76 research outputs found

    Coralline algae in a naturally acidified ecosystem persist by maintaining control of skeletal mineralogy and size

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    To understand the effects of ocean acidification (OA) on marine calcifiers, the trade-offs among different sublethal responses within individual species and the emergent effects of these trade-offs must be determined in an ecosystem setting. Crustose coralline algae (CCA) provide a model to test the ecological consequences of such sublethal effects as they are important in ecosystem functioning, service provision, carbon cycling and use dissolved inorganic carbon to calcify and photosynthesize. Settlement tiles were placed in ambient pH, low pH and extremely low pH conditions for 14 months at a natural CO2 vent. The size, magnesium (Mg) content and molecular-scale skeletal disorder of CCA patches were assessed at 3.5, 6.5 and 14 months from tile deployment. Despite reductions in their abundance in low pH, the largest CCA from ambient and low pH zones were of similar sizes and had similar Mg content and skeletal disorder. This suggests that the most resilient CCA in low pH did not trade-off skeletal structure to maintain growth. CCA that settled in the extremely low pH, however, were significantly smaller and exhibited altered skeletal mineralogy (high Mg calcite to gypsum (hydrated calcium sulfate)), although at present it is unclear if these mineralogical changes offered any fitness benefits in extreme low pH. This field assessment of biological effects of OA provides endpoint information needed to generate an ecosystem relevant understanding of calcifying system persistence

    Settlement pattern of Posidonia oceanica epibionts along a gradient of ocean acidification: an approach with mimics

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    Effects of ocean acidification (OA on the colonization/settlement pattern of the epibiont community of the leaves and rhizomesof the Mediterranean seagrass,Posidoniaoceanica, have been studied at volcanic CO2vents off Ischia (Italy), using "mimics"as artificial substrates. The experiments were conducted in shallowPosidoniastands (2-3 m depth), in three stations on the northand three on the south sides of the study area, distributed along a pH gradient. At each station, 4 rhizome mimics and 6 artificialleaves were collected every three months (Sept 2009-Sept 2010). The epibionts on both leaf and rhizome mimics showed clearchanges along the pH gradient; coralline algae and calcareous invertebrates (bryozoans, serpulid polychaetes and barnacles) weredominant at control stations but progressively disappeared at the most acidified stations. In these extremely low pH sites theassemblage was dominated by filamentous algae and non calcareous taxa such as hydroids and tunicates. Settlement pattern onthe artificial leaves and rhizome mimics over time showed a consistent distribution pattern along the pH gradient and highlightedthe peak of recruitment of the various organisms in different periods according to their life history.Posidoniamimics at theacidified station showed a poor and very simplified assemblage where calcifying epibionts seemed less competitive for space. Thisprofound difference in epiphyte communities in low pH conditions suggests cascading effects on the food web of the meadow and,consequently, on the functioning of the syste

    Biology and new records of the invasive species Branchiomma bairdi (Annelida: Sabellidae) in the Mediterranean Sea

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    First observations on the reproductive biology of the alien polychaete Branchiomma bairdi (McIntosh, 1885) (Sabellidae) in the Mediterranean Sea are provided as well as additional Mediterranean records of the species which can help to understand its introduction and spreading. Re-examination of the specimens from Miseno harbour (Tyrrhenian Sea, Italy) revealed the presence of B. bairdi in the central-Mediterranean since September 2004. The histological study of individuals collected in Malta revealed that the species is a simultaneous hermaphrodite, developing male and female gametes in the same body segments; embryos are brooded inside the parent tube. However, there is evidence also for asexual reproduction. The species shows a different reproductive pattern from the previously reported population from the eastern-Pacific; this demonstrates its great plasticity and adaptability. Branchiomma bairdi has an invasive behaviour, colonizing large areas in relatively short-time, and reaching relatively high densities (c.a. 50 individuals/m2). Its expansion throughout several Mediterranean localities is largely a consequence of the high capacity of this species to colonize extremely different habitats and substrates, to the occurrence of sexual and asexual reproductive strategies, and the combination of both. Further, B. bairdi appears to be particularly abundant in confined and anthropogenic degraded areas. Finally, our findings strongly suggest that the pathway of introduction in the Mediterranean, previously hypothesized as the Suez Canal (Lessepsian migration), is most likely via the Gibraltar Strait

    Alien species in the Mediterranean Sea by 2012. A contribution to the application of European Union's Marine Strategy Framework Directive (MSFD). Part 2. Introduction trends and pathways

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    More than 60 marine non-indigenous species (NIS) have been removed from previous lists and 84 species have been added, bringing the total to 986 alien species in the Mediterranean [775 in the eastern Mediterranean (EMED), 249 in the central Mediterranean (CMED), 190 in the Adriatic Sea (ADRIA) and 308 in the western Mediterranean (WMED)]. There were 48 new entries since 2011 which can be interpreted as approximately one new entry every two weeks. The number of alien species continues to increase, by 2-3 species per year for macrophytes, molluscs and polychaetes, 3-4 species per year for crustaceans, and 6 species per year for fish. The dominant group among alien species is molluscs (with 215 species), followed by crustaceans (159) and polychaetes (132). Macrophytes are the leading group of NIS in the ADRIA and the WMED, reaching 26-30% of all aliens, whereas in the EMED they barely constitute 10% of the introductions. In the EMED, molluscs are the most species-rich group, followed by crustaceans, fish and polychaetes. More than half (54%) of the marine alien species in the Mediterranean were probably introduced by corridors (mainly Suez). Shipping is blamed directly for the introduction of only 12 species, whereas it is assumed to be the most likely pathway of introduction (via ballasts or fouling) of another 300 species. For approximately 100 species shipping is a probable pathway along with the Suez Canal and/or aquaculture. Approximately 20 species have been introduced with certainty via aquaculture, while >50 species (mostly macroalgae), occurring in the vicinity of oyster farms, are assumed to be introduced accidentally as contaminants of imported species. A total of 18 species are assumed to have been introduced by the aquarium trade. Lessepsian species decline westwards, while the reverse pattern is evident for ship-mediated species and for those introduced with aquaculture. There is an increasing trend in new introductions via the Suez Canal and via shipping.The research leading to these results was partly supported by funding from the European Community’s Seventh Framework Programme ([FP7/2007-2013]) under grant agreement n° 287600 - PERSEUS project (Policy-oriented marine Environmental Research for the Southern European Seas). MAMIAS has been developed for the Regional Activity Centre for Specially Protected Areas of the UNEP/ Mediterranean Action Plan under contracts No 67, 68, 69, 70 and 71 /2011/RAC/RPA

    Errata to the Review Article (Medit. Mar. Sci. 11/2, 2010, 381-493): "Alien species in the Mediterranean Sea by 2010. A contribution to the application of European Union’s Marine Strategy Framework Directive (MSFD). Part I. Spatial distribution"

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    The state-of-art on alien species in the Mediterranean Sea is presented, making distinctions among the four subregions defined in the EU Marine Strategy Framework Directive: (i) the Western Mediterranean Sea (WMED); (ii) the Central Mediterranean Sea (CMED); (iii) the Adriatic Sea (ADRIA); and (iv) the Eastern Mediterranean Sea (EMED). The updated checklist (December 2010) of marine alien species within each subregion, along with their acclimatization status and origin, is provided. A total of 955 alien species is known in the Mediterranean, the vast majority of them having being introduced in the EMED (718), less in the WMED (328) and CMED (267) and least in the Adriatic (171). Of these, 535 species (56%) are established in at least one area.Despite the collective effort of experts who attempted in this work, the number of introduced species remains probably underestimated. Excluding microalgae, for which knowledge is still insufficient, aliens have increased the total species richness of the Mediterranean Sea by 5.9%. This figure should not be directly read as an indication of higher biodiversity, as spreading of so many aliens within the basin is possibly causing biotic homogenization. Thermophilic species, i.e. Indo-Pacific, Indian Ocean, Red Sea, Tropical Atlantic, Tropical Pacific, and circum(sub)tropical, account for 88.4% of the introduced species in the EMED, 72.8% in the CMED, 59.3% in the WMED and 56.1% in the Adriatic. Cold water species, i.e. circumboreal, N Atlantic, and N Pacific, make up a small percentage of the introduced species, ranging between 4.2% and 21.6% and being more numerous in the Adriatic and less so in the EMED.Species that are classified as invasive or potentially invasive are 134 in the whole of the Mediterranean: 108 are present in the EMED, 76 in the CMED, 53 in the Adriatic and 64 in the WMED. The WMED hosts most invasive macrophytes, whereas the EMED has the lion’s share in polychaetes, crustaceans, molluscs and fish

    Descriptors of Posidonia oceanica meadows: Use and application

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    The conservation of the coastal marine environment requires the possession of information that enables the global quality of the environment to be evaluated reliably and relatively quickly. The use of biological indicators is often an appropriate method. Seagrasses in general, and Posidonia oceanica meadows in particular, are considered to be appropriate for biomonitoring because of their wide distribution, reasonable size, sedentary habit, easy collection and abundance and sensitivity to modifications of littoral zone. Reasoned management, on the scale of the whole Mediterranean basin, requires standardized methods of study, to be applied by both researchers and administrators, enabling comparable results to be obtained. This paper synthesises the existing methods applied to monitor P. oceanica meadows, identifies the most suitable techniques and suggests future research directions. From the results of a questionnaire, distributed to all the identified laboratories working on this topic, a list of the most commonly used descriptors was drawn up, together with the related research techniques (e.g. standardization, interest and limits, valuation of the results). It seems that the techniques used to study meadows are rather similar, but rarely identical, even though the various teams often refer to previously published works. This paper shows the interest of a practical guide that describes, in a standardized way, the most useful techniques enabling P. oceanica meadows to be used as an environmental descriptor. Indeed, it constitutes the first stage in the process. (c) 2005 Elsevier Ltd. All rights reserved.Peer reviewe

    Spatio-temporal variability in Posidonia oceanica seagrass meadows of the Western Mediterranean: shoot density and plant features

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    The spatial and temporal variability of shoot density and selected plant features of Posidonia oceanica seagrass were assessed in 2 different meadows off the Island of Ischia (Naples, Italy), subjected to different degrees of both human impact and hydrological conditions. A nested hierarchical sampling design was used (1) to examine patterns of distribution of shoot density and plant features at different spatial scales and (2) to analyze temporal patterns of variability along the 2 principal seasons, showing the minimum and maximum development of the plant canopy (summer and winter; 2 sampling dates for each season). The shoot density showed 2 main spatial scales of variability: between the 2 beds (a few km apart) and within each meadow (10s of m); how- ever, there were no seasonal differences. Most morphometric features showed multiple spatial scales of variability, especially at the smallest scale (10s of cm), but none of these parameters var- ied significantly between the meadows. Most of the morphometric parameters also displayed vari- ations with season and date of sampling, likely related to the growth cycle of the plant. A permu- tational analysis of variance identified several scales of variability for all features across the suite of scales from 10s to 100s of meters and for seasons and sampling dates. The present study pro- vides evidence of the high spatio-temporal variability of P. oceanica plant features despite the dif- ferent ecological status of the meadows. It is advisable to take this high variability into account during monitoring studies to avoid misinterpretation of natural variation

    Cognetti's syllid collection (Polychaeta: Syllidae) deposited at the Museum of the Stazione Zoologica "Anton Dohrn" (Naples, Italy), with descriptions of two new species of Autolytus

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    A total of 36 syllid specimens preserved on permanent slides, which were collected and identified by G. Cognetti, and deposited at the Museum of the Stazione Zoologica "Anton Dohrn" in Naples, Italy, were re-examined. Among the material, two new species of Autolytus, Autolytus antondohrni sp. nov. and A. cognettii sp. nov., were found and are described. Three new combinations are assigned: Autolytus mediterraneus (Cognetti, 1953), Exogone (Parexogone) meridionalis (Cognetti, 1955) and Syllis alternata Moore, 1908. Four lectotypes are designated for Autolytus convolutus Cognetti, 1953, A. mediterraneus (Cognetti, 1953), A. neapolitanus Cognetti, 1953 and Exogone (Parexogone) meridionalis (Cognetti, 1955). Proceraea scapularis (Claparède, 1864) is resurrected
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