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1. Field experiments have enhanced our understanding of drought impacts on terrestrial ecosystems—But where do we go from here?

   https://doi.org/10.1111/1365-2435.14460  

   Knapp, Alan K. ; Condon, Kathleen V. ; Folks, Christine C. ; Sturchio, Matthew A. ; Griffin‐Nolan, Robert J. ; Kannenberg, Steven A. ; Gill, Amy S. ; Hajek, Olivia L. ; Siggers, J. Alexander ; Smith, Melinda D. ( October 2023 , Functional Ecology)

   We review results from field experiments that simulate drought, an ecologically impactful global change threat that is predicted to increase in magnitude, extent, duration and frequency. Our goal is to address, from primarily an ecosystem perspective, the questions ‘What have we learned from drought experiments?’ and ‘Where do we go from here?’.

   Drought experiments are among the most numerous climate change manipulations and have been deployed across a wide range of biomes, although most are conducted in short‐statured, water‐limited ecosystems. Collectively, these experiments have enabled ecologists to quantify the negative responses to drought that occur for most aspects of ecosystem structure and function. Multiple meta‐analyses of responses have also enabled comparisons of relative effect sizes of drought across hundreds of sites, particularly for carbon cycle metrics. Overall, drought experiments have provided strong evidence that ecosystem sensitivity to drought increases with aridity, but that plant traits associated with aridity are not necessarily predictive of drought resistance. There is also intriguing evidence that as drought magnitude or duration increases to extreme levels, plant strategies may shift from drought tolerance to drought escape/avoidance.

   We highlight three areas where more drought experiments are needed to advance our understanding. First, because drought is intensifying in multiple ways, experiments are needed that address alterations in drought magnitude versus duration, timing and/or frequency (individually and interactively). Second, drivers of drought may be shifting—from precipitation deficits to rising atmospheric demand for water—and disentangling how ecosystems respond to changes in hydrological ‘supply versus demand’ is critical for understanding drought impacts in the future. Finally, more attention should be focussed on post‐drought recovery periods since legacies of drought can affect ecosystem functioning much longer than the drought itself.

   We conclude with a call for a fundamental shift in the focus of drought experiments from those designed primarily as ‘response experiments’, quantifying the magnitude of change in ecosystem structure and function, to more ‘mechanistic experiments’—those that explicitly manipulate ecological processes or attributes thought to underpin drought responses.

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2. Trade‐offs in rooting strategy dimensions along an edaphic gradient in a grassland ecosystem

   https://doi.org/10.1111/1365-2435.14514  

   Yang, Yuguo ; Russo, Sabrina E. ( February 2024 , Functional Ecology)

   Roots are essential to the diversity and functioning of plant communities, but trade‐offs in rooting strategies are still poorly understood.

   We evaluated existing frameworks of rooting strategy trade‐offs and tested their underlying assumptions, guided by the hypothesis that community‐level rooting strategies are best described by a combination of variation in organ‐level traits, plant‐level root:shoot allocation and symbiosis‐level mycorrhizal dependency. We tested this hypothesis using data on plant community structure, above‐ and below‐ground biomass, eight root traits including mycorrhizal colonisation and soil properties from an edaphic gradient driven by elevation and water availability in sandhills prairie, Nebraska, USA.

   We found multidimensional trade‐offs in rooting strategies represented by a two‐way productivity‐durability trade‐off axis (captured by root length density and root dry matter content) and a three‐way resource acquisition trade‐off between specific root length, root:shoot mass ratio and mycorrhizal dependence. Variation in rooting strategies was driven to similar extents by interspecific differences and intraspecific responses to soil properties.

   Organ‐level traits alone were insufficient to capture community‐level trade‐offs in rooting strategies across the edaphic gradient. Instead, trait variation encompassing organ, plant and symbiosis levels revealed that consideration of whole‐plant phenotypic integration is essential to defining multidimensional trade‐offs shaping the functional variation of root systems.

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3. Regulation of reproductive processes with dynamic energy budgets

   https://doi.org/10.1111/1365-2435.13298  

   Muller, Erik B. ; Lika, Konstadia ; Nisbet, Roger M. ; Schultz, Irvin R. ; Casas, Jérôme ; Gergs, André ; Murphy, Cheryl A. ; Nacci, Diane ; Watanabe, Karen H. ; Smallegange, ed., Isabel ( February 2019 , Functional Ecology)

   Linking organismal‐level processes to underlying suborganismal mechanisms at the molecular, cellular and organ level constitutes a major challenge for predictive ecological risk assessments. This challenge can be addressed with the simple bioenergetic models in the family of dynamic energy budget (DEB), which consist of a small number of state equations quantifying universal processes, such as feeding, maintenance, development, reproduction and growth.

   Motivated by the need for process‐based models to evaluate the impact of endocrine disruptors on ecologically relevant endpoints, this paper develops and evaluates two general modelling modules describing demand‐driven feedback mechanisms within the DEB modelling framework exerted by gonads on the allocation of resources to production of reproductive matter.

   These modules describe iteroparous, semelparous and batch‐mode reproductive strategies. The modules have a generic form with both positive and negative feedback components; species‐ and sex‐specific attributes of endocrine regulation can be added without changing the core of the modules.

   We demonstrate that these modules successfully describe time‐resolved measurements of wet weight of body, ovaries and liver, egg diameter and plasma content of vitellogenin and oestradiol in rainbow trout (Oncorynchus mykiss) by fitting these models to published and new data, which require the estimation of less than two parameters per data type.

   We illustrate the general applicability of the concept of demand‐driven allocation of resources to reproduction by evaluating one of the modules with data on growth and seed production of an annual plant, the common bean (Phaseolisvulgaris).

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4. Ecological strategies begin at germination: Traits, plasticity and survival in the first 4 days of plant life

   https://doi.org/10.1111/1365-2435.13543  

   Larson, Julie E. ; Anacker, Brian L. ; Wanous, Sara ; Funk, Jennifer L. ; Baltzer, ed., Jennifer ( March 2020 , Functional Ecology)

   We commonly use trait variation to characterize plant function within and among species and understand how vegetation responds to the environment. Seedling emergence is an especially vulnerable window affecting population and community dynamics, yet trait‐based frameworks often bypass this earliest stage of plant life. Here we assess whether traits vary in ecologically meaningful ways when seedlings are just days old. How do shared evolutionary history and environmental conditions shape trait expression, and can traits explain which seedlings endure drought?

   We measured seedling traits in the first 4 days of life for 16 annual plant species under two water treatments, exploring trait trade‐offs, species‐level plasticity and the ability of traits to predict duration of survival under drought.

   Nearly half of traits showed the imprint of evolutionary history (i.e. significant phylogenetic signal), often reflecting differences between grasses and forbs, two groups separated by a deep evolutionary split. Water availability altered trait expression in most cases, though species‐level plastic responses also reflected evolutionary history.

   On average, new seedlings exhibited substantial trait variation structured as multiple trade‐offs like those found in mature plants. Some species invested in thick roots and shoots, whereas others invested in more efficient tissues. Separately, some invested in tougher roots and others in deeper roots. We also observed trade‐offs related to growth rates (fast or slow) and biomass allocation (above‐ or below‐ground). Drought survival time was correlated most strongly with seed mass, root construction and allocation traits, and phylogeny (grasses vs. forbs).

   Synthesis.Our results show that seed and seedling trait variation among annual species is substantial, and that a few attributes could capture major dimensions of ecological strategies during emergence. With seedling survival times ranging twofold among annuals (from 7.5 to 14.5 days), these strategies could mitigate recruitment responses to more frequent or longer dry spells. Multivariate trait and plasticity strategies should be further explored in studies designed to assess trait‐fitness linkages during recruitment.

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5. Drought response in herbaceous plants: A test of the integrated framework of plant form and function

   https://doi.org/10.1111/1365-2435.14495  

   Funk, Jennifer L. ; Larson, Julie E. ; Blair, Megan D. ; Nguyen, Monica A. ; Rivera, Ben J. ( January 2024 , Functional Ecology)

   Multidimensional trait frameworks are increasingly used to understand plant strategies for growth and survival. However, it is unclear if frameworks developed at a global level can be applied in local communities and how well these frameworks—based largely on plant morphological traits—align with plant physiology and response to stress.

   We tested the ability of an integrated framework of plant form and function to characterise seedling trait variation and drought response among 22 grasses and forbs common in a semi‐arid grassland. We measured above‐ground and below‐ground traits, and survival to explore how drought response is linked to three trait dimensions (resource conservation, microbial collaboration, and plant size) associated with the framework as well as non‐morphological dimensions (e.g. physiological traits) that are under‐represented in global trait frameworks.

   We found support for three globally‐recognised axes representing trade‐offs in strategies associated with tissue investment (leaf nitrogen, leaf mass per area, root tissue density), below‐ground resource uptake (root diameter, specific root length), and size (shoot mass). However, in contrast to global patterns, above‐ground and below‐ground resource conservation gradients were oppositely aligned: root tissue density was positively correlated with leaf N rather than leaf mass per area. This likely reflects different investment strategies of annual and perennial herbaceous species, as fast‐growing annual species invested in lower density roots and less nitrogen‐rich leaves to maximise plant‐level carbon assimilation. Species with longer drought survival minimised water loss through small above‐ground size and low leaf‐level transpiration rates, and drought survival was best predicted by a principal component axis representing plant size.

   Contrary to our expectations, drought survival in seedlings did not align with the conservation or collaboration axes suggesting that seedlings with different functional strategies can achieve similar drought survival, as long as they minimise water loss. Our results also show that within local communities, expected trait relationships could be decoupled as some plant groups achieve similar performance through different trait combinations. The effectiveness of species mean trait values in predicting drought response highlights the value of trait‐based methods as a versatile tool for understanding ecological processes locally across various ecosystems.

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