Cycloid crack sequences on Europa: Relationship to stress history and constraints on growth mechanics based on cusp angles

The original model developed to explain cycloidal cracks on Europa interprets cycloids as tensile fractures that grow in a curved path in response to the constantly rotating diurnal tidal stress field. Cusps form when a new cycloid crack segment propagates at an angle to the first in response to a rotation of the principal tidal stress orientation during a period of no crack growth. A recent revised model states that a cycloid cusp forms through the creation of a secondary fracture called a tailcrack at the tip of an existing cycloid segment during shearing motion induced by the rotating tidal stress field. As the tailcrack propagates away from the cusp, it becomes the next cycloid segment in the chain. The qualitative tailcrack model uniquely accounts for the normal and shear stresses that mechanically must resolve onto the tip of an existing cycloid segment at the instant of cusp formation. In this work, we provide a quantitative framework and test of the hitherto purely conceptual tailcrack model. We first present a relative age sequence inferred from geologic mapping of multiply cross-cutting cycloids in Europa's trailing hemisphere and place this into the context of the global stress history. The age sequence requires a cumulative minimum of 630° of shell reorientation due to nonsynchronous rotation to account for the observed range of orientations of cycloids of different ages. We determined the back-rotated longitudes of formation of two cycloid chain examples and used mathematical modeling of europan tidal stresses to show that the tailcrack model for cusp formation is not only viable, but places constraints on the overall development of a cycloid chain by controlling the timing of cusp development within Europa's orbit. For all cusps analyzed, the exact ratio of resolved shear to normal stress required to form the cusp angles by a process of tailcracking, as governed by the principles of linear elastic fracture mechanics, is produced at the tip of a shearing cycloid segment during Europa's orbit. Cusp formation occurs after the point in the orbit at which the maximum tensile principal tidal stress occurs, implying that tensile tidal stresses are not directly responsible for cusp development. Instead, cusps develop when a tailcrack forms at the tip of a cycloid segment in response to the highly perturbed stress field induced during concomitant opening and shearing at the tip of the cycloid segment.     

Faecal-indicator bacteria and sedimentary processes in estuarine mudflats (Seine, France)

Over a three-year period, quantification of faecal indicators and the molecular detection of Escherichia coli and Salmonella were monitored in sediments from three contrasting mudflats of the Seine estuary (France). The elevation of the mudflat surface was monitored concurrently using a high-resolution altimeter. During the period of the study, estuarine mudflats were areas of deposition for faecal-indicator bacteria and were mainly controlled by sedimentary processes. In the intertidal freshwater and subtidal mudflats, the highest abundances of faecal-indicator bacteria were counted during a depositional period. Maximum levels were observed in the freshwater mudflats during periods of high flow: thermotolerant coliforms: 3.9 x 10(4) cfu cm(-2), enterococci: 1.2 x 10(4) cfu cm(-2), Clostridium perfringens spores: 9.8 x 10(5) spores cm(-2). Loss of culturability of enteric bacteria in sediment microcosms demonstrated the remediatory capacity of the mudflats, even if they might be a secondary source of bacteria-forming spores to the water column through erosion and resuspension events.     

Nutrient availability in support of Karenia brevis blooms on the central West Florida Shelf: What keeps Karenia blooming?

Identifying nutrient sources, primarily nitrogen (N) and phosphorus (P), sufficient to support high biomass blooms of the red tide dinoflagellate, Karenia brevis, has remained problematic. The West Florida Shelf is oligotrophic, yet populations >10⁶ cells L⁻¹ frequently occur and blooms can persist for months. Here we examine the magnitude and variety of sources for N and P that are available to support blooms. Annual average in situ or background concentrations of inorganic N in the region where blooms occur range 0.02–0.2 μM while inorganic P ranges 0.025–0.24 μM. Such concentrations would be sufficient to support the growth of populations up to ∼3×10⁴ cells L⁻¹ with at least a 1 d turnover rate. Organic N concentrations average 1–2 orders of magnitude greater than inorganic N, 8–14 μM while organic P concentrations average 0.2–0.5 μM. Concentrations of organic N are sufficient to support blooms >10⁵ cells L⁻¹ but the extent to which this complex mixture of N species is utilizable is unknown. Other sources of nutrients included in our analysis are aerial deposition, estuarine flux, benthic flux, zooplankton excretion, N₂-fixation, and subsequent release of organic and inorganic N by Trichodesmium spp., and release of N and P from dead and decaying fish killed by the blooms. Inputs based on atmospheric deposition, benthic flux, and N₂-fixation, were minor contributors to the flux required to support growth of populations >2.6×10⁴ cells L⁻¹. N and P from decaying fish could theoretically maintain populations at moderate concentrations but insufficient data on the flux and subsequent mixing rates does not allow us to calculate average values. Zooplankton excretion rates, based on measured zooplankton population estimates and excretion rates could also supply all of the N and P required to support populations of 10⁵ and 10⁶ cells L⁻¹, respectively, but excretion is considered as “regenerated” nutrient input and can only maintain biomass rather than contribute to “new” biomass. The combined estuarine flux from Tampa Bay, Charlotte Harbor, and the Caloosahatchee River can supply a varying, but at times significant level of N and P to meet growth and photosynthesis requirements for populations of approximately 10⁵ cells L⁻¹ or below. Estimates of remineralization of dead fish could supply a significant proportion of bloom maintenance requirements but the rate of supply must still be determined. Overall, a combination of sources is required to maintain populations >10⁶ cells L⁻¹.     

Oceanographic and climatic implications of the Palaeocene carbon isotope maximum

We have compared detailed planktonic and benthonic foraminiferal carbon and oxygen isotope records from the Palaeocene and early Eocene successions at DSDP Site 577 (Shatsky Rise, North Pacific), a composite section derived from DSDP Leg 74 sites (Walvis Ridge, South Atlantic) and a composite section from ODP Leg 113 sites (Maud Rise, Weddell Sea). The δ¹³C records of Palaeocene and early Eocene Foraminifera at Site 577 and the Leg 74 sites show that an increase in δ¹³C values in surface waters at 64 Ma (end of Zone P1) resulted in increased vertical carbon isotope gradients (δ¹³C) between surface and deeper dwelling planktonic foraminifera, and between surface-dwelling planktonics and benthonic foraminifera which became progressively steeper until the iniddle Late Palaeocene (Zone P4). This steepening also occurs in the latest Palaeocene of the composite Leg 113 section and can be explained by an increase in surface ocean productivity. This increase in productivity probably resulted in an expansion of the oxygen minimum zone (OMZ). Benthonic δ¹³C values increased during the late Palaeocene in Site 577 and the composite Leg 74 section, suggesting that the Palaeocene carbon isotope maximum was composed of both within-ocean reservoir (increased surface water productivity) and between-reservoir (organic carbon burial) ftactionation effects. The benthonic δ¹³C increase lags the surface ocean δ¹³C increase in the early Palaeocene (63–64 Ma) suggesting that surface water productivity increase probably led an increase in the burial rate of organic carbon relative to carbonate sedimentation. Moreover, inter-site δ¹³C comparisons suggest that the locus of deep to intermediate water formation for the majority of the Palaeocene and the earliest Eocene was more likely to have been in the high southern latitudes than in the lower latitudes. Oxygen isotope data show a decline in deeper water temperatures in the early and early late Palaeocene, followed by a temperature increase in the late Palaeocene and across the PalaeoceneEocene boundary. We speculate that these changes in deeper water temperatures were related to the flux of CO₂ between the oceans and the atmosphere through a mechanism operating at the high southern latitudes.     

Identification of a c-Ki-ras oncogene in a neoplasm isolated from winter flounder

It has been shown that a high incidence of hepatomas are present in winter flounder (Pseudopleuronectes americanus) obtained from Boston Harbor. It has been suggested that this may be a consequence of locally high levels of polycyclic aromatic hydrocarbons found in the sediment. The purpose of this study was to determine whether transforming DNA sequences (oncogenes) could be identified in liver neoplasms isolated from feral fish and to study their relationship to their corresponding proto-oncogenes. The ultimate aim of this study is to characterize novel mutations in oncogenes derived from these hepatomas to correlate these genetic changes with chemical exposure history. Genomic DNA was isolated from liver neoplasms and transfected into NIH3T3 mouse fibroblasts to assay for the formation of transformed foci. DNA was prepared from transformed foci and analyzed by Southern blot hybridization to viral DNA probes specific for c-Ki-ras and c-Ha-ras DNA sequences. A c-Ki-ras oncogene was identified in a transformant derived from one of the two tumors assayed. Comparison of c-Ki-ras DNA sequences of tumor and tumor-derived transformants indicate that the activated oncogene in the transformant is of flounder origin. We are currently analyzing the flounder oncogene for activating point mutations by primer-directed enzymatic amplification and direct sequence analysis.