Relations of mineral-soil C and N to climate and texture: regional differences within the conterminous USA

Soil is a prominent component of terrestrial C and N budgets. Soil C and N pools are influenced by, and may reciprocally influence, many environmental factors. Our objective was to determine the quantitative relations of surface mineral-soil organic C, N, and C/N ratios to climate and soil texture across seven ecological regions that make up the conterminous USA. Up to 608 soil profiles per region and their corresponding climates were evaluated with regression analysis. The organic C pool (kg C m⁻²) in the upper 20 cm of mineral soil was positively related to mean annual precipitation, evapotranspiration and clay content in all regions. It was negatively related to a temperature/precipitation index in all regions and negatively related to mean annual temperature, except in the northwest temperate forest region. Soil C/N ratios were negatively related to clay or silt content in all regions. These relations are consistent with concepts of moisture and temperature controls on detrital production, differential effects of temperature on detrital production and decomposition, and stabilization of organic matter by clay and silt. Differences in quantitative relations among regions may be related to vegetation-composition effects on soil organic matter processes, clay mineralogy, and faunal mixing of surface organic horizons with mineral soil. Regional differences also occurred in the importance of climate vs. soil texture in explaining the variability in soil C. The regional differences indicate the importance of using region-specific, rather than generalized, equations for projecting long-term soil responses to climate change and for conducting ecosystem-model calibration or validation.     

Clay Mineralogy of Central Victorian (Creswick) Soils: Clay Mineral Contents as a Possible Tool of Environmental Indicator

The clay mineralogy and heavy metal/metalloid (As, Pb and Cu) contents of soils developed on the various rock units in a central highlands environment in Victoria (Creswick, Australia) have been investigated. The clay minerals identified showed an order of abundance as: kaolinite ? illite > smectite > mixed-layer (ML) ≈ vermiculite. The soil clay mineralogy did not change systematically with depth (0～ 10, 10～ 20 and 20～ 30 cm) and showed large variations spatially. The high proportion of kaolinite was probably due to the removal of 2:1 phyllosilicates by the formation of 1:1 kaolinite through weathering, which also reduced the cation exchange capacity (CEC) and electrical conductivity (EC, soil: water ratio of 1:5) of soils by aging. Soils were classified as silty loam to loam with a low clay size (≤ 2μ m) fraction. The soils were acidic to moderately acidic with pH ranging from 4.5 to 7.1, averaging 5.7. Concentrations of As, Pb, and Cu (average values 24.3, 16.7 and 11.0 mg/kg, respectively) did not show an association with the clay mineral contents except vermiculite. The occurrence of smectite and mixed-layer clay contents, although far lower than kaolinite and illite, contributed significantly to CEC of soils. The study area was affected by mining, high natural background As values dominate the area and the role of clay minerals in fixation of metalloid/metals was found to be less significant. Low organic matter content (average ～ 6.5%), low soil surface area (average ～ 1.0 m²/g) and the high proportion of kaolinite mineral content result in a limited ability to fix heavy metals. The role of Fe oxides appeared to be a key influence in the fixation of As and other potentially toxic metals, rather than the clay minerals, and therefore requires further research. This work highlighted the importance of the determination of types and amounts of clay minerals of natural soils in environmental management.     

Similar composition but differential stability of mineral retained organic matter across four classes of clay minerals

Adsorption of dissolved organic compounds onto mineral surfaces is increasingly recognized as a significant, if not dominant, carbon stabilisation mechanism in many soils. By utilising carbon-13 enriched dissolved organic carbon (DOC) source materials in a repeated leaching-sorption-incubation study, we show here that the biochemical composition of mineral-retained organic matter (OM) is similar across four different classes of clay minerals but the quantity and stability of this OM is both a function of source material and clay mineralogy. Three to eight times as much carbon was retained on a mass basis when the same amount of DOC derived from eucalyptus versus wheat litter was applied, and the retained wheat-derived OM was up to 2.4 times more degradable than that of the eucalyptus source. For both litter types, carbon retention across the clay types was not significantly different; whereas, the stability of the retained OM was different but depended on which litter extract had been applied. The wheat-derived DOC was more stable when retained by allophane and oxides than by illite and smectite. Solid-state ¹³C NMR spectroscopic results indicated that despite large compositional differences in both source litter and resultant DOC, the composition of the mineral-retained OM was similar across clay classes with lignin-derived aromatic and carboxylic compounds dominating. Differences in the amount of carbon retained were related to differences in the proportions of aromatic, phenolic and carboxylic C in the DOC produced from the two litter sources. Differences in the stability across the clay classes were correlated with the abundance of metals and short-range ordered minerals. These results suggest that whenever reactive mineral surfaces and metals are present in a soil, a similar form of relatively unaltered litter derived OM can be adsorbed but that the longer term stability of sorbed OM, and thus in situ composition, will be a function of the mineralogy (reactivity) of the specific minerals involved in the binding process.     

Clay minerals as a soil potassium reservoir: observation and quantification through X-ray diffraction

Potassium (K) is a major element for plant growth. The K⁺ ions fixed in soil 2:1 clay mineral interlayers contribute to plant K nutrition. Such clay minerals are most often the majority in temperate soils. Field and laboratory observations based on X-ray diffraction techniques suggest that 2:1 clay minerals behave as a K reservoir. The present work investigated this idea through data from a replicated long term fertilization experiment which allowed one to address the following questions: (1) Do fertilization treatments induce some modifications (as seen from X-ray diffraction measurements) on soil 2:1 clay mineralogy? (2) Are soil 2:1 clay mineral modifications related to soil K budget in the different plots? (3) Do fertilizer treatments modify clay Al, Si, Mg, Fe or K elemental content? (4) Are clay mineral modifications related to clay K content modifications? (5) Are clay mineral changes related to clay Al, Si, Mg or Fe content as well as those of K content? Our results showed that K fertilization treatments considered in the context of soil K budget are very significantly related to 2:1 soil clay mineralogy and clay K content. The 2:1 clay mineral modifications observed through X-ray measurements were quantitatively correlated with chemically analyzed clay K content. Clay K content modifications are independent from clay Al, Si, Mg or Fe contents. These results show that the soil chemical environment can modify interlayer site occupations (illite content) which suggests that high level accumulation of potassium can occur without any modification of the clay sheet structure. This study therefore validates the view of 2:1 clay minerals as a K reservoir easily quantifiable through X-ray observations.     

Status of copper in some calcareous and non-calcareous soils of Egypt

Summary To assess the status of copper in Egyptian soils, surface and subsurface soil samples were collected from various geographical regions of Egypt and of various genesis. The samples were analyzed for the total Cu, water-soluble plus exchangeable as well as the acid-extractable and EDTA-extractable Cu. The total Cu varied between 3.5 and 72.3 ppm. Less than 2% of this copper was in the soluble plus exchangeable form. The highest values of total and soluble plus exchangeable copper were found in the alluvial soils while the sandy soils had the least amounts. This was attributed to the high clay and organic matter content of the alluvial soils in addition to the dominance of montmorillonitic clay minerals in their fine fraction. The calcareous soils showed intermediate values of total and soluble plus exchangeable Cu due to their lower organic matter and clay mineral content. The clay mineralogy of these soils revealed the dominance of illitic and kaolinitic minerals which are relatively poor in Cu and other trace elements.Because of their relatively higher organic matter content, the alluvial soils had a large percentage (up to 43%) of their total Cu in the EDTA extractable form. The calcareous soils, on the other hand, had a large percentage (up to 52%) of their Cu in the acid-extractable form. The EDTA extractable Cu was correlated with the organic matter content of the soils. Since the pH of the EDTA extract was found to be dependent on the CaCO₃ content of the soils, it was suggested that the method be modified so that the final pH of the extract is constant for all soils.     

The role of clay minerals in the preservation of Precambrian organic-walled microfossils

Precambrian organic-walled microfossils (OWMs) are primarily preserved in mudstones and shales that are low in total organic carbon (TOC). Recent work suggests that high TOC may hinder OWM preservation, perhaps because it interferes with chemical interactions involving certain clay minerals that inhibit the decay of microorganisms. To test if clay mineralogy controls OWM preservation, and if TOC moderates the effect of clay minerals, we compared OWM preservational quality (measured by pitting on fossil surfaces and the deterioration of wall margins) to TOC, total clay, and specific clay mineral concentrations in 78 shale samples from 11 lithologic units ranging in age from ca. 1650 to 650 million years ago. We found that the probability of finding well-preserved microfossils positively correlates with total clay concentrations and confirmed that it negatively correlates with TOC concentrations. However, we found no evidence that TOC influences the effect of clay mineral concentrations on OWM preservation, supporting an independent role of both factors on preservation. Within the total clay fraction, well-preserved microfossils are more likely to occur in shales with high illite concentrations and low berthierine/chamosite concentrations; however, the magnitude of their effect on preservation is small. Therefore, there is little evidence that bulk clay chemistry is important in OWM preservation. Instead, we propose that OWM preservation is largely regulated by physical properties that isolate organic remains from microbial degradation such as food scarcity (low TOC) and low sediment permeability (high total clay content): low TOC increases the diffusive distances between potential carbon sources and heterotrophic microbes (or their degradative enzymes), while high clay concentrations reduce sediment pore space, thereby limiting the diffusion of oxidants and degradative enzymes to the sites of decay.     

Accumulation and soil-to-plant transfer of radionuclides in the Nile Delta coastal black sand habitats

The radionuclide content was estimated in the soil of three black sand habitats in the Mediterranean coast of Egypt, namely, sand mounds and coastal sand planes and dunes. In addition, a total of 14 heavy minerals found in the soils were characterized. The soil to plant transfer of uranium and thorium was tested on three black sand species, namely, Cakile maritima Scop., Senecio glaucus L. and Rumex Pictus Forssk. The transfer of thorium and uranium radionuclides from the soil to plant is complex process that is subjected to many variables; among which are the organic matter and clay content of the soil, the type of radionuclides and plant species. The study revealed a strong negative relationship between uranium and thorium uptake by S. glaucus and R. pictus and the clay and organic matter content of soil. Concentration of thorium in the soil has a negative correlation with soil-to-plant transfer factor. The study results suggest the possibility of using black sand species for phytoremediation of soils contaminated with radioactive elements. The potentiality of S. glaucus as phytoremediator of radionuclides polluted soils is greater than R. pictus which in turn outweigh C. maritima.     

Visible near-infrared reflectance spectroscopy as a predictive indicator of soil properties

It is becoming increasingly important to improve spatial resolutions of soil maps as a fundamental information layer for studying ecological processes and to tackle land degradation. There is growing interest in the use of remote sensing technologies to assist the identification and delineation of spatial variation in soils. This paper investigates whether selected properties of extensively weathered, low fertility soils can be predicted using high-resolution reflectance spectra over the range 400–2500 nm. Clay content, carbonate concentration, organic carbon content and iron oxide content were analysed for 300 soil samples collected from the Jamestown, Belalie district, South Australia. The paper also examines the efficacy of this soil analysis methodology to supplement or replace traditional soil sampling in soil survey to increase sampling density and improve the spatial resolution of soil maps.Reflectance spectra were obtained from air-dried samples under controlled laboratory conditions using an ASD FieldSpec Pro spectroradiometer. Partial least squares regression was used to examine relationships between soil mineralogy, clay content and organic carbon and the reflectance spectra and identify the wavelengths contributing to prediction of these soil properties. Results show that it is possible to predict clay content, soil organic carbon, iron oxide content and carbonate content. Cross-validation R² values for all analyses were above 0.5 and the residual prediction difference (RPD) was acceptable for all soil properties. Carbonate and clay content were more accurately predicted than iron oxide and organic carbon. All samples were collected from the same geographical area such that they represented physical properties over a naturally occurring range and provide a prediction that could be related to subsequent image analysis or be used to carry out local scale soil survey. A rapid and reliable form of soil mapping could be developed from this methodology.     

Geochemistry and clay mineralogy of soils eaten by Japanese macaques

Three groups of soils from two Japanese monkey parks at Arashiyama (Honshu) and Takasakiyama (Kyushu) were analyzed for their geochemistry and clay and primary mineral content. Two groups (Y and T) of soils are regularly eaten by Japanese macaques; a third group (N) is not eaten. Of the elements analyzed, soil group N (not eaten) is within the range of all elements in the Y group, and is very different from the T group. These preliminary data suggest there is no chemical stimulus in soil eating behaviour. We also analyzed the mineralogy of the clay fraction (<2 μm) but could find only a possible stimulus from ingesting plagioclase and orthoclase minerals. The clay mineral content consists of small to trace amounts of metahalloysite that might play a role in countering the effects of diarrhea. However, from the available data there are no clear trends that would provide a stimulus for geophagic behaviour.     

Temperature and vegetation effects on soil organic carbon quality along a forested mean annual temperature gradient in North America

Both climate and plant species are hypothesized to influence soil organic carbon (SOC) quality, but accurate prediction of how SOC process rates respond to global change will require an improved understanding of how SOC quality varies with mean annual temperature (MAT) and forest type. We investigated SOC quality in paired hardwood and pine stands growing in coarse textured soils located along a 22 °C gradient in MAT. To do this, we conducted 80‐day incubation experiments at 10 and 30 °C to quantify SOC decomposition rates, which we used to kinetically define SOC quality. We used these experiments to test the hypotheses that SOC quality decreases with MAT, and that SOC quality is higher under pine than hardwood tree species. We found that both SOC quantity and quality decreased with increasing MAT. During the 30 °C incubation, temperature sensitivity (Q₁₀) values were strongly and positively related to SOC decomposition rates, indicating that substrate supply can influence temperature responsiveness of SOC decomposition rates. For a limited number of dates, Q₁₀ was negatively related to MAT. Soil chemical properties could not explain observed patterns in soil quality. Soil pH and cation exchange capacity (CEC) both declined with increasing MAT, and soil C quality was positively related to pH but negatively related to CEC. Clay mineralogy of soils also could not explain patterns of SOC quality as complex (2 : 1), high CEC clay minerals occurred in cold climate soils while warm climate soils were dominated by simpler (1 : 1), low CEC clay minerals. While hardwood sites contained more SOC than pine sites, with differences declining with MAT, clay content was also higher in hardwood soils. In contrast, there was no difference in SOC quality between pine and hardwood soils. Overall, these findings indicate that SOC quantity and quality may both decrease in response to global warming, despite long‐term changes in soil chemistry and mineralogy that favor decomposition.     

Short-term effects of biological and physical forces on aggregate formation in soils with different clay mineralogy

The mechanisms resulting in the binding of primary soil particles into stable aggregates vary with soil parent material, climate, vegetation, and management practices. In this study, we investigated short-term effects of: (i) nutrient addition (Hoagland's solution), (ii) organic carbon (OC) input (wheat residue), (iii) drying and wetting action, and (iv) root growth, with or without dry–wet cycles, on aggregate formation and stabilization in three soils differing in weathering status and clay mineralogy. These soils included a young, slightly weathered temperate soil dominated by 2:1 (illite and chlorite) clay minerals; a moderately weathered soil with mixed [2:1 (vermiculite) and 1:1 (kaolinite)] clay mineralogy and oxides; and a highly weathered tropical soil dominated by 1:1 (kaolinite) clay minerals and oxides. Air-dried soil was dry sieved through a 250 m sieve to break up all macroaggregates and 100 g-subsamples were brought to field capacity and incubated for 42 days. After 14 and 42 days, aggregate stability was measured on field moist and air-dried soil, to determine unstable and stable aggregation respectively. In control treatments (i.e., without nutrient or organic matter addition, without roots and at constant moisture), the formation of unstable and stable macroaggregates (> 250 m) increased in the order: 2:1 clay soil < mixed clay soil < 1:1 clay soil. After 42 days of incubation, nutrient addition significantly increased both unstable and stable macroaggregates in the 2:1 and 1:1 clay soils. In all soils, additional OC input increased both unstable and stable macroaggregate formation. The increase in macroaggregation with OC input was highest for the mixed clay soil and lowest for the 1:1 clay soil. In general, drying and wetting cycles had a positive effect on the formation of macroaggregates. Root growth caused a decrease in unstable macroaggregates in all soils. Larger amounts of macroaggregates were found in the mixed clay and oxides soil when plants were grown under 50% compared to 100% field capacity conditions. We concluded that soils dominated by variable charge clay minerals (1:1 clays and oxides) have higher potential to form stable aggregates when OC concentrations are low. With additional OC inputs, the greatest response in stable macroaggregate formation occurred in soils with mixed mineralogy, which is probably a result of different binding mechanisms occurring: i.e., electrostatic bindings between 2:1 clays, 1:1 clays and oxides (i.e. mineral-mineral bindings), in addition to OM functioning as a binding agent between 2:1 and 1:1 clays.     

Secular distribution of Burgess-Shale-type preservation

Burgess-Shale-type preservation is defined as a taphonomic pathway involving the exceptional organic preservation of non-mineralizing organisms in fully marine siliciclastic sediments. In the Phanerozoic it occurs widely in Lower and Middle Cambrian sequences but subsequently disappears as a significant taphonomic mode. The hypothesis that this distribution derives solely from a secular increase in the depth of bioturbation is falsified: low bioturbation indices do not prevent the rapid enzymatic degradation of organic structure, nor do they account for the conspicuous absence of comparable preservation during the Vendian. An earlier, Late Riphean (ca. 750–850 Ma), interval of enhanced organic-walled fossil preservation suggests a long-term recurrence in Burgess-Shale-type taphonomy that is independent of metazoan activity. A model based on the potentially powerful anti-enzymatic and/or stabilizing effects of clay minerals on organic molecules is proposed to account for Burgess-Shale-type preservation. Long-term changes in average clay mineralogies and the ocean chemistry that determines their interaction with organic molecules are likely to have induced the pronounced secular distribution of these fossil biotas, while regional variations in tectonism, weathering, etc., explain their non-uniform geographic distribution; the close correlation between exceptional, organic-walled fossil preservation and volcano-genic sedimentation in Tertiary lake deposits provides a compelling analogue. Recognition of a temporal control on Burgess-Shale-type preservation constrains the evolutionary scenarios that can be drawn from such biotas; significantly, neither the initial rate of appearance, nor the ultimate fate of Burgess-Shale-type taxa can be directly assessed. □ Taphonomy, exceptional preservation, organic preservation, fossil Lagerstätten, Burgess Shale, clay mineralogy, clay-organic interactions, secular change, Cambrian, Proterozoic.     

Possible effect between the molecular packing of collagen and the composition of bony tissues

The weight fractions of the organic, mineral and water components of bone have been shown to be uniquely related to the wet bone density, except for a small variation possibly due to structure, for the range of bone densities from 1.7 g/cm³ for deer antler to 2.7 g/cm³ for porpoise petrosal. In this report the mathematical expression for the organic weight fraction is shown to depend on three factors, each a function of bone density. The first factor can be ralated to the mineral fraction, the second to the volume fraction of the organic component and the third to the density of the organic component. The influence of these factors is not obvious, since the change in the organic weight fraction could be due to an absolute loss of organic matter alone, or to a combination of increased mineral concentration together with some loss of organic matter. The mathematical development is based on the generalized packing model for collagen. It is demonstrated that the mineralization process requires a decrease of the organic component as well as a compaction of the collagen fibrils and these vary with the bone density.     

Relationship between the weathering of clay minerals and the nitrification rate: a rapid tree species effect

We compared the properties of the clay mineral fraction and the composition of soil solutions in a Fagus sylvatica coppice (native forest) and four adjacent plantations of Pseudotsuga menziesii, Pinus nigra, Picea abies and Quercus sessiliflora planted in 1976. The results revealed changes of clay fraction properties due to tree species effect. Clay samples from Douglas fir and pine stands differ when compared to other species. Twenty-eight years after planting, we observed the following changes: a more pronounced swelling after citrate extraction and ethylene glycol solvation, a higher CEC and a smaller poorly crystallised aluminium content. All these changes affecting the clay fraction agreed well with soil solution analyses which revealed high NO₃ ^?, H⁺ and Al concentrations under Douglas fir and pine. These changes were explained by a strong net nitrification under Douglas fir and pine stands when compared with other tree species. The higher NO₃ ^? concentrations in soil solutions should be linked to the presence, type and activity of ammonia-oxiding bacteria which are likely influenced by tree species. The production of NO₃ ^? in excess of biological demand leads to a net production of hydrogen ion and enhances the dissolution of poorly crystallised Al-minerals. Secondary Al-bearing minerals constituted the principal acid-consuming system in these soils. As a consequence, the depletion of interlayer spaces of hydroxyinterlayered minerals increases the number of sites for exchangeable cation fixation and increases CEC of the clay fraction. The dissolution of Al oxy-hydroxides explain the increase in Al concentrations of soil solutions under Douglas fir and pine stands when compared to other species. Nitrate and dissolved aluminium were conjointly leached in the soil solutions. A change in environmental conditions, like an introduction of tree species, enough modifies soil processes to induce significant changes in the soil mineralogical composition even over a period of time as short as some tens of years. Generally, mineral weathering has been considered to be very slow and unlikely to change over tens of years, resulting in few studies capable of detecting changes in mineralogy. This study appears to have detected changes in clay mineralogy during a period of 28 years after the planting of forest species. Our study represents a single location with a limited block design, but causes us to conclude that the observed changes could be widely representative. Where available, archived samples should be utilized and long-term experiments set up so that similar changes can be tested for and detected using more robust designs. The plausible hypothesis we present to explain apparent changes in clay mineralogy has strong relevance to the sustainable management of land.     

Geochemistry and clay mineralogy of termite mound soil and the role of geophagy in chimpanzees of the Mahale Mountains,Tanzania

Earth from a termite mound in the Mahale Mountains National Park, Tanzania, eaten by chimpanzees, was analyzed to determine the possible stimulus, or stimuli, for geophagy. The termite mound sample contains relatively high aluminum (10.0%), iron (3.0%), and sodium (0.5%). This correlates well with the mineralogy of the clay (<2 μm) fraction, which is high in metahalloysite, a 1:1 (Si:Al=1:1) clay mineral similar in chemical composition to the clay mineral kaolinite, and smectite (montmorillonite), which is a 2:1 expandable clay mineral. The combination of metahalloysite and smectite produces a substance much like the pharmaceutical Kaopectate^™ widely used by humans as an anti-diarrheal agent. These analyses and preliminary observations linking geophagy with instances of severe diarrhea, and other signs of gastrointestinal upset in the Mahale chimpanzees, suggest that one function for the ingestion of this substance by chimpanzees may be to help provide temporary relief from gastrointestinal ailments. Further detailed investigations into the relationship between health and geophagy should provide important insights into the diverse roles of this behavior as a form of self-medication.     

Bacterial trace fossils in eocene kaolin of the huber formation of Georgia; phylloderma microsphaeroides,n. ichnogen., n. ichnosp.

An Eocene kaolin deposit in Georgia contains microspheres of tangentially oriented kaolinite enclosing authigenic cristobalite/tridymite overgrown with kaolinite. These structures resemble cutans of clay minerals that surround polysaccharide‐covered bacteria in recent soils and sediments. Bacteria actively synthesize anionic mucopolysaccharides as adhesives for attachment to surfaces. Empty cutans are common; these polymer‐bound clay mineral microspheres persist following cell death and lysis. Even though the void space thus created and associated organic material influence subsequent diagenetic changes, sedimentary microfabrics attributable to bacterial activity are preserved.     

新疆其木干剖面中新世-上新世沉积物粘土矿物特征及其古气候指示意义

为重建新疆其木干地区中新世-上新世古气候,采用X射线衍射、扫描电子显微分析方法,对该区中新世-上新世沉积物中粘土矿物的相对含量、组合类型及显微形貌等进行了研究。结果显示:中新世早期-早中新世中期,沉积物中粘土矿物以伊利石和绿泥石为主,含少量的蒙脱石,表明以干旱气候为特征;晚中新世中期-早中新世晚期,伊利石的相对含量逐渐降低,且含有少量的蒙脱石和高岭石,指示相对温湿的气候条件;中新世晚期的粘土矿物组分与中新世早期相似,以伊利石和绿泥石为主,指示古气候以干旱为主导;晚中新世晚期至上新世伊利石相对含量降低,而蒙脱石和高岭石的相对含量升高,但由于粘土矿物中伊利石、绿泥石的含量仍然较高,指示古气候仍然以干旱为主导,但相对于中新世而言,这段时期为相对湿润期。以上结果表明,新疆其木干地区中新世-上新世古气候以干旱为主,并且气候经历了干旱-相对湿润-干旱-相对湿润的演化过程,但总体而言,本区中新世比上新世要更为干旱。     

Calcite and aragonite seas and the de novo acquisition of carbonate skeletons

A longstanding question in paleontology has been the influence of calcite and aragonite seas on the evolution of carbonate skeletons. An earlier study based on 21 taxa that evolved skeletons during the Ediacaran through Ordovician suggested that carbonate skeletal mineralogy is determined by seawater chemistry at the time skeletons first evolve in a clade. Here I test this hypothesis using an expanded dataset comprising 40 well‐defined animal taxa that evolved skeletons de novo in the last 600 Myr. Of the 37 taxa whose mineralogy is known with some confidence, 25 acquired mineralogies that matched seawater chemistry of the time, whereas only two taxa acquired non‐matching mineralogies. (Ten appeared during times when seawater chemistry is not well constrained.) The results suggest that calcite and aragonite seas do have a strong influence on carbonate skeletal mineralogy, however, this appears to be true only at the time mineralized skeletons first evolve. Few taxa switch mineralogies (from calcite to aragonite or vice versa) despite subsequent changes in seawater chemistry, and those that do switch do not appear to do so in response to changing aragonite–calcite seas. This suggests that there may be evolutionary constraints on skeletal mineralogy, and that although there may be increased costs associated with producing a mineralogy not favored by seawater, the costs of switching mineralogies are even greater.     

Rhizospheric Processes Influencing the Biogeochemistry of Forest Ecosystems

In the rhizosphere, biotic and abiotic processes interact to create a zone distinct from the bulk soil that may strongly influence the biogeochemistry of forest ecosystems. This paper presents a conceptual model based upon three operationally defined soil-root compartments (bulk soil, rhizosphere and soil-root interface) to assess nutrient availability in the mineral soil-root system. The model is supported by chemical and mineralogical analyses from bulk and rhizosphere soils collected from a Norway spruce forest. The rhizosphere was more intensively weathered and had accumulated more acidity, base cations and phosphorus than the bulk soil. The quantity and quality of organic matter regulate the reciprocal relationships between soil and roots with their associated biota. However, the biogeochemical role of organic matter in the rhizosphere still remains as an area in which more future research is needed. The mechanisms that may regulate nutrient availability in the rhizosphere are also discussed and related to nutrient cycling and adaptation of forests growing under nutrient poor or perturbed conditions. We suggest that the rhizosphere is not an ephemeral environment in the soil, but persists over time and is resilient against perturbation as evinced by consistent differences between rhizosphere and bulk chemistry and mineralogy over wide range of field treatments.     

Potential role of soil properties in the spread of CWD in western Canada

Chronic wasting disease (CWD) is a horizontally transmissible prion disease of free ranging deer, elk and moose. Recent experimental transmission studies indicate caribou are also susceptible to the disease. CWD is present in southeast Alberta and southern Saskatchewan. This CWD-endemic region is expanding, threatening Manitoba and areas of northern Alberta and Saskatchewan, home to caribou. Soil can serve as a stable reservoir for infectious prion proteins; prions bound to soil particles remain infectious in the soils for many years. Soils of western Canada are very diverse and the ability of CWD prions to bind different soils and the impact of this interaction on infectivity is not known. In general, clay-rich soils may bind prions avidly and enhance their infectivity comparable to pure clay mineral montmorillonite. Organic components of soils are also diverse and not well characterized, yet can impact prion-soil interaction. Other important contributing factors include soil pH, composition of soil solution and amount of metals (metal oxides). In this review, properties of soils of the CWD-endemic region in western Canada with its surrounding terrestrial environment are described and used to predict bioavailability and, thus, potential spread of CWD. The major soils in the CWD-endemic region of Alberta and Saskatchewan are Chernozems, present in 60% of the total area; they are generally similar in texture, clay mineralogy and soil organic matter content, and can be characterized as clay loamy, montmorillonite (smectite) soils with 6–10% organic carbon. The greatest risk of CWD spread in western Canada relates to clay loamy, montmorillonite soils with humus horizon. Such soils are predominant in the southern region of Alberta, Saskatchewan and Manitoba, but are less common in northern regions of the provinces where quartz-illite sandy soils with low amount of humus prevail.