ALBERT

Description: Wildfires are natural or anthropogenic phenomena increasing at alarming rates globally due to land-use alterations, droughts, climatic warming, hunting and biological invasions. Whereas wildfire effects on terrestrial ecosystems are marked and relatively well-studied, ash depositions into aquatic ecosystems have often remained overlooked but have the potential to significantly impact bottom-up processes. This study assessed ash-water-phytoplankton biomass dynamics using six plant species [i.e., three natives (apple leaf Philenoptera violacea, Transvaal milk plum Englerophytum magalismontanum, quinine tree Rauvolfia caffra) and three aliens (lantana Lantana camara, gum Eucalyptus camaldulensis, guava Psidium guajava)] based on a six-week mesocosm experiment with different ash concentrations (1 and 2 g L-1). We assessed concentrations of chemical elements, i.e., N, P, K, Ca, Mg, Na, Mn, Fe, Cu, Zn and B from ash collected, and we have observed significant differences among the species. High concentrations of P, K, Mn, Fe, Cu, Zn and B were recorded from Transvaal milk plum ash and low concentrations of P, K, Ca, Mg, Cu and Zn were recorded from apple leaf. An increase in phytoplankton biomass (using chlorophyll-a concentration as a proxy) for all treatments i.e., 1 and 2 g L-1 for all plant species ash was observed a week after, followed by decreases in the following weeks, with the exception of 2 g L-1 for lantana, gum and control. Silicate concentrations (i.e., used as a proxy for diatom abundance) showed increasing patterns among all ash treatments, with exception of controls. However, no clear patterns were observed between native and alien plant ash on both chl-a and silicate concentrations. We found that ash has notable effects on water chemistry, particularly nitrate, which increased throughout the weeks, whereas, pH and conductivity were high at low ash concentrations. The impacts of ash on water chemistry, chl-a and silicate concentrations vary with individual species and the amount of ash deposited into the system.

Description: Phytoplankton form the base of the pelagic food web in inland waters. Unlike rooted plants with access to nutrients in the sediment, phytoplankton depend on the open water as their sole direct source of minerals. Phytoplankton comprise cyanobacteria and phylogenetically diverse eukaryotic algae that convert light energy and mineral nutrients into organic matter. Many species also exploit the elements and energy within dissolved organic compounds and particles produced in the catchment or within the water. Here, we describe the nutrient requirements of phytoplankton, their different modes of nutrition, the mechanisms they employ to acquire nutrients and the ecological consequences of their varying ability to exploit an often scarce and spatially and temporally variable resource. When nutrients are abundant, often as a result of human disruption of nutrient cycles, phytoplankton productivity, and often biomass, increases to the point that it causes a range of ecological consequences that reduce the value of the water resource for mankind.

Description: Quantification of phthalates or phthalic acid esters (PAEs) might be problematic due to matrix overlap, auto-self absorbance and background scattering noise by the plastic lab materials although plastics have been reported in the release of PAEs. These materials (ambient air, reagents bottles, sampling devices, and various analytical instruments), are ubiquitous in the laboratory environment, thereby making it more difficult to reliably analyze of trace concentration of PAEs. Thus, in the current study, a straight forward and reliable protocol has been established for the analysis of PAEs including control of blank contamination, and the experimental conditions such as extraction time and temperature were optimized. The mass of PAEs in blank tests of selected materials ranged from 3±0.7 to 35±6 ng for liquid-liquid extraction (LLE) and from 5±1.8 to 63±15 ng for solid-phase extraction (SPE). For both extraction methods, higher blank values were measured for dibutyl phthalate (DBP) (35±6 ng, 12±3 ng), and DEHP (63±12 ng, 23±5 ng) in LLE and SPE, respectively. Average recoveries of PAEs in LLE were 90-97% and obtained with successive aliquots of 2 mL, 1 mL, and 1 mL dichloromethane (DCM). For SPE, recoveries up to 86-90% were achieved with successive aliquots of 5, 3, and 2 mL DCM at a sample flow rate of 5 mL min -1 . Under the optimized conditions, the method quantification limits (MQL) for PAEs was 10-20 ng L -1 for LLE and 10-35 ng L -1 for SPE. Moreover, the dissolved concentrations of PAEs from LDPE measured by the LLE method ranged 〈 1.5 to 5.83 ng cm -2, and those measured by SPE ranged from 1.0to256ngL -1 , in seawater samples of Sharm Obhur. The method has lower MQL values for LLE and SPE than average reported values of 10-100 ng L -1 and 30-100 ng L -1 , respectively.

Description: A key requirement for geological CO2 storage is site integrity management and monitoring during operation through to the post decommissioning period. This paper focuses on monitoring deformation of the ground surface and seabed as a proxy for overall deformation in the reservoir and surrounding layers. The objective is to inform, based on deformation data, on how the reservoir is responding to CO2 injection and to ensure any issues with regard to storage integrity are rapidly detected. The magnitude and pattern of deformation at the surface reveals geomechanical/hydromechanical processes that occur in reservoir due to CO2 injection. We acquired deformation data from the In Salah CO2 injection site and from four additional study cases during the course of this study; one in the onshore UK, the other a combined campaign onshore Norway and offshore Germany, and the third in onshore Japan. Significant developments in measurement techniques, processing tools and interpretation algorithms were developed through this project. Models were then developed to simulate the observed data and to couple surface deformation to displacement in the subsurface. The results show millimeter-scale deformations in the subsurface have a signature at the surface that can be captured by the tools and workflows developed in this project. These deformations, particularly the patterns, are important factors to consider when monitoring a CO2 storage site.

Description: New sedimentological data of facies and diagenesis as well as chronological data including strontium (87Sr/86Sr)-isotope ratios and uranium (U)-series dating, radiocarbon (14C) accelerator mass spectrometry (AMS) dating and biostratigraphy from elevated reef terraces (makatea) in the southern Cook Islands of Mangaia, Rarotonga and Aitutaki contribute to controversial discussions regarding age and sea-level relationships of these occurrences during the Neogene and Quaternary. The oldest limestones of the uplifted makatea island of Mangaia include reef-related facies which are mid-Miocene in age, based on new Sr-isotope and biostratigraphical data. In between these older deposits and the lowest coastal reef terrace of marine isotope stage (MIS) 5e, various older Pleistocene reef-related facies were identified. Based on Sr-isotope ratios, these were deposited during earlier Pleistocene highstands (as old as 2.28 Ma). Rare reef terraces on Rarotonga belong to the Plio-Pleistocene and the late Miocene, according to 87Sr/86Sr ratios. The late Miocene age is enigmatic as it exceeds the age of subaerially exposed volcanic rocks of Rarotonga island. The fossil reef could have formed on an older submarine volcanic high that was later displaced by younger volcanism to its present position, or the Sr-age could be too old due to diagenetic resetting. The Plio-Pleistocene Rarotonga reef terraces are overlain irregularly by Holocene reef deposits that are interpreted as storm rubble. Reef terraces on Aitutaki represent evidence of a higher-than-present (up to 1 m) sea-level during the late Holocene, based on 14C AMS age data. They are very similar to elevated late Holocene reefs of adjacent French Polynesia with regard to composition, elevation and age.

Description: Using the fault plane mechanisms of the shallow earthquakes occurring along the Hellenic arc and the extent of the intermediate seismic belt, we make a quantitative estimate of the relative motion occurring between the Hellenic arc and the adjacent sea floor. This estimate is then used to evaluate the deformation in the Aegean area and to reconstruct the pattern of motion over the Eastern Mediterranean region for the last 13 m.y. It is shown that this pattern is compatible with the neotectonic and seismicity studies in Aegea. We then discuss the dynamics of the area and propose that, since Serravallian-Tortonian time, Aegea has been spreading gravitationally in front of the southwestward advancing Turkey. The reasons for this gravitational spreading are discussed.

Description: Data gathered by recent “Islas Orcadas” cruises reveal the seafloor spreading pattern for a region south of the Agulhas/Falkland fracture zone system. The presence of a magnetic anomaly bight about the Agulhas Plateau indicates that the Agulhas Plateau may have developed at the site of a tectonic plate triple junction during the Late Cretaceous. A westward jump in the seafloor spreading center during the Late Maestrichtian (anomaly 34−31) reduced the offset across the Falkland/Agulhas fracture zone system and resulted in the formation of two conjugate aseismic ridges here described as the Meteor and Islas Orcadas Rises. The magnetic lineation pattern in the Agulhas Basin suggests that a tectonic plate (Malvinas Plate) existed during Campanian to Maestrichtian times. Relative rates of motion are calculated for Antarctica, South America, and Africa for the Late Cretaceous.

Description: This chapter discusses the carbon turnover, calcification, and growth in coral reefs. Carbon turnover within a total reef community is a function of two distinct, biochemically interacting cycles. The first is the metabolic cycle consisting of the photosynthetic fixation of CO2 and the release of CO2 by respiration and decomposition processes. Superimposed on this are the direct incorporation of organic compounds (dissolved or particulate; living or non-living) originating outside the reef systems (in the adjacent ocean waters), and the loss of organic compounds from the reef system into the out-flowing water. The second is the inorganic carbonate cycle involving the biological and non-biological precipitation and dissolution of carbonates. Superimposed on this is the loss of particulate carbonates in suspension in the out-flowing water. The main chemical component of a coral-reef system is calcium carbonate, which occurs either as high-Mg calcite, aragonite, or low-Mg calcite. The mean calcification values in various environments at One Tree Reef are presented in the chapter. These data may be converted to an implied vertical growth rate potential assuming that accrual is dominantly aragonite (density = 2.89 g cm–3) and that there is 50% porosity after normal compaction.

Description: Microbial decomposition of organic matter in recent sediments of the Landsort Deep—an anoxic basin of the central Baltic Sea—resulted in the formation of a characteristic assemblage of authigenic mineral precipitates of carbonates, sulfides. phosphates and amorphous silica, The dominant crystalline phases are a mixed Mn-carbonate [(Mn0.85Ca0.10Mg0.05)CO3]. Mn-sulfide [MnS] and Fecarbonate [FeCO3]. Amorphous Fe-sulfide [FeS]. Mn-phosphate [Mn3(PO4)2] and a mixed Fe-Ca-phosphate [(Fe0.86Ca0.14)3(PO4)2] were identified by their chemical compositions only. The variability in composition of these solid phases and their mode of occurrence as a co-existing assemblage constrains the conditions and solution composition from which they precipitated. Estimates of activities for dissolved Fe. Mn. PO4, CO3 and S in equilibrium with such an assemblage are close to those found in recent anoxic interstitial water-sediment systems. It is important to have detailed knowledge of the composition and stability conditions of these solid precipitates in order to refine stoichiometric models of interstitial nutrient regeneration in anoxic sediments.

Description: Goban Spur lies on the continental margin of northwest Europe, southwest of Ireland. It is a marginal plateau underlain by Hercynian granites and Palaeozoic sediments, which form large horsts, grabens and tilted fault blocks with a trend that is approximately parallel to the main Celtic/Armorican Shelf edge. The spur is thought to be a westward continuation of the buoyant Cornubian Ridge, and is bounded to the north and south by large fault lines which probably represent reactivation of Hercynian structural trends. The continental basement is further divided longitudinally into a low-lying outer zone (Intermediate Zone) and a high inner region (Goban Spur proper). The ocean/continent boundary is thought to lie at the outer edge of the Intermediate Zone, Sea-floor spreading anomalies immediately west of the Intermediate Zone suggest that the adjacent ocean crust was created prior to anomaly 33 (say at ca. 90 m.y. B.P.). The sedimentary sequence on Goban Spur can be subdivided into four layers which can be tentatively correlated with the stratigraphic succession on the Meriadzek Terrace (IPOD sites). Such a correlation suggests that the lowermost sediment layer (?Jurassic-Albian) represents a tectono-sedimentary rift infill, and that Layers 2–4 (Upper Cretaceous to Quaternary) were deposited during slow epeirogenic downwarping of the plateau and that the sedimentary processes involved both draping and strong current moulding. The relatively buoyant nature of Inner Goban Spur has inhibited the accumulation of a thick post-rifting sedimentary sequence (700–1000 m), and has shielded the Intermediate Zone from downslope mass movements of material. This has resulted in the accumulation of an anomalously thin post-rift stage outer margin sediment prism (ca. 1000 m) compared to most continent rises (up to 10 km).

Description: A bathymetric map of the deep-sea floor off southeastern Africa shows the Agulhas Plateau to be separated from the continental margin of southeastern Africa by a narrow (50 km) elongate depression, the Agulhas Passage, which acts as a deep-water connection between the Agulhas and Transkei basins. Three regionally developed sediment layers occur in the deep (〉 4500 m) Transkei Basin/Agulhas Passage area. With the aid of a simple ocean crust sinking/carbonate compensation level (CCL) model these layers are related to the sedimentation history of the area. The model suggests that acoustic basement (Horizon X) represents Lower Cretaceous limestones draped over oceanic basement, and that this is overlain by an acoustically transparent sequence of pelagic/terrigenous material (Horizon A) that was deposited during a lengthy period (95 m.y.) beneath the carbonate compensation level. Post-Late Miocene sedimentation (Horizons B and C) has probably taken place above the CCL. Local sedimentation has always been influenced by strong sea-floor currents, but since middle Palaeogene times these currents have operated on a regional scale and have generated numerous large ridge and billow-like bed forms.

Description: The ratio of compressional wavevelocityV p to shear wavevelocityV s , and Poisson’s ratio in marine sediments and rocks are important in modeling the sea floor for underwater acoustics,geophysics, and foundation engineering. V p and V s versus depth information was linked at common depths in terrigenous sediments (to 1000 m) and in sands (to 20 m) to yield data on V p vs V s , and V p /V s and Poisson’s ratios versus depth. Soft, terrigenous sediments usually grade with depth into mudstones and shales; V p /V s ratios vary from about 13 or more at the sea floor to about 2.6 at 1000 m. Poisson’s ratios vary from above 0.49 at the sea floor to about 0.41 at 1000 m. In sands, V p , V s , and V p /V s have very high gradients in the first few meters; below about 5 m, V p /V s ratios decrease from about 9 to about 6 at 20 m; Poisson’s ratios vary from above 0.49 at the surface to above 0.48 at 20 m. The mean value of V p /V s in 30 laboratory samples of chalk and limestone is 1.90 (standard error: 0.03); mean Poisson’s ratio is 0.31. Literature data on basalts from the sea floor are reviewed. Equations relating V p to V s are given for terrigenous sediments, sands, and basalts.

Description: An estimate of average river particulate matter (RPM) composition was bàsed on analyses of more than 40 elements in the Amazon, Congo, Ganges, Magdalena, Mekong, Parana and Orinoco rivers, to which were added literature data for 13 other major world rivers, covering the whole spectrum of morphoclimatic features. Geographic variations of major elements in RPM are mostly linked to weathering types and to the balance between weathering rate and river transport. As a result of chemical erosion, Al, Fe and Ti are enriched in RPM with respect to the average parent rock, while Na, Ca, Mg and Sr are strongly depleted. These figures are directly related to the relative importance of dissolved and particulate transport in rivers; this has been computed for each of 40 elements. In order to study weathering on a global scale, the total observed elemental fluxes (dissolved + particulate) have been computed and compared to theoretical ones. The latter were derived from the elemental content in the average parent rock and the total quantity of weathered material, computed from the Al ratio in RPM and in parent rock. Observed and theoretical fluxes are balanced for the less mobilized elements (rare earths, Co, Cr, Cs, Fe, Mn, Rb, Si, Th, Ti, U and V) for which no enrichment relative to Al is noted in RPM, and for B, Ba, Ca, K, Mg, Na, Sr which are relatively depleted in RPM due to their high dissolved transport. Additional fluxes have been found for Br, Sb, Pb, Cu, Mo, Zn and are possible also for Ni and P. This is reflected by marked enrichments in RPM relative to Al for the poorly or moderately dissolved transports (Pb, Cu, Zn). Several hypotheses involving either the natural origin (volcanic dust, marine aerosols, geochemical fractionation) or the artificial origin (worldwide pollution) are discussed to explain these discrepancies, assuming river transport and weathering either to be in a steady state on a global scale or not. However, none of them can fully account for these additional fluxes. It is most likely that these excesses have multiple origins, anthropogenic or natural or both. The comparison between RPM and deep-sea clay compositions emphasizes the prime influence of river input on oceanic sedimentation of Si, Al, Fe, Ti, lanthanides, Sc, Rb, V, etc. A few elements such as Zn, Sb, occur in excess in RPM as compared to deep-sea clays; in order to balance this excess, a remobilization of these elements out of the sediment can be considered. Finally, the enrichment of Co, Cu, Mn and Ni in deep-sea clays compared to RPM is discussed and attributed to several sources and processes.