22 research outputs found

    Changes in host ant communities of Alcon Blue butterflies in abandoned mountain hay meadows

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    1. Land use intensification is a general threat to biodiversity, but many species depend on low-intensity agricultural ecosystems. One example is European mountain meadow ecosystems, traditionally managed by hay harvesting or livestock grazing. Abandoning management often causes population declines, local extinctions and biotic homogenisation in these meadows. 2. We studied changes in the Myrmica host ant communities of the xerophilic form of the ant-parasitic Alcon Blue butterfly (Maculinea alcon) in four hay meadows in the BĂŒkk mountains of Hungary between 2000–2007 and 2018. Abandonment started in this region in the 1970s, accelerated in the 1980s, and culminated in the 1990s. 3. We found that the Myrmica ant community has changed substantially in less than two decades. Diversity of the ant community always decreased, and species composition became more homogeneous at two sites. Habitat suitability for Maculinea butterflies decreased at three sites and increased at only one site, where management was restarted 20 years after abandonment. 4. The number of M. alcon caterpillars and pupae, the rate of infestation of ant nests and the mean number of caterpillars and pupae per ant nest decreased between the two periods, whereas host ant specificity did not differ from random in either period. 5. We conclude that the unfavourable changes in the host ant community due to abandonment have negative consequences for the persistence of Maculinea populations. Our study highlights the need for detailed monitoring, and the maintenance of low-intensity management by mowing or grazing to avoid the decline of biodiversity dependent on low-intensity agriculture

    Setting the Trade Policy Agenda: What Roles for Economists?

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    Effects of CD2 locus control region sequences on gene expression by retroviral and lentiviral vectors

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    Locus control region (LCR) sequences are involved in the establishment of open chromosomal domains. To evaluate the possibility of exploiting the human CD2 LCR to regulate gene expression by Moloney murine leukemia virus (Mo-MLV)-based retroviral vectors in T cells, it was included in vectors carrying the enhanced green fluorescence protein (EGFP) reporter gene; then transduction in vitro of lymphoid and nonlymphoid cell lines was performed. Deletion of the viral enhancer in the Mo-MLV long terminal repeat was necessary to detect LCR activity in the context of these retroviral vectors. It was found that a full-length (2.1 kb), but not a truncated (1.0 kb), CD2 LCR retained the ability to modulate reporter gene expression by Mo-MLV-derived retroviral vectors, leading to a homogeneous, unimodal pattern of EGFP expression that remained unmodified in culture over time, specifically in T-cell lines; on the other hand, viral titer was strongly reduced compared with vectors not carrying the LCR. Lentiviral vectors containing the CD2 LCR could be generated at higher titers and were used to analyze its effects on gene expression in primary T cells. Subcutaneous implantation of genetically modified cells in immunodeficient mice showed that retroviral vectors carrying the CD2 LCR conferred an advantage in terms of transgene expression in vivo, compared with the parental vector, by preventing the down-modulation of EGFP expression. These findings suggest a potential application of this LCR to increase gene expression by retroviral and lentiviral vectors in T lymphocytes
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