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Considering the complexity of the<br />

EMED, we validate the use of Sr/Ca ratios<br />

as productivity proxy and unravel<br />

the varied processes which may influence<br />

it. We examined the relationship<br />

between the seasonal peaks in export<br />

fluxes and the Sr/Ca ratio in coccoliths<br />

of three upper photic zone coccolithophores<br />

species collected in the traps,<br />

Calcidiscus leptoporus, Helicosphaera<br />

carteri and Emiliania huxleyi. We aimed<br />

at testing whether high export fluxes are<br />

correlated with high Sr/Ca ratios, suggestive<br />

of higher nutrient-stimulated<br />

production, or Sr/Ca ratios are unchanged<br />

during high export periods,<br />

suggestive of increased export efficiency<br />

or scavenging. Periods of enhanced trap<br />

fluxes in March and June result from<br />

surface water blooms recognized in satellite<br />

imagery. An additional peak flux<br />

was found in January, but this peak<br />

represents re-suspended or recycled material<br />

in the water column.<br />

The amplitude of seasonal variations<br />

in the Sr/Ca ratios of the three investigated<br />

species is small in both traps. In<br />

the shallow trap, a decrease in the Sr/Ca<br />

ratio of C. leptoporus occurred synchronously<br />

with minimal fluxes. The other<br />

two species were not measured for this<br />

period. In the deep trap, no such decrease<br />

in Sr/Ca was observed during<br />

minimal fluxes, in either C. leptoporus<br />

or H. carteri, probably due to a long<br />

residence of coccoliths in the water column,<br />

recycling and low export efficiency.<br />

Absolute Sr/Ca ratios for all species<br />

are lower than in other more productive<br />

environments like the Bay of<br />

Bengal, Arabian Sea, or Sargasso Sea.<br />

We conclude that Sr/Ca ratios in coccoliths<br />

of surface sediments in the EMED<br />

reflect mainly spring–summer bloom<br />

conditions averaged over hundreds to<br />

thousands of years.<br />

In addition, the origin of varying calcite<br />

thickness in H. carteri was investigated.<br />

The similarity of average Sr/Ca<br />

ratios in differently-calcified specimens<br />

confirms that coccolith thickness variations<br />

in this species result from primary<br />

biomineralization processes and not<br />

from variable overgrowth by (low Sr)<br />

abiogenic calcite in the water column or<br />

the sediments.<br />

2010010103<br />

横 贯 阿 尔 泰 山 戈 壁 沙 漠 ( 蒙 古 ) 晚 古<br />

新 世 轮 藻 = Charophytes from the Upper<br />

Paleocene of the Trans-Altai Gobi<br />

Desert (Mongolia). ( 英 文 ). Gereltsetseg<br />

L. Paleontological Journal, 2009, 43(6):<br />

699-701 1 图 版 .<br />

Charophyte assemblage is described<br />

from the Naran Member of the Tsagaan<br />

sair section (Upper Paleocene). A new<br />

species, Mesochara cornuta, is described.<br />

2010010104<br />

西 伯 利 亚 二 叠 三 叠 纪 暗 色 玄 武 岩 地 层<br />

中 的 细 菌 化 石 = Fossil bacteria from<br />

the Permotriassic Trappean strata of Siberia.<br />

( 英 文 ). Astafieva M M; Rozanov<br />

A Yu; Sadovnikov G N; Sapova E V.<br />

Paleontological Journal, 2009, 43(8):<br />

896-904 6 图 版 .<br />

The strata of the Permotriassic Trappean<br />

Complex of Siberia (Ilimpeya<br />

River and Kapchan locality) are studied.<br />

The water-lava and water-tuff boundaries<br />

are shown to be promising for bacterial<br />

paleontological studies. The analysis<br />

of fossilized microbial communities<br />

shows that they vary depending on<br />

sedimentation conditions. This example<br />

is important for a better understanding<br />

of the prospects for the study of similar<br />

situations in the Archean and Proterozoic.<br />

2010010105<br />

卡 累 利 阿 太 古 代 的 细 菌 古 生 物 学 研 究<br />

= Bacterial Paleontological study of Archaean<br />

of Karelia. ( 英 文 ). Astafieva M<br />

M; Rozanov A Yu. Paleontological<br />

Journal, 2009, 43(8): 905-910 8 图 版 .<br />

39

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