Experimental study of terrestrial plant litter interaction with aqueous solutions

Quantification of silicon and calcium recycling by plants is hampered by the lack of physico-chemical data on reactivity of plant litter in soil environments. We applied a laboratory experimental approach for determining the silica and calcium release rates from litter of typical temperate and boreal plants: pine (Pinus laricio), birch (Betula pubescens), larch (Larix gmelinii), elm (Ulmus laevis Pall.), tree fern (Dicksonia squarrosa), and horsetail (Equisetum arvense) in 0.01 M NaCl solutions, pH of 2-10 and temperature equals to 5, 25 and 40 °C. Open system, mixed-flow reactors equipped with dialysis compartment and batch reactors were used. Comparative measurements were performed on intact larch needles and samples grounded during different time, sterilized or not and with addition or not of sodium azide in order to account for the effect of surface to mass ratio and possible microbiological activity on the litter dissolution rates. Litter degradation results suggest that the silica release rate is independent on dissolved organic carbon release (cell breakdown) which implies the presence of phytoliths in a pure “inorganic” pool not complexed with organic matter. Calcium and DOC are released at the very first stage of litter dissolution while Si concentration increases gradually suggesting the presence of Ca and Si in two different pools. The dry-weight normalized dissolution rate at circum-neutral pH range (approx. 1-10 μmol/g_DW/day) is 2 orders of magnitude higher than the rates of Si release from common soil minerals (kaolinite, smectite, illite). Minimal Ca release rates evaluated from batch and mixed-flow reactors are comparable with those of most reactive soil minerals such as calcite and apatite, and several orders of magnitude higher than the dissolution rates of major rock-forming silicates (feldspars, pyroxenes). The activation energy for Si liberation from plant litter is approx. 50 kJ/mol which is comparable with that of surface-controlled mineral dissolutions. It is shown that the Si release rate from the above-ground forest biomass is capable of producing the Si concentrations observed in soil solutions of surficial horizons and contribute significantly to the Si flux from the soil to the river.     

Identifying the δO signature of precipitation in grass cellulose and phytoliths: Refining the paleoclimate model

Cellulose and silica phytoliths were extracted from the leaves and stems of Calamovilfa longifolia, a C₄ grass, grown under varying climatic conditions across the North American prairies. The oxygen-isotope compositions of both cellulose and silica record a complex signal of the isotopic composition of the soil water that feeds the plants and the relative humidity conditions that influence transpiration rates, stomatal conductance, and ultimately the ¹⁸O-enrichment of leaf water. As the initial stages of cellulose formation occur in the leaves, cellulose in both the leaves and stems forms primarily from leaf water and does not differ greatly in its oxygen-isotope composition between these locations. In contrast, the δ¹⁸O values of leaf phytoliths are significantly enriched in ¹⁸O relative to stem phytoliths, reflecting the varying isotopic composition of the water in these tissues. The oxygen-isotope compositions of leaf cellulose may be used as a proxy for the isotopic composition of water involved in leaf phytolith formation, while the δ¹⁸O values of stem phytoliths can be used to determine the δ¹⁸O values of stem water involved in partial exchange reactions during the transport of carbohydrates through the plant. A comparison of the isotopic compositions of phytoliths with cellulose allows for the deduction of soil and leaf water δ¹⁸O values as well as temperature and relative humidity conditions during plant growth. This approach has application in paleoclimate studies that traditionally have required estimations of one or more of these variables because direct measurements were unavailable.     

Volcanic and anthropogenic contributions to global weathering budgets

We evaluate whether the global weathering budget is near steady state for the pre-anthropogenic modern environment by assessing the magnitude of acidity-generating volcanic exhalations. The weathering rate induced by volcanic acid fluxes, of which the CO₂ flux is the most important, can be expressed as an average release rate of dissolved silica, based on a model feldspar-weathering scheme, and the ratio of carbonate-to-silicate rock weathering. The theoretically predicted flux of silica from chemical weathering is slightly smaller than the estimated global riverine silica flux. After adjustment for carbonate weathering, the riverine dissolved bicarbonate flux is larger than the volcanic carbon degassing rate by a factor of about three. There are substantial uncertainties associated with the calculated and observed flux values, but the modern system may either not be in steady state, or additional, “unknown” carbon sources may exist. The closure errors in the predicted budgets and observed riverine fluxes suggest that continental weathering rates might have had an impact on atmospheric CO₂ levels at a time scale of 10³-10⁴ years, and that enhanced weathering rates during glacial periods might have been a factor in the reduced glacial atmospheric CO₂ levels. Recent anthropogenic emissions of carbon and sulfur have a much larger acid-generating capacity than the natural fluxes. Estimated potential weathering budgets to neutralize these fluxes are far in excess of observed values. A theoretical scenario for a return to steady state at the current anthropogenic acidity emissions (disregarding the temporary buffering action of the ocean reservoir) requires either significantly lower pH values in continental surface waters as a result of storage of strong acids, and/or higher temperatures as a result of enhanced atmospheric CO₂ levels in order to create weathering rates that can neutralize the total flux of anthropogenic and natural background acidity.     

Surface properties, solubility and dissolution kinetics of bamboo phytoliths

Although phytoliths, constituted mainly by micrometric opal, exhibit an important control on silicon cycle in superficial continental environments, their thermodynamic properties and reactivity in aqueous solution are still poorly known. In this work, we determined the solubility and dissolution rates of bamboo phytoliths collected in the Réunion Island and characterized their surface properties via electrophoretic measurements and potentiometric titrations in a wide range of pH. The solubility product of “soil” phytoliths ( at 25 °C) is equal to that of vitreous silica and is 17 times higher than that of quartz. Similarly, the enthalpy of phytoliths dissolution reaction is close to that of amorphous silica but is significantly lower than the enthalpy of quartz dissolution. Electrophoretic measurements yield isoelectric point pH_IEP = 1.2 ± 0.1 and 2.5 ± 0.2 for “soil” (native) and “heated” (450 °C heating to remove organic matter) phytoliths, respectively. Surface acid-base titrations allowed generation of a 2-pK surface complexation model. Phytoliths dissolution rates, measured in mixed-flow reactors at far from equilibrium conditions at 2 ? pH ? 12, were found to be intermediate between those of quartz and vitreous silica. The dissolution rate dependence on pH was modeled within the concept of surface coordination theory using the equation:

     

Experimental evidence for eukaryotic fossil preservation: Onion skin cells in silica solution

Research on the origin of eukaryotes often focuses on the exceptional preservation found in silicified Precambrian fossils. Nuclei like subcellular structures in well-preserved fossil becomes confusion and arguments, which focus on whether the partial degradation of prokaryotes produces artifacts that resemble a ‘nucleus’, or fossilized nuclei of eukaryotes. In order to understand the mechanisms of silicification and identify the fossilized subcellular and microstructures in rocks, a series of laboratory controlled experiments were performed for simulating the silicification process. The effects of different silica solutions in eukaryote fossilization were studied in our experiments by exposing onion skin cells (epidermis) to silica solutions. Onion skin provides a good experimental model because of its well characterized cellular structures which are easily observed. The designed experiments revealed that the possibility of onion cell preserved as a “fossil” with nuclear structures, the first week fossilization, or mineralization as rapid as 1 week is important. And the experiment also revealed interactions between silica and the onion skin cell wall surface functional groups were weak. The preservation of nuclei in the onion skin model was due to precipitation in highly supersaturated silica solutions rather than simply the high silica concentration. When the silica gel precipitates slowly at low supersaturation states, the nuclei were not well preserved, but the rapid precipitation at high supersaturated silica conditions preserved nuclear structures. A better understanding of the processes involved in onion skin fossilization will further contribute to issues concerning the silicification of other eukaryotic materials.     

Reflections on interviewing foreign elites: praxis, positionality, validity, and the cult of the insider

Using open-ended interviews to conduct research on foreign elites raises methodological questions which conducting research on non-foreign elites and foreign non-elites does not. In this paper I first reflect upon some of the practical issues I have encountered when conducting interviews with members of foreign elites. I then examine the issue of positionality to suggest that the dualism of “insider” knowledge and status versus “outsider” knowledge and status is not as stable as it is often assumed to be, and that it should not be presumed that an “insider” will necessarily produce “better” knowledge than will an “outsider” simply by dint of their positionality. Indeed, given that the interview process is about constructing social meaning – a process that involves both the researcher and the source – in many ways such a dualism is meaningless.     

Dissolution kinetics of biogenic silica from the water column to the sediments

Stirred flow-through experiments were conducted for the first time with planktonic biogenic silica (BSi). We investigated the dissolution kinetics of uncleaned and chemically cleaned BSi collected in ocean surface water, sediment traps, and sediments from the Norwegian Sea, the Southern Ocean, and the Arabian Sea. The solubility at 2°C is rather constant (1000 to 1200 μM). The dissolution rates are, however, highly variable, declining with water depth, and phytoplankton reactivity is two to three orders of magnitude higher than pure siliceous oozes. The reactivity decrease correlates well with an increase in the integrated peak intensity ratios of Si-O-Si/Si-OH measured by Fourier transform infrared (FTIR) spectroscopy. The removal of organic or inorganic coatings enhance the reactivity by at least an order of magnitude. Atomic Al/Si ratios of 0.03 to 0.08 in sedimentary diatom frustules decrease significantly to 0.02 as a result of removal of inorganic coatings and detritals present. Near equilibrium, the dissolution rates exhibit a linear dependence on the degree of undersaturation. At higher degrees of undersaturation—that is, at low concentrations of dissolved silica—the dissolution rates of uncleaned samples define a nonlinear trend.The nonlinear kinetics imply that the dissolution of natural BSi is strongly accelerated in silica-depleted surface waters. The FTIR results suggest that internal condensation reactions reduce the amount of surface reaction sites and are partly responsible for the reactivity decrease with depth. The high content of Al in sedimentary BSi is likely caused by precipitation of dissolved silica with Al dissolved from minerals in sediment. Nonbiogenic silica as coatings or detritals are partly responsible for the solubility and reactivity decrease of BSi in sediments. One order of magnitude different rate constants measured in Norwegian Sea and Southern Ocean sediment trap material support the so-called opal paradox—that is, high BSi accumulation rates in sediments in spite of low BSi production rates in surface waters of the Southern Ocean.     

Surface chemistry and reactivity of plant phytoliths in aqueous solutions

In order to better understand the reactivity of plant phytoliths in soil solutions, we determined the solubility, surface properties (electrophoretic mobilities and surface charge) and dissolution kinetics of phytoliths extracted from fresh biomass of representative plant species (larch tree and elm, horsetail, fern, and four grasses) containing significant amount of biogenic silica. The solubility product of larch, horsetail, elm and fern phytoliths is close to that of amorphous silica and soil bamboo phytoliths. Electrophoretic measurements yield isoelectric point pH_IEP = 0.9, 1.1, 2.0 and 2.2 for four grasses, elm, larch and horsetail phytoliths respectively, which is very close to that of quartz or amorphous silica. Surface acid–base titrations allowed generation of a 2-pK surface complexation model (SCM) for larch, elm and horsetail phytoliths. Phytoliths dissolution rates, measured in mixed-flow reactors at far from equilibrium conditions at 1 ≤ pH ≤ 8, were found to be very similar among the species, and close to those of soil bamboo phytoliths. Mechanistic treatment of all plant phytoliths dissolution rates provided three-parameters equation sufficient to describe phytoliths reactivity in aqueous solutions:$R(\text{mol}/{\text{cm}}^2/\text{s})=6?{10}^{?16}?a_{\text{H+}}+5.0?{10}^{?18}+3.5?{10}^{?13}?a_{\text{OH}?}^{0.33}$Alternatively, the dissolution rate dependence on pH can be modeled within the concept of surface coordination theory assuming the rate proportional to concentration of > SiOH₂⁺, > SiOH⁰ and > SiO^? species. In the range of Al concentration from 20 to 5000 ppm in the phytoliths, we have not observed any correlation between their Al content and solubility, surface acid–base properties and dissolution kinetics.It follows from the results of this study that phytoliths dissolution rates exhibit a minimum at pH ～ 3. Mass-normalized dissolution rates are similar among all four types of plant species studied and these rates are an order of magnitude higher than those of typical soil clay minerals. The minimal half life time of larch and horsetail phytoliths in the interstitial soil solution ranges from 10–12 years at pH = 2–3 to < 1 year at pH above 6, comparable with mean residence time of phytoliths in soil from natural observations.     

竹亚科植硅体形态学研究及其生态学意义

选择我国常见的竹亚科19属64种进行系统的植硅体形态学研究,对竹亚科特有的长鞍型植硅体的长度、宽度、高度(侧面宽)和硅质颗粒数目等参数进行了测量。研究发现,合轴散生竹长鞍型植硅体个体最大(长度20.6±0.2m,宽度12.8±0.5m,高度12.4±0.1m,颗粒数2.8±0.5),单轴散生竹次之(长度18.8±0.8m,宽度11.7±0.4m,高度11.8±0.3m,颗粒数1.9±0.1),复轴混生竹再次(长度18.3±1.5m,宽度11.2±1.5m,高度11.4±1.7m,颗粒数1.8±0.4),合轴丛生竹最小(长度18.0±1.8m,宽度9.7±0.5m,侧面宽10.1±1.4m,颗粒数2.6±0.3)。经判别分析显示以长鞍型植硅体三维形态参数和硅质颗粒数目为变量可以区分竹亚科植物各生态型,并初步明确了长鞍型植硅体形态与竹亚科生态型的对应关系,探讨了其与竹亚科植物生境条件之间的对应关系,以及在竹亚科植物演化序列中的意义,为利用竹亚科长鞍型植硅体形态进行古环境分析提供了基础性资料。     

植硅体在河流硅输送中的作用

高等植物产生的植硅体是古气候和古环境研究的重要手段,也是陆地硅循环中重要的硅的储库;植硅体通过河流的跨区域输送在全球硅的生物地球化学循环中起着重要作用,是区域硅循环研究的重要载体,然而这方面的关注却很少。河流输送的生物硅大致分为自源和异源两种类别。"自源"生物硅主要包括河流水体本身自生浮游植物(主要是淡水硅藻)产生的硅质颗粒;"异源"生物硅主要由流域土壤的侵蚀输出到河流的植硅体所构成。流域地表过程是使得部分土壤中的植硅体进入河流的主要途径,并成为河流生物硅输送中重要的形式,这对河流-河口水循环体系的硅生物地球化学循环过程产生了重要的影响,但人们对河流输送的植硅体在硅循环中的作用的研究还不够。文章着眼于陆海相互作用研究,以河流中水体携带的植硅体为中心,总结了河流植硅体输送在地表水体硅循环系统中贡献的研究进展,分析了长江与黄河植硅体入海通量与河口行为及对近海海洋环境的影响。最后,对未来河流输送的植硅体参与硅循环研究可能需要加强的科学问题提出了建议。     

Climatic influences on the oxygen isotopic composition of biogenic silica in prairie grass

Samples of Calamovilfa longifolia were collected from across the North American prairies to investigate the relationship between the oxygen-isotope composition of biogenic silica (phytoliths) deposited in this grass and relative humidity, temperature, and the oxygen-18 enrichment of soil water relative to local precipitation. The δ¹⁸O values of silica in nontranspiring tissues were controlled by soil-water composition and temperature, whereas the oxygen-18 content of silica formed in leaf and inflorescence tissues was enriched further by transpiration. Accurate calculation of growing temperature was possible only when the oxygen-isotope compositions of both stem silica and soil water were known. However, the oxygen-isotope values of stem phytoliths can be used to calculate the variation in the isotopic composition of soil water across a North American temperature gradient.As plant organic matter decays and phytoliths are transferred to the soil, the temperature and soil-water signals carried by the oxygen-isotope composition of silica from nontranspiring tissues can be masked by the oxygen-18 enrichment of phytoliths from transpiring tissues. However, the overall oxygen-isotope composition of a soil-phytolith assemblage can be related to temperature using an empirical relationship based on temperature and the difference between soil-phytolith and estimated soil-water oxygen-isotope compositions.     

Evaluation of silica-water surface chemistry using NMR spectroscopy

We have combined traditional batch and flow-through dissolution experiments, multinuclear nuclear magnetic resonance (NMR) spectroscopy, and surface complexation modeling to re-evaluate amorphous silica reactivity as a function of solution pH and reaction affinity in NaCl and CsCl solutions. The NMR data suggest that changes in surface speciation are driven by solution pH and to a lesser extent alkali concentrations, and not by reaction time or saturation state. The ²⁹Si cross-polarization NMR results show that the concentration of silanol surface complexes decreases with increasing pH, suggesting that silanol sites polymerize to form siloxane bonds with increasing pH. Increases in silica surface charge are offset by sorption of alkali cations to ionized sites with increasing pH. It is the increase in these ionized sites that appears to control silica polymorph dissolution rates as a function of pH. The ²³Na and ¹³³Cs NMR results show that the alkali cations form outersphere surface complexes and that the concentration of these complexes increases with increasing pH. Changes in surface chemistry cannot explain decreases in dissolution rates as amorphous silica saturation is approached. We find no evidence for repolymerization of the silanol surface complexes to siloxane complexes at longer reaction times and constant pH.     

Opaline and Al–Si phytoliths from a tropical mire system of West Malaysia: abundance, habit, elemental composition, preservation and significance

Abundant and unique opaline and Al–Si phytoliths and opaline bioliths have been discovered in Holocene peat deposits of tropical Tasek Bera in Peninsular Malaysia. These are secreted mainly by plants (higher plants and algae) and incorporated in the sediment cycle during the rapid biomass turnover. Many wetland plants have entire skeletons secreted. The study shows that differing plant parts of same species as well as same parts of differing plant species incorporate different amounts of elements. Whilst deciduous trees of the swamp forest have phytoliths enriched in Al, most phytoliths of palms, sedges and grasses of the littoral swamp are composed of opaline silica. Incorporation of Al and many other elements into relatively stable phytoliths is the result of high evapotranspiration rate and ample plant-available elements and can serve to detoxify the soil solution. Because of the abundance of such opaline and Al–Si structures, spongillid and algal remains in acid peat-accumulating environments, tropical peatlands represent repositories of Si and Al, which together with variable amounts of other elements could provide the prime material for silicate neoformation during later diagenetic processes. Neoformation of minerals from bioliths would explain the scarcity of biogenic remains in Carboniferous and Tertiary coal deposits. Furthermore, incorporation of major elements in phytoliths may limit the rate of leaching of these elements in an environment where biomass turnover is rapid, thus reducing the loss of nutrients and other plant-essential elements. Most nutrients of tropical peats are recycled by plants within the top 150 cm and an upward migration of plant-essential elements, such as Mg, Ca, or P, but also of Si and Al, occurs during peat accumulation. Such elemental cycling strongly influences the geochemical composition of the peats during mire evolution. Utilizing Al for normalization of major and minor elements of tropical peats for paleoclimatic and paleodepositional analyses may thus result in incorrect interpretations.     

Evolution of organic matter indicators in response to major environmental changes: The case of a formerly cut-over peat bog (Le Russey, Jura Mountains, France)

To assess whether the biochemical characteristics of peat can provide clues for past ecosystem changes or not, a study was carried out combining elemental analysis, micro-morphological counts and neutral monosaccharide determination of peat organic matter (OM) and the dominant living plants from a formerly cut-over peat bog in the Jura Mountains. Peat profiles (up to 50 cm depth) from two distinctive zones (bare peat, FRA and a regenerating stage, FRC) were compared with the reference profile (FRD) taken from an unexploited area of the bog. The results show contrasting OM composition along the profiles. In the upper sections of the FRD and FRC profiles, high C/N ratios and sugar contents (in the same range as in the source plants) and the large predominance of well preserved plant tissues indicate good preservation of primary biological inputs. In contrast, in peat from the FRA profile and deeper levels of the FRC profile, lower C/N ratios, lower amounts of sugars and a predominance of amorphous OM and mucilage suggest more extensive OM degradation. These features delineate a clear threshold between an uppermost “new” regenerating peat section and an “old” catotelm peat below. Nevertheless, even in the latter, the sugar contents remain relatively high (>80 mg/g) compared with other organic and mineral soils. Analysis of typical peat-forming plants and of bulk peat and fine grained fractions allowed identification of the following source indicators: xylose and arabinose for Cyperaceae; rhamnose, galactose and mannose for mosses; and ribose (and to a lesser extent, hemicellulosic glucose) possibly for microbial synthesis.     

Evaluation of lake sediment surveys using the relationship of metal tenor to organic content

In geochemical surveys, including those of lake sediments, it is convenient to classify logarithmic cumulative frequency distributions of elements as anomalous, background, or intermediate. The third, and commonest, group presents the dilemma - Is a given distribution in that group tending towards an anomalous or a background distribution? Data from a series of surveys suggest that the relationship of loss on ignition to metal tenor can be used as an indicator of an element's “potential” or “availability” in the region of the survey. In turn, increased availability implies an anomalous source, such as an ore deposit. Areas with the best potential are considered to be those where logarithmic cumulative distributions of particular elements have the same or greater positive slopes than the associated loss on ignition distribution. The method does not define areas within the survey that can be considered more anomalous, only whether or not the given survey area exhibits a greater than expected concentration of a given element.     

Pliocene and Quaternary regional uplift in western Turkey: the Gediz River terrace staircase and the volcanism at Kula

Along the upper reaches of the Gediz River in western Turkey, in the eastern part of the Aegean extensional province, the land surface has uplifted by 400 m since the Middle Pliocene. This uplift is revealed by progressive gorge incision, and its rate can be established because river terraces are capped by basalt flows that have been K–Ar and Ar–Ar dated. At present, the local uplift rate is 0.2 mm a⁻¹. Uplift at this rate began around the start of the Middle Pleistocene, following a span of time when the uplift was much slower. This was itself preceded by an earlier uplift phase, apparently in the late Late Pliocene and early Early Pleistocene, when the uplift rate was comparable to the present. The resulting regional uplift history resembles what is observed in other regions and is analogously interpreted as the isostatic response to changing rates of surface processes linked to global environmental change. We suggest that this present phase of surface uplift, amounting so far to 150 m, is being caused by the nonsteady-state thermal and isostatic response of the crust to erosion, following an increase in erosion rates in the late Early Pleistocene, most likely as a result of the first large northern-hemisphere glaciation during oxygen isotope stage 22 at 870 ka. We suggest that the earlier uplift phase, responsible for the initial 250 m of uplift, resulted from a similar increase in erosion rates caused by the deterioration in local climate at 3.1 Ma. This uplift thus has no direct relationship to the crustal extension occurring in western Turkey, the rate and sense of which are thought not to have changed significantly on this time scale. Our results thus suggest that the present, often deeply incised, landscape of western Turkey has largely developed from the Middle Pleistocene onwards, for reasons not directly related to the active normal faulting that is also occurring. The local isostatic consequences of this active faulting are instead superimposed onto this “background” of regional surface uplift. Modelling of this surface uplift indicates that the effective viscosity of the lower continental crust beneath this part of Turkey is of the order of 10¹⁹ Pa s, similar to a recent estimate for beneath central Greece. The lower uplift rates observed in western Turkey, compared with central Greece, result from the longer typical distances of fluvial sediment transport, which cause weaker coupling by lower-crustal flow between offshore depocentres and eroding onshore regions that provide the sediment source.     

长白山区湿地表土植硅体特征及其环境意义*

湿地在全球环境变化中扮演着十分重要的角色,湿地表土中的植硅体分析是恢复第四纪古环境的重要途径。文中选取长白山区的桦南到哈尼一线的6处湿地表土,并采用PCA和CA分析植硅体组合的环境指示意义,结果显示：温度因子是造成长白山不同湿地表土植硅体组合差异的第1环境因子,且植硅体的种类和含量与采样点上覆植被、湿度与海拔等环境条件都存在相关性。结合方差分析和植硅体大小变化趋势分析曲线可以看出,不同表土中符合方差分析条件的植硅体类型的大小随着温度的升高而增大。总体来看,长白山区6处湿地中,植硅体类型基本相同,但温暖指数和植硅体的大小差异较显著,说明植硅体大小及其组合对温度都有较敏感的响应。     

Controls on herbaceous litter decomposition in the estuarine ecotones of the Florida Everglades

The effects of nutrient availability and litter quality on litter decomposition were measured in two oligotrophic phosphorus (P)-limited Florida Everglades esturies, United States. The two estuaries differ, in that one (Shark River estuary) is directly connected to the Gulf of Mexico and receives marine P, while the other (Taylor Slough estuary) does not receive marine P because Florida Bay separates it from the Gulf of Mexico. Decomposition of three macrophytes.Cladium jamaicense, Eleochaaris spp., andJuncus roemerianus, was studied using a litter bag technique over 18 mo. Litter was exposed to three treatments: soil surface+macroinvertebrates (=macro), soil surface without macroinvertebrates (=wet), and above the soil and water (=aerial). The third treatment replicated the decomposition of standing dead leaves. Decomposition rates showed that litter exposed to the wet and macro treatments decomposed significantly faster than the aerial treatment, where atmospheric deposition was the only source of nutrients. Macroinvertebrates had no influence on litter decompostion rates.C. jamaicense decomposed faster at sites, with higher P, andEleocharis spp. decomposed significantly faster at sites with higher nitrogen (N). Initial tissue C:N and C:P molar ratios revealed that the nutrient quality of litter of bothEleocharis spp. andJ. roemerianus was higher thanC. jamaicense, but onlyEleocharis spp. decomposed faster thanC. jamaicense. C. jamaicense litter tended to immobilize P, whileEleocharis spp. litter showed net remineralization of N and P. A comparison with other estuarine and wetland systems revealed the dependence of litter decomposition on nutrient availability and litter quality. The results from this experiment suggest that Everglades restoration may have an important effect on key ecosystem processes in the estuarine ecotone of this landscape.     

Horsetails (equisetum) as indirect indicators of gold mineralization

The alleged reputation of the horsetail (Equisetum) as an accumulator of gold was studied by analysis of a number of specimens from various localities, mainly from Nova Scotia. None of the samples had appreciable gold concentrations but with one exception, all the specimens collected from auriferous ground had high concentrations of arsenic ranging up to 738 μg/g dry mass. To a lesser extent this was also true for antimony. The evidence tends to refute the previous belief that horsetails accumulate gold, but does show that the genus is not only tolerant of arseniferous ground but is also an arsenic accumulator. Because of the common geochemical association of gold and arsenic, it is suggested that analysis of horsetails for arsenic may be a useful prospecting tool where geologic or other evidence suggests the possible presence of auriferous ground.     

Petrographic constraints on models of intergranular pressure solution in quartzose sandstones

Petrographic and SEM observations on 478 samples of six quartzose sandstones provide a data base that can be used to evaluate the role of intergranular pressure solution (IPS) in sandstone diagenesis and to constrain predictive models of the pressure solution process. SEM examination of grain contacts that have experienced pressure solution suggests that IPS occurs at the interior portions of contacts where the greatest stress is concentrated and that granulation of quartz grains at points of contact may contribute to the process. The chemical compaction fabrics that result from IPS suggest that the process is most commonly induced by effective lithostatic stress and that the resulting strain is uniaxial.Numerous geological variables influence IPS. Grain size exerts a fundamental influence, with finer grained samples experiencing more IPS than coarser grained samples. On both local and regional scales, IPS is inhibited by poor sorting, an abundance of ductile grains, the presence of “shallow” cement, slow rates of shallow burial, and overpressured conditions. In contrast, IPS is enhanced by the presence of illite grain coatings, increased maximum burial depth, rapid rates of shallow burial, longer times spent at great depths, higher temperatures, and high volumes and rates of fluid flow.Silica budgets indicate that some of the analyzed sandstones approximate mass balance whereas others have exported silica. Calculations of fluid flow requirements indicate that advanced stages of IPS are favored by high volume, high velocity fluid flow. Such flow can occur as a result of uplift of basin margins, which is typical of foreland and intractonic basins.