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Developing an understanding of vegetation change and carbon budgets in semi-arid environments Alan Puttock Research aims and objectives Aim: Using an ecohydrological approach, develop an understanding of vegetation change and associated soil carbon dynamics across the dominant vegetation transitions occurring within the Sevilleta Long Term Ecological Research Site (LTER), New Mexico, USA (sev.lternet.edu). Objective 1: Use carbon isotope ratios/plant biomarker techniques to develop an understanding of vegetation change and sediment (particularly associated carbon) dynamics in response to rainfall events. There remains a lack of quantitative understanding of the biotic-abiotic interactions and resulting, water, sediment and carbon fluxes across semi-arid vegetation transitions, particularly in response to rainfall events. While models provide a means to develop this understanding, additional field data is required both to understand the processes occurring and provide data for model calibration and evaluation. The use of carbon isotope ratios and plant biomarkers provides a means to fingerprint sources of eroded sediment, in addition to the type of vegetation under which the sediment was formed. Previous research has identified the significant potential for using δ13C carbon isotope ratios to develop an understanding of vegetation change and carbon dynamics, due to its ability to differentiate between C3 and C4 input vegetation (Turnbull et al. 2008). However, Turnbull et al identified the difficulties in using such a technique in these environments where soils are not in a steady state, highlighting the need for methodological refinement to derive usable unique signatures. This project will address this using fraction specific analysis of samples, specifically the extraction of n-alkane lipid fractions. N-alkanes have been chosen due to their ease of extraction, resistance to degradation and because C3 woody species and C4 grass species produce distinctive n-alkane signatures. Objective 2: Compare and contrast ecosystem structure and function over both grass-tocreosotebush and grass-to-piñon-juniper transitions. Previous research has demonstrated the need to adopt an ecohydrological approach to understanding grass to woody species transitions. However, many studies and conceptual models addressing these transitions refer broadly to grass-to-shrub transitions. It is important to be aware that many sites in transition exhibit a mixture of characteristics (Michaelides et al. 2009) and also that different shrub/woody species have different characteristics affecting both ecohydrological interactions and carbon dynamics. Therefore, it would be erroneous to assume that the characteristics of one end-member species are generic. In order to develop an understanding of vegetation transitions occurring in semi-arid environments, it is essential to move beyond basing conclusions, on the transition to one vegetation endmember. Specifically in the Sevilleta LTER, there is a need to consider the transitions from grass dominated landscapes, to not only creosotebush dominated shrubland but also piñon-juniper woodland. By expanding beyond a one site, one view perspective, this study aims to address both key vegetation transitions occurring in the Sevilleta LTER, within a common methodological framework. A key conclusion from previous studies over both transitions is that they result in an increased heterogeneity of resources, reinforced by a series of feedbacks, particularly, increased bare inter-plant areas and an increased vulnerability to runoff and erosion. However, the different vegetation types present over the Sevilleta ecotones can result in different ecohydrological interactions, as a result of their physiological characteristics and physical scale. This study will characterise the changes in both vegetation and soil properties for both the dominant transitions, followed by monitoring of the temporal and spatial variation in fluxes as a result of monsoon rainfall events. Justification for research 1. Dryland environments are estimated to cover around 40% of the global land surface, and are home to approximately 2.4 billion people (Okin et al. 2009). Many of these areas have recently experienced extensive land degradation (Van Auken 2000, Jackson et al. 2002, Turnbull et al. 2009). In the US Southwest (US-SW), degradation over the past 150 years has been characterised by the invasion of woody vegetation into areas previously dominated by grasslands. Research suggests that due to the potential for catastrophic shifts, these vegetation transitions are often persistent and irreversible. 2. The research outlined is of major significance to understanding the ecosystem processes occurring in the Sevilleta LTER and by inference semi-arid areas both in the US-SW and worldwide. By addressing both key vegetation transitions occurring in the Sevilleta LTER within a common methodological framework this study will address whether grass-woody species transitions show common interactions between biotic and abiotic structure and function. This information in turn will be used to evaluate the use of generic conceptual models for representing these grass-woody plant transitions, with widespread relevance both to future research frameworks and management strategies. 3. Soil erosion is a poorly understood component of the carbon cycle (Lal 2005). With vegetation change we tend to see significant increases in runoff and erosion, resulting in the loss of key nutrients including carbon from the soil, with implications for carbon sequestration and its resulting local and global implications. The use of n-alkane biomarkers and carbon isotope ratios provides a means to develop a greater understanding of the spatial redistribution and loss of soil and associated carbon over the vegetation transitions occurring within the Sevilleta LTER. Additionally this quantitative data, fingerprinting the source of eroded sediment provides a valuable database for the construction and calibration of modelling approaches designed to address these transitions. April 2010 trip to the Sevilleta LTER This two week trip to the research site accomplished multiple objectives: 1. The refurbishment of existing runoff plots over the grass to shrub transition so as to be ready to collect results during the summer monsoon season. (Working at Plot 4 the shrub (creosotebush) vegetation endmember) 2. The collection of vegetation samples from which to derive biomarker signatures. (Dominant vegetation types; top-left: black grama, top-right: creosotebush, bottom left: piñon, bottom-right: juniper) 3. The construction of an initial runoff plot in the piñon-juniper woodland endmember (Transportation of water/sediment collecting tank to piñon-juniper site) (Construction of runoff plot at piñon-juniper site) References Jackson, R. B., J. L. Banner, E. G. Jobbagy, W. T. Pockman, and D. H. Wall. 2002. Ecosystem carbon loss with woody plant invasion of grasslands. Nature 418:623-626. Lal. 2005. Soil erosion and carbon dynamics. Soil & Tillage Research 81:137-142. Michaelides, K., D. Lister, J. Wainwright, and A. J. Parsons. 2009. Vegetation controls on small-scale runoff and erosion dynamics in a degrading dryland environment. Hydrological Processes 23:1617–1630. Okin, G. S., A. J. Parsons, J. Wainwright, J. E. Herrick, B. Bestelmeyer, T., D. C. Peters, and E. L. Fredrickson. 2009. Do Changes in Connectivity Explain Desertification? Bioscience 59:237244. sev.lternet.edu. Sevilleta Long Term Ecological Research: Where Edges Meet. http://sev.lternet.edu/. Last accessed 15th December 2009. Turnbull, L., R. E. Brazier, J. Wainwright, L. Dixon, and R. Bol. 2008. Use of carbon isotope analysis to understand semi-arid erosion dynamics and long-term semi-arid land degradation. Rapid Communications in Mass Spectrometry 22:1-6. Turnbull, L., J. Wainwright, and R. E. Brazier. 2009. Changes in hydrology and erosion over a transition from grassland to shrubland. Hydrological Processes, online in advance of print: http://dx.doi.org/10.1002/hyp.7491. Van Auken, O. W. 2000. Shrub invasions of North American grasslands. Annu. Rev. Ecol. Syst. 31:197215.