1,298 publications from this institution
Better land stewardship is needed to achieve the Paris Agreement's temperature goal, particularly in the tropics, where greenhouse gas emissions from the destruction of ecosystems are largest, and where the potential for additional land carbon storage is greatest. As countries enhance their nationally determined contributions (NDCs) to the Paris Agreement, confusion persists about the potential contribution of better land stewardship to meeting the Agreement's goal to hold global warming below 2°C. We assess cost-effective tropical country-level potential of natural climate solutions (NCS)—protection, improved management and restoration of ecosystems—to deliver climate mitigation linked with sustainable development goals (SDGs). We identify groups of countries with distinctive NCS portfolios, and we explore factors (governance, financial capacity) influencing the feasibility of unlocking national NCS potential. Cost-effective tropical NCS offers globally significant climate mitigation in the coming decades (6.56 Pg CO 2 e yr −1 at less than 100 US$ per Mg CO 2 e). In half of the tropical countries, cost-effective NCS could mitigate over half of national emissions. In more than a quarter of tropical countries, cost-effective NCS potential is greater than national emissions. We identify countries where, with international financing and political will, NCS can cost-effectively deliver the majority of enhanced NDCs while transforming national economies and contributing to SDGs. This article is part of the theme issue ‘Climate change and ecosystems: threats, opportunities and solutions’.
Abstract Since 1970 global agricultural production has more than doubled; contributing ~1/4 of total anthropogenic greenhouse gas ( GHG ) burden in 2010. Food production must increase to feed our growing demands, but to address climate change, GHG emissions must decrease. Using an identity approach, we estimate and analyse past trends in GHG emission intensities from global agricultural production and land‐use change and project potential future emissions. The novel Kaya–Porter identity framework deconstructs the entity of emissions from a mix of multiple sources of GHG s into attributable elements allowing not only a combined analysis of the total level of all emissions jointly with emissions per unit area and emissions per unit product. It also allows us to examine how a change in emissions from a given source contributes to the change in total emissions over time. We show that agricultural production and GHG s have been steadily decoupled over recent decades. Emissions peaked in 1991 at ~12 Pg CO 2 ‐eq. yr −1 and have not exceeded this since. Since 1970 GHG emissions per unit product have declined by 39% and 44% for crop‐ and livestock‐production, respectively. Except for the energy‐use component of farming, emissions from all sources have increased less than agricultural production. Our projected business‐as‐usual range suggests that emissions may be further decoupled by 20–55% giving absolute agricultural emissions of 8.2–14.5 Pg CO 2 ‐eq. yr −1 by 2050, significantly lower than many previous estimates that do not allow for decoupling. Beyond this, several additional costcompetitive mitigation measures could reduce emissions further. However, agricultural GHG emissions can only be reduced to a certain level and a simultaneous focus on other parts of the food‐system is necessary to increase food security whilst reducing emissions. The identity approach presented here could be used as a methodological framework for more holistic food systems analysis.
Soil organic carbon (SOC) is vital for terrestrial ecosystems, affecting biogeochemical processes, and soil health. It is known that soil salinity impacts SOC content, yet the specific direction and magnitude of SOC variability in relation to soil salinity remain poorly understood. Analyzing 43,459 mineral soil samples (SOC < 150 g kg −1 ) collected across different land covers since 1992, we approximate a soil salinity increase from 1 to 5 dS m −1 in croplands would be associated with a decline in mineral soils SOC from 0.14 g kg −1 above the mean predicted SOC ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:msub><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover><mml:mi>c</mml:mi></mml:msub></mml:math> = 18.47 g kg −1 ) to 0.46 g kg −1 below <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:msub><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover><mml:mi>c</mml:mi></mml:msub></mml:math> (~−430%), while for noncroplands, such decline is sharper, from 0.96 above <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:msub><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover><mml:mrow><mml:mi mathvariant="italic">nc</mml:mi></mml:mrow></mml:msub></mml:math> = 35.96 g kg −1 to 4.99 below <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:msub><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover><mml:mrow><mml:mi mathvariant="italic">nc</mml:mi></mml:mrow></mml:msub></mml:math> (~−620%). Although salinity’s significance in explaining SOC variability is minor (<6%), we estimate a one SD increase in salinity of topsoil samples (0 to 7 cm) correlates with respective <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover></mml:math> declines of ~4.4% and ~9.26%, relative to <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:msub><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover><mml:mi>c</mml:mi></mml:msub></mml:math> and <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:msub><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover><mml:mrow><mml:mi mathvariant="italic">nc</mml:mi></mml:mrow></mml:msub></mml:math> . The <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover></mml:math> decline in croplands is greatest in vegetation/cropland mosaics while lands covered with evergreen needle-leaved trees are estimated with the highest <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" display="inline" overflow="scroll"><mml:mover accent="true"><mml:mrow><mml:mi mathvariant="italic">SOC</mml:mi></mml:mrow><mml:mrow><mml:mo stretchy="true">¯</mml:mo></mml:mrow></mml:mover></mml:math> decline in noncroplands. We identify soil nitrogen, land cover, and precipitation Seasonality Index as the most significant parameters in explaining the SOC’s variability. The findings provide insights into SOC dynamics under increased soil salinity, improving understanding of SOC stock responses to land degradation and climate warming.
Abstract Species distribution models (SDMs) have been widely used to predict species ranges and their future distribution under climate change scenarios. In this study we applied Maxent, one of the most used SDMs, to project the distribution of some rare bryophyte species in Scotland in the 2050s. Most of these species are strongly linked to the blanket bog habitat, which is threatened by climate change in the near future. To assess the extent to which changes in habitat distribution leads to a different modelled distribution of the selected bryophytes, blanket bog distribution was included in the model as one of the explanatory variables for some species, and Maxent was run for three 2050s scenarios: once with the current blanket bog distribution and two other runs using the blanket bog distribution derived from two bioclimatic models (Lindsay modified and Blanket Bog Tree model) under the same climate change scenario. For seven out of nine of our studied bryophyte species, the modelled distribution in Scotland was predicted to decline, with some species retreating towards the north-west and other species almost disappearing. When the change in blanket bog distribution was also accounted for, further areas in the north/centre east of Scotland and in the south were predicted to be unfavourable for many of the species considered. Our findings suggest that when modelling species distributions, habitat distribution also needs to be considered, especially when there is a strong relationship between the species and a particular habitat.
A questionnaire was used to survey methods and protocols currently employed by laboratories involved in determining the antimicrobial susceptibility of bacteria associated with fish disease. Thirty-one laboratories in 18 countries reported the methods they employed for non-fastidious (Group 1) organisms. Of these 29 reported the use of disc diffusion methods and only 8 reported the use of MIC methods. Of these 8, only 4 reported using MIC methods in routine testing of clinical isolates. There was significant, but not complete, harmony in the protocols used for disc diffusion studies. Seventy-six percent of the laboratories reported the use of either the M42-R (CLSI, 2003) or other closely related protocols. The changes that will be required to increase the harmony in test protocols are discussed. The most significant will be the inclusion of control strains and the QA procedures associated with M42-R (CLSI, 2003) and in the harmonisation of the content of the discs.
ACKNOWLEDGEMENTS We would like to thank Dr Peter Long for assistance extracting input parameters from spatial data products and Dr Paul Bürkner for advice on Bayesian statistics in the brms package. We would also like to thank the anonymous reviewers for their comments which greatly improved the manuscript. This work was supported by the Biotechnology and Biological Sciences Research Council (BBSRC) [grant number BB/M011224/1]. The funder had no role in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the article for publication. The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
One of the greatest challenges we face in the twenty-first century is to sustainably feed nine to ten billion people by 2050 while at the same time reducing environmental impact (e.g. greenhouse gas (GHG) emissions, biodiversity loss, land use change and loss of ecosystem services). To this end, food security must be delivered. According to the United Nations definition, ‘food security exists when all people, at all times, have physical and economic access to sufficient, safe and nutritious food to meet their dietary needs and food preferences for an active and healthy life’. At the same time as delivering food security, we must also reduce the environmental impact of food production. Future climate change will make an impact upon food production. On the other hand, agriculture contributes up to about 30% of the anthropogenic GHG emissions that drive climate change. The aim of this review is to outline some of the likely impacts of climate change on agriculture, the mitigation measures available within agriculture to reduce GHG emissions and outlines the very significant challenge of feeding nine to ten billion people sustainably under a future climate, with reduced emissions of GHG. Each challenge is in itself enormous, requiring solutions that co-deliver on all aspects. We conclude that the status quo is not an option, and tinkering with the current production systems is unlikely to deliver the food and ecosystems services we need in the future; radical changes in production and consumption are likely to be required over the coming decades.