Release into the environment of metals by two vascular salt marsh plants

Metals in contaminated salt marshes are mainly locked in the anaerobic layer of sediments, where they are tightly bound as sulfides and organic complexes. Vascular plants survive in saturated soils in part by pumping O2 into their root zones, changing their microenvironment to an oxic one. This, along with chelating exudates, mobilizes metals, allowing uptake by the roots. We compared the common reed Phragmites australis and cordgrass Spartina alterniflora in lab and field studies for ways in which they handle trace metals. Both plants store most of their metal burden in their roots, but some is transported to aboveground tissues. Spartina leaves contain approximately 2-3 x more Cr, Pb, and Hg than Phragmites leaves, but equivalent Cu and Zn. Furthermore, Spartina leaves have salt glands, so leaf excretion of all metals is twice that of Phragmites. In-depth studies with Hg indicate that Hg excretion correlates with Na release but not with transpiration, which is 2.2 x higher in Phragmites; and that more Hg accumulates in early-appearing leaves than in upper (i.e. later) leaves in both species. Spartina thus makes more metals available to salt marsh ecosystems than Phragmites by direct excretion and via dead leaves which will enter the food web as detritus.     

The partial molal volume of silicic acid in 0.725 m NaCl

The partial molal volume ($\text{V}\text{?}$) of silicic acid in 0.725 m NaCl at 20°C has been calculated from (1) direct volume changes due to the dissolution of anhydrous sodium silicate and (2) some literature values for the partial molal volumes of NaOH and water. , unconnected for electrostriction effects, was found to be 53 ± 2 ml mole^?1. , corrected for volume changes due to solvent electrostriction by charged Si species, was estimated to be in the range 58–62 ml mole^?1; this range is 7–11 ml mole^?1 greater than the calculated from Willey's (Mar. Chem. 2, 239–250, 1974) solubility data obtained from the dissolution, in seawater, of amorphous silica subjected to hydrostatic pressure. Our does, however, agree within experimental error with the calculated from Jones and Pytkowicz's (Bull. Soc. Roy. Sci. Liege 42, 118–120, 1973) data for the solubility of amorphous silica in seawater at high pressure and is nearly in agreement with Willey's (Ph.D. thesis, Dalhousie University, 1975) solubility data for amorphous silica in 0.6 m NaCl.     

Emplacement ages and sources of kimberlites and related rocks in southern Africa: U–Pb ages and Sr–Nd isotopes of groundmass perovskite

Groundmass perovskite has been dated by LA-ICPMS in 135 kimberlites and related rocks from 110 localities across southern Africa. Sr and/or Nd isotopes have been analysed by LA-MC-ICPMS in a subset of these and integrated with published data. The age distribution shows peaks at 1,600–1,800, 1,000–1,200, 500–800 and 50–130 Ma. The major “bloom” of Group I kimberlites at ca 90 ± 10 Ma was preceded by a slow build-up in magmatic activity from ca 180 Ma. The main pulse of Group II kimberlites at 120–130 Ma was a distinct episode within this build-up. Comparison of the isotopic data with seismic tomography images suggests that metasomatized subcontinental lithospheric mantle (SCLM) with very low ε _Nd and high ⁸⁷Sr/⁸⁶Sr, (the isotopic signature of Group II kimberlites) was focused in low-Vs zones along translithospheric structures. Such metasomatized zones existed as early as 1,800 Ma, but were only sporadically tapped until the magmatic build-up began at ca 180 Ma, and contributed little to the kimberlitic magmas after ca 110 Ma. We suggest that these metasomatized volumes resided in the deep SCLM and that their low-melting point components were “burned off” by rising temperatures, presumably during an asthenospheric upwelling that led to SCLM thinning and a rise in the ambient geotherm between 120 and 90 Ma. The younger Group I kimberlites therefore rarely interacted with such SCLM, but had improved access to shallower volumes of differently metasomatized, ancient SCLM with low ⁸⁷Sr/⁸⁶Sr and intermediate ε _Nd (0–5). The kimberlite compositions therefore reflect the evolution of the SCLM of southern Africa, with metasomatic-enrichment events from as early as 1.8 Ga, through a major thermal and compositional change at ca 110 Ma, and the major kimberlite “bloom” around 90 Ma.     

Palaeomagnetic study of Archaean Banded Hematite Jasper Rocks from the Singhbhum-Orissa Craton, India

The Banded Hematite Jasper Formation within the Iron Ore Supergroup of the Singhbhum Craton in eastern India comprises fine alternating layers of jasper and specularite. It was deposited at 3000 Ma and deformed by a mobile episode at 2700 Ma. Hematite pigment (<1 μm) mixed with cryptocrystalline silica and specularite (> 10 μm) is chiefly responsible for red to brown rhythmic bands in the hematite jasper facies although thermomagnetic study also shows that minor amounts (1–2%) of magnetite are present. Palaeomagnetic study identifies a dual polarity remanence resident in hematite (D/I = 283/60°, α₉₅ = 12°) which predates deformation. Studies of the fabric of magnetic susceptibility and rock magnetic results suggest a diagenetic origin for this magnetisation with the hematite formed from oxidation of primary magnetite. The palaeopole (32°E, 24°N, dp/dm = 14/18°) records the earliest post-metamorphic magnetisation event in the Orissa Craton. A minimum apparent polar wander motion of the Orissa-Singhbhum craton of through 80° is identified during Late Archaean times (2900-2600 Ma).     

Multi-species chemical data assimilation with the Danish Eulerian hemispheric model: system description and verification

Satellite retrievals of atmospheric composition provide a wealth of data on a global scale. These complement results from atmospheric chemistry-transport models (CTMs), and can be combined using data assimilation. We present two assimilation schemes coupled to the Danish Eulerian Hemispheric Model (DEHM), a three-dimensional, off-line CTM with full photochemistry: a variant on the ensemble Kalman filter and the three-dimensional variational scheme. The aim of this paper is to describe the two schemes and present an initial assessment of their impacts on model skill. Retrievals of multiple atmospheric trace gases are assimilated, namely: NO₂ tropospheric column densities, CH₄ total column densities, and partial column concentrations of O₃, CO and CH₄; these data are retrieved from four satellite sensors. Data for each species are assimilated independently of one another, and other species are only adjusted indirectly via the model’s chemistry and dynamics. Assimilation results are compared with measurements from surface monitoring stations and other satellite retrievals, and preliminary validation results are presented.Reference simulations (without assimilation) grossly underestimate surface CO concentrations, and both assimilation schemes eliminate this large and systematic model bias. The assimilation improves the spatial correlation of modelled CO with surface observations, and improves the spatial correlation between forecasts and retrievals for CO, NO₂ and O₃. Results for CH₄ show a loss of skill due to a mismatch in model bias between two assimilated CH₄ data-sets. Finally, we discuss differences in methodology and results between this paper and a recent study on multi-species chemical data assimilation. Joint optimisation of initial conditions and emission rates offers a promising direction for improving modelled boundary-layer concentrations.     

Bound and mobile soil water isotope ratios are affected by soil texture and mineralogy,whereas extraction method influences their measurement

Questions persist about interpreting isotope ratios of bound and mobile soil water pools, particularly relative to clay content and extraction conditions. Interactions between pools and resulting extracted water isotope composition are presumably related to soil texture, yet few studies have manipulated the bound pool to understand its influence on soil water processes. Using a series of drying and spiking experiments, we effectively labelled bound and mobile water pools in soils with varying clay content. Soils were first vacuum dried to remove residual water, which was then replaced with heavy isotope-enriched water prior to oven drying and spiking with heavy isotope-depleted water. Water was extracted via centrifugation or cryogenic vacuum distillation (at four temperatures) and analysed for oxygen and hydrogen isotope ratios via isotope ratio mass spectrometry. Water from centrifuged samples fell along a mixing line between the two added waters but was more enriched in heavy isotopes than the depleted label, demonstrating that despite oven drying, a residual pool remains and mixes with the mobile water. Soils with higher clay + silt content appeared to have a larger bound pool. Water from vacuum distillation samples have a significant temperature effect, with high temperature extractions yielding progressively more heavy isotope-enriched values, suggesting that Rayleigh fractionation occurred at low temperatures in the vacuum line. By distinctly labelling bound and mobile soil water pools, we detected interactions between the two that were dependent on soil texture. Although neither extraction method appeared to completely extract the combined bound and mobile (total water) pool, centrifugation and high temperature cryogenic vacuum distillations were comparable for both δ²H and δ¹⁸O of soil water isotope ratios.     

Mass Spectrometric Isotope Dilution Analyses Of Barium in Geochemical Reference Samples

Twenty-four geochemical reference samples have been analysed far barium using the stable isotope dilution technique. These include five CRPG, ten ANRT, six Nimroc and two CCRMP samples together with the Tonalite from Tanzania, Duplicate analyses have been made in each case and our values for barium are believed to be accurate to approximately 3 %. In general, our results are in good agreement with the published data except for Nimroc samples where our data are consistently lower than the presently accepted values. No evidence of sample inhomogeneities was observed in the present work.     

Non-monotonic Responses of Phytoplankton Biomass Accumulation to Hydrologic Variability: A Comparison of Two Coastal Plain North Carolina Estuaries

Freshwater inputs often play a more direct role in estuarine phytoplankton biomass (chlorophyll a) accumulation than nitrogen (N) inputs, since discharge simultaneously controls both phytoplankton residence time and N loading. Understanding this link is critical, given potential changes in climate and human activities that may affect discharge and watershed N supply. Chlorophyll a (chla) relationships with hydrologic variability were examined in 3-year time series from two neighboring, shallow (<5?m), microtidal estuaries (New and Neuse River estuaries, NC, USA) influenced by the same climatic conditions and events. Under conditions ranging from drought to floods, N concentration and salinity showed direct positive and negative responses, respectively, to discharge for both estuaries. The response of chla to discharge was more complex, but was elucidated through conversion of discharge to freshwater flushing time, an estimate of transport time scale. Non-linear fits of chla to flushing time revealed non-monotonic, unimodal relationships that reflected the changing balance between intrinsic growth and losses through time and along the axis of each estuary. Maximum biomass occurred at approximately 10-day flushing times for both systems. Residual analysis of the fitted data revealed positive relationships between chla and temperature, suggesting enhanced growth rates at higher temperatures. N loading and system-wide, volume-weighted chla were positively correlated, and biomass yields per N load were greater than other marine systems. When combined with information on loss processes, these results on the hydrologic control of phytoplankton biomass will help formulate mechanistic models necessary to predict ecosystem responses to future climate and anthropogenic changes.     

Aircraft observations in the planetary boundary layer under stable conditions

An analysis of observations of airflow over Lake Ontario in a stably stratified atmosphere is presented. The relationship with theory is mentioned only in terms of what may be important to future work. Detailed air motion, potential temperature and mixing-ratio measurements are presented which show pervasive variability in the horizontal. There is no evidence of gravity waves. It is suggested that vertical mixing of the atmosphere may occur in stable conditions by a mechanism quite apart from the usual concept of the small-scale random eddy motion usually associated with surface convection. Vertical soundings are analyzed as well as two long constant-height observational runs.