only loosely corresponded with the frequency at which a moth species was included in the subsets. Thus, certain uncommon species contribute importantly to species composition patterns. Our results show unexpectedly extensive structural redundancies in complex floodplain forest moth communities, which may also indicate strong functional redundancies.

opencc-zeroDec 2014View details →

dryad32/100

Tropical montane forest in South Asia: Composition, structure and dieback in relation to soils and topography

We evaluated the composition, structure and dieback of a montane forest in relation to soils and physiography of an important biogeographic region that has been sparsely studied. Our objectives were to: 1. Describe the forest composition and structure; 2. Assess the current extent of dieback; and 3. Relate tree composition, structure, and dieback proneness to edaphic and physiographic measures. We enumerated all live and dead standing plants ≥ 3 cm diameter at breast height (DBH), in thirty 20×15 m2 over story plots. We measured all regeneration < 1m height in subplots, sampled soils and measures of physiography, and visually rated the proportion of crown die-back, and recorded standing dead trees.

opencc-zeroMar 2022View details →

zenodo32/100

Changes in structure and composition of protected forest habitats after 10 years: Analyzes from different Natura 2000 sites in Saxony-Anhalt, Germany

The data utilized in the paper "Wild et al. (2024)," submitted in Ecology and Evolution, are provided herein. The study examines the alterations in forest structure and species composition in Natura 2000 sites over a period of approximately ten years in the Harz and Harz foreland regions of Saxony-Anhalt, Germany. The data were collected as part of the research project "Possibilities and Methods for the Promotion of Tree Species and Habitats of Native Forests as a Building Block for Adaptation to Climate Change and for Coping with Forest Damage Using the Example of Selected Natura 2000 Areas in Saxony-Anhalt" (10/2020 – 06/2023) (project no. 407.1.10-60128/630120000006) funded by the European Agricultural Fund for Rural Development and the State Administration Office of Saxony-Anhalt.  The surveys were conducted between the months of July and September in the years 2021 and 2022.

opencc-by-4.0Sep 2024View details →

dryad32/100

The vegetation composition, structure and regeneration status of Gole Natural Forest, West Arsi Zone, Oromia Regional State, Ethiopia

This study was conducted in Gole natural forest (Dodola) West Arsi Zone of Oromia Regional State, Ethiopia. The study was intended to investigate the vegetation composition, structure, community types and the regeneration status. To collect the vegetation data, systematically 62 plots 20 m × 20 m (400 m2) were established at 100 m interval, starting from the top of the mountain. Tree and shrub species were counted and their cover abundance value was estimated. The data for herbaceous species were collected from five 2 m × 2 m sub-plots laid at the four corners each and one at the centre of the main plot. Height and diameter at breast height (DBH) of all woody species taller than 1.5 m and thicker than 2 cm were measured. R package was applied for cluster analysis. Indicator species analysis was performed in R Interpolated species accumulation curves. Estimate S 8.2 Software and Microsoft Excel were used to analyze the data. Rarefaction was applied to compare the species richness of the plant communities in the study area. Sorensen's similarity coefficient was used to detect similarities and dissimilarities among communities. A total of 114 plant species belonging to 57 families and 94 genera were identified. The most dominant families were Asteraceae, followed by Acanthaceae and Lamiaceaae. Out of 114 species 17 were endemic to Ethiopia. The study showed that high density was seen at lower height and DBH classes. Five plant community types were identified. The rarefaction revealed that there is difference in species richness among communities. The Sorensen's similarity index showed that, there was a difference in the distribution of plant species composition among the five plant communities.

opencc-zeroJan 2020View details →

dryad32/100

Data from: BIOVERA-Tree: tree diversity, community composition, forest structure and functional traits along gradients of forest-use intensity and elevation in Veracruz, Mexico

Here, we describe BIOVERA-Tree, a database on tree diversity, community composition, forest structure, and functional traits collected in 120 forest plots distributed along an extensive elevational gradient in Veracruz State, Mexico. BIOVERA-Tree includes information on forest structure from three levels of forest-use intensity, namely old-growth, degraded, and secondary forest, replicated across eight elevations from sea-level to near the tree line at 3500 m and on size and location of 4549 tree individuals with a diameter at breast height ≥ 5 cm belonging to 216 species, 154 genera, and 80 families. We also report measurements of eight functional traits, namely wood density for 143 species, maximum height for 216 species and leaf traits including: specific leaf area, lamina density, leaf thickness, chlorophyll content, and leaf area for 148 species and leaf dry matter content for 145 species.

opencc-zeroAug 2021View details →

dryad32/100

Fire alters diversity, composition and structure of dry tropical forests in the Eastern Ghats

Fire is known to have dramatic consequences on forest ecosystems around the world, and on the livelihoods of forest-dependent people. While the Eastern Ghats of India have high abundances of fire-prone dry tropical forests, little is known about how fire influences the diversity, composition and structure of these communities. Our study aims to fill this knowledge gap by examining the effects of presence and absence of recent fire on tropical dry forest communities within Kadiri watershed, Eastern Ghats. We sampled plots with and without evidence of recent fire in the Eswaramala Reserve Forest in 2008 and 2018. Our results indicate that even though stem density increases in the recently burned areas, species richness is lower because communities become dominated by a few species with fire resistance and tolerance traits, such as thick bark and clonal sprouting. Further, in the presence of fire, the size structure of these fire-tolerant species shifts towards smaller-sized, resprouting individuals. Our results demonstrate that conservation actions are needed to prevent further degradation of forests in this region and the ecosystem services they provide.

opencc-zeroMar 2022View details →

zenodo32/100

Data set of 1) plant abundance in the herb layer and 2) Shrub and tree composition and structure following forest management along a chronosequence

In each site (1200 m²), three circular plots (400 m²) were established (total of 198 plots). Data presented here for 1) plant of the herb layer and 2) shrub and tree are grouped by site (addition of three plots).  In the herb layer, total plant species identity and abundance (percentage cover) were sampled in each plot using eight circular micro-plots of 4 m². Data were collected in 2016 and 2017, between June and August. To minimize seasonal variability and allow detection of early spring species, plants (identity and abundance) in the herb layer were measured twice (once in June to early-July, and once in late-July to August). For tree, in each plot, species identity, diameter at breast height (DBH, 1.3 m) and locations of each tree > 9.1 cm DBH were determined. In each plot, species identity and DBH of shrubs and small trees (DBH range: 1.1 to 9.1 cm) were measured in three circular micro-plots of 25 m². Data that were related to the shrub-canopy layer included all trees and shrubs with DBH > 1.1 cm. Here, in each site, forest composition and structure is represented by different combinations of DBH classes (1.1-4 cm, 4-9.1 cm, 9.1-20 cm, 20-35 cm, >35 cm) and species. Plant community composition and abundance were assessed in unmanaged forests (sites of old-growth forest > 100 years, with dominant and co-dominant trees older than 200 years, and no obvious sign of past harvesting), and in even-aged and uneven-aged managed forests along a chronosequence (< 5 years, 15 years, 30 years after forest harvesting).

opencc-by-4.0Oct 2021View details →

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