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"Forest ecology"
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Forest habitats
Introduces forest habitats, covering such topics as the history of forests from 354 million years ago, the different types of forests, and the current deforestation due to population growth and agricultural and urban development.
Book
Can retention forestry help conserve biodiversity? A meta‐analysis
Industrial forestry typically leads to a simplified forest structure and altered species composition. Retention of trees at harvest was introduced about 25 years ago to mitigate negative impacts on biodiversity, mainly from clearcutting, and is now widely practiced in boreal and temperate regions. Despite numerous studies on response of flora and fauna to retention, no comprehensive review has summarized its effects on biodiversity in comparison to clearcuts as well as un‐harvested forests. Using a systematic review protocol, we completed a meta‐analysis of 78 studies including 944 comparisons of biodiversity between retention cuts and either clearcuts or un‐harvested forests, with the main objective of assessing whether retention forestry helps, at least in the short term, to moderate the negative effects of clearcutting on flora and fauna. Retention cuts supported higher richness and a greater abundance of forest species than clearcuts as well as higher richness and abundance of open‐habitat species than un‐harvested forests. For all species taken together (i.e. forest species, open‐habitat species, generalist species and unclassified species), richness was higher in retention cuts than in clearcuts. Retention cuts had negative impacts on some species compared to un‐harvested forest, indicating that certain forest‐interior species may not survive in retention cuts. Similarly, retention cuts were less suitable for some open‐habitat species compared with clearcuts. Positive effects of retention cuts on richness of forest species increased with proportion of retained trees and time since harvest, but there were not enough data to analyse possible threshold effects, that is, levels at which effects on biodiversity diminish. Spatial arrangement of the trees (aggregated vs. dispersed) had no effect on either forest species or open‐habitat species, although limited data may have hindered our capacity to identify responses. Results for different comparisons were largely consistent among taxonomic groups for forest and open‐habitat species, respectively. Synthesis and applications. Our meta‐analysis provides support for wider use of retention forestry since it moderates negative harvesting impacts on biodiversity. Hence, it is a promising approach for integrating biodiversity conservation and production forestry, although identifying optimal solutions between these two goals may need further attention. Nevertheless, retention forestry will not substitute for conservation actions targeting certain highly specialized species associated with forest‐interior or open‐habitat conditions.
Journal Article
What are temperate deciduous forests?
Forests fascinate readers and hikers alike. And the deciduous forest, perhaps the \"classic\" forest biome, fills our stories and is the go-to spot for many outdoor activities. This informative book describes the forest many think they know, presenting the abundant life within, including trees, animals, plants, and even moss. Readers will learn about its iconic four seasons, as well as why trees drop their leaves and change from green to the brilliant hues of autumn. Thought-provoking sidebars prompt further investigation.
Book
Diversity and carbon storage across the tropical forest biome
Tropical forests are global centres of biodiversity and carbon storage.Many tropical countries aspire to protect forest to fulfil biodiversity and climate mitigation policy targets, but the conservation strategies needed to achieve these two functions depend critically on the tropical forest tree diversity-carbon storage relationship. Assessing this relationship is challenging due to the scarcity of inventories where carbon stocks in aboveground biomass and species identifications have been simultaneously and robustly quantified.Here, we compile a unique pan-tropical dataset of 360 plots located in structurally intact old-growth closed-canopy forest, surveyed using standardised methods, allowing a multi-scale evaluation of diversity-carbon relationships in tropical forests. Diversity-carbon relationships among all plots at 1 ha scale across the tropics are absent, and within continents are either weak (Asia) or absent (Amazonia, Africa). A weak positive relationship is detectable within 1 ha plots, indicating that diversity effects in tropical forests may be scale dependent.The absence of clear diversity-carbon relationships at scales relevant to conservation planning means that carbon-centred conservation strategies will inevitably miss many high diversity ecosystems. As tropical forests can have any combination of tree diversity and carbon stocks both require explicit consideration when optimising policies to manage tropical carbon and biodiversity.
Journal Article
Temperate forests
Introduces temperate forests, discusses the threats to them, and describes how the animals that live there survive.
Book
Components of tree resilience: effects of successive low-growth episodes in old ponderosa pine forests
Recent world-wide episodes of tree dieback have been attributed to increasing temperatures and associated drought. Because these events are likely to become more common, improved knowledge of their cumulative effects on resilience and the ability to recover pre-disturbance conditions is important for forest management. Here we propose several indices to examine components of individual tree resilience based on tree ring growth: resistance (inverse of growth reduction during the episode), recovery (growth increase relative to the minimum growth during the episode), resilience (capacity to reach pre-episode growth levels) and relative resilience (resilience weighted by the damage incurred during the episode). Based on tree ring analyses, we analyzed historical patterns of tree resilience to successive drought-induced low growth periods in ponderosa pine trees growing in unmanaged, remote forests of the Rocky Mountains. Low-growth periods registered in tree rings were related to anomalies in the Palmer drought severity index (PDSI) and were attributed to drought. Independently of the impact of a specific event, subsequent growth after a single low-growth episode was related to the growth prior to the event. Growth performance differed with tree age: young trees were overall more resistant to low-growth periods, but older trees recovered better from more recent events. Regardless of tree age, recently burned sites exhibited lower post-episode growth and lower resistance and resilience than unburned ones. We found mixed evidence for the cumulative effect of past low-growth episodes: overall, greater impacts of a prior event and greater cumulative effects of past low-growth periods caused a decrease in resistance. However, we did not find a progressive decrease in resilience over time in old trees. Our results highlight the value of using a combination of estimators to evaluate the different components of resilience. Specifically, while tree responses to disturbance depend on past disturbance episodes, the response is context-specific and depends on the impact the capacity to recover after disturbance. This suggests that recent increases in forest mortality under current climate trends could relate to thresholds on specific components of resilience (resistance, recovery, resilience itself) rather than to an overall loss of resilience over time. Identifying such thresholds and their underlying mechanisms is a promising area of research with important implications for forest management.
Journal Article
Welcome to the forest
Explores the ecosystem of the forest and how plants, animals and trees are interdependent.
Book
Forest productivity increases with evenness, species richness and trait variation: a global meta‐analysis
1. Although there is ample support for positive species richness–productivity relationships in planted grassland experiments, a recent 48‐site study found no diversity–productivity relationship (DPR) in herbaceous communities. Thus, debate persists about diversity effects in natural versus planted systems. Additionally, current knowledge is weak regarding the influence of evenness on the DPRs, how DPRs are affected by the variation in life‐history traits among constituent species in polycultures and how DPRs differ among biomes. The impacts of these factors on DPRs in forest ecosystems are even more poorly understood. 2. We performed a meta‐analysis of 54 studies to reconcile DPRs in forest ecosystems. We quantified the net diversity effect as log effect size [ln(ES)], the log ratio of the productivity in polycultures to the average of those in monocultures within the same type of mixture, site condition and stand age of each study. The first use of a boosted regression tree model in meta‐analysis, a useful method to partition the effects of multiple predictors rather than relying on vote‐counting of individual studies, unveiled the relative influences of individual predictors. 3. Global average ln(ES) was 0.2128, indicating 23.7% higher productivity in polycultures than monocultures. The final model explained 21% of the variation in ln(ES). The predictors that substantially accounted for the explained variation included evenness (34%), heterogeneity of shade tolerance (29%), richness (13%) and stand age (15%). In contrast, heterogeneity of nitrogen fixation and growth habits, biome and stand origin (naturally established versus planted) contributed negligibly (each ≤ 4%). Log effect size strongly increased with evenness from 0.6 to 1 and with richness from 2 to 6. Furthermore, it was higher with heterogeneity of shade tolerance and generally increased with stand age. 4. Synthesis. Our analysis is, to our knowledge, the first to demonstrate the critical role of species evenness, richness and the importance of contrasting traits in defining net diversity effects in forest polycultures. While testing the specific mechanisms is beyond the scope of our analysis, our results should motivate future studies to link richness, evenness, contrasting traits and life‐history stage to the mechanisms that are expected to produce positive net biodiversity effects such as niche differentiation, facilitation and reduced Janzen–Connell effects.
Journal Article
Forests and vegetation
Everything that we need, Earth provides. All across our planet, plants grow. Earth's forests and plants are one of our valuable natural resources. We pick their fruit, leaves, and seeds for food. We cut their wood for lumber. We harvest them for medicine. Even when we do nothing, plants give us oxygen to breathe. Natural resources are a gift from Earth, but we must use them responsibly. Just as Earth takes care of us, we must take care of its plants. Color photos, fact boxes, a hands-on activity, and 'Words to Know' round out this earth science volume.
Book
Successional changes in functional composition contrast for dry and wet tropical forest
We tested whether and how functional composition changes with succession in dry deciduous and wet evergreen forests of Mexico. We hypothesized that compositional changes during succession in dry forest were mainly determined by increasing water availability leading to community functional changes from conservative to acquisitive strategies, and in wet forest by decreasing light availability leading to changes from acquisitive to conservative strategies. Research was carried out in 15 dry secondary forest plots (5-63 years after abandonment) and 17 wet secondary forest plots (<1-25 years after abandonment). Community-level functional traits were represented by community-weighted means based on 11 functional traits measured on 132 species. Successional changes in functional composition are more marked in dry forest than in wet forest and largely characterized by different traits. During dry forest succession, conservative traits related to drought tolerance and drought avoidance decreased, as predicted. Unexpectedly acquisitive leaf traits also decreased, whereas seed size and dependence on biotic dispersal increased. In wet forest succession, functional composition changed from acquisitive to conservative leaf traits, suggesting light availability as the main driver of changes. Distinct suites of traits shape functional composition changes in dry and wet forest succession, responding to different environmental filters.
Journal Article