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Isaac Barshad

Bio: Isaac Barshad is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: Vermiculite & Montmorillonite. The author has an hindex of 13, co-authored 18 publications receiving 653 citations.

Papers
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Journal ArticleDOI
20 Dec 1968-Science
TL;DR: Oxidation of octahedral ferrous to ferric iron in soil vermiculite clays and biotites increases the potassium-fixation capacity of vermicULites and increases the difficulty of replacing interlayer potassium in biotite.
Abstract: Oxidation of octahedral ferrous to ferric iron in soil vermiculite clays and biotites increases the potassium-fixation capacity of vermiculites and increases the difficulty of replacing interlayer potassium in biotites. This unexpected effect is believed to be related to an increase in the attractive forces between potassium ions and oxygen ions of the surface layers which is brought about by a tilting of the dipole of the octahedral hydroxyl ions from a perpendicular position to an inclined position with respect to the cleavage plane.

51 citations


Cited by
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Journal ArticleDOI
01 Nov 2003-Geoderma
TL;DR: The generic framework, which the authors call the scorpanSSPFe (soil spatial prediction function with spatially autocorrelated errors) method, is particularly relevant for those places where soil resource information is limited.

2,527 citations

Journal ArticleDOI
15 May 2010-Geoderma
TL;DR: The conventional factor of 1.724, based on the assumption that soil organic matter contains 58% carbon, applies only to some soils or only to particular components of organic matter as mentioned in this paper.

699 citations

Journal ArticleDOI
TL;DR: In this paper, a review of the literature concerning selective sorption and fixation of K and similar cations by clay minerals and soil clays and the mechanisms of these reactions are reviewed.
Abstract: Investigations concerning selective sorption and fixation of K and similar cations by clay minerals and soil clays and the mechanisms of these reactions are reviewed. In particular, recent observations on selective sorption of these ions in dilute solutions by weathered micas and vermiculite in relation to the interlayer structures are discussed in detail. Also, implications of the resistance to weathering of small mica particles to cation selectivity by soils are described. Despite the increased understanding of sorption and fixation reactions, the following aspects remain unclear. First, the mechanism of the collapse of alternate layers in vermiculite on K or Cs sorption has not been unequivocally established. Second, factors that impart stability to the central core of mica particles so that K extraction becomes progressively difficult are not known. Third, inability of Ca or Mg ions to expand interlayers of Cs-saturated vermiculite in contrast to K-saturated vermiculite is not completely understood.

602 citations

Book ChapterDOI
01 Jan 1986

440 citations

Book ChapterDOI
TL;DR: In this paper, a review brings together fundamental aspects of soil acidification and recent developments on the implications of liming in relation to soil processes, particularly nutrient and heavy metal transformation and bioavailability in soils.
Abstract: “ No other single chemical soil characteristic is more important in determining the chemical environment of higher plants and soil microbes than the pH There are few reactions involving any component of the soil or of its biological inhabitants that are not sensitive to soil pH This sensitivity must be recognized in any soil-management system” “ Lime is truly a foundation for much of modern humid-region agriculture Knowing how pH is controlled, how it influences the supply and availability of essential plant nutrients as well as toxic elements, how it affects higher plants and human beings, and how it can be ameliorated is essential for the conservation and sustainable management of soils throughout the world” (Brady and Weil, 1999) Under areas where rainfall exceeds evapotranspiration, soil acidification is an ongoing natural process, which can either be accelerated by the activity of plants, animals and humans or can be impeded by careful management practices In areas affected by industrial activities, soil acidification is caused by acid drainage from pyrite oxidation and also from acid precipitation In areas that remain unaffected by industrial pollution, soil acidification in managed ecosystems is mainly caused by the release of protons (H + ) during the transformation and cycling of carbon (C), nitrogen (N) and sulfur (S) Just like in managed ecosystems, soil acidification in natural ecosystems caused by acid drainage and acid precipitation can have adverse impacts where soils have low pH buffering capacity Liming is the most common management practice aimed at neutralizing the acid produced, thereby overcoming the adverse impacts of soil acidification This review brings together fundamental aspects of soil acidification and recent developments on the implications of liming in relation to soil processes, particularly nutrient and heavy metal transformation and bioavailability in soils The article first outlines the various soil, plant and microbial processes that generate acid (protons; H + ions) both under natural and managed ecosystems It then discusses the effects of soil acidity on soil chemical and biological properties The effect of liming to overcome the problems associated with soil acidity is examined in relation to the transformation of nutrient ions and heavy metals The practical implications of liming to overcome heavy metal toxicity have been discussed in relation to the adsorption, leaching and phytoavailability of these metal ions Future research should aim to focus on the development of methods to quantify lime-enhanced (im)mobilization of nutrient ions and heavy metals in soils and to explore further the role of liming in remediating contaminated soils

433 citations