2,583 research outputs found
Will a 385 million year-struggle for light become a struggle for water and for carbon? - How trees may cope with more frequent climate change-type drought events
Trees are exceptional organisms that have evolved over some 385 million years and have overtaken other plants in order to harvest light first. However, this advantage comes with a cost: trees must transport water all the way up to their crowns and inherent physical limitations make them vulnerable to water deficits. Because climate change scenarios predict more frequent extreme drought events, trees will increasingly need to cope with water stress. Recent occurrences of climate change-type droughts have had severe impacts on several forest ecosystems. Initial experimental studies have been undertaken and show that stomatal control of water loss hinders carbon assimilation and could lead to starvation during droughts. Other mechanisms of drought-induced mortality are catastrophic xylem dysfunction, impeded long-distance transport of carbohydrates (translocation) and also symplastic failure (cellular breakdown). However, direct empirical support is absent for either hypothesis. More experimental studies are necessary to increase our understanding of these processes and to resolve the mystery of drought-related tree mortality. Instead of testing the validity of particular hypothesis as mechanisms of drought-induced tree mortality, future research should aim at revealing the temporal dynamics of these mechanisms in different species and over a gradient of environmental conditions. Only such studies will reveal whether the struggle for light will become a struggle for water and/or for carbon in drought-affected areas
Interannual variation in competitive interactions from natural and anthropogenic disturbances in a temperate forest tree species: Implications for ecological interpretation
Competition is a major determinant of plant growth and is often used in studies of tree growth and species coexistence. However, these approaches are usually temporally static, i.e., assessed at a single point or period in time. While constantly changing forest conditions due to natural and human-induced disturbances potentially alter competition among individuals, static approaches cannot qualify the temporal variability of competitive interactions. Here we present a longitudinal analysis of competitive interactions among trees and discuss the implication of our results for ecological interpretation. Spatially-explicit tree growth data were obtained from 18 study plots (0.4 ha each) in sugar maple (Acer saccharum Marsh.) stands in Quebec, Canada. During the studied period (1980-2003), these stands had been disturbed by insect outbreaks (forest tent caterpillar, Malacosoma disstria Hubner) and by commercial partial harvest. We analyzed radial growth rates (outcome of competition) on an annual basis and as a function of tree biology (bole diameter, crown position), competition (above- and belowground competition from neighbours) and environmental conditions (light availability, harvest disturbance). Competitive interactions changed throughout the studied period. Canopy disturbance from partial harvest interacted with defoliators and influenced competition symmetry by favoring smaller trees. Competitive interactions seemed to have switched from below- to above-ground following canopy recovery after harvest. Release from competition due to partial harvest increase neighbourhood size (radius of effective competition) and enhanced the competitive pressure from larger individuals. The temporal variability in parameter estimates may be used for setting confidence intervals on competitive success (growth rates), thereby yielding a more robust basis for ecological interpretation. Our results also show that temporal variability in competitive interactions could contribute to the maintenance of high tree species diversity and structural complexity in some ecosystems by temporally altering species-specific responses to environmental change and disturbance
Understanding the roles of nonstructural carbohydrates in forest trees – from what we can measure to what we want to know
Carbohydrates provide the building blocks for plant structures as well as versatile resources for metabolic processes. The nonstructural carbohydrates (NSC), mainly sugars and starch, fulfil distinct functional roles, including transport, energy metabolism and osmoregulation, and provide substrates for the synthesis of defence compounds or exchange with symbionts involved in nutrient acquisition or defence. At the whole-plant level, NSC storage buffers the asynchrony of supply and demand on diel, seasonal or decadal temporal scales and across plant organs. Despite its central role in plant function and in stand-level carbon cycling, our understanding of storage dynamics, its controls and response to environmental stresses is very limited, even after a century of research. This reflects the fact that often storage is defined by what we can measure, that is, NSC concentrations, and the interpretation of these as a proxy for a single function, storage, rather than the outcome of a range of NSC source and sink functions.Newisotopic tools allow direct quantification of timescales involved in NSC dynamics, and show that NSC-C fixed years to decades previously is used to support tree functions. Here we review recent advances, with emphasis on the context of the interactions between NSC, drought and tree mortality
The role of forest tent caterpillar defoliations and partial harvest in the decline and death of sugar maple
Natural and anthropogenic disturbances can act as stresses on tree vigour. According to Manion's conceptual model of tree disease, the initial vigour of trees decreases as a result of predisposing factors that render these trees more vulnerable to severe inciting stresses, stresses that can then cause final vigour decline and subsequent tree death. This tree disease model was tested in sugar maple (Acer saccharum) by assessing the roles of natural and anthropogenic disturbances in tree decline and death
Detours on the phloem sugar highway: stem carbon storage and remobilization
For trees to survive, they must allocate resources between sources and sinks to maintain proper function. The vertical transport pathway in tree stems is essential for carbohydrates and other solutes to move between the canopy and the root system. To date, research and models emphasize the role of tree stems as ‘express’ sugar highways. However, recent investigations using isotopic markers suggest that there is considerable storage and exchange of phloem-transported sugars with older carbon (C) reserves within the stem. Thus, we suggest that stems play an important role not only in long-distance transport, but also in the regulation of the tree's overall C balance. A quantitative partitioning of stem C inputs among storage and sinks, including tissue growth, respiration, and export to roots, is still lacking. Combining methods to better quantify the dynamics and controls of C storage and remobilization in the stem will help to resolve central questions of allocation and C balance in trees
Negative or positive effects of plantation and intensive forestry on biodiversity: A matter of scale and perspective
Using longitudinal survival probabilities to test field vigour estimates in sugar maple (Acer saccharum Marsh.).
Tree mortality is a major force driving forest dynamics. To foresters, however, tree mortality is often considered a loss in productivity. To reduce tree mortality, silvicultural systems, such as selection cuts, aim at removing trees that are more likely to die. In order to identify trees with higher risks of mortality, field classifications are employed that assess vigour based on external characteristics of trees. We used a novel longitudinal approach for estimating survival probabilities based on ring-width measurements, initially developed by Bigler and Bugmann [Bigler, C., Bugmann, H., 2004. Predicting the time of tree death using dendrochronological data. Ecol. Appl. 14 (3), 902–914], to parameterize a survival probability model for sugar maple (Acer saccharum Marsh.) and to test whether field-assessed tree vigour classes are corroborated by survival probabilities determined from radial growth history. Data from 56 dead and 321 live sugar maples were collected in stands in western Quebec (Canada) that had undergone a selection cut ≈10 years prior to sampling. Our results showed that tree vigour established from external defects and pathological symptoms, using the classification of Boulet [Boulet, B., 2005. Défauts externes et indices de la carie des arbres: guide d’interprétation. Publication du Québec, Sainte-Foy, Quebec. 291 pp.], is partially corroborated by growth-driven survival probabilities. Moribund trees had lower survival probabilities than vigorous trees over several years in the period prior to vigour assessment. Intermediate vigour classes showed less obvious tendencies, but this may be due to the growth-independent nature of some defects used for their classification. Although the timing of tree death may not be correctly predicted by the vigour classification (i.e., our results suggest that time of death generally was overestimated), its general agreement with survival probabilities determined from growth series make it a useful tool for tree selection in sugar maple stands under selection management
Lethal drought leads to reduction in nonstructural carbohydrates in Norway spruce tree roots but not in the canopy
Heat waves and droughts are expected to increase in frequency and severity in many regions with future climate change, threatening the survival of a number of forest ecosystems. However, our understanding of the physiological processes and mechanisms underlying drought-induced tree mortality is incomplete. Here, we present results on the physiological response of young Norway spruce trees exposed to lethal drought stress. We applied three levels of drought treatment (control, dryingrewetting, complete drought) and monitored relevant physiological functions and processes of carbon and water relations at high temporal resolution until tree death occurred. Only trees subjected to continuous drought died in our experiment. Trees subjected to dryingrewetting cycles consistently recovered in their ability to transport water, indicating that these trees do not suffer permanent damage to the hydraulic system. In all cases, drought reduced carbon assimilation, caused changes in carbon allocation and appeared to have severely reduced phloem functioning and carbon translocation. Structural growth was sacrificed for carbon investment in maintenance respiration and osmoprotection. Severe drought caused trees to rely on stored carbon reserves but, in contrast to above-ground tissues, only root carbon pools were strongly reduced when trees died. Our results indicate that drought-induced changes in carbon allocation, use and transport differ between above- and below-ground tissues in trees. While root death may have been caused by carbon depletion, this was definitely not the case in above-ground tissues. Our findings indicate that mortality mechanisms are not defined at the organism level but rather within tree compartments
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