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Geology topics

Research about North Pacific Ocean

Source-linked reports with geographic coverage including North Pacific Ocean.

6 recordsLinked to original sources

Cycles in adult steelhead length suggest interspecific competition in the North Pacific Ocean

Anadromous fishes rely on abundant prey in the ocean to grow large quickly, but prey limitation leads to interspecific competition. When species interactions are difficult to observe, growth can be studied to detect otherwise cryptic signals of competition. We describe a previously undocumented two-year cycle in the lengths of adult natural-origin steelhead ( Oncorhynchus mykiss ) returning to spawn in the Snake River Basin. Returning steelhead were 38 mm shorter on odd return years, not accounting for sex, stock, and years of ocean residence. The well-known cycle in abundance of Pink Salmon from eastern Kamchatka and North America had statistically significant negative effects on returning steelhead lengths that depended on sex and the number of years of ocean residence. These results suggest that competition for limited resources occurs well after initial ocean entry and that interactions during later stages of ocean residence can be influential. Interspecific competition has implications for future returns of steelhead from the ocean, especially as metabolic demands for steelhead increase as the ocean warms.

North Pacific Ocean

Food of Flesh-footed shearwaters Puffinus carneipes associated with high-seas driftnets in the central North Pacific Ocean

We examined digestive tract contents and stable nitrogen isotope ratios in breast muscles of Flesh-footed Shearwaters Puffinus carneipes associated with high-seas driftnet fisheries in the central North Pacific Ocean. Small fish, Lanternfish (Myctophidae) and Pacific Saury Cololabis saira , were the principal prey found in the digestive tracts. Pieces of unidentified fish, possibly Pacific Pomfret Brama japonica , and shredded squid tissue, mostly Neon Flying Squid Ommastrephes bartrami , in the digestive tracts indicate scavenging at driftnet fishing operations. Although soft-bodied animals such as Velella sp. were rare in the digestive tracts, low stable nitrogen isotope values (δ 15 N) suggest Flesh-footed Shearwaters feed heavily on such low trophic level animals.

Emu

Foods, trophic relationships, and migration of Sooty and Short-tailed Shearwaters associated with squid and large-mesh driftnet fisheries in the North Pacific Ocean

We salvaged dead birds from high seas driftnets in the Central North Pacific Ocean during a study of the impact of high seas driftnet fishing on marine ecosystems. Digestive tract contents and stable isotopes of nitrogen and carbon in breast muscles of these birds were analyzed to assess the effect of driftnets on the trophic relationships of marine birds. The diets of Sooty ( Puffinus griseus ) and Short-tailed ( P. tenuirostris ) Shearwaters associated with high seas driftnets in the transitional region of the North Pacific Ocean overlap broadly. The principal differences between them include 1) Sooties prey more heavily on immature stages of invertebrates, especially the barnacle Lepas fascicularis than do Short-tails, 2) Pacific saury ( Cololabis saira ) are the primary fish taken by Sooties while lanternfish ( Myctophidae ) are the primary fish taken by Short-tails, and 3) Sooties take a wider variety of prey than do Short-tails. During the last years of extensive high seas driftnet fishing (early 1990's), both shearwaters augmented their diets with about 15% offal and discards from fishing vessels. Values for stable isotopes of nitrogen and carbon in breast muscle tissues (δ 15 N and δ 15 C) indicate the extent and timing of movements of Sooty Shearwaters: including arrival of migrants from the south Pacific (April-May), east to west movement from the eastern Pacific (May-June), and west to east movement from Japan (August-September). Fall migrant Sooties were not detected. The only movements of Short-tails that we detected were a few south-bound migrants in September-November.

Waterbirds

Sea otters in the northern Pacific Ocean

About 250 years ago sea otters ( Enhydra lutris ) were distributed continuously from central Baja California, north and west along the Pacific Rim to Machatka Peninsula in Russia, and south along the Kuril Island to northern Japan (Kenyon 1969; Fig. 1a). Several hundred thousand sea otters may have occurred in the north Pacific region when commercial hunting began in the 18th century (Riedman and Estes 1990). At least two attributes of the sea otter have influenced humans, likely for as long as they have resided together along the coast of the north Pacific Ocean. First, sea otters rely on a dense fur, among the finest in the world, for insulation in the cold waters of the Pacific Ocean. The demand for sea otter fur led to their near extinction in the 19th century. The fur harvest, begun about 1740 and halted by international treaty in 1911, left surviving colonies, each likely numbering less than a few hundred animals, in California, south-central Alaska, and the Aleutian, Medney, and Kuril Islands (Fig. 1a). These individuals provided the nucleus for the recovery of the species. Today more than 100,000 sea otters occur throughout about 75% of their original range (fig. 1b). Immigration has resulted in near-complete occupation of the Aleutian and Kuril archipelagos and the Alaska peninsula. Successful translocations have resulted in viable populations in southeast Alaska, Washington, and British Columbia. Large amounts of unoccupied habitat remain along the coasts of Russia, Canada, the United States, and Mexico. The second potential source of conflict between sea otters and humans is that sea otters prey on and often limit some benthic invertebrate populations. Because some of these invertebrates are aso used by humans (Estes and VanBlaricom 1985), human perceptions about the effects of sea otter foraging on invertebrates sometimes differ. By limiting populations of herbivorous invertebrates ( e.g. , sea urchins [Echinoidea]) otters help maintain the integrity of kelp forest communities. At the same time, sea otter predation on other marine invertebrates can lead to direct competition with humans for resources. These interactions add complex dimensions to the conservation and management of sea otters, in large part because of wide-ranging social, ecological, and economic consequences of sea otter foraging. Long-term data on abundance and distribution are available for relatively few sea otter populations. Here we summarize such data from three populations: Being Island, Russia; Prince William Sound, Alaska; and Olympic Peninsula, Washington. The Bering Island population resulted from natural emigration and represents complete recovery. Prince William Sounds represents near recovery of a remnant population, whereas the Washington population was established via translocations from Alaska and is just beginning to recover. We will compare growth rates and current status among these populations. Because of its unique status and growth characteristics, the California sea otter is not treated in this article.

Book chapter

Interactions between seabirds and fisheries in the North Pacific Ocean

Interactions between commercial fisheries and seabirds in the northern Pacific Ocean are increasing with rising consumption of fishery products. As fishing expands into remote areas previously not fished, additional populations of seabirds may be affected. Some interactions such as introduction of fish processing wastes into the environment may be beneficial for seabirds, while others such as competition for fish prey and incidental take by fishing nets may have negatively affected seabird populations.

Book chapter

Seabirds between Alaska and Hawaii

Seabirds were observed between Alaska and Hawaii along 158°W longitude from 24 October to 6 November 1976. Their distributions and abundances corresponded remarkably well to oceanographic regions. Indices of seabird density dropped in a series of plateaus from 44 birds/km 2 in the Alaska Current System to less than 1 bird/km 2 in subtropic waters. Northern distribution records were found for six species. The Subarctic Boundary marked the center of the separation between subarctic and subtropic pelagic avifaunas.

Alaska, Hawaii