英文摘要: | The models used by the IPCC are yet to provide realistic predictions for nitrogen emissions from the land to the air and water. Natural isotopic benchmarks offer a simple solution to this emerging global imperative.
We must make progress in our ability to represent nitrogen (N) in global models if we are to reduce uncertainty in climate change projections and develop more insightful impact scenarios for decision-makers. Nitrogen can both warm and cool the climate system, depending on its form, phase and flux, and interaction with the biosphere's natural CO2 sinks1, with non-trivial effects on Earth's heat balance2, 3. For instance, gaseous N emissions from the soil limit the availability of this nutrient for plant CO2 capture — an indirect warming effect — yet can simultaneously cool global temperatures via the N-based aerosols that alter the planet's reflectance4. Once in the atmosphere, gaseous N species can directly increase the Earth's greenhouse effect, particularly when incomplete soil denitrification releases nitrous oxide (N2O), the third most important greenhouse gas in modern climate change2. Moreover, downstream and downwind transport of N accelerates eutrophication, decreases aquatic biodiversity, impairs water- and air-quality for human health, and contributes to N2O emissions in coastal ecosystems1, 5, 6. A recent assessment7 in the European Union (EU27) showed that the externality damages associated with excess N spillovers are roughly equivalent to the gross profits attributable to enhanced food production via N-based fertilizers, at around 100 billion annually. Terrestrial N fates are therefore vital to many aspects of the environment, society and climate system; but the models used by the IPCC have been criticized for their lack of constraint on terrestrial N balances and loss pathways8. We suggest that including the ratios of natural N isotopes (15N/14N or δ15N = [(15N/14Nsample)/(15N/14Nstandard) ] – 1 where the standard is atmospheric N2) can improve the efficacy of Earth system models generally, and N-based projections of modern climate change in particular. As a case study, we demonstrate here how natural N isotope composition can be used to validate and advance N cycle predictions in the Community Land Model with Coupled Carbon Nitrogen (CLM-CN, hereafter just CLM)9. We focused on this model because of its historical importance in setting climate science and policy: CLM was the only model to consider the effect of N in CO2 and climate change simulations in the Fifth Assessment Report from the IPCC (ref. 2).
We conducted our investigation in two sequential steps. First, we used empirical relationships to project patterns of soil δ15N throughout the land surface and thereby develop an observation against which the efficacy of global models can be quantitatively appraised. The δ15N of plant and soil pools varies systematically as a function of mean annual temperature and precipitation (r2= 0.39)10; hence climate correlations have been widely used to estimate soil δ15N globally, capturing biome-scale patterns to within ~1‰ of empirical observations and latitudinal differences in soil δ15N equal to ~10‰ (ref. 11). Such patterns in soil δ15N reflect N losses to fractionating (denitrification) relative to non-fractionating (leaching) pathways11, with the highest proportions of denitrification (relative to total N losses) observed for desert ecosystems, and lowest denitrification proportions in high-latitude boreal regions where N leaching losses are generally high (Fig. 1a,b).
- Sutton, M. A. et al. (eds) The European Nitrogen Assessment (Cambridge Univ. Press, 2011).
- Ciais, P. et al. in Climate Change 2013: The Physical Science Basis (eds Stocker, T. et al.) 465–570 (IPCC, Cambridge Univ. Press, 2013).
- Wang, Y. P. & Houlton, B. Z. Geophys. Res. Lett. 36, L24403 (2009).
- Pinder R. et al. Biogeochemistry 114, 25–40 (2013).
- Galloway, J. N. et al. Biogeochemistry 70, 153–226 (2004).
- Vitousek, P. M. et al. Ecol. Appl. 7, 737–751 (1997).
- Brink, C. et al. The European Nitrogen Assessment (eds Sutton, M. A. et al.) 513–540 (Cambridge Univ. Press, 2011).
- Hungate, B., Dukes, J., Shaw, M., Luo, Y. & Field, C. Science 302, 1512–1513 (2003).
- Thornton, P. E., Lamarque, J-F., Rosenbloom, N. A. & Mahowald, N. M. Global Biogeochem. Cycles 21, GB4018 (2007).
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