An integrated genetic linkage map for E. nitens was constructed in an outbred three-generation pedigree. Analysis of 210 RFLP, 125 RAPD and 4 isozyme loci resulted in 330 markers linked in 12 linkage groups covering 1462 cM (n=11 in eucalypts). The 12th linkage group is comprised of only 5 markers and will probably coalesce with another linkage group when further linked loci are located. Co-dominant RFLP loci segregating in both parents were used to integrate linkages identified in the male and female parents. Differences in recombination frequencies in the two parents were observed for a number of pairs of loci, and duplication of sequences was identified both within and between linkage groups. The markers were distributed randomly across the genome except for the RFLPs in linkage group 10 and for some loci showing segregation distortion, which were clustered into three regions of the map. The use of a large number of co-dominant RFLP loci in this map enables it to be used in other pedigrees of E. nitens and forms a basis for the detection and location of QTL in E. nitens and other eucalypt species.

Two snow and ice cores from the Rennick Glacier area, Antarctica (study area center point lat 71 ·15'S, long 162 ·30' E) were analyzed for the chemical species: chloride, sodium, reactive silicate, sulfate and nitrate .

While some investigators have attempted to use isozyme electrophoresis to gain information on the genetics of brown algae, most have reported unsatisfactory results. Through exhaustive screening and modification of sample preparation techniques, gel and tray buffers systems, plus staining recipes, we have developed procedures that consistently provide scorable bands for over 20 enzyme systems in several laminarian algae. We have used our procedures to examine geographically diverse populations of Laminaria saccharina and L. longicruris, as well as L. digitata, L. groenlandica, Agarum cribrosum, Alaria esculenta, Chorda tomentosa, and Macrocystispyrifera. Overall, these kelp species seem to have an extremely low degree of enzyme polymorphism, both within and between populations. While some 'rare alleles' occurred in several enzyme systems, only 3-5 loci were found to be polymorphic. Our results are consistent with the few reported studies that have used molecular genetic techniques to look at the intraspecific variability of laminarian algae. We suggest that at the species level the Laminariales, and perhaps other groups of brown algae, are genetically extremely conservative as compared to other divisions of plants. We further suggest that isozyme electrophoresis provides a quick and useful tool for algal population genetic studies.

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