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Effects of grazing on grassland soil carbon: a global review
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Soils of grasslands represent a large potential reservoir for storing CO2, but this potential likely depends on how grasslands are managed for large mammal grazing. Previous studies found both strong positive and negative grazing effects on soil organic carbon (SOC) but explanations for this variation are poorly developed. Expanding on previous reviews, we performed a multifactorial meta-analysis of grazer effects on SOC density on 47 independent experimen- tal contrasts from 17 studies. We explicitly tested hypotheses that grazer effects would shift from negative to positive with decreasing precipitation, increasing fineness of soil texture, transition from dominant grass species with C3 to C4 photosynthesis, and decreasing grazing intensity, after controlling for study duration and sampling depth. The six variables of soil texture, precipitation, grass type, grazing intensity, study duration, and sampling depth explained 85% of a large variation (`150 g m␣2 yr␣1) in grazing effects, and the best model included significant interactions between precipitation and soil texture (P = 0.002), grass type, and grazing intensity (P = 0.012), and study duration and soil sampling depth (P = 0.020). Specifically, an increase in mean annual precipitation of 600 mm resulted in a 24% decrease in grazer effect size on finer textured soils, while on sandy soils the same increase in precipitation pro- duced a 22% increase in grazer effect on SOC. Increasing grazing intensity increased SOC by 6–7% on C4-dominated and C4–C3 mixed grasslands, but decreased SOC by an average 18% in C3-dominated grasslands. We discovered these patterns despite a lack of studies in natural, wildlife-dominated ecosystems, and tropical grasslands. Our results, which suggest a future focus on why C3 vs. C4-dominated grasslands differ so strongly in their response of SOC to grazing, show that grazer effects on SOC are highly context-specific and imply that grazers in different regions might be managed differently to help mitigate greenhouse gas emissions.
Keywords: carbon sequestration, grasslands, grazing, grazing intensity, precipitation, soil organic carbon, soil texture
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Millennium Ecosystem Assessment: Research Needs
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The research community needs to develop analytical tools for projecting future trends and evaluating the success of interventions as well as indicators to monitor biological, physical, and social changes.
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Migration and Dispersal: Science Special Section
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INTRODUCTION: When to Go, Where to Stop
THE ABILITY TO MOVE, AT SOME STAGE IN THE LIFE CYCLE, IS FUNDAMENTAL TO SUCCESS in life. Passive drift in water columns conferred a selective advantage for early life, offering an escape from starvation and genetic uniformity. Since then, organisms have evolved many ways to disperse and migrate in response to the pressures of finding resources, escaping predators, seeking out mates and suitable breeding grounds, and distancing themselves from family. Dispersal in its broadest sense means movement away from the birthplace. Strictly speaking, migration involves travel in a periodically and geographically predictable way, whether it occurs just once or many times. In this issue, Science deals with what we know, what we need to know, and how we are going to find out more about both of these movement types.
In plants, the spore, seed, or fruit is typically the unit of dispersal. Although the many morphological adaptations for their dispersal are known, until now, researchers have been unable to determine the distances traveled or the proportion of dispersal events that lead to seedlings. In one Perspective (p. 786), Nathan describes recent developments in the modeling and measurement of the long-distance dispersal of plants. A News story by Holden (p. 779) discusses the push to come up with a theoretical framework, not just for plants, but for all moving organisms. Organisms also disperse in reaction to changing habitats and climate. The Perspective by Kokko and López-Sepulcre (p. 789) discusses the selective forces affecting this ability in animals and how dispersal translates into range expansions and contractions. Kintisch (p. 776) describes the challenges for marine scientists assessing how climate change may affect oceangoing species.
Humans have been great dispersers. Colonizing new habitat has been a hallmark of human ecology over the past million years or so. In a Review (p. 796), Mellars considers recent advances in archaeology and genetics that are illuminating the controversies over the routes taken by ancient peoples in the colonization of Asia 40,000 to 60,000 years ago. Two Perspectives consider migration: Holland et al. (p. 794) focus on migrating insects, which tend to travel in established geographical patterns across several generations rather than returning to their birthplace, and Alerstam (p. 791) discusses the accumulating and sometimes conflicting evidence about the navigational mechanisms used by animals (particularly birds) in long-distance annual migrations. In a related Report (p. 837), Muheim et al. describe the role of polarized light at dawn and sunset in calibrating the magnetic compasses of migrating birds. A News story by Morell (p. 783) describes a new model that will clarify the mix of genes and environmental responses underlying successful bird migration.
As News stories by Blackburn and Holden (p. 780) and Unger (p. 784) point out, ingenuity and persistence are beginning to pay off in new techniques for following organisms, be they fish, crabs, jellyfish, rhinos, or polar bears. Thanks to these advances, the study of the ecology and evolution of movement is charging ahead and unearthing the challenges faced by organisms in dispersing and migrating in a world undergoing anthropogenic change.
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On the Hydrologic Adjustment of Climate-Model Projections: The Potential Pitfall of Potential Evapotranspiration
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Hydrologic models often are applied to adjust projections of hydroclimatic change that come from climate models. Such adjustment includes climate-bias correction, spatial refinement (‘‘downscaling’’), and consideration of the roles of hydrologic processes that were neglected in the climate model. Described herein is a quantitative analysis of the effects of hydrologic adjustment on the projections of runoff change associated with projected twenty-first-century climate change. In a case study including three climate models and 10 river basins in the contiguous United States, the authors find that relative (i.e., fractional or percentage) runoff change computed with hydrologic adjustment more often than not was less positive (or, equivalently, more negative) than what was pro- jected by the climate models. The dominant contributor to this decrease in runoff was a ubiquitous change in runoff (median 211%) caused by the hydrologic model’s apparent amplification of the climate-model-implied growth in potential evapotranspiration. Analysis suggests that the hydrologic model, on the basis of the empirical, temperature-based modified Jensen–Haise formula, calculates a change in potential evapotranspiration that is typically 3 times the change implied by the climate models, which explicitly track surface energy budgets. In com- parison with the amplification of potential evapotranspiration, central tendencies of other contributions from hydrologic adjustment (spatial refinement, climate-bias adjustment, and process refinement) were relatively small. The authors’ findings highlight the need for caution when projecting changes in potential evapotranspiration for use in hydrologic models or drought indices to evaluate climate change impacts on water.
KEYWORDS: Hydrologic model; Climate change; Potential evapotranspi- ration
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Temperature Mediated Moose Survival in Northeastern Minnesota
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The earth is in the midst of a pronounced warming trend and temperatures in Minnesota, USA, as elsewhere, are projected to increase. Northern Minnesota represents the southern edge to the circumpolar distribution of moose (Alces alces), a species intolerant of heat. Moose increase their metabolic rate to regulate their core body temperature as temperatures rise. We hypothesized that moose survival rates would be a function of the frequency and magnitude that ambient temperatures exceeded the upper critical temperature of moose. We compared annual and seasonal moose survival in northeastern Minnesota between 2002 and 2008 with a temperature metric. We found that models based on January temperatures above the critical threshold were inversely correlated with subsequent survival and explained .78% of variability in spring, fall, and annual survival. Models based on late-spring temperatures also explained a high proportion of survival during the subsequent fall. A model based on warm-season temperatures was important in explaining survival during the subsequent winter. Our analyses suggest that temperatures may have a cumulative influence on survival. We expect that continuation or acceleration of current climate trends will result in decreased survival, a decrease in moose density, and ultimately, a retreat of moose northward from their current distribution.
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CARBON CYCLE : Fertilizing change
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Carbon cycle–climate feedbacks are expected to diminish the size of the terrestrial carbon sink over the next century. Model simulations suggest that nitrogen availability is likely to play a key role in mediating this response.
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First signs of carbon sink saturation in European forest biomass
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European forests are seen as a clear example of vegetation rebound in the Northern Hemisphere; recovering in area and growing stock since the 1950s, after centuries of stock decline and deforestation. These regrowing forests have shown to be a persistent carbon sink, projected to continue for decades, however, there are early signs of saturation. Forest policies and management strategies need revision if we want to sustain the sink.
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Earth system sensitivity inferred from Pliocene modelling and data
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Here we use a coupled atmosphere–ocean general circulation model to simulate the climate of the mid-Pliocene warm period (about three million years ago), and analyse the forcings and feedbacks that contributed to the relatively warm temperatures. Furthermore, we compare our simulation with proxy records of mid-Pliocene sea surface temperature. Taking these lines of evidence together, we estimate that the response of the Earth system to elevated atmospheric carbon dioxide concentrations is 30–50% greater than the response based on those fast-adjusting components of the climate system that are used traditionally to estimate climate sensitivity. We conclude that targets for the long-term stabilization of atmospheric greenhouse gas concentrations aimed at preventing a dangerous human interference with the climate system should take into account this higher sensitivity of the Earth system.
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A general integrative model for scaling plant growth, carbon flux, and functional trait spectra
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Linking functional traits to plant growth is critical for scaling attributes of organisms to the dynamics of ecosystems (1,2) and for understanding how selection shapes integrated botanical phenotypes (3). However, a general mechanistic theory showing how traits specifically influence carbon and biomass flux within and across plants is needed. Building on foundational work on relative growth rate (4–6), recent work on functional trait spectra (7–9), and metabolic scaling theory (10,11), here we derive a generalized trait-based model of plant growth. In agreement with a wide variety of empirical data, our model uniquely predicts how key functional traits interact to regulate variation in relative growth rate, the allometric growth normalizations for both angiosperms and gymnosperms, and the quantitative form of several functional trait spectra relationships. The model also provides a general quantitative framework to incorporate additional leaf-level trait scaling relationships (7,8) and hence to unite functional trait spectra with theories of relative growth rate, and metabolic scaling. We apply the model to calculate carbon use efficiency. This often ignored trait, which may influence variation in relative growth rate, appears to vary directionally across geographic gradients. Together, our results show how both quantitative plant traits and the geometry of vascular transport networks can be merged into a common scaling theory. Our model provides a framework for predicting not only how traits covary within an integrated allometric phenotype but also how trait variation mechanistically influences plant growth and carbon flux within and across diverse ecosystems.
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Snowball Earth termination by destabilization of equatorial permafrost methane clathrate
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The start of the Ediacaran period is defined by one of the most severe climate change events recorded in Earth history—the recov- ery from the Marinoan ‘snowball’ ice age, ,635 Myr ago (ref. 1). Marinoan glacial-marine deposits occur at equatorial palaeolati- tudes2, and are sharply overlain by a thin interval of carbonate that preserves marine carbon and sulphur isotopic excursions of about 25 and 115 parts per thousand, respectively3–5; these deposits are thought to record widespread oceanic carbonate precipitation during postglacial sea level rise1,3,4. This abrupt transition records a climate system in profound disequilibrium3,6 and contrasts shar- ply with the cyclical stratigraphic signal imparted by the balanced feedbacks modulating Phanerozoic deglaciation. Hypotheses accounting for the abruptness of deglaciation include ice albedo feedback3, deep-ocean out-gassing during post-glacial oceanic overturn7 or methane hydrate destabilization8–10. Here we report the broadest range of oxygen isotope values yet measured in mar- ine sediments (225% to 112%) in methane seeps in Marinoan deglacial sediments underlying the cap carbonate. This range of values is likely to be the result of mixing between ice-sheet-derived meteoric waters and clathrate-derived fluids during the flushing and destabilization of a clathrate field by glacial meltwater. The equatorial palaeolatitude implies a highly volatile shelf permafrost pool that is an order of magnitude larger than that of the present day. A pool of this size could have provided a massive biogeochem- ical feedback capable of triggering deglaciation and accounting for the global postglacial marine carbon and sulphur isotopic excur- sions, abrupt unidirectional warming, cap carbonate deposition, and a marine oxygen crisis. Our findings suggest that methane released from low-latitude permafrost clathrates therefore acted as a trigger and/or strong positive feedback for deglaciation and warming. Methane hydrate destabilization is increasingly suspected as an important positive feedback to climate change11–13 that coincides with critical boundaries in the geological record14,15 and may represent one particularly important mechanism active during conditions of strong climate forcing.
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