The effect of transient storage on nitrate uptake lengths in streams: an inter‐site comparison

Surface water–groundwater interaction in the hyporheic zone may enhance biogeochemical cycling in streams, and it has been hypothesized that streams exchanging more water with the hyporheic zone should have more rapid nitrate utilization. We used simultaneous conservative solute and nitrate addition tracer tests to measure transient storage (which includes hyporheic exchange and in‐stream storage) and the rate of nitrate uptake along three reaches within the Red Canyon Creek watershed, Wyoming. We calibrated a one‐dimensional transport model, incorporating transient storage (OTIS‐P), to the conservative solute breakthrough curves and used the results to determine the degree of transient storage in each reach. The nitrate uptake length was quantified from the exponential decrease in nitrate concentration with distance during the tracer tests. Nitrate uptake along the most downstream reach of Red Canyon Creek was rapid (turnover time K^?1_c = 32 min), compared with nitrate uptake reported in other studies (K^?1_c = 12 to 551 min), but other sites within the watershed showed little nitrate retention or loss. The uptake length S_w‐NO^?₃ for the most downstream reach was 500 m and the mass transfer coefficient V_f‐NO^?₃ was 6·3 m min^?1. Results from 15 other nitrate‐addition tracer tests were used to create a regression model relating transient storage and measures of stream flow to nitrate uptake length. The model, which includes specific discharge and transient storage area, explains almost half the variability in nitrate uptake length (adjusted R² = 0·44) and is most effective for comparing sites with very different stream characteristics. Although large differences in specific discharge and storage zone area explain inter‐site differences in nitrate uptake, other unmeasured variables, such as available organic carbon and microbial community composition, are likely important for predicting differences in nitrate uptake between sites with similar specific discharge rates and storage zone areas, such as when making intra‐site comparisons. Copyright © 2007 John Wiley & Sons, Ltd.     

Sedimentary vs. diagenetic control on rhythmic calcareous successions (Pliensbachian of Asturias, Spain)

The diagenetic overprint in rhythmic hemipelagic successions can either enhance or change the original distribution of CaCO₃, but it is difficult to evaluate its effect because in most field examples, it is not possible to distinguish between sedimentary and diagenetic features. The rhythmic succession of the Pliensbachian of Asturias (Spain) shows alternation of bioclastic and laminated/burrowed intervals. The original content of carbonate brought by storms from shallow areas was larger in the bioclastic horizons. However, there is a widespread mismatch between facies alternations and the observed lithological rhythms. The diagenetic redistribution of CaCO₃ resulted in successive limestone–marl/clay couplets that do not match (either in number or in the location of the boundaries) the sedimentary cycles defined by facies alternations. We conclude that interpreting the limestone–marl rhythms as a direct response to primary changes is highly questionable, unless there is unequivocal proof of a sedimentary origin of the alternation of the two lithologies.     

Preliminary paleolimnological study of rocha lagoon, SE Uruguay

Physical, chemical and biological data from a sedimentary profile of Rocha lagoon (Uruguay) are presented. Analyses of silica remains showed that opal phytoliths, diatoms, sponge spicules and chrysophyte cysts were the most important contributors to biogenic silica. Organic matter, total nitrogen and total phosphorus were used to infer past trophic development. Physical analysis of sediments allowed us to identify five lithological units related to sea level variation and climatic events.     

U and Th concentrations and isotope ratios in modern carbonates and waters from the Bahamas

The short residence times of Th and Pa in seawater make them very responsive to changes in the ocean environment. We use a new multi-ion-counting technique to make Th and Pa isotope measurements in seawaters from a near-shore environment in which oceanic chemical tracers are not overwhelmed by terrestrial inputs (the Bahamas). An unusual feature of the Bahamas setting is the shallow depth of water residing on the bank tops. These waters have significantly lower ²³²Th/²³⁰Th (∼10,000) than those immediately adjacent to the banks (24,000-31,000) and a (²³¹Pa/²³⁰Th) near the production ratio (∼0.1). The change in ²³²Th/²³⁰Th and (²³¹Pa/²³⁰Th) on the bank tops is explained by almost quantitative removal of Th and Pa by scavenging, and their replacement with a mixture of ²³⁰Th and ²³¹Pa alpha-recoiled from the underlying carbonates, together with Th from dust dissolution. Analysis of a water profile in the Tongue of the Ocean, which separates the Great and Little Bahama Banks, allows us to trace the movement of bank-top water to depth. A distinct minimum in both ²³²Th/²³⁰Th (∼13,000) and (²³¹Pa/²³⁰Th) (∼0.5) is observed at ∼430 m and is interpreted to reflect density cascading of bank-top water with entrained carbonate sediment. These results suggest that Th and Pa can be used as water-mass tracers in near-shore environments. Uranium concentration measurements on the same waters demonstrate that U is conservative across a range in salinity of 2 psu, with a concentration of 3.33 ppb (at a salinity of 35).The incorporation of U and Th isotopes into marine carbonates has also been assessed by analyzing carbonate samples from the same location as these Bahamas waters. Such incorporation is critical for U-Th geochronology. U isotope analyses demonstrate that seawater δ²³⁴U averages 146.6 and does not vary by more than 2.5%o, and that carbonates capture this value. Additional high precision measurements (≈±1%o) on modern carbonates confirm that all oceans have identical δ²³⁴U. Modern marine carbonates are shown to have ²³²Th/²³⁰Th ratios that reflect the local seawater in which they formed.     

Habitat requirements for submerged aquatic vegetation in Chesapeake Bay: Water quality, light regime, and physical-chemical factors

We developed an algorithm for calculating habitat suitability for seagrasses and related submerged aquatic vegetation (SAV) at coastal sites where monitoring data are available for five water quality variables that govern light availability at the leaf surface. We developed independent estimates of the minimum light required for SAV survival both as a percentage of surface light passing though the water column to the depth of SAV growth (PLW _min) and as a percentage of light reaching reaching leaves through the epiphyte layer (PLL _min). Value were computed by applying, as inputs to this algorithm, statistically dervived values for water quality variables that correspond to thresholds for SAV presence in Chesapeake Bay. These estimates ofPLW _min andPLL _min compared well with the values established from a literature review. Calcultations account for tidal range, and total light attenuation is partitioned into water column and epiphyte contributions. Water column attenuation is further partitioned into effects of chlorophylla (chla), total suspended solids (TSS) and other substances. We used this algorithm to predict potential SAV presence throughout the Bay where calculated light available at plant leaves exceededPLL _min. Predictions closely matched results of aerial photographic monitoring surveys of SAV distribution. Correspondence between predictions and observations was particularly strong in the mesohaline and polythaline regions, which contain 75–80% of all potential SAV sites in this estuary. The method also allows for independent assessment of effects of physical and chemical factors other than light in limiting SAV growth and survival. Although this algorithm was developed with data from Chesapeake Bay, its general structure allows it to be calibrated and used as a quantitative tool for applying water quality data to define suitability of specific sites as habitats for SAV survival in diverse coastal environments worldwide.     

Cu isotopic fractionation in the supergene environment with and without bacteria

The isotopic composition of dissolved Cu and solid Cu-rich minerals [δ⁶⁵Cu (‰) = (⁶⁵Cu/⁶³Cu_sample/⁶⁵Cu/⁶³Cu_std) - 1)*1000] were monitored in batch oxidative dissolution experiments with and without Thiobacillus ferrooxidans. Aqueous copper in leach fluids released during abiotic oxidation of both chalcocite and chalcopyrite was isotopically heavier (δ⁶⁵Cu = 5.34‰ and δ⁶⁵Cu = 1.90‰, respectively, [±0.16 at 2σ]) than the initial starting material (δ⁶⁵Cu = 2.60 ± 0.16‰ and δ⁶⁵Cu = 0.58 ± 0.16‰, respectively). Isotopic mass balance between the starting material, aqueous copper, and secondary minerals precipitated in these experiments explains the heavier isotopic values of aqueous copper. In contrast, aqueous copper from leached chalcocite and chalcopyrite inoculated with Thiobacillus ferrooxidans was isotopically similar to the starting material. The lack of fractionation of the aqueous copper in the biotic experiments can best be explained by assuming a sink for isotopically heavy copper present in the bacteria cells with δ⁶⁵Cu = 5.59 ± 0.16‰. Consistent with this inference, amorphous Cu-Fe oxide minerals are observed surrounding cell membranes of Thiobacillus grown in the presence of dissolved Cu and Fe.Extrapolating these experiments to natural supergene environments implies that release of isotopically heavy aqueous Cu from oxidative leach caps, especially under abiotic conditions, should result in precipitates in underlying enrichment blankets that are isotopically heavy. Where iron-oxidizing cells are involved, isotopically heavy oxidized Cu entrained in cellular material may become associated with leach caps, causing the released aqueous Cu to be less isotopically enriched in the heavy isotope than predicted for the abiotic system. Rayleigh fractionation trends with fractionation factors calculated from our experiments for both biotic and abiotic conditions are consistent with large numbers of individual abiotic or biotic leaching events, explaining the supergene chalcocites in the Morenci and Silver Bell porphyry copper deposits.     

Observations of physical effects from tsunamis of December 30, 2002 at Stromboli volcano, southern Italy

On December 30, 2002, following an intense period of activity of Stromboli volcano (south Tyrrhenian Sea, Italy), complex mass failures occurred on the northwest slope of the mountain which also involved the underwater portion of the volcanic edifice for a total volume of about 2–3×10⁷ m³. Two main landslides occurred within a time separation of 7 min, and both set tsunami waves in motion that hit the coasts of Stromboli causing injuries to three people and severe damage to buildings and structures. The tsunamis also caused damage on the island of Panarea, some 20 km to the SSE from the source. They were observed all over the Aeolian archipelago, at the island of Ustica to the west, along the northern Sicily coasts to the south as well as along the Tyrrhenian coasts of Calabria to the east and in Campania to the north. This paper presents field observations that were made in the days and weeks immediately following the events. The results of the quantitative investigations undertaken in the most affected places, namely along the coasts of Stromboli and on the island of Panarea, are reported in order to highlight the dynamics of the attacking waves and their impact on the physical environment, on the coastal structures and on the coastal residential zone. In Stromboli, the tsunami waves were most violent along the northern and northeastern coastal belt between Punta Frontone and the village of Scari, with maximum runup heights of about 11 m measured on the beach of Spiaggia Longa. Measured runups were observed to decay rapidly with distance from the source, typical of tsunami waves generated by limited-area sources such as landslides.     

The Ross orogeny of the transantarctic mountains: a northern Victoria Land perspective

Northern Victoria Land (Antarctica) is made up of three terranes of Cambrian–Ordovician rocks: the Wilson (WT), Bowers (BT) and Robertson Bay terranes (RBT). The WT comprises a low- to high-grade metasedimentary sequence intruded by calc-alkaline plutons with magmatic arc affinity; the BT is composed of low-grade metavolcanic and metasedimentary rocks usually interpreted as an intra-oceanic arc; the RBT is a very low-grade flysch-like sequence. Terrane juxtaposition has traditionally been attributed to accretion during the Cambro-ordovician Ross orogeny. We propose a new model in which the WT, BT and RBT are interpreted as an arc/back-arc/trench system, developed in the context of a SW-dipping subduction zone. The subducting plate carried a continent originally located outboard of the turbidite fan of the RBT. Collision between this continent and the East Antarctic craton caused partial subduction of the intervening back-arc basin and, ultimately, the end of Ross-orogenic subduction. The turbidite fan of the RBT originally sedimented above the trench and on the subducting oceanic plate; due to collision it was thrusted on the continent, that constitutes, at least in part, the present basement of the RBT turbidite. The eastern portions of this continental mass were later dissected by the tensile tectonics related to the opening of the of the Southern Ocean.     

Building stone employed in the historical monuments of Eastern Sicily (Italy). An example: the ancient city centre of Catania

An archaeometric study of the stone materials employed in the Late Baroque historical monuments of the ancient city centre of Catania was carried out. Lithological maps of a selection of monuments, transferred to a digital format, revealed that the stone materials are both magmatic and sedimentary rocks, the colours of which are matched in a peculiar type of bichromy. Particular attention focused on sedimentary rocks, which consist of various types of limestone quarried near the city of Syracuse (Hyblean Plateau, south-eastern Sicily). Carbonate rocks were characterised in terms of mineralogy, petrography and geochemistry, by studying rock samples from both monuments and historical extraction sites. Results showed that, although only one name was historically attributed to the above lithotypes (i.e. “Pietra di Siracusa‘’), they were quarried from many locations and, as they belong to various geological formations, they therefore exhibit great variety. In order to examine the durability of Hyblean limestones employed in works of cultural heritage interest, salt crystallisation tests were carried out according to standard procedure norms (UNI EN 12370 (1999) Determination of resistance to crystallisation of salts, 6p). Results are consistent with the forms of deterioration observed in the monuments, and highlight the close relationship between textural characteristics and damage. Our purpose is to provide a basic tool, which may be useful both for conserving monuments of cultural heritage and for their restoration.