The volcano-magnetic effect

Summary A geometrically simple volcano is considered, havig a spherical magma chamber of 2.5 km radius centred at 10 km depth. The Curie point isotherm is assumed to be a plane at 20 km depth, except for the spherical volume which is also non-magnetic. The stress pattern in the vicinity of the spherical chamber, due to regional stress of sufficient intensity to cause an eruptions, is used to calculate the change in magnetization which results from the piezomagnetic effect through the volume of solid rock. The consequent magnetic field anomaly at the surface is then obtaied by numerical integration of the dipole law of force over the stressed volume. For rocks of the type found on the volcanic island of St. Vincent (West Indies), this model gives a maximum local volcano-magnet c effect of about 7 gammas.     

Partitioning of polycyclic aromatic hydrocarbons between water and particles compared to bioaccumulation in mussels: a harbour case

Water and particles from three sites located in Halifax Harbour, near and further away from combined municipal sewage effluents (CMSE) were analysed for parental and alkylated polycyclic aromatic hydrocarbons (par and alkPAH). Bioavailability of PAH was compared for inter-tidal mussels collected at the same sites in April and November. The PAH fingerprint determined over 9 sampling times covering a period of 19 months differed more between phases (water and particles) and seasons, than between sites. In the spring, more alkPAH associated with diesel and gasoline were detected in the soluble phase, along with more bioaccumulation of alkPAH in inter-tidal mussels. A broader number of parPAH were detected in mussels collected in the fall. The mean sum of dissolved alkPAH concentrations was higher in water at the site closer to raw CMSE than at the other two sites and particles of that site. However, lowest bioconcentration factors (BCF) were determined in mussels of this more contaminated site. Similar biota-particle accumulation factors (BPAF) were determined for parPAH in mussels from the three sites, all lower than the BCF of alkPAH. The study indicates that sewage treatment plants will reduce the amount of parPAH especially larger than fluoranthene and pyrene from being deposited in the harbour; that alk naphthalenes and fluorenes present in water will continue to be discharged; that the disturbance of sediments can make particle-bound PAH available to mussels.     

Inter-annual variability in larval supply to populations of three invertebrate taxa in the northern California Current

We investigated sources of inter-annual variability in larval supply to crab and sea urchin populations at Bodega Head and Point Reyes in northern California. During the spring and summer upwelling seasons of the years 1992 through 1997 we monitored the weekly settlement rates of nine species of crabs and two species of sea urchins. As observed in previous studies, daily values of alongshore windstress, temperature and salinity provided evidence for the poleward flow of relatively warm, low salinity water from south of Point Reyes, an apparent retention zone, during upwelling relaxation events. In years dominated by these events (1992, 1993, 1995 and 1996) we observed that alongshore windstress, temperature and salinity were coherent and temperature was significantly correlated with cancrid crab settlement. During these years the magnitude of cancrid crab settlement and the fraction of cancrid crabs relative to other crab species settling were high. Over four years of concurrent sampling there was consistently greater cancrid crab settlement at the Point Reyes site, within the retention zone, than at Bodega Head. Settlement of non-cancrid crabs (porcellanids, grapsids, pagurids and majids) was not as closely linked to intra-annual patterns of upwelling and relaxation, possibly due to the shorter seasonal availability of larvae allowing for the influence of fewer relaxation events. Settlement of this group among years was positively correlated with environmental indicators of strong seasonal upwelling; high salinity, Bakun upwelling index and low temperature. Sea urchin settlement events were observed in June and July of 1992, 1994 and 1997 during warming periods when salinity and temperature were increasing and alongshore windstress was low. Across the six years of the study, we found that cancrid crab larvae had a more even seasonal availability than larvae of non-cancrid species, which settled in greatest numbers during the early portion of the upwelling season. Sea urchins settled in greatest numbers during the later part of the upwelling season. Together these patterns demonstrate the taxon-specific way that inter-annual variability in larval supply is forced by the coincidence of larval availability with favorable physical transport mechanisms.     

Properties of structure and function of cadmium-binding proteins/peptides from Euglena gracilis

Euglena gracilis makes two small Cd-binding proteins/peptides (Cd-BP I and Cd-BP II) in response to exposure to Cd²⁺. These proteins migrate slower than mammalian Cd-metallothionein (Cd-Mt) through Sephadex G-75, but like Cd-Mt also contain Zn and are separated into two species when chromatographed over a DEAE column. Both BPs are much less stable than Cd-Mt under acidic conditions. One source of this instability is that at least Cd-BP II contains acid-labile sulfide co-ordinated to the metals. It has been quantitated in Cd-BP II and shown to have a value of 1·25 ± 0·10 S²⁻/Cd. The reactivity of the Cd-binding sites in ligand substitution and thioldisulfide exchange reactions has been assessed. The reactions of Cd-BP I and II with pyridylazoresorcinol (PAR) were slow and displayed complex kinetic behavior. Similarly, both Cd-BPs react slowly and with complicated kinetics with 5,5′-dithiobis-(2-nitrobenzoate).     

Direct determination of organic carbon in modern reef sediments and calcareous organisms after dissolution of carbonate

An improved method for the direct determination of organic carbon in calcareous marine sediments, organisms and particulate matter is described. Samples are dissolved in phosphoric acid to remove carbonates, purged with oxygen to remove CO₂, and the resulting acidic solution is analysed for total (dissolved and particulate) organic carbon. The method is rapid, involves minimal sample manipulation, and is both accurate (better than ± 2%) and precise (better than ± 0.2 mg organic carbon/g sediment). The method is especially suitable for modern carbonate sediments which have low levels of predominantly acid-soluble organic carbon.     

Recovery of thermohaline circulation under CO2 stabilization and overshoot scenarios

In this study we examine the behavior of the thermohaline circulation, as simulated by the Community Climate System Model version 3 (CCSM3), for several centuries following CO₂ stabilization for the SRES B1 and A1B scenarios and for an “overshoot” scenario in which CO₂ levels temporarily reach the same level as in the A1B scenario before declining to an ultimate stabilization level that is identical to the B1 case. While we find no evidence for irreversible changes of the thermohaline circulation in the overshoot experiment, the interplay of the different timescales of the temperature response of the surface and interior ocean does lead to a number of differences in the long-term response of the ocean between it and the B1 stabilization scenario where the same GHG levels are approached by different paths. The stronger initial warming and its slow penetration into the deeper ocean, followed by a transient surface cooling in the overshoot scenario leads to lower static stability, deeper mixing, and a more rapid recovery of the thermohaline circulation than in the B1 stabilization scenario. While the overshoot scenario recovers surface conditions (e.g. SST, sea ice extent) very similar to the B1 scenario shortly after reaching the same GHG levels, the additional accumulation of heat in the interior ocean during the period of higher forcing causes the global mean ocean temperature and steric sea level to remain higher than in the B1 stabilization scenario for at least another several centuries.     

Volatile halocarbons released from Arctic macroalgae

Twenty-two different species of Arctic brown, red and green macroalgae, collected in the Kongsfjord at Ny-Ålesund (Spitsbergen), were incubated under polar conditions and investigated for their release of volatile halogenated organic compounds (VHOC). Bromoform, dibromomethane, dibromochloromethane, bromodichloromethane, 1,2-dibromoethane, diiodomethane and chloroiodomethane have been identified and their net releases during incubations were determined. Generally, brown and green macroalgae showed higher VHOC release, while red macroalage had only low release. Bromoform was released in relatively large quantities from all species studied, with the highest release observed from the brown algae Dictyosyphon foeniculaceus (0.3 μg g⁻¹ wet algal weight day⁻¹) and Laminaria saccharina (0.15 μg g⁻¹ wet algal weight day⁻¹), and from the green algae Monostroma arcticum (0.3 μg g⁻¹ wet algal weight day⁻¹) and Blidingia minima (0.27 μg g⁻¹ wet algal weight day⁻¹). Dibromomethane, diiodomethane, dibromochloromethane and 1,2-dibromoethane showed lower net release during the incubations. The net release of chloroiodomethane and bromodichloromethane was very low for the most algae species investigated. Based on the distribution of these algae in the Arctic environment, Dictyosiphon foeniculaceus and Laminaria saccharina may be important sources for VHOC because of high release and high biomass. Release of VHOC could be detected from all parts of the thallus of the macroalga. This may provide some evidence for a possible role of VHOC production as a chemical protection mechanism in algae.     

The dissociation constants of carbonic acid in seawater at salinities 5 to 45 and temperatures 0 to 45°C

The pK₁^* and pK₂^* for the dissociation of carbonic acid in seawater have been determined from 0 to 45°C and S = 5 to 45. The values of pK₁^* have been determined from emf measurements for the cell:

Pt](1 − X)H2 + XCO2|NaHCO3, CO2 in synthetic seawater|AgC1; Ag

where X is the mole fraction of CO₂ in the gas. The values of pK₂^* have been determined from emf measurements on the cell:

Pt, H2(g, 1 atm)|Na2CO3, NaHCO3 in synthethic seawater|AgC1; Ag

The results have been fitted to the equations:

lnK^*₁ = 2.83655 − 2307.1266/T − 1.5529413 lnT + (−0.20760841 − 4.0484/T)S^0.5 + 0.08468345S − 0.00654208S¹

InK^*₂ = −9.226508 − 3351.6106/T− 0.2005743 lnT + (−0.106901773 − 23.9722/T)S^0.5 + 0.1130822S − 0.00846934S^1.5

where T is the temperature in K, S is the salinity, and the standard deviations of the fits are σ = 0.0048 in lnK₁^* and σ = 0.0070 in lnK₂^*.Our new results are in good agreement at S = 35 (±0.002 in pK₁^*and ±0.005 in pK₂^*) from 0 to 45°C with the earlier results of Goyet and Poisson (1989). Since our measurements are more precise than the earlier measurements due to the use of the Pt, H₂|AgCl, Ag electrode system, we feel that our equations should be used to calculate the components of the carbonate system in seawater.