This book is written as a reference on organic substances in natural waters and as a supplementary text for graduate students in water chemistry. The chapters address five topics: amount, origin, nature, geochemistry, and characterization of organic carbon. Of these topics, the main themes are the amount and nature of dissolved organic carbon in natural waters (mainly fresh water, although seawater is briefly discussed). It is hoped that the reader is familiar with organic chemistry, but it is not necessary. The first part of the book is a general overview of the amount and general nature of dissolved organic carbon. Over the past 10 years there has been an exponential increase in knowledge on organic substances in water, which is the result of money directed toward the research of organic compounds, of new methods of analysis (such as gas chromatography and mass spectrometry), and most importantly, the result of more people working in this field. Because of this exponential increase in knowledge, there is a need to pull together and summarize the data that has accumulated from many disciplines over the last decade.

Organic geochemistry of natural waters

Dissolved organic matter (DOM) in soils plays an important role in the biogeochemistry of carbon, nitrogen, and phosphorus, in pedogenesis, and in the transport of pollutants in soils. The aim of this review is to summarize the recent literature about controls on DOM concentrations and fluxes in soi

Controls on the dynamics of dissolved organic matter in soils: a review.

Interpretation of X-ray Powder Diffraction Patterns . By H. Lipson and H. Steeple. Pp. viii + 335 + 3 plates. (Mac-millan: London; St Martins Press: New York, May 1970.) £4.

X-Ray Diffraction

http://andrewsforest.oregonstate.edu/pubs/pdf/pub1374.pdf

Stabilization and destabilization of soil organic matter: mechanisms and controls

Organic Matter Characterization

Adsorption isotherms were obtained for fulvic and humic acids on synthetic gibbsite and goethite and on a natural imogolite. The results were interpreted with the help of spectra of the adsorption complexes, and measurements of hydroxyl displaced. The mechanism of adsorption involved ligand exchange with the surface hydroxyl groups and hydrogen bonding. The hydroxyl groups displaced included singly coordinated species on the (100) face of goethite and on the edge faces of gibbsite. The doubly coordinated hydroxyl groups on the (001) face of gibbsite were not replaced, and this face adsorbed only un-ionized fulvic acid probably by a hydrogen bonding mechanism. Imogolite adsorbed most fulvic acid because of its high porosity. Only isolated places on its surface reacted with fulvic acid to form carboxylate groups.

Adsorption on hydrous oxides.III.Fulvic acid and humic acid on goethite,gibbsite and imogolite

Replacement of kaolinite by dickite has been observed to occur with increasing depth of burial in sandstones from three different basins on the Norwegian continental shelf. In the Garn Formation (Middle Jurassic) of Haltenbanken, samples from 1.4-2-7 km below the sea floor (110°C) contain kaolinite, whereas deeper than 3.2 km (130°C) mainly dickite is present. In the Statfjord Formation (Late Triassic-Early Jurassic) from Gullfaks and Gullfaks Sor Fields, transformation of kaolinite to dickite occurs at ~3.1 km below the sea floor (120°C) From the Sto and Nordmela Formations (Lower to Middle Jurassic) to the Troms Area, kaolin polytypes have been identified in only two shallow and two deep samples, but the results are consistent with the transformation depth determined in two other areas studied. These occurrences are significant because they allow the temperature of the kaolinite/dickite transformation to be established with greater confidence than had been possible previously. Also the observation of this transformation in all three areas so far examined indicates that it may be a general and predictable feature of kaolinbearing sandstones worldwide and therefore a potentially reliable paleogeothermometer. In most cases, the kaolinite occurs as relatively large vermicular crystals, whereas dickite forms more euhedral, blockier crystals. This morphological difference, together with the nature of the structural difference in octahedral occupancy between the kaolinite and dickite, suggests that the transformation occurs by dissolution and reprecipitation, rather then in the solid state.

Depth-dependent transformation of kaolinite to dickite in sandstones of the Norwegian continental shelf

Mossbauer and i.r. spectra of a series of nontronites show that Fe3+ and Al3+ are distributed between tetrahedral and octahedral sites. The Mossbauer results have reaffirmed the occupation by Fe3+ of octahedral sites at which these ions are coordinated to pairs of OH groups in both cis and trans configurations. The distribution of Fe3+ between these two sites varies considerably but in all of the nontronites some Fe3+ occurs in the trans site in contrast to the all cis occupancy of the centro-symmetric structure proposed by Mering and Oberlin (1967). In one of the nontronites the distribution of Fe3+ between these two sites approaches that in the ideal non-centrosymmetric structure proposed for montmorillonite.

A Mössbauer and I.R. Spectroscopic Study of the Structure of Nontronite

Heating weakly acidic dilute solutions containing hydroxyaluminium orthosilicate complexes gives a fibrous polymer, each fibre consisting of tubes about 2·2 nm external diameter and 1·0 nm internal diameter, essentially identical with those of the natural mineral, imogolite.

Synthesis of imogolite: a tubular aluminium silicate polymer

INFRARED studies of surface hydroxyls on solids of high area have been limited to almost anhydrous materials prepared at elevated temperatures. These studies have made an important contribution to the understanding of surface catalysis, but have little relevance to adsorption processes that occur on moist surfaces at ambient temperatures. Such processes contribute to a wide range of everyday phenomena, including the retention of fertilisers and pesticides in soils.

Anthony R. Fraser

Papers

Adsorption on hydrous oxides.III.Fulvic acid and humic acid on goethite,gibbsite and imogolite

Depth-dependent transformation of kaolinite to dickite in sandstones of the Norwegian continental shelf

A Mössbauer and I.R. Spectroscopic Study of the Structure of Nontronite

Synthesis of imogolite: a tubular aluminium silicate polymer

Surface structures of gibbsite goethite and phosphated goethite