Peter Hawthorne
University of Minnesota
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Publication
Featured researches published by Peter Hawthorne.
Science | 2008
Joseph Fargione; Jason Hill; David Tilman; Stephen Polasky; Peter Hawthorne
Increasing energy use, climate change, and carbon dioxide (CO2) emissions from fossil fuels make switching to low-carbon fuels a high priority. Biofuels are a potential low-carbon energy source, but whether biofuels offer carbon savings depends on how they are produced. Converting rainforests, peatlands, savannas, or grasslands to produce food crop–based biofuels in Brazil, Southeast Asia, and the United States creates a “biofuel carbon debt” by releasing 17 to 420 times more CO2 than the annual greenhouse gas (GHG) reductions that these biofuels would provide by displacing fossil fuels. In contrast, biofuels made from waste biomass or from biomass grown on degraded and abandoned agricultural lands planted with perennials incur little or no carbon debt and can offer immediate and sustained GHG advantages.
PLOS ONE | 2010
Erik Nelson; Heather A. Sander; Peter Hawthorne; Marc Conte; Driss Ennaanay; Stacie Wolny; Steven M. Manson; Stephen Polasky
Background As the global human population grows and its consumption patterns change, additional land will be needed for living space and agricultural production. A critical question facing global society is how to meet growing human demands for living space, food, fuel, and other materials while sustaining ecosystem services and biodiversity [1]. Methodology/Principal Findings We spatially allocate two scenarios of 2000 to 2015 global areal change in urban land and cropland at the grid cell-level and measure the impact of this change on the provision of ecosystem services and biodiversity. The models and techniques used to spatially allocate land-use/land-cover (LULC) change and evaluate its impact on ecosystems are relatively simple and transparent [2]. The difference in the magnitude and pattern of cropland expansion across the two scenarios engenders different tradeoffs among crop production, provision of species habitat, and other important ecosystem services such as biomass carbon storage. For example, in one scenario, 5.2 grams of carbon stored in biomass is released for every additional calorie of crop produced across the globe; under the other scenario this tradeoff rate is 13.7. By comparing scenarios and their impacts we can begin to identify the global pattern of cropland and irrigation development that is significant enough to meet future food needs but has less of an impact on ecosystem service and habitat provision. Conclusions/Significance Urban area and croplands will expand in the future to meet human needs for living space, livelihoods, and food. In order to jointly provide desired levels of urban land, food production, and ecosystem service and species habitat provision the global society will have to become much more strategic in its allocation of intensively managed land uses. Here we illustrate a method for quickly and transparently evaluating the performance of potential global futures.
Ecology Letters | 2013
Forest Isbell; David Tilman; Stephen Polasky; Seth Binder; Peter Hawthorne
Although nutrient enrichment frequently decreases biodiversity, it remains unclear whether such biodiversity losses are readily reversible, or are critical transitions between alternative low- and high-diversity stable states that could be difficult to reverse. Our 30-year grassland experiment shows that plant diversity decreased well below control levels after 10 years of chronic high rates (95-270 kg N ha(-1) year(-1)) of nitrogen addition, and did not recover to control levels 20 years after nitrogen addition ceased. Furthermore, we found a hysteretic response of plant diversity to increases and subsequent decreases in soil nitrate concentrations. Our results suggest that chronic nutrient enrichment created an alternative low-diversity state that persisted despite decreases in soil nitrate after cessation of nitrogen addition, and despite supply of propagules from nearby high-diversity plots. Thus, the regime shifts between alternative stable states that have been reported for some nutrient-enriched aquatic ecosystems may also occur in grasslands.
Journal of Animal Ecology | 2008
Meggan E. Craft; Peter Hawthorne; Craig Packer; Andrew P. Dobson
1. We provide the first theoretical analysis of multihost disease dynamics to incorporate social behaviour and contrasting rates of within- and between-group disease transmission. 2. A stochastic susceptible-infected-recovered (SIR) model of disease transmission involving one to three sympatric species was built to mimic the 1994 Serengeti canine distemper virus outbreak, which infected a variety of carnivores with widely ranging social structures. The model successfully mimicked the erratic and discontinuous spatial pattern of lion deaths observed in the Serengeti lions under a reasonable range of parameter values, but only when one to two other species repeatedly transmitted the virus to the lion population. 3. The outputs from our model suggest several principles that will apply to most directly transmitted multihost pathogens: (i) differences in social structure can significantly influence the size, velocity and spatial pattern of a multihost epidemic; and (ii) social structures that permit higher intraspecific neighbour-to-neighbour transmission are the most likely to transmit disease to other species; whereas (iii) species with low neighbour-to-neighbour intraspecific transmission suffer the greatest costs from interspecific transmission.
PLOS ONE | 2009
William C. Ratcliff; Peter Hawthorne; Michael Travisano; R. Ford Denison
Background Stresses like dietary restriction or various toxins increase lifespan in taxa as diverse as yeast, Caenorhabditis elegans, Drosophila and rats, by triggering physiological responses that also tend to delay reproduction. Food odors can reverse the effects of dietary restriction, showing that key mechanisms respond to information, not just resources. Such environmental cues can predict population trends, not just individual prospects for survival and reproduction. When population size is increasing, each offspring produced earlier makes a larger proportional contribution to the gene pool, but the reverse is true when population size is declining. Principal Findings We show mathematically that natural selection can favor facultative delay in reproduction when environmental cues predict a decrease in total population size, even if lifetime fecundity decreases with delay. We also show that increased reproduction from waiting for better conditions does not increase fitness (proportional representation) when the whole population benefits similarly. Conclusions We conclude that the beneficial effects of stress on longevity (hormesis) in diverse taxa are a side-effect of delaying reproduction in response to environmental cues that population size is likely to decrease. The reversal by food odors of the effects of dietary restriction can be explained as a response to information that population size is less likely to decrease, reducing the chance that delaying reproduction will increase fitness.
Science Advances | 2016
Christina M. Kennedy; Daniela A. Miteva; Leandro Baumgarten; Peter Hawthorne; Kei Sochi; Stephen Polasky; James R. Oakleaf; Elizabeth M. Uhlhorn; Joseph M. Kiesecker
Landscape-level mitigation provides cost-effective conservation and can be used to promote sustainable development. Impact mitigation is a primary mechanism on which countries rely to reduce environmental externalities and balance development with conservation. Mitigation policies are transitioning from traditional project-by-project planning to landscape-level planning. Although this larger-scale approach is expected to provide greater conservation benefits at the lowest cost, empirical justification is still scarce. Using commercial sugarcane expansion in the Brazilian Cerrado as a case study, we apply economic and biophysical steady-state models to quantify the benefits of the Brazilian Forest Code (FC) under landscape- and property-level planning. We find that FC compliance imposes small costs to business but can generate significant long-term benefits to nature: supporting 32 (±37) additional species (largely habitat specialists), storing 593,000 to 2,280,000 additional tons of carbon worth
Environmental Research Letters | 2016
Jesse Gourevitch; Peter Hawthorne; Bonnie L. Keeler; Craig Beatty; Michelle Greve; Michael A Verdone
69 million to
Evolution | 2015
William C. Ratcliff; Peter Hawthorne; Eric Libby
265 million (
Archive | 2017
Christina M. Kennedy; Peter Hawthorne; Kei Sochi; Daniela A. Miteva; Leandro Baumgarten; Elizabeth M. Uhlhorn; Joseph M. Kiesecker
pertains to U.S. dollars), and marginally improving surface water quality. Relative to property-level compliance, we find that landscape-level compliance reduces total business costs by
Biological Conservation | 2016
Christina M. Kennedy; Peter Hawthorne; Daniela A. Miteva; Leandro Baumgarten; Kei Sochi; Marcelo Matsumoto; Jeffrey S. Evans; Stephen Polasky; Perrine Hamel; Emerson M. Vieira; Pedro Ferreira Develey; Cagan H. Sekercioglu; Ana D. Davidson; Elizabeth M. Uhlhorn; Joseph M. Kiesecker
19 million to
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International Union for Conservation of Nature and Natural Resources
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