3,638 research outputs found

    Mediterranean developed coasts: what future for the foredune restoration?

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    The feasibility and efficacy of soft engineering foredune restoration approaches still lack insight from research and monitoring activities, especially in areas where dunes are under persisting human disturbance. We evaluated the efficacy of Mediterranean foredune restoration in dune areas freely accessible to tourists. Foredunes were reconstructed using only sand already available at nearby places and consolidated through the plantation of seedlings of native ecosystem engineer species and foredune focal species. We monitored transplanted and spontaneous seedlings for one year to assess their mortality and growth in relation to the distance from the closest beach access, either formal or informal, as proxy of human disturbance.We also tested whether species differing in their ecology (i.e., affinity to a given habitat) and growth form showed different response to human disturbance. The relationship between seedling mortality and growth and the distance from the closest beach access was tested through Generalized Linear Mixed Models. We found a clear spatial pattern of seedling survival and growth, which decreased as the proximity to the closest beach access increased. Only invasive alien plants and erect leafy species showed to better perform at lower distances from beach accesses. In dune areas with a strong tourist vocation, foredune restoration should be coupled with the implementation of integrated management plans aiming at optimising the relationship between protection and use. Management plans should not only rely on passive conservation measures; rather they should include educational activities to stimulate a pro-environmental behaviour, increase the acceptance of behaviour rules and no entry zones, and actively engage stakeholders in long-term conservation

    Growth-survival trade-offs and the restoration of non-forested open ecosystems

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    The growth-survival trade-off has been extensively documented for phanerophyte species, whereas there is little evidence for non-phanerophyte species. However, information on the growth-survival trade-offs in non-phanerophyte species could be of great use in non-forested open ecosystem restoration by providing insights for plant production and transplantation, thus impacting the planning of cost-effective restoration actions. In this study, we explored the relationship between growth and survival of individual plants of non-phanerophyte species used in a coastal dune restoration project, and we investigated whether plant functional traits explained patterns of trade-off between growth and survival. We monitored 355 individual plants of 13 perennial non-phanerophyte species belonging to foredune and transition dune communities every 30 days after planting and calculated relative growth and survival rates. In addition, we regressed the relationship between growth and survival on values of leaf and floral traits. We found that, besides being a widely recognised axis of life history variation in phanerophyte species, the growth-survival trade-off can also be observed in perennial non-phanerophyte species. Species of different coastal dune communities (i.e., foredune vs. transition dune communities) differed with respect to the growth-survival trade-off, with plant species of foredune communities exhibiting higher growth but lower survival rates than plant species of transition dune communities. Leaf dry matter content and mean number of floral displays explained species position on the growth-survival trade-off axis; species with relatively high growth and low survival rates exhibited an acquisitive strategy, with low values of leaf dry matter content, but also a low sexual reproductive effort, as revealed by low number of floral displays. In contrast, plant species with relatively low growth and high survival rates exhibited a conservative strategy but also high sexual reproductive effort, suggesting that trade-offs occur in resource allocation among vegetative and reproductive plant structures. The trade-off we found between growth and survival in perennial non-phanerophyte species provides useful insights for planning cost-effective ecosystem restoration actions of non-forested open ecosystems, especially when the actions are nature-based and involve planting individual plants. The results of this study suggest that individual plant production for coastal dune restoration should disproportionately target plant species of foredune communities because they have low survival rates associated with low sexual reproductive effort. Planning plant production based on ecological knowledge of plant species’ growth and survival after planting in the field could help achieve restoration goals while meeting project cost-effectiveness requirements

    Analysis of peripheral blood dendritic cells as a non-invasive tool in the follow-up of patients with chronic hepatitis C

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    Hepatitis C virus (HCV) has a high propensity to establish chronic infections. Failure of HCV-infected individuals to activate effective antiviral immune responses is at least in part related to HCV-induced impairment of dendritic cells (DCs) that play a central role in activating T cell responses. Although the impact of HCV on DC phenotype and function is likely to be more prominent in the liver, major HCV-induced alterations are detectable in peripheral blood DCs (pbDCs) that represent the most accessible source of DCs. These alterations include numerical reduction, impaired production of inflammatory cytokines and increased production of immunosuppressive IL10. These changes in DCs are relevant to our understanding the immune mechanisms underlying the propensity of HCV to establish persistent infection. Importantly, the non-invasive accessibility of pbDCs renders the analysis of these cells a convenient procedure that can be serially repeated in patient follow-up. Accordingly, the study of pbDCs in HCV-infected patients during conventional treatment with pegylated interferon and ribavirin indicated that restoration of normal plasmacytoid DC count may represent an additional mechanism contributing to the efficacy of the dual therapy. It also identified the pre-treatment levels of plasmacytoid DCs and IL10 as putative predictors of response to therapy. Treatment of chronic HCV infection is changing, as new generation direct-acting antiviral agents will soon be available for use in interferon-free therapeutic strategies. The phenotypic and functional analysis of pbDCs in this novel therapeutic setting will provide a valuable tool for investigating mechanisms underlying treatment efficacy and for identifying predictors of treatment response

    Crustal blocks and seismicity in the Central Apennines of Italy

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    Kinematics and geodynamics of crustal-block structures separated by compliant zones with viscoelastic rheology play an important role in defining the conditions for many deformation events such as ordinary seismic ruptures, silent and slow earthquakes and aseismic fault creep phenomena. New seismological data from the Latium-Abruzzi carbonatic platform of central Italy fit a block-tectonic modelling previously proposed for this area on the basis of structural and paleomagnetic evidences

    Aerobic training and angiogenesis activation in patients with stable chronic heart failure: a preliminary report.

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    The pathophysiology of chronic heart failure (CHF) involves multiple hystologic and molecular alterations. To determine the effects of physical training on circulating endothelial progenitor cells (EPCs), angiogenesis (angiogenin, angiopoietin-1 and -2, VEGF, Tie-2, SDF-1α) and inflammation (IL-6, CRP), we compared data obtained from 11 CHF pts before and after 3 months aerobic exercise training, to those from 10 non trained CHF pts (CHF-C group, age 64 + 2 years, NYHA 2). At the end of the study, EPCs count and AP-2 serum levels significantly increased in the CHF-TR group. These preliminary data suggest a significant effect of even a short program of physical training on angiogenic activation and endothelial dysfunction

    Moraxella catarrhalis-specific Th1 cells in BAL fluids of chronic obstructive pulmonary disease patients

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    In chronic obstructive pulmonary disease (COPD) patients' airway mucosa is infiltrated by macrophages and T lymphocytes, potentially reactive to pathogens. We studied the antigen-specificity and the effector functions of in vivo activated T lymphocytes isolated from BAL (Bronchoalveolar lavage) of 5 Moraxella catarrhalis (Mc)-infected and 5 Mc-non-infected COPD patients. Mc-specific T cells were detected only in BAL or peripheral blood of Moraxella catarrhalis-infected patients. The majority of BAL Mc-specific T cells expressed the T helper type 1 (Th1) cytokine profile with high cytotoxic and pro-apoptotic activity. Upon antigen stimulation, all Me-specific T clones were able to help the immunoglobulin production by autologous B cells and the MMP (Matrix MetalloProteinase)-12 activity by monocytes. Our results suggest a role for Th1-driven response to Moraxella catarrhalis in the genesis of COPD

    Circulating endothelial progenitor cells are increased in patients with classic Kaposi’s Sarcoma

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    Accumulating evidence indicates that tumor angiogenesis is supported by the mobilization and incorporation of endothelial progenitor cells (EPCs), highly proliferative elements derived from the bone marrow. EPCs have been detected at increased frequency in the circulation of patients with different types of cancer. Circulating EPCs have never been quantified in patients with Kaposi’s sarcoma (KS), an angioproliferative malignancy characterized by typical spindle-shaped tumor cells of endothelial origin. In this study, we analyzed the number of EPCs in the peripheral blood of 29 patients with classic KS (cKS) compared with 27 matched healthy controls. EPCs were measured by flow cytometry on fresh blood samples at a single time point. The number of circulating EPCs was significantly higher in cKS patients than controls. EPC count did not correlate with the plasmatic levels of the main proangiogenic factors possibly involved in EPC proliferation and mobilization, thus suggesting that the increased number of EPCs in cKS patients may rather be related to direct or indirect effects of viral environment sustained by HHV-8, the causative agent for KS. The increase of EPCs was significantly more pronounced in cKS patients with slowly evolving than rapidly evolving disease, likely reflecting a localization of EPCs within the lesions during the active phases of KS. Overall, this study demonstrates that EPCs are increased in the peripheral blood of cKS patients and may suggest that changes in the number of circulating EPCs may predict disease progression and may therefore be proposed as a biomarker in the follow-up of KS patients

    Are interleukin-16 and thrombopoietin new tolls for the in vitro generation of dendritic cells?

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    The effects of interleukin 16 (IL-16) on dendritic cell (DC) generation from human CD34+ progenitor cells are not known. Here, we show that IL-16 added to a basal cocktail comprised of granulocyte-macrophage colony-stimulating factor (GM-CSF), IL-4, Flt-3 ligand (Flt3L), and tumor necrosis factor \u3b1 (TNF-\u3b1) does induce the CD34+ hematopoietic cells to proliferate in vitro and to differentiate into phenotypically and functionally mature DCs. IL-16 exerts this function more efficiently than stem cell factor (SCF) as a control, thrombopoietin (TPO), or IL-16 plus TPO. Moreover, we show that the combination of IL-16 plus TPO induces the generation of tolerogenic DCs, able to induce an anergic state in T cells that persists when T cells are rechallenged with immunogenic DCs. An altered pattern of cytokine production, a reduced expression of the C-type lectin DC-SIGN, and an increased surface expression of the inhibitory molecules immunoglobulin-like transcript 2 (ILT-2), ILT-3, and ILT-4 may all contribute to confer the tolerogenic properties of these DCs. Generation of tolerogenic DCs may aid the exploration of new therapeutic strategies to promote tolerance to autoantigens and prevent disease development. (Blood. 2004;104:4020-4028
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