[THIS DATASET HAS BEEN WITHDRAWN]. This dataset consists of 4,397 insect species associated with 679 native plant species, 120 archaeophytes, and 223 neophytes from the Database of Insects and their Food Plants (DBIF). The DBIF details approximately 60,000 interactions between phytophagous insect (and mite) species and plants recorded in Great Britain over the last century, based on a wide variety of sources, including entomological journals and field guides. The data here represents a reduced subset of the full DBIF (13,277 interactions), only including interactions resolved to the species level (insect species x associated with host plant species y), records that have been expertly verified as reliable and included in previous large-scale analyses (Ward 1988; Ward & Spalding 1993; Ward et al. 1995; Ward et al. 2003), and records that are certain to have occurred in Great Britain. Any records originating from captive breeding studies are excluded. Finally, only plants with associated phylogenetic data and native status are included. Host plant distribution size is also included, in addition to a quantification of the distinctiveness of the insect communities found on a subset of the non-native plants. This work was supported by the Natural Environment Research Council award number NE/R016429/1 as part of the UK-SCAPE programme delivering National Capability. Full details about this dataset can be found at https://doi.org/10.5285/cc6b5e83-a1f4-40d6-bbbb-64366b002418

This dataset consists of 4,397 insect species associated with 679 native plant species, 120 archaeophytes, and 234 neophytes from the Database of Insects and their Food Plants (DBIF). The DBIF details approximately 60,000 interactions between phytophagous insect (and mite) species and plants recorded in Great Britain over the last century, based on a wide variety of sources, including entomological journals and field guides. The data here represents a reduced subset of the full DBIF (13,277 interactions), only including interactions resolved to the species level (insect species x associated with host plant species y), records that have been expertly verified as reliable and included in previous large-scale analyses (Ward 1988; Ward & Spalding 1993; Ward et al. 1995; Ward et al. 2003), and records that are certain to have occurred in Great Britain. Any records originating from captive breeding studies are excluded. Finally, only plants with associated phylogenetic data and native status are included. Host plant distribution size is also included, in addition to a quantification of the distinctiveness of the insect communities found on a subset of the non-native plants. This work was supported by the Natural Environment Research Council award number NE/R016429/1 as part of the UK-SCAPE programme delivering National Capability. Full details about this dataset can be found at https://doi.org/10.5285/33a825f3-27cb-4b39-b59c-0f8182e8e2e4

Genetic variation on a spatial scale was assessed, using both DNA fingerprinting and sequencing-based approaches, in the Antarctic endemics Buellia frigida, Carbonia vorticosa and Amandinea petermananii, and in the bipolar species Caloplaca saxicola, Umbilicaria decussata and Cladonia galindezii. PCR-based (Polymerase Chain Reaction) molecular biology techniques, were used as they are ideal for working with lichens because little starting material is required. See Fabian et al. 2007 for further information on analyses and results.

The majority of Antarctic lichens produce sexual organs, and in many species sexual ascospores appear to be the only reproductive propagule. However, it is unknown whether sexual reproduction involves selfing (homothallism) or outcrossing (heterothallism). To investigate this issue we have established axenic cultures of sexual progeny in order to generate DNA fingerprints and thereby determine the breeding system.

The fieldwork involved collection of fertile lichens from a range of sites across the Antarctic Peninsula and isolation of the lichen-forming fungi into pure culture in a laboratory at Rothera. Approximately 5,600 monospore cultures were isolated, including B frigida. Approximately 400 thalli of Usnea species, and 3 O. frigida thalli have also been collected for whole thallus analysis. Logarithmic sampling transects of B frigida were conducted at Rothera (2 transects) and on Anchorage Island (one transect) to examine the genetic variation and geographic variation. All thalli of B frigida collected from the transects were successfully used to generate viable spores from four individual apothecia from each thallus. 16 spores were subcultured and maintained from each apothecium.

DNA sequencing data from octopus samples collected in the Southern Ocean. A small tissue sample was taken from the mantle of each octopus and placed immediately in 70 - 80 % ethanol for preservation, in preparation for DNA extraction.

Genetic profiling data relating to studies on Antarctic krill, Euphausia superba, that document the sequence of expression of genes over the moult cycle and the spatial-temporal expression of clock genes. This work was carried out to examine rhythmic behaviour patterns in this species - namely diel vertical migration and the moult cycle - and the functioning of the genes that underlie these behaviours. Circadian entrainment experiments were carried out twice during the Discovery 2010 summer cruise (cruise no JR177) using krill caught in nets at latitudes of 60S and 52S. Krill samples from each net were processed and preserved for subequent analysis using molecular biology technique to isolate canonical clock genes.