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  • Energy Research
  • 2021-2025
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  • 2. Zero hunger

  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: Long, Marc; Lelong, Aurélie; Bucciarelli, Eva; Le Grand, Fabienne; +2 Authors

    This dataset contains the data used in the manuscript "Physiological adaptation of the diatom Pseudo-nitzschia delicatissima under copper starvation" accepted for publication in April 2023 in Marine Environmental Research. In the open ocean and particularly in iron (Fe)-limited environment, copper (Cu) deficiency might limit the growth of phytoplankton species. Cu is an essential trace metal used in electron-transfer reactions, such as respiration and photosynthesis, when bound to specific enzymes. Some phytoplankton species, such as the diatom Pseudo-nitzschia spp. can cope with Cu starvation through adaptative strategies. This dataset contains the data collected during the experimental starvation of a strain of the diatom P. delicatissima under laboratory controlled conditions.

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    https://dx.doi.org/10.17882/94...
    Dataset . 2023
    License: CC BY NC
    Data sources: Datacite
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    SEANOE
    Dataset . 2023
    License: CC BY NC
    Data sources: SEANOE
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      https://dx.doi.org/10.17882/94...
      Dataset . 2023
      License: CC BY NC
      Data sources: Datacite
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      SEANOE
      Dataset . 2023
      License: CC BY NC
      Data sources: SEANOE
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    Authors: Klatt, Björn; de La Vega, Bernardo; Smith, Henrik;

    Data set and R script for the published article: Altered winter conditions impair plant development and yield in oilseed rape. The data set includes data about plant development, growth and yield resulting from an experiment where plants were grown at different winter conditions and exposed to an extreme weather event.The R script contains the analyses used for obtaining the results in the published article. Linear models within the R package glmmTMB are used for alla analyses.

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    4TU.ResearchData | science.engineering.design
    Dataset . 2022
    License: CC BY
    Data sources: Datacite
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    4TU.ResearchData | science.engineering.design
    Dataset . 2022
    License: CC BY
    Data sources: Datacite
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    4TU.ResearchData | science.engineering.design
    Dataset . 2022
    License: CC BY
    Data sources: Datacite
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      4TU.ResearchData | science.engineering.design
      Dataset . 2022
      License: CC BY
      Data sources: Datacite
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      4TU.ResearchData | science.engineering.design
      Dataset . 2022
      License: CC BY
      Data sources: Datacite
      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
      4TU.ResearchData | science.engineering.design
      Dataset . 2022
      License: CC BY
      Data sources: Datacite
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    Authors: Rodriguez Alarcon, Slendy Julieth; Tamme, Riin; Perez Carmona, Carlos;

    Seeds of 52 species of herbaceous plants typical from European grassland ecosystems were obtained from a commercial supplier (Planta naturalis). When species germinated in Petri dishes the seedlings were then transplanted to plastic pots (11 x 11 x 12 cm height, 1L volume). Pots were filled with a mixture of a potting substrate (Biolan Murumuld) and sand. Pots were randomly placed in the greenhouse of the University of Tartu, Estonia. Then, we established monocultures with seven individuals of a single species per pot which were grown under well-watered conditions. One month after transplanting the seedlings to the pots, a drought treatment was applied to half of the pots (five pots per species). The experiment was harvested in late July 2020, when the first individuals started flowering, after month-long drought treatment. Plant traits related to drought responses and resource use strategies were selected and measured for each species following established protocols. These included seven above- and belowground traits: Vegetative plant height (H, cm), Leaf Area (LA, mm2), Specific Leaf Area (SLA, mm2 mg-1), Leaf Dry Matter Content (LDMC, mg g-1), Specific Root Length (SRL, cm g-1), Average root Diameter (AvgD, mm), Root Dry Matter Content (RDMC, mg g-1). Before harvesting, we measured the plant height and collected one leaf per individual for three individuals per pot. Afterward, we collected the aboveground biomass and belowground biomass of all the individuals in each pot. Due to the difficulty in untangling the roots of the different individuals in a pot, root traits were estimated at the pot level. Roots were washed and a sample of finest roots (10-50mg) was collected. Leaves and fine roots were scanned at 300dpi and 600dpi, respectively, using an Epson perfection 3200 Photo scanner for leaves and Epson V700 Photo scanner for fine roots. After scanning, leaves and roots were oven-dried at 60°C for 72h. AvgD and root length were determined using WinRHIZO Pro 2015 (Regent Instruments Inc., Canada), and leaf area with ImageJ software. We averaged all traits values at the species level, attaining a single value for each trait in each treatment. The total aboveground biomass and total belowground biomass of each pot were oven-dried at 60°C for 72h and weighed. Drought is expected to increase in future climate scenarios. Although responses to drought of individual functional traits are relatively well-known, simultaneous changes across multiple traits in response to water scarcity remain poorly understood despite its importance to understand alternative strategies to resist drought. We grew 52 herbaceous species in monocultures under drought and control treatments and characterized the functional space using seven measured above- and belowground traits: plant height, leaf area, specific leaf area, leaf dry matter content, specific root length, average root diameter, and root dry matter content. Then, we estimated how each species occupied this space and the amount of functional space occupied in both treatments using trait probability density functions. We also estimated intraspecific trait variability (ITV) for each species as the dissimilarity in trait values between the individuals of each treatment. We then mapped drought resistance and ITV in the functional space using generalized additive models. The response of species to drought strongly depended on their traits, with species that invested more in root tissues and conserved small size being both more resistant to drought and having higher ITV. We also observed a significant trend of trait displacement towards less conservative strategies. However, these changes depended strongly on the trait values of species in the control treatment, with species with different traits having opposing responses to drought. These contrasting responses resulted in lower trait variability in the species pool in drought compared to control conditions. Our results suggest strong trait filtering acting on conservative species as well as the existence of an optimal part in the functional space to which species converge under drought. Our results show that changes in species trait-space occupancy are key to understand plant strategies to withstand drought, highlighting the importance of individual variation in response to environmental changes, and suggest that community-wide functional diversity and biomass productivity could decrease in a drier future. Knowing these shifts will help to anticipate changes in ecosystem functioning facing climate change. The complete dataset is in the file.

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    ZENODO
    Dataset . 2022
    License: CC 0
    Data sources: ZENODO
    DRYAD
    Dataset . 2022
    License: CC 0
    Data sources: Datacite
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      ZENODO
      Dataset . 2022
      License: CC 0
      Data sources: ZENODO
      DRYAD
      Dataset . 2022
      License: CC 0
      Data sources: Datacite
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    Authors: Barreaux, Antoine; Higginson, Andrew; Bonsall, Michael; English, Sinead;

    Here, we investigate how stochasticity and age-dependence in energy dynamics influence maternal allocation in iteroparous females. We develop a state-dependent model to calculate the optimal maternal allocation strategy with respect to maternal age and energy reserves, focusing on allocation in a single offspring at a time. We introduce stochasticity in energetic costs– in terms of the amount of energy required to forage successfully and individual differences in metabolism – and in feeding success. We systematically assess how allocation is influenced by age-dependence in energetic costs, feeding success, energy intake per successful feeding attempt, and environmentally-driven mortality. First, using stochastic dynamic programming, we calculate the optimal amount of reserves M that mothers allocate to each offspring depending on their own reserves R and age A. The optimal life history strategy is then the set of allocation decisions M(R, A) over the whole lifespan which maximizes the total reproductive success of distant descendants. Second, we simulated the life histories of 1000 mothers following the optimisation strategy and the reserves at the start of adulthood R1, the distribution of which was determined, the distribution of which was determined using an iterative procedure as described . For each individual, we calculated maternal allocation Mt, maternal reserves Rt, and relative allocation Mt⁄Rt at each time period t. The relative allocation helps us to understand how resources are partitioned between mother and offspring. Third, we consider how the optimal strategy varies when there is age-dependence in resource acquisition, energetic costs and survival. Specifically, we include varying scenarios with an age-dependent increase or a decrease with age in energetic costs (c_t), feeding success (q_t), energy intake per successful feeding attempt (y_t), and environmentally-driven extrinsic mortality rate (d_t) (Table 2). We consider the age-dependence of parameters one at a time or in pairs, altering the slope, intercept, or asymptote of the age-dependence (linear or asymptotic function). Our aim is to identify whether the observed reproductive senescence can arise from optimal maternal allocation. As such, we do not impose a decline in selection in later life as all offspring are equally valuable at all ages (for a given maternal allocation), and there are no mutations. For each scenario, we run the backward iteration process with these age-dependent functions, obtain the allocation strategy, and simulate the life history of 1000 individuals based on the novel strategy. We then fit quadratic and linear models to the reproduction of these 1000 individuals using the lme function, nlme package in R. For these models, the response variable is the maternal allocation Mt and explanatory variables are the time period t and t2 (for the quadratic fit only), with individual identity as a random term. We use likelihood ratio tests to compare linear and quadratic models using the anova function (package nlme) with the maximum-likelihood method. If the comparison is significant (p-value <0.05), we considered the quadratic model to have a better fit, otherwise the linear model is considered more parsimonious. We were particularly interested in identifying scenarios where the fit was quadratic with a negative quadratic term. For each scenario, the pseudo R2 conditional value (proportion of variance explained by the fixed and random terms, accounting for individual identity) is calculated to assess the goodness-of-fit of the lme model, on a scale from 0 to 1, using the “r.squared” function, package gabtool. All calculations and coding are done in R. Iteroparous parents face a trade-off between allocating current resources to reproduction versus maximizing survival to produce further offspring. Optimal allocation varies across age, and follows a hump-shaped pattern across diverse taxa, including mammals, birds and invertebrates. This non-linear allocation pattern lacks a general theoretical explanation, potentially because most studies focus on offspring number rather than quality and do not incorporate uncertainty or age-dependence in energy intake or costs. Here, we develop a life history model of maternal allocation in iteroparous animals. We identify the optimal allocation strategy in response to stochasticity when energetic costs, feeding success, energy intake, and environmentally-driven mortality risk are age-dependent. As a case study, we use tsetse, a viviparous insect that produces one offspring per reproductive attempt and relies on an uncertain food supply of vertebrate blood. Diverse scenarios generate a hump-shaped allocation: when energetic costs and energy intake increase with age; and also when energy intake decreases, and energetic costs increase or decrease. Feeding success and mortality risk have little influence on age-dependence in allocation. We conclude that ubiquitous evidence for age-dependence in these influential traits can explain the prevalence of non-linear maternal allocation across diverse taxonomic groups.

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    ZENODO
    Dataset . 2022
    License: CC 0
    Data sources: ZENODO
    DRYAD
    Dataset . 2022
    License: CC 0
    Data sources: Datacite
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      ZENODO
      Dataset . 2022
      License: CC 0
      Data sources: ZENODO
      DRYAD
      Dataset . 2022
      License: CC 0
      Data sources: Datacite
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    Authors: Villegas-Torres, M (via Mendeley Data);

    This data corresponds to the manuscript titled: Sustainable sugarcane vinasse biorefinement toward biobased chemicals and bioenergy generation

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    Mendeley Data
    Dataset . 2021
    License: CC BY
    Data sources: Datacite
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    Mendeley Data
    Dataset . 2021
    License: CC BY
    Data sources: Datacite
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    B2FIND
    Dataset . 2021
    Data sources: B2FIND
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      Mendeley Data
      Dataset . 2021
      License: CC BY
      Data sources: Datacite
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      Mendeley Data
      Dataset . 2021
      License: CC BY
      Data sources: Datacite
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      B2FIND
      Dataset . 2021
      Data sources: B2FIND
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    Authors: Roth, Jamila; Osborne, Todd; Reynolds, Laura;

    The ecological impacts of multiple stressors are hard to predict but important to understand. When multiple stressors influence foundation species, the effects can cascade throughout the ecosystem. Gulf of Mexico seagrass ecosystems are currently experiencing a suite of novel stressors, including warmer water temperatures and increased herbivory due to tropicalization and conservation efforts. We investigated the impact of warming temperatures and grazing history on plant performance, morphology, and palatability by integrating a mesocosm study using the seagrass Thalassia testudinum with feeding trials using the sea urchin Lytechinus variegatus. Warming temperatures negatively impacted T. testudinum tolerance traits, reducing belowground biomass by 34%, productivity by 74%, shoot density by 10%, and the number of leaves per plant by 24%, and negatively impacted resistance traits through 13% lower toughness of young leaves and a trend for reduced leaf carbon:nitrogen. Lytechinus variegatus individuals preferred to consume plants grown under heated conditions, which supports findings of enhanced palatability. Simulated turtle grazing impacted more plant traits than grazing by other herbivores, potentially diminishing plant resilience to future disturbances through reduced rhizome non-structural carbohydrate concentrations and increasing palatability through reduced fiber content and 23% lower leaf carbon:phosphorus. Simulated turtle, simulated parrotfish, and urchin grazing reduced leaf carbon:nitrogen by 11%, also potentially increasing nutritive value. Interactions between warming temperatures and grazers on plant traits were additive for 16 out of 19 response variables. However, the stressors non-additively impacted the number of leaves per plant, fiber content, and epiphyte load. We suggest that the impacts of grazers on leaf turnover rate and leaf age may vary based on water temperature, potentially driving these interactions. Overall, increased temperatures and grazing pressure will likely reduce seagrass resilience, structure, and biomass, potentially impacting feedback systems and producing negative consequences for seagrass cover, associated species, and ecosystem services.

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    ZENODO
    Dataset . 2023
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    DRYAD
    Dataset . 2023
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    Data sources: Datacite
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      ZENODO
      Dataset . 2023
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      DRYAD
      Dataset . 2023
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    Authors: Shuai ZHANG;

    Climate trends during maize growing period and their impacts on spring maize yield in North China was investigated. This dataset contains: 1) information of stations in cultivation region for spring maize in North China; 2) Trend in temperature and its effect on yield in cultivation region for spring maize in North China; 3) Trend in radiation and its effect on yield in cultivation region for spring maize in North China; 4) Trend in precipitation and its effect on yield in cultivation region for spring maize in North China. Climate trends during maize growing period and their impacts on spring maize yield in North China was investigated. This dataset contains: 1) information of stations in cultivation region for spring maize in North China; 2) Trend in temperature and its effect on yield in cultivation region for spring maize in North China; 3) Trend in radiation and its effect on yield in cultivation region for spring maize in North China; 4) Trend in precipitation and its effect on yield in cultivation region for spring maize in North China.

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    https://dx.doi.org/10.57760/sc...
    Dataset . 2022
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      https://dx.doi.org/10.57760/sc...
      Dataset . 2022
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    Authors: Shao, Junjiong; Zhou, Xuhui; van Groenigen, Kees; Zhou, Guiyao; +9 Authors

    Aim: Climate warming and biodiversity loss both alter plant productivity, yet we lack an understanding of how biodiversity regulates the responses of ecosystems to warming. In this study, we examine how plant diversity regulates the responses of grassland productivity to experimental warming using meta-analytic techniques. Location: Global Major taxa studied: Grassland ecosystems Methods: Our meta-analysis is based on warming responses of 40 different plant communities obtained from 20 independent studies on grasslands across five continents. Results: Our results show that plant diversity and its responses to warming were the most important factors regulating the warming effects on plant productivity, among all the factors considered (plant diversity, climate and experimental settings). Specifically, warming increased plant productivity when plant diversity (indicated by effective number of species) in grasslands was lesser than 10, whereas warming decreased plant productivity when plant diversity was greater than 10. Moreover, the structural equation modelling showed that the magnitude of warming enhanced plant productivity by increasing the performance of dominant plant species in grasslands of diversity lesser than 10. The negative effects of warming on productivity in grasslands with plant diversity greater than 10 were partly explained by diversity-induced decline in plant dominance. Main Conclusions: Our findings suggest that the positive or negative effect of warming on grassland productivity depends on how biodiverse a grassland is. This could mainly owe to differences in how warming may affect plant dominance and subsequent shifts in interspecific interactions in grasslands of different plant diversity levels.

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    ZENODO
    Dataset . 2023
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    DRYAD
    Dataset . 2022
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      ZENODO
      Dataset . 2023
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      DRYAD
      Dataset . 2022
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    Authors: Shuai ZHANG;

    Changes in late rice phenology during 1981–2009 were investigated using observed phenological data from agro-meteorological stations across China. This dataset contains 1) details of late rice agrometeorological experiment stations; 2) mean date of late rice phenology date and trend in phenology date during the period of 1981–2009; 3) trends in length of late rice growing period during the period of 1981-2009. Changes in late rice phenology during 1981–2009 were investigated using observed phenological data from agro-meteorological stations across China. This dataset contains 1) details of late rice agrometeorological experiment stations; 2) mean date of late rice phenology date and trend in phenology date during the period of 1981–2009; 3) trends in length of late rice growing period during the period of 1981-2009.

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    https://dx.doi.org/10.57760/sc...
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      https://dx.doi.org/10.57760/sc...
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    Authors: Guindo, Samuel; Dossou-Yovo, Elliott Ronald;

    The data used in this article are related to the rice yield following the use of the RiceAdvice technology recommendation and the rice yield following the recommended level of fertilizer recommendations. The data were collected in 5 sites in Mali. In all sites, rice yield with RiceAdvice was higher than rice yield following the conventional levels of fertilizer. On average, rice yield with RiceAdvice was 0.7 t/ha higher than rice yield with the conventional level of fertilizer recommendations.

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    Harvard Dataverse
    Dataset . 2022
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    Authors: Long, Marc; Lelong, Aurélie; Bucciarelli, Eva; Le Grand, Fabienne; +2 Authors

    This dataset contains the data used in the manuscript "Physiological adaptation of the diatom Pseudo-nitzschia delicatissima under copper starvation" accepted for publication in April 2023 in Marine Environmental Research. In the open ocean and particularly in iron (Fe)-limited environment, copper (Cu) deficiency might limit the growth of phytoplankton species. Cu is an essential trace metal used in electron-transfer reactions, such as respiration and photosynthesis, when bound to specific enzymes. Some phytoplankton species, such as the diatom Pseudo-nitzschia spp. can cope with Cu starvation through adaptative strategies. This dataset contains the data collected during the experimental starvation of a strain of the diatom P. delicatissima under laboratory controlled conditions.

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    https://dx.doi.org/10.17882/94...
    Dataset . 2023
    License: CC BY NC
    Data sources: Datacite
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    SEANOE
    Dataset . 2023
    License: CC BY NC
    Data sources: SEANOE
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      https://dx.doi.org/10.17882/94...
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      SEANOE
      Dataset . 2023
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    Authors: Klatt, Björn; de La Vega, Bernardo; Smith, Henrik;

    Data set and R script for the published article: Altered winter conditions impair plant development and yield in oilseed rape. The data set includes data about plant development, growth and yield resulting from an experiment where plants were grown at different winter conditions and exposed to an extreme weather event.The R script contains the analyses used for obtaining the results in the published article. Linear models within the R package glmmTMB are used for alla analyses.

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    4TU.ResearchData | science.engineering.design
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    4TU.ResearchData | science.engineering.design
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      4TU.ResearchData | science.engineering.design
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      4TU.ResearchData | science.engineering.design
      Dataset . 2022
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    Authors: Rodriguez Alarcon, Slendy Julieth; Tamme, Riin; Perez Carmona, Carlos;

    Seeds of 52 species of herbaceous plants typical from European grassland ecosystems were obtained from a commercial supplier (Planta naturalis). When species germinated in Petri dishes the seedlings were then transplanted to plastic pots (11 x 11 x 12 cm height, 1L volume). Pots were filled with a mixture of a potting substrate (Biolan Murumuld) and sand. Pots were randomly placed in the greenhouse of the University of Tartu, Estonia. Then, we established monocultures with seven individuals of a single species per pot which were grown under well-watered conditions. One month after transplanting the seedlings to the pots, a drought treatment was applied to half of the pots (five pots per species). The experiment was harvested in late July 2020, when the first individuals started flowering, after month-long drought treatment. Plant traits related to drought responses and resource use strategies were selected and measured for each species following established protocols. These included seven above- and belowground traits: Vegetative plant height (H, cm), Leaf Area (LA, mm2), Specific Leaf Area (SLA, mm2 mg-1), Leaf Dry Matter Content (LDMC, mg g-1), Specific Root Length (SRL, cm g-1), Average root Diameter (AvgD, mm), Root Dry Matter Content (RDMC, mg g-1). Before harvesting, we measured the plant height and collected one leaf per individual for three individuals per pot. Afterward, we collected the aboveground biomass and belowground biomass of all the individuals in each pot. Due to the difficulty in untangling the roots of the different individuals in a pot, root traits were estimated at the pot level. Roots were washed and a sample of finest roots (10-50mg) was collected. Leaves and fine roots were scanned at 300dpi and 600dpi, respectively, using an Epson perfection 3200 Photo scanner for leaves and Epson V700 Photo scanner for fine roots. After scanning, leaves and roots were oven-dried at 60°C for 72h. AvgD and root length were determined using WinRHIZO Pro 2015 (Regent Instruments Inc., Canada), and leaf area with ImageJ software. We averaged all traits values at the species level, attaining a single value for each trait in each treatment. The total aboveground biomass and total belowground biomass of each pot were oven-dried at 60°C for 72h and weighed. Drought is expected to increase in future climate scenarios. Although responses to drought of individual functional traits are relatively well-known, simultaneous changes across multiple traits in response to water scarcity remain poorly understood despite its importance to understand alternative strategies to resist drought. We grew 52 herbaceous species in monocultures under drought and control treatments and characterized the functional space using seven measured above- and belowground traits: plant height, leaf area, specific leaf area, leaf dry matter content, specific root length, average root diameter, and root dry matter content. Then, we estimated how each species occupied this space and the amount of functional space occupied in both treatments using trait probability density functions. We also estimated intraspecific trait variability (ITV) for each species as the dissimilarity in trait values between the individuals of each treatment. We then mapped drought resistance and ITV in the functional space using generalized additive models. The response of species to drought strongly depended on their traits, with species that invested more in root tissues and conserved small size being both more resistant to drought and having higher ITV. We also observed a significant trend of trait displacement towards less conservative strategies. However, these changes depended strongly on the trait values of species in the control treatment, with species with different traits having opposing responses to drought. These contrasting responses resulted in lower trait variability in the species pool in drought compared to control conditions. Our results suggest strong trait filtering acting on conservative species as well as the existence of an optimal part in the functional space to which species converge under drought. Our results show that changes in species trait-space occupancy are key to understand plant strategies to withstand drought, highlighting the importance of individual variation in response to environmental changes, and suggest that community-wide functional diversity and biomass productivity could decrease in a drier future. Knowing these shifts will help to anticipate changes in ecosystem functioning facing climate change. The complete dataset is in the file.

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    ZENODO
    Dataset . 2022
    License: CC 0
    Data sources: ZENODO
    DRYAD
    Dataset . 2022
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    Data sources: Datacite
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      ZENODO
      Dataset . 2022
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      Dataset . 2022
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    Authors: Barreaux, Antoine; Higginson, Andrew; Bonsall, Michael; English, Sinead;

    Here, we investigate how stochasticity and age-dependence in energy dynamics influence maternal allocation in iteroparous females. We develop a state-dependent model to calculate the optimal maternal allocation strategy with respect to maternal age and energy reserves, focusing on allocation in a single offspring at a time. We introduce stochasticity in energetic costs– in terms of the amount of energy required to forage successfully and individual differences in metabolism – and in feeding success. We systematically assess how allocation is influenced by age-dependence in energetic costs, feeding success, energy intake per successful feeding attempt, and environmentally-driven mortality. First, using stochastic dynamic programming, we calculate the optimal amount of reserves M that mothers allocate to each offspring depending on their own reserves R and age A. The optimal life history strategy is then the set of allocation decisions M(R, A) over the whole lifespan which maximizes the total reproductive success of distant descendants. Second, we simulated the life histories of 1000 mothers following the optimisation strategy and the reserves at the start of adulthood R1, the distribution of which was determined, the distribution of which was determined using an iterative procedure as described . For each individual, we calculated maternal allocation Mt, maternal reserves Rt, and relative allocation Mt⁄Rt at each time period t. The relative allocation helps us to understand how resources are partitioned between mother and offspring. Third, we consider how the optimal strategy varies when there is age-dependence in resource acquisition, energetic costs and survival. Specifically, we include varying scenarios with an age-dependent increase or a decrease with age in energetic costs (c_t), feeding success (q_t), energy intake per successful feeding attempt (y_t), and environmentally-driven extrinsic mortality rate (d_t) (Table 2). We consider the age-dependence of parameters one at a time or in pairs, altering the slope, intercept, or asymptote of the age-dependence (linear or asymptotic function). Our aim is to identify whether the observed reproductive senescence can arise from optimal maternal allocation. As such, we do not impose a decline in selection in later life as all offspring are equally valuable at all ages (for a given maternal allocation), and there are no mutations. For each scenario, we run the backward iteration process with these age-dependent functions, obtain the allocation strategy, and simulate the life history of 1000 individuals based on the novel strategy. We then fit quadratic and linear models to the reproduction of these 1000 individuals using the lme function, nlme package in R. For these models, the response variable is the maternal allocation Mt and explanatory variables are the time period t and t2 (for the quadratic fit only), with individual identity as a random term. We use likelihood ratio tests to compare linear and quadratic models using the anova function (package nlme) with the maximum-likelihood method. If the comparison is significant (p-value <0.05), we considered the quadratic model to have a better fit, otherwise the linear model is considered more parsimonious. We were particularly interested in identifying scenarios where the fit was quadratic with a negative quadratic term. For each scenario, the pseudo R2 conditional value (proportion of variance explained by the fixed and random terms, accounting for individual identity) is calculated to assess the goodness-of-fit of the lme model, on a scale from 0 to 1, using the “r.squared” function, package gabtool. All calculations and coding are done in R. Iteroparous parents face a trade-off between allocating current resources to reproduction versus maximizing survival to produce further offspring. Optimal allocation varies across age, and follows a hump-shaped pattern across diverse taxa, including mammals, birds and invertebrates. This non-linear allocation pattern lacks a general theoretical explanation, potentially because most studies focus on offspring number rather than quality and do not incorporate uncertainty or age-dependence in energy intake or costs. Here, we develop a life history model of maternal allocation in iteroparous animals. We identify the optimal allocation strategy in response to stochasticity when energetic costs, feeding success, energy intake, and environmentally-driven mortality risk are age-dependent. As a case study, we use tsetse, a viviparous insect that produces one offspring per reproductive attempt and relies on an uncertain food supply of vertebrate blood. Diverse scenarios generate a hump-shaped allocation: when energetic costs and energy intake increase with age; and also when energy intake decreases, and energetic costs increase or decrease. Feeding success and mortality risk have little influence on age-dependence in allocation. We conclude that ubiquitous evidence for age-dependence in these influential traits can explain the prevalence of non-linear maternal allocation across diverse taxonomic groups.

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    ZENODO
    Dataset . 2022
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    DRYAD
    Dataset . 2022
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      ZENODO
      Dataset . 2022
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      Dataset . 2022
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    Authors: Villegas-Torres, M (via Mendeley Data);

    This data corresponds to the manuscript titled: Sustainable sugarcane vinasse biorefinement toward biobased chemicals and bioenergy generation

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    Mendeley Data
    Dataset . 2021
    License: CC BY
    Data sources: Datacite
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    Mendeley Data
    Dataset . 2021
    License: CC BY
    Data sources: Datacite
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    B2FIND
    Dataset . 2021
    Data sources: B2FIND
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      Mendeley Data
      Dataset . 2021
      License: CC BY
      Data sources: Datacite
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      Mendeley Data
      Dataset . 2021
      License: CC BY
      Data sources: Datacite
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      B2FIND
      Dataset . 2021
      Data sources: B2FIND
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    Authors: Roth, Jamila; Osborne, Todd; Reynolds, Laura;

    The ecological impacts of multiple stressors are hard to predict but important to understand. When multiple stressors influence foundation species, the effects can cascade throughout the ecosystem. Gulf of Mexico seagrass ecosystems are currently experiencing a suite of novel stressors, including warmer water temperatures and increased herbivory due to tropicalization and conservation efforts. We investigated the impact of warming temperatures and grazing history on plant performance, morphology, and palatability by integrating a mesocosm study using the seagrass Thalassia testudinum with feeding trials using the sea urchin Lytechinus variegatus. Warming temperatures negatively impacted T. testudinum tolerance traits, reducing belowground biomass by 34%, productivity by 74%, shoot density by 10%, and the number of leaves per plant by 24%, and negatively impacted resistance traits through 13% lower toughness of young leaves and a trend for reduced leaf carbon:nitrogen. Lytechinus variegatus individuals preferred to consume plants grown under heated conditions, which supports findings of enhanced palatability. Simulated turtle grazing impacted more plant traits than grazing by other herbivores, potentially diminishing plant resilience to future disturbances through reduced rhizome non-structural carbohydrate concentrations and increasing palatability through reduced fiber content and 23% lower leaf carbon:phosphorus. Simulated turtle, simulated parrotfish, and urchin grazing reduced leaf carbon:nitrogen by 11%, also potentially increasing nutritive value. Interactions between warming temperatures and grazers on plant traits were additive for 16 out of 19 response variables. However, the stressors non-additively impacted the number of leaves per plant, fiber content, and epiphyte load. We suggest that the impacts of grazers on leaf turnover rate and leaf age may vary based on water temperature, potentially driving these interactions. Overall, increased temperatures and grazing pressure will likely reduce seagrass resilience, structure, and biomass, potentially impacting feedback systems and producing negative consequences for seagrass cover, associated species, and ecosystem services.

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    ZENODO
    Dataset . 2023
    License: CC 0
    Data sources: ZENODO
    DRYAD
    Dataset . 2023
    License: CC 0
    Data sources: Datacite
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      ZENODO
      Dataset . 2023
      License: CC 0
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      Dataset . 2023
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    Authors: Shuai ZHANG;

    Climate trends during maize growing period and their impacts on spring maize yield in North China was investigated. This dataset contains: 1) information of stations in cultivation region for spring maize in North China; 2) Trend in temperature and its effect on yield in cultivation region for spring maize in North China; 3) Trend in radiation and its effect on yield in cultivation region for spring maize in North China; 4) Trend in precipitation and its effect on yield in cultivation region for spring maize in North China. Climate trends during maize growing period and their impacts on spring maize yield in North China was investigated. This dataset contains: 1) information of stations in cultivation region for spring maize in North China; 2) Trend in temperature and its effect on yield in cultivation region for spring maize in North China; 3) Trend in radiation and its effect on yield in cultivation region for spring maize in North China; 4) Trend in precipitation and its effect on yield in cultivation region for spring maize in North China.

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    https://dx.doi.org/10.57760/sc...
    Dataset . 2022
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      https://dx.doi.org/10.57760/sc...
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    Authors: Shao, Junjiong; Zhou, Xuhui; van Groenigen, Kees; Zhou, Guiyao; +9 Authors

    Aim: Climate warming and biodiversity loss both alter plant productivity, yet we lack an understanding of how biodiversity regulates the responses of ecosystems to warming. In this study, we examine how plant diversity regulates the responses of grassland productivity to experimental warming using meta-analytic techniques. Location: Global Major taxa studied: Grassland ecosystems Methods: Our meta-analysis is based on warming responses of 40 different plant communities obtained from 20 independent studies on grasslands across five continents. Results: Our results show that plant diversity and its responses to warming were the most important factors regulating the warming effects on plant productivity, among all the factors considered (plant diversity, climate and experimental settings). Specifically, warming increased plant productivity when plant diversity (indicated by effective number of species) in grasslands was lesser than 10, whereas warming decreased plant productivity when plant diversity was greater than 10. Moreover, the structural equation modelling showed that the magnitude of warming enhanced plant productivity by increasing the performance of dominant plant species in grasslands of diversity lesser than 10. The negative effects of warming on productivity in grasslands with plant diversity greater than 10 were partly explained by diversity-induced decline in plant dominance. Main Conclusions: Our findings suggest that the positive or negative effect of warming on grassland productivity depends on how biodiverse a grassland is. This could mainly owe to differences in how warming may affect plant dominance and subsequent shifts in interspecific interactions in grasslands of different plant diversity levels.

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    ZENODO
    Dataset . 2023
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    DRYAD
    Dataset . 2022
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      image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/ ZENODOarrow_drop_down
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      ZENODO
      Dataset . 2023
      License: CC 0
      Data sources: ZENODO
      DRYAD
      Dataset . 2022
      License: CC 0
      Data sources: Datacite
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    Authors: Shuai ZHANG;

    Changes in late rice phenology during 1981–2009 were investigated using observed phenological data from agro-meteorological stations across China. This dataset contains 1) details of late rice agrometeorological experiment stations; 2) mean date of late rice phenology date and trend in phenology date during the period of 1981–2009; 3) trends in length of late rice growing period during the period of 1981-2009. Changes in late rice phenology during 1981–2009 were investigated using observed phenological data from agro-meteorological stations across China. This dataset contains 1) details of late rice agrometeorological experiment stations; 2) mean date of late rice phenology date and trend in phenology date during the period of 1981–2009; 3) trends in length of late rice growing period during the period of 1981-2009.

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    https://dx.doi.org/10.57760/sc...
    Dataset . 2022
    License: CC BY NC
    Data sources: Datacite
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      https://dx.doi.org/10.57760/sc...
      Dataset . 2022
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      Data sources: Datacite
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    Authors: Guindo, Samuel; Dossou-Yovo, Elliott Ronald;

    The data used in this article are related to the rice yield following the use of the RiceAdvice technology recommendation and the rice yield following the recommended level of fertilizer recommendations. The data were collected in 5 sites in Mali. In all sites, rice yield with RiceAdvice was higher than rice yield following the conventional levels of fertilizer. On average, rice yield with RiceAdvice was 0.7 t/ha higher than rice yield with the conventional level of fertilizer recommendations.

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    Harvard Dataverse
    Dataset . 2022
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      Dataset . 2022
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      Data sources: Datacite
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