The identification of nursery grounds and other essential fish habitats of exploited stocks is a key requirement for the development of spatial conservation planning aimed at reducing the adverse impact of fishing on the exploited populations and ecosystems. The reduction in juvenile mortality is particularly relevant in the Mediterranean and is considered as one of the main prerequisites for the future sustainability of trawl fisheries. The distribution of nursery areas of 11 important commercial species of demersal fish and shellfish was analysed in the European Union Mediterranean waters using time series of bottom trawl survey data with the aim of identifying the most persistent recruitment areas. A high interspecific spatial overlap between nursery areas was mainly found along the shelf break of many different sectors of the Northern Mediterranean indicating a high potential for the implementation of conservation measures. Overlap of the nursery grounds with existing spatial fisheries management measures and trawl fisheries restricted areas was also investigated. Spatial analyses revealed considerable variation depending on species and associated habitat/depth preferences with increased protection seen in coastal nurseries and minimal protection seen for deeper nurseries (e.g. Parapenaeus longirostris 6%). This is partly attributed to existing environmental policy instruments (e.g. Habitats Directive and Mediterranean Regulation EC 1967/2006) aiming at minimising impacts on coastal priority habitats such as seagrass, coralligenous and maerl beds. The new knowledge on the distribution and persistence of demersal nurseries provided in this study can support the application of spatial conservation measures, such as the designation of no-take Marine Protected Areas in EU Mediterranean waters and their inclusion in a conservation network. The establishment of no-take zones will be consistent with the objectives of the Common Fisheries Policy applying the ecosystem approach to fisheries management and with the requirements of the Marine Strategy Framework Directive to maintain or achieve seafloor integrity and good environmental status.
Bioconstructions such as coralligenous outcrops and maërl beds are typical Mediterranean underwater seascapes. Fine-scale knowledge on the distribution of these sensitive habitats is crucial for their effective management and conservation. In the present study, a thorough review of existing spatial datasets showing the distribution of coralligenous and maërl habitats across the Mediterranean Sea was undertaken, highlighting current gaps in knowledge. Predictive modelling was then carried out, based on environmental predictors, to produce the first continuous maps of these two habitats across the entire basin. These predicted occurrence maps for coralligenous outcrops and maërl beds provide critical information about where the two habitats are most likely to occur. The collated occurrence data and derived distribution model outputs can help addressing the challenge of developing basin-wide spatial plans and to guide cost-effective future surveys and monitoring efforts towards areas that are presently poorly-sampled
Identification of the potential habitat of European anchovy (Engraulis encrasicolus) at different life stages in relation to environmental conditions is an interesting subject from both ecological and management points of view. For this purpose, acoustic data from different seasons and different parts of the Mediterranean Sea along with satellite environmental and bathymetry data were modelled using generalized additive models. Similarly, egg distribution data from summer ichthyoplankton surveys were used to model potential spawning habitat. Selected models were used to produce maps presenting the probability of anchovy presence (adults, juveniles and eggs) in the entire Mediterranean basin, as a measure of habitat adequacy. Bottom depth and sea surface chlorophyll concentration were the variables found important in all models. Potential anchovy habitats were located over the continental shelf for all life stages examined. An expansion of the potential habitat from the peak spawning (early summer) to the late spawning season (early autumn) was observed. However, the most suitable areas for the presence of anchovy spawners seem to maintain the same size between seasons. Potential juvenile habitats were associated with highly productive inshore waters, being less extended and closer to coast during winter than late autumn. Potential spawning habitat in June and July based on ichthyoplankton surveys overlapped but were wider in extent compared with adult potential habitat from acoustics in the same season. Similarities and dissimilarities between the anchovy habitats as well as comparisons with sardine habitats in the oligotrophic Mediterranean Sea and other ecosystems with higher productivity are discussed.
Each year, a phytoplankton spring bloom starts just north of the North Atlantic Subtropical Gyre, and then expands northwards across the entire North Atlantic. Here, we investigate whether the timing of the spring migration of baleen whales is related to the timing of the phytoplankton spring bloom, using 4 yr of dedicated whale observations at the Azores in combination with satellite data on ocean chlorophyll concentration. Peak abundances of blue whale Balaenoptera musculus, fin whale B. physalus, humpback whale Megaptera novaeangliae and sei whale B. borealis were recorded in April-May. The timing of their presence tracked the onset of the spring bloom with mean time lags of 13, 15, 15 and 16 wk, respectively, and was more strongly related to the onset of the spring bloom than to the actual time of year. Baleen whales were actively feeding on northern krill Meganyctiphanes norvegica in the area, and some photo-identified individuals stayed in Azorean waters for at least 17 d. Baleen whales were not observed in this area in autumn, during their southward migration, consistent with low chlorophyll concentrations during summer and autumn. Our results support the hypothesis that baleen whales track the secondary production generated by the North Atlantic spring bloom, utilizing mid-latitude areas such as the Azores as foraging areas en route towards their summer feeding grounds.KEY WORDS: Baleen whales · Balaenopteridae · Phytoplankton spring bloom · Whale migration · Feeding area · Satellite remote sensing · North Atlantic Ocean · Azores Resale or republication not permitted without written consent of the publisherMar Ecol Prog Ser 440: [267][268][269][270][271][272][273][274][275][276][277][278][279] 2011 tune their migration to the timing of the North Atlantic spring bloom. Baleen whales need dense aggregations of krill or fish to enable efficient foraging (Whitehead & Carscadden 1985, Friedlaender et al. 2006, Goldbogen et al. 2011, and temporal synchrony with the presence of suitable prey is evident in these species. Most baleen whale species undertake extensive north-south migrations associated with feeding at mid-to high latitudes in summer and breeding in (sub)tropical regions during winter (Kellogg 1929, Norris 1967; but see Simon et al. 2010 for a counterexample). Seasonal presence of baleen whales at the summer feeding grounds coincides with increased food availability in these waters. Nevertheless, migratory patterns over the North Atlantic are still largely unknown for most species of baleen whales.The North Atlantic spring bloom could temporarily produce sufficient prey densities to induce foraging of baleen whales during their spring migration towards the high-latitude feeding grounds. This might particularly apply to areas where the phytoplankton spring bloom combines with physical factors to con- centrate prey. Physical conditions conducive to concentrating prey may include coastal zones, upwelling areas, fronts and seamounts. For example, offshore regions of high marine productivit...
We review the variety of existing modelling approaches applied to species habitat mapping and we discuss issues arising from the availability and nature of sampled biological data and corresponding ecological and environmental habitat descriptors, as well as the different spatial analysis approaches that are selected according to specific hypotheses. We focus on marine species habitat mapping, presenting an overview of work on modelling fish habitat carried out through a European Communities Policy-Support Action, EnviEFH 'Environmental Approach to Essential Fish Habitat (EFH) Designation' (2005)(2006)(2007)(2008). The selection of the appropriate habitat model is dataset-specific and the resulting EFH maps are often similar in spite of using different models. Derived EFH maps are based on either environmental ranges (used as minimum and maximum environmental habitat descriptors) or probability of occurrence values. We apply model outputs to regions larger than sampled areas making use of the capacity of satellite data to cover wide areas.
Integrated information from different parts of the Mediterranean Sea was used to model the spatial and temporal variability of the distribution grounds of the sardine population. Acoustic data from the North Aegean Sea (Eastern Mediterranean), the Adriatic Sea (Central Mediterranean), the Sicily Channel (Central Mediterranean) and Spanish Mediterranean waters (Western Mediterranean) were analysed along with satellite environmental and bathymetric data to model the potential habitat of sardine during summer, autumn and early winter. Generalized additive models were applied in a presence−absence approach. Models were validated in terms of their predictive ability and used to construct maps exhibiting the probability of sardine presence throughout the entire Mediterranean basin as a measure of habitat adequacy for sardine. Bottom depth and sea surface temperature were the environmental variables that explained most of the data variability. Several areas along the Mediterranean coastline were indicated as suitable habitat for sardine in different seasons. An expansion of these areas over the continental shelf, up to 100 m depth, was consistently noticed from summer to winter. This was attributed to the horizontal movements of sardine related to spawning (i.e. winter period) and the peculiarities of the Mediterranean Sea where areas favouring growth, feeding and spawning processes tend to be localised and prevent a long range, offshore migration as opposed to large upwelling ecosystems. Moreover, within the study period, a positive relationship between the extent of sardine preferred habitat and landings was revealed for both summer and winter seasons throughout the entire Mediterranean Sea.
Cephalopods are highly sensitive to environmental conditions and changes at a range of spatial and temporal scales. Relationships documented between cephalopod stock dynamics and environmental conditions are of two main types: those concerning the geographic distribution of abundance, for which the mechanism is often unknown, and those relating to biological processes such as egg survival, growth, recruitment and migration, where mechanisms are sometimes known and in a very few cases demonstrated by experimental evidence. Cephalopods seem to respond to environmental variation both 'actively' (e.g. migrating to areas with more favoured environmental conditions for feeding or spawning) and 'passively' (growth and survival vary according to conditions experienced, passive migration with prevailing currents). Environmental effects on early life stages can affect life history characteristics (growth and maturation rates) as well as distribution and
Identification of potential juvenile grounds of shortlived species such as European sardine (Sardina pilchardus) in relation to the environment is a crucial issue for effective management. In the current work, habitat suitability modelling was applied to acoustic data derived from both the western and eastern part of the Mediterranean Sea. Early summer acoustic data of sardine juveniles were modelled using generalized additive models along with satellite environmental and bathymetry data. Selected models were used to construct maps that exhibit the probability of presence in the study areas, as well as throughout the entire Mediterranean basin, as a measure of habitat adequacy. Areas with high probability of supporting sardine juvenile presence persistently within the study period were identified throughout the Mediterranean Sea. Furthermore, within the study period, a positive relationship was found between suitable habitat extent and the changes in abundance of sardine juveniles in each study area.
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