Seagrass meadows are considered to be among the most important marine ecosystems, with regard to both ecology and biodiversity and for the services they provide. Seven species occur in the Mediterranean Sea: Posidonia oceanica (the most common in the open sea), Cymodocea nodosa (particularly common in the eastern basin), Ruppia cirrhosa, R. maritima, Zostera marina and Zostera noltii (mainly in estuaries and brackish lagoons), and Halophila stipulacea (introduced from the Red Sea). Seagrass regression may be due to natural processes and/or natural or anthropogenic disturbances and stress. It can also be due to long-term climate trends, e.g., the post-Last Glacial Maximum rise in sea-level, the Little Ice Age (LIA) cooling and the post-LIA warming, resulting in possible misinterpretation. Human-induced losses of P. oceanica have been mainly related to coastal development, pollution, trawling, fish farming, moorings, dredging, dumping and introduced species. All other seagrasses have also undergone more or less dramatic regression events. In fact, accurate data are generally of very local value and they are lacking for most of the Mediterranean Sea. In the absence of a reliable baseline, some widely cited cases of regression are questionable. Relatively healthy P. oceanica meadows, whose limits have changed little since the 1950s, may thrive in highly anthropized areas. In addition, the decline of one species can benefit another, so that the overall seagrass balance may remain unchanged (e.g., Cymodocea replacing Posidonia). However, to conclude that everything is for the best would be erroneous. First, the lack of data supporting the general regression hypothesis does not invalidate the hypothesis. Indisputably dramatic seagrass losses have been documented (e.g., P. oceanica and Z. marina). Second, the Posidonia regression is irreversible at human scales, while other seagrasses can rapidly recover, and the expansion of some seagrasses (e.g., Cymodocea) cannot counterbalance, in terms of ecosystem services, the decline of the P. oceanica meadows. Third, human pressure (demography, tourism, etc.) on Mediterranean seagrass ecosystems is destined to strongly increase in the coming decades. Finally, the rise in sea-level due to global climate change will automatically induce a withdrawal of the lower limit of seagrass meadows whenever the limit is beyond the compensation depth. So the regression trend observed in Mediterranean seagrasses, even if it proves to be currently weaker than postulated, will significantly increase and become a major concern in the future. There is therefore an urgent need for the adoption of a set of efficient indicators and the setting up of a robust comparative baseline in order to draw up an accurate assessment of the losses and, for seagrasses other than Posidonia, possible gains at Mediterranean scale. In addition, seagrasses and seagrass habitats should be granted legal protection and, where such protection already exists, it should be implemented.
Recent morphological and genetic studies on the Caulerpa racemosa (Forsska˚l) J. Agardh complex have demonstrated that three taxa occur in the Mediterranean Sea. One of them, the 'invasive variety', provisionally regarded as close to C. racemosa var. occidentalis J. Agardh, is currently spreading spectacularly throughout the Mediterranean. On the basis of new morphological and molecular studies (rDNA ITS1, 5.8S and ITS2 sequences), we confirm here that this invasion is the result of a recent introduction and we identify the invasive variety as Caulerpa cylindracea Sonder, endemic to south-west Australia, and currently known as C. racemosa var. laetevirens f. cylindracea (Sonder) Weber-van Bosse. C. cylindracea differs from the tropical north Australian C. laetevirens Montagne by its slender thallus, lack of large rhizoidal pillars, the slight inflation of the basal part of the upright axes immediately above the attachment to the stolon, by the range of morphological variations (branchlets clavate to cylindrical but never trumpet-like or shield-like) and by the rDNA ITS sequence data. The new combination C. racemosa var. cylindracea (Sonder) Verlaque, Huisman et Boudouresque is therefore proposed.
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