Landscape-scale species monitoring of agri-environment schemes (LandSpAES project). Final project report, 2022

In this project, we applied a novel, pseudo-experimental design in order to collect a baseline survey dataset of the responses of mobile taxa to local and landscape AES gradients over four years, from 54 survey squares across six regions (NCAs) in England. This is the first project to monitor the responses of multiple mobile taxa to generalised AES gradients across large spatial extents, which were applied to arable, grassland and upland agricultural systems, in order specifically to address impacts beyond AES option or agreement boundaries. This baseline dataset supported a spatial assessment of relationships between the AES gradients and taxon abundance (or activity), species richness and diversity. Strong evidence for relationships with local and / or landscape AES gradients were found for one or more response variable for butterflies, moths and bats. Little or no evidence of AES gradient relationships were found for either bees or hoverflies and weak evidence for associations with bird metrics. A future resurvey would allow analyses of the longer-term changes in target taxa in response to AES management, against this baseline. The identification of various spatial relationships is encouraging in terms of the likely power to detect AES effects on biodiversity change in the future

Role of cell-cycle regulated expression in the localized incorporation of cell wall proteins in yeast.

The yeast cell wall is an essential organelle that protects the cell from mechanical damage and antimicrobial peptides, participates in cell recognition and adhesion, and is important for the generation and maintenance of normal cell shape. We studied the localization of three covalently bound cell wall proteins in Saccharomyces cerevisiae. Tip1p was found only in mother cells, whereas Cwp2p was incorporated in small-to-medium–sized buds. When the promoter regions of TIP1 and CWP2 (responsible for transcription in early G(1) and S/G(2) phases, respectively) were exchanged, the localization patterns of Tip1p and Cwp2p were reversed, indicating that the localization of cell wall proteins can be completely determined by the timing of transcription during the cell cycle. The third protein, Cwp1p, was incorporated into the birth scar, where it remained for several generations. However, we could not detect any role of Cwp1p in strengthening the birth scar wall or any functional interaction with the proteins that mark the birth scar pole as a potential future budding site. Promoter-exchange experiments showed that expression in S/G(2) phase is necessary but not sufficient for the normal localization of Cwp1p. Studies of mutants in which septum formation is perturbed indicate that the normal asymmetric localization of Cwp1p also depends on the normal timing of septum formation, composition of the septum, or both

A magnetic, neutron diffraction, and Mossbauer spectral study of the Tb2Co17-xGax solid solutions

The compositional dependence of the Curie temperature of the Tb2Fe17-xGax solid solutions shows a primary maximum for x equal to three and a secondary maximum for x equal to eight. The Mössbauer spectra and powder neutron diffraction patterns of Tb2Fe9Ga8 indicate that gallium avoids the 9d site, completely fills the 6c site, and occupies preferentially the 18f site over the 18h site. This gallium preferential substitution leads to a nearly ordered two-dimensional antiferromagnetic arrangement of the terbium and iron magnetic moments, an increase in Curie temperature, and a surprisingly sharp Mössbauer spectrum

Identification of molecular mechanisms used by Finegoldia magna to penetrate and colonise human skin.

Finegoldia magna is a Gram-positive anaerobic commensal of the human skin microbiota, but also known to act as an opportunistic pathogen. Two primary virulence factors of F. magna are the subtilisin-like extracellular serine protease SufA and the adhesive protein FAF. This study examines the molecular mechanisms F. magna uses when colonising or establishing an infection in the skin. FAF was found to be essential in the initial adherence of F. magna to human skin biopsies. In the upper layers of the epidermis FAF mediates adhesion through binding to galectin-7 - a keratinocyte cell marker. Once the bacteria moved deeper into the skin to the basement membrane layer, SufA was found to degrade collagen IV which forms the backbone structure of the basement membrane. It also degraded collagen V, whereby F. magna could reach deeper dermal tissue sites. In the dermis, FAF interacts with collagen V and fibrillin, which presumably helps the bacteria to establish infection in this area. The findings of this study paint a clear picture of how F. magna interacts with human skin and explain how it is such a successful opportunistic pathogen in chronic wounds and ulcers