Ecologists have long been intrigued by the ways co-occurring species divide limiting resources. Such resource partitioning, or niche differentiation, may promote species diversity by reducing competition. Although resource partitioning is an important determinant of species diversity and composition in animal communities, its importance in structuring plant communities has been difficult to resolve. This is due mainly to difficulties in studying how plants compete for below-ground resources. Here we provide evidence from a 15N-tracer field experiment showing that plant species in a nitrogen-limited, arctic tundra community were differentiated in timing, depth and chemical form of nitrogen uptake, and that species dominance was strongly correlated with uptake of the most available soil nitrogen forms. That is, the most productive species used the most abundant nitrogen forms, and less productive species used less abundant forms. To our knowledge, this is the first documentation that the composition of a plant community is related to partitioning of differentially available forms of a single limiting resource.
Variations of the 13C content of marine participate organic carbon (δ13CPOC) in the modern ocean were studied using literature data to test the assumptions underlying the calculation of atmospheric pCO2 through geological time from the δ13C of sedimentary organic matter. These assumptions are that (1) concentrations of CO2 in the atmosphere and the surface ocean are at equilibrium at all times and latitudes and that (2) carbon isotopic fractionation of phytoplankton (ϵp) covaries primarily with concentrations of dissolved molecular CO2 ([CO2]aq). Previous studies and compilations have shown that the first assumption does not strictly hold, although [CO2]aq may be predicted with a reasonable degree of accuracy from sea surface temperature for specific regions of the world ocean. The second assumption is shown to be questionable due to the weak covariation of ϵp and [CO2]aq in the modern ocean. The large residual variance for regressions of ϵp against [CO2]aq suggests that factors other than [CO2]aq strongly affect carbon isotopic fractionation in phytoplankton. It is concluded that the relationship between ϵp and [CO2]aq cannot be easily calibrated using δ13CPOC data from the modern ocean.
Compound-specific isotopic analysis of amino acids (CSIA-AA) has emerged in the last decade as a powerful approach for tracing the origins and fate of nitrogen in ecological and biogeochemical studies. This approach is based on the empirical knowledge that source AAs (i.e., phenylalanine), fractionate 15 N very little (<0.5‰) during trophic transfer, whereas trophic AAs (i.e., glutamic acid), are greatly (~6-8‰) enriched in 15 N during each trophic step. The differential fractionation of these two AA groups can provide a valuable estimate of consumer trophic position that is internally indexed to the baseline δ 15 N value of the integrated food web. In this paper, we critically review the analytical methods for determining the nitrogen isotopic composition of AAs by gas chromatography/isotope-ratio mass spectrometry. We also discuss methodological considerations for accurate trophic position assessment of organisms using CSIA-AA. We then discuss the advantages and challenges of the CSIA-AA approach by examining published studies including trophic position assessment in various ecosystems, reconstruction of ancient human diets, reconstruction of animal migration and environmental variability, and assessment of marine organic matter dynamics. It is clear that the CSIA-AA approach can provide unique insight into the sources, cycling, and trophic modification of organic nitrogen as it flows through systems. However, some uncertainty still exists in how biochemical, physiological, and ecological mechanisms affect isotopic fractionation of trophic AAs. We end this review with a call for continued exploration of the mechanisms of AA isotopic fractionation, through various studies to promote the evolution of the rapidly growing field of CSIA-AA.
Statistical mixing models have been developed to help ecologists deal with isotope tracer data and to estimate source contributions in complex systems such as food webs and sediments. However, there are often too few tracer measurements and too many sources, so that unique solutions are not possible in underdetermined mixing models. This review highlights 3 approaches for solving otherwise underdetermined mixing models. The approaches include frequency-based statistics, calculations based on sectors measured in mixing polygons, and linear mixing between central and sidewall points in the mixing polygons. All approaches have some assumptions that allow extrapolation of mean solutions from measured data, with the simplest assumption being that any uncertainty in source contributions is divided in an even-handed manner among sources. A new graphical approach is proposed that allows scientists to critically recognize and separate datasupported aspects of solutions from any assumed aspects of solutions. The data-supported aspects of solutions can be tracked conservatively as the sum of the minimum source contributions, ΣMIN , and for the many cases where ΣMIN is low, additional ways to approach mixing problems are summarized from the published literature. Many underdetermined mixing problems do not have robust mean solutions with tracers employed thus far, so that there is a longerterm need for additional tracers and methodologies to really solve these complex ecological problems. This review concludes with several practical steps one can take to interpret isotope tracer information from underdetermined systems.
Abstract. We sampled consumers and organic matter sources (mangrove litter, freshwater swamp-forest litter, seagrasses, seagrass epiphytes, and marine particulate organic matter [MPOM]) from four estuaries on Kosrae, Federated States of Micronesia for stable isotope (␦ 13 C and ␦ 34 S) analysis. Unique mixing solutions cannot be calculated in a dualisotope, five-endmember scenario, so we tested IsoSource, a recently developed statistical procedure that calculates ranges in source contributions (i.e., minimum and maximum possible). Relatively high minimum contributions indicate significant sources, while low maxima indicate otherwise. Litter from the two forest types was isotopically distinguishable but had low average minimum contributions (0-8% for mangrove litter and 0% for swampforest litter among estuaries). Minimum contribution of MPOM was also low, averaging 0-13% among estuaries. Instead, local marine sources dominated contributions to consumers. Minimum contributions of seagrasses averaged 8-47% among estuaries (range 0-88% among species). Minimum contributions of seagrass epiphytes averaged 5-27% among estuaries (range 0-69% among species). IsoSource enabled inclusion of five organic matter sources in our dual-isotope analysis, ranking trophic importance as follows: seagrasses Ͼ seagrass epiphytes Ͼ MPOM Ͼ mangrove forest Ͼ freshwater swamp-forest. IsoSource is thus a useful step toward understanding which of multiple organic matter sources support food webs; more detailed work is necessary to identify unique solutions.
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