(Table 1) Compressional-wave velocities and anisotropies and wet-bulk densities of calcareous rocks and some cherts at DSDP Holes 62-463 and 62-465A

Anisotropy in compressional-wave velocities in sedimentary rocks recovered by DSDP has been recognized by several investigators (Boyce, 1976; Tucholke et al., 1976; Carlson and Christensen, 1977). The anisotropy is also observed at elevated pressures in laboratory experiments, and thus probably persists at depth in some calcareous rocks (Schreiber et al., 1972; Christensen et al., 1973; Carlson and Christensen, 1979). Carlson and Christensen (1979) suggested that the observed velocity anisotropy was produced not by the alignment of cracks but by the alignment of c axes of calcite perpendicular to bedding during compaction, diagenesis, and recrystallization. On DSDP Leg 62, calcareous rocks were recovered from the western Mid-Pacific Mountains (sub-bottom depths of 452-823 m, Site 463) and southern Hess Rise (276-412 m, Site 465). Most of the calcareous rocks are horizontally laminated and color-banded, and ages are early Cenomanian to late Barremian (Site 463 and 465 reports, this volume). The purpose of this study is to confirm the velocity anisotropy in the calcareous rocks and to identify any relationship of anistropy to bulk density, mean velocity, and burial depth.

Diversity and identification of heterotrophic bacteria from Antarctic Rocks of the McMurdo Dry Valleys (Ross Desert)

Diversity of endolithic Dry Valley rock microorganisms was studied by evaluating the presence of morphotypes in enrichments. Storage of rock samples for 16 h over dry ice affected the diversity of endolithic organisms, especially that of algae and fungi. Diversity in various samples depended on rock location and exposure, on the rock type, and to some extent on the pH of the pulverized rock samples. In most cases sandstone contained more morphotypes than dolerite or granite. Presence of many different phototrophs resulted in greater diversity of the heterotrophs in the enrichments. Samples from Linnaeus Terrace and Battleship Promontory had higher morphotype (MT) numbers than those from more exposed sites such as New Mountain, University Valley, Dais, or Mt. Fleming. Beacon sandstone (13 samples) from Linnaeus Terrace varied greatly with respect to MT numbers, although the pH values ranged only from 4.2-5.3. The highest MT number of 24 per sample was obtained from the upper surface of a flat boulder tilted to the North. Only two MT's were found in a hard sandstone sample from the wind-exposed and more shaded east side of the Terrace. 15 sandstone samples from Battleship Promontory contained more diverse populations: there occurred a total of 131 different MT's in these samples as compared to only 68 in Linnaeus Terrace samples. Cysts of colorless flagellates were found in some Battleship Promontory samples; rnost samples were populated with a wealth of different cyanobacteria. Studies on the distribution of actinomycete morphotypes in Linnaeus Terrace sandstone revealed great differences between individual boulders. Identification tests and lipid analyses made with representative strains of the isolated 1500 pure cultures led to genus names such as Caulobacter, Blastobacter, Hyphomicrobium, Micrococcus, Arthrobacter, Brevibacterium, Corynebacterium, Bifidobacterium, Mycobacterium, Nocardia (Amycolata), Micromonospora, Streptomyces, Blastococcus, and Deinococcus. Our data demonstrate the great diversity of Antarctic endolithic microbial populations.