The mid-ocean ridge axial valley as a steady-state neck

In this paper the mid-ocean ridge axial valley is modelled as a steady-state lithospheric neck in which lithospheric stretching balances lithospheric accretion. Conversely, the axial high is a steady-state lithospheric bulge. The lithosphere is modelled as a thin plate with a Newtonian rheology. It is shown that an axial valley will occur if the rate of viscosity increase away from the ridge axis is faster than the rate at which accretion decreases. An axial high will occur if the opposite condition holds. This is consistent with the observation that axial valleys occur at low spreading rates and axial highs at high spreading rates. By fitting our model to profiles across the Mid-Atlantic Ridge and the East Pacific Rise and assuming the lithospheric thickness at the ridge axis to be 5 km, we find accretion widths of 6–8 km. We find the width over which there is a significant increase in lithospheric viscosity to be also 6–8 km.     

The 1982 eruptions of El Chichon volcano,Mexico (2): Observations and numerical modelling of tephra-fall distribution

Tephra fallout from the A-1 (March 29, 0532 UT), B (April 4, 0135 UT), and C (April 4, 1122 UT) 1982 explosive eruptions of El Chichon produced three tephra fall deposits over southeastern Mexico. Bidirectional spreading of eruption plumes, as documented by satellite images, was due to a combination of tropospheric and stratospheric transport, with heaviest deposition of tephra from the ENE tropospheric lobes. Maximum column heights for the eruptions of 27, 32, and 29 km, respectively, have been determined by comparing maximum lithic-clast dispersal in the deposits with predicted lithic isopleths based on a theoretical model of pyroclast fallout from eruption columns. These column heights suggest peak mass eruption rates of 1.1 × 10⁸, 1.9 × 10⁸, and 1.3 × 10⁸ kg/s. Maximum column heights and mass eruption rates occured early in each event based on the normal size grading of the fall deposits. Sequential satellite images of plume transport and the production of a large stratospheric aerosol plume indicate that the eruption columns were sustained at stratospheric altitudes for a significant portion of their duration. New estimates of tephra fall volume based on integration of isopach area and thickness yield a total volume of 2.19 km³ (1.09 km³ DRE, dense rock equivalent) or roughly twice the amount of the deposit mapped on the ground. Up to one-half of the erupted mass was therefore deposited elsewhere as highly dispersed tephra.     

Petrochemistry of the silicic-mafic complexes at Vesturhorn and Austurhorn, Iceland: evidence for zoned/stratified magma

Within the Austurhorn and Vesturhorn silicic intrusions of southeastern Iceland are composite complexes that consist of pillow-like bodies of mafic and intermediate rock entirely surrounded by silicic rock. The pillows with cuspate and chilled boundaries are interpreted to indicate a liquid-liquid relationship with a silicic magma. Some pillow-like bodies have a chilled and sharp cuspate boundary, whereas others have a distinct chemical and visible gradational contact with the silicic rock. The visible scale of mixing is of the same order of magnitude as the size of the pillows enclosed in the silicic rock (mm to meters).Two important types of chemical variation in the pillows are recognized. The first type of variation occurs from mafic pillow interiors to margins and into the surrounding silicic rock. These variations are due to mechanical mixing between mafic magma and the silicic magma. The second type of chemical variation occurs between individual pillows. Large variations occur between pillows in P and Ti at nearly constant silica. These variations cannot have resulted from in situ simple magma mixing or crystal fractionation, and must have originated at depth below the present level of exposure. These compositions could have been derived from separate mafic (or intermediate) magma bodies or from a single zoned and/or stratified magma body. Because the Austurhorn, Vesturhorn, and Ardnamurchan composite complexes all exhibit similar variations in P and Ti and because these occurrences are separated in space and time, they are thought to have had similar processes occur during their evolution. The chemical variations are interpreted to have resulted from mafic magma that has underplated silicic magma and become zoned/stratified due to the effects of magma mixing and cooling-crystallization.     

A chemical survey of the Mississippi estuary

A “snap shot” survey of the Mississippi estuary was made during a period of low river discharge, when the estuarine mixing zone was within the deltaic channels. Concentrations of H⁺, Ca²⁺, inorganic phosphorus and inorganic carbon suggest that the waters of the river and the low salinity (<5‰) portion of the estuary are near saturation with respect to calcite and sedimentary calcium phosphate. An input of oxidized nitrogen species and N₂O was observed in the estuary between 0 and 4‰ salinity. The concentrations of dissolved NH₄ ⁺ and O₂, over most of the estuary, appeared to be influenced by decomposition of terrestrial organic matter in bottom sediments. The estuarine bottom also appears to be a source of CH₄ which has been suggested to originate from petroleum shipping and refining operations. Estuarine mixing with offshore Gulf waters was the dominant influence on distributions of dissolved species over most of the estuary (i.e., from salinities >5‰). The phytoplankton abundance (measured as chlorophylla) increased as the depth of the mixed layer decreased in a manner consistent with that expected for a light-limited ecosystem. Fluxes of NO₃ ^?+NO₂ ^? and soluble inorganic phosphorus to the Gulf of Mexico were estimated to be 3.4±0.2×10³ g N s^?1 and 1.9±0.2 g P s^?1 respectively, at the time of this study.     

A revised identification of the oldest sea-floor spreading anomalies between Australia and Antarctica

We propose that magnetic anomalies south of Australia and along the conjugate margin of Antarctica that were originally identified as anomalies 19 to 22 may be anomalies 20 to 34. The original anomaly identification has two troublesome aspects: (1) it does not account for an “extra” anomaly between anomalies 20 and 21, and (2) it provides no explanation for the rough topography comprising the Diamantina Zone. With our revised identification there is no “extra” anomaly and the Diamantina Zone is attributed to a period of very slow spreading (～4.5mm/yr half rate) between 90 and 43 m.y. The ages bounding the interval of slow spreading (90 and 43 m.y.) correspond to times of global plate reorganizations. Our revised identification opens up the possibility that part of the magnetic quiet zone south of Australia formed during the Cretaceous long normal polarity interval. Breakup of Australia and Antarctica probably occurred sometime between 110 and 90 m.y. B.P. The “breakup unconformity” identified by Falvey in the Otway Basin may correspond to a eustastic sea level change.     

Environmental oxidation rate of manganese(II): bacterial catalysis

A simple mass balance for dissolved manganese(II) in waters containing low levels of oxygen in Saanich Inlet indicates that the residence time for Mn(II) removal to the solid phase is on the order of a few days. The average oxidation state of Mn in particulate material sampled from the region of Mn removal was 2.3–2.7, and electron micrographs revealed structures characteristic of bacterially formed Mn precipitates. Radiotracer experiments utilizing ⁵⁴Mn(II) indicated that removal of Mn from solution in the region of active uptake was substantially blocked by a poison mixture, demonstrating that Mn(II) binding to particulates is catalyzed by bacteria in this environment.     

The present day formation of apatite in Mexican continental margin sediments

Results of pore water and sediment analyses from the western Mexican continental margin strongly suggest the present day formation of apatite. The interstitial water phosphate and fluoride profiles indicate chemical removal at a depth which corresponds to a large maximum in the phosphorus content of the sediments. Apatite is identified within this maximum via X-ray diffraction but is elsewhere undetectable in the core. Radioisotopic thorium, uranium, and radium data support the conclusion that this deposit is modern. The present day depositional environment is consistent with those reported by other workers for phosphorite formation with the exception that pore water magnesium is not depleted below its seawater value.     

ENCORE: the effect of nutrient enrichment on coral reefs. Synthesis of results and conclusions

Coral reef degradation resulting from nutrient enrichment of coastal waters is of increasing global concern. Although effects of nutrients on coral reef organisms have been demonstrated in the laboratory, there is little direct evidence of nutrient effects on coral reef biota in situ. The ENCORE experiment investigated responses of coral reef organisms and processes to controlled additions of dissolved inorganic nitrogen (N) and/or phosphorus (P) on an offshore reef (One Tree Island) at the southern end of the Great Barrier Reef, Australia. A multi-disciplinary team assessed a variety of factors focusing on nutrient dynamics and biotic responses. A controlled and replicated experiment was conducted over two years using twelve small patch reefs ponded at low tide by a coral rim. Treatments included three control reefs (no nutrient addition) and three + N reefs (NH4Cl added), three + P reefs (KH2PO4 added), and three + N + P reefs. Nutrients were added as pulses at each low tide (ca twice per day) by remotely operated units. There were two phases of nutrient additions. During the initial, low-loading phase of the experiment nutrient pulses (mean dose = 11.5 microM NH4+; 2.3 microM PO4(-3)) rapidly declined, reaching near-background levels (mean = 0.9 microM NH4+; 0.5 microM PO4(-3)) within 2-3 h. A variety of biotic processes, assessed over a year during this initial nutrient loading phase, were not significantly affected, with the exception of coral reproduction, which was affected in all nutrient treatments. In Acropora longicyathus and A. aspera, fewer successfully developed embryos were formed, and in A. longicyathus fertilization rates and lipid levels decreased. In the second, high-loading, phase of ENCORE an increased nutrient dosage (mean dose = 36.2 microM NH4+; 5.1 microM PO4(-3)) declining to means of 11.3 microM NH4+ and 2.4 microM PO4(-3) at the end of low tide) was used for a further year, and a variety of significant biotic responses occurred. Encrusting algae incorporated virtually none of the added nutrients. Organisms containing endosymbiotic zooxanthellae (corals and giant clams) assimilated dissolved nutrients rapidly and were responsive to added nutrients. Coral mortality, not detected during the initial low-loading phase, became evident with increased nutrient dosage, particularly in Pocillopora damicornis. Nitrogen additions stunted coral growth, and phosphorus additions had a variable effect. Coral calcification rate and linear extension increased in the presence of added phosphorus but skeletal density was reduced, making corals more susceptible to breakage. Settlement of all coral larvae was reduced in nitrogen treatments, yet settlement of larvae from brooded species was enhanced in phosphorus treatments. Recruitment of stomatopods, benthic crustaceans living in coral rubble, was reduced in nitrogen and nitrogen plus phosphorus treatments. Grazing rates and reproductive effort of various fish species were not affected by the nutrient treatments. Microbial nitrogen transformations in sediments were responsive to nutrient loading with nitrogen fixation significantly increased in phosphorus treatments and denitrification increased in all treatments to which nitrogen had been added. Rates of bioerosion and grazing showed no significant effects of added nutrients. ENCORE has shown that reef organisms and processes investigated in situ were impacted by elevated nutrients. Impacts were dependent on dose level, whether nitrogen and/or phosphorus were elevated and were often species-specific. The impacts were generally sub-lethal and subtle and the treated reefs at the end of the experiment were visually similar to control reefs. Rapid nutrient uptake indicates that nutrient concentrations alone are not adequate to assess nutrient condition of reefs. Sensitive and quantifiable biological indicators need to be developed for coral reef ecosystems. The potential bioindicators identified in ENCORE should be tested in future research on coral reef/nutrient interactions. Synergistic and cumulative effects of elevated nutrients and other environmental parameters, comparative studies of intact vs. disturbed reefs, offshore vs. inshore reefs, or the ability of a nutrient-stressed reef to respond to natural disturbances require elucidation. An expanded understanding of coral reef responses to anthropogenic impacts is necessary, particularly regarding the subtle, sub-lethal effects detected in the ENCORE studies.