Landscape Partnership Resources Library
Permanent storage of carbon dioxide in geological reservoirs by mineral carbonation
Anthropogenic greenhouse-gas emissions continue to increase rapidly despite efforts aimed at curbing the release of such gases. One potentially long-term solution for offsetting these emissions is the capture and storage of carbon dioxide. In principle, fluid or gaseous carbon dioxide can be injected into the Earth’s crust and locked up as carbonate minerals through chemical reactions with calcium and magnesium ions supplied by silicate minerals. This process can lead to near-permanent and secure sequestration, but its feasibility depends on the ease and vigour of the reactions. Laboratory studies as well as natu- ral analogues indicate that the rate of carbonate mineral formation is much higher in host rocks that are rich in magnesium- and calcium-bearing minerals. Such rocks include, for example, basalts and magnesium-rich mantle rocks that have been emplaced on the continents. Carbonate mineral precipitation could quickly clog up existing voids, presenting a challenge to this approach. However, field and laboratory observations suggest that the stress induced by rapid precipitation may lead to fracturing and subsequent increase in pore space. Future work should rigorously test the feasibility of this approach by addressing reaction kinetics, the evolution of permeability and field-scale injection methods.
Importance of methane and nitrous oxide for Europe’s terrestrial greenhouse-gas balance
Climate change negotiations aim to reduce net greenhouse-gas emissions by encouraging direct reductions of emissions and crediting countries for their terrestrial greenhouse-gas sinks. Ecosystem carbon dioxide uptake has offset nearly 10% of Europe’s fossil fuel emissions, but not all of this may be creditable under the rules of the Kyoto Protocol. Although this treaty recognizes the importance of methane and nitrous oxide emissions, scientific research has largely focused on carbon dioxide. Here we review recent estimates of European carbon dioxide, methane and nitrous oxide fluxes between 2000 and 2005, using both top-down estimates based on atmospheric observations and bottom-up estimates derived from ground-based measure- ments. Both methods yield similar fluxes of greenhouse gases, suggesting that methane emissions from feedstock and nitrous oxide emissions from arable agriculture are fully compensated for by the carbon dioxide sink provided by forests and grass- lands. As a result, the balance for all greenhouse gases across Europe’s terrestrial biosphere is near neutral, despite carbon sequestration in forests and grasslands. The trend towards more intensive agriculture and logging is likely to make Europe’s land surface a significant source of greenhouse gases. The development of land management policies which aim to reduce greenhouse-gas emissions should be a priority.
Stronger winds over a large lake in response to weakening air-to-lake temperature gradient
The impacts of climate change on the world’s large lakes are a cause for concern1–4. For example, over the past decades, mean surface water temperatures in Lake Superior, North America, have warmed faster than air temperature during the thermally stratified summer season, because decreasing ice cover has led to increased heat input2,5. However, the effects of this change on large lakes have not been studied extensively6. Here we analyse observations from buoys and satellites as well as model reanalyses for Lake Superior, and find that increasing temperatures in both air and surface water, and a reduction in the temperature gradient between air and water are destabilizing the atmospheric surface layer above the lake. As a result, surface wind speeds above the lake are increasing by nearly 5% per decade, exceeding trends in wind speed over land. A numerical model of the lake circulation suggests that the increasing wind speeds lead to increases in current speeds, and long-term warming causes the surface mixed layer to shoal and the season of stratification to lengthen. We conclude that climate change will profoundly affect the biogeochemical cycles of large lakes, the mesoscale atmospheric circulation at lake–land boundaries and the transport of airborne pollutants in regions that are rich in lakes.
Quantifying the benefit of early climate change mitigation in avoiding biodiversity loss
Climate change is expected to have significant influences on terrestrial biodiversity at all system levels, including species-level reductions in range size and abundance, especially amongst endemic species1–6. However, little is known about how mitigation of greenhouse gas emissions could reduce biodiversity impacts, particularly amongst common and widespread species. Our global analysis of future climatic range change of common and widespread species shows that without mitigation, 57 ± 6% of plants and 34 ± 7%of animals are likely to lose ≥50% of their present climatic range by the 2080s. With mitigation, however, losses are reduced by 60% if emissions peak in 2016 or 40% if emissions peak in 2030. Thus, our analyses indicate that without mitigation, large range contractions can be expected even amongst common and widespread species, amounting to a substantial global reduction in biodiversity and ecosystem services by the end of this century. Prompt and stringent mitigation, on the other hand, could substantially reduce range losses and buy up to four decades for climate change adaptation.
Human land-use-driven reduction of forest volatiles cools global climate
Human conversion of forest ecosystems to agriculture is a major driver of global change. Conventionally, the impacts of the historical cropland expansion on Earth’s radiation balance have been quantified through two opposing effects: the release of stored carbon to the atmosphere as CO2 (warming) versus the increase in surface albedo (cooling)1. Changing forest cover has a third effect on the global radiation balance by altering emissions of biogenic volatile organic compounds (BVOCs) that control the loadings of multiple warming and cooling climate pollutants: tropospheric ozone (O3 ), methane (CH4 ) and aerosols. Although human land cover change has dominated BVOC emission variability over the past century2–4, the net effect on global climate has not been quantified. Here, I show that the effects of the global cropland expansion between the 1850s and 2000s on BVOC emissions and atmospheric chemistry have imposed an additional net global radiative impact of −0.11 ± 0.17 W m−2 (cooling). This magnitude is comparable to that of the surface albedo and land carbon release effects. I conclude that atmospheric chemistry must be considered in climate impact assessments of anthropogenic land cover change and in forestry for climate protection strategies.
Predictive traits to the rescue
Climate change poses new challenges to the conservation of species, which at present requires data-hungry models to meaningfully anticipate future threats. Now a study suggests that species traits may offer a simpler way to help predict future extinction risks.
Inhomogeneous forcing and transient climate sensitivity
Understanding climate sensitivity is critical to projecting climate change in response to a given forcing scenario. Recent analyses1–3 have suggested that transient climate sensitivity is at the low end of the present model range taking into account the reduced warming rates during the past 10–15 years during which forcing has increased markedly4. In contrast, comparisons of modelled feedback processes with observations indicate that the most realistic models have higher sensitivities5,6. Here I analyse results from recent climate modelling intercomparison projects to demonstrate that transient climate sensitivity to historical aerosols and ozone is substantially greater than the transient climate sensitivity to CO2 . This enhanced sensitivity is primarily caused by more of the forcing being located at Northern Hemisphere middle to high latitudes where it triggers more rapid land responses and stronger feedbacks. I find that accounting for this enhancement largely reconciles the two sets of results, and I conclude that the lowest end of the range of transient climate response to CO2 in present models and assessments7 (<1.3 ◦ C) is very unlikely.
Life history and spatial traits predict extinction risk due to climate change
There is an urgent need to develop effective vulnerability assessments for evaluating the conservation status of species in a changing climate1. Several new assessment approaches have been proposed for evaluating the vulnerability of species to climate change 2–5 based on the expectation that established assessments such as the IUCN Red List6 need revising or superseding in light of the threat that climate change brings. However, although previous studies have identified ecological and life history attributes that characterize declining species or those listed as threatened7–9, no study so far has undertaken a quantitative analysis of the attributes that cause species to be at high risk of extinction specifically due to climate change. We developed a simulation approach based on generic life history types to show here that extinction risk due to climate change can be predicted using a mixture of spatial and demographic variables that can be measured in the present day without the need for complex forecasting models. Most of the variables we found to be important for predicting extinction risk, including occupied area and population size, are already used in species conservation assessments, indicating that present systems may be better able to identify species vulnerable to climate change than previously thought. Therefore, although climate change brings many new conservation challenges, we find that it may not be fundamentally different from other threats in terms of assessing extinction risks.
Observed and predicted effects of climate change on species abundance in protected areas
The dynamic nature and diversity of species’ responses to climate change poses significant difficulties for developing robust, long-term conservation strategies. One key question is whether existing protected area networks will remain effective in a changing climate. To test this, we developed statistical models that link climate to the abundance of internationally important bird populations in northwestern Europe. Spatial climate–abundance models were able to predict 56% of the variation in recent 30-year population trends. Using these models, future climate change resulting in 4.0 ◦C global warming was projected to cause declines of at least 25% for more than half of the internationally important populations considered. Nonetheless, most EU Special Protection Areas in the UK were projected to retain species in sufficient abundances to maintain their legal status, and generally sites that are important now were projected to be important in the future. The biological and legal resilience of this network of protected areas is derived from the capacity for turnover in the important species at each site as species’ distributions and abundances alter in response to climate. Current protected areas are therefore predicted to remain important for future conservation in a changing climate.
Shifts in Arctic vegetation and associated feedbacks under climate change
Climate warming has led to changes in the composition, density and distribution of Arctic vegetation in recent decades1–4. These changes cause multiple opposing feedbacks between the biosphere and atmosphere5–9, the relative magnitudes of which will have globally significant consequences but are unknown at a pan-Arctic scale10. The precise nature of Arctic vegetation change under future warming will strongly influence climate feedbacks, yet Earth system modelling studies have so far assumed arbitrary increases in shrubs (for example, +20%; refs 6,11), highlighting the need for predictions of future vegetation distribution shifts. Here we show, using climate scenarios for the 2050s and models that utilize statistical associations between vegetation and climate, the potential for extremely widespread redistribution of vegetation across the Arctic. We predict that at least half of vegetated areas will shift to a different physiognomic class, and woody cover will increase by as much as 52%. By incorporating observed relationships between vegetation and albedo, evapotranspiration and biomass, we show that vegetation distribution shifts will result in an overall positive feedback to climate that is likely to cause greater warming than has previously been predicted. Such extensive changes to Arctic vegetation will have implications for climate, wildlife and ecosystem services.
Impacts of biofuel cultivation on mortality and crop yields
Ground-level ozone is a priority air pollutant, causing ∼22,000 excess deaths per year in Europe1, significant reductions in crop yields2 and loss of biodiversity3. It is produced in the troposphere through photochemical reactions involving oxides of nitrogen (NOx) and volatile organic compounds (VOCs). The biosphere is the main source of VOCs, with an estimated 1,150 TgC yr−1 (∼90% of total VOC emissions) released from vegetation globally4 . Isoprene (2-methyl-1,3-butadiene) is the most significant biogenic VOC in terms of mass (around 500 TgC yr−1 ) and chemical reactivity4 and plays an important role in the mediation of ground-level ozone concentrations5. Concerns about climate change and energy security are driving an aggressive expansion of bioenergy crop production and many of these plant species emit more isoprene than the traditional crops they are replacing. Here we quantify the increases in isoprene emission rates caused by cultivation of 72 Mha of biofuel crops in Europe. We then estimate the resultant changes in ground-level ozone concentrations and the impacts on human mortality and crop yields that these could cause. Our study highlights the need to consider more than simple carbon budgets when considering the cultivation of biofuel feedstock crops for greenhouse-gas mitigation.
Projections of declining surface-water availability for the southwestern United States
Global warming driven by rising greenhouse-gas concentrations is expected to cause wet regions of the tropics and mid to high latitudes to get wetter and subtropical dry regions to get drier and expand polewards 1–4. Over southwest North America, models project a steady drop in precipitation minus evapotranspiration, P − E, the net flux of water at the land surface5–7, leading to, for example, a decline in Colorado River flow8–11. This would cause widespread and important social and ecological consequences12–14. Here, using new simulations from the Coupled Model Intercomparison Project Five, to be assessed in Intergovernmental Panel on Climate Change As- sessment Report Five, we extend previous work by examining changes in P, E, runoff and soil moisture by season and for three different water resource regions. Focusing on the near future, 2021–2040, the new simulations project declines in surface-water availability across the southwest that translate into reduced soil moisture and runoff in California and Nevada, the Colorado River headwaters and Texas.
The challenge to keep global warming below 2 °C
The latest carbon dioxide emissions continue to track the high end of emission scenarios, making it even less likely global warming will stay below 2 °C. A shift to a 2 °C pathway requires immediate significant and sustained global mitigation, with a probable reliance on net negative emissions in the longer term.
Response of snow-dependent hydrologic extremes to continued global warming
Snow accumulation is critical for water availability in the Northern Hemisphere 1,2, raising concern that global warming could have important impacts on natural and human systems in snow-dependent regions1,3. Although regional hydrologic changes have been observed (for example, refs 1,3–5), the time of emergence of extreme changes in snow accumulation and melt remains a key unknown for assessing climate- change impacts3,6,7. We find that the CMIP5 global climate model ensemble exhibits an imminent shift towards low snow years in the Northern Hemisphere, with areas of western North America, northeastern Europe and the Greater Himalaya showing the strongest emergence during the near- term decades and at 2 ◦ C global warming. The occurrence of extremely low snow years becomes widespread by the late twenty-first century, as do the occurrences of extremely high early-season snowmelt and runoff (implying increasing flood risk), and extremely low late-season snowmelt and runoff (implying increasing water stress). Our results suggest that many snow-dependent regions of the Northern Hemisphere are likely to experience increasing stress from low snow years within the next three decades, and from extreme changes in snow-dominated water resources if global warming exceeds 2 ◦ C above the pre-industrial baseline.
Focus on poleward shifts in species’ distribution underestimates the fingerprint of climate change
Species are largely predicted to shift poleward as global temperatures increase, with this fingerprint of climate change being already observed across a range of taxonomic groups and, mostly temperate, geographic locations1–5. However, the assumption of uni-directional distribution shifts does not account for complex interactions among temperature, precipitation and species-specific tolerances 6, all of which shape the direction and magnitude of changes in a species’ climatic niche. We analysed 60 years of past climate change on the Australian continent, assessing the velocity of changes in temperature and precipitation, as well as changes in climatic niche space for 464 Australian birds. We show large magnitude and rapid rates of change in Australian climate over the past 60 years resulting in high-velocity and multi-directional, including equatorial, shifts in suitable climatic space for birds (ranging from 0.1 to 7.6kmyr−1, mean 1.27kmyr−1). Overall, if measured only in terms of poleward distribution shifts, the fingerprint of climate change is underestimated by an average of 26% in temperate regions of the continent and by an average of 95% in tropical regions. We suggest that the velocity of movement required by Australian species to track their climatic niche may be much faster than previously thought and that the interaction between temperature and precipitation changes will result in multi-directional distribution shifts globally.
Regional carbon dioxide implications of forest bioenergy production
Strategies for reducing carbon dioxide emissions include substitution of fossil fuel with bioenergy from forests1, where carbon emitted is expected to be recaptured in the growth of new biomass to achieve zero net emissions 2, and forest thinning to reduce wildfire emissions 3. Here, we use forest inventory data to show that fire prevention measures and large-scale bioenergy harvest in US West Coast forests lead to 2–14% (46–405 Tg C) higher emissions compared with current management practices over the next 20 years. We studied 80 forest types in 19 ecoregions, and found that the current carbon sink in 16 of these ecoregions is sufficiently strong that it cannot be matched or exceeded through substitution of fossil fuels by forest bioenergy. If the sink in these ecoregions weakens below its current level by 30–60 g C m−2 yr−1 owing to insect infestations, increased fire emissions or reduced primary production, management schemes including bioenergy production may succeed in jointly reducing fire risk and carbon emissions. In the remaining three ecoregions, immediate implementation of fire prevention and biofuel policies may yield net emission savings. Hence, forest policy should consider current forest carbon balance, local forest conditions and ecosystem sustainability in establishing how to decrease emissions.
Shrinking body size as an ecological response to climate change
Determining how climate change will affect global ecology and ecosystem services is one of the next important frontiers in environmental science. Many species already exhibit smaller sizes as a result of climate change and many others are likely to shrink in response to continued climate change, following fundamental ecological and metabolic rules. This could negatively impact both crop plants and protein sources such as fish that are important for human nutrition. Furthermore, heterogeneity in response is likely to upset ecosystem balances. We discuss future research directions to better understand the trend and help ameliorate the trophic cascades and loss of biodiversity that will probably result from continued decreases in organism size.
The temperature response of soil microbial efficiency and its feedback to climate
Soils are the largest repository of organic carbon (C) in the terrestrial biosphere and represent an important source of carbon dioxide (CO2)totheatmosphere,releasing60–75PgC an- nually through microbial decomposition of organic materials1,2. A primary control on soil CO2 flux is the efficiency with which the microbial community uses C. Despite its critical importance to soil–atmosphere CO2 exchange, relatively few studies have examined the factors controlling soil microbial efficiency. Here, we measured the temperature response of microbial efficiency in soils amended with substrates varying in lability. We also examined the temperature sensitivity of microbial efficiency in response to chronic soil warming in situ. We find that the efficiency with which soil microorganisms use organic matter is dependent on both temperature and substrate quality, with efficiency declining with increasing temperatures for more recalcitrant substrates. However, the utilization efficiency of a more recalcitrant substrate increased at higher temperatures in soils exposed to almost two decades of warming 5 ◦ C above ambient. Our work suggests that climate warming could alter the decay dynamics of more stable organic matter compounds, thereby having a positive feedback to climate that is attenuated by a shift towards a more efficient microbial community in the longer term.
Global diversity of drought tolerance and grassland climate-change resilience
Drought reduces plant productivity, induces widespread plant mortality and limits the geographic distribution of plant species1–7. As climates warm and precipitation patterns shift in the future8,9, understanding the distribution of the diversity of plant drought tolerance is central to predicting future ecosystem function and resilience to climate change10–12 . These questions are especially pressing for the world’s 11,000 grass species13, which dominate a large fraction of the terrestrial biosphere14, yet are poorly characterized with respect to re- sponses to drought. Here, we show that physiological drought tolerance, which varied tenfold among 426 grass species, is well distributed both climatically and phylogenetically, sug- gesting most native grasslands are likely to contain a high diversity of drought tolerance. Consequently, local species may help maintain ecosystem functioning in response to changing drought regimes without requiring long-distance migrations of grass species. Furthermore, physiologically drought-tolerant species had higher rates of water and carbon dioxide exchange than intolerant species, indicating that severe droughts may generate legacies for ecosystem functioning. In all, our findings suggest that diverse grasslands throughout the globe have the potential to be resilient to drought in the face of climate change through the local expansion of drought-tolerant species.
Increased soil emissions of potent greenhouse gases under increased atmospheric CO2
Increasing concentrations of atmospheric carbon dioxide (CO2) can affect biotic and abiotic conditions in soil, such as microbial activity and water content 1,2. In turn, these changes might be expected to alter the production and consumption of the important greenhouse gases nitrous oxide (N2O) and methane (CH4) (refs 2, 3). However, studies on fluxes of N2O and CH4 from soil under increased atmo- spheric CO2 have not been quantitatively synthesized. Here we show, using meta-analysis, that increased CO2 (ranging from 463 to 780 parts per million by volume) stimulates both N2O emissions from upland soils and CH4 emissions from rice paddies and natural wetlands. Because enhanced greenhouse-gas emissions add to the radiative forcing of terrestrial ecosystems, these emissions are expected to negate at least 16.6 per cent of the climate change mitigation potential previously predicted from an increase in the terrest- rial carbon sink under increased atmospheric CO2 concentrations4. Our results therefore suggest that the capacity of land ecosystems to slow climate warming has been overestimated.