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  1. Eddy covariance data are invaluable for determining ecosystem water use strategies under soil water stress. However, existing stress inference methods require numerous subjective data processing and model specification assumptions whose effect on the inferred soil water stress signal is rarely quantified. These uncertainties may confound the stress inference and the generalization of ecosystem water use strategies across multiple sites and studies. In this research, we quantify the sensitivity of soil water stress signals inferred from eddy covariance data to the prevailing data and modeling assumptions (i.e., their robustness) to compile a comprehensive list of sites with robust soil water stress signals and assess the performance of current stress inference methods. To accomplish this, we identify the most prevalent assumptions from the literature and perform a digital factorial experiment to extract probability distributions of plausible soil water stress signals and model performance at 151 FLUXNET2015 and AmeriFlux-FLUXNET sites. We develop a new framework that summarizes these probability distributions to classify and rank the robustness of each site’s soil water stress signal, which we display with a user-friendly heat map. We estimate that only 5%–36% of sites exhibit a robust soil water stress signal due to deficient model performance and poorly constrained ecosystem water use parameters. We also find that the lack of robustness is site-specific, which undermines grouping stress signals by broad ecosystem categories or comparing results across studies with differing assumptions. Lastly, existing stress inference methods appear better suited for eddy covariance sites with grass/annual vegetation. Our findings call for more careful and consistent inference of ecosystem water stress from eddy covariance data. 
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    Free, publicly-accessible full text available December 1, 2024
  2. A previous study demonstrated that atmospheric rivers (ARs) generate substantial air-sea fluxes in the northeast Pacific. Since the southeast Indian Ocean is one of the active regions of ARs, similar air-sea fluxes could be produced. However, the spatial pattern of sea surface temperature (SST) in the southeast Indian Ocean, especially along the west coast of Australia, is different from that in the northeast Pacific because of the poleward flowing Leeuwin Current, which may cause different air-sea fluxes. This study investigates AR-associated air-sea fluxes in the southeast Indian Ocean and their relation with SST variability. The large-scale spatial pattern of latent heat flux (evaporation) associated with ARs in the southeast Indian Ocean is similar to that in the northeast Pacific. A significant difference is however found near the coastal area where relatively warm SSTs are maintained in all seasons. While AR-induced latent heat flux is close to zero around the west coast of North America where the equatorward flowing coastal current and upwelling generate relatively cold SSTs, a significant latent heat flux induced by ARs is evident along the west coast of Australia due to the relatively warm surface waters. Temporal variations of coastal air-sea fluxes associated with landfalling ARs are investigated based on the composite analysis. While the moisture advection reduces the latent heat during landfalling, the reduction of air humidity with strong winds enhances large evaporative cooling (latent heat flux) after a few days of the landfalling. A significant SST cooling along the coast is found due to the enhanced latent heat flux.

     
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    Free, publicly-accessible full text available July 12, 2024
  3. Abstract

    Observations show vulnerability segmentation between stems and leaves is highly variable within and between environments. While a number of species exhibit conventional vulnerability segmentation (stem leaf ), others exhibit no vulnerability segmentation and others reverse vulnerability segmentation (stem leaf ). We developed a hydraulic model to test hypotheses about vulnerability segmentation and how it interacts with other traits to impact plant conductance. We do this using a series of experiments across a broad parameter space and with a case study of two species with contrasting vulnerability segmentation patterns:Quercus douglasiiandPopulus trichocarpa. We found that while conventional vulnerability segmentation helps to preserve conductance in stem tissues, reverse vulnerability segmentation can better maintain conductance across the combined stem‐leaf hydraulic pathway, particularly when plants have more vulnerable s and have hydraulic segmentation with greater resistance in the leaves. These findings show that the impacts of vulnerability segmentation are dependent upon other plant traits, notably hydraulic segmentation, a finding that could assist in the interpretation of variable observations of vulnerability segmentation. Further study is needed to examine how vulnerability segmentation impacts transpiration rates and recovery from water stress.

     
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    Free, publicly-accessible full text available September 1, 2024
  4. Abstract

    Stomata have recently been theorized to have evolved strategies that maximize turgor-driven growth over plants’ lifetimes, finding support through steady-state solutions in which gas exchange, carbohydrate storage and growth have all reached equilibrium. However, plants do not operate near steady state as plant responses and environmental forcings vary diurnally and seasonally. It remains unclear how gas exchange, carbohydrate storage and growth should be dynamically coordinated for stomata to maximize growth. We simulated the gas exchange, carbohydrate storage and growth that dynamically maximize growth diurnally and annually. Additionally, we test whether the growth-optimization hypothesis explains nocturnal stomatal opening, particularly through diel changes in temperature, carbohydrate storage and demand. Year-long dynamic simulations captured realistic diurnal and seasonal patterns in gas exchange as well as realistic seasonal patterns in carbohydrate storage and growth, improving upon unrealistic carbohydrate responses in steady-state simulations. Diurnal patterns of carbohydrate storage and growth in day-long simulations were hindered by faulty modelling assumptions of cyclic carbohydrate storage over an individual day and synchronization of the expansive and hardening phases of growth, respectively. The growth-optimization hypothesis cannot currently explain nocturnal stomatal opening unless employing corrective ‘fitness factors’ or reframing the theory in a probabilistic manner, in which stomata adopt an inaccurate statistical ‘memory’ of night-time temperature. The growth-optimization hypothesis suggests that diurnal and seasonal patterns of stomatal conductance are driven by a dynamic carbon-use strategy that seeks to maintain homeostasis of carbohydrate reserves.

     
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  5. Abstract

    Green infrastructure (GI) practices improve stormwater quality and reduce urban flooding, but as urban hydrology is highly controlled by its associated gray infrastructure (e.g., stormwater pipe network), GI's watershed‐scale performance depends on its siting within its associated watershed. Although many stormwater practitioners have begun considering GI's spatial configuration within a larger watershed, few approaches allow for flexible scenario exploration, which can untangle GI's interaction with gray infrastructure network and assess its effects on watershed hydrology. To address the gap in integrated gray‐green infrastructure planning, we used an exploratory model to examine gray‐green infrastructure performance using synthetic stormwater networks with varying degrees of flow path meandering, informed by analysis on stormwater networks from the Minneapolis‐St. Paul Metropolitan Area, MN, USA. Superimposed with different coverage and placements of GI (e.g., bioretention cells), these gray‐green stormwater networks are then subjected to different rainfall intensities within Environmental Protection Agency's Storm Water Management Model to simulate their hydrological benefits (e.g., peak flow reduction, flood reduction). Although only limited choices of green and gray infrastructure were explored, the results show that the gray infrastructure's spatial configuration can introduce tradeoffs between increased peak flow and increased flooding, and further interacts with GI coverage and placement to reduce peak flow and flooding at low rainfall intensity. However, as rainfall intensifies, GI ceases to reduce peak flow. For integrated gray‐green infrastructure planning, our results suggest that physical constraints of the stormwater networks and the range of rainfall intensities must be considered when implementing GI.

     
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  6. Abstract. Elevated atmospheric CO2 concentration is expectedto increase leaf CO2 assimilation rates, thus promoting plant growthand increasing leaf area. It also decreases stomatal conductance, allowingwater savings, which have been hypothesized to drive large-scale greening,in particular in arid and semiarid climates. However, the increase in leafarea could reduce the benefits of elevated CO2 concentration through soilwater depletion. The net effect of elevated CO2 on leaf- andcanopy-level gas exchange remains uncertain. To address this question, wecompare the outcomes of a heuristic model based on the Partitioning ofEquilibrium Transpiration and Assimilation (PETA) hypothesis and three modelvariants based on stomatal optimization theory. Predicted relative changes in leaf-and canopy-level gas exchange rates are used as a metric of plant responsesto changes in atmospheric CO2 concentration. Both model approaches predictreductions in leaf-level transpiration rate due to decreased stomatalconductance under elevated CO2, but negligible (PETA) or no(optimization) changes in canopy-level transpiration due to the compensatoryeffect of increased leaf area. Leaf- and canopy-level CO2 assimilationis predicted to increase, with an amplification of the CO2fertilization effect at the canopy level due to the enhanced leaf area. Theexpected increase in vapour pressure deficit (VPD) under warmer conditions isgenerally predicted to decrease the sensitivity of gas exchange toatmospheric CO2 concentration in both models. The consistentpredictions by different models that canopy-level transpiration varieslittle under elevated CO2 due to combined stomatal conductancereduction and leaf area increase highlight the coordination ofphysiological and morphological characteristics in vegetation to maximizeresource use (here water) under altered climatic conditions. 
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  7. Abstract. Plant transpiration downregulation in the presence of soil water stress is a critical mechanism for predicting global water, carbon, and energy cycles. Currently, many terrestrial biosphere models (TBMs) represent this mechanism with an empirical correction function (β) of soil moisture – a convenient approach that can produce large prediction uncertainties. To reduce this uncertainty, TBMs have increasingly incorporated physically based plant hydraulic models (PHMs). However, PHMs introduce additional parameter uncertainty and computational demands. Therefore, understanding why and when PHM and β predictions diverge would usefully inform model selection within TBMs. Here, we use a minimalist PHM to demonstrate that coupling the effects of soil water stress and atmospheric moisture demand leads to a spectrum of transpiration responses controlled by soil–plant hydraulic transport (conductance). Within this transport-limitation spectrum, β emerges as an end-member scenario of PHMs with infinite conductance, completely decoupling the effects of soil water stress and atmospheric moisture demand on transpiration. As a result, PHM and β transpiration predictions diverge most for soil–plant systems with low hydraulic conductance (transport-limited) that experience high variation in atmospheric moisture demand and have moderate soil moisture supply for plants. We test these minimalist model results by using a land surface model at an AmeriFlux site. At this transport-limited site, a PHM downregulation scheme outperforms the β scheme due to its sensitivity to variations in atmospheric moisture demand. Based on this observation, we develop a new “dynamic β” that varies with atmospheric moisture demand – an approach that overcomes existing biases within β schemes and has potential to simplify existing PHM parameterization and implementation. 
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