Grace M. Wilkinson
University of Virginia
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Featured researches published by Grace M. Wilkinson.
Science Advances | 2017
Andrew J. Tanentzap; Brian W. Kielstra; Grace M. Wilkinson; Martin Berggren; Nicola Craig; Paul A. del Giorgio; Jonathan Grey; John M. Gunn; Stuart E. Jones; Jan Karlsson; Christopher T. Solomon; Michael L. Pace
There is widespread evidence that aquatic consumers use terrestrial resources depending on the features of surrounding catchments. Widespread evidence that organic matter exported from terrestrial into aquatic ecosystems supports recipient food webs remains controversial. A pressing question is not only whether high terrestrial support is possible but also what the general conditions are under which it arises. We assemble the largest data set, to date, of the isotopic composition (δ2H, δ13C, and δ15N) of lake zooplankton and the resources at the base of their associated food webs. In total, our data set spans 559 observations across 147 lakes from the boreal to subtropics. By predicting terrestrial resource support from within-lake and catchment-level characteristics, we found that half of all consumer observations that is, the median were composed of at least 42% terrestrially derived material. In general, terrestrial support of zooplankton was greatest in lakes with large physical and hydrological connections to catchments that were rich in aboveground and belowground organic matter. However, some consumers responded less strongly to terrestrial resources where within-lake production was elevated. Our study shows that multiple mechanisms drive widespread cross-ecosystem support of aquatic consumers across Northern Hemisphere lakes and suggests that changes in terrestrial landscapes will influence ecosystem processes well beyond their boundaries.
Proceedings of the National Academy of Sciences of the United States of America | 2017
Michael L. Pace; Ryan D. Batt; Cal D. Buelo; Stephen R. Carpenter; Jonathan J. Cole; Jason T. Kurtzweil; Grace M. Wilkinson
Significance Blooms of cyanobacteria in lakes and reservoirs cause fish kills and pose toxicity risk for humans, livestock, and wildlife. Theory suggests that blooms may be anticipated in advance by calculating resilience indicators using high-frequency observations of pigments in lake water. However, it is not known whether management can prevent blooms once indicators are detected. We measured these indicators while gradually enriching a lake until a bloom was triggered. When indicators passed a preset threshold, nutrient input was stopped. This action reversed the bloom, showing that monitoring of resilience indicators followed by prompt action when limits are exceeded can be useful in management. However, in practice, the risk of blooms may best be prevented by reducing inputs of nutrients. Directional change in environmental drivers sometimes triggers regime shifts in ecosystems. Theory and experiments suggest that regime shifts can be detected in advance, and perhaps averted, by monitoring resilience indicators such as variance and autocorrelation of key ecosystem variables. However, it is uncertain whether management action prompted by a change in resilience indicators can prevent an impending regime shift. We caused a cyanobacterial bloom by gradually enriching an experimental lake while monitoring an unenriched reference lake and a continuously enriched reference lake. When resilience indicators exceeded preset boundaries, nutrient enrichment was stopped in the experimental lake. Concentrations of algal pigments, dissolved oxygen saturation, and pH rapidly declined following cessation of nutrient enrichment and became similar to the unenriched lake, whereas a large bloom occurred in the continuously enriched lake. This outcome suggests that resilience indicators may be useful in management to prevent unwanted regime shifts, at least in some situations. Nonetheless, a safer approach to ecosystem management would build and maintain the resilience of desirable ecosystem conditions, for example, by preventing excessive nutrient input to lakes and reservoirs.
Inland Waters | 2014
Carol Yang; Grace M. Wilkinson; Jonathan J. Cole; Stephen A. Macko; Michael L. Pace
Abstract Studies designed to assess the resources supporting aquatic consumers using stable isotope analysis require measurements of the potential end members (basal resources). While some basal resources are easily measured, it is often difficult to physically separate phytoplankton (one potential end member) from other components in seston. Further, terrestrial materials entering aquatic ecosystems undergo diagenetic change, potentially altering isotope composition and making it difficult to assign end member values. We tested techniques for determining the isotopic hydrogen (δ2H), carbon (δ13C), and nitrogen (δ15N) values of terrestrial and phytoplankton end members in seston. Long term in situ leaf decomposition experiments were performed. No appreciable change was found in the isotope values of degraded material (mean change 3.6‰ for δ2H, 0.0‰ for δ13C, and −0.1‰ for δ15N). We conclude that the isotope values of terrestrial plant material can be used to assign end members for terrestrial detritus. Using samples collected from 10 lakes with phytoplankton-dominated seston, we compared 3 published methods for estimating the δ13C and δ15N of phytoplankton. One method, which corrected bulk particulate organic matter (POM) isotope values based on a δ2H mixing model, accurately predicted measured phytoplankton δ13C. Another method, which used a C:N mixing model to correct bulk POM, also performed well. A new method, proposed here, modified seston isotope values using the difference in C:N of phytoplankton and terrestrial material in a δ2H mixing model and correctly predicted measured phytoplankton δ15N. We recommend estimating phytoplankton δ13C and δ15N by correcting bulk POM using a δ2H mixing model, with the C:N modification proposed here for δ15N.
Geophysical Research Letters | 2016
Grace M. Wilkinson; Cal D. Buelo; Jonathan J. Cole; Michael L. Pace
It is well established that lakes are typically sources of CO2 to the atmosphere. However, it remains unclear what portion of CO2 efflux is from endogenously processed organic carbon or from exogenously produced CO2 transported into lakes. We estimated high-frequency CO2 and O2 efflux from three north temperate lakes in summer to determine the proportion of the total CO2 efflux that was exogenously produced. Two of the lakes were amended with nutrients to experimentally enhance endogenous CO2 uptake. In the unfertilized lake, 50% of CO2 efflux was from exogenous sources and hydrology had a large influence on efflux. In the fertilized lakes, endogenous CO2 efflux was negative (into the lake) yet exogenous CO2 made the lakes net sources of CO2 to the atmosphere. Shifts in hydrologic regimes and nutrient loading have the potential to change whether small lakes act primarily as reactors or vents in the watershed.
Ecosphere | 2015
Ryan D. Batt; Stephen R. Carpenter; Jonathan J. Cole; Michael L. Pace; Robert A. Johnson; Jason T. Kurtzweil; Grace M. Wilkinson
Theory suggests that alternative resources may begin to support a food web when highly used resources become less available relative to alternatives. To test the potential for alternative resources to support consumers, we experimentally darkened a lake whose consumers had relied heavily on algal resources (phytoplankton and benthic algae). We estimated the support consumers received from resources before and after darkening using a Bayesian mixing model and stables isotopes of carbon, nitrogen, and hydrogen. Between a prior year and the darkened year, phytoplankton biomass diminished by 60%, and surface dissolved oxygen saturation, pCO2, and net ecosystem production indicated a shift from autotrophy to heterotrophy. Although a specialist copepod maintained a high reliance on phytoplankton after darkening, a generalist zooplankton predator (Chaoborus spp.) derived more support from terrestrial sources. Fishes received less support from benthic algae after darkening, and received greater support from float...
Hydrobiologia | 2015
Kyle A. Emery; Grace M. Wilkinson; Flannery G. Ballard; Michael L. Pace
Aquatic food webs are supported by primary production from within the system (autochthony) as well as organic matter produced outside of and transported into the system (allochthony). Zooplankton use allochthonous resources, especially in systems with high terrestrial loading and moderate to low internal primary production. We hypothesized that due to high terrestrial loads and remnant submerged terrestrial material, allochthonous resource use by zooplankton would be significant in all reservoirs and would decline along an increasing reservoir age gradient. Using hydrogen stable isotopes and a Bayesian mixing model, we estimated the contribution of allochthonous sources to organic matter pools and crustaceous zooplankton biomass for ten reservoirs. Dissolved organic matter (DOM) in all systems was dominated by allochthonous sources (posterior distribution median >92% allochthonous), while particulate organic matter (POM) composition varied (2–68% allochthonous) and had a lower allochthonous fraction in older reservoirs. There was no relationship between zooplankton allochthony and reservoir age. Crustaceous zooplankton allochthony varied among systems from 26 to 94%, and Chaoborus allochthony, measured in four reservoirs, was similarly variable (33–94%). Consumer allochthony was higher than POM allochthony in some reservoirs, potentially due to terrestrial DOM pathways being important and/or algal resources being inedible (e.g., cyanobacteria). As with many lakes, in the reservoirs we studied, allochthonous inputs account for a significant fraction of the organic matter of basal consumers.
Scientific Reports | 2018
Grace M. Wilkinson; Alice F. Besterman; Cal D. Buelo; Jessica A. Gephart; Michael L. Pace
Organic carbon accumulation in the sediments of inland aquatic and coastal ecosystems is an important process in the global carbon budget that is subject to intense human modification. To date, research has focused on quantifying accumulation rates in individual or groups of aquatic ecosystems to quantify the aquatic carbon sinks. However, there hasn’t been a synthesis of rates across aquatic ecosystem to address the variability in rates within and among ecosystems types. Doing so would identify gaps in our understanding of accumulation rates and potentially reveal carbon sinks vulnerable to change. We synthesized accumulation rates from the literature, compiling 464 rate measurements from 103 studies of carbon accumulated in the modern period (ca. 200 years). Accumulation rates from the literature spanned four orders of magnitude varying substantially within and among ecosystem categories, with mean estimates for ecosystem categories ranging from 15.6 to 73.2 g C m−2 y−1 within ecosystem categories. With the exception of lakes, mean accumulation rates were poorly constrained due to high variability and paucity of data. Despite the high uncertainty, the estimates of modern accumulation rate compiled here are an important step for constructing carbon budgets and predicting future change.
Archive | 2016
Kyle A. Emery; Jessica A. Gephart; Grace M. Wilkinson; Alice F. Besterman; Michael L. Pace
The living organisms of an ecosystem interact within food webs, transferring energy and nutrients through trophic (i.e., feeding) linkages. Human impacts on the environment may lead to disturbances that alter food webs, which may in turn affect important ecosystem services such as the availability of clean water. Anthropogenic changes at one trophic level of a food web may cause a trophic cascade, affecting all other levels of the food web. Lakes exhibit these trophic cascades which may be caused by human disturbance. The goal of this learning activity is for students to discover how anthropogenic perturbations can induce trophic cascades in a lake food web. Using a spreadsheet model, students explore how overfishing, stocking fish, fertilizer runoff, and invasive species impact lake food webs. After completing this activity students should be able to (1) describe a food web and trophic cascades; (2) distinguish between predatory and resource controls on food webs; (3) state hypotheses and interpret model output; (4) evaluate management strategies that sustain ecosystem services; and (5) predict the causes of trophic cascades in diverse ecosystems and the consequences for ecosystem services and human health.
Global Biogeochemical Cycles | 2013
Grace M. Wilkinson; Michael L. Pace; Jonathan J. Cole
Freshwater Biology | 2013
Grace M. Wilkinson; Stephen R. Carpenter; Jonathan J. Cole; Michael L. Pace; Carol Yang