Bioaccumulation and histopathological effects of oil on a stony coral

Colonies of the shallow-water Caribbean coral Manicina areolata incorporated petroleum hydrocarbons into their tissues during exposure to water accommodated fractions of No. 2 fuel oil for three months. This contamination was not removed after depuration periods of up to two weeks. Although these corals remained alive, evidence of pathological responses was found which included impaired development of reproductive tissues, degeneration and loss of symbiotic zooxanthellae, and atrophy of mucous secretory cells and muscle bundles.     

Analysis of development and depth of backward erosion pipes in the presence of a coarse sand barrier

Backward erosion piping (BEP) is a failure mechanism that can affect the safety of water-retaining structures. It can occur when a local anomaly on the downstream side of an embankment causes a concentration of seepage flow at that location. Shallow pipes may then form, progressing in the upstream direction and leading to a collapse of the water-retaining structure. A novel and economically appealing measure against BEP is the coarse sand barrier (CSB), which is now being developed in a multiscale experimental programme in the Netherlands. The method involves placing a trench filled with coarse sand below the blanket layer on the downstream side of the embankment. The CSB prevents the upstream progression of the pipe and significantly enhances resistance to BEP. This paper presents medium-scale laboratory tests involving a range of sands, barrier depths and relative densities. The piping process and the observations of pipe progression in the presence of a CSB are presented, followed by a conceptual model. The presence of a CSB changed the erosion pattern. It resulted in pipe formation perpendicular to the flow direction over the entire width of the barrier before the barrier was damaged. The findings also demonstrate the effect of material properties on pipe initiation, progression and pipe depth. Measurements of the pipe depth are presented and analysed, revealing the significance of pipe depth for understanding the piping process. This analysis shows considerable erosion in the downstream background sand and demonstrates that erosion profiles and measured pipe depths are significantly larger than in BEP tests without a CSB.

     

Assessment of ERA5 and ERA-Interim in Reproducing Mean and Extreme Climates over West Africa

In situ data in West Africa are scarce, and reanalysis datasets could be an alternative source to alleviate the problem of data availability. Nevertheless, because of uncertainties in numerical prediction models and assimilation methods, among other things, existing reanalysis datasets can perform with various degrees of quality and accuracy. Therefore, a proper assessment of their shortcomings and strengths should be performed prior to their usage. In this study, we examine the performance of E...     

Hydrothermal processes in partially serpentinized peridotites from Costa Rica: evidence from native copper and complex sulfide assemblages

Native metals and metal alloys are common in serpentinized ultramafic rocks, generally representing the redox and sulfur conditions during serpentinization. Variably serpentinized peridotites from the Santa Elena Ophiolite in Costa Rica contain an unusual assemblage of Cu-bearing sulfides and native copper. The opaque mineral assemblage consists of pentlandite, magnetite, awaruite, pyrrhotite, heazlewoodite, violarite, smythite and copper-bearing sulfides (Cu-pentlandite, sugakiite [Cu(Fe,Ni)₈S₈], samaniite [Cu₂(Fe,Ni)₇S₈], chalcopyrite, chalcocite, bornite and cubanite), native copper and copper–iron–nickel alloys. Using detailed mineralogical examination, electron microprobe analyses, bulk rock major and trace element geochemistry, and thermodynamic calculations, we discuss two models to explain the formation of the Cu-bearing mineral assemblages: (1) they formed through desulfurization of primary sulfides due to highly reducing and sulfur-depleted conditions during serpentinization or (2) they formed through interaction with a Cu-bearing, higher temperature fluid (350–400 °C) postdating serpentinization, similar to processes in active high-temperature peridotite-hosted hydrothermal systems such as Rainbow and Logatchev. As mass balance calculations cannot entirely explain the extent of the native copper by desulfurization of primary sulfides, we propose that the native copper and Cu sulfides formed by local addition of a hydrothermal fluid that likely interacted with adjacent mafic sequences. We suggest that the peridotites today exposed on Santa Elena preserve the lower section of an ancient hydrothermal system, where conditions were highly reducing and water–rock ratios very low. Thus, the preserved mineral textures and assemblages give a unique insight into hydrothermal processes occurring at depth in peridotite-hosted hydrothermal systems.     

Phase relations in the greenschist-blueschist-amphibolite-eclogite facies in the system Na2O-CaO-FeO-MgO-Al2O3-SiO2-H2O (NCFMASH), with application to metamorphic rocks from Samos, Greece

Calculated phase equilibria among the minerals sodic amphibole, calcic amphibole, garnet, chloritoid, talc, chlorite, paragonite, margarite, omphacite, plagioclase, carpholite, zoisite/clinozoisite, lawsonite, pyrophyllite, kyanite, sillimanite, quartz and H₂O are presented for the model system Na₂O-CaO-FeO-MgO-Al₂O₃-SiO₂-H₂O (NCFMASH), which is relevant for many greenschist, blueschist, amphibolite and eclogite facies rocks. Using the activity-composition relationships for multicomponent amphiboles constrained by Will and Powell (1992), equilibria containing coexisting calcic and sodic amphiboles could be determined. The blueschist–greenschist transition reaction in the NCFMASH system, for example, is defined by the univariant reaction sodic amphibole + zoisite = calcic amphibole + chlorite + paragonite + plagioclase (+ quartz + H₂O) occurring between approximately 420 and 450 °C at 9.5 to 10 kbar. The calculated petrogenetic grid is a valuable tool for reconstructing the PT-evolution of metabasic rocks. This is shown for rocks from the island of Samos, Greece. On the basis of mineral and whole rock analyses, PT-pseudosections were calculated and, together with the observed mineral assemblages and reaction textures, are used to reconstruct PT-paths. For rocks from northern Samos, pseudomorphs after lawsonite preserved in garnet, the assemblage sodic amphibole-garnet-paragonite-chlorite-zoisite-quartz and the retrograde appearance of albitic plagioclase and the formation of calcic amphibole around sodic amphibole constrain a clockwise PT-path that reaches its thermal maximum at some 520 °C and 19 kbar. The derived PT-trajectory indicates cooling during exhumation of the rocks and is similar to paths for rocks from the western part of the Attic-Cycladic crystalline complex. Rocks from eastern Samos indicate lower pressures and are probably related to high-pressure rocks from the Menderes Massif in western Turkey. Received: 8 July 1997 / Accepted: 11 February 1998     

First identification and characterization of Borrobol‐type tephra in the Greenland ice cores: new deposits and improved age estimates

Contiguous sampling of ice spanning key intervals of the deglaciation from the Greenland ice cores of NGRIP, GRIP and NEEM has revealed three new silicic cryptotephra deposits that are geochemically similar to the well‐known Borrobol Tephra (BT). The BT is complex and confounded by the younger closely timed and compositionally similar Penifiler Tephra (PT). Two of the deposits found in the ice are in Greenland Interstadial 1e (GI‐1e) and an older deposit is found in Greenland Stadial 2.1 (GS‐2.1). Until now, the BT was confined to GI‐1‐equivalent lacustrine sequences in the British Isles, Sweden and Germany, and our discovery in Greenland ice extends its distribution and geochemical composition. However, the two cryptotephras that fall within GI‐1e ice cannot be separated on the basis of geochemistry and are dated to 14358 ± 177 a b2k and 14252 ± 173 a b2k, just 106 ± 3 years apart. The older deposit is consistent with BT age estimates derived from Scottish sites, while the younger deposit overlaps with both BT and PT age estimates. We suggest that either the BT in Northern European terrestrial sequences represents an amalgamation of tephra from both of the GI‐1e events identified in the ice‐cores or that it relates to just one of the ice‐core events. A firm correlation cannot be established at present due to their strong geochemical similarities. The older tephra horizon, found within all three ice‐cores and dated to 17326 ± 319 a b2k, can be correlated to a known layer within marine sediment cores from the North Iceland Shelf (ca. 17179‐16754 cal a BP). Despite showing similarities to the BT, this deposit can be distinguished on the basis of lower CaO and TiO₂ and is a valuable new tie‐point that could eventually be used in high‐resolution marine records to compare the climate signals from the ocean and atmosphere.     

The spatial and temporal distribution of grain‐size breaks in turbidites

Grain‐size breaks are surfaces where abrupt changes in grain size occur vertically within deposits. Grain‐size breaks are common features in turbidites around the world, including ancient and modern systems. Despite their widespread occurrence, grain‐size breaks have been regarded as exceptional, and not included within idealized models of turbidity current deposition. This study uses ca 100 shallow sediment cores, from the Moroccan Turbidite System, to map out five turbidite beds for distances in excess of 2000 km. The vertical and spatial distributions of grain‐size breaks within these beds are examined. Five different types of grain‐size break are found: Type I – in proximal areas between coarse sand and finer grained structureless sand; Type II – in proximal areas between inversely graded sand overlain by finer sand; Type III – in proximal areas between sand overlain by ripple cross‐laminated finer sand; Type IV – throughout the system between clean sand and mud; and Type V – in distal areas between mud‐rich (debrite) sand and mud. This article interprets Types I and V as being generated by sharp vertical concentration boundaries, controlled by sediment and clay concentrations within the flows, whilst Types II and III are interpreted as products of spatial/temporal fluctuations in flow capacity. Type IV are interpreted as the product of fluid mud layers, which hinder the settling of non‐cohesive grains and bypasses them down slope. Decelerating suspensions with sufficient clay will always form cohesive layers near to bed, promoting the generation of Type IV grain‐size breaks. This may explain why Type IV grain‐size breaks are widespread in all five turbidites examined and are commonplace within turbidite sequences studied elsewhere. Therefore, Type IV grain‐size breaks should be understood as the norm, not the exception, and regarded as a typical feature within turbidite beds.     

Current‐aligned dewatering sheets and ‘enhanced’ primary current lineation in turbidite sandstones of the Marnoso‐arenacea Formation

Turbidite sandstones of the Miocene Marnoso‐arenacea Formation (northern Apennines, Italy) display centimetre to decimetre long, straight to gently curved, 0·5 to 2·0 cm regularly spaced lineations on depositional (stratification) planes. Sometimes these lineations are the planform expression of sheet structures seen as millimetre to centimetre long vertical ‘pillars’ in profile. Both occur in the middle and upper parts of medium‐grained and fine‐grained sandstone beds composed of crude to well‐defined stratified facies (including corrugated, hummocky‐like, convolute, dish‐structured and dune stratification) and are aligned sub‐parallel to palaeoflow direction as determined from sole marks often in the same beds. Outcrops lack a tectonic‐related fabric and therefore these structures may be confidently interpreted to be sedimentary in origin. Lineations resemble primary current lineations formed by the action of turbulence during bedload transport under upper stage plane bed conditions. However, they typically display a larger spacing and micro‐topography compared to classic primary current lineations and are not associated with planar‐parallel, finely laminated sandstones. This type of ‘enhanced lineation’ is interpreted to develop by the same process as primary current lineations, but under relatively high near‐bed sediment concentrations and suspended load fallout rates, as supported by laboratory experiments and host facies characteristics. Sheets are interpreted to be dewatering structures and their alignment to palaeoflow (only noted in several other outcrops previously) inferred to be a function of vertical water‐escape following the primary depositional grain fabric. For the Marnoso‐arenacea beds, sheet orientation may be linked genetically to the enhanced primary current lineation structures. Current‐aligned lineation and sheet structures can be used as palaeoflow indicators, although the directional significance of sheets needs to be independently confirmed. These indicators also aid the interpretation of dewatered sandstones, suggesting sedimentation under a traction‐dominated depositional flow – with a discrete interface between the aggrading deposit and the flow – as opposed to under higher concentration grain or hindered‐settling dominated regimes.     

The rise of the diptera‐microbial mat interactions during the Cenozoic: consequences for the sedimentary record of saline lakes

Shoreline gypsiferous sediments of an inland lake in central Spain furnishes valuable insight into reconstructions of early sedimentary changes related to shore fly–microbial mat interactions in fossil gypsum precipitating saline lake systems. The association of adult and larval forms of Ephydra (Diptera) with microbial matgrounds overlying the lake margin results in the formation of gypsiferous meniscate back‐filled burrows that provide an analogue for recurring, extensively developed trace fossils that occur in Cenozoic, but not older, lacustrine gypsum rocks. In this setting, sediment burrowing by ephydridae hinders significant preservation of microbialites. The overwhelming rise of Diptera at the onset of the Cenozoic resulted in extensive feeding and dwelling activity and contributed to reshape the saline aquatic habitat where microbial mats thrived, thus leading to the formation of specific trace fossils that are illustrative of the existence of microbes in the paleoenvironment.