652 resultados para Celebes (Indonesia)
Resumo:
This paper presents the planktonic foraminifer biostratigraphy of the sites drilled during Ocean Drilling Program Leg 124 in the Celebes and Sulu Seas. It discusses preservation of foraminifers in pelagic sediments and in calcareous turbidites. In the Celebes Sea, pelagic carbonates are only found in the Eocene and Oligocene at Site 770. The faunas are poorly preserved due to severe dissolution and offer little biostratigraphic detail. In the Sulu Sea, pelagic carbonates are found in the upper Pliocene and Pleistocene at Sites 768 and 769 and throughout the recovered sequence at the shallower Site 771. The foraminifer faunas from these sediments allow for recognition of most standard zones. Variations in preservation of pelagic foraminifer faunas with time are due to changes in the depth of the lysocline. Shifts to improved preservation at Sites 768 and 769 are synchronous in the upper Pliocene/Pleistocene and may be related to global sea-level cycles. Planktonic foraminifers are also abundant in calcareous turbidites, which were deposited in both basins from the late Miocene onward. However, the turbidites are fine-grained, and biostratigraphic marker species are absent as a result of size-sorting during transport. In the Celebes Sea, shelf-derived material was a major component of early-late Miocene and middle Pliocene to early Pleistocene turbidites. Changes in the composition of the turbidites may correspond to global sea-level changes. In the Sulu Sea, a shift from shelf-derived material in Pliocene calcareous turbidites to a pelagic source in the Pleistocene may be related to subsidence of the Cagayan Ridge.
Resumo:
During Leg 124, off the Philippines, volcanic material was recovered in deep-sea sediments dating from the late Oligocene in the Celebes Sea Basin, and from the early Miocene in the Sulu Sea Basin. Chemical and petrological studies of fallout ash deposits are used to characterize volcanic pulses and to determine their possible origin. All of the glass and mineral compositions belong to medium-K and high-K calc-alkaline arc-related magmatic suites including high-Al basalts, pyroxene-hornblende andesites, dacites, and rhyolites. Late Oligocene and early Miocene products may have originated from the Sunda arc or from the Sabah-Zamboanga old Sulu arc. Late early Miocene Sulu Sea tuffs originated from the Cagayan arc, whereas early late Miocene fallout ashes are attributed to the Sulu arc. A complex magmatic production is distinguished in the Plio-Quaternary with three sequences of basic to acidic lava suites. Early Pliocene strata registered an important activity in both Celebes Sea and Sulu Sea areas, from the newly born Sangihe arc (low-alumina andesite series) and from the Sulu, Zamboanga, and Negros arcs (high-alumina basalt series and high-K andesite series). In the late Pliocene and the early Pleistocene, renewal of activity affects the Sangihe-Cotobato arc as well as the Sulu and Negros arcs (same magmatic distinctions). The last volcanic pulse took place in the late Pleistocene with revival of all the present arc systems.
Resumo:
All sample sites were situated at the northern tip of Napu Valley in Central Sulawesi, Indonesia. After an initial mapping of the study area, we selected 15 smallholder cacao plantations as sites for bird and bat exclosure experiments in March 2010. On each study site, we established 4 treatments for these exclosure experiments (bird exclosure - closed during daytime and open during night; bat exclosure - closed overnight and opened during daytime; full exclosure of both birds and bats - always closed and unmanipulated/open control treatments - always open). In each treatment, there were 2 cacao trees (total of 8 cacao trees per study site), surrounded by nylon filament (2x2 cm mesh size) that was opened and closed according to the activity period of day and night active flying vertebrates (05:00-06:00 am and 17:00-18:00 pm) on a daily basis. The mean tree height and diameter at breast height (dbh) result from two measures of all study trees at the beginning of the exclosure experiment (June 2010) and 6 months later (February 2011).