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"

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

Observation of Scaling Violations in Scaled Momentum Distributions at HERA

Charged particle production has been measured in deep inelastic scattering (DIS) events over a large range of $x$ and $Q^2$ using the ZEUS detector. The evolution of the scaled momentum, $x_p$, with $Q^2,$ in the range 10 to 1280 $GeV^2$, has been investigated in the current fragmentation region of the Breit frame. The results show clear evidence, in a single experiment, for scaling violations in scaled momenta as a function of $Q^2$.Comment: 21 pages including 4 figures, to be published in Physics Letters B. Two references adde

D* Production in Deep Inelastic Scattering at HERA

This paper presents measurements of D^{*\pm} production in deep inelastic scattering from collisions between 27.5 GeV positrons and 820 GeV protons. The data have been taken with the ZEUS detector at HERA. The decay channel $D^{*+}\to (D^0 \to K^- \pi^+) \pi^+$ (+ c.c.) has been used in the study. The $e^+p$ cross section for inclusive D^{*\pm} production with $5<Q^2<100 GeV^2$ and $y<0.7$ is 5.3 \pms 1.0 \pms 0.8 nb in the kinematic region {$1.3<p_T(D^{*\pm})<9.0$ GeV and $| \eta(D^{*\pm}) |<1.5$}. Differential cross sections as functions of p_T(D^{*\pm}), $\eta(D^{*\pm}), W$ and $Q^2$ are compared with next-to-leading order QCD calculations based on the photon-gluon fusion production mechanism. After an extrapolation of the cross section to the full kinematic region in p_T(D^{*\pm}) and $\eta$(D^{*\pm}), the charm contribution $F_2^{c\bar{c}}(x,Q^2)$ to the proton structure function is determined for Bjorken $x$ between 2 $\cdot$ 10$^{-4}$ and 5 $\cdot$ 10$^{-3}$.Comment: 17 pages including 4 figure

11. Simposio iberico de estudios del bentos marino Libro de resumenes

Centro de Informacion y Documentacion Cientifica (CINDOC). C/Joaquin Costa, 22. 28002 Madrid. SPAIN / CINDOC - Centro de Informaciòn y Documentaciòn CientìficaSIGLEESSpai

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

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

Temporal changes of mollusc populations from a Zostera marina bed in southern Spain (Alboran Sea), with biogeographic considerations

Molluscs associated with a Zostera marina bed from Cantarriján bay (Southern Spain, Alboran Sea) at 14–16 m depth were sampled monthly from October 1996 to September 1997. A total of 44,819 individuals belonging to 80 species were identified. In spite of the high species richness, only seven species of gastropods showed a dominance value (D) higher than 1%. Jujubinus striatus was the dominant species of the assemblage with 70.8% of the total abundance. The other dominant species were Rissoa membranacea (9.8%), Nassarius pygmaeus (5.8%), Mitrella minor (4%), Smaragdia viridis (1.9%), Rissoa monodonta (1.4%), Bittium reticulatum (1.3%). The dynamic pattern of the mollusc populations showed a temporal trend with monthly values of species richness and abundance ranging between 10 and 25 species and between 178 and 4412 individuals·222 m−2. The species richness and abundance were higher in the spring and summer months than in the autumn and winter ones. The diversity (Shannon–Wiener, H') follows a similar trend, with increases from April to September and decreases from October to March. H' values (ranging from 0.45 to 3.10) are more influenced by the evenness (J) than by the species richness. A multivariate analysis (Cluster, Multi-dimensional Scaling) based on both presence/absence and quantitative data has also pointed out a temporal trend, with spring–summer samples significantly different from autumn–winter samples. The temporal changes in abundance seem related with the species' biology, such as recruitment events, as well as to the canopy features and shoot density variation in the Zostera meadow. From the biogeographical point of view, most of the molluscs (65%) found in the Cantarriján bed, have a Lusitanian–Mediterranean distribution (sensuEkman 1953). The proximity to Africa is shown by the presence of four species with a mainly West African distribution. Only R. membranacea has a typical Atlantic distribution, driven by that of Z. marina in NW Europe

Electroweak measurements in electron–positron collisions at w-boson-pair energies at lep

Contains fulltext : 121524.pdf (preprint version ) (Open Access

Measurement of the diffractive cross section in deep inelastic scattering using ZEUS 1994 data

The DIS diffractive cross section, dσdiffγ*p→XN/dMx, has been measured in the mass range Mx < 15 GeV for γ*p c.m. energies 60 < W < 200 GeV and photon virtualities Q2 = 7 to 140 GeV2. For fixed Q2 and Mx, the diffractive cross section rises rapidly with W, dσdiffγ*p→X N (Mx, W, Q2)/dMx ∝ Wadiff with adiff = 0.507 ± 0.034 (stat) +0.155-0.046 (syst) corresponding to a t-averaged pomeron trajectory of ̄αℙ = 1.127 ± 0.009 (stat) +0.039-0.012 (syst) which is larger than ̄αℙ observed in hadron-hadron scattering. The W dependence of the diffractive cross section is found to be the same as that of the total cross section for scattering of virtual photons on protons. The data are consistent with the assumption that the diffractive structure function FD(3)2 factorizes according to cursive greek chiℙFD(3)2(cursive greek chiℙ, β, Q2) = (cursive greek chi0//cursive greek chiℙ)nFD(2)2(β, Q2). They are also consistent with QCD based models which incorporate factorization breaking. The rise of cursive greek chiℙFD(3)2 with decreasing cursive greek chiℙ and the weak dependence of FD(2)2 on Q2 suggest a substantial contribution from partonic interactions