Determining and improving the analytical blank for radiocarbon analyses of small foraminifera samples using MICADAS and the gas interface system

Author(s):  
Gesine Mollenhauer ◽  
Hendrik Grotheer ◽  
Elizabeth Bonk ◽  
Torben Gentz

<p>Foraminifera isolated from deep-sea sediments are among the most common materials in AMS radiocarbon analysis. These results are used to determine accurate age models for sediment sequences as well as to detect changes in deep-sea ventilation. Often, only small numbers of (monospecific) foraminifera shells can be isolated, in particular when studying benthic species in sediments from the polar regions. Therefore, these samples are often analyzed as CO<sub>2</sub> gas using MICADAS instruments, and the method can typically be used for samples of up to around 40 ka in age. For reliable results, an accurate determination and minimization of processing blanks is required.</p><p>Processing blanks for foraminifera samples may in part derive from acid hydrolysis of the carbonates. It has, however, been shown that contamination of the carbonate fossils, mainly from atmospheric CO<sub>2</sub> adsorbed on the porous surfaces of foraminifera, is the largest source of blank found in foraminifera samples. The removal of such contamination has been attempted by various leaching methods, which come at the risk of introducing additional contaminations. Alternatively, blank correction of AMS results may be achieved using fossil foraminifera from ancient deposits much beyond the range of the radiocarbon method.</p><p>Here we report results of a systematic test comparing the F<sup>14</sup>C levels obtained for fossil (>130 ka) and sub-modern monospecific planktic and benthic foraminifera samples using different blank correction approaches. Specifically, we compare leaching with dilute hydrochloric acid, blank correction relative to a leached and an un-leached fossil foraminifera standard, and blank correction relative to the IAEA-C1 certified carbonate standard. </p>

Zootaxa ◽  
2009 ◽  
Vol 2096 (1) ◽  
pp. 287-298 ◽  
Author(s):  
ELKE WILLEN ◽  
JANINE DITTMAR

A new species of the new genus Keraia gen. nov. from the Guinea Basin is described in the present paper. The new taxon belongs to the Pseudomesochrinae Willen, 1996, which until now has contained only the genus Pseudomesochra T. Scott, 1902. Both genera are prevalent in the deep sea. Whereas Pseudomesochra reaches quite high individual and species numbers in the investigated samples of the DIVA 1, DIVA 2 and ANDEEP deep-sea expeditions, Keraia is found only occasionally and as single specimens. Keraia is characterised among others by a modified antenna exopodite and the shape of P1. Pseudomesochra on the other hand can still be identified as a monophylum by specialised setation on the P1 endopodite and the lack of the inner setae of the first segment of swimming leg exopodites. Other species of Keraia gen. nov. are K. longiseta (Vasconcelos, George & Santos 2008) and the type species K. tamara (Smirnov, 1946). The available records implicate a widespread occurrence of Keraia gen. nov. from the northern to the southern Atlantic, and even reaching both northern and southern polar regions. Up to now all individuals that have been found occur exclusively at deep-sea sites and in very low abundances.


ChemBioChem ◽  
2018 ◽  
Vol 19 (6) ◽  
pp. 540-544 ◽  
Author(s):  
Christopher P. Lepper ◽  
Martin A. K. Williams ◽  
David Penny ◽  
Patrick J. B. Edwards ◽  
Geoffrey B. Jameson
Keyword(s):  
Deep Sea ◽  

1953 ◽  
Vol 6 (2) ◽  
pp. 156 ◽  
Author(s):  
JWT Merewether

Ethanol lignin-A from the ethanolysis of Eucalyptus regnans P. Muell. has been hydrolysed with dilute hydrochloric acid with the object of ascertaining whether the combined ethoxyl is present as an acetal or as ether. Hydrolysis with 12 per cent. hydrochloric acid was found to split off one ethoxyl group, while hydrolysis with 20 per cent. acid brought about complete de-ethylation. The de-ethylated ethanol lignin-A contained one carbonyl group less and two hydroxyl groups more than the original ethanol lignin-A. These results lend no support to the hypothesis that alcohol lignins are acetals, and favour the theory that the combined alkoxyl is probably present as ether.


Nature ◽  
1997 ◽  
Vol 385 (6617) ◽  
pp. 624-627 ◽  
Author(s):  
T. M. Cronin ◽  
M. E. Raymo

2006 ◽  
Vol 62 (4) ◽  
pp. o1490-o1491
Author(s):  
Xin-Biao Mao ◽  
Tie-Han Li ◽  
Chun-An Ma ◽  
Qing-Bao Song

The title compound, C5H4ClNO3S, was obtained by hydrolysis of 4-chloropyridine-3-sulfonamide in dilute hydrochloric acid. In the crystal structure, one-dimensional chains are formed via N—H...O hydrogen bonds. In addition, weak C—H...Cl hydrogen bonds link these chains into a two-dimensional network


Palaios ◽  
2020 ◽  
Vol 35 (10) ◽  
pp. 403-420
Author(s):  
TOBIAS B. GRUN ◽  
MORANA MIHALJEVIĆ ◽  
GREGORY E. WEBB

ABSTRACT The infaunal living clypeasteroid echinoid genus Echinocyamus is considered a model organism for various ecological and paleontological studies since its distribution ranges from the polar regions to the tropics, and from shallow-marine settings to the deep-sea. Deep-sea analyses of this genus are rare, but imperative for the understanding and function of these important ecosystems. During the 2012 Southern Surveyor expedition, 35 seamounts off the east coast of Australia were dredged in depths greater than 800 m. Of these, six dredges contained a total of 18 deep-sea Echinocyamus tests. The tests have been analyzed for taphonomic alterations including abrasion patterns, macro-borings, micro-borings, depressions on the test, test staining, test filling, encrustation, and fragmentation. Findings are interpreted in the context of the deep-sea setting and are compared to Echinocyamus samples from shallow-water environments. Results show that abrasion in deep-sea environments is generally high, especially in ambulacral and genital pores indicating that tests can persist for a long time on the seafloor. This contrasts with shallow-water Echinocyamus that show lower abrasion due to early test destruction. Macro-borings are present as single or paired holes with straight vertical profiles resembling Lithophaga borings. Micro-borings are abundant and most likely the result of sponge or fungal activity. Depressions on the tests, such as scars or pits, are likely the result of trauma or malformation during ontogeny. Test staining is common, but variable, and is associated with FE/Mn oxidation and authigenic clays based on elemental analyses. Test filling occurs as loose or lithified sediment. Encrustation is present in the form of rudimentary crusts and biofilms. No macro-organisms were found on the tests. Biofilm composition differs from shallow-water environments in that organisms captured in the biofilm reflect aphotic conditions or sedimentation of particles from higher in the water column (e.g., coccoliths). Fragmentation is restricted to the apical system and pore regions. Results of this first comparative study on deep-sea Echinocyamus from Australian seamounts show that the minute tests can survive for a long time in these settings and undergo environmental specific taphonomic processes reflected in various taphonomic alterations.


2014 ◽  
Vol 64 (Pt_1) ◽  
pp. 116-121 ◽  
Author(s):  
Yue-Hong Wu ◽  
Lin Xu ◽  
Fan-Xu Meng ◽  
Dong-Sheng Zhang ◽  
Chun-Sheng Wang ◽  
...  

A Gram-stain-negative, short rod-shaped bacterium, designated 26DY36T, was isolated from a deep-sea sediment sample collected from the North Atlantic Rise. The isolate required NaCl and grew best with 2 % (w/v) sea salts at a temperature of 30–35 °C and at pH 7.0. It formed yellow colonies, produced carotenoid-like pigments and did not produce bacteriochlorophyll a. Strain 26DY36T was positive for hydrolysis of aesculin, gelatin, tyrosine and Tweens 20, 40, 60 and 80, but negative for hydrolysis of casein, DNA and starch. The major respiratory quinone was ubiquinone-10. The major polar lipid profile consisted of sphingoglycolipid, diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylcholine and two unidentified glycolipids. The principal fatty acids (>5 %) were C18 : 1ω7c, C17 : 1ω6c, C15 : 0 2-OH and C16 : 0. The genomic DNA G+C content was 59.4 mol%. Phylogenetic analysis based on the 16S rRNA gene sequences indicated that strain 26DY36T should be assigned to the genus Altererythrobacter . 16S rRNA gene sequence similarities between the isolate and the type strains of species of the genus Altererythrobacter were in the range 92.7–96.5 %. On the basis of phenotypic and genotypic data, strain 26DY36T represents a novel species of the genus Altererythrobacter , for which the name Altererythrobacter atlanticus sp. nov. (type strain, 26DY36T = CGMCC 1.12411T = JCM 18865T) is proposed.


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