The fishes of the Indo-Australian Archipelago ...

Mode of access: Internet.

The Hawaiian archipelago; six months among the palm groves, coral reefs, and volcanoes of the Sandwich Islands,

Mode of access: Internet.

Narrative of a whaling voyage round the globe, from the year 1833 to 1836. Comprising sketches of Polynesia, California, the Indian Archipelago, etc. with an account of southern whales, the sperm whale fishery, and the natural history of the climates visited.

Master negative available (Box 564:8)

Bismarck Archipelago.

Shipping list no.: 94-0318-P.

Alaska : its southern coast and the Sitkan archipelago /

Author's letters to various newspapers on her two summer cruises in 1883-84 assembled and amplified by reference to published information to form an informative tourist guide to the region.

A record of the Buddhist religion as practised in India and the Malay archipelago (A. D. 671-695) /

Half-title: Buddhist practices in India.

The Journal of the Indian archipelago and eastern Asia

Mode of access: Internet.

The Eastern archipelago. A description of the scenery, animal and vegetable life, people, and physical wonders of the islands of the eastern seas.

Mode of access: Internet.

Literature on wildlife research in the Madrean Archipelago : 1800s-1994 /

"March 1997."

A list of lecturers on southeast Asia (Burma, Siam, French Indo-China, Malay Peninsula, Malay Archipelago, Philippines) and adjacent areas.

Pub. by the institute under its earlier name: East Indies Institute of America.

Spatial and temporal variability in somatic growth of green sea turtles (Chelonia mydas) resident in the Hawaiian Archipelago

The somatic growth dynamics of green turtles ( Chelonia mydas) resident in five separate foraging grounds within the Hawaiian Archipelago were assessed using a robust non-parametric regression modelling approach. The foraging grounds range from coral reef habitats at the north-western end of the archipelago, to coastal habitats around the main islands at the southeastern end of the archipelago. Pelagic juveniles recruit to these neritic foraging grounds from ca. 35 cm SCL or 5 kg ( similar to 6 years of age), but grow at foraging-ground-specific rates, which results in quite different size- and age-specific growth rate functions. Growth rates were estimated for the five populations as change in straight carapace length ( cm SCL year) 1) and, for two of the populations, also as change in body mass ( kg year) 1). Expected growth rates varied from ca. 0 - 2.5 cm SCL year) 1, depending on the foraging-ground population, which is indicative of slow growth and decades to sexual maturity, since expected size of first-time nesters is greater than or equal to 80 cm SCL. The expected size- specific growth rate functions for four populations sampled in the southeastern archipelago displayed a non-monotonic function, with an immature growth spurt at ca. 50 - 53 cm SCL ( similar to 18 - 23 kg) or ca. 13 - 19 years of age. The growth spurt for the Midway atoll population in the northwestern archipelago occurs at a much larger size ( ca. 65 cm SCL or 36 kg), because of slower immature growth rates that might be due to a limited food stock and cooler sea surface temperature. Expected age-at-maturity was estimated to be ca. 35 - 40 years for the four populations sampled at the south-eastern end of the archipelago, but it might well be > 50 years for the Midway population. The Hawaiian stock comprises mainly the same mtDNA haplotype, with no differences in mtDNA stock composition between foraging-ground populations, so that the geographic variability in somatic growth rates within the archipelago is more likely due to local environmental factors rather than genetic factors. Significant temporal variability was also evident, with expected growth rates declining over the last 10 - 20 years, while green turtle abundance within the archipelago has increased significantly since the mid-1970s. This inverse relationship between somatic growth rates and population abundance suggests a density-dependent effect on somatic growth dynamics that has also been reported recently for a Caribbean green turtle stock. The Hawaiian green turtle stock is characterised by slow growth rates displaying significant spatial and temporal variation and an immature growth spurt. This is consistent with similar findings for a Great Barrier Reef green turtle stock that also comprises many foraging-ground populations spanning a wide geographic range.

The east/west archipelagic sea lanes passage through the Indonesian archipelago

The Law of the Sea Convention (LOSC) contained a number of new navigational rights of which archipelagic sea lanes passage was but one. There had previously been no established rules under international law for passage through mid-ocean archipelagos. This article explains about the East/West Archipelagic Sea lanes passage through the Indonesian Archipelago.

Geochemistry, fatty acid content and phylogenetic affiliation of soil samples from Livingston Island, South Shetland Archipelago, Antarctica

Microorganisms inhabit very different soil habitats in the ice-free areas of Antarctica, playing a major role in nutrient cycling in cold environments. We studied the soil characteristics and the dominant bacterial composition from nine different soil profiles located on Livingston Island (maritime Antarctica). The total carbon (TC) and total nitrogen (TN) values were high for the vegetated soils, decreasing with depth, whereas the values for the mineral soils were generally low. Soil pH was more acidic for moss-covered soils and neutral to alkaline for mineral soils. Numbers of culturable heterotrophic bacteria were higher at vegetated sites, but significant numbers were also detectable in carbon-depleted soils. Patterns of denaturing gradient gel electrophoresis (DGGE) revealed a highly heterogeneous picture throughout the soil profiles. Subsequent sequencing of DGGE bands revealed in total 252 sequences that could be assigned to 114 operational taxonomic units, showing the dominance of members of the Bacteroidetes and Acidobacteria. The results of phospholipid fatty acid analysis showed a lack of unsaturated fatty acids for most of the samples. Samples with a prevalence of unsaturated over saturated fatty acids were restricted to several surface samples. Statistical analysis showed that the dominant soil bacterial community composition is most affected by TC and TN contents and soil physical factors such as grain size and moisture, but not pH. Keywords

Tab. 1: Radiocarbon ages of samples from the Canadian archipelago

A sediment-sampling program was carried out in the Nares Strait region during the Nares 2001 Expedition to obtain cores for high-resolution palaeoceanographic studies of late Pleistocene-Holocene climate change. Long cores (>4 m) were obtained from basins near Coburg Island, Jones Sound, John Richardson Fiord off Kane Basin, and in northeastern Hall Basin. Short cores and grab samples were taken on shelves east and west of northern Smith Sound and in Kennedy Channel. Detailed studies of sediment texture, stable isotopes, microfossils and palynomorphs were made on the longest cores from Jones Sound and Hall Basin at the southern and northern ends of the Nares Strait region.