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132 records · Page 8Linked to original sources
USGS1982

Diatom biostratigraphy and paleoecology of the type section of the Luisian Stage, central California

Diatoms from the type section of the Luisian Stage in central California correlate with the lowermost part of the Denticulopsis lauta Zone through the lower part of subzone "a" of the Denticulopsis hustedtii-D. lauta Zone and are early Middle Miocene in age (about 6.0 to 14.0 Ma), Rocks assigned to the Luisian Stage by benthic foraminifers elsewhere in California exhibit little diachroneity in terms of diatom biostratigraphy, however, detailed studies of boundaries have not been done. Planktic diatoms dominate the assemblages, although an increase in benthic and tychopelagic diatoms in the overlying Hames Member of the Monterey Formation probably reflects shoaling. A cooling trend is suggested by diatom assemblages in the upper part of the section and is most marked near the top of the type Luisian. This cooling trend is supported by data elsewhere in the Pacific Basin as well as by both megafossil and microfossil studies in California. One hundred four diatom taxa are documented, and one new species, Coscinodiscus volutus Baldauf, is described.

California↗
USGS2016

Some contrasting biostratigraphic links between the Baker and Olds Ferry Terranes, eastern Oregon

New stratigraphic and paleontologic data indicate that ophiolitic melange windows in the Olds Ferry terrane of eastern Oregon contain limestone blocks and chert that are somewhat different in age than those present in the adjacent Baker terrane melange. The melange windows in the Olds Ferry terrane occur as inliers in the flyschoid Early and Middle Jurassic age Weatherby Formation, which depositionally overlies the contact between the melange-rich Devonian to Upper Triassic rocks of the Baker terrane on the north, and Upper Triassic and Early Jurassic volcanic arc rocks of the Huntington Formation on the south. The Baker terrane and Huntington Formation represent fragments of a subduction complex and related volcanic island arc, whereas the Weatherby Formation consists of forearc basin sedimentary deposits. The tectonic blocks in the melange windows of the Weatherby Formation (in the Olds Ferry terrane) are dated by scarce biostratigraphic evidence as Upper Pennsylvanian to Lower Permian and Upper Triassic. In contrast, tectonic blocks of limestone in theBaker terrane yield mostly fusulinids and small foraminifers of Middle Pennsylvanian Moscovian age at one locality.Middle Permian (Guadalupian) Tethyan fusulinids and smaller foraminifers (neoschwagerinids and other Middle Permian genera) are present at a few other localities. Late Triassic conodonts and bryozoans are also present in a few of the Baker terrane tectonic blocks. These limestone blocks are generally embedded in Permian and Triassic radiolarian bearing chert or argillite. Based on conodont, radiolarian and fusulinid data, the age limits of the meange blocks in the Weatherby Formation range from Pennsylvanian to Late Triassic.

Oregon↗
USGS1980

Diatoms and stratigraphically significant silicoflagellates from the Atlantic Margin Coring Project and other Atlantic margin sites

In 1976, 19 sites were cored along the U.S. Atlantic Continental Shelf and Slope by the Oceanographic Branch of the U.S. Geological Survey aboard the Glomar Conception. Only 6 sites contained siliceous microfossil assemblages of sufficient quantity and quality for biostratigraphic study. Two of the sites, AMCOR (Atlantic Margin Coring Project) 6002 and AMCOR 6011, contained good Miocene assemblages: a small Pleistocene assemblage occurred at the top of AMCOR 6002. A Late Miocene to Early Pliocene assemblage was encountered in AMCOR 6007B. AMCOR 6013, 6019, and 6021 contained Pleistocene assemblages. In addition to the AMCOR cores, 3 additional Atlantic Margin cores were studied. These were the JOIDES 1 (Caldrill) core, and Atlantic Slope Project (ASP) cores 10 and 22. JOIDES 1 contains a Middle Miocene assemblage similar to AMCOR 6002. ASP 10 contains a Lower Pliocene assemblage and ASP 22 contains a Middle to Late Oligocene and a Pleistocene assemblage. Siliceous assemblages at all sites consisted mainly of shallow shelf species, including brackish and marine benthics and occasionally freshwater forms. Although planktonic forms were present, they were few and most were extant cosmopolitan species. This makes it difficult to correlate the biostratigraphy of the sediments with siliceous microfossil zonations from other oceans. The only biostratigraphic zonations for Atlantic Shelf diatom assemblages are for the Miocene.

Micropaleontology↗
USGS2018

The occurrence of the invasive foraminifera Trochammina hadai Uchio in Flamengo Inlet, Ubatuba, São Paulo State, Brazil

The agglutinated foraminifera Trochammina hadai Uchio (1962), a dominant species in Japan, first appeared as an invasive species in San Francisco Bay, US, in 1983. Trochammina hadai's first appearance in the Brazilian coastal waters of Flamengo Inlet, Ubatuba, Sao Paulo State, is recorded nearly three decades later, in two of thirty-four sediment samples collected in the western portion known as "Saco do Ribeira" in 2010. By 2014 and 2015, the species was found alive in 78% of the samples with relative abundance reaching 18%. We suggest this recent colonization was most likely the result of an introduction by anchor mud on commercial fishing boats and recreational vessels or from fishing bait, and the species' proliferation due to its suitability to live in anthropogenically-induced stressed environmental conditions of the inlet that has affected the ecological dominance of this benthic community.

Sao Paulo↗
USGS2018

Initial dispersal (1986-1987) of the invasive foraminifera Trochammina hadai Uchio in San Francisco Bay, California, USA

A time series of three closely-spaced data sets are used to track the early expansion of the invasive Japanese benthic foraminifera Trochammina hadai in the southern portion of San Francisco Bay known as South Bay. The species initially appeared in 1983, comprising only 1.5% of the assemblage in one of four samples that were dominated by the native species Ammonia tepida and Cribroelphidium excavatum (means = 60.2% and 33.8%, respectively). By 1986, census counts and R- andQ-mode cluster analyses document the explosive growth of the invasive as T. hadai now dominates the assemblage (mean = 42.7%;max = 88.7%)with associated declines in abundance of A. tepida (by greater than one-half; mean = 26.8%) and C. excavatum (by greater than one-third; mean = 20.6%). The invasive continued to dominant the assemblage in 1987, spreading even further to the north and south in South Bay, although its average abundance dropped slightly (~2%) as did those of A. tepida (~3%) and C. excavatum (0.4%). A rare increase in abundance of Elphidiella hannai and the appearance of numerous coastalmarine species in the central portion of the bay are thought to be the result of an incursion ofmarine waters into South Bay due to the prevalent drought conditions in 1987. Clearly, the rapid decline in abundance of the formerly dominant species A. tepida and C. excavatum in South Bay from 1983 to 1986 that continued into 1987 suggests the introduction of T. hadai in the bay severely impacted the native population.

California↗
USGS2019

The benthic foraminifera cassidulina from the Arctic Ocean: Application to paleoceanography and biostratigraphy

We investigated the morphology, biostratigraphy, shell stable isotope composition and paleogeography of the common Arctic benthic foraminifera, Cassidulina teretis (Tappan 1951) (sometimes assigned to Islandiella (Nørvang 1958), for application to Quaternary paleoceanography. Cassidulina teretis, which has been studied by several generations of Arctic foraminiferal specialists, is used in Arctic Ocean paleoceanographic reconstructions based on foraminiferal assemblages and, increasingly, isotope shell chemistry. Here we review its modern and fossil distribution including discussions of its taxonomy, ecology, biostratigraphy and shell chemistry. Cassidulina teretis Tappan 1951, originally described from the Gubik Formation, northern Alaska coastal plain, has variability in test size, apertural morphology and development of an umbilical boss representing intra- and inter-population differences across the Arctic and subarctic in modern, Quaternary and Pliocene assemblages. Nonetheless, our studies and those previously published lead us to conclude that populations from the Arctic Ocean represent a single species proposed by Tappan as Cassidulina teretis. Its modern distribution is mainly 200 to 1000 m water depth, often living within the core of the relatively warm Atlantic Layer. However, shallower occurrences suggest other factors, such as food supply, are also critical to its ecology. The Holocene distribution of Cassidulina teretis in the Beaufort Sea boundary indicate millennial-scale changes in relative abundance related to changing Atlantic Layer influence, sea-ice cover, surface productivity and food availability. There are extremely large changes in its abundance during the last deglacial interval on the Yermak Plateau, Barents Sea slope and the Laptev Sea reflecting rapid ocean changes during the Bølling-Allerød, Younger Dryas, and Preboreal. Similarly, C. teretis abundance changes during the last 300,000 years allow us to use it, at least regionally, as a useful biostratigraphic marker. The stable isotopic composition of Cassidulina teretis tests holds promise for establishing an isotope stratigraphy across the Arctic Ocean and perhaps also in the Nordic Seas, off Iceland and in the northern North Atlantic Ocean, once disequilibrium values and offsets from other Arctic benthic species are more firmly established.

Micropaleontology↗