The Intergovernmental Panel on Climate Change (IPCC) Technical Paper Climate Change and Water draws together and evaluates the information in IPCC Assessment and Special Reports concerning the impacts of climate change on hydrological processes and regimes, and on freshwater resources – their availability, quality, use and management. It takes into account current and projected regional key vulnerabilities, prospects for adaptation, and the relationships between climate change mitigation and water. Its objectives are:

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Climate change and water.

Agricultural lands occupy 37% of the earth's land surface. Agriculture accounts for 52 and 84% of global anthropogenic methane and nitrous oxide emissions. Agricultural soils may also act as a sink or source for CO2, but the net flux is small. Many agricultural practices can potentially mitigate greenhouse gas (GHG) emissions, the most prominent of which are improved cropland and grazing land management and restoration of degraded lands and cultivated organic soils. Lower, but still significant mitigation potential is provided by water and rice management, set-aside, land use change and agroforestry, livestock management and manure management. The global technical mitigation potential from agriculture (excluding fossil fuel offsets from biomass) by 2030, considering all gases, is estimated to be approximately 5500–6000 Mt CO2-eq. yr−1, with economic potentials of approximately 1500–1600, 2500–2700 and 4000–4300 Mt CO2-eq. yr−1 at carbon prices of up to 20, up to 50 and up to 100 US$ t CO2-eq.−1, respectively. In addition, GHG emissions could be reduced by substitution of fossil fuels for energy production by agricultural feedstocks (e.g. crop residues, dung and dedicated energy crops). The economic mitigation potential of biomass energy from agriculture is estimated to be 640, 2240 and 16 000 Mt CO2-eq. yr−1 at 0–20, 0–50 and 0–100 US$ t CO2-eq.−1, respectively.

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Greenhouse gas mitigation in agriculture

B6nassy, C., 1955. R6marques sur deux Aphelinid6s: Aphelinus mytilaspidis Le Baron et Aphytis proclia Walker. Annls l~piphyt. 6: 11-17. Lord, F. T. & MacPhee, A. W., 1953. The influence of spray programs on the fauna of apple orchards in Nova Scotia II. Oyster shell scale. Can. Ent. 79: 196-209. Pickett, A. D., 1946. A progress report on long term spray programs. Rep. Nova Scotia Fruit Grow. Ass. 83 : 27-31. Pickett, A. D., 1967. The influence of spray programs on the fauna of apple orchards in Nova Scotia XIV. Can. Ent. 97: 816-821. Tothill, J. D., 1918. The predacious mite Hemisarcoptes malus Shimer and its relation to the natural control of the oyster shell scale Lepidosaphes ulmi L. Agric. Gaz. Can. 5 : 234-239.

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Soil enzymes: Kuprevich, V. F. & Shcherbakova, T. A.: Translated from the Russian edition (1966), published by the Indian National Scientific Documentation Centre, New Delhi 1971. 392 pp., offset printing from type script, paper cover. Obtainable from U.S. Department of Commerce, National Technical Information Service, Springfield, Va. 22151

Soil biota, ecosystem services and land productivity

With anthropogenic nutrient inputs to ecosystems increasing globally, there are long-standing, fundamental questions about the role of nutrients in the decomposition of organic matter. We tested the effects of exogenous nitrogen and phosphorus inputs on litter decomposition across a broad suite of litter and soil types. In one experiment, C mineralization was compared across a wide array of plants individually added to a single soil, while in the second, C mineralization from a single substrate was compared across 50 soils. Counter to basic stoichiometric decomposition theory, low N availability can increase litter decomposition as microbes use labile substrates to acquire N from recalcitrant organic matter. This "microbial nitrogen mining" is consistently suppressed by high soil N supply or substrate N concentrations. There is no evidence for phosphorus mining as P fertilization increases short- and long-term mineralization. These results suggest that basic stoichiometric decomposition theory needs to be revised and ecosystem models restructured accordingly in order to predict ecosystem carbon storage responses to anthropogenic changes in nutrient availability.

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Microbial nitrogen limitation increases decomposition

Increases in the concentrations of greenhouse gases, carbon dioxide (CO2), methane (CH4), nitrous oxide (N2O), and halocarbons in the atmosphere due to human activities are associated with global climate change. The concentration of N2O has increased by 16% since 1750. Although the atmospheric concentration of N2O is much smaller (314 ppb in 1998) than of CO2 (365 ppm), its global warming potential (cumulative radiative forcing) is 296 times that of the latter in a 100-year time horizon. Currently, it contributes about 6% of the overall global warming effect but its contribution from the agricultural sector is about 16%. Of that, almost 80% of N2O is emitted from Australian agricultural lands, originating from N fertilisers (32%), soil disturbance (38%), and animal waste (30%). Nitrous oxide is primarily produced in soil by the activities of microorganisms during nitrification, and denitrification processes. The ratio of N2O to N2 production depends on oxygen supply or water-filled pore space, decomposable organic carbon, N substrate supply, temperature, and pH and salinity. N2O production from soil is sporadic both in time and space, and therefore, it is a challenge to scale up the measurements of N2O emission from a given location and time to regional and national levels. Estimates of N2O emissions from various agricultural systems vary widely. For example, in flooded rice in the Riverina Plains, N2O emissions ranged from 0.02% to 1.4% of fertiliser N applied, whereas in irrigated sugarcane crops, 15.4% of fertiliser was lost over a 4-day period. Nitrous oxide emissions from fertilised dairy pasture soils in Victoria range from 6 to 11 kg N2O-N/ha, whereas in arable cereal cropping, N2O emissions range from <0.01% to 9.9% of N fertiliser applications. Nitrous oxide emissions from soil nitrite and nitrates resulting from residual fertiliser and legumes are rarely studied but probably exceed those from fertilisers, due to frequent wetting and drying cycles over a longer period and larger area. In ley cropping systems, significant N2O losses could occur, from the accumulation of mainly nitrate-N, following mineralisation of organic N from legume-based pastures. Extensive grazed pastures and rangelands contribute annually about 0.2 kg N/ha as N2O (93 kg/ha per year CO2-equivalent). Tropical savannas probably contribute an order of magnitude more, including that from frequent fires. Unfertilised forestry systems may emit less but the fertilised plantations emit more N2O than the extensive grazed pastures. However, currently there are limited data to quantify N2O losses in systems under ley cropping, tropical savannas, and forestry in Australia. Overall, there is a need to examine the emission factors used in estimating national N2O emissions; for example, 1.25% of fertiliser or animal-excreted N appearing as N2O (IPCC 1996). The primary consideration for mitigating N2O emissions from agricultural lands is to match the supply of mineral N (from fertiliser applications, legume-fixed N, organic matter, or manures) to its spatial and temporal needs by crops/pastures/trees. Thus, when appropriate, mineral N supply should be regulated through slow-release (urease and/or nitrification inhibitors, physical coatings, or high C/N ratio materials) or split fertiliser application. Also, N use could be maximised by balancing other nutrient supplies to plants. Moreover, non-legume cover crops could be used to take up residual mineral N following N-fertilised main crops or mineral N accumulated following legume leys. For manure management, the most effective practice is the early application and immediate incorporation of manure into soil to reduce direct N2O emissions as well as secondary emissions from deposition of ammonia volatilised from manure and urine. Current models such as DNDC and DAYCENT can be used to simulate N2O production from soil after parameterisation with the local data, and appropriate modification and verification against the measured N2O emissions under different management practices.

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Nitrous oxide emission from Australian agricultural lands and mitigation options: a review

The roles of microbial biomass (MBC) and substrate supply as well as their interaction with clay content in determining soil respiration rate were studied using a range of soils with contrasting properties. Total organic C (TOC), water-soluble organic carbon, 0.5 M K2SO4-extractable organic C and 33.3 mM KMnO4-oxidisable organic carbon were determined as C availability indices. For air-dried soils, these indices showed close relationship with flush of CO2 production following rewetting of the soils. In comparison, MBC determined with the chloroform fumigation–extraction technique had relatively weaker correlation with soil respiration rate. After 7 d pre-incubation, soil respiration was still closely correlated with the C availability indices in the pre-incubated soils, but poorly correlated with MBC determined with three different techniques—chloroform fumigation extraction, substrate-induced respiration, and chloroform fumigation–incubation methods. Results of multiple regression analyses, together with the above observations, suggested that soil respiration under favourable temperature and moisture conditions was principally determined by substrate supply rather than by the pool size of MBC. The specific respiratory activity of microorganisms (CO2-C/MBC) following rewetting of air-dried soils or after 7 d pre-incubation was positively correlated with substrate availability, but negatively correlated with microbial pool size. Clay content had no significant effect on CO2 production rate, relative C mineralization rate (CO2-C/TOC) and specific respiratory activity of MBC during the first week incubation of rewetted dry soils. However, significant protective effect of clay on C mineralization was shown for the pre-incubated soils. These results suggested that the protective effect of clay on soil organic matter decomposition became significant as the substrate supply and microbial demand approached to an equilibrium state. Thereafter, soil respiration would be dependent on the replenishment of the labile substrate from the bulk organic C pool.

Relationships of soil respiration to microbial biomass, substrate availability and clay content

Improved understanding of the interactive relationships of plant material decomposition kinetics to biochemical characteristics and nitrogen availability is required for terrestrial C accounting and sustainable land management. In this study, 15 typical and/or native Australian plant materials were finely ground and incubated with a sandy soil at 25 °C and 55% water holding capacity without nitrogen (−N) or with nitrogen (+N) addition (77 mg N kg−1 soil as KNO3). The C mineralisation dynamics were monitored for 356 days and the initial biochemical characteristics of the plant materials were determined by NMR and wet-chemical analyses. Under the −N treatment, C mineralisation rates of the plant materials were positively correlated with their initial N contents during the first several weeks, and then negatively correlated with lignin and polyphenols contents during the late stages of incubation. Thus the ratios of lignin/N, polyphenols/N and (lignin+polyphenols)/N had more consistent correlation with the cumulative amounts of C mineralised throughout the incubation than did any single component. In terms of the C types determined by NMR analysis, the C mineralisation rates were initially related positively to carbonyl C contents, and then negatively to aryl and O-aryl C contents from day 3 onwards. Addition of NO3−–N accelerated C mineralisation during the early stages, but resulted in lower cumulative C mineralisation at the end of the incubation for most plant materials. Under the +N treatment, the decomposition rates were correlated with the contents of lignin and the sum of cellulose+acid detergent-extractable non-phenolic compounds, or with aryl, O-aryl and N-alkyl+methoxyl C contents. Regardless of the N treatment, the ratios of aryl/carbonyl, O-aryl/carbonyl and (aryl+O-aryl)/carbonyl C had the closest and most consistent correlations with the cumulative C mineralisation among all biochemical indices examined. A double exponential model with defined mineralisation rate constants for the active and slow pools was used to describe the C mineralisation dynamics. The biological meanings of the kinetically estimated active and slow pool sizes are interpreted and their relationships to the initial chemical/biochemical composition of the plant materials are explored.

Decomposition dynamics of plant materials in relation to nitrogen availability and biochemistry determined by NMR and wet-chemical analysis

Aggregation often provides physical protection and stabilisation of soil organic carbon (C). No tillage (NT) coupled with stubble retention (SR) and nitrogen (N) fertiliser application (90 N, 90 kg N ha−1 application) can help improve soil aggregation. However, information is lacking on the effect of long‐term NT, SR and N fertiliser (NT, SR + N) application on soil aggregation and C distribution in different aggregates in vertisols. We analysed the soil samples collected from 0‐ to 30‐cm depth from a long‐term (47 years) experiment for soil aggregation and aggregate‐associated C and N. This long‐term field experiment originally consisted of 12 treatments, having plot size of 61·9 × 6·4 m, and these plots were arranged in a randomised block design with four replications, covering an area of 1·9 ha. Soil organic C concentrations as well as stocks were significantly higher under the treatment of NT, SR + N only in 0–10 cm compared with other treatments such as conventional tillage, stubble burning + 0 N (no N application) and conventional tillage, SR + 0 N. Mineral‐associated organic C (MOC) of 0·053 mm) in the 0‐ to 30‐cm layer. We found that NT, SR + N treatment had a positive impact on soil aggregation, as measured by the mean weight diameter (MWD) through wet sieving procedure, but only in the top 0‐ to 10‐cm depth. MWD had significant positive correlation with water stable aggregates (r = 0·67, p 2 mm) had significantly higher organic C and N concentrations than small macroaggregates (0·25–2 mm) or microaggregates (0·053–0·25 mm). We also found that N application had a significant effect on MWD and soil organic C in vertisols. It is evident that better soil aggregation was recorded under NTSR90N could have a positive influence on soil C sequestration. Our results further highlight the importance of soil aggregation and aggregate‐associated C in relation to C sequestration. Copyright © 2016 John Wiley & Sons, Ltd.

Weijin Wang

Papers

Nitrous oxide emission from Australian agricultural lands and mitigation options: a review

Relationships of soil respiration to microbial biomass, substrate availability and clay content

Decomposition dynamics of plant materials in relation to nitrogen availability and biochemistry determined by NMR and wet-chemical analysis

Impact of 47 Years of No Tillage and Stubble Retention on Soil Aggregation and Carbon Distribution in a Vertisol

Autotrophic and symbiotic diazotrophs dominate nitrogen-fixing communities in Tibetan grassland soils.