冷泉区底栖有孔虫研究进展

海底冷泉区是海洋能源和生物资源同时富集的一类特殊区域。底栖有孔虫群落及其地球化学组成是海底冷泉区发育的重要指示标志之一。海底冷泉区的底栖有孔虫及其碳同位素研究,对于探讨冷泉演化、评估古冷泉甲烷排放对全球气候变化的影响有重要的研究意义。综述了全球一些主要冷泉区的底栖有孔虫研究方法及其进展,对比了各冷泉区底栖有孔虫群落结构的主要特征及地域差异,评述了冷泉区底栖有孔虫的碳同位素记录特征、影响因素及其对冷泉活动的潜在指示意义,最后提出了南海北部冷泉活动区底栖有孔虫方面的研究展望。     

热带西太平洋碳酸盐溶跃深度及其变化规律

碳酸盐的溶解与保存是全球碳循环的重要组成部分,研究碳酸盐溶解作用对探索碳循环机制、理解全球气候变化机理等具有重要意义。本文通过西太平洋暖池核心区雅浦海沟南部附近海域108个表层沉积物和3个柱状沉积物样品中浮游有孔虫、底栖有孔虫和碳酸钙含量等变化特征分析了海底碳酸盐溶跃深度、补偿深度及其自中更新世以来的变化规律。表层沉积物碳酸盐含量、浮游与底栖有孔虫丰度、底栖有孔虫占有孔虫全群比例、底栖有孔虫群中胶结质壳比例等多种指标变化表明,本区现代碳酸盐溶跃面(carbonate lysocline depth, CLD)位于水深3800m附近,碳酸盐补偿深度(carbonate compensation depth, CCD)约为4800m。柱状样有孔虫溶解指数(foraminifera dissolution index, FDX）的变化表明,冰期碳酸盐溶解作用减弱,碳酸盐溶跃面和补偿深度变深;冰消期碳酸盐溶解作用增强,溶跃面和补偿深度变浅。位于现代溶跃面附近的柱状岩心碳酸盐含量呈现冰期高、间冰期低的“太平洋型”旋回特征,同时古生产力替代性指标的变化曲线与碳酸盐含量没有明显的相关性,说明中更新世以来的碳酸盐含量变化主要受溶解作用的控制,特别是在冰期- 间冰期转换时期更为明显。     

海洋低氧环境底栖有孔虫研究进展

全球变暖和人为活动不断加剧海洋低氧环境发生的频率和范围,低氧对全球海洋底栖生物群落结构造成重大影响。底栖有孔虫能够广泛适应生存在各种海洋低氧环境中,是极少数能适应低氧环境的真核生物之一,底栖有孔虫对低氧环境的响应及适应机制研究是海洋研究领域的前沿和热点话题,至今仍存在很多谜团。本文总结了不同海洋低氧环境活体底栖有孔虫分布特征、活体底栖有孔虫对人为诱导低氧环境的响应、低氧环境下底栖有孔虫外壳化学组成特征、低氧环境下底栖有孔虫的生存机理,期望为后续推进海洋低氧环境下底栖有孔虫相关研究进一步开展提供参考和借鉴。底栖有孔虫作为古海洋环境重建的重要工具,对我们了解全球海洋低氧环境的历史演化进程具有非常重要的意义。展望未来我们需要进一步加强有孔虫细胞生理学和分子生物学对低氧环境的适应机制研究,从系统发生学上认识真核生物对低氧环境适应的历史演化进程,为利用有孔虫作为工具更好地重建和预测海洋低氧环境变化提供理论依据。     

晚上新世以来南海北部深部水团演化

对南海北部大洋钻探184航次1146站晚上新世以来底栖有孔虫属种组合的Q型因子分析, 发现底栖有孔虫组合以2.1Ma, 1.5Ma和0.7Ma为界, 分为Stilostomella-Globocassidulina subglobosa-Nodogenerina, Bulimina alazanensis, Uvigerina perigrina和Melonis barleeanus-Globobulimina affinis-Bulimina aculeata4个组合.结合底层水溶解氧含量和浮游、底栖有孔虫碳同位素分析, 认为底栖有孔虫组合的变化是南海底层水影响所致, 以及南海北部表层和底层海水营养盐含量变化的共同结果.      

南海晚第四纪表层古生产力与东亚季风变迁

根据南海南北陆坡两个站位的柱状样中底栖有孔虫分布,结合有机碳、稳定同位素分析,获得南海近4万年来高分辨率的表层古生产力记录,进而探讨晚第四纪东亚古季风的变迁。研究表明,由于冬季风在本次冰期、夏季风在全新世早期约10000aB．P．急剧增强,分别在南海南北陆坡产生海岸上升流,加上陆源营养物输入增多,使得表层古生产力明显增高、有机碳通量增大至3．5gC／(m²·10³a)以上,从而底栖有孔虫群中Buliminaaculeata和Uvigerinaperegrina占绝对优势。     

南黄海北部晚第四纪底栖有孔虫群落 分布特征及对古冷水团的指示

底栖有孔虫和粒度分析结果表明,南黄海北部DLC70 3孔（36°38′15″ N,123°32′56″ E,水深7200 m）7120 m长的柱状样保存了130 ka以来的沉积记录。依据349个样品的底栖有孔虫丰度和特征种的分布,结合岩性粒度变化,可识别9个底栖有孔虫组合,对应5个海相层和4个陆相至过渡相层;结合AMS14C和OSL测年数据建立了钻孔晚更新世以来的年代地层,可以与南黄海其他钻孔的地层进行对比。应用属种组合和不同生态种的丰度变化,探讨了研究区末次间冰期以来的古环境变化,认为海平面频繁波动是该地区不同成因类型地层从陆相、潮间、滨岸、滨海、近岸浅海、到浅海反复演替的关键。孔段2040~2780 m（MIS3早期）和5500~7120 m（MIS5e）的底栖有孔虫优势种是 Buccella frigida和Protelphidium tuberculatum,代表了与目前相似的冷涡边缘的冷水环境,指示南黄海古冷水团在MIS5e和MIS3早期高海平面时期已经存在。     

南海北部天然气水合物远景区末次冰期以来底栖有孔虫稳定同位素特征及其影响因素

底栖有孔虫碳同位素负偏移是地质记录中天然气水合物释放的重要证据之一.对南海北部西沙海槽和东沙陆坡等天然气水合物远景区XH-27PC和DS-4PC柱状样分别进行顶空气甲烷含量分析、有机碳含量分析、粒度分析和有孔虫氧碳同位素分析.结合碳酸盐含量及AMS 14C测年,揭示研究区末次冰期以来底栖有孔虫的稳定同位素特征.结果显示:西沙海槽BSR区沉积物中甲烷含量较低;底栖有孔虫碳同位素负偏不明显,与顶空气甲烷含量呈弱正相关(R=0.32),与有机碳含量有强负相关(R=-0.82),说明低通量甲烷不足以引起底栖有孔虫碳同位素显著偏移,在无甲烷或甲烷轻微渗漏的环境中有机碳的厌氧氧化是影响底栖有孔虫碳同位素组成的主要因素.东沙陆坡BSR区沉积物中含有大量的甲烷气体;底栖有孔虫氧同位素记录在末次冰期异常偏重,可能与天然气水合物的分解释放有关;同时可识别出多期碳同位素快速负偏事件,其成因很可能是末次冰期海平面下降导致海底沉积物的温度、压力条件发生变化,从而引发水合物甲烷失稳分解,底栖有孔虫吸收富12C的甲烷源碳致使壳体碳同位素负偏移.     

高有机质输入对底栖有孔虫的抑制作用——以西北太平洋菲律宾海MD06-3054孔为例

底栖有孔虫古生产力指标-底栖有孔虫堆积速率(Benthic Foraminifera Accumulation Rate,简称BFAR)和小泡虫超科的Uvigerina与Bulimina两属在种群中的百分含量(简称"U+B含量")是目前古海洋学研究的常用方法.然而,从MD06-3054孔的记录中发现,两指标与有机质输入之间不仅不存在很好的线性关系.而且当有机质输入大于阀值时,两指标均随沉积物中总有机碳(Total Organic Carbon,简称TOC)含量的增加而明显地降低,说明过高有机质的输入还会抑制底栖有孔虫的生长和繁盛.另外,还发现当TOC含量较高时,U+B含量指标较BFAR指标相对更适用.     

南海西部浮游有孔虫含量与水深关系定量研究

南海西部4°～18°N,1085～115°E海域表层沉积物中有孔虫定量分析表明,从陆架至深海盆区,随着水深增加,底栖有孔虫丰度总体呈下降趋势;而浮游有孔虫在上陆坡区水深200～2 000 m处最丰富,向浅水和深水方向,其丰度均下降,浮游有孔虫百分含量（P）与水深（D）有明显的相关关系。但在陆架区和陆坡－深海盆区,两者关系完全不同：在陆架区随水深增加浮游有孔虫百分含量明显增大,而在陆坡－深海盆区,两者呈负相关关系。经定量拟合水深小于200 m的陆架区,浮游有孔虫含量与水深满足关系式：lnD＝0.021P＋3.208;而在水深大于200 m的陆坡－深海盆区,两者满足D＝－5263P＋52 105.2。这主要是由于陆架区随水深增加,浮游有孔虫增加,但水深大于200 m后,碳酸盐的溶解起主要作用,浮游有孔虫比底栖有孔虫更易于溶解,造成其含量随水深增加而下降。     

南海北部崖19-1-1井晚第三纪有孔虫动物群演替与古水深变化

依据现代海洋中有孔虫动物群的分布与环境之间的关系 ,即在一定限度内有孔虫动物群的丰度和分异度随水深增加而增加 ,有孔虫动物群的组合面貌随之发生规律性变化 ,对南海北部琼东南盆地崖 1 9-1 -1井晚第三纪有孔虫动物群进行了定量研究。通过对有孔虫动物群的丰度、分异度、辛普松指数、信息函数熵、多变度、优势度、浮游有孔虫百分含量及底栖有孔虫内生种与外生种的比值逐样计算和统计 ,讨论了陆架海区有孔虫动物群的演替与古水深变化的关系。研究认为崖 1 9-1 -1井晚第三纪以来古水深变化的总趋势为逐渐增大 ,至上新世早中期出现外浅海至半深海环境 ,为古水深最大时期 ,随后水深则逐渐减小。     

Species diversity variations in Neogene deep-sea benthic foraminifera at ODP Hole 730A,western Arabian Sea

Deep-sea benthic foraminifera are an important and widely used marine proxy to understand paleoceanographic and paleoclimatic changes on regional and global scales, owing to their sensitivity to oceanic and climatic turnovers. Some species of benthic foraminifera are sensitive to changes in water mass properties whereas others are sensitive to organic fluxes and deep-sea oxygenation. Benthic faunal diversity has been found closely linked to food web, bottom water oxygen levels, and substrate and water mass stability. The present study is aimed at analyzing species diversity trends in benthic foraminifera and their linkages with Indian monsoon variability during the Neogene. Species diversity of benthic foraminifera is examined in terms of number of species (S), information function (H), equitability (E) and Sanders’ rarefied values, which were combined with relative abundances of high and low productivity benthic foraminifera at Ocean Drilling Program Hole 730A, Oman margin, western Arabian Sea. The Oman margin offers the best opportunity to understand monsoon-driven changes in benthic diversity since summer monsoon winds have greater impact on the study area. The species diversity was higher during the early Miocene Climatic Optimum (～17.2–16.4 Ma) followed by a decrease during 16.4–13 Ma coinciding with a major increase in Antarctic ice volume and increased formation of Antarctic Bottom Water. All the diversity parameters show an increase during 13–11.6 Ma, a gradual decrease during 11.6–9 Ma and then an increase with a maximum at 7 Ma. Thereafter the values show little change until 1.2 Ma when all the parameters abruptly decrease. The benthic foraminiferal populations and diversity at Hole 730A were mainly driven by the Indian monsoon, and polar waters might have played a minor or no role since early Neogene period as the Arabian Sea is an enclosed basin.     

东西特提斯晚白垩世深水底栖有孔虫生物相和岩相

白垩纪深水古海洋学研究仍处于早期发展阶段,一方面是由于来自钙质底栖有孔虫的稳定同位素和地球化学数据的缺乏,其原因在于白垩纪高碳酸盐补偿深度;另一方面在于深水有机质胶结有孔虫示踪古海洋还没有充分发展起来。深海环境深水胶结有孔虫的分布主要取决于碳酸盐可利用状况、原始生产的输入通量、深水交换、环境波动(深海洋流、浊流和快速沉积事件)和底层沉积类型,因此对于重建深海环境具有非常巨大的潜力。东、西特提斯Campanian Maastrichtian深水底栖有孔虫组合的统计分析揭示出6个生物相,代表着明显不同的沉积环境。包括:深海红色泥岩与矮小深海生物组合(生物相1);红色深海泥灰岩(“Couches Rouges”相),含钙质胶结有孔虫组合(生物相3);深水远洋灰岩(“Scaglia Rossa”相),含易碎的Rhizammina组合(生物相2);绿色灰色半远洋泥灰岩,含适应高输出通量生物组合(生物相4);半远洋泥岩和粉砂岩,含Aschemocella Nothia 组合(生物相5);陆源浊积层序,含“复理石型”Rhabdammina组合(生物相6)。Campanian Maastrichtian红色氧化深水环境动物组合与现今深海类似,而白垩纪贫氧深海环境胶结组合在现今无法找到相类似物。随着古生态信息的增加和数据库的扩展,深水胶结有孔虫有望成为揭示古海洋条件的重要工具,尤?     

Paleoceanographic changes of surface and deep water based on oxygen and carbon isotope records during the last 130 kyr identified in MD179 cores,off Joetsu,Japan Sea

We reconstructed the paleoenvironmental history of surface and deep water over the last 130 kyr from oxygen and carbon isotope ratios of planktonic and benthic foraminifera in two cores (MD179-3312 and MD179-3304) from the Joetsu Basin, eastern margin of the Japan Sea. Our data showed that paleoceanographic changes such as influx of surface currents and vertical circulation were associated with global glacial–interglacial sea level change. Surface water conditions were influenced by the influx of Tsushima Current, East China Sea coastal or off-shore waters through the Tsushima Strait during interglacial or interstadial stages, and strongly affected by freshwater input during the glacial maximum. During interglacial maximums such as Marine Isotope Stages 1 and 5e, development of well-oxygenated bottom water was indicated. A density-stratified ocean with weak ventilation was inferred from the isotopic records of benthic foraminifera during the Last Glacial Maximum. Local negative excursions in carbon isotopes during deglacial or interglacial periods may suggest the dissolution of gas hydrates or methane seep activities.     

Rapid climatic shifts of the northern Norwegian Sea during the last deglaciation and the Holocene

High resolution cores from the upper continental slope, northern Norwegian Sea, document rapid climatic fluctuations during the latest deglaciation and the Holocene. Based on down-core analysis of planktic and benthic foraminifera, stable oxygen and carbon isotopes, carbonate and organic carbon and radiocarbon dating, the following evolution is proposed: sea-ice cover broke up, the surface ocean warmed and an in situ benthic foraminiferal fauna was established at 12 500 BP. The Younger Dryas was characterized by reduced sedimentaion and foraminiferal production, due to surface ocean cooling. At the end of the Younger Dryas there were major shifts in both surface and bottom water conditions. The surface ocean warmed to temperatures similar to modern levels within < 100 years, reaching a maximum at about 9200 BP when foraminiferal production was high. A benthic foraminiferal assemblage indicative of bottom water conditions similar to present conditions was established at 10 000 BP. This was followed by a gradual decline in nutrients or an increase in ventilation of the bottom water throughout the Holocene. A gradual surface ocean cooling of c . 2°C ended around 6500 BP followed by a second warming that culminated at 2000 BP. The warming at the end of the Younger Dryas and the succeeding older Holocene temperature maximum correlate to a June insolation maximum in the northern hemisphere. In addition, fluctuating surface temperatures in the Holocene may be driven by variations in inflow of Atlantic Water.     

Pleistocene oceanographie changes indicated by deep sea benthic foraminifera in the northern Indian Ocean

An attempt has been made to understand the Pleistocene bottom water history in response to the paleoclimatic changes in the northern Indian Ocean employing quantitative analyses of deep sea benthic foraminifera at the DSDP sites 219 and 238. Among the 150 benthic foraminifera recorded a few species show dominance with changing percent frequencies during most of the sequence. The dominant benthic foraminiferal assemblages suggest that most of the Pleistocene bottom waters at site 219 and Early Pleistocene bottom waters at site 238 are of North Indian Deep Water (NIDW) origin. However, Late Pleistocene assemblage at site 238 appears to be closely associated with a water mass intermediate between North Indian Deep Water (NIDW) and Antarctic Bottom Water (AABW). Uvigerina proboscidea is the most dominant benthic foraminiferal species present during the Pleistocene at both the sites. A marked increase in the relative abundance ofU. proboscidea along with less diverse and equitable fauna during Early Pleistocene suggests a relative cooling, an intensified oceanic circulation and upwelling of nutrient rich bottom waters resulting in high surface productivity. At the same time, low sediment accumulation rate during Early Pleistocene reveals increased winnowing of the sediments possibly due to more corrosive and cold bottom waters. The Late Pleistocene in general, is marked by relatively warm and stable bottom waters as reflected by low abundance ofU. proboscidea and more diverse and equitable benthic fauna. The lower depth range for the occurrence ofBulimina aculeate in the Indian Ocean is around 2300 m, similar to that of many other areas.B. aculeata also shows marked increase in its abundance near the Pliocene/Pleistocene boundary while a sudden decrease in the relative abundance ofStilostomella lepidula occurs close to the Early/Late Pleistocene boundary.     

Palaeoenvironmental turnover across the Palaeocene/Eocene boundary at the Stratotype section in Dababiya (Egypt) based on benthic foraminifera

The Global Stratotype Section and Point for the Palaeocene/Eocene (P/E) boundary was defined at Dababiya Quarry (Egypt) at the base of the carbon isotope excursion (CIE). We present the first detailed analysis of Palaeocene–Eocene benthic foraminifera from Dababiya, in order to infer the palaeoenvironmental turnover across the P/E boundary. At Dababiya, the CIE coincides with a major turnover in foraminiferal assemblages; the last occurrence of Angulogavelinella avnimelechi, at the base of the CIE, may be correlated to the main phase of extinction of deep-sea benthic foraminifera. Benthic foraminifera indicate that stressful conditions such as oxygen deficiency, carbonate dissolution, and changes in food supply, persisted at the sea floor over most of the CIE interval. The main phase of recovery of benthic foraminifera is recorded c. 250 cm above the P/E boundary, and it may be linked to increased productivity and oxygenation at the sea floor.     

Calculating surface water PCO2 from foraminiferal organic δC

The δ¹³C of organic matter bound within the crystal lattice of foraminiferal calcite tests may provide a potential tracer of the isotopic composition of the surface water primary photosynthate. Using δ¹³C of the organic matter extracted from the crystal lattice and the calcite test, it is theoretically possible to estimate the paleo-surface water pCO₂. We have tailored this technique initially for the subpolar planktonic foraminifera species Globigerina bulloides. Initial surface water pCO₂ estimates from deep-sea core BOFS 5K (50°41.3′N, 21°51.9′W, water depth 3547 m) indicate that the northeast Atlantic Ocean may have been a greater sink for CO₂ during the last glacial than during the Holocene. Greatly reduced benthic foraminifera abundances, especially phytodetritus feeders, in BOFS 5K during the last glacial indicates low surface productivity. This rules out a productivity-driven CO₂ sink. The enhanced glacial CO₂ sink must, therefore, have results from a southwards shift of the centre of deep water formation.     

Late Pleistocene paleo-oceanography of the Norwegian-Greenland Sea: Benthic foraminiferal evidence

Fluctuations in benthic foraminiferal faunas over the last 130,000 yr in four piston cores from the Norwegian Sea are correlated with the standard worldwide oxygen-isotope stratigraphy. One species, Cibicides wuellerstorfi, dominates in the Holocene section of each core, but alternates downcore with Oridorsalis tener, a species dominant today only in the deepest part of the basin. O. tener is the most abundant species throughout the entire basin during periods of particularly cold climate when the Norwegian Sea presumably was ice covered year round and surface productivity lowered. Portions of isotope Stages 6, 3, and 2 are barren of benthic foraminifera; this is probably due to lowered benthic productivity, perhaps combined with dilution by ice-rafted sediment; there is no evidence that the Norwegian Sea became azoic. The Holocene and Substage 5e (the last interglacial) are similar faunally. This similarity, combined with other evidence, supports the presumption that the Norwegian Sea was a source of dense overflows into the North Atlantic during Substage 5e as it is today. Oxygen-isotope analyses of benthic foraminifera indicate that Norwegian Sea bottom waters warmer than they are today from Substage 5d to Stage 2, with the possible exception of Substage 5a. These data show that the glacial Norwegian Sea was not a sink for dense surface water, as it is now, and thus it was not a source of deep-water overflows. The benthic foraminiferal populations of the deep Norwegian Sea seem at least as responsive to near-surface conditions, such as sea-ice cover, as they are to fluctuations in the hydrography of the deep water. Benthic foraminiferal evidence from the Norwegian Sea is insufficient in itself to establish whether or not the basin was a source of overflows into the North Atlantic at any time between the Substage 5e/5d boundary at 115,000 yr B.P. and the Holocene.     

The transition from the Younger Dryas to the Preboreal: a case study from the Kattegat, Scandinavia

A two-step climatic warming and oceanographic change during the Younger Dryas/Preboreal transition was registered by diatom, foraminiferal, mollusc, lithologic data and sediment accumulation rates in a high resolution sediment core from the Swedish west coast. An abrupt climatic warming in the surface water of the Kattegat occurred at c . 10 200 BP, resulting in a rapid increase in sea surface water temperatures. The attenuation of meltwater discharge into the Kattegat led to an increase in sea surface salinity. Consequently, the difference in salinity through the water column diminished. This change happened within less than 80 years. The warming of bottom water in the deeper parts of the region took place a few hundred years after the surface water warming. The climatic amelioration was recorded by increased meltwater discharge and a slight increase in abundance of relatively warm diatoms around 10 600 BP at the time of the recession of the Fennoscandian ice sheet. An increase in the number of arctic/subarctic benthic foraminifera shows that the bottom water temperature during this period was still relatively low.