He diffusion in olivine

Helium diffusion in olivine (dunite xenolith) has been measured in the temperature range 1180–1460°C; a linear Arrhenius function was obtained with an activation energy of 120₋₂₇⁺³² kcal/mole, and a pre-exponential factor (D₀) = 2.2 × 10⁸ cm²/s.

Diffusion mechanisms are not a viable means of degassing He from the mantle. Olivine phenocrysts can be expected to retain previously trapped He, during cooling in extrusive basalts, provided the flow units are thinner than 50 m; xenoliths will retain mantle He signatures only if magma transport times are less than 50 years, or if the He fugacity in the magma is high enough to prevent xenolith degassing. The lower oceanic crust is probably substantially degassed of He. Trapped He will be qualitatively retained in quenched submarine basalt glass only if the cooling rate is faster than 5 × 10¹⁴°C/m.y.; glass at several centimeters depth in a basalt flow (near the spherulite zone) will have cooling rates lower than this, so He loss may be significant in many basalt glass samples.     

Ocean crust vein mineral deposition: Rb/Sr ages, U-Th-Pb geochemistry, and duration of circulation at DSDP sites 261, 462 and 516

Cation exchange experiments (ammonium acetate and cation resin) on celadonite-smectite vein minerals from three DSDP holes demonstrate selective removal of common Sr relative to Rb and radiogenic Sr. This technique increases the Rb/Sr ratio by factors of 2.3 to 22 without significantly altering the age of the minerals, allowing easier and more precise dating of such vein minerals. The ages determined by this technique (site 261—121.4 ±1.6 m.y.; site 462A—105.1 ±2.8 m.y.; site 516F—69.9 ±2.4 m.y.) are 34, 54 and 18 m.y. younger, respectively, than the age of crust formation at the site; in the case of site 462A, the young age is clearly related to off-ridge emplacement of a massive sill/flow complex. At the other sites, either the hydrothermal circulation systems persisted longer than for normal crust (10–15 m.y.), or were reactivated by off-ridge igneous activity.

Celadonites show U and Pb contents and Pb isotopic compositions little changed from their basalt precursors, while Th contents are significantly lower. Celadonites thus have unusually high alkali/U,Th ratios and low Th/U ratios. If this celadonite alteration signature is significantly imprinted on oceanic crust as a whole, it will lead to very distinctive Pb isotope signatures for any hot spot magmas which contain a component of aged subducted recycled oceanic crust.

Initial Sr isotope ratios of ocean crust vein minerals (smectite, celadonite, zeolite, calcite) are intermediate between primary basalt values and contemporary sea water values and indicate formation under seawaterdominated systems with effective water/rock ratios of 20–200.     

Detecting Changes in Ground Water Quality at Regulated Facilities

The Resource Conservation and Recovery Act (PL 94–580) and related federal and state legislation have mandated routine monitoring of ground water quality at regulated facilities. The objective of the required monitoring activities is detection of adverse changes in ground water quality caused by the facilities.
Both failure to detect pollution and an incorrect determination of pollution can be very expensive. It is crucial, therefore, that monitoring programs be designed and operated to provide statistically sound information. It is equally important that users of ground water quality data understand the nature and limitations of information from monitoring.
To address the preceding issues, the authors present a general approach to analyzing ground water quality data in light of the stated monitoring objective. The suggested approach accounts for "natural" variation in background water quality through pairing of observations. The limitations of quarterly sampling for detecting small changes in quality over a short time frame are discussed.     

Chemical structure and evolution of the mantle and continents determined by inversion of Nd and Sr isotopic data,I. Theoretical methods

While the chemical structure of the earth's mantle is probably rather complex, multi-box models have been used as a first approximation to evaluate this structure. Most commonly, a three-box model is used, involving the continental crust, the upper mantle and the lower mantle. The depleted upper mantle and the continental crust are assumed to represe1nt complementary reservoirs, related by crust formation processes occurring during geologic history.Here we investigate the Rb/Sr and Sm/Nd isotopic systematics of several three-box models, using mass balance equations and the definition of the mean age of the reservoirs. The geochemical uniqueness of the models, chosen from a large family of possible models, is evaluated from elementary graph theory, and these models are then solved using a total inversion approach. This paper (Part I) describes the methodology of the procedure; the companion paper (Part II) discusses the application of this approach to multi-box mantle models.     

Possible contribution of leakage currents from the Atlantic Ocean to the magnetic-field variations observed in Devon

It is suggested that leakage currents flow across Devon, north of Exeter, from large-scale electric-current systems induced in the Atlantic Ocean by the geomagnetic variations incident on the Atlantic Ocean from the ionosphere. This model can account for the variation with period of the contribution of induced current flow to the differences in the magnetic H variations of period > 30 s observed at Exeter and Sidmouth.     

Subtidal distribution of barnacles (Cirripedia: Balanidae) in Chesapeake Bay,Maryland

From 1977 to 1980, samples of barnacles were collected (as opportunities arose) from 61 subtidal locations (mostly oyster beds) around Chesapeake Bay, Maryland. Three species were identified from the area.Balanus improvisus dominated, comprising 83% of the 8,231 barnacles identified, and was collected at all locations but one. It occurred over a collection salinity range of 0.8‰ to 17.9‰.Balanus subalbidus (14% of the barnacles identified) was collected over the same salinity range, but mainly in lower salinity waters.Balanus eburneus was scarce (2% of the barnacles identified) and was collected at higher salinities (8.5‰ to 17.1‰).     

Alteration of basaltic glass: Mechanisms and significance for the oceanic crust-seawater budget

Alteration of basaltic glass to palagonite is characterized by a nearly isomolar exchange of SiO₂, Al₂O₃, MnO, MgO, CaO, Na₂O, P₂O₅, Zn, Cu, Ni, Cr, Hf, Sc, Co and REE for H₂O and K₂O, whilst TiO₂ and FeO are passively accumulated during removal of the remaining cations. The network forming cations Al and Si are removed from the glass in proportion to the gain in Ti and Fe, whilst the other cations do not show a significant relationship to the amount of Ti and Fe accumulation. Sr isotopic data show that during palagonite formation approximately 85% of the basaltic Sr is lost to the hydrous solutions and 40% of seawater Sr is added to the glass, yielding an average loss of the same order of magnitude as of the network forming cations. Losses and gains of oxides yield an average increase of +105% TiO₂.K, Rb, and Cs show high increases, but $\text{K}\text{Rb}$ and $\text{K}\text{Cs}$ ratios indicate two different alteration processes: (1) formation of palagonite involves a drastic decrease in these ratios, indicating structural similarities between palagonite and smectite; (2) surface alteration of glass is characterized by an increase in $\text{K}\text{Rb}$ and $\text{K}\text{Cs}$ ratios, probably best interpreted as sorption of alkalies in ratios approximating those of seawater.The total fluxes involved in alteration of glass in the upper portion of the oceanic crust are estimated from the modal abundance of palagonite in the oceanic crust and the abundance of the vein materials smectite and carbonate. Smectite and carbonates act as a sink for a significant portion of the elements liberated up during alteration of basaltic glass except for Na and Al, which are probably taken up by zeolites and/or albite, possibly hidden in the macroscopic estimate of carbonate. Formation of the observed quantity of secondary phases requires additional sources for Si, Fe. Ca and K. K is provided in excess from the inflowing seawater at reasonable water/rock ratios. The remaining excess Ca, Si and Fe required may be derived by alteration of interstitial glass and breakdown of anorthite rich plagioclase and titano-magnetite, and/or by supply of deeper seated metamorphic reactions.