We studied a guild of desert winter annual plants that differ in long-term variation in per capita reproductive success (lb, the product of per capita survival from germination to reproduction, l, times per capita reproduction of survivors, b) to relate individual function to population and community dynamics. We hypothesized that variation in lb should be related to species' positions along a trade-off between relative growth rate (RGR) and photosynthetic water-use efficiency (WUE) because lb is a species-specific function of growing-season precipitation. We found that demographically variable species have greater RGR and greater leaf carbon isotope discrimination (Delta, a proxy inversely related to WUE). We examined leaf nitrogen and photosynthetic characteristics and found that, in this system, variation in Delta is a function of photosynthetic demand rather than stomatal regulation of water loss. The physiological characteristics that result in low Delta in some species may confer greater photosynthetic performance during the reliably moist but low temperature periods that immediately follow winter rainfall in the Sonoran Desert or alternatively during cool periods of the day or early growing season. Conversely, while species with high Delta and high RGR exhibit low leaf N, they have high biomass allocation to canopy leaf area display. Such trait associations may allow for greater performance during the infrequent conditions where high soil moisture persists into warmer conditions, resulting in high demographic variance. Alternatively, high variance could arise from specialization to warm periods of the day or season. Population dynamic buffering via stress tolerance (low RGR and Delta) correlates negatively with buffering via seed banks, as predicted by bet-hedging theory. By merging analyses of population dynamics with functional trait relationships, we develop a deeper understanding of the physiological, ecological, and evolutionary mechanisms involved in population and community dynamics.
Summary• Night-time stomatal conductance (g night ) occurs in many ecosystems, but the g night response to environmental drivers is relatively unknown, especially in deserts.• Here, we conducted a Bayesian analysis of stomatal conductance (g) (N = 5013) from 16 species in the Sonoran, Chihuahuan, Mojave and Great Basin Deserts (North America). We partitioned daytime g (g day ) and g night responses by describing g as a mixture of two extreme (dark vs high light) behaviors.• Significant g night was observed across 15 species, and the g night and g day behavior differed according to species, functional type and desert. The transition between extreme behaviors was determined by light environment, with the transition behavior differing between functional types and deserts. Sonoran and Chihuahuan C 4 grasses were more sensitive to vapor pressure difference (D) at night and soil water potential (W soil ) during the day, Great Basin C 3 shrubs were highly sensitive to D and W soil during the day, and Mojave C 3 shrubs were equally sensitive to D and W soil during the day and night.• Species were split between the exhibition of isohydric or anisohydric behavior during the day. Three species switched from anisohydric to isohydric behavior at night. Such behavior, combined with differential D, W soil and light responses, suggests that different mechanisms underlie g day and g night regulation.
Belowground processes and associated plant-microbial interactions play a critical role in how ecosystems respond to environmental change. However, the mechanisms and factors controlling processes such as soil carbon turnover can be difficult to quantify due to methodological or logistical constraints. Soil incubation experiments have the potential to greatly improve our understanding of belowground carbon dynamics, but relating results from laboratorybased incubations to processes measured in the field is challenging. This study has two goals: (1
While there were effects of timing of defoliation and differences between species, the nature of these effects did not precisely fit our predictions. Our results suggest that differences in the length and flexibility of the life cycles of the two species allowed for unexpected variation in responses. For example, because flower production continued after the last treatment in S. vesicaria, responses were not constrained to reductions in individual seed mass.
Ecohydrological connectivity is a system level property that results from the linkages in the networks of water transport through ecosystems, by which feedbacks and other emergent system behaviours may be generated. We created a system dynamics model that represents primary ecohydrological networks to examine how connectivity between ecosystem components impacts ecosystem processes. Here, we focused on the savanna ecosystems, although the analyses may be expanded to other ecosystem types in the future. To create the model, a set of differential equations representing ecohydrological processes was programmed into the dynamic solver Vensim. Stocks of water storage (e.g. atmospheric and soil moisture) were linked by flows [e.g. precipitation and evapotranspiration (ET)] that were in turn dynamically controlled by the amount of water stored. Precipitation was forced stochastically, and soil moisture and potential ET controlled actual ET. The model produced extended, probabilistic time series of stocks and flows, including precipitation, soil moisture, runoff, transpiration, and groundwater recharge. It was used to describe the behaviour of several previously studied savanna ecosystems in North America and Africa. The model successfully reproduced seasonal patterns of soil moisture dynamics and ET at the California site. It also demonstrated more complex, system level behaviours, such as multiyear persistence of drought and synergistic or antagonistic responses to disconnection of system components. Future improvements to the model will focus on capturing other important aspects of long-term system behaviour, such as changes in physiology or phenology, and spatial heterogeneity, such as the patchwork nature of savannas. Figure 6. Comparison of (a) volumetric water content and (b) ET results from initial testing to data from the Arizona riparian shrubland. In this test case, the model was driven by the actual precipitation data, rather than a random time series, to demonstrate its validity. The model was calibrated using the ] Measured ET [mm d -1 ]
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