The Subglacial Antarctic Lakes Scientific Access (SALSA) Project accessed Mercer Subglacial Lake using environmentally clean hot-water drilling to examine interactions among ice, water, sediment, rock, microbes and carbon reservoirs within the lake water column and underlying sediments. A ~0.4 m diameter borehole was melted through 1087 m of ice and maintained over ~10 days, allowing observation of ice properties and collection of water and sediment with various tools. Over this period, SALSA collected: 60 L of lake water and 10 L of deep borehole water; microbes >0.2 μm in diameter from in situ filtration of ~100 L of lake water; 10 multicores 0.32–0.49 m long; 1.0 and 1.76 m long gravity cores; three conductivity–temperature–depth profiles of borehole and lake water; five discrete depth current meter measurements in the lake and images of ice, the lake water–ice interface and lake sediments. Temperature and conductivity data showed the hydrodynamic character of water mixing between the borehole and lake after entry. Models simulating melting of the ~6 m thick basal accreted ice layer imply that debris fall-out through the ~15 m water column to the lake sediments from borehole melting had little effect on the stratigraphy of surficial sediment cores.

Callianassid fossils, preserved within their burrows, collected from Mount Discovery, East Antarctica, provide the first such occurrence in Antarctica as well as evidence for deposition in a shallow marine environment distal to a deltaic system. The age of the specimens, based upon associated dinoflagellate cysts, is late early to middle Eocene.

Recent studies suggest that sand can serve as a vehicle for exposure of humans to pathogens at beach sites, resulting in increased health risks. Sampling for microorganisms in sand should therefore be considered for inclusion in regulatory programmes aimed at protecting recreational beach users from infectious disease. Here, we review the literature on pathogen levels in beach sand, and their potential for affecting human health. In an effort to provide specific recommendations for sand sampling programmes, we outline published guidelines for beach monitoring programmes, which are currently focused exclusively on measuring microbial levels in water. We also provide background on spatial distribution and temporal characteristics of microbes in sand, as these factors influence sampling programmes. First steps toward establishing a sand sampling programme include identifying appropriate beach sites and use of initial sanitary assessments to refine site selection. A tiered approach is recommended for monitoring. This approach would include the analysis of samples from many sites for faecal indicator organisms and other conventional analytes, while testing for specific pathogens and unconventional indicators is reserved for high-risk sites. Given the diversity of microbes found in sand, studies are urgently needed to identify the most significant aetiological agent of disease and to relate microbial measurements in sand to human health risk.

New information and discussions regarding Mesozoic diatoms presented over the last decade advanced our knowledge of their origin and early history. The oldest confirmed centric diatom fossils are presented here from the earliest Cretaceous, and araphid and raphid pennate diatoms now date from the Late Cretaceous; all from terrestrial sediments. Molecular sequencing helped clarify relationships between diatom lineages, and verify the position of diatoms within the heterokontophytes. Molecular clock approaches estimate a diatom origin near ~135 Ma, but not before 240 Ma. Biomarkers in marine sediments are able to trace a diatom presence back to the mid-Cretaceous, even when siliceous fossils are absent. Seasonal growth and encystment cycles in Late Cretaceous planktonic marine diatoms are now well documented. A biostratigraphic framework for the Late Cretaceous Arctic will aid regional and global biostratigraphic correlations. The systematic position of many new taxonomic groups is now included within a more natural classification scheme that better reflects phylogenetic relationships evident in molecular data and affirmed by biostratigraphic micropaleontology. Discussions regarding the impact of diatoms on several global systems are maturing, as more information becomes available. Four stages in diatom evolution are proposed to explain the history of radiation, extinction, and expansion into new environments and habitats during the Mesozoic.

Fossil marine diatom assemblages from the Sørsdal Formation, a deposit of diatomaceous sand from Marine Plain in the Vestfold Hills, provide age and palaeoenvironmental information from a Pliocene coastal setting in East Antarctica. Benthic and meroplanktic diatom taxa suggest deposition in a shallow coastal embayment with water depths of 20–25 m. Diatom biostratigraphy indicates that the Sørsdal Formation belongs to the Fragilariopsis barronii Zone (4.5 to 4.1 Ma), through correlation to reference sections in the Ross Sea and Southern Ocean. Features of the other biota suggest higher sea-surface temperatures and reduced sea-ice cover, consistent with global records of higher sea level.

Late Neogene Sirius Group strata from Tillite Spur and Quartz Hills in the Reedy Glacier area, Antarctica, demonstrate the variability in Sirius Group facies and contrasts Sirius Group strata deposited at high and low paleo-elevation, respectively. The Tillite Spur and Quartz Hills Formations (Pliocene) are formally defined here.The Tillite Spur Formation type section crops out on the edge of the Wisconsin Plateau overlooking Tillite Spur. It comprises 32m of alternating coarse gray conglomerate and muddy olive-brown diamictites. The Quartz Hills Formation type section crops out above the western margin of Reedy Glacier in a pre-existing cirque towards the southern end of the Quartz Hills. It comprises c.100m of alternating massive diamictites and rhythmically interbedded sandstone and laminated mudstones which were deposited close to sea level and subsequently rapidly uplifted (>500 m Myr−1) to their present elevation at c. 1500 m. Three orders of paleoclimatic variability are recorded in the Sirius Group strata from Reedy Valley: (1) recycled marine microfloras in glacial diamictites indicate intervals of marine incursion into the Antarctic cratonic interior co-occurring with reductions in the East Antarctic ice sheet; (2) an advancing and retreating paleo-Reedy Glacier deposited a glacial/interglacial sequence alternating on a 10-100 kyr scale; 3) Centimeter and millimeter stratification in strata of the Quartz Hills Formation record annual kyr scale variability.

The Cretaceous record of the diatoms presented here outlines our understanding of their early morphological development. Recent documentation of well preserved Lower Cretaceous (Aptian/Albian) diatom assemblages provides a window into the early history of the diatoms and serves as a base for comparing their subsequent morphological changes. A brief review of diatom biology and morphology is provided to introduce this paper and that of Barron and Baldauf (this volume). Additional background information on the diatoms can be found in the works of Schrader and Schuette (1981), Tappan (1980), Bach and Burkhardt (1984), Barron (1985a, 1993), Fenner (1985), Ricard (1987), Bradbury (1988), Round et al. (1990), and Picket-Heaps et al. (1990).