Coral communities and reefs from Guerrero,Southern Mexican Pacific

Corals in the Eastern Pacific extend south from the Gulf of California to Ecuador and oceanic Chile, and west from Colombia to Clipperton Atoll. Nevertheless, large stretches of the Mexican Pacific remain fundamentally unstudied. Therefore, to assess the current conditions of coral communities, a coastal fringe ～300 km long (17°40′ N, 101°39′ W to 16°46′ N, 99°49′ W) was surveyed within the Southern Mexican Pacific, between 2005 and 2009. Fifteen stony coral species were identified at 13 coral communities and six Pocillopora‐dominated fringing reefs, with Pocillopora verrucosa and Pocillopora damicornis the primary contributing taxa. Reef development was identified in embayments or behind rocks or islands that offered shelter from northern and northwestern winds. Observations of Pocillopora effusus, Pocillopora inflata, Porites lobata, Pavona clavus, and Pavona varians expanded the species known geographic ranges by several degrees of latitude, suggesting reef building fauna comprised a mixture of widespread and relatively rare Eastern Pacific corals. Results indicated greater live coral cover in the Ixtapa‐Zihuatanejo area (15–73%) than in the Acapulco localities, which had high algal dominance; the reefs in the latter region exhibited high erosion. Regional differences are likely the result of long‐standing anthropogenic pressures around Acapulco since 1950, when it became an important tourist destination. This paper is the first detailed report of ecologically stressed corals and coral reefs from the state of Guerrero on the Mexican Southern Pacific coast.     

Population dynamics of cryptogenic calcarean sponges (Porifera,Calcarea) in Southeastern Brazil

The calcarean sponge Paraleucilla magna is classified as being an invasive species on the Mediterranean Sea, where it causes economic damages to mollusc farms. On the Brazilian coast, this species is considered to be cryptogenic, and information on its ecology is scarce. The same is true for Sycettusa hastifera, another calcarean sponge with a worldwide distribution. Data on the ecology of these species could help in elucidating their potential to become a threat if they are found to be exotic species in Brazil. In the present work, we studied habitat selection, growth and mortality of early juveniles of P. magna and habitat selection of S. hastifera in a Marine Reserve from Southeastern Brazil, where these species are abundant in the benthic community. Granite plates were used for habitat selection analysis, varying in substrate inclination (vertical and horizontal) and exposure to light and hydrodynamism (exposed and sheltered). To analyse the growth and mortality rates, sponges were mapped and then measured once a week for 10 weeks. If a monitored sponge was not found in the following week, it was considered to be dead. Our results showed that, although P. magna and S. hastifera are capable of inhabiting substrates exposed to different environmental conditions, they showed habitat preferences. Growth of the juveniles of P. magna seemed not to have damaged any neighbouring invertebrates. The mortality of juveniles of this species was higher during the first 2 weeks of life but its causes could not be elucidated.     

The effect of human use of sandy beaches on developmental stability of Talitrus saltator (Montagu, 1808) (Crustacea, Amphipoda). A study on fluctuating asymmetry

In recent years, there has been an increasing intensity of human use of coastal areas in Galicia (NW Spain). Actually, there is great concern about rapid and unplanned urban and industrial development on certain locations, as this can generate adverse impacts on those areas. In this study, we selected three sandy beaches along the Galician coast (Chanteiro, Insuela and Valieros) facing different levels of anthropic pressure, and we analysed Talitrus saltator individuals with the aim of elucidating whether anthropogenic pressures on beaches such as tourism or pollution have an influence on the incidence of morphological developmental alterations in sandhoppers in the field. Specifically, levels of fluctuating asymmetry were selected as indicators of environmental stress. Results of two sampling dates (May and September) show that individuals collected at the most touristy and polluted beach were those showing the highest asymmetry values, although results were only statistically significant for samples collected during spring. Results are in accordance with the hypothesis that beach management and pollution reduce symmetry in sandhoppers living in altered beaches.     

Morphometric and molecular data on two mitochondrial genes of a newly discovered chimaeran fish (Hydrolagus melanophasma, Chondrichthyes)

Fresh and preserved (type material) specimens of the black ghost chimaera Hydrolagus melanophasma were compared for morphometric characteristics. A molecular comparison was also performed on two mitochondrial gene sequences (12S rRNA and 16S rRNA gene sequences). While significant differences in measurements were found, the differences were not attributable to sexual dimorphism or the quality of the specimens, but to the sample size and the type of statistical tests. The result of the genetic characterization showed that 12S rRNA and 16S rRNA genes represented robust molecular markers that characterized the species.     

Morphosedimentary features and recent depositional architectural model of the Cantabrian continental margin

Multibeam bathymetry, high (sleeve airguns) and very high resolution (parametric system-TOPAS-) seismic records were used to define the morphosedimentary features and investigate the depositional architecture of the Cantabrian continental margin. The outer shelf (down to 180–245 m water depth) displays an intensively eroded seafloor surface that truncates consolidated ancient folded and fractured deposits. Recent deposits are only locally present as lowstand shelf-margin deposits and a transparent drape with bedforms. The continental slope is affected by sedimentary processes that have combined to create the morphosedimentary features seen today. The upper (down to 2000 m water depth) and lower (down to 3700–4600 m water depth) slopes are mostly subject to different types of slope failures, such as slides, mass-transport deposits (a mix of slumping and mass-flows), and turbidity currents. The upper slope is also subject to the action of bottom currents (the Mediterranean Water — MW) that interact with the Le Danois Bank favouring the reworking of the sediment and the sculpting of a contourite system. The continental rise is a bypass region of debris flows and turbidity currents where a complex channel-lobe transition zone (CLTZ) of the Cap Ferret Fan develops.The recent architecture depositional model is complex and results from the remaining structural template and the great variability of interconnected sedimentary systems and processes. This margin can be considered as starved due to the great sediment evacuation over a relatively steep entire depositional profile. Sediment is eroded mostly from the Cantabrian and also the Pyrenees mountains (source) and transported by small stream/river mountains to the sea. It bypasses the continental shelf and when sediment arrives at the slope it is transported through a major submarine drainage system (large submarine valleys and mass-movement processes) down to the continental rise and adjacent Biscay Abyssal Plain (sink). Factors controlling this architecture are tectonism and sediment source/dispersal, which are closely interrelated, whereas sea-level changes and oceanography have played a minor role (on a long-term scale).     

Structure of the South Powell Ridge (NE Antarctic Peninsula): new clues for changing tectonic regimes near the Scotia/Antarctica Plate boundary

The structure of the South Powell Ridge (SPR), separating the Late Cenozoic ocean-floored Powell Basin and the Mesozoic Weddell Sea domain, is revealed by multichannel seismic data. The SPR appears as a basement high, bounded northward by transtensional faults and by normal and major reverse faults to the south. These margin features seem to be linked to the Powell Basin southern strike-slip margin and to the Jane Arc paleotrench, respectively. We suggest the ridge evolved from the Antarctic Peninsula passive margin to become the deformational front of the Scotia/Antarctica Plate boundary, later being welded to the Antarctic Plate. Received: 18 August 1997 / Revision received: 4 May 1998     

Large-Scale and Mesoscale Distribution of Plankton Biomass and Metabolic Activity in the Northeastern Central Atlantic

Plankton biomass and indices of metabolism and growth [electron transport system (ETS), glutamate dehydrogenase (GDH) and aspartate transcarbamylase (ATC) activities] were studied over a 2,800 km east-west section of the tropical North Atlantic Ocean (21°N) in <200, 200–500 and >;500 µm size classes. On the large-scale, zooplankton (>;200 µm) enzymatic activities increased westward in the study section, where large cyanobacteria chains (Trichodesmium spp.) were observed. Parallel to it, an increase in medium calanoids (1–2 mm length) was observed towards the western part of the transect, whereas small calanoids (<1 mm) were dominant throughout the boundary area of the subtropical gyre. Microplankton ETS and mesoplankton ETS and ATC activities seemed to match the wave length of low frequency waves. Our results suggest that such waves are related to the observed enhancement of metabolic activity of micro- and mesoplankton. The large-scale and mesoscale variability observed give evidence of the inadequacy of assuming a steady-state picture of the euphotic zone of tropical and subtropical waters.     

Coastal vulnerability in barrier islands: The high risk areas of the Ria Formosa (Portugal) system

Coastal vulnerability in barrier island systems is extremely high. The barrier island shoreline is exposed to many threats, such as storm erosion, reductions in sediment longshore drift and sea level rise. Many of these threats to coastal areas, such as Ria Formosa, are likely to increase in the near future. The main objectives of the present study are to identify the areas in the system that are at most risk by assessing the evolution of the Ria Formosa barrier island system since the 1940s, and determine which interventions would be necessary to protect these areas.The coastal vulnerability of the system was assessed based on current literature, data available from official institutions, and aerial and terrestrial in situ examination. The results obtained for the evolution of the Ria Formosa coastal system reveal that there are several vulnerable areas that have very dynamic processes, such as extremely high evolution rates of islands and inlets. Human actions that affect the whole system, namely the construction of many physical structures, are the main cause of the instability. Moreover, as several stakeholders are involved, efficient management of the coastal system is imperative. Extensive and careful interventions are urgently needed to avoid irreversible negative impacts on the barrier island system. Three types of techniques could be adopted to deal with the threats to barrier islands: hard stabilization, soft techniques, and non-structural alternatives. However, using hard techniques has many negative effects compared to soft techniques, and as a result it is necessary to remove existing structures from the areas at most risk.     

Sediment bioavailable organic matter,deposition rates and mixing intensity in the Setúbal–Lisbon canyon and adjacent slope (Western Iberian Margin)

The role of the Setúbal–Lisbon canyon in accumulation and transport of labile organic matter from the coastal sea and ocean surface water towards the deep sea was assessed by investigating the distribution of organic matter of different quality in sedimentary aggregates and surface sediments of the canyon and adjacent slopes. Total hydrolysable amino acids (THAA) and organic carbon (Corg) were measured from aggregates, and contents of Corg, chlorophyll a (chl a), phaeopigments (phaeo), chloroplastic pigment equivalents (CPE) from sediments. As indices of organic matter (OM) quality THAA:Corg, degradation index (DI), chl a:phaeo, chl a:Corg and C:N ratio were determined. Sediment profiles of chl a and the isotope 210 of lead (²¹⁰Pb) were used as tracers in a transport model to estimate deposition rates and background levels of the tracers, and sediment mixing rates (Db). Whereas bulk Corg contents of canyon and slope sediments were practically similar at all depths, higher contents of THAA, chl a and CPE, as well as higher THAA:Corg, DI and chl a:Corg, in aggregates and sediments from the upper reaches of the canyon indicate that labile organic matter accumulates in the upper canyon. This is confirmed by higher chl a and ²¹⁰Pb deposition and Db calculated from the model. Hence, the Setúbal–Lisbon canyon, specially the upper region, acts as a natural trap of organic matter that is transported to the region via lateral transport and vertical settling from primary productivity. Organic matter might be further transported in downward canyon direction via rebound processes. The chl a and ²¹⁰Pb profiles reveal active sediment mixing by physical processes and/or animal reworking.     

Automatic tracing of the foot of the continental slope

The UNCLOS III (Article 76, Section 4(b)) defines the foot of the continental slope as the point of maximum change in the gradient at its base. It is impossible to locate so defined afoot and thus to trace the foot‐line objectively by eye. In this study we show a method designed automatically to detect and trace the foot‐line of the continental slope from an irregular array of bathymetrical data. Our algorithm first transforms the bathymetric surface to a maximum curvature surface. On this new surface, the foot‐line corresponds to one of the ridges; instead of tracing the foot‐line on the bathymetric surface, we now can trace the ridges on the maximum curvature surface. The tracing of the ridges can be done automatically and objectively and the foot‐line is identified as being one of these ridges. We devote particular attention to the case when the ridge‐line is not defined, i.e., to the case when the point of maximum gradient change becomes a region of maximum gradient change.