294 resultados para Nepenthes.
Resumo:
From October to December in 1996, Sites 1039 through 1043 were drilled on the lower continental slope and the bottom of the Middle American Trench. Planktonic foraminifers were obtained from 377 samples of the total 487 examined. The Pliocene- to Pleistocene-age sediments of Sites 1039 and 1043 are continuous from Zones N19 through N23. At Sites 1039 and 1040, middle Miocene sediments are also continuous, encompassing Zones N8 through N12. The sequences of the upper part of Sites 1040, 1041, 1042, and 1043 are décollements, tentatively assignable to Zone N19 for Sites 1040, 1041, and 1042 and to Zone N22 for Site 1043. The oldest sediments of these sites are assigned to Zone N7 (latest early Miocene), ~17 Ma in age.
Resumo:
Early Miocene to Quaternary benthic foraminifers have been quantitatively studied (>63 ?m size fraction) in a southwest Pacific traverse of DSDP sites at depths from about 1300 to 3200 m down the Lord Howe Rise (Site 590,1299 m; Site 591, 2131 m; Site 206, 3196 m). Benthic foraminiferal species smaller than 150 µm are by far dominant in the samples, averaging from 78 to 89% of the total benthic foraminiferal assemblages in the three sites examined. Although about 150 benthic foraminiferal species or taxonomic groups have been identified, only a few species dominate the assemblages. These dominant species include Epistominella exigua, E. rotunda, and Globocassidulina subglobosa, which prevail in the three sites, and Oridorsalis umbonatus, E. umbonifera, and Cassidulina carinata, which occur usually in frequencies of between 10 and 30%. Faunal changes in Neogene benthic foraminiferal assemblages are not similar in each of the three sites, but faunal successions are most similar between the two shallowest sites. The deepest site differs in composition and distribution of dominant species. There are three intervals during which the most important changes occur in benthic foraminiferal assemblages: the early middle Miocene (14 Ma; the Orbulina suturalis Zone and the Globorotalia fohsi s.l. Zone); the late Miocene (6 Ma; the Globigerina nepenthes Zone) and near the Pliocene/Pleistocene boundary at about 2 Ma. A Q-mode factor analysis of the faunal data has assisted in recognizing assemblage changes during the Neogene at each of the sites. Early Miocene assemblages were dominated by Globocassidulina subglobosa at Site 590 (1299 m), by G. subglobosa and Oridorsalis umbonatus at Site 591 (2131 m), and by G. subglobosa, E. exigua, and Bolivina pusilla at Site 206 (3196 m). In the early middle Miocene at Sites 590 and 591, a marked increase occurred in the frequencies of E. exigua. Epistominella exigua reached maximum abundance in the early Miocene in the deeper Site 206, and in the middle and early late Miocene in the shallower Sites 590 and 591. In the late Miocene, a spike occurred in the frequencies of E. umbonifera in Site 206, whereas the dominant species changed from E. exigua to E. rotunda at Site 590. Latest Miocene to late Pliocene assemblages were dominated by E. rotunda at Site 590, by E. exigua at Site 591, and by G. subglobosa-E. exigua (early Pliocene) and E. rotunda-E. exigua (late Pliocene) at Site 206. At the Pliocene/Pleistocene boundary, E. exigua temporarily diminished in importance at Sites 591 and 206. Quaternary assemblages were dominated by E. rotunda and Cassidulina carinata at Site 590, by E. rotunda at Site 591, and by E. exigua at Site 206. These major faunal changes are all associated with known major paleoceanographic events-the middle Miocene development of the Antarctic ice sheet; the latest Miocene global cooling and increased polar glaciation; and the onset of quasiperiodic glaciation of the Northern Hemisphere. These major paleoceanographic events undoubtedly had a profound effect on the intermediate and deep water mass structure of the Tasman Sea as recorded by changes in benthic foraminiferal assemblages.
Resumo:
Planktonic foraminifers were examined from 27 holes situated at 12 separate sites in the tropical Atlantic. The sites are located in various environments, including areas of upwelling, areas affected by cool currents, areas of strong dissolution, and areas that show little dissolution in warm-water settings. Paleomagnetic results were variable at these sites, but accumulation rate curves have been produced by combining the existing paleomagnetic data with the available microfaunal data. Determinations of the ages of the planktonic foraminifer datums from these accumulation rate curves show some species to be strongly diachronous, while others provide good stratigraphic markers. The warmest water sites with the least dissolution show the most complete ranges of species.
Resumo:
The 136 m of calcareous oozes recovered in Hole 810C span the interval from upper Maastrichtian to middle Pleistocene. Three major hiatuses interrupt the sequence, with the topmost part of the Maastrichtian through the entire lower Paleocene, most of the lower Eocene, and the entire middle Eocene through most of the middle Miocene missing. Severe reworking and displacement affected the lower part of the succession from the Maastrichtian through the middle Miocene. Reworking and displacement gradually decreased in the upper portion. Calcareous nannofossil biostratigraphy enabled us to calibrate precisely the nearly complete magnetic reversal sequence of the Pliocene to the late Pleistocene. Two minor hiatuses detected by calcareous nannofossils across the Pliocene/Pleistocene boundary and in the upper lower Pleistocene, respectively, resulted in shortening of the Olduvai and Jaramillo Events within the Matuyama Chron of the magnetic reversal sequence.
Resumo:
Cores from four Ocean Drilling Program (ODP) sites were examined for planktonic foraminifers. One sample per core (from core-catchers in Holes 806B and 807B and from Section 4 in Holes 847B and 852B) was examined through the interval representing the last 5.8 m.y. Sites 806 (0°19.1'N; 159°21.7'E) and 847 (0o12.1'N; 95°19.2'W) are beneath the equatorial divergence zone. Sites 807 (3°36.4'N; 156°37.5'E) and 852 (5°19.6'N; 110°4.6'W) are located north of the equator in the convergence zone created by the interaction of the westward-flowing South Equatorial Current (SEC) and the eastward-flowing North Equatorial Countercurrent (NECC). Specimens were identified to species and then grouped according to depth habitat and trophic level. Species richness and diversity were also calculated. Tropical neogloboquadrinids have been more abundant in the eastern than in the western equatorial Pacific Ocean throughout the last 5.8 m.y. During the mid-Pliocene (3.8-3.2 Ma), their abundance increased at all sites, while during the Pleistocene (after ~ 1.6 Ma), they expanded in the east and declined in the west. This suggests an increase in surface-water productivity across the Pacific Ocean during the closing of the Central American seaway and an exacerbation of the productivity asymmetry between the eastern and western equatorial regions during the Pleistocene. This faunal evidence agrees with eolian grain-size data (Hovan, 1995) and diatom flux data (Iwai, this volume), which suggest increases in tradewind strength in the eastern equatorial Pacific that centered around 3.5 and 0.5 Ma. The present longitudinal zonation of thermocline dwelling species, a response to the piling of warm surface water in the western equatorial region of the Pacific, seems to have developed after 2.4 Ma, not directly after the closing of the Panama seaway (3.2 Ma). Apparently, after 2.4 Ma, the piling warm water in the west overwhelmed the upwelling of nutrients into the photic zone in that region, creating the Oceanographic asymmetry that exists in the modern tropical Pacific and is reflected in the microfossil record. In the upper Miocene and lower Pliocene sediments, the ratio of thermocline-dwelling species to mixed-layer dwellers is 60%:40%. During the mid-Pliocene, the western sites became 40% thermocline and 60% mixed-layer dwellers. Subsequent to -2.4 Ma, the asymmetry increased to 20%: 80% in the west and the reverse in the east. This documents the gradual thickening of the warm-water layer piled up in the western tropical Pacific over the last 5.8 m.y. and reveals two "steps" in the biotic trend that can be associated with specific events in the physical environment.
Resumo:
One hundred and sixty core samples were analyzed from Hole 832B to evaluate planktonic foraminiferal datum levels, and to zone and correlate the borehole succession. A total of 32 biostratigraphic events were recognized in the interval from Core 134-832B-59R through 134-832B-73R (702.49 through 846.4 meters below seafloor [mbsf]). These include 17 first appearance datum levels (FAD), 10 last appearance datum levels (LAD), and 5 coiling-change events in trochospiral species. The studied succession has been subdivided into nine planktonic foraminiferal zones (viz. downsequence N.22, N.21, N.20, N.19, N.18, N.17B, N.17A-N.16, N.15, N.8). The zonal index species occur in the expected stratigraphic order for zonal correlation, but some of the zonal boundaries may be diachronous compared to other localities in the western Pacific region. The FAD of Globorotalia (Truncorotalia) truncatulinoides (d' Orbigny) at 714.10 mbsf defines the boundary between the Zone N.22 and N.21; the boundary between Zones N.21 and N.20 at 741.73 mbsf is marked by the FAD of Globorotalia (Truncorotalia) tosaensis Takayanagi and Saito. The lower boundary of Zone N.20 is placed at 747.65 mbsf, based on the FAD of Globorotalia (Truncorotalia) crassaformis s.s. (Galloway and Wissler); the FAD of Sphaeroidinella dehiscens (Parker and Jones) at 756.61 mbsf defines the boundary between Zones N.18 and N.19. The FAD of Globorotalia (Globorotalia) tumida tumida (Brady) at 811.15 mbsf marks the boundary between Zones N.18 and N.17B. The boundary between Zones N.17B and N.17Ais placed at 843.52 mbsf, based on the FAD of Pulleniatina primalis Banner and Blow. A change in depositional conditions occurs at 846.4 mbsf just below the Zone N.17B lower boundary and is marked by the first appearance of abundant planktonic foraminifers in the region. The interval between 849.13 and 856.1 mbsf is placed in undifferentiated Zones N.17A and N.16, based on the rare occurrence of Neogloboquadrina acostaensis (Blow). The sparsely fossiliferous volcanic sandstone unit between 934.19 and 955.67 mbsf is positioned within Zone N.15 based on the presence of Globigerina (Zeaglobigerina) nepenthes Todd and Globigerinoides (Zeaglobigerina) druryi Arkers, and absence of N. acostaensis and Globorotalia (Jenkinsella) siakensis LeRoy. An unconformity between 955.67 and 971.80 mbsf may explain the absence of Zones N.14 through N.9. Basal Zone N.8 is recognized at 971.80 to 1008.60 mbsf by the presence of Globigerinoides sicanus De Stefani and the absence of Praeorbulina and Orbulina spp. The age of the succession between 702.49 and 1008.6 mbsf extends from the latest Pliocene or earliest Pleistocene (Zone N.22) to the earliest middle Miocene (Zone N.8). Among the datum levels evaluated here, the following events are considered to be the most reliable for time correlation in the studied region: the FADs of G. (T.) truncatulinoides, G. (T.) tosaensis, G. (T.) crassaformis, S. dehiscens, G. conglobatus (Brady), G. (G.) tumida tumida, and P. primalis; and the LADs of Globorotalia (Menardella) multicamerata Cushman and Jarvis, and Dentoglobigerina altispira altispira (Cushman and Jarvis). Application of a chronometric scale to part of the succession, suggests that the interval of calcareous sediment between 702.49 and 846.4 mbsf accumulated at about 30 m/m.y.
Resumo:
The late Miocene sediments of the Tyrrhenian ODP Site 654 encompass a deepening sequence which begins with glauconite shallow water sands followed by a rapid transition to deep water sediments and culminates with dolomitic mudstones associated with Messinian evaporites. The sequence compares well with the so-called 'Sahelian cycle' and with post-orogenic cycles recognized in peninsular Italy and Sicily. The studied interval, consisting of 55 m thick nannofossil oozes, belongs to the Globorotalia suterae subzone and lower part of the Globorotalia conomiozea Zone, indicating late Tortonian and early Messinian age, respectively. Biomagnetostratigraphic correlation assigns the Tortonian/ Messinian boundary an age of 6.44-6.45 Ma. In addition, six main events have been recognized, based on the range of keeled globorotaliids and coiling direction changes of keeled and unkeeled globorotaliids, which have been correlated to the geomagnetic time-scale. Comparison with North Atlantic sites and land sections of the Guadalquivir basin and northern Morocco provides good correlations with the events documented in these areas. In particular, Event IV, which predates the FO of Globorotalia conomiozea, may be used to recognize the Tortonian/Messinian boundary in extra-Mediterranean areas where G. conomiozea is missing. Variations in the distribution of different species of Globigerinoides are related to changes in the surficial marine environment. Although no clear trends can be recognized on the oxygen and carbon isotope records of Globigerinoides obliquus, the parallelism between the occurrence of low salinity species (G. sacculifer) and peaks of low 5180 values, as well as that of normal salinity species (G. obliquus) and peaks of high d18O values, suggests strong local changes of environmental conditions. The high amplitude of the fluctuations of d18O values suggests important variations in the salinity of the Tyrrhenian Sea, related to a rapidly changing water budget. The major feature of the carbon isotope record is a large decrease between 7.0 and 6.95 Ma, which therefore predates the 6.2 Ma global 'carbon shift'.
Resumo:
Diverse, warm-water planktonic foraminiferal faunas prevailed on the Wombat and Exmouth plateaus during the Neogene, in spite of the northward drift of Australia across 10° to 15° latitude since the early Miocene. Invasions of cool-water species occurred during periods of global cooling in the late middle Miocene, late Miocene, and Pleistocene, and reflect periods of increased northward transport of cool surface water, probably via the West Australian Current. The sedimentary record of the Neogene on Wombat and Exmouth Plateau is interrupted by two hiatuses (lower Miocene, Zone N5, and upper middle to upper Miocene, Zones N15-N17), and one redeposited section of upper Miocene to uppermost Pliocene sediments. Mechanical erosion or nondeposition by increased deep-water flow or tilting and uplift of Wombat and Exmouth plateaus, resulting in sediment shedding, are the most likely explanations for these Miocene hiatuses, but which of these processes were actually operative on the Wombat and Exmouth plateaus is uncertain. The redeposited section of upper Miocene to uppermost Pliocene sediments in Hole 761B, however, certainly reflects a latest Pliocene period of uplift and tilting of the Wombat Plateau. An important finding was the occurrence of Zone N15-correlative sediments in Hole 762B without any representative of Neogloboquadrina. Similar findings in Java and Jamaica indicate that the earliest spreading of Neogloboquadrina acostaensis in the tropical region resulted from migration. The evolution of this species, therefore, must have taken place in higher latitudes. I suggest that Neogloboquadrina acostaensis evolved from Neogloboquadrina atlantica in the North Atlantic within Zone NN9, but how and where in the region this speciation took place is still uncertain
Resumo:
We document the waxing and waning of a "proto-warm pool" in the western equatorial Pacific (WEP) based on a study of multi-species planktic foraminiferal isotope ratios and census data spanning the 13.2-5.8 Ma interval at ODP Site 806. We hypothesize that the presence or absence of a proto-warm pool in the WEP, caused by the progressive tectonic constriction of the Indonesian Seaway and modulated by sea level fluctuations, created El Niño/La Niña-like alternations of hydrographic conditions across the equatorial Pacific during the late Miocene. This hypothesis is supported by the general antithetical relationship observed between carbonate productivity and preservation in the western and eastern equatorial Pacific, which we propose is caused by these alternating ocean-climate states. Warming of thermocline and surface waters, as well as a major change in planktic foraminferal assemblages record a two-step phase of proto-warm pool development ~11.6-10 Ma, which coincides with Miocene isotope events Mi5 and Mi6, and sea-level low stands. We suggest that these changes in the biota and structure of the upper water column in the WEP mark the initiation of a more modern equatorial current system, including the development of the Equatorial Undercurrent (EUC), as La Niña-like conditions became established across the tropical Pacific. This situation sustained carbonate and silica productivity in the eastern equatorial Pacific (EEP) at a time when carbonate preservation sharply declined in the Caribbean. Proto-warm pool weakening after ~10 Ma may have contributed to the nadir of a similar "carbonate crash" in the EEP. Cooling of the thermocline and increased abundances of thermocline taxa herald the decay of the proto-warm pool and higher productivity in the WEP, particularly ~ 9.0-8.8 Ma coincident with a major perturbation in tropical nannofossil assemblages. We suggest that this interval of increased productivity records El Niño-like conditions across the tropical Pacific and the initial phase of the widespread "biogenic bloom". Resurgence of a later proto-warm pool in the WEP ~6.5-6.1 Ma may have spurred renewed La Niña-like conditions, which contributed to a strong late phase of the "biogenic bloom" in the EEP.
Resumo:
During Leg 41 Neogene sediments were recovered from five sites off northwest Africa. On the Sierra Leone Rise (Site 366), Neogene sediments consist of nanno oozes, nanno chalk, and calcareous clays 230 meters thick, resting conformably on the late Oligocene sediments. The common succession of zones occurs with two hiatuses. The lower gap corresponds to an interval around the lower/middle Miocene boundary (the Praeorbulina glomerosa and Orbulina suturalis-Globorotalia peri-pheroronda zones are absent) and the upper gap coincides with an interval around the middle/upper Miocene boundary (the Sphaeroidinellopsis sub-dehiscens-GIobigerina druryi, Globigerina nepenthes-Globorotalia siakensis and Globorotalia conlinuosa zones are missing). In the Cape Verde Basin (Site 367) deep-water Neogene turbidites (about 200-250 m thick) contain poor fauna of redeposited and sorted Cretaceous, Eocene, Oligocene, and Neogene species. On the Cape Verde Rise (Site 368) the Neogene section starts with slightly calcareous and non-calcareous clays with poor planktonic foraminifers of the lower Miocene. Later on this area was uplifted and clayey sediments have been replaced upsection in order by more shallow-water clayey nanno and nanno-foraminifer oozes and marls and pure calcareous oozes. In the middle Miocene, planktonic foraminifers are still not diverse, but since the level of the Globigerina nepenthes-Globorotalia siakensis Zone, almost all Neogene zones have been traced. The minimum thickness of the Neogene sediments is about 230 meters. On the continental slope off Spanish Sahara (Site 369) monotonous calcareous pelagic sediments of Neogene age (164 m thick) overlie the late Oligocene comformably, or with a small time gap. A set of zones beginning from the Globigerinoides primordis-Globorotaiia kugleri Zone up to the Globorotalia fohsi fohsi Zone has been revealed with a gap corresponding to the Globigerinita stainforthi and the Globigerinatella insueta-Globigerinoides irilobus zones. Above that follow sediments with heterogeneous microfauna which result from redeposition or mixing of sediments during drilling. The section ends with sediments of the late Miocene and lower Pliocene with abundant planktonic foraminifers. The latter are unconformably overlain by the Quaternary ooze. In the Morocco basin (Site 370) deep-water marls and calcareous clays of the lower Miocene contain poor assemblages of planktonic foraminifers. The middle and upper Miocene are represented by turbidites (alternation of nanno oozes, clays, siltstones, and sands) with heterogeneous microfauna. Total thickness of Neogene is up to 200 meters. In general the Neogene foraminifer microfauna of the area studied includes the majority of species which developed within the tropical-subtropical belt. The entire succession of the Miocene and Pliocene foraminifer zones occurs. The only exclusion is the Sphaeroidinellopsis subdehiscens-Globigerina druryi Zone of the middle Miocene. The distribution of species is shown on three tables. Comments are given for 47 species and subspecies of foraminifers (stratigraphic ranges, peculiarities of morphology, and ultrastructure of the shell wall).
Resumo:
The mid-Piacenzian (MP) warm period (3.264-3.025 Ma) has been identified as the most recent time in geologic history during which mean global surface temperatures were considerably warmer than today for a sustained period. This interval has therefore been proposed as a potential (albeit imperfect) analog for future climate change and as such, has received much scientific attention over the past two decades. Central to this research effort is the Pliocene Research, Interpretation, and Synoptic Mapping (PRISM) project, an iterative paleoenvironmental reconstruction of the MP focused on increasing our understanding of warm-period climate forcings, dynamics, and feedbacks by providing three-dimensional data sets for general circulation models. A mainstay of the PRISM project has been the development of a global sea surface temperature (SST) data set based primarily upon quantitative analyses of planktic foraminifer assemblages, supplemented with geochemical SST estimates wherever possible. In order to improve spatial coverage of the PRISM faunal data set in the low and mid-latitude North Atlantic, this study provides a description of the MP planktic foraminifer assemblage from five Ocean Drilling Program sites (951, 958, 1006, 1062, and 1063) in the subtropical gyre, a region critical to Atlantic Ocean circulation and tropical heat advection. Assemblages from each core provide evidence for a temperature- and circulation-driven 5-10° northward displacement of MP faunal provinces, as well as regional shifts in planktic foraminifer populations linked to species ecology and interactions. General biogeographic trends also indicate that, relative to modern conditions, gyre circulation was stronger (particularly the Gulf Stream, North Atlantic Current, and North Equatorial Current) and meridionally broader. A comparison of mid-Piacenzian and modern North Atlantic planktic foraminifer assemblages suggests that low latitude western boundary currents were less than 1 °C warmer while eastern boundary currents were ~1-2 °C warmer, supporting the hypothesis of enhanced northward heat advection along western boundary currents and warming of high latitude Northeast Atlantic source regions for the Canary Current. These findings are consistent with a model of reduced meridional SST gradients, with little-to-no low latitude warming, and more vigorous ocean circulation. Results therefore support the theory that enhanced meridional overturn circulation and associated northward heat advection made an important contribution, in conjunction with elevated atmospheric CO2 concentrations, to the 2-3 °C global surface temperature increase (relative to today) and strong polar amplification of SST warmth during the MP warm period.