“单特异性”和接近单特异性的底栖有孔虫动物群,新西兰

Pub Date : 2014-07-01 DOI:10.2113/GSJFR.44.3.300
B. Hayward
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引用次数: 18

摘要

在新西兰,13种底栖有孔虫在现代“单特异性”动物群中占主导地位(在>63 μm样品中,一个物种的死亡动物群占>80%)。这些动物群出现在隐蔽的,通常是半咸淡水,潮间带或浅潮下环境中,深度不超过25米。没有发生在裸露的海岸或开阔的海洋。在不同盐度和海拔范围的盐沼中,7种凝集种(黑毛芽孢菌、褐毛芽孢菌、马尼拉芽孢菌、褐毛芽孢菌、斜斑芽孢菌、膨胀芽孢菌、salsa芽孢菌)在“单种”动物群中占主导地位。除马尼拉猿人外,其他所有猿人都至少有一种动物群的99% - 100%被记录。6种(Ammobaculites exiguus, Ammotium aoteana, Ammotium fragile, Elphidium excavatum clavatum, E. williamsoni, E. gunteri)在无植被的潮间带和浅滩潮下(Amb.)占主导地位。据推测,残存的动物群是由钙质成分溶解而产生的。另有17种主宰着现代近单种的动物群(一个物种的50-80%),11种在深海。在新西兰北部,6种主宰着早中新世的“单种”动物群:在隐蔽的砾石沙滩上的Elphidium crispum;Nonionella novozealandica在深水(50-100米),可能缺氧的港口;以及三种更大、更健壮的物种(奥克兰Amphistegina aucklandica、orakilepidocyclina、Miogypsina intermedia),生长在水流或波浪集中的海滩或浅海沉积物中。唯一的深海或深海“单种”动物群以出现在化石烃渗漏环境中的Amphimorphinella butonensis为主。许多现代的“单一”动物群(特别是那些在盐沼中的)是世界性的,而大多数化石和一些现代动物群是新西兰地区特有的。这些高优势动物群是由地学和生态过程产生的。地学原因包括在高能量、浅海环境中,波浪或水流因过滤或运输而集中,以及在低pH值、微咸、盐沼或深海环境中碳酸盐溶解。生态驱动因素包括高度特定的适应,使物种能够在压力(潮间带)、强变化(涨潮微咸)或不寻常(碳氢化合物渗漏)的环境中胜过所有其他物种。有时,机会性物种的高测试生产力可能导致接近单一的动物群。
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“MONOSPECIFIC” AND NEAR-MONOSPECIFIC BENTHIC FORAMINIFERAL FAUNAS, NEW ZEALAND
Thirteen benthic foraminiferal species dominate modern “monospecific” faunas (dead faunas with >80% of one species in >63-μm samples) in New Zealand. These faunas occur in sheltered, often brackish, intertidal or shallow-subtidal environments, never deeper than 25 m. None occurs along exposed coasts or in the open ocean. Seven agglutinated species ( Entzia macrescens , Haplophragmoides wilberti , H. manilaensis , Miliammina fusca , M. obliqua , Trochammina inflata , Trochamminita salsa ) dominate “monospecific” faunas in salt marshes with varying salinity and elevational ranges. All but H. manilaensis have been recorded comprising 99–100% of at least one fauna. A further six species ( Ammobaculites exiguus , Ammonia aoteana , Ammotium fragile , Elphidium excavatum clavatum , E. williamsoni , E. gunteri ) dominate “monospecific” faunas in unvegetated intertidal and shallow-subtidal ( Amb. exiguus faunas are inferred to have been produced by dissolution of calcareous components. A further 17 species dominate modern near-monospecific faunas (50–80% of one species), 11 at depths Six species dominate “monospecific” early Miocene faunas in northern New Zealand: Elphidium crispum in a sheltered gravel beach; Nonionella novozealandica in a deep-water (50–100 m), possibly dysoxic harbour; and three larger, more robust species ( Amphistegina aucklandica, Lepidocyclina orakiensis, Miogypsina intermedia ) in current- or wave-concentrated beach or shallow-marine deposits. The only bathyal or abyssal “monospecific” fauna is dominated by Amphimorphinella butonensis occurring in a fossil hydrocarbon seep setting. Many of the modern “monospecific” faunas (especially those in salt marshes) are cosmopolitan, whilst most of the fossil and some of the modern faunas are endemic to the New Zealand region. These high-dominance faunas are produced by taphonomic and ecological processes. Taphonomic causes include wave or current concentration by winnowing or transport in high energy, shallow-marine environments and carbonate dissolution in low pH, brackish, salt marsh or deep-sea settings. Ecological drivers include highly specific adaptations that allow species to outcompete all others in stressful (intertidal), strongly variable (high-tidal brackish), or unusual (hydrocarbon seep) environments. Sometimes high test productivity of opportunistic species may result in near-monospecific faunas.
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