A Coupled Ice-Ocean Model in the Pan-Arctic and North Atlantic Ocean: Simulation of Seasonal Cycles

A coupled ice-ocean model is configured for the pan-Arctic and northern North Atlantic Ocean with a 27.5 km resolution. The model is driven by the daily atmospheric climatology averaged from the 40-year NCEP reanalysis (1958–1997). The ocean model is the Princeton Ocean Model (POM), while the sea ice model is based on a full thermodynamical and dynamical model with plastic-viscous rheology. A sea ice model with multiple categories of thickness is utilized. A systematic model-data comparison was conducted. This model reasonably reproduces seasonal cycles of both the sea ice and the ocean. Climatological sea ice areas derived from historical data are used to validate the ice model performance. The simulated sea ice cover reaches a maximum of 14 × 10⁶ km² in winter and a minimum of 6.7 × 10⁶ km² in summer. This is close to the 95-year climatology with a maximum of 13.3 × 10⁶ km² in winter and a minimum of 7 × 10⁶ km² in summer. The simulated general circulation in the Arctic Ocean, the GIN (Greenland, Iceland, and Norwegian) seas, and northern North Atlantic Ocean are qualitatively consistent with historical mapping. It is found that the low winter salinity or freshwater in the Canada Basin tends to converge due to the strong anticyclonic atmospheric circulation that drives the anticyclonic ocean surface current, while low summer salinity or freshwater tends to spread inside the Arctic and exports out of the Arctic due to the relaxing wind field. It is also found that the warm, saline Atlantic Water has little seasonal variation, based on both simulation and observations. Seasonal cycles of temperature and salinity at several representative locations reveals regional features that characterize different water mass properties.     

Acoustics in Fisheries and Aquatic Ecology: Part 1 Introduction

The ICES Symposium on Acoustics in Fisheries and Aquatic Ecology(SAFAE) was held in Montpellier, France, from 10 to 14 June2002. There were 303 participants from 37 countries, emphasizingthe strongly international character of the meeting. This Symposiumwas the fifth organized by ICES in a series concerned with acousticsin fisheries and related fields. The first two were held inBergen (1973 and 1982), the third in Seattle (1987), and thefourth in Aberdeen     

Theory of interaction intensities,buffer capacities,and pH stability in aqueous systems,with application to the pH of seawater and a heterogeneous model ocean system

The choice of convenient basic constituents for evaluating pH stability of aqueous systems is discussed, and two useful interaction parameters are defined and related to the buffer capacity: the interaction capacity, $\text{δ′}{}_{\mathrm{X,Y}}\text{=}\text{?}\text{p}\text{X}\text{?}\text{TOT}\text{Y}$, and the interaction intensity, $\text{δ}{}_{\mathrm{X,\; Y}}\text{=}\text{?}\text{p}\text{X}\text{?}\text{pTOT}\text{Y}$; for pH and TOTH, δ′_{H, H} = ?β_H^?1, where β_H is the pH buffer capacity. A method is presented for the computation of exact values of all interaction capacities and intensities through inversion of the Jacobian matrix of the system of non-linear equations describing the aqueous system. The major species of an aqueous system (H₂O, H⁺, solid phases, gases, and the most abundant solute species) are shown to constitute a useful set of basic constituents for evaluation of approximate pH buffer capacities according to a simple rule: the major-minor species rule for zeroth order pH-TOTH interaction. The concepts of buffering and pH-statting are examined and contrasted; it is demonstrated that the buffer capacity of an aqueous system cannot be infinite: it is limited by the concentration of solutes in solution. The effect upon pH of variations in constituents other than H⁺ is described in terms of first order interactions via complex formation and solid formation; approximate formulas for calculation are derived. Higher order interactions are derived from combinations of first order ones. The pH stability of the ocean system is examined in terms of an aqueous phase model including ion-association reactions and a heterogeneous model incorporating CO₂ in the gas phase, quartz, kaolinite, calcite, chlorite, and illite, in addition to the aqueous phase. There is an approximately three-fold enhancement of buffer capacity in the aqueous model as a consequence of ion-association. Only a few interaction pathways are of quantitative significance in establishing the buffer capacity. Results for the heterogeneous ocean model lend quantitative support to Sillén's notion of pH stability: the buffer capacity is about four hundred times greater than that of the aqueous phase model.     

Biotite stability in peraluminous granitic melts: Compositional dependence and application to the generation of two-mica granites in the South Bohemian batholith (Bohemian Massif, Czech Republic)

Crystallization experiments have been conducted in the system Na₂O–K₂O–MgO–FeO–Al₂O₃–SiO₂–H₂O (with 4% normative corundum) in order to constrain the stability of biotite as a function of water activity and the Mg# of biotite [Mg/(Mg +Fe_total)] in equilibrium with peraluminous granitic melts. The temperature at which biotite breakdown starts is strongly dependent on the Mg# of biotite. At 500 MPa, the temperature of biotite breakdown to form orthopyroxene increases from 750 °C to 830 °C, as the Mg# of biotite increases from 0.4 to 0.5. Considering that the system investigated is relevant for Ca-poor peraluminous biotite-bearing rocks (metapelites), the biotite dehydration curves obtained are used to discuss the melting reactions and the temperatures that lead to the formation of two distinct types of two-mica granites found in the South Bohemian batholith (specifically the Eisgarn and Deštná granites). The phase relationships were determined experimentally for the composition of these two granites in order to constrain the composition of the biotite in equilibrium with the melt in the protoliths. We demonstrate that Eisgarn granitic melts may have been generated at temperatures in the range 830–850 °C from melting reactions involving biotite with a Mg# up to 0.5 as a reactant. In contrast, Deštná granitic melts cannot have been generated from dehydration melting reactions involving biotite.     

煤矸石堆周围土壤重金属污染特征分析--以焦作市中马村矿为例

利用扇形布点法采集了焦作市中马村矿矸石堆周围土壤，对其中的Cr、Pb、Cu、Mn4种重金属含量进行了研究。结果表明：煤矸石的堆放对周围土壤造成不同程度的污染，重金属的含量随离矸石堆距离增大呈减小的趋势，主要受到风向的影响。     

Carbonation of alkaline paper mill waste to reduce CO2 greenhouse gas emissions into the atmosphere

The global warming of Earth’s near-surface, air and oceans in recent decades is a direct consequence of anthropogenic emission of greenhouse gases into the atmosphere such as CO₂, CH₄, N₂O and CFCs. The CO₂ emissions contribute approximately 60% to this climate change. This study investigates experimentally the aqueous carbonation mechanisms of an alkaline paper mill waste containing about 55 wt% portlandite (Ca(OH)₂) as a possible mineralogical CO₂ sequestration process. The overall carbonation reaction includes the following steps: (1) Ca release from portlandite dissolution, (2) CO₂ dissolution in water and (3) CaCO₃ precipitation. This CO₂ sequestration mechanism was supported by geochemical modelling of final solutions using PHREEQC software, and observations by scanning electron microscope and X-ray diffraction of final reaction products. According to the experimental protocol, the system proposed would favour the total capture of approx. 218 kg of CO₂ into stable calcite/ton of paper waste, independently of initial CO₂ pressure. The final product from the carbonation process is a calcite (ca. 100 wt%)-water dispersion. Indeed, the total captured CO₂ mineralized as calcite could be stored in degraded soils or even used for diverse industrial applications. This result demonstrates the possibility of using the alkaline liquid–solid waste for CO₂ mitigation and reduction of greenhouse effect gases into the atmosphere.     

Reversible surface-sorption-induced electron-transfer oxidation of Fe(II) at reactive sites on a synthetic clay mineral

The sorption of ⁵⁷Fe(II) onto an Fe-free, mineralogically pure and Ca-saturated synthetic montmorillonite sample (structural formula: Ca_0.15(Al_1.4Mg_0.6)(Si₄)O₁₀(OH,F)₂), was studied as a function of pH under strictly anoxic conditions (N₂ glove box atmosphere, O₂ content <1 ppm), using wet chemistry and cryogenic (T = 77 K) ⁵⁷Fe Mössbauer spectrometry. No Fe(III) was detected in solution at any pH. However, in pH conditions where Fe(II) is removed from solution, a significant amount of surface-bound Fe(III) was produced, which increased with pH from 0% to 3% of total Fe in a pre-sorption edge region (i.e. at pH < 7.5 where about 15% of total Fe is sorbed) to 7% of total Fe when all Fe is sorbed. At low pH, where the pre-sorption edge plateau occurs (2 < pH < 7.5), the total sorbed-Fe amount remained constant but, within this sorbed-Fe pool, the Fe(III)/Fe(II) ratio increased with pH, from 0.14 at pH 2 up to 0.74 at pH 7. The pre-sorption edge plateau is interpreted as cation exchange on interlayer surfaces together with a sorption phenomenon occurring on highly reactive (i.e. high affinity) surface sites. As pH increases and protons are removed from the clay edge surface, we propose that more and more of these highly reactive sites acquire a steric configuration that stabilizes Fe(III) relative to Fe(II), thereby inducing a Fe to clay particle electron transfer. A sorption model based on cation exchange combined with surface complexation and electron transfers reproduces both wet chemical as well as the Mössbauer spectrometric results. The mechanism is fully reversible: sorbed-Fe is reduced as pH decreases (Mössbauer solid-state analyses) and all Fe returned to solution is returned as Fe(II) (solution analyses). This would not be the case if the observed oxidations were due to contaminant oxidizing agents in solution. The present work shows that alternating pH may induce surface redox phenomena in the absence of an electron acceptor in solution other than H₂O.     

Ecotoxicological effects of a semi-submerged municipal dump (Castle harbour, Bermuda) on the Calico scallop Argopecten gibbus

A biomarker study was undertaken using the Calico scallop Argopecten gibbus to assess the ecotoxicological effects of a semi-submerged municipal dump on the adjacent patch reef lagoon ecosystem (Castle harbour, Bermuda). Caged scallops were deployed in situ for 2 months at various distances from the dump (50 m, 900 m and 2.7 km) and at a reference site (14 km). A suite of biomarkers comprising metallothionein (MT), lipid peroxidation (LPO), vitellin-like proteins (Vn), glutathione S-transferase (GST), DNA strand breaks and condition factor (CF) were investigated in various tissues of the scallop (gill, digestive gland and gonad). Levels of heavy metals were also measured in the whole scallop soft tissue. While there was some variation in response between tissues, in general the results indicated that the dump was negatively impacting scallops deployed in the adjacent marine environment: elevated levels of MT, DNA strand breaks, Vn and GST and reduced condition factor were found for scallops deployed nearest to the dump and at the site 1.5 km from this point source of contamination (Tuckers town) in Castle harbour, with respect to the reference site, North Rock (although this exhibited some degree of metal contamination). The gills from scallops deployed at the dump site were the most responsive tissue, with the highest expression of MT, LPO and DNA damage. This study indicates the potential of the Calico scallop as a convenient bioindicator species in the marine tropical benthos.     

Fe(II)-Na(I)-Ca(II) Cation Exchange on Montmorillonite in Chloride Medium: Evidence for Preferential Clay Adsorption of Chloride – Metal Ion Pairs in Seawater

Fe(II)–Ca(II), Fe(II)–Na(I), and Fe(II)–Ca(II)–Na(I) exchange experiments on montmorillonite were performed in chloride background. These experiments show the possible sorption of Fe²⁺ and FeCl⁺ ion pairs in exchange site positions, a result confirmed with 77 K ⁵⁷Fe Mössbauer experiments. The sorption data were modeled and the cation exchange selectivity for Fe(II) were found to be nearly equal to that of Ca(II). Vanselow selectivity coefficients, for Na–Fe²⁺ and Na–FeCl⁺ reactions, were found to be equal to 0.4 (0.5 for Ca²⁺) and 2.3 (2.5 for CaCl⁺) respectively. High affinity of montmorillonite for chloride ion pairs seems to be a common mechanism as first stated by Sposito et al., (Soil Sci. Soc. Am. J. 47, 51–56, 1983a), and should have implications e.g., on the chemistry of suspended particles in seawater. Exchange selectivity coefficients derived from this study and others were used to model experimental data on river water and seawater equilibrated particles. The agreement between simulations and experimental data is very good. The simulation shows the predominance of monovalent ion (Na⁺ and chloride ion pairs) sorption on clay particles in seawater. This sorption of monovalent ions leads to the dispersion of particles in seawater and to the extension of a plume of particles spreading away from river deltas, such as that of the River Amazon.