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Plankton chemical composition

The unique chemical composition of cosmogenous debris has provided some insight into why approximately 70% of the species of organisms on Earth were driven extinct over a relatively short time interval approximately 66 million years ago. Evidence for this mass extinction has been observed in marine sediments throughout all the ocean basins. In a contemporaneous layer deposited at the end of the Cretaceous period, the hard parts of many species of marine plankton abruptly vanished from the sedimentary record. This sedimentary layer is also characterized by a large enrichment in the rare element iridium. [Pg.342]

In some sediments, downcore variations in the bulk chemical composition are interpretable as records of temporal shifts in the elemental composition of the sinking POM. Such shifts are caused by changes in the production of sinking POM, which are in turn the result of fluctuations in the abundance and diversity of the overlying plankton community. In nearshore sediments, fluctuations in river runoff and lateral transport can lead to shifts in the supply rate of terrigenous organic matter. An example of a nearshore sediment core in which such fluctuations have been recorded is shown in Figure 23.18. [Pg.649]

The chemical composition of the organic matter derived from lake plankton typically is considerably higher in proteins and fats than that derived from terrestrial vegetation. [Pg.49]

Table II. Average Chemical Composition of Plankton, Detritus Settled at the 11-Meter level, and Surface Bottom Sediments, in lake Lauzon,... Table II. Average Chemical Composition of Plankton, Detritus Settled at the 11-Meter level, and Surface Bottom Sediments, in lake Lauzon,...
The process of removal of calcium by marine organisms in the water column is well known. Production of calcium carbonate by water column biological processes may be estimated from primary productivity and from the mean chemical composition of plankton. After death of the organisms and removal of the organic protective layer, the skeletons may undergo dissolution if they encounter water undersaturated with respect to their mineral composition. Active dissolution of calcium carbonate occurs mainly near the sediment-water interface in deep waters that are undersaturated with respect to both calcite and aragonite (see Chapter 4). Thus, calcium is regenerated from calcareous skeletons and, finally, only a small fraction of the initial production of these materials accumulates in sediments. An... [Pg.500]

If the chemical composition of the samples is known or at least partly known (in a stepwise TIE approach) or existing data allow for QSAR calculation, the samples can be ranked by TUs. Arts et al. (2006) studied, in 12 outdoor ditch mesocosms, the effects of sequential contamination with 5 pesticides in a regression design. They applied dosages equivalent with 0.2%, 1%, and 5% of the predicted environmental concentration (PEC) subsequently over 17 weeks. Endpoints recorded over 30 weeks included community composition of macroinvertebrates, plankton, and macrophytes, and leaf litter decomposition as functional ecosystem parameters. TUs were calculated in relation to acute toxicity data for the most sensitive standard species Daphnia magna and Lemna minor. Principal response curves (PRCs), a special form of constrained PCA, and Williams test (NOEC, class 2 LOEC) were used to identify the most sensitive taxa. Next to direct effects on certain species, also indirect effects, for example, how the change in abundance of a sensitive species affects the abundance of another, more tolerant species, can be detected only in mesocosm or in situ experiments. All observed effects were summarized in effect classes in a descriptive manner. [Pg.152]

The bulk chemical composition of seawater DOM (Table 8.8), however, is not consistent with a predominant riverine origin. In particular, seawater DOM is depleted in C and enriched in C and compared with most DOM discharged by rivers (with the Amazon being taken here as an example). Seawater DOM is also depleted in aromatic carbon (as measured by C NMR) and lignin phenol structural units (as determined by CuO oxidation), possibly as a consequence both of the low phenol content of marine plankton, and of selective alteration of aromatic carbon by photodegradation. Thus all evidence to date, including elevated total concentrations in surface marine waters (Fig. 8.19), indicates that seawater DOM is largely... [Pg.296]

Several studies support the idea that the chemical composition of biogenic carbonate is modified by partial dissolution under the infiuence of bottom waters or porewaters that are undersaturated with respect to calcium carbonate (e.g. Rosenthal et al. 2000). In a study of planktonic foraminifera conducted by Brown Elderfield (1996), artificial partial dissolution of G. tumida tests resulted in a decrease in both Mg/Ca and Sr/Ca, but there was no significant change for G. sacculifer. The cause of this reduction is thought to be preferential dissolution of high-Mg inner (chamber) calcite, which forms in warmer waters than the low-Mg calcite crust (keel). In theory, it should be possible to correct for such effects if the extent of dissolution can be quantified. A number of dissolution indicators, including foraminiferal test weights (e.g. Broecker Clark 2001) and calcite crystallinity (Bassinot et al. 2004), have been tested, but none have been widely applied to date. [Pg.21]

Harris, E., and Riley, G. A. (1956). Oceanography of Long Island Sound, 1952-1954. VIII. Chemical composition of the plankton. Bull. Bingham Oceanogr. Collect. 15,315-323. [Pg.346]

Other roles for noxious metabolites produced by certain phytoplankton species include mediation of allelopathic interactions [47]. Allelopathy covers biochemical interactions among different primary producers or between primary producers and microorganisms. These can provide an advantage for the producer in the competition among different photoautotrophs for resources. Although not directly involved in chemical defense, allelopathic metabolites can affect the dominance and succession of species in phytoplankton therefore they are crucial for understanding plankton composition. In contrast to the fresh water environment, the location of many studies on the role of allelopathic interactions, which have identified active compounds [47], only few studies have addressed this topic in the marine environment. [Pg.190]

King, K., and Hare, P. E. Amino acid composition of planktonic foraminifera A paleobio-chemical approach to evolution. Science 175, 1461—1463 (1972). [Pg.97]


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