Properties of sea grass and sand flat sediments from the intertidal zone of St. Andrew Bay,Florida

Organic and carbonate carbon and textural properties of the substrates underlyingHalodule wrightii andThalassia testudinum sea grass beds in the intertidal zone of St. Andrew Bay, Florida were compared to adjacent unvegetated sand flats by physiographic divisions within the bay and to the subtidal slopes of the bay. Sea grass and sand flat sediments were principally fine-grained quartz sands. The mean particle-size of the sea grass sediments were finer-grained than those of the sand flats only in the west arm and lagoon of the bay. Size-frequency distributions of the sea grass sediments were generally slightly more negatively skewed and more leptokurtic than those of the sand flats. The sea grass sediments were less well sorted than were the sand flat sediments. The average organic and carbonate carbon contents of the sea grass beds were 1.9-fold greater than that of the sand flats but much less than that of the subtidal sea grass meadows. In the areas of pollution, sea grasses were absent; near this areaHalodule wrightii was the dominant sea grass.     

The major‐ and trace‐element whole‐rock fingerprints of Egyptian basalts and the provenance of Egyptian artefacts

Discrimination diagrams have been developed that source Egyptian basaltic artefacts using whole‐rock major element geochemistry. These include K₂O versus SiO₂, TiO₂ and P₂O₅ against MgO/Fe₂O₃^t (total Fe as Fe₂O₃), and a discriminant analysis diagram using SiO₂, Fe₂O₃^t, CaO, and MnO. A complementary set of diagrams uses easily obtained trace element data (Nb/Y versus Zr/Nb; Zr [ppm] versus Rb/Sr; TiO₂ [wt % volatile free] versus V; and Cr [ppm] versus Zr/Y) to determine the bedrock sources. These diagrams have been applied to seven First Dynasty basalt vessels (Abydos), two Fourth Dynasty basalt paving stones (Khufu's funerary temple, Giza), and two Fifth Dynasty paving stones (Sahure's complex, Abu Sir). They show that the bedrock source for all the artefacts was the Haddadin flow in northern Egypt. Multidimensional scaling and cluster analysis applied to the whole‐rock data (major elements and trace elements together) and previously published mineral fingerprinting studies confirm these results. Comparing mineral versus whole‐rock fingerprinting techniques, a major advantage of the former is the small sample size required (0.001 g compared to ≥ 0.1 g). Analytical costs are similar for both methods assuming that a comparison (bedrock) database can be assembled from the literature. For most archaeological problems, a whole‐rock bedrock database is more likely to exist than a mineral database, and whole‐rock analyses on artefacts will generally be easier to obtain than mineral analyses. Whole‐rock fingerprinting may be more sensitive than mineral‐based fingerprinting. Thus, if sample quantity is not an issue, whole‐rock analysis may have a slight cost, convenience, and technical advantage over mineral‐based methods. Our results also emphasize that the Egyptians cherished their Haddadin basalt flow and used it extensively and exclusively for manufacturing basalt vessels and paving stones for at least 600 years (∼3150 B.C. to 2500 B.C., approximate ages of the vessels and Abu Sir paving stones, respectively). © 2001 John Wiley & Sons, Inc.     

Tidal intrusion fronts

A tidal intrusion front forms as a dense seawater inflow plunges (subducts) beneath ambient estuarine water during flood tide. The associated foam lines and color changes have been observed on many smaller estuaries with constricted mouths. Internal hydraulic theory and laboratory experiments are reviewed and expressions are obtained for the position of plunging and the amount of associated mixing. The existence of a tidal intrusion front and its structure are discussed in terms of densimetric Froude numbers. These fronts are particularly important in smaller estuaries in which the intrusion process may dominate wind and tidal mixing and thus determine the overall stratification of the estuary. Three classes of three-dimensional plunging flow are identified and discussed. In particular, it is suggested that the peculiar, cursive V-shape plunge line is characteristic of strongly plunging flow.     

Provincialism and correlations between some properties of vitrinites

Optical and chemical properties for hand-picked samples of vitrinite from a number of British coalfields are correlated and the correlations compared with previously published data. The form of the relationship found for the properties of British vitrinites is generally similar to that exhibited by a number of other sets of analyses, but some significant differences also exist in several of the correlations. For maximum reflectance as a function of carbon content, the present data indicate that at medium and low ranks, maximum reflectance is lower than the level suggested by most previous studies. The relationships of volatile-matter yield to reflectance and carbon content suggest that at low ranks, volatile-matter yield is strongly dependent upon the nature of the coalification history of the vitrinite. Furthermore, these correlations are likely to show provincialism, in that correlations which hold for one coalfield may not be representative of the relationship in other coalfields. Similarly, major differences in relationships involving bireflectance are associated with the tectonic setting at the time of effective coalification. The data presented here indicate that for low-rank coals at least, correlations between properties of vitrinites must take account of provincialism if they are to be sufficiently reliable to be useful. The measurement of a number of rank-sensitive variables can yield additional information about rank, as compared with the use of a single rank-sensitive variable.     

Inter‐laboratory Characterisation of Apatite Reference Materials for Chlorine Isotope Analysis

Here we report on a set of six apatite reference materials (chlorapatites MGMH#133648, TUBAF#38 and fluorapatites MGMH#128441A, TUBAF#37, 40, 50) which we have characterised for their chlorine isotope ratios; these RMs span a range of Cl mass fractions within the apatite Ca₁₀(PO₄)₆(F,Cl,OH)₂ solid solution series. Numerous apatite specimens, obtained from mineralogical collections, were initially screened for ³⁷Cl/³⁵Cl homogeneity using SIMS followed by δ³⁷Cl characterisation by gas source mass spectrometry using both dual‐inlet and continuous‐flow modes. We also report major and key trace element compositions as determined by EPMA. The repeatability of our SIMS results was better than ± 0.10‰ (1s) for the five samples with > 0.5 % m/m Cl and ± 0.19‰ (1s) for the low Cl abundance material (0.27% m/m). We also observed a small, but significant crystal orientation effect of 0.38‰ between the mean ³⁷Cl/³⁵Cl ratios measured on three oriented apatite fragments. Furthermore, the results of GS‐IRMS analyses show small but systematic offset of δ³⁷Cl_SMOC values between the three laboratories. Nonetheless, all studied samples have comparable chlorine isotope compositions, with mean 10³δ³⁷Cl_SMOC values between +0.09 and +0.42 and in all cases with 1s ≤ ± 0.25.     

Denitrification rates measured along a salinity gradient in the eutrophic Neuse River estuary, North Carolina, USA

Denitrification rates along a salinity gradient in the eutrophic Neuse River Estuary, North Carolina, were quantified using membrane inlet mass spectrometry (MIMS) within short-term batch incubations. Denitrification rates within the system were highly variable, ranging from 0 to 275 μmol N m⁻² h⁻¹. Intrasite variability increased with salinity, but no significant differences were observed across the salinity gradient. Denitrification rates were positively correlated with sediment oxygen demand at the upstream sampling site where sediment organic carbon levels were lowest. This relationship was not observed in the more saline sampling sites. Denitrification rates were highest during winter. On an annual basis, denitrification accounted for 26% of the dissolved inorganic nitrogen and 12% of the total nitrogen supplied to the system.     

Phase equilibria in the system CO2-H2O I: New equilibrium relations at low temperatures

Graphical analysis of free-energy relationships involving binary quadruple points and their associated univariant equilibria in the system CO₂-H₂O suggests the presence of at least 2 previously unrecognized quadruple points and a degenerate binary invariant point involving an azeotrope between CO₂-rich gas and liquid. Thermodynamic data extracted from the equilibrium involving clathrate (hydrate), gas, and ice (H = G+I) are employed along with published data to calculate the P-T range of the 3-ice equilibrium curve, S+I = H, where S is solid CO₂. This equilibrium curve intersects the H = G+I curve approximately where the latter curve intersects the S+H = G curve, thus confirming the existence of one of the inferred quadruple points involving the phases S, G, H, and I. Recognition of some binary equilibria probably have been hampered by extremely low mutual solubilities of CO₂ and H₂O in the fluids phases which, for example, render the S+H = G virtually indistinguishable from the CO₂-sublimation curve.To make the published portion of the L(liquid CO₂)-G-H equilibrium “connect” with the other new quadruple point involving S, L, G, and H, it is necessary to change the sense of the equilibrium from L = G+H at higher pressures to L+H = G at lower pressures by positing a L = G azeotrope at very low concentrations of H₂O. At the low-pressure origin of the azeotrope, which is only a few bars above the CO₂-triple point, the azeotrope curve intersects the 3-phase curve tangentially, creating a degenerate invariant point at which the 3-phase equilibrium changes from L+H = G at lower pressures to L = G+H at higher pressures. The azeotrope curve is offset at slightly lower temperature from the L = G+H curve until the 3-phase equilibrium terminates at the quadruple point involving G, L, H, and W (water). With further increase in pressure the azeotrope curve tracks the L = G+W equilibrium and apparently terminates at a critical end point in close proximity to critical endpoints for the CO₂-saturation curve and the L = G+W curve.Thermodynamic data for clathrate extracted from the slope of the H = G+I curve are consistent with a solid-state phase transformation in CO₂-clathrate between 235 and 255 K. Published work shows that the type-I clathrate phase, whose atomic structure is a framework of water molecules with CO₂ molecules situated in large “guest” sites within the framework, is variable in composition with ∼1 guest site vacancy per unit cell at the high-temperature limit of its stability; the number of water molecules, however, remains constant. The formula (CO₂)_8-y·46H₂O, where y is the number of vacancies per unit cell, is in keeping with the atomic structure, whereas the traditional formula, CO₂·nH₂O, where n (hydration number) = 5.75, is misleading.Ambient P-T conditions in the Antarctic and Greenland ice sheets are compatible with sequestering large amounts of carbon as liquid CO₂ and/or clathrate.     

A hybrid discrete-continuum approach to model hydro-mechanical behaviour of jointed rocks

A hybrid discrete-continuum approach has been presented in this paper to simulate water flow in the near and far fields of deformable fractured rocks. In the near field, the discrete model is used; while in the far field, the equivalent continuum model is employed. The discrete element method (with the static relaxation algorithm) is used in the near field and the boundary integral equation method in the far field. Along the interface of these two domains, both mechanical and hydraulic compatibility conditions are satisfied. Fully coupled hydro-mechanical analysis can be conducted in the combined near and far fields. Application to a dam foundation problem has demonstrated the capability of the developed approach.     

Effects of salinity and temperature on the bioenergetics of adult stages of the grass shrimp (Palaemonetes pugio Holthuis) from the North Inlet Estuary, South Carolina

The influence of temperature, salinity, body size, and sex on the bioenergetics and life-history parameters of grass shrimp (Palaemonetes pugio Holthuis) was determined under laboratory conditions. Sex and/or size show a highly significant effect only on energy allocation for metabolism. Temperature, salinity and their interaction are the main effects on most energetic parameters, with temperature showing the strongest influence on both life-history parameters and energetics. The adult grass shrimp's energy budget is different from that of larval or juvenile stages, in that most of the energy ingested by adults is allocated to reproduction. Under optimal conditions (25°C and 28‰), allocation of ingested energy in the adult grass shrimp is 51.7% for reproduction, 25.4% for respiration, 14.1% for somatic growth, 4.8% for exoskeletons, and 1.8% for excretion.     

Chemical fractionations in meteorites—X. Ureilites

Four ureilites (Dyalpur, Goalpara, Haverö, and Novo Urei) were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Rb, Re, Sb, Se, Te, Tl, and U. An attempt has been made to resolve the data into contributions from the parent ultramafic rock and the injected, carbon- and gas-rich vein material. Interelement correlations, supported by analyses of separated vein material (WANKE et al, 1972), suggest that the vein material is enriched about 10-fold in refractory Ir and Re over moderately volatile Ni and Au, and is low in volatiles except Ge, C, and noble gases. It appears to be a refractory-rich nebular condensate that precipitated carbon by surface catalytic reactions at ˜500K and trapped noble gases but few other volatiles. The closest known analogue is a Cr- and C-rich fraction from the Allende meteorite, highly enriched in heavy noble gases and noble metals. By analogy with Allende, the gas-bearing phase in ureilites may have been an Fe, Cr-sulfide.

The ultramafic rock contains siderophiles and chalcophiles (Ni, Au, Ge, S, Se) at ˜0.05 of Cl chondrite level, and highly volatile elements (Rb, Cs, Bi, Tl, Br, Te, In, Cd) at ˜0.01 Cl level. It probably represents the residue from partial melting of a C3V-like chondrite body, under conditions where phase separation was incomplete so that some liquid was retained. The vein material was injected into this rock at some later time.