This chapter reviews the present-day composition of the continental crust, the methods employed to derive these estimates, and the implications of the continental crust composition for the formation of the continents, Earth differentiation, and its geochemical inventories. We review the composition of the upper, middle, and lower continental crust. We then examine the bulk crust composition and the implications of this composition for crust generation and modification processes. Finally, we compare the Earth's crust with those of the other terrestrial planets in our solar system and speculate about what unique processes on Earth have given rise to this unusual crustal distribution.

/pdf/composition-of-the-continental-crust-2hxz49vsod.pdf

Composition of the Continental Crust

The stable isotopes of nitrogen (8'5N) and carbon (8'3C) provide powerful tools for estimating the trophic positions of and carbon flow to consumers in food webs; however, the isotopic signature of a consumer alone is not generally sufficient to infer trophic position or carbon source without an appropriate isotopic baseline. In this paper, I develop and discuss methods for generating an isotopic baseline and evaluate the assump- tions required to estimate the trophic position of consumers using stable isotopes in multiple ecosystem studies. I test the ability of two primary consumers, surface-grazing snails and filter-feeding mussels, to capture the spatial and temporal variation at the base of aquatic food webs. I find that snails reflect the isotopic signature of the base of the littoral food web, mussels reflect the isotopic signature of the pelagic food web, and together they provide a good isotopic baseline for estimating trophic position of secondary or higher trophic level consumers in lake ecosystems. Then, using data from 25 north temperate lakes, I evaluate how 815N and 8'3C of the base of aquatic food webs varies both among lakes and between the littoral and pelagic food webs within lakes. Using data from the literature, I show that the mean trophic fractionation of b'5N is 3.4%o (1 SD = 1%M) and of 8'3C is 0.4%o (1 SD = 1.3%o), and that both, even though variable, are widely applicable. A sen- sitivity analysis reveals that estimates of trophic position are very sensitive to assumptions about the trophic fractionation of '5 N, moderately sensitive to different methods for gen- erating an isotopic baseline, and not sensitive to assumptions about the trophic fractionation of 8'3C when 8'3C is used to estimate the proportion of nitrogen in a consumer derived from two sources. Finally, I compare my recommendations for generating an isotopic baseline to an alternative model proposed by M. J. Vander Zanden and J. B. Rasmussen. With an appropriate isotopic baseline and an appreciation of the underlying assumptions and model sensitivity, stable isotopes can help answer some of the most difficult questions in food web ecology.

/pdf/using-stable-isotopes-to-estimate-trophic-position-models-16ajs0cxhj.pdf

Using stable isotopes to estimate trophic position: models, methods, and assumptions

The influence of diet on the distribution of nitrogen isotopes in animals was investigated by analyzing animals grown in the laboratory on diets of constant nitrogen isotopic composition. 
The isotopic composition of the nitrogen in an animal reflects the nitrogen isotopic composition of its diet. The δ^(15)N values of the whole bodies of animals are usually more positive than those of their diets. Different individuals of a species raised on the same diet can have significantly different δ^(15)N values. The variability of the relationship between the δ^(15)N values of animals and their diets is greater for different species raised on the same diet than for the same species raised on different diets. Different tissues of mice are also enriched in ^(15)N relative to the diet, with the difference between the δ^(15)N values of a tissue and the diet depending on both the kind of tissue and the diet involved. The δ^(15)N values of collagen and chitin, biochemical components that are often preserved in fossil animal remains, are also related to the δ^(15)N value of the diet. 
The dependence of the δ^(15)N values of whole animals and their tissues and biochemical components on the δ^(15)N value of diet indicates that the isotopic composition of animal nitrogen can be used to obtain information about an animal's diet if its potential food sources had different δ^(15)N values. The nitrogen isotopic method of dietary analysis probably can be used to estimate the relative use of legumes vs non-legumes or of aquatic vs terrestrial organisms as food sources for extant and fossil animals. However, the method probably will not be applicable in those modern ecosystems in which the use of chemical fertilizers has influenced the distribution of nitrogen isotopes in food sources. 
The isotopic method of dietary analysis was used to reconstruct changes in the diet of the human population that occupied the Tehuacan Valley of Mexico over a 7000 yr span. Variations in the δ^(15)C and δ^(15)N values of bone collagen suggest that C_4 and/or CAM plants (presumably mostly corn) and legumes (presumably mostly beans) were introduced into the diet much earlier than suggested by conventional archaeological analysis.

Influence of Diet On the Distribtion of Nitrogen Isotopes in Animals

The use of stable isotopes to solve biogeochemical problems in ecosystem analysis is increasing rapidly because stable isotope data can contribute both source-sink (tracer) and process information: The elements C, N, S, H, and all have more than one isotope, and isotopic compositions of natural materials can be measured with great precision with a mass spectrometer. Isotopic compositions change in predictable ways as elements cycle through the biosphere. These changes have been exploited by geochemists to understand the global elemental cycles. Ecologists have not until quite recently employed these techniques. The reasons for this are, first, that most ecologists do not have the background in chemistry and geochemistry to be fully aware of the possibilities for exploiting the natural variations in stable isotopic compositions, and second, that stable isotope ratio measurements require equipment not normally available to ecologists. This is unfortunate because some of the more intractable problems in ecology can be profitably addressed using stable isotope measurements. Stable isotopes are ideally suited to increase our understanding of element cycles in ecosystems. This review is written for ecologists who would like to learn more about how stable isotope analyses have been and can be used in ecosystem studies. We begin with an explanation of isotope terminology and fractionation, then summarize isotopic distributions in the C, N, and S biogeochemical cycles, and conclude with five case studies that show how stable isotope measurements can provide crucial information for ecosystem analysis. We restrict this review to studies of natural variations in C, N, and S isotopic abundances, cxcluding from consideration ~5N enrichment studies and hydrogen and oxygen isotope studies. Our focus on C, N, and S derives in part from our

Stable isotopes in ecosystem studies

Oxygen isotope records of five stalagmites from Hulu Cave near Nanjing bear a remarkable resemblance to oxygen isotope records from Greenland ice cores, suggesting that East Asian Monsoon intensity changed in concert with Greenland temperature between 11,000 and 75,000 years before the present (yr. B.P.). Between 11,000 and 30,000 yr. B.P., the timing of changes in the monsoon, as established with 230Th dates, generally agrees with the timing of temperature changes from the Greenland Ice Sheet Project Two (GISP2) core, which supports GISP2's chronology in this interval. Our record links North Atlantic climate with the meridional transport of heat and moisture from the warmest part of the ocean where the summer East Asian Monsoon originates.

http://science.sciencemag.org/content/sci/294/5550/2345.full.pdf

A High-Resolution Absolute-Dated Late Pleistocene Monsoon Record from Hulu Cave, China

The stable-carbon isotope ratios for the flesh of marine and terrestrial animals from Canada's Pacific coast differ by 7.9 +/- 0.4 per mil, reflecting the approximately 7 per mil difference between oceanic and atmospheric carbon. This difference is passed on to human consumers. The carbon isotopic values (delta(13)C) for human collagen thus yield direct information on the relative amounts of marine and terrestrial foods in prehistoric diets.

https://science.sciencemag.org/content/sci/216/4550/1131.full.pdf

Stable-Carbon Isotope Ratios as a Measure of Marine Versus Terrestrial Protein in Ancient Diets

Extracting nutrients is of upmost importance to the sur- vival of any individual or species. One of the distinguishing characteristics of the order Primates is the vast range of nutritional adaptations it exhibits. Within our own species all manner of adaptations are practiced and it has been a major focus of research to determine when and where these various patterns originated. We present one method based on stable isotope analysis in human tissues and discuss its contributions. The ratios of l3C/''C and 15N/14N vary among various pools (i.e., the atmosphere, the oceans, plant communities, trophic levels). These differences are transferred to humans via the foods they eat. The major differences in carbon occur between two photosynthetic pathways (C3 and C4), which in the New World permits tracing the introduction of maize (a C4 plant) and in Asia permits tracing the introduction of millet (also a C4 plant). The marine and terrestrial systems have distinctive isotope ratios of both carbon and nitrogen. Thus, the dependence on marine resources has been traced throughout several areas of the New and Old Worlds. We discuss several potential sources of variation including sex, age, nutritional status, among others. We conclude with some suggestions for future research.

/pdf/stable-isotope-analyses-in-human-nutritional-ecology-1q2es4xc05.pdf

Stable isotope analyses in human nutritional ecology

Fractionations of carbon and oxygen isotopes and magnesium between coexisting dolomite and calcite have been determined for marbles and calcareous schists of a wide variety of metamorphic environments from Vermont and the Grenville Province of Ontario. Concordant equilibrium fractionations are given by 83% of the samples. Calibration of the isotopic thermometers using the Mg-calcite solvus thermometer gave in the temperature range: 650°>T°>100°C 

$$ \begin{gathered} 1,000\ln \alpha _{D - Ct}^{O^{18} } = 0.45 (10^6 T^{ - 2} ) - 0.40 \hfill \\ 1,000\ln \alpha _{D - Ct}^{O^{18} } = 0.18 (10^6 T^{ - 2} ) + 0.17. \hfill \\ \end{gathered} $$

Fractionation of carbon and oxygen isotopes and magnesium between coexisting metamorphic calcite and dolomite

This paper investigates the utility of stable carbon and oxygen isotopes in human dental enamel to reveal patterns of breastfeeding and weaning in prehistory. Enamel preserves a record of childhood diet that can be studied in adult skeletons. Comparing different teeth, we used delta13C to document the introduction of solid foods to infant diets and delta18O to monitor the decline of breastfeeding. We report enamel carbonate delta13C and delta18O of 33 first molars, 35 premolars, and 25 third molars from 35 burials from Kaminaljuyu, an early state in the valley of Guatemala. The skeletons span from Middle Preclassic through Late Postclassic occupations, ca. 700 B.C. to 1500 A.D. Sections of enamel were removed from each tooth spanning from the cusp to the cemento-enamel junction. Stable isotope ratios were measured on CO2 liberated by reaction of enamel with H3PO4 in an automated carbonate system attached to a VG Optima mass spectrometer. Within a skeleton, teeth developing at older ages are more enriched in 13C and more depleted in 18O than teeth developing at younger ages. Premolars average 0.5/1000 [corrected] higher in delta13C than first molars from the same skeleton (P = 0.0001), but third molars are not significantly enriched over premolars. The shift from first molars to premolars may be due to the shift to solid foods from lipid-rich milk. After 2 years, when premolars begin to mineralize, the delta13C in childhood diets did not change systematically. First molars and premolars are similar in delta18O, but third molars average 0.7/1000 [corrected] lower than first molars (P = 0.0001) and 0.5/1000 [corrected] lower than premolars (P = 0.0003). First molar and premolar delta18O is heavier, because breast milk is more enriched in 18O than is drinking water. Hence, many children continued to nurse during the period of premolar formation. Together, these results indicate that Kaminaljuyu children had begun to eat solid maize foods before the age of 2 years but continued to drink breast milk until much later.

Henry P. Schwarcz

Papers

Stable-Carbon Isotope Ratios as a Measure of Marine Versus Terrestrial Protein in Ancient Diets

Stable isotope analyses in human nutritional ecology

Fractionation of carbon and oxygen isotopes and magnesium between coexisting metamorphic calcite and dolomite

Stable carbon and oxygen isotopes in human tooth enamel : identifying breastfeeding and weaning in prehistory

Infrared and Isotopic Evidence for Diagenesis of Bone Apatite at Dos Pilas, Guatemala: Palaeodietary Implications