Paleopedology as a Tool for Reconstructing Paleoenvironments and Paleoecology

Soils form as a product of physical, chemical, and biological activity at the outermost veneer of Earth’s surface. Once buried and incorporated into the sedimentary record, these soils, now paleosols, preserve archives of ancient climates, ecosystems, and sedimentary systems. Paleopedology, the study of paleosols, includes qualitative interpretation of physical characteristics and quantitative analysis of geochemical and mineralogical assays. In this chapter, the paleosol macroscopic, micromorphological, mineralogical, and geochemical indicators of paleoecology are discussed with emphasis on basic analytical and interpretative techniques. These data can reveal a breadth of site-specific interpretations of vegetation, sedimentary processes, climatic variables, and durations of landscape stability. The well-known soil-forming factors are presented as a theoretical framework for understanding landscape-scale soil evolution through time. Vertical and lateral patterns of stacked paleosols that appear in the rock record are discussed in order to address practical approaches to identifying and describing paleosols in the field. This chapter emphasizes a robust multi-proxy approach to paleopedology that combines soil stratigraphy, morphology, mineralogy, biology, and chemistry to provide an in-depth understanding of paleoecology

Pedogenic Iron Oxides in Iron-Rich Oxisols Developed from Mafic Rocks

Despite the considerable amount of information on the mineralogical characteristics of pedogenic Fe oxides in Brazilian soils, there are few studies on Fe-rich soils developed from mafic rocks with taxonomic identities at lower categorical levels. This study evaluated the mineralogical characteristics of pedogenic Fe oxides in B horizons (Bw) of Fe-rich Oxisols developed from several mafic rocks in the state of Minas Gerais, Brazil. The Bw horizons were sampled at a 0.8-1.0 m depth in 13 Ferric and Perferric Rhodic Oxisols along with a Mesoferric Typic Oxisol originating from basalt, gabbro, tuffite, amphibolite and itabirite in Minas Gerais. The selected soils have taxonomic identities up to the fourth categorical level of the Brazilian System of Soil Classification. In the laboratory, the following analyses were made: a) powder X ray diffraction (XRD) of the clay fraction before and after selective concentration of Fe oxides by silicate alkaline dissolution (5 mol L^-1 NaOH); b) selective chemical dissolution of the clay fraction by citrate-bicarbonate-dithionite (CBD), acid ammonium oxalate (AAO), and sulfuric acid (H2SO4 1.8 mol L^-1); c) quantitative estimation of minerals in the clay fraction through allocation of phases from the XRD patterns, magnetic susceptibility of the clay fraction, and quantification of elements after sulfuric acid digestion (H2SO4 1:1) of the air-dried fine earth and treatment of the clay fraction with CBD; and d) estimation of the mean crystal size (MCS), specific surface area (SSA), and isomorphic Al-substitution (IS) of hematite, goethite, and maghemite from the XRD patterns obtained from concentrates of Fe oxides. The results showed that estimation of Fe content of maghemite by selective dissolution with 1.8 mol L^-1 H2SO4 may not be accurate enough to realistically reflect the maghemite contents in the soil sample. The Al content extracted may also be influenced by other minerals that are sources of this element. Hematite crystals were predominantly placoid in shape in all Rhodic Oxisols and had smaller SSA compared to goethite, which showed both isodimensional and asymmetric habit. Higher crystallinity of maghemite and the IS values generally lower than those of hematite and goethite suggest that in well-drained soils derived from mafic rocks, the IS phenomenon in maghemites seems to result from pedogenetic advancement after its formation from magnetite oxidation