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34 results for “leaf gas exchange”
Leaf Gas Exchange in the Clearcut Site at Harvard Forest 2010-2012
Clearcutting a forest ecosystem can result in a drastic reduction of the stand’s productivity. Despite the severity of this disturbance type, past studies have found that the productivity of young regenerating stands can quickly rebound, approaching that of mature undisturbed stands within a few years. One of the obvious reasons is increased leaf area with each year of recovery. However, a less obvious reason may be the variability in species composition and distribution during the natural regeneration process. The purpose of this study was to investigate to what extent the increase in GEP, observed during the first four years of recovery, in a naturally regenerating clearcut stand was due to 1) an overall expansion of leaf area, and 2) an increase in the canopy’s photosynthetic capacity stemming from either species compositional shifts or drift in physiological traits within species. We found that the multi-year rise in GEP following harvest was clearly attributed to the expansion of leaf area rather than a change in vegetation composition. Sizeable changes in relative abundance of species were masked by remarkably similar leaf physiological attributes for a range of vegetation types present in this early successional environment. Comparison of upscaled leaf-chamber to eddy-covariance-based light-response curves revealed broad consistency in both maximum photosynthetic capacity and quantum yield efficiency. The approaches presented here illustrate how chamber- and ecosystem-scale measurements of gas exchange can be blended with species-level leaf area data to draw conclusive inferences about changes in ecosystem processes over time in a highly dynamic environment.
Black Rock Forest Spring Freeze Defoliation Radial Growth and Leaf-Level Gas Exchange
These data are from a study conducted at Black Rock Forest in Cornwall, New York, USA during 2020 and 2021. This study was conduct to assess the ecophysiological responses of red oak (Quercus rubra) and red maple (Acer rubrum) trees in a temperate broadleaf forests to a spring frost in 2020 that that defoliated red oak trees, but not red maples. We used 2021—a year without a defoliation event—as a reference year. The datasets include tree-level measurements of (1) basal area increment for the early growing season, late growing season, and entire growing season and (2) leaf-level gas exchange (Amax, gsw, and WUE) for red oak (Quercus rubra) and red maple (Acer rubrum). These data are associated with the manuscript “Compensatory Responses of Leaf Physiology Reduce Effects of Spring Frost Defoliation on Temperate Forest Tree Carbon Uptake” by Reinmann et al.2023 in Frontiers in Forests and Global Change.
Effect of the aspen leaf miner feeding damage on aspen leaf gas exchange and water relations from south-facing site on the University of Alaska Fairbanks campus: Fairbanks, Alaska 2018
This dataset addresses the effects of epidermal leaf mining by the aspen leaf miner (Phyllocnistis populiella) on the physiology and water relations of aspen leaves. The dataset contains measurements of gas exchange, water potential, water content, and delta13C of aspen leaves manipulated to bear leaf mining damage on the top (adaxial) leaf surface only, the bottom (abaxial) leaf surface only, or no mining damage.
FCE LTER Taylor Slough/Panhandle-7 Site Scrub Red Mangrove (Rhizophora mangle) Leaf Gas Exchange Data, Florida, USA from January-December 2019
Rates of leaf gas exchange were measured monthly during the 2019 calendar year in a scrub Red mangrove (Rhizophora mangle (L.) L.) forest site (TS/Ph-7) near the mouth of Taylor River in southeastern Florida Everglades. Sampling of green mature leaves was designed to target scrub mangrove tree branches growing on slightly higher elevation mangrove island centers versus permanently inundated island edge habitats. Concurrent measurements of water depth and surface and porewater salinity were collected at each of the mangrove island habitats, with the research objective of assessing the effect of physicochemical variables on rates of leaf gas exchange (i.e., assimilation and stomatal conductance). Leaf gas exchange data were collected using the Li-6800 portable photosynthesis system (Li-COR, Lincoln, NE). Additional data on leaf functional traits and nutrient concentrations and environmental data from the site are included. Data are presented in five datasets (.csv).
Seasonal trends in leaf level physiological parameters, obtained through gas exchange, reflectance spectroscopy and, functional trait analysis
This data package contains leaf level gas exchange, reflectance spectroscopy, and functional trait measurements collected in six common deciduous tree species across the full 2021 growth season (May -October) at the Black Rock Forest in Cornwall, New York, USA. Branches were sampled predawn using the shotgun method of branch retrieval, and re-cut under water to preserve hydraulic function before transport to the lab. Gas exchange data included in this package are stomatal response curves (irradiance response) which can be used to estimate stomatal slope and intercept. Spectroscopic data are full-range (350 – 2500 nm) leaf reflectance spectra collected on all leaves sampled for gas exchange and traits. Leaf level trait measurements include leaf mass per area (LMA), leaf dry matter content (LDMC), elemental nitrogen and carbon expressed on a per mass basis, and fitted values of Asat, Vcmax, and Rdark scaled to a reference temperature of 25C. Data from these three data tables (stomatal responce, spectra, leaf traits) can be cross referenced using the unique SampleID. Additional data tables include stomatal anatomy (stomatal density, length, and width of the guard cells), hydraulic properties estimated from pressure volume curves (relative water deficit at the turgor loss point), and predawn water potential for all sampled branches. Site level data includes the dGPS location of each sampled tree, its species, and DBH. Each tabular data file (*.csv) is accompanied by a data description (*_dd.csv) which includes relevant metadata (unit, definition, data type). Copies of all raw instrument output (spectroradiometer, LICOR, pressure chamber) and included as .zip files.
Gnuplot scripts for plotting selected leaf gas exchange and morphological data of industrial hemp
<p>Gnuplot code (scripts) for reproducing the eight figures of Sunoj et al. 2025 "Foliar gas exchange, morphology, and cannabinoid contents of three hemp varieties in southwest Texas," Agrosystems, Geosciences & Environment, 8, e70101. https://doi.org/10.1002/agg2.70101. Here is a list of the authors of the manuscript: John Sunoj V. S. (1), Xuejun Dong (1), Madhumita Joshi (1), Russell W. Jessup (2), Daniel I. Leskovar (1), and David D. Baltensperger (2). Texas A&M AgriLife Research at Uvalde, Texas, USA (1); Department of Soil and Crop Sciences, Texas A&M University, College Station, Texas, USA (2).</p> <p>The revised upload includes updated gnuplot scripts for reproducing Figures 2, 3, and 8, and Supplemental Figures 1-5 and Supplemental Tables 1-5 of the accepted manuscript by AGE.</p> <p>Code and data to reproduce Figure 2 (pnf_rev.eps): pn_dat_rev.txt, pnf_rev.txt</p> <p>Code and data to reproduce Figure 3 (fmf_rev.eps): fm_dat.txt, fm_rev.txt</p> <p>Code and data to reproduce Figure 8 (allom_1.eps): allom_1.txt, allom_data.csv</p> <p> </p> <p> </p> <p> </p> <p> </p>
Figure 2 in Root deformation affects mineral nutrition but not leaf gas exchange and growth of Genipa americana seedlings during the recovery phase after soil flooding
Figure 2. Concentrations of P in leaves for G. americana seedlings without or with root deformation (RD) after 28 days of soil drainage (recovery). N = 3. Means followed by the same letter are not significantly different according to Tukey's test (p <0.05). Capital letters represent comparisons water effects within root conditions and lower case letters represent comparisons of roots effects within water conditions.
Figure 1 in Root deformation affects mineral nutrition but not leaf gas exchange and growth of Genipa americana seedlings during the recovery phase after soil flooding
Figure 1. Four months old seedlings of G. americana without (A) and with (B) root deformation (RD) caused by errors in the pricking out process, and a detail of the RD (C).
Gas exchange, dieback, leaf water potential and chlorophyll content during a greenhouse drought experiment: An evolutionary perspective on functional diversity in co-occuring willow(salix) species
Thirteen willow (Salix) species occur in southeastern Minnesota and often co-occur within the same wetlands. This high local diversity is challenging to explain since closely related species are often functionally similar and density-dependent interactions such as competition and susceptibility to pests and pathogens should limit their co-occurrence. However, if willow species are partitioning resources, or if they are phylogenetically structured so that closely related species rarely co-occur, then the impact of these density-dependent processes could be reduced. In this study, I examined the role of niche partitioning in maintaining local willow diversity by comparing species physiology in a greenhouse.
Data from: Leaf morphological traits show greater responses to changes in climate than leaf physiological traits and gas exchange variables
<p>Adaptation to changing conditions is one of the strategies plants use to survive climate change. Here, we ask whether plants' leaf morphological and physiological traits/gas exchange variables have changed in response to recent, anthropogenic climate change. We grew seedlings from resurrected historic seeds from <em>ex-situ </em>seed banks and paired modern seeds in a common-garden experiment. Species pairs were collected from regions that had undergone differing levels of climate change using an emerging framework – Climate Contrast Resurrection Ecology, allowing us to hypothesise that regions with greater changes in climate (including temperature, precipitation, climate variability and climatic extremes) there would be greater trait responses in leaf morphology and physiology over time. Our found that in regions where there were greater changes in climate, there were greater changes in average leaf area, leaf margin complexity, leaf thickness and leaf intrinsic water use efficiency. Changes in leaf roundness, photosynthetic rate, stomatal density and the leaf economic strategy of our species were not correlated with changes in the climate. Our results show that leaves do have the ability to respond to changes in climate, however, there are greater inherited responses in morphological leaf traits than in physiological traits/variables, and greater responses to extreme measures of climate than gradual changes in climatic means. It is vital for accurate predictions of species' responses to impending climate change to ensure that future climate change ecology studies utilise knowledge about the difference in both leaf trait and gas exchange responses, and the climate variables that they respond to.</p>
Data from: Genomic regions associate with major axes of variation driven by gas exchange and leaf construction traits in cultivated sunflower (Helianthus annuus L.)
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Data from: Leaf morphological traits show greater responses to changes in climate than leaf physiological traits and gas exchange variables
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TeRaCON Leaf Gas Exchange:E141 - BioCON: Biodiversity, CO2, and Nitrogen
BioCON (Biodiversity, CO2, and Nitrogen) is an ecological experiment started in 1997 at the University of Minnesota's Cedar Creek Ecosystem Science Reserve. BioCON's goal is to explore the ways in which plant communities will respond to three environmental changes that are known to be occurring on a global scale: increasing nitrogen deposition, increasing atmospheric CO2, and decreasing biodiversity. Why Biodiversity, CO2, and Nitrogen? While there are many uncertainties in global change biology, there are also some well documented facts. Some of these are: 1. The amount of carbon dioxide (CO2) in the atmosphere is rising. Since the industrial revolution, the CO2 concentration in the atmosphere has increased from approximately 275 parts per million (ppm) to about 378 ppm today. This has been largely the result of fossil fuel burning. It is expected that CO2 levels will continue to rise, and that by the year 2050 these levels will be approximately 550 ppm. CO2 is the raw material for photosynthesis and is known to affect plant growth and development. 2. The amount of nitrogen moving through terrestrial ecosystems has increased in the recent past. While natural "background" levels of nitrogen fixation have remained constant, human additions to the system through fertilizer production and fossil fuel use have increased dramatically. Nitrogen is a key nutrient for plant growth and plays a critical role in plant community structure and composition in many environments. 3. Biodiversity levels are falling. While the research and data are not as complete as they are for CO2 and nitrogen, data indicate that the number of species globally, is being reduced. Perhaps more important for ecosystem function, diversity levels on local to regional scales have fallen due to land use change, biotic invasion and many other drivers. While much is known about how each of these factors affects ecosystem functioning, many questions remain. There is also little data on how these issues affe
Data from: Gas exchange and leaf anatomy of a C3-CAM hybrid, Yucca gloriosa (Asparagaceae)
While the majority of plants use the typical C3 carbon metabolic pathway, ~6% of angiosperms have adapted to carbon limitation as a result of water stress by employing a modified form of photosynthesis known as Crassulacean acid metabolism (CAM). CAM plants concentrate carbon in the cells by temporally separating atmospheric carbon acquisition from fixation into carbohydrates. CAM has been studied for decades, but the evolutionary progression from C3 to CAM remains obscure. In order to better understand the morphological and physiological characteristics associated with CAM photosynthesis, phenotypic variation was assessed in Yucca aloifolia, a CAM species, Yucca filamentosa, a C3 species, and Yucca gloriosa, a hybrid species derived from these two yuccas exhibiting intermediate C3–CAM characteristics. Gas exchange, titratable leaf acidity, and leaf anatomical traits of all three species were assayed in a common garden under well-watered and drought-stressed conditions. Yucca gloriosa showed intermediate phenotypes for nearly all traits measured, including the ability to acquire carbon at night. Using the variation found among individuals of all three species, correlations between traits were assessed to better understand how leaf anatomy and CAM physiology are related. Yucca gloriosa may be constrained by a number of traits which prevent it from using CAM to as high a degree as Y. aloifolia. The intermediate nature of Y. gloriosa makes it a promising system in which to study the evolution of CAM.
Genetic variation in leaf traits and gas exchange response to vapor pressure deficit in two contrasting conifer species
<p>1. Mechanistically predicting the evolutionary response of tree species to climate change requires an understanding of genetic variation in relevant traits. Here we compared the phenotypic and genetic variation in the Leaf Economics Spectrum (LES) traits and the response of gas exchange to vapor pressure deficit (VPD) in lodgepole pine (Pico) and white spruce (Pigl), an early and a late successional species dominating the boreal forests of western Canada. 2. We measured gas exchange, foliar nitrogen, and lamina mass to area ratio in 697 app. 30-year-old trees in two field progeny trials. We analyzed the response of gas exchange rates to VPD using a novel quantitative genetic model, the function-valued trait approach. 3. Pico showed greater phenotypic variation in the LES traits and greater genetic variation in photosynthetic rate than Pigl, but the species showed no significant difference in their phenotypic correlations between the LES traits. Pico showed a less sensitive stomatal response to VPD than Pigl and no significant genetic variation in stomatal sensitivity. In contrast, Pigl showed a positive correlation between the genetic values of stomatal sensitivity to VPD and stomatal conductance under low VPD. 4. Our study region is projected to see an increase in VPD with climate change; the less sensitive and genetically diverse stomatal response to VPD in Pico could make this species more vulnerable to climate change-induced droughts. </p>
"Field integration of shoot gas exchange and leaf chlorophyll fluorescence measurements to study the long-term regulation of photosynthesis in situ" data set
<p>The main data used in the "Field integration of shoot gas exchange and leaf chlorophyll fluorescence measurements to study the long-term regulation of photosynthesis in situ" publication, as well as the readme-file for the dataset. Supplementary figures are available at the Tree Physiology website.</p>
Data from: Influence of leaf trichomes on boundary layer conductance and gas-exchange characteristics in Metrosideros polymorpha (Myrtaceae)
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Genetic variation in leaf traits and gas exchange response to vapor pressure deficit in two contrasting conifer species
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Data from: Gas exchange and leaf anatomy of a C3-CAM hybrid, Yucca gloriosa (Asparagaceae)
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Leaf gas exchange in Ipomopsis aggregata under manipulated snowmelt timing and summer precipitation
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