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32 results for “plant water use”
The role of the intraspecific variability of hydraulic traits for modelling the plant water use in different European forest ecosystems: scripts, model output, and parameter files
<p>This repository contains the model outputs and R scripts used to process the data to analyze the impact of the plant hydraulic parameterization of the manuscript: "The role of the intraspecific variability of hydraulic traits for modelling the plant water use in different European forest ecosystems". The following is a detailed description of the content of this repository:</p> <p>model_output.zip: This compressed file contains the results of all the individual numerical experiments per experimental site as produced by the Comunity Land Model version 5. The files are stored in NETCDF format per year. The folder is arranged with subfolders containing the individual results from each experimental site as follows:</p> <ul> <li>rc: model output with the results of the resistant configuration of experiment 1 (RC)</li> <li>vc: model output with the results of the vulnerable configuration of experiment 1 (VC)</li> <li>k_dc: model output with the results of the default configuration used for experiments 1 and 2 (DC or DC<em>k</em><sub>max</sub>)</li> <li>k_rc: model output with the results of the low plant hydraulic conductance (L<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_irc: model output with the results of the intermediate low plant hydraulic conductance (IL<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_vc: model output with the results of the high plant hydraulic conductance (H<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_ivc: model output with the results of the intermediate high plant hydraulic conductance (IH<em>k</em><sub>max</sub>) for experiment 2</li> <li>k_iirc: model output with the results of the additional intermediate low plant hydraulic conductance (IIL<em>k</em><sub>max</sub>) for experiment 2</li> <li>ko_dc: model output with the results of the best <em>k</em><sub>max</sub> and the default configuration of the PVC used in experiment 3</li> <li>ko_rc: model output with the results of the best <em>k</em><sub>max</sub> and the resistant configuration of the PVC used in experiment 3</li> <li>ko_vc: model output with the results of the best <em>k</em><sub>max</sub> and the vulnerable configuration of the PVC used in experiment 3</li> </ul> <p>The scripts were written for use in RStudio, and each contains a detailed description of the data requirements and outputs. Each script was developed to read directly the netcdf files of the model output and the csv files containing the transpiration estimates calculated from the SAPFLUXNET per experimental site (script 1).</p>
Satellite-derived chlorophyll-a concentrations for Western Water Treatment Plant (Melbourne, Australia) using Mixture Density Networks and Sentinel-2 and Landsat 8 imagery
<p>This dataset contains satellite-derived chlorophyll-a data of the Western Water Treatment Plant (Melbourne, Australia) for the period 21 Mar. 2013 - 01 Feb. 2021. Chlorophyll-a concentrations have been calculated using Mixture Density Networks and Sentinel-2 and Landsat 8 imagery.</p> <p>Mixture Density Networks are a class of neural networks that tackle the inverse problem by modelling the multimodal distribution of target variables using a mixture of Gaussians. For more information, please refer to the following:</p> <ul> <li>Pahlevan, N., Smith, B., Alikas, K., Anstee, J., et al. (2022). Simultaneous retrieval of selected optical water quality indicators from Landsat-8, Sentinel-2, and Sentinel-3. <em>Remote Sensing of Environment, 270</em>, 112860</li> <li>Smith, B., Pahlevan, N., Schalles, J., et al. (2021). A Chlorophyll-a Algorithm for Landsat-8 Based on Mixture Density Networks. <em>Frontiers in Remote Sensing, 1</em></li> <li>Pahlevan, N., Smith, B., Schalles, J., et al. (2020). Seamless retrievals of chlorophyll-a from Sentinel-2 (MSI) and Sentinel-3 (OLCI) in inland and coastal waters: A machine-learning approach. <em>Remote Sensing of Environment, 240</em>, 111604</li> </ul>
High water use in desert plants exposed to extreme heat
<p>Many plant water use models predict leaves maximize carbon assimilation while minimizing water loss via transpiration. Alternate scenarios may occur at high temperature, including heat avoidance, where leaves increase water loss to evaporatively cool regardless of carbon uptake; or heat failure, where leaves non-adaptively lose water also regardless of carbon uptake. We hypothesized that these alternative scenarios are common in species exposed to hot environments, with heat avoidance more common in species with high construction-cost leaves. Diurnal measurements of leaf gas exchange and temperature for 11 Sonoran Desert species revealed 37% of these species increased transpiration in the absence of increased carbon uptake. High leaf mass per area partially predicted this behavior (<i>r</i><sup>2</sup>=0.39). These data are consistent with heat avoidance and heat failure, but failure is less likely given the ecological dominance of the focal species. These behaviors are not yet captured in any extant plant water use model.</p> <p> </p>
Data from: Species-specific variation in germination rates contributes to spatial coexistence more than adult plant water use in four closely-related annual flowering plants
1. Spatial partitioning is a classic hypothesis to explain plant species coexistence, but evidence linking local environmental variation to spatial sorting, demography, and species' traits is sparse. If co-occurring species' performance is optimized differently along environmental gradients because of trait variation, then spatial variation might facilitate coexistence. 2. We used a system of four naturally co-occurring species of Clarkia (Onagraceae) to ask if distribution patchiness corresponds to variation in two environmental variables that contribute to hydrological variation. We then reciprocally sowed Clarkia into each patch type and measured demographic rates in the absence of congeneric competition. Species sorted in patches along one or both gradients, and in three of the four species, germination rate in the "home" patch was higher than all other patches. 3. Spatially variable germination resulted in the same three species exhibiting the highest population growth rates in their home patches. 4. Species' trait values related to plant water use, as well as indicators of water stress in home patches, differed among species and corresponded to home patch attributes. However, post-germination survival did not vary among species or between patch types, and fecundity did not vary spatially. 5. Synthesis Our research demonstrates the likelihood that within-community spatial heterogeneity affects plant species coexistence, and presents novel evidence that differential performance in space is explained by what happens in the germination stage. Despite the seemingly obvious link between adult plant water-use and variation in the environment, our results distinguish the germination stage as important for spatially variable population performance.
Data from: Plant water use affects competition for nitrogen: why drought favors invasive species in California
Classic resource competition theory typically treats resource supply rates as independent; however, nutrient supplies can be affected by plants indirectly, with important consequences for model predictions. We demonstrate this general phenomenon by using a model in which competition for nitrogen is mediated by soil moisture, with competitive outcomes including coexistence and multiple stable states as well as competitive exclusion. In the model, soil moisture regulates nitrogen availability through soil moisture dependence of microbial processes, leaching, and plant uptake. By affecting water availability, plants also indirectly affect nitrogen availability and may therefore alter the competitive outcome. Exotic annual species from the Mediterranean have displaced much of the native perennial grasses in California. Nitrogen and water have been shown to be potentially limiting in this system. We parameterize the model for a Californian grassland and show that soil moisture–mediated competition for nitrogen can explain the annual species' dominance in drier areas, with coexistence expected in wetter regions. These results are concordant with larger biogeographic patterns of grassland invasion in the Pacific states of the United States, in which annual grasses have invaded most of the hot, dry grasslands in California but perennial grasses dominate the moister prairies of northern California, Oregon, and Washington.
Plant water use strategies predict restoration success across degraded drylands
<ul> <li>Plant strategies for coping with water limitation are likely to mediate restoration outcomes in degraded dryland ecosystems. Tradeoffs in traits related to water acquisition and use can intensify in more arid environments, making their effects on dryland restoration success even more salient. However, isolating the effects of drought responses from those of other environmental factors, as well as identifying the specific drought resistance traits that influence restoration success, can be difficult.</li> <li>In the present study, we couple a controlled dry-down experiment with a cross-site restoration field trial of out-planted seedlings (RestoreNet) using a suite of dryland herbaceous plant species from the same seed sources. We quantified interspecific variation in physiological responses to drought, specifically reductions in stomatal conductance (g<sub>s</sub>) and stem water potential (SWP), by comparing well-watered control plants to those experiencing decreasing soil moisture.</li> <li>Drought responses of SWP and g<sub>s</sub> varied independently among species, but both were related to survival in the cross-site restoration field trial when effect sizes were aggregated across all sites. Responses were consistent with acquisitive water use strategies resulting in greater success, where species with greater declines in SWP or weaker declines in g<sub>s</sub> under drought had greater survival. The correlation between SWP drought response and survival also intensified in sites with lower accumulated precipitation following restoration.</li> <li>Differences among functional groups revealed two different paths to restoration success: forbs that maintain high g<sub>s</sub> and narrow safety margins to maximize exploitation of moisture pulses before going into drought dormancy, or C<sub>4</sub> grasses that maintain efficient water uptake in drying soils while risking cavitation. C<sub>3</sub> grass species varied between these two strategies.</li> <li> <em>Synthesis and applications</em>: Taken together, the results of this study and others conducted at RestoreNet sites indicate that while a diversity of physiological responses to drought may exist in dryland plant communities, successfully restoring herbaceous species through out-planting in degraded conditions is likely to be achieved with species that maximize water uptake via one of two strategies, with tolerance of low SWP being particularly important in the most arid settings.</li> </ul>
Novel cropping system strategies in China can increase plant protein with higher economic value but lower greenhouse gas emissions and water use
<p> This database contains the average crop residue, manure nitrogen, manure organic carbon, net greenhouse gas emissions, and cropland area for 17 cropping systems at prefecture level during the period 2014-2018. In addition, it contained the changes of net greenhouse gas emissions caused by the optimization at prefecture level and province level.</p> <p> We also shared the key code for optimizing cropping systems at prefecture level and provided the all data. Users can run it the Matlab platform.</p>
Data from: Species-specific variation in germination rates contributes to spatial coexistence more than adult plant water use in four closely-related annual flowering plants
Open the record for dataset details and reuse information.
Balancing water yield and water use efficiency between planted and natural forests: A global analysis
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Plant water use strategies predict restoration success across degraded drylands
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Data from: Plant water use affects competition for nitrogen: why drought favors invasive species in California
Open the record for dataset details and reuse information.
High water use in desert plants exposed to extreme heat
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Analyzing coastal fog effects on carbon and water fluxes in a California agricultural system using approaches in biometeorology, remote sensing, and plant physiology
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Water Use and flooding in central Arizona-Phoenix: comparison of water and carbon dioxide uptake by selected plant species among residential patch transition types, from 1998 to 1999.
Compare the primary productivity (rate of of production of plant material) and uptake of water and carbon dioxide by selected plant species, at sites selected to represent the transition between desert or agriculture and new residential development.
Stand age rather than soil moisture gradient dominantly regulates the compromise between plant growth and water use of Eucalyptus urophylla in hilly South China
<p>These files contain the clinate data, the morphology characteristics, soil water content and tree normalized transpiration collected in our studied site.</p>
Data from: Can intercropping with the world's three major beverage plants help improve the water use of rubber trees?
The dramatic expansion of rubber plantations in mainland South-East Asia and south-west China has caused many eco-environmental problems, especially negative hydrological consequences. These problems have gradually worsened and pose formidable threats to rubber agriculture, especially in the light of increasingly frequent extreme weather events. Although rubber-based agroforestry systems are regarded as the best solution for improving the sustainability of rubber agriculture and environmental conservation, plant water use and related interactions have rarely been examined in such systems. We primarily used stable isotope (δD, δ18O and δ13C) methods to test whether intercropping could improve the water use and extreme weather tolerance (extreme cold and drought in our study) of rubber trees in three types of promising agroforestry systems (i.e. rubber with tea, coffee and cocoa) in Xishuangbanna, China. We found that the rubber tree is a drought-avoidance plant with strong plasticity with respect to water uptake. This characteristic is reflected by its ability to cope with serious seasonal drought, allowing it to avoid interspecific competition for water. The rubber trees showed wasteful water behaviour unless they were intercropped with tea or coffee. However, these intercropped species exhibited drought-tolerance strategies and maintained lower water use efficiencies to strengthen their competitive capacity for surface soil water. The stable δ13C values of the intercrop leaves indicated that all the agroforestry systems have stable internal microclimatic environments or higher resistance. Synthesis and applications. This study suggests that interspecific competition for water can enhance the water use efficiency of drought-avoidance plants (i.e. rubber trees) and lead to complementarity between the root distributions of plants in rubber agroforestry systems (i.e. rubber with tea, coffee and cocoa). All agroforestry systems have higher resistance, but tea was the most suitable intercrop in terms of water use because the interspecific competition for water was moderate and the agroforestry system retained much more soil water and improved the water use efficiency of the rubber tree. Considering the root characteristics of the tea trees, we suggest that the crops selected for intercropping with rubber trees should have a relatively fixed water use pattern, short lateral roots and a moderate amount of fine roots that overlap with the roots of the rubber trees in the shallow soil layer.
Data from: Epiphytes improve host plant water use by microenvironment modification
1. Epiphytes have the potential to modify the canopy environments in which they grow. Accurately evaluating the impact of epiphytes can be challenging, since plants without epiphytes may also otherwise differ from host plants, and experimental removal is impractical and difficult to replicate in many forests. 2. We studied the impacts of epiphytes (primarily fruticose lichens and Tillandsia spp.) on host plants (Eulychnia saint-pieana and Caesalpinia spinosa) in two fog ecosystems in Chile (Pan de Azucar) and Peru (Atiquipa). These desert ecosystems sustain very high epiphyte loads and depend heavily on fog-water inputs. Using a combination of artificial substrates and epiphyte removals we show significant impacts of epiphytes on their host plants. 3. The presence of epiphytes reduced throughfall volumes, reducing fog and rainfall inputs to the soil beneath host plant canopies. 4. Soil moisture loss rate was increased below cacti after removal of epiphytes from sun-facing but not shade-facing branches. This suggests epiphyte effects on hosts are microclimatic. 5. Epiphytes also buffered temperature fluctuations and reduced daytime vapour pressure deficit (VPD). 6. Epiphytes can have strong effects on host plant ecophysiology and forest ecosystem processes, making them an important component for models and studies of canopy environments.
Data from: Plant functional types broadly describe water use strategies in the Caatinga, a seasonally dry tropical forest in northeast Brazil
<ol> <li><span>In seasonally dry tropical forests, plant functional type can be classified as deciduous low wood density, deciduous high wood density, or evergreen high wood density species. While deciduousness is often associated with drought-avoidance and low wood density is often associated with tissue water storage, the degree to which these functional types may correspond to diverging and unique water use strategies has not been extensively tested. </span></li> <li><span>We examined (1) tolerance to water stress, measured by pre-dawn and mid-day leaf water potential; (2) water use efficiency, measured via foliar δ<sup>13</sup>C; and (3) access to soil water,<i> </i>measured via stem water δ<sup>18</sup>O.</span></li> <li><span>We found that deciduous low wood density species maintain high leaf water potential and low water use efficiency. Deciduous high wood density species have lower leaf water potential and variable water use efficiency. Both groups rely on shallow soil water. Evergreen high wood density species have low<i> </i>leaf water potential, higher water use efficiency, and access alternative water sources. These findings indicate that deciduous low wood density species are drought avoiders, with a specialized strategy for storing root and stem water. Deciduous high wood density species are moderately drought tolerant, and evergreen high wood density species are the most drought tolerant group. </span></li> <li><span><i>Synthesis. </i>Our results broadly support the plant functional type framework as a way to understand water use strategies, but also highlight species-level differences. </span></li> </ol>
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925). in Muridae
Distribution. Now restricted to the Channel Country of SW Queensland and the Lake Eyre Basin in NE South Australia. Descriptive notes. Head-body 95-120 mm, tail 105-160 mm, ear 23-29 mm, hindfoot 32-37 mm; weight 30-50 g. The Fawn Hopping Mouse has body form typical of hopping mice, with very long hindfeet, long tail with distal brush of longer hairs, very long ears, and large protruberant eyes. Dorsal fur is of variable color, from pale pinkish fawn to gray; ventral fur white. Unlike most other hopping mice, it has no throat pouch, but males have a glandular area of naked skin on the chest. Habitat. Occurs in low shrublands and tussock grasslands on stony ("gibber") plains and claypans. Shows marked habitat segregation from the Dusky Hopping Mouse (N. fuscus), which is closely associated with sandy substrates. Food and Feeding. The Fawn Hopping Mouse is mostly granivorous, but also eats other plant material (stems, leaves) and occasionally invertebrates. It uses succulent, salt-adapted plants around edges of claypans as a source of water. Breeding. Reproduction is probably largely opportunistic and aseasonal, with high reproductive output from near-continuous breeding after periods of high rainfall; reported littersize is 1-5, most commonly three; gestation period 38-43 days for nonlactating females. Females may mature later than other hopping mice, with reproductive maturity reached at about six months. Activity patterns. Terrestrial and nocturnal. Fawn Hopping Mice shelter during day in burrow systems that are typically simpler and shallower than those of other hopping mice. Movements, Home range and Social organization. Fawn Hopping Mice generally live singly or in small groups; typically uncommon within range, but population density may increase by an order of magnitude following periods of high rainfall. Status and Conservation. Classified as Near Threatened on The IUCN Red List. The Fawn Hopping Mouse has shown marked decline in range (estimated at greater than 50%), and presumably population size, since European settlement of Australia. This is mostlikely due to predation by the introduced house cat and Red Fox (Vulpes vulpes), and to habitat degradation associated with pastoralism. Bibliography. Brazenor (1934), Burbidge et al. (2008), Finlayson (1939), Gould (1853), Jackson & Groves (2015), Murray et al. (1999), Ogilby (1892), Thomas (1921h), Van Dyck & Strahan (2008), Waite (1898), Watts & Aslin (1981), Woinarski et al. (2014), Wood Jones (1925).
Techno-economic comparison of power-to-Ammonia and biomass- to-Ammonia plants using electrolyzer, CO 2 capture and water-gas- shift membrane reactor
<p>A set of imput data used for the paper entitled: Techno-economic comparison of power-to-Ammonia and biomass-<br>to-Ammonia plants using electrolyzer, CO 2 capture and water-gas-shift membrane reactor </p>
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