Five test runs were performed to assess possible bias when performing the loss on ignition (LOI) method to estimate organic matter and carbonate content of lake sediments. An accurate and stable weight loss was achieved after 2 h of burning pure CaCO3 at 950 °C, whereas LOI of pure graphite at 530 °C showed a direct relation to sample size and exposure time, with only 40-70% of the possible weight loss reached after 2 h of exposure and smaller samples losing weight faster than larger ones. Experiments with a standardised lake sediment revealed a strong initial weight loss at 550 °C, but samples continued to lose weight at a slow rate at exposure of up to 64 h, which was likely the effect of loss of volatile salts, structural water of clay minerals or metal oxides, or of inorganic carbon after the initial burning of organic matter. A further test-run revealed that at 550 °C samples in the centre of the furnace lost more weight than marginal samples. At 950 °C this pattern was still apparent but the differences became negligible. Again, LOI was dependent on sample size. An analytical LOI quality control experiment including ten different laboratories was carried out using each laboratory's own LOI procedure as well as a standardised LOI procedure to analyse three different sediments. The range of LOI values between laboratories measured at 550 °C was generally larger when each laboratory used its own method than when using the standard method. This was similar for 950 °C, although the range of values tended to be smaller. The within-laboratory range of LOI measurements for a given sediment was generally small. Comparisons of the results of the individual and the standardised method suggest that there is a laboratory-specific pattern in the results, probably due to differences in laboratory equipment and/or handling that could not be eliminated by standardising the LOI procedure. Factors such as sample size, exposure time, position of samples in the furnace and the laboratory measuring affected LOI results, with LOI at 550 °C being more susceptible to these factors than LOI at 950 °C. We, therefore, recommend analysts to be consistent in the LOI method used in relation to the ignition temperatures, exposure times, and the sample size and to include information on these three parameters when referring to the method.

/pdf/loss-on-ignition-as-a-method-for-estimating-organic-and-6sj1elmojb.pdf

Loss on ignition as a method for estimating organic and carbonate content in sediments: reproducibility and comparability of results.

http://www.highstand.org/erohling/Rohling-papers/2004-Mayewski%20et%20al%20Holocene%20climate%20variability%20QR62.pdf

Holocene climate variability

Several explanations for the 200 to 280 ppm glacial/interglacial change in atmospheric CO2 concentrations deal with variations in southern ocean phytoplankton productivity and the related use or nonuse of major plant nutrients. An hypothesis is presented herein in which arguments are made that new productivity in today's southern ocean (7.4 × 1013g yr−1) is limited by iron deficiency, and hence the phytoplankton are unable to take advantage of the excess surface nitrate/phosphate that, if used, could result in total southern ocean new production of 2−3 × 1015 g C yr−1. As a consequence of Fe-limited new productivity, Holocene interglacial CO2 levels (preindustrial) are as high as they were during the last interglacial (≈ 280 ppm). In contrast, atmospheric dust Fe supplies were 50 times higher during the last glacial maximum (LGM). Because of this Fe enrichment, phytoplankton growth may have been greatly enhanced, larger amounts of upwelled nutrients may have been used, and the resulting stimulation of new productivity may have contributed to the LGM drawdown of atmospheric CO2 to levels of less than 200 ppm. Background information and arguments in support of this hypothesis are presented.

glacial-interglacial Co2 change : the iron hypothesis

Hydrological changes in the African tropics since the Last Glacial Maximum

1. Introduction.- 2. Taxonomy and Species Features.- 2.1 Introduction.- 2.2 Species List.- 2.2.1 Spinose Planktonic Foraminifera.- 2.2.2 Non-spinose Planktonic Foraminifera.- 3. Collecting and Culture Methods.- 3.1 Introduction.- 3.2 Collection for Ecological Studies.- 3.3 Fixation and Storing of Samples.- 3.4 Laboratory Preparations.- 3.5 Collection for Physiological and Ecological Studies.- 3.5.1 Net Collection.- 3.5.2 SCUBA Collection.- 3.6 Isolation and Preparation for Maintenance Culture.- 3.7 Maintenance Cultures.- 3.8 Monitoring Vitality and Growth of the Cultures.- 3.9 Feeding Techniques.- 3.9.1 Algal Prey.- 3.9.2 Animal Prey.- 3.10 Cataloguing and Storing Shells.- 3.11 Summary.- 4. Cellular Ultrastructure.- 4.1 Introduction.- 4.2 Fixation of Planktonic Foraminifera for Fine Structure Analysis.- 4.3 Cytoplasmic Streaming.- 4.4 Peripheral Cytoplasm and Rhizopodial Morphology.- 4.4.1 Cytoskeletal Structures.- 4.4.2 Filaments.- 4.5 Fine Structure of Cytoplasmic Organelles.- 4.5.1 Nucleus.- 4.5.2 Mitochondria.- 4.5.3 Peroxisomes.- 4.5.4 Endoplasmic Reticulum, Golgi Complex, and Vacuolar System.- 4.5.5 Fibrillar Bodies.- 4.5.6 Lipids and Various Cytoplasmic Inclusions.- 4.6 Comparative Fine Structure Data of Benthic and Planktonic Species.- 4.7 Comparative Fine Structure of Planktonic Foraminifera and Radiolaria.- 4.8 Summary.- 5. Host and Symbiont Relationships.- 5.1 Introduction.- 5.2 Symbiosis, Commensalism and Parasitism.- 5.3 Symbiont Morphology and Structural Association with Host.- 5.3.1 Dinoflagellate Symbiont Fine Structure.- 5.3.2 Chrysophycophyte Symbiont Fine Structure.- 5.4 Symbiont and Host Physiological Interactions.- 5.5 Origin of Symbionts.- 5.6 Major Features of Algal Symbionts.- 5.7 Summary.- 6. Trophic Activity and Nutrition.- 6.1 Introduction.- 6.2 Natural Prey.- 6.3 Laboratory Studies of Trophic Activity.- 6.3.1 Prey Acceptance and Rate of Digestion.- 6.3.2 Cannibalism.- 6.3.3 Fine Structure Studies of Prey Capture and Digestion.- 6.3.4 Trophic Activity and Longevity.- 6.3.5 Laboratory Studies of Omnivorous Feeding.- 6.4 Prey Abundance and Foraminiferal Distribution.- 6.5 Predators on Planktonic Foraminifera.- 6.6 Comparative Data with Benthic Foraminifera and Radiolaria.- 6.7 Summary.- 7. Reproduction.- 7.1 Introduction.- 7.2 Gametogenesis.- 7.2.1 Light Microscopic Data.- 7.2.2 Fine Structure Data.- 7.3 Morphological Changes during Gametogenesis.- 7.4 Reproductive Cycles.- 7.5 Comparisons with Benthic Foraminifera and Radiolaria.- 7.6 Summary.- 8. Shell Ontogeny.- 8.1 Introduction.- 8.2 Ontogenetic Concept for Spinose Species.- 8.2.1 Five Stage Concept.- 8.2.2 Ontogeny of Globigerinoides sacculifer.- 8.3 Variations in Developmental Morphology of Spinose Species.- 8.4 Variations in Developmental Morphology of Non-spinose Species.- 8.5 Quantitative Ontogeny.- 8.6 Coiling Directions.- 8.7 Taxonomic Applications.- 8.8 Summary.- 9. Shell Architecture.- 9.1 Introduction.- 9.2 Chamber Deposition and Pore Formation.- 9.2.1 Chamber Formation in Non-spinose Species.- 9.2.2 Pore Formation and Wall Thickening.- 9.2.3 Keel Development.- 9.2.4 Pustule Formation.- 9.3 Chamber Formation in Spinose Species.- 9.3.1 Spine Types.- 9.4 Wall Thickening and Gametogenic Calcification.- 9.5 Physiological Mechanism and Rates of Calcification.- 9.6 Organic Composition of the Calcitic Wall.- 9.7 Resorption and Repair Processes.- 9.8 Abnormal Shell Growth.- 9.9 Summary.- 10. Ecology.- 10.1 Introduction.- 10.2 Statistical Treatment and the Transfer Function.- 10.3 Stable Isotopes.- 10.4 Distributional Pattern of Planktonic Foraminifera.- 10.4.1 Horizontal Distribution.- 10.4.2 Seasonal Distribution.- 10.4.3 Vertical Distribution.- 10.4.4 Patchiness and Daily Vertical Migration.- 10.4.5 General Sea Surface Temperature in the Past.- 10.5 Population Dynamics.- 10.5.1 Reproductive Strategies.- 10.5.1.1 Lunar Periodicity.- 10.5.1.2 Annual Periodicity.- 10.5.2 Water Mass Boundary Effects.- 10.6 Experimental Studies.- 10.7 Summary.- 11. Sedimentation - Settlement of Shells.- 11.1 Introduction.- 11.2 Shells Released by Reproduction and Juvenile Mortality.- 11.3 Aggregates - Sedimentation.- 11.4 Predation.- 11.5 Residence Time and Sinking Velocity.- 11.6 Seasonal Fluctuations in the Settlement.- 11.7 Dissolution in the Deep Water.- 11.8 Summary.- 12. Concluding Remarks.- 12.1 Effects Influencing the Isotopic Signal.- 12.1.1 Temperature Effect.- 12.1.2 GlacialEffect.- 12.1.3 Water Mass Effect.- 12.1.4 VitalEffect.- 12.1.5 Selective Production.- 12.1.6 Differential Dissolution.- 12.2 Carbon Isotopes.- 12.3 Summative Perspective.- 13. References.- 14. Glossary.- 15. Index.

Modern Planktonic Foraminifera

Calibration of the alkenone paleotemperature index U37K′ based on core-tops from the eastern South Atlantic and the global ocean (60°N-60°S)

An automated leaching method for the analysis of biogenic silica (opal) in sediments and particulate matter is described. The opaline material is extracted with 1 M NaOH at 85°C in a stainless steel vessel under constant stirring, and the increase in dissolved silica is continuously monitored. For this purpose, a minor portion of the leaching solution is cycled to an autoanalyzer and analyzed for dissolved silicon by molybdate-blue spectrophotometry. The resulting absorbance versus time plot is then evaluated according to the extrapolation procedure of DeMaster (1981).

The method has been tested on sponge spicules, radiolarian tests. Recent and Pliocene diatomaceous ooze samples, clay minerals and quartz, artificial sediment mixtures, and on various plankton, sediment trap and sediment samples. The results show that the relevant forms of biogenic opal in Quaternary sediments are quantitatively recovered. The time required for an analysis is dependent on the sample type, ranging from 10 to 20 min for plankton and sediment trap material and up to 40–60 min for Quaternary sediments. The silica co-extracted from silicate minerals is largely compensated for by the applied extrapolation technique. The remaining degree of uncertainty is on the order of 0.4 wt% SiO2 or less, depending on the clay mineral composition and content.

An automated leaching method for the determination of opal in sediments and particulate matter

Evidence for abrupt climate changes on millennial and shorter timescales is widespread in marine and terrestrial climate records1,2,3,4. Rapid reorganization of ocean circulation is considered to exert some control over these changes5, as are shifts in the concentrations of atmospheric greenhouse gases6. The response of the climate system to these two influences is fundamentally different: slowing of thermohaline overturn in the North Atlantic Ocean is expected to decrease northward heat transport by the ocean and to induce warming of the tropical Atlantic7,8, whereas atmospheric greenhouse forcing should cause roughly synchronous global temperature changes9. So these two mechanisms of climate change should be distinguishable by the timing of surface-water temperature variations relative to changes in deep-water circulation. Here we present a high-temporal-resolution record of sea surface temperatures from the western tropical North Atlantic Ocean which spans the past 29,000 years, derived from measurements of temperature-sensitive alkenone unsaturation in sedimentary organic matter. We find significant warming is documented for Heinrich event H1 (16,900–15,400 calendar years bp) and the Younger Dryas event (12,900–11,600 cal. yr bp), which were periods of intense cooling in the northern North Atlantic. Temperature changes in the tropical and high-latitude North Atlantic are out of phase, suggesting that the thermohaline circulation was the important trigger for these rapid climate changes.

Warming of the tropical Atlantic Ocean and slowdown of thermohaline circulation during the last deglaciation

Paleosalinity and terrigenous sediment input changes reconstructed on two sediment cores from the northernmost Red Sea were used to infer hydrological changes at the southern margin of the Mediterranean climate zone during the Holocene. Between approximately 9.25 and 7.25 thousand years ago, about 3 per thousand reduced surface water salinities and enhanced fluvial sediment input suggest substantially higher rainfall and freshwater runoff, which thereafter decreased to modern values. The northern Red Sea humid interval is best explained by enhancement and southward extension of rainfall from Mediterranean sources, possibly involving strengthened early-Holocene Arctic Oscillation patterns and a regional monsoon-type circulation induced by increased land-sea temperature contrasts. We conclude that Afro-Asian monsoonal rains did not cross the subtropical desert zone during the early to mid-Holocene.

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Mediterranean Moisture Source for an Early-Holocene Humid Period in the Northern Red Sea

THE oxygen isotope (δ18O) composition of foraminiferal tests from deep-sea sediments is widely used as a palaeoclimate proxy, but it includes contributions from sea surface temperature, global ice volume and local salinity, which are difficult to separate. Recently a new technique for deriving palaeotemperatures has been developed which is based on the abundance ratios of unsaturated alkenones in phytoplankton algae1,2. Here we use a combination of oxygen isotope and alkenone records in a deep-sea core from the juncture of the Arabian Sea and the Bay of Bengal to extract the salinity signal from the former record. Variations in salinity are related to the balance between evaporation and precipitation3, and are thus a sensitive indicator of climate change. Our 170-kyr salinity record enables us to reconstruct changes in the Indian monsoon over this period, considerably extending earlier studies (which reached back to 18 kyr ago)4–8. Like these previous studies, we find that large variations in the monsoon occurred during the transition from the last glacial period to the present interglacial, but our results also provide a view of the monsoon throughout the last glacial and demonstrate the potential of this approach for reconstructing palaeosalinity.

Peter J Müller

Papers

Calibration of the alkenone paleotemperature index U37K′ based on core-tops from the eastern South Atlantic and the global ocean (60°N-60°S)

An automated leaching method for the determination of opal in sediments and particulate matter

Warming of the tropical Atlantic Ocean and slowdown of thermohaline circulation during the last deglaciation

Mediterranean Moisture Source for an Early-Holocene Humid Period in the Northern Red Sea

Reconstructing sea surface temperature and salinity using δ 18 O and alkenone records