The global-average production rate ofBe

Precipitation collected in continuously open containers for about a year at seven sites around the United States was analyzed for¹⁰Be,⁹⁰Sr,²¹⁰Pb and²³⁸U. Based on these data and long-term precipitation,⁹⁰Sr and²¹⁰Pb delivery patterns, the stratospheric, tropospheric and recycled¹⁰Be components in the collections were estimated and the global¹⁰Be production rate was assessed. Single station production rate estimates range from 0.52 × 10⁶ atoms cm⁻² yr⁻¹ to 2.64 × 10⁶ atoms cm⁻² yr⁻¹. The mean value is 1.21 × 10⁶ atoms cm⁻² yr⁻¹ with a standard error of 0.26 × 10⁶ atoms cm⁻² yr⁻¹.     

Chemical characteristics of the crater lakes of Popocatetetl, El Chichon, and Nevado de Toluca volcanoes, Mexico

Three crater lakes from Mexican volcanoes were sampled and analyzed at various dates to determine their chemical characteristics. Strong differences were observed in the chemistry among the three lakes: Nevado de Toluca, considered as dormant, El Chichón at a post-eruptive stage, and Popocatépetl at a pre-eruptive stage. Not surprisingly, no influence of volcanic activity was found at the Nevado de Toluca volcano, while the other volcanoes showed a correlation between the changing level of activity and the evolution of chemical trends. Low pHs (<3.0) were measured in the water from the active volcanoes, while a pH of 5.6 was measured at the Nevado de Toluca Sun lake. Changes with time were observed at Popocatépetl and El Chichón. Concentrations of volcanic-gas derived species like Cl⁻, SO₄²⁻ and F⁻ decreased irregularly at El Chichón from 1983 until 1997. Major cations concentrations also diminished at El Chichón. A 100% increase in the SO₄²⁻ content was measured at Popocatépetl between 1985 and 1994. An increase in the Mg/Cl ratio between 1992 (Mg/Cl=0.085) and 1994 (Mg/Cl=0.177) was observed at Popocatépetl, before the disappearance of the crater lake in 1994. It is concluded that chemical analysis of crater lakes may provide a useful additional tool for active-volcano monitoring.     

Sulfur isotopic effects in the disproportionation reaction of sulfur dioxide in hydrothermal fluids: implications for the δS variations of dissolved bisulfate and elemental sulfur from active crater lakes

Sulfur isotope effects during the SO₂ disproportionation reaction to form elemental sulfur (3SO₂+3H₂O→2HSO₄⁻+S+2H⁺) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO₄⁻ and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln α_HSO4⁻–S=6.21×10⁶/T²+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ³⁴S values of HSO₄⁻ and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). Δ_HSO4⁻–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO₂ disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high Δ_HSO4⁻–S values, whereas contribution of HSO₄⁻ produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower Δ_HSO4⁻–S values. Currently, Noboribetsu crater lake contains no HSO₄⁻ of magmatic origin. A 40-year period observation of δ³⁴S_HSO4⁻ and δ³⁴S_S values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO₂ to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ³⁴S_HSO4⁻ values. The δ¹⁸O values of HSO₄⁻ and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.     

Neodymium isotopic study of Baffin Bay water: sources of REE from very old terranes

Water samples were collected from Baffin Bay and surrounding areas in order to evaluate this region as a potential source of Nd from old continental material to Atlantic water. The isotopic data ranged from ε_Nd(0) = −9.0 to −26 with most of the data around ε_Nd(0) = −20 compared with values of North Atlantic Deep Water (NADW) with ε_Nd(0) = −13.5. The concentration of Nd in Baffin Bay waters was as high as 6 × 10⁻¹² g/g compared with 2.5 × 10⁻¹² g/g for NADW. The combination of low ε_Nd and high Nd concentration indicates that Baffin Bay may be a significant source of Nd from very old crustal material. A simple box model was used to evaluate the contribution to the Nd budget of NADW and it was concluded that a substantial fraction of the Nd from ancient crustal sources that is required to maintain the isotopic composition of NADW could be supplied by Baffin Bay outflow.     

High-resolution garnet chronometry and the rates of metamorphic processes

Garnets in an amphibolite-facies metasediment from Sulitjelma, North Norway yield precise and concordant SmNd, UPb and RbSr ages that relate directly to the pressure (P) and temperature (T) conditions of mineral growth. Differential mineral reaction between graphitic and non-graphitic layers within this sample preserves a record of theP-T and time (t) history experienced during Barrovian regional metamorphism. Garnets in graphitic layers grew during prograde metamorphism at462 ± 16°C and5.2 ± 0.5 kbar under conditions of lowaH₂O, and yield indistinguishable¹⁴⁷Sm¹⁴³Nd and²³⁸U²⁰⁶Pb ages of434.1 ± 1.2 Ma and433.9 ± 1.0 Ma, respectively. In contrast, garnet growth in adjacent graphite-free layers did not occur untilP-T conditions of540 ± 18°C and8.0 ± 1.0 kbar were attained, with continued growth in response to minor heating and decompression with final matrix equilibration at544 ± 16°C and7.0 ± 1.0 kbar. The inclusion-free garnet rims in this assemblage record indistinguishable¹⁴⁷Sm¹⁴³Nd and²³⁸U²⁰⁶Pb ages of424.6 ± 1.2 Ma and423.4± 1.7 Ma, respectively. These results provide precise estimates for average heating and burial rates during prograde metamorphism of 8.6_−4.4^+7.5°C Ma⁻¹ and 0.8_−0.5^+0.9 km Ma⁻¹, respectively. Rb and Sr exchange between coexisting silicates in the graphite-free assemblage continued for some 37 Ma after the “peak” of metamorphism, and require an average cooling rate of about 4.0°C Ma⁻¹ during uplift. These results illustrate a clear relationship between reaction history and the timing of mineral growth and provide definitive constraints on the rates of thermal and tectonic processes accompanying regional metamorphism.     

Airborne measurements of particle and gas emissions from the December 1994–January 1995 eruption of Popocatépetl volcano (Mexico)

Airborne and ground-based (correlation spectrometer, cascade impactor, and photoelectric counter together with intake filter probes) measurements are described for the volcanic emissions from Popocatépetl volcano (Mexico) from December 23, 1994 to January 28, 1995. Measurements of SO₂ restarted 48 h after the eruption onset of December 21, 1994. Maximum sulfur dioxide (4560 t d⁻¹) plus 3.8×10⁴ t d⁻¹ of particulate matter were ejected on December 24, 1994. The maximum rate of ejection occurred coincidentally with the maximum amplitude of harmonic tremor and the maximum number of seismic type B events. Sulfur dioxide emission rates ranged from 1790 to 2070 t d⁻¹ (December 23–24, 1994). Afterwards, sulfur dioxide emission rates clearly indicated a consistent decline. However, frequent gas and ash emission puffs exhibited SO₂ fluxes reaching values as high as 3060 t d⁻¹. The emission SO₂ baseline for the period of study (February 1994–January 1995) was about 1000 t d⁻¹. Ejection velocity of particulate matter was approximately 270 m s⁻¹ reaching a height of about 2.5 km over the summit. The immediate aerosol dispersion area was estimated at 6.0×10⁴ km² maximum. The microscopic structure of particles (aerosol and tephra) showed a fragile material, probably coming from weathered crustal layers. X-ray fluorescence and neutron-activation analysis from the impactor samples found the following elements: Si, Al, Ca, S, P, Cl, K, Ni, Fe, Ti, Sc, Cu, Zn, Mn, Sr, Cr, Co, Y, Br, Se, Ga, Rb, Hg and Pb. Morphological analysis shows that ash samples might be from pulverized basaltic rock indicating that the Popocatépetl eruption of December 21, 1994 was at low temperature. The microscopic structure of puff material showed substance aggregates consisted of fragile rock, water and adsorbed SO₂. These aggregates were observed within water droplets of approximately 1 mm and even larger. Sulfur transformations in the droplets occurred intensively. Volcanic ash contained 5–6% of sulfur during the first expulsion hours. Elemental relative concentrations with respect to Al show that both Si and S have relative concentrations >1, i.e., 13.73 and 2.17, respectively in agreement with the photoelectric counter and COSPEC measurements.     

Thermal equation of state of magnesite to 32 GPa and 2073 K

Pressure–volume–temperature relations have been measured to 32 GPa and 2073 K for natural magnesite (Mg_0.975Fe_0.015Mn_0.006Ca_0.004CO₃) using synchrotron X-ray diffraction with a multianvil apparatus at the SPring-8 facility. A least-squares fit of the room-temperature compression data to a third-order Birch–Murnaghan equation of state (EOS) yielded K₀ = 97.1 ± 0.5 GPa and K′ = 5.44 ± 0.07, with fixed V₀ = 279.55 ± 0.02 Å³. Further analysis of the high-temperature compression data yielded the temperature derivative of the bulk modulus (∂K_T/∂T)_P = −0.013 ± 0.001 GPa/K and zero-pressure thermal expansion α = a₀ + a₁T with a₀ = 4.03 (7) × 10⁻⁵ K⁻¹ and a₁ = 0.49 (10) × 10⁻⁸ K⁻². The Anderson–Grüneisen parameter is estimated to be δ_T = 3.3. The analysis of axial compressibility and thermal expansivity indicates that the c-axis is over three times more compressible (K_Tc = 47 ± 1 GPa) than the a-axis (K_Tc = 157 ± 1 GPa), whereas the thermal expansion of the c-axis (a₀ = 6.8 (2) × 10⁻⁵ K⁻¹ and a₁ = 2.2 (4) × 10⁻⁸ K⁻²) is greater than that of the a-axis (a₀ = 2.7 (4) × 10⁻⁵ K⁻¹ and a₁ = −0.2 (2) × 10⁻⁸ K⁻²). The present thermal EOS enables us to accurately calculate the density of magnesite to the deep mantle conditions. Decarbonation of a subducting oceanic crust containing 2 wt.% magnesite would result in a 0.6% density reduction at 30 GPa and 1273 K. Using the new EOS parameters we performed thermodynamic calculations for magnesite decarbonation reactions at pressures to 20 GPa. We also estimated stability of magnesite-bearing assemblages in the lower mantle.     

Leaf breakdown in two tropical streams: Differences between single and mixed species packs

We assessed leaf breakdown of five native riparian species from Brazilian Cerrado (Myrcia guyanensis, Ocotea sp., Miconia chartacea, Protium brasiliense, and Protium heptaphyllum), incubated in single and mixed species packs in two headwater streams with different physico-chemical properties in the Espinhaço Mountain range (Southeastern Brazil). Leaves were placed in plastic litter bags (15 cm×20 cm, 10 mm mesh size) and the experiments were carried out during the dry seasons of 2003 and 2004. Leaf nitrogen and phosphorus contents were similar in all species, but polyphenolic contents were different (P<0.001). M. guyanensis showed higher polyphenolics content (8.48% g⁻¹ dry mass) and leaf toughness. Individually, higher breakdown rates were found in M. guyanensis at Indaiá stream (k=0.0063±0.0005 d⁻¹) and in Ocotea sp. at Garcia stream (k=0.0088±0.0006 d⁻¹). However, P. brasiliense and P. heptaphyllum showed lower breakdown rates at Indaiá and Garcia streams (Indaiá: k=0.0020±0.0002 and 0.0019±0.0001 d⁻¹; Garcia: k=0.0042±0.0001 and 0.0040±0.0002 d⁻¹). Single and mixed breakdown processes of each species were not statistically different on both streams. However, all species showed higher breakdown rates at Garcia stream (P<0.01). These results suggest that leaf breakdown is not altered when litter benthic patches are composed by a mixture of species in the same proportions that they occur on riparian leaf falls.     

Cosmogenic chlorine-36 production rates in terrestrial rocks

Chlorine-36 is produced in rocks exposed to cosmic rays at the earth surface through thermal neutron activation of ³⁵Cl, spallation of ³⁹K and ⁴⁰Ca, and slow negative moun capture by ⁴⁰Ca. We have measured the ³⁶Cl content of ¹⁴C-dated glacial boulders from the White Mountains in eastern California and in a ¹⁴C-dated basalt flow from Utah. Effective, time-intergrated production parameters were calculated by simultaneous solution of the ³⁶Cl production equations. The production rates due to spallation are 4160 ± 310 and 3050 ± 210 atoms ³⁶Cl yr⁻¹ mol⁻¹³⁹K and ⁴⁰Ca, respectively. The thermal neutron capture rate was calculated to be (3.07 ± 0.24) × 10⁵ neutrons (kg of rock)⁻¹ yr⁻¹. The reported values are normalized to sea level and high geomagnetic latitudes. Production of ³⁶Cl at different altitudes and latitudes can be estimated by appropriate scaling of the sea level rates. Chlorine-36 dating was performed on carbonate ejecta from Meteor Crater, Arizona, and late Pleistocene morainal boulders from the Sierra Nevada, California. Calculated ³⁶Cl ages are in good agreement with previously reported ages obtained using independent methods.     

Viscosity of a Teide phonolite in the welding interval

The viscosity of a natural phonolitic composition with variable amounts of H₂O has been experimentally determined. The starting materials were crystal-free phonolitic glasses from Montaña Blanca, situated within the Las Cañadas caldera of Teide. Dry phonolitic melt viscosities were determined using concentric cylinder viscometry in the low viscosity range. The glassy quench products of these runs were then hydrated by high pressure synthesis in a piston–cylinder apparatus to generate a suite of samples with water contents ranging from 0.02 to 3.75 wt%. Samples thus hydrated were quenched rapidly and prepared (cut and polished) for the determination of water contents by infrared spectroscopy before and after experimental viscometry. The viscosities of the melts (dry and hydrated) were determined at 1 bar using a micropenetration technique. Samples were stable under the measurement conditions up to 3.75 wt% H₂O. Homogeneity of water content was confirmed by infrared spectroscopy and total water contents were calculated using absorptivity coefficients for compositions extremely close to that investigated here. The variation of viscosity as a function of water content and temperature can be described in the high viscosity interval of relevance to many welding processes by the non-Arrhenian expression:

(1)

log₁₀ η=−5.900−0.286 ln (H₂O)+(10775.4−394.8(H₂O))/(T−148.7+21.65 ln (H₂O))

whereas the high viscosity range alone is adequately described by the Arrhenian expression

(2)

log₁₀ η=−10.622−0.738 ln (H₂O)+(17114.3−590.4(H₂O))×1/T

where η is the viscosity in Pa s, H₂O is the water content in wt% and T is the temperature in K.These results are particularly useful for the scaling of conditions extant during the welding of phonolitic products of Montaña Blanca. The welding of glassy phonolitic rocks is enhanced by the lower viscosity of these melts with respect to calcalkaline rhyolites. The ratio of viscosities of phonolitic to calcalkaline rhyolitic melts is a complex function of temperature and water content and reaches up to 10^4.5 at 0.1 wt% H₂O and 500°C. Abundant evidence of welding and remobilisation of pyroclastic and spatter products of Teide system volcanism are consistent with these experimental observations.     

Helium accumulation in groundwater, III. Limits on helium transfer across the mantle-crust boundary beneath Australia and the magnitude of mantle degassing

The groundwaters of the Great Artesian Basin (Australia) have been previously shown to be accumulating in-situ production helium for groundwaters ages < 50 kyr and an external helium flux equivalent to whole crustal production for groundwater ages > 100 kyr [1,2]. New helium isotope measurements show that the observed in-situ production helium (³He/⁴He 1.6 × 10⁻⁸) is isotopically distinct from the crustal degassing helium flux (³He/⁴He 6.6 × 10⁻⁸). Furthermore, the crustal degassing helium isotope ratio is marginally in excess of the whole crustal production ratio (³He/⁴He= 3.5 × 10⁻⁸) and the production ratio in a variety of continental rock types. This suggests that the upper limit on volatile transport across the mantle-crust boundary beneath the (relatively) stable and “complacent” Australian continent can be characterized by a “conductive-diffusive” helium/heat flux ratio of 2.6 × 10⁶⁴He atoms mW⁻¹ s⁻¹ which is two orders of magnitude less than the “intrusive-volcanic” ratio of 2.9 × 10⁸⁴He atoms mW⁻¹ s⁻¹ measured at the Galapagos [16]. These results constrain the transcrustal mantle degassing fluxes of⁴He and⁴⁰Ar to be much less than the mid-ocean ridge degassing fluxes; which are much less than the degassing of⁴He and⁴⁰Ar from continental crust. Thus, the degassing of the Earth's interior is dominated by magmatic processes but the dominant fluxes of⁴He and⁴⁰Ar to the atmosphere must come from the continental crust.     

Hydrothermal vent waters at 13°N on the East Pacific Rise: isotopic composition and gas concentration

Gas concentrations and isotopic compositions of water have been measured in hydrothermal waters from 13°N on the East Pacific Rise. In the most Mg-depleted samples ( 5 × 10⁻³ moles/kg) the gas concentrations are: 3–4.5 × 10⁻⁵ cm³ STP/kg helium, 0.62–1.24 cm³ STP/kg CH₄, 10.80–16.71 × 10⁻³ moles/kg CO₂. The samples contain large quantities (95–126 cm³/kg) of H₂ and some carbon monoxide (0.26–0.36 cm³/kg) which result from reaction with the titanium sampling bottles. δ¹³C in methane and CO₂ (−16.6 to −19.5 and −4.1 to −5.5 respectively) indicate temperatures between 475 and 550°C, whereas δ¹³C_CO is compatible with formation by reduction of CO₂ on Ti at 350°C close to the sampling temperature.³He/⁴He are very homogeneous at (7.5 ± 0.1)R_A(³He/⁴He = 1.0 × 10⁻⁵) and very similar to already published data as well as CH₄/³He ratios between 1.4 and 2.1 × 10⁶.¹⁸O and D in water show enrichments from 0.39 to 0.69‰ and from 0.62 to 1.49‰ respectively. These values correspond to W/R ratios of 0.4–7. The distinct¹⁸O enrichments indicate that the isotopic composition of the oceans is not completely buffered by the hydrothermal circulations. The³He-enthalpy relationship is discussed in terms of both hydrothermal heat flux and³He mantle flux.     

Oxygen diffusion rates in quartz exchanged with CO2

Oxygen self diffusion rates were determined in quartz samples exchanged with¹⁸O-enriched CO₂ between 745 and 900°C and various pressures, and the diffusion profiles were measured using an ion microprobe. The activation energy (Q) and preexponential factor (D₀) at P(CO₂) = P(tot) = 100 bar, for diffusion parallel to the c-axis are 159 ( ± 13) kJ/g atom and 2.10 (+0.75/ −0.55) × 10⁻⁸ cm²/s. This rate is approximately 100 times slower than that obtained from hydrothermal experiments and 100 times faster than a previous 1-bar quartz-O₂ exchange experiment. The oxygen diffusion rate measured at 0.6 bar, 888°C, and at 900°C in vacuum is in agreement with the previous 1-bar exchange experiments with¹⁸O₂. The effect of higher CO₂ pressures is small. At 900°C, the diffusion rate exchanged with CO₂ is = 2.35 × 10⁻¹⁵ cm²/s at 100 bar, 2.24 × 10⁻¹⁵ cm²/s at 3.45 kbar and 8.13 × 10⁻¹⁵ cm²/s at 7.2 kbar.There is probably a diffusing species, other than oxygen, that enhances the oxygen diffusion rate in these quartz-CO₂ systems, relative to that occurring at very low pressures or in a vacuum. The effect of this diffusing species, however, is not as strong as that associated with H₂O. Preserved oxygen isotope fractionations between coexisting minerals in a slowly cooled, high-grade metamorphic terrane will vary depending upon whether a water-rich phase was present or not. Closure temperatures will be approximately 100°C higher in rocks where no water-rich phase was present during cooling. The measured fractionations between coexisting minerals in metamorphic rocks may potentially be used as a sensor of water presence during retrogression.     

Mesoscalic estimation of nitrogen discharge via drainage systems

A complex approach has been developed for estimating mesoscalic nitrogen discharges via drainage systems using spatial information about land use, drainage areas, nitrogen balances and soil and site characteristics. Determining the total drainage area involves certain difficulties for larger areas, as on the one hand, the available databases are incomplete, and on the other hand the localisation and digitalisation of large subsurface drainage areas is a very time-consuming process. Knowledge of the history and causes of drainage systems in landscapes is required. To solve this problem a method has been developed to calculate the drainage areas for large catchments. In order to obtain a complete data set of subsurface drainage areas, representative areas were selected to enable the proportion of subsurface drainage area to be determined for various soil and site characteristics. These proportions were extrapolated to the entire area and the approach tested in the Mulde River Catchment Area in Germany.The rate of drained arable land is about 25.2% of the total area, which can be broken down into grassland (19.0%) and arable land (27.4%). The results differ for sandy soils with up to 8% drained areas and 57.8% for stagnant soils. This shows that the proportion of drained land is highly dependent on the nature of the soil in the catchment area, which has profound implications for approaches to nitrogen modelling.Average nitrogen discharge for the whole catchment area via drainage water was 33 kg ha⁻¹ yr⁻¹ in the 1980s and 10 kg ha⁻¹ yr⁻¹ in the 1990s. The nitrogen discharge varies from one soil type to another: in regions with sandy substrate (11,900 ha) discharge was 34 kg ha⁻¹ yr⁻¹ in the 1980s (14 kg ha⁻¹ yr⁻¹ in the 1990s), while in areas with loess lessivé soils (89,200 ha) it was about 26 kg ha⁻¹ yr⁻¹ in the 1980s (9 kg ha⁻¹ yr⁻¹ in the 1990s). The reduction can be explained by the complete change in farming strategy since the demise of the former German Democratic Republic (GDR).The approach shown is well suited to future model approaches on a regional scale. By creating and integrating new data sets derived from modern GIS operations the approach reduces the uncertainty of water and nitrogen modelling. This gives us a better understanding of nitrogen discharges into surface and groundwater and temporal discharge dynamics. The discharge data are highly valuable to predict environmental protection measurements for streams, lakes, coastal waters and groundwaters.     

Riparian alder fens — source or sink for nutrients and dissolved organic carbon? — 2. Major sources and sinks

Natural riparian forest wetlands are known to be effective in their ability to remove nitrate by denitrification and sediments with attached phosphorus via sedimentation. On the other hand, litter input and decomposition is a process of crucial importance in cycling of nitrogen and phosphorus in a forest ecosystem.In this study we investigated the amount of nitrogen and phosphorus entering the alder fen ecosystem through leaf litter and its decomposition and the removal capacity of nitrogen and phosphorus by measuring denitrification and sedimentation in the alder fen.We found an average input of leaf litter during fall 1998 of 226 g m⁻² yr⁻¹ DW with nutrient concentration of 0.17% P and 1.6% N. This means a yearly input of 0.4 g m⁻² yr⁻¹ P and 3.6 g m⁻² yr⁻¹ N. The decomposition of leaf litter using litter bags with small and large mesh size resulted in bags with macroinvertebrates (large mesh size) and without macroinvertebrates (small mesh size). After 57 days the litter bags with macroinvertebrates had a decomposition rate of 79%.Denitrification was measured in May and June of 1997 using the acetylene inhibition technique on intact soil cores and slurry-experiments. The average annual denitrification rate was 0.2 g m⁻² yr⁻¹ N using data from the core experiments. The denitrification rate was higher after addition of nitrate, indicating that denitrification in the riparian alder fen is mainly controlled by nitrate supply.The sedimentation rate in the investigated alder fen ranged from 0.47 kg m⁻² yr⁻¹ DW to 4.46 kg m⁻² yr⁻¹ DW in 1998 depending on the study site and method we used. Sedimentation rates were lower in newly designed plate traps than in cylinder traps. The alder fen also showed lower rates than the adjacent creek Briese. Average phosphorus removal rate was 0.33 g m⁻² yr⁻¹ P.Input sources for the surface water of the alder fen are sediment mineralization and decomposition of leaf litter; output sources are sedimentation and denitrification. This study showed that a nutrient input of 24.58 kg ha⁻¹ yr⁻¹ N, 8.8 kg ha⁻¹ yr⁻¹ P and 419 kg ha⁻¹ yr⁻¹ DOC into the surface water of the alder fen is possible. Alder fens cannot improve water quality of an adjacent river system. This is only true for a nearly pristine alder fen with the hydrology of 10 months flooded conditions and 2 months non-flooding conditions a year.     

Development of Archaean lithosphere deduced from chronology and isotope chemistry of Scourie Dykes

The chronology and isotope geochemistry of a selection of Proterozoic Scourie dykes has been investigated in order to specify both their time of emplacement within the thermal history of the Archaean crust of N.W. Scotland, and to attempt to characterise the evolution of continental lithosphere. SmNd, RbSr and UPb isotope analyses are presented. Primary, major igneous minerals separated from four well preserved dykes yield SmNd ages of 2.031 ± 0.062Ga, 2.015 ± 0.042Ga, 1.982 ± 0.044Ga and 2.101 ± 0.078Ga, which are interpreted as crystallisation ages.The initial Nd isotope compositions in the dykes at their emplacement age of 2.0 Ga, range from +3.4 to −6.8, indicating the presence of an older lithospheric component. SmNd whole-rock isotope data for fifteen dykes, if interpreted to have age significance, yield an “age” of 3.05 ± 0.27 Ga. SmNd crustal residence ages for the same dykes average 2.95 Ga, which is interpreted as the time that small melts were added to the Lewisian lithosphere. The possibility that correlated¹⁴⁷Sm/¹⁴⁴Nd and¹⁴³Nd/¹⁴⁴Nd ratios are an artifact of mixing between depleted mantle melts generated at 2.0 Ga, and an older enriched lithospheric component is not eliminated by the data, but the relationship between 1/Nd and¹⁴³Nd/¹⁴⁴Nd ratios rules out any simple mixing. UPb isotope data for plagioclase feldspars and whole-rock samples of dykes provide useful estimates of initial Pb-isotope composition of the dykes at the time of their emplacement. Initial²⁰⁶Pb/²⁰⁴Pb and²⁰⁷Pb/²⁰⁴Pb ratios vary considerably and range from 13.98 to 15.78, and 14.72 to 15.56 respectively, and suggest that the UPb fractionation responsible must have occurred at least 2.5 Ga ago.The Scourie dykes have inherited a trace element enriched component from the Lewisian lithosphere, which has resided there since ca. 3 Ga ago. Whether the dykes inherited this material from the crust or the mantle portions of the lithosphere or both, it seems likely that small basaltic melts derived from asthenospheric mantle were ultimately responsible for the enrichment. The simplest view is that these small melt fractions had been resident in the mantle part of the Lewisian lithosphere. In this case the Archaean trace-element enrichment and element fractionation in the Lewisian lithospheric mantle sampled by the dykes was closely associated in time with the generation of the 2.9 Ga old crustal portion of the lithosphere [36,37].     

The ClBrI composition of 3.23 Ga modified seawater: implications for the geological evolution of ocean halide chemistry

Fluid inclusion leachates obtained from vug and vein quartz samples from an Archean (3.23 Ga) Fe-oxide hydrothermal deposit in the west-central part of the Barberton greenstone belt, South Africa, were analyzed by ion chromatography for chloride, bromide, and iodide. The deposit, known as the ironstone pods, formed by seafloor hydrothermal activity and fluid discharge. Quartz is dominated by type I liquid-vapor, aqueous inclusions with a bimodal salinity distribution (0–0.25 M_Cl⁻ and 0.9–1.8 M_Cl⁻). Bulk analytical salinities range from 0.45 to 0.99 M_Cl⁻ represent averages of type I inclusions. Bulk fluid inclusion bromide and iodide concentrations are 1.44–3.32 mM and 0.01–0.12 mM, respectively. For comparison, modern seawater has halogen contents of 590 mM chloride, 0.9 mM bromide, and 0.5 μM total iodine. In the fluids from the ironstone pods, bromide and iodide are enriched relative to chloride, when compared with modern seawater.Approximate Br⁻Cl⁻ and I⁻Cl⁻ ratios of 3.2 Ga Barberton seawater are 2.5 × 10⁻³ and 40 × 10⁻⁶, respectively. Dispersion to higher values was caused principally by reaction with organic sediments whose trends are similar to those seen for modern vent fluids at unsedimented and sedimented ridges, relative to modern seawater. These halide ratios are greater than those of modern seawater, suggesting a change in the halide ratios of seawater over geological time. The analytical data are consistent with a model in which marine organic sedimentation has fractionated bromine and iodine out of seawater relative to chloride, thereby causing the halide ratios of seawater to decrease from high early and mid-Archean values towards their present day values.     

Efficient trapping of organic carbon in sediments on the continental margin with high fluvial sediment input off southwestern Taiwan

Accumulation rates of marine and terrigenous organic carbon in the continental margin sediments off southwestern Taiwan were estimated from the measured concentrations and isotopic compositions of total organic carbon (TOC) and previously reported sedimentation rates. Surficial sediments were collected from the study area spanning from the narrow shelf near the Kaoping River mouth to the deep slope with depths reaching almost 3000 m. The average sediment loading of Kaoping River is 17 Mt/yr, which yields high sediment accumulation rates ranging from 0.08 to 1.44 g cm⁻² yr⁻¹ in the continental margin. About half of the discharged sediments were deposited on the margin within 120 km of the river mouth. Carbon isotopic compositions of terrestrial and marine end-members of organic matter were determined, respectively, based on suspended particulate matter (SPM) collected from three major rivers in the southwestern Taiwan and from an offshore station. All samples were analyzed for the TOC content and its isotopic composition (δ¹³C_org). The SPM samples were also analyzed for the total nitrogen (TN) content. TOC content in marine sediments ranges from 0.45% to 1.35% with the highest values on the upper slope near the Kaoping River mouth. The TOC/TN ratio of the SPM samples from the offshore station is 6.8±0.6, almost identical to the Redfield ratio, indicating their predominantly marine origin; their δ¹³C_org values are also typically marine with a mean of −21.5±0.3‰. The riverine SPM samples exhibit typical terrestrial δ¹³C_org values around −25‰. The δ¹³C_org values of surficial sediments range from −24.8‰ to −21.2‰, showing a distribution pattern influenced by inputs from the Kaoping River. The relative contributions from marine and terrestrial sources to sedimentary organic carbon were determined by the isotope mixing model with end-member compositions derived from the riverine and marine SPM. High fluvial sediment inputs lead to efficient trapping of organic carbon over a wide range of water depth in this continental margin. The marine organic accumulation rate ranges from 1.6 to 70 g C m⁻² yr⁻¹ with an area weighted mean of 4.2 g C m⁻² yr⁻¹, which is on a par with the mean terrestrial contribution and accounts for 2.3% of mean primary production. The depth-dependent accumulation rate of marine organic carbon can be simulated with a function involving primary productivity and mineral accumulation rate, which may be applicable to other continental margins with high sedimentation rates. Away from the nearshore area, the content of terrigenous organic carbon in surficial sediments decreases with distance from the river mouth, indicating its degradation in marine environments.     

Turbulence measurements in a submarine canyon

Profiles of velocity turbulence in Monterey Canyon, made with a recently developed expendable probe, show the existence of a very turbulent bottom boundary layer. The turbulent flow is up to 170 m thick and has peak microscale shears of 1 m s⁻¹ per meter. The rate of dissipation of kinetic energy, based on the observed shear variance, averaged over the depth of the turbulent boundary layer ranged from 70 to 500 × 10⁻⁶W m⁻³. Temperature measurements indicate that the flow was up canyon at a time of low tide. The upper bound for the vertical eddy viscosity is estimated to be17 × 10⁻⁴m²s⁻¹ and for the vertical eddy diffusivity is estimated to be 15 × 10⁻⁴m²s⁻¹. The large vertical scale and the intensity of the observed boundary layer suggest that the flow in Monterey Canyon may be important for the renewal and circulation of water over the continental shelf in the bay area.     

Crustal strain observation for nine years with a laser strainmeter in Kobe, Japan

We carried out precise crustal strain observation using a laser strainmeter system at the Rokko-Takao station in Kobe, Japan from 1989 to 1997. The long-term strain record is characterized by remarkable annual changes of the order of 2–3×10⁻⁶ and linear strain accumulation of −4.4×10⁻⁷/year (in contraction). The annual strain changes are inversely proportional to temperature changes that precede the strain changes by about 1 month. The apparent annual strain changes were mainly caused by refractive-index changes in the light path due to the ambient temperature changes. After eliminating the annual temperature effect, linear strain accumulation is corrected to be −6.3−6.7×10⁻⁷/year. Residual strains show the oscillating behavior, in which the oscillating cycle seems to become shorter and shorter as time goes by. During the period, a destructive earthquake of M=7.2 occurred near the Kobe City on 17 January 1995. We investigated the oscillating behavior in secular variations of ground-strains by introducing the deterministic approach of earthquake prediction to search for the “critical point” of the occurrence of an earthquake in the extended power law equation. However, we could not obtain a unique solution to determine eight unknown parameters including the “critical point”. This may be mainly due to lack of data for 4 months from August to November in 1994 by the failure of the laser source before the occurrence of earthquake on 17 January 1995. After removing environmental effects and tidal components, we carefully re-examined strain changes in 7 days and 1 day before the occurrence of the earthquake, but we could not detect anomalous strain changes exceeding 1×10⁻⁸ before the earthquake.