The biogeochemistry of major elements of the suspended particulate matter of the Cretan Sea

The biogeochemistry of the following elements Al, Fe, Si_bio, POC, PN_tot, Ca_bio, S_org, P and Mn has been studied within waters of the Cretan Sea in March and September 1994, as part of the PELAGOS project. Particulate aluminosilicate concentrations, exemplified by Al, are very low (<1 μgl⁻¹) especially in the upper waters. Higher concentrations occur below 200 m, especially at depths of 200 m and 500–700 m in the central and eastern areas, and are thought to result from sediment injections from the shelf edge and slope. The results for Si_bio, Ca_bio, P and S_org show much higher concentrations within the photic waters. Temporal and spatial high concentrations in these waters closely relate to the existence of cyclonic eddies on the east and west sides of the sea, while low concentrations are associated with an intervening anticyclonic eddy. However in September, discharge of Black Sea Water in the west sufficiently suppresses the thermocline to prevent upwelled water from reaching the surface and hence these substances are prevented from forming.Particulate Fe (expressed as Fe_excess) concentrations show much higher concentrations relative to Al in September, and are thought to result from additional atmospheric inputs. The low particulate Mn concentrations in the upper water compared with deeper waters are considered to be a product of photoinhibition of MnO_x precipitation from Mn(II).An attempt has been made to assess input/output budgets of Al, Ca, Fe and Mn through the Antikithira and Kassos Straits. Much of the outflows leave through the Kassos Strait and, except for Ca, net outflows through the Antikithira Straits are negligible.     

Some effects of certain metals on development and mortality within the moult cycle of crangon crangon (L.)

Crangon crangon (L.) (Crustacea: Decapoda) were subjected to three metals (Cd, Cu and Zn) at respective concentrations (0·35, 1·6 and 14·4mg/litre) that would induce 50% mortality in 5–6 days. Significantly different (P < 0·05) rates of mortality occurred in the three groups, although their ET₅₀'s were almost identical. No moultstage-dependent mortality was observed for Cd, but in Cu and Zn the post-moult stages (A and B) were more susceptible than either the intermoult (C_a and C_b) or premoult (D₀–D₄) stages.No significant (P> 0·05) sex- or size-dependent mortality was evident at the tested concentrations of these metals.Feeding and ecdysis were inhibited in all metals after day 3 and development from one moult-stage to the next was greatly reduced in Cd.Possible modes of toxicity have been discussed in terms of the physiological condition inferred from the moult-stage at the time of death.     

Evaporation from a blanket bog in a foggy coastal environment

Frequent fog severely restricts evaporation from blanket bogs in Newfoundland because it more than halves the radiant energy input, and it eliminates the vapor pressure deficit, resulting in evaporation at the equilibrium rate (average = 0.99 during fog). During these periods, there is no surface resistance to evaporation because the bog has been wetted by fog drip, and although the latent heat flux dominates over sensible heat (average = 0.8), both are small. In contrast, the surface dries during clear periods, increasing the surface resistance to evaporation so that sensible heat becomes more important ( = 1.05). When the mosses are dry, evaporation is below the equilibrium rate ( = 0.87), although the higher available energy ensures that actual evaporation is higher. During clear periods, daily evaporation averaged 2.5 mm, compared to 1.1 and 0.7 mm for fog and rain, respectively. The suppressed evaporation at this site is important in maintaining appropriate hydrological conditions for blanket bog development.     

Comparative study of dissolved organic matter from groundwater and surface water in the Florida coastal Everglades using multi-dimensional spectrofluorometry combined with multivariate statistics

Dissolved organic matter (DOM) in groundwater and surface water samples from the Florida coastal Everglades were studied using excitation–emission matrix fluorescence modeled through parallel factor analysis (EEM-PARAFAC). DOM in both surface and groundwater from the eastern Everglades S332 basin reflected a terrestrial-derived fingerprint through dominantly higher abundances of humic-like PARAFAC components. In contrast, surface water DOM from northeastern Florida Bay featured a microbial-derived DOM signature based on the higher abundance of microbial humic-like and protein-like components consistent with its marine source. Surprisingly, groundwater DOM from northeastern Florida Bay reflected a terrestrial-derived source except for samples from central Florida Bay well, which mirrored a combination of terrestrial and marine end-member origin. Furthermore, surface water and groundwater displayed effects of different degradation pathways such as photodegradation and biodegradation as exemplified by two PARAFAC components seemingly indicative of such degradation processes. Finally, Principal Component Analysis of the EEM-PARAFAC data was able to distinguish and classify most of the samples according to DOM origins and degradation processes experienced, except for a small overlap of S332 surface water and groundwater, implying rather active surface-to-ground water interaction in some sites particularly during the rainy season. This study highlights that EEM-PARAFAC could be used successfully to trace and differentiate DOM from diverse sources across both horizontal and vertical flow profiles, and as such could be a convenient and useful tool for the better understanding of hydrological interactions and carbon biogeochemical cycling.     

The geochemistry of the Dunedin Volcano,East Otago,New Zealand: Rare earth elements

A variety of alkaline lavas from the Dunedin Volcano have been analyzed for the rare earth elements (REE) La-Yb. The compositions analyzed were: basalt-hawaiite-mugearite-benmoreite; basanite, nepheline hawaiite, nepheline trachyandesite and nepheline benmoreite; trachyte; phonolite. The series from basalt to mugearite shows continuous enrichment in the REE, consistent with a crystal fractionation model involving removal of olivine and clinopyroxene. From mugearite to benmoreite there is a depletion in the REE which is explained by the appearance of apatite as a liquidus phase. The chondrite normalized REE patterns for the phonolites are characterized by strong enrichment and fractionation coupled with a sharp depletion in Eu. Removal of plagioclase from benmoreite magma is suggested for the derivation of the phonolites. The series basanite-nepheline hawaiite, and basanite-nepheline hawaiite-nepheline benmoreite appear to be high pH₂O analogues of the series basalt-ben-moreite, with enrichment of the REE being achieved by removal of clinopyroxene, kaersutite and olivine. Compared with other lavas the trachyte has low REE abundances and is characterized by a striking positive Eu anomaly.     

The geochemistry of iodine in oxidised and reduced recent marine sediments

Surface sediments from the South West Africa shelf and the Gulf of California have been analysed for iodine and organic carbon. The iodine contents range from 96 to 1990 ppm. While iodine and organic carbon show certain anomalies on the South West Africa shelf, the trend of the $\text{I}\text{C}$ ratios is smooth and decreases from the shelf edge, an area of oxidising surface sediment, shorewards to reducing sediments, formed as a result of intense water upwelling. In the Gulf of California, a similar distribution of $\text{I}\text{C}$ ratios with surface sediment type occurs; lowest values occur in the reduced sediments and highest in oxidised sediments. Values of the $\text{I}\text{C}\text{(× 10}{}^4\text{)}$ ratio of the oxidised sediments (~250) are more than an order of magnitude higher than in reduced sediments, and are similar to some other surface oxidised sediments.The high I content of oxidised sediments is mostly due to uptake of I on to plankton seston on the seabed. In reduced sediments, I contained in planktonic matter originating in surface waters forms the bulk of iodine in the sediment.With sediment burial, oxidised sediments lose most of the iodine through degradation of unspecified organic constituents. This does not happen to the same extent in reduced sediments. The geological implications of these reactions are briefly discussed.     

Radiation damage in Luna 20 soil

Micron-sized soil grains from the Luna 20 mission are the most lightly irradiated we have examined, in contrast to micron-sized grains from the Luna 16 soil, which are the most heavily irradiated. Radiation damage in micron-sized grains is inversely correlated with albedo of the soil. The absence of angular, amorphous grains in Luna 20 supports our previous contention that such grains in Luna 16 were produced by intense radiation damage.     

A close-interval sampler for collection of sediment pore waters for nutrient analyses

An in situ sediment pore water sampler is described. It can simultaneously and continuously sample at four discrete 1 cm levels at one location without disturbing the sediment or the sample. The sampler can maintain an anaerobic environment, and can be used over extended periods of time. Laboratory tests indicate 98 to 100 percent recoveries for ammonium, silicate, reactive phosphate, nitrate and nitrite. Vertical profiles for ammonium, reactive phosphate and silicate are shown from field studies.     

Geochemistry and evolution of Iherzolite-bearing phonolitic lavas from Nigeria,Australia, East Germany and New Zealand

The major and trace element chemistry of phonolites containing spinel Iherzolite xenoliths from Bokkos (Nigeria), Phonolite Hill (northeastern Australia) and Heldburg (East Germany) is consistent with an origin by fractional crystallization of basanitic magmas at upper mantle pressures (10–15 kbar). At Bokkos, spatially associated lavas ranging from hawaiitic nepheline mugearite to nepheline benmoreite can be modeled very well by fractional crystallization of kaersutitic amphibole + olivine + Fe-Ti-spinel + apatite, a crystal extract consistent with experimentally-determined near-liquidus phase relationships for mugearitic liquids. Further fractional crystallization of aluminous clinopyroxene + mica + apatite will yield the phonolites. A similar model relating the unusual Iherzolite-bearing mafic nepheline benmoreite from Pigroot (New Zealand) to basanitic lavas of the East Otago province is not supported by major and trace element data. The Pigroot lava is possibly the product of melting of a mantle source region previously enriched in Sr and light rare earth elements, with subsequent minor fractional crystallization of olivine + kaersutite. Dynamic flow crystallization processes operating within conduit systems from mantle pressures are capable of yielding large volumes of evolved phonolitic liquids from primary basanitic liquids, if magma flow rates are appropriate. This mechanism may provide an explanation for the volumetric bias towards salic differentiates in some alkalic provinces.