Air photography Samoylov Island

For the qualitative description of surface properties like vegetation cover or land-water-ratio of Samoylov Island as well as for the evaluation of fetch homogeneity considerations of the eddy covariance measurements and for the up-scaling of chamber flux measurements, a detailed surface classification of the island at the sub-polygonal scale is necessary. However, up to know only grey-scale Corona satellite images from the 1960s with a resolution of 2 x 2 m and recent multi-spectral LandSat images with a resolution of 30 x 30 m were available for this region. Both are not useable for the desired classification because of missing spectral information and inadequate resolution, respectively. During the Lena 2003 expedition, a survey of the island by air photography was carried out in order to obtain images for surface classification. The photographs were taken from a helicopter on 10.07.2002, using a Canon EOS100 reflex camera, a Soligor 19-23 mm lens and colour slide film. The height from which the photographs were taken was approximately 600 meters. Due to limited flight time, not all the area of the island could be photographed and some regions could only be photographed with a slanted view. As a result, the images are of a varying quality and resolution. In Potsdam, after processing the films were scanned using a Nikon LS-2000 scanner at maximal resolution setting. This resulted in a ground resolution of the scanned images of approximately 0.3x0.3 m. The images were subsequently geo-referenced using the ENVI software and a referenced Corona image dating from 18.07.1964 (Spott, 2003). Geo-referencing was only possible for the Holocene river terrace areas; the floodplain regions in the western part of the island could not be referenced due to the lack of ground reference points. In Figure 3.7-1, the aerial view of Samoylov Island composed of the geo-referenced images is shown. Further work is necessary for the classification and interpretation of the images. If possible, air photography surveys will be carried out during future expeditions in order to determine changes in surface pattern and composition.

(Table 1) Chemical analyses of rock samples from low atolls of the Western Indian Ocean

Compositions, structures, and microstructures of different types of phosphorites and poorly phosphatized rocks from low atolls in the near-equatorial part of the Western Indian Ocean are described. The rocks were examined under optical and scanning microscopes using microprobe techniques and etching of selected samples with weak solvents as well as with the help of chemical analyses. It is proved that phosphorites have been formed owing to the uneven phosphatization of primary carbonate rocks; degree of their phosphatization ranges from traces to 40% P2O5. In the phosphorites numerous organic remains were encountered; they included fragments of plankton, debris of tortoise shells, and coccoidal and filamentous bacteria-like formations. It is suggested that the phosphorites formed due to high local biological productivity over the outer edges of coral reefs and are not related to guano accumulation or to endoupwelling.

Multilocus DNA fingerprinting reveals high rate of heritable genetic mutation in herring gulls nesting in an industrialized urban site.

Genotoxins, such as polycyclic aromatic compounds, are ubiquitous in urban and industrial environments. Our understanding of the role that these chemicals play in generating DNA sequence mutations is predominantly derived from laboratory studies with specific genotoxins or extracts of contaminants from environmental media. Most assays are not indicative of the germinal effects of exposure in situ to complex mixtures of common environmental mutagens. Using multilocus DNA fingerprinting, we found the mutation rate in herring gulls inhabiting a heavily industrialized urban harbor (Hamilton Harbour, Ontario) to be more than twice as high as three rural sites: Kent Island, Bay of Fundy; Chantry Island, Lake Huron; and Presqu'ile Provincial Park in Lake Ontario. Overall we found a mutation rate of 0.017 +/- 0.004 per offspring band in Hamilton, 0.006 +/- 0.002 at Kent Island, 0.002 +/- 0.002 from Chantry Island, and 0.004 +/- 0.002 from Presqu'ile Provincial Park. The mutation rate from the rural sites (pooled) was significantly lower than the rate observed in Hamilton Harbour (Fisher's exact test, two-tailed; P = 0.0006). These minisatellite DNA mutations may be important biomarkers for heritable genetic changes resulting from in situ exposure to environmental genotoxins in a free-living vertebrate species.

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands.

Precise mapping of DNA methylation patterns in CpG islands has become essential for understanding diverse biological processes such as the regulation of imprinted genes, X chromosome inactivation, and tumor suppressor gene silencing in human cancer. We describe a new method, MSP (methylation-specific PCR), which can rapidly assess the methylation status of virtually any group of CpG sites within a CpG island, independent of the use of methylation-sensitive restriction enzymes. This assay entails initial modification of DNA by sodium bisulfite, converting all unmethylated, but not methylated, cytosines to uracil, and subsequent amplification with primers specific for methylated versus unmethylated DNA. MSP requires only small quantities of DNA, is sensitive to 0.1% methylated alleles of a given CpG island locus, and can be performed on DNA extracted from paraffin-embedded samples. MSP eliminates the false positive results inherent to previous PCR-based approaches which relied on differential restriction enzyme cleavage to distinguish methylated from unmethylated DNA. In this study, we demonstrate the use of MSP to identify promoter region hypermethylation changes associated with transcriptional inactivation in four important tumor suppressor genes (p16, p15, E-cadherin, and von Hippel-Lindau) in human cancer.