Evidence for initial calcite-aragonite composition of Lower Algal Chert Member ooids and stromatolites, Paleoproterozoic Gunflint Formation, Ontario, Canada

2000 ◽  
Vol 37 (9) ◽  
pp. 1229-1243 ◽  
Author(s):  
M G Sommers ◽  
S M Awramik ◽  
K S Woo

The chert members of the Paleoproterozoic Gunflint Formation, Ontario, Canada, are commonly regarded as examples of primary silica chemical sediments. This interpretation is founded upon the ubiquitous nature of silica, high fidelity of preservation of microfossils found within, and lack of observed primary carbonate. Previous arguments for silica replacement of carbonate are based on indirect evidence and are largely dismissed. Thus, Gunflint microfossils are regarded as having lived in a silica-rich environment, which makes them unusual compared to most other pre-Phanerozoic microfossils that are known from silicified carbonates. We present evidence that carbonate was a primary mineral species of the Lower Algal Chert Member (where most of the microbiota are found). Most compelling are iron-stained, low-Mg calcite ooids containing (1) well-preserved growth laminae, (2) textures indicating a disrupted tangential fabric of growth laminae, and (3) quartz crosscutting the growth laminae. These indicate the initial mineral was a carbonate, possibly aragonite. Less-compelling evidence is found in stromatolite columns. Specularite crystals in low-Mg calcite display crosscutting relationships with calcite and quartz indicating that calcite was primary, specularite secondary, and quartz tertiary. The crosscutting relations show that silicification took place in at least two stages. One of the silicification events took place very early in diagenesis. Thus the Gunflint microbiota may not have existed in a radically different environment (silica precipitating) than those of most other known Proterozoic microbiota. High fidelity of preservation of microfossils does not always indicate that the mineral entombing them was the primary mineral precipitated from aqueous solution.

2008 ◽  
Vol 72 (5) ◽  
pp. 1083-1101 ◽  
Author(s):  
W. H. Paar ◽  
Y. Moëlo ◽  
N. N. Mozgova ◽  
N. I. Organova ◽  
C. J. Stanley ◽  
...  

AbstractCoiraite, ideally (Pb,Sn2+)12.5As3Fe2+Sn4+S28, occurs as an economically important tin ore in the large Ag-Sn-Zn polymetallic Pirquitas deposit, Jujuy Province, NW-Argentina. The new mineral species is the As derivative of franckeite and belongs to the cylindrite group of complex Pb sulphosalts with incommensurate composite-layered structures. It is a primary mineral, frequently found in colloform textures, and formed from hydrothermal solutions at low temperature. Associated minerals are franckeite, cylindrite, pyrite-marcasite, as well as minor amounts of hocartite, Ag-rich rhodostannite. arsenopyrite and galena. Laminae of coiraite consist of extremely thin bent platy crystals up to 50 urn long. Electron microprobe analysis (n = 31) gave an empirical formula Pb11.21As2.99Ag0.13Fe1.10Sn6.13S28.0 close to the ideal formula (Pb11.3Sn2+1.2)Σ=12.5As3Fe2+Sn4+S28. Coiraite has two monoclinic sub-cells, Q (pseudotetragonal) and H (pseudohexagonal). Q: a 5.84(1) Å, b 5.86(1) Å, c 17.32(1) Å, β 94.14(1)°, F 590.05(3) Å3, Z = 4, a:b:c = 0.997:1:2.955; H (orthogonal setting): a 6.28(1) Å, b 3.66(1) Å, c 17.33(1) Å, β 91.46(1)°, V398.01(6) Å3, Z = 2, a∶b∶c = 1.716∶1∶4.735. The strongest Debye-Scherrer camera X-ray powder-diffraction lines [d in Å, (I), (hkl)] are: 5.78, (20), (Q and H 003); 4.34, (40), (Q 004); 3.46, (30), (Q and H 005); 3.339, (20), (Q 104); 2.876, (100), (Q and H 006); 2.068, (60), (Q 220).


1979 ◽  
Vol 16 (3) ◽  
pp. 421-439 ◽  
Author(s):  
B. J. Fryer ◽  
R. Kerrich ◽  
R. W. Hutchinson ◽  
M. G. Peirce ◽  
D. S. Rogers

The Porcupine District, Abitibi Greenstone Belt is one of the most extensive areas of Archaean auriferous mineralization. At least two stages of lode gold emplacement may be recognized. The first involves gold-bearing ferroan dolomite layers with subordinate chert, sulphides, and graphite deposited as laterally extensive chemical sediments at interflow horizons within the mafic volcanic sequence. The second stage is represented by major gold-bearing hydrothermal quartz–albite–dravite veins which transect diverse host rocks including the carbonate chemical sediments. Differences between gold-bearing chemical sediment and auriferous hydrothermal veins, in terms of texture, mineralogy, and nature of inclusions, together with considerations of chemistry are not compatible with local derivation of veins from enveloping chemical sediments or adjacent host rocks. The chemical sediments display slump structures and predate all tectonic deformation. In general, auriferous hydrothermal quartz veins transect bedding and/or schistosity, and are at a low state of internal strain. They appear to have been emplaced late during the second regional fold episode.Au, Ag, and Pd average 10, 2, and 0.1 ppm respectively in ore types at the Dome mine; representing concentration factors of 10 000,40, and 10 times background values in unmineralized metabasalt, and primary igneous rocks worldwide. Au and Ag are inhomogeneously distributed.Mineralized metabasic rocks adjacent to vein stockworks have Ti/Zr and Ti/Al2O3 ratios comparable to tholeiitic basalts, but display variable enrichment or depletion of silica, systematic depletion in Na2O, and where intensely altered significant extraction of calcium. The low Ni and Cr contents of the carbonate layers, together with low Ti/Zr ratios (43–78) of the carbonates and their enveloping mafic schists, are not consistent with the hypothesis that these auriferous rocks are carbonated ultramafics. Massive banded quartz–fuchsite–dravite veins have Cr and Ni abundances averaging 350 ppm, implying hydrothermal transport of these elements. Ti/Zr ratios of 120, together with high Mg, Cr, and Ni abundances in magnesite–dolomite–quartz– chlorite schists which host the banded veins are compatible with a primary komatiitic composition. Mineralized metabasic rocks are reduced (Fe2+/ΣFe = 0.9) relative to rocks with primary background abundances of precious metals (Fe2+/ΣFe = 0.7). This change of oxidation state implies that large volumes of reducing hydrothermal solutions were involved in vein mineralization.


Author(s):  
Igor Yanovich

The chapter traces two stages of the rise of the may-under-hope construction of Late Modern English, present in examples like (i) Dearest, I hope we may be on such terms twenty years hence. Despite the archaic feel to it, this construction is in fact a very recent innovation that arose not earlier than the sixteenth century. I conjecture that its elevated flavor does not stem from its old age, but rather was inherited from another construction, with the inflectional subjunctive under hope. Along the way, I also present evidence that the textual absence of may under verbs of hoping before the rise of this construction was not due to narrow compositional semantics.


Porphyrins have been shown to be stronger bases than previously supposed, two protons being added in two stages to the nitrogen atoms in the conjugated tetrapyrrolic ring as the pH of an aqueous solution is decreased from pH 12 to 0. The existence of mono-cations of certain porphyrins in aqueous solution with characteristic visible and ultra-violet absorption spectra has been established, p K' a values for the two more basic ring nitrogen atoms of coproporphyrin I, deuteroporphyrin IX dimethyl ester disulphonic acid, N -methyl coproporphyrin I free acid and its tetramethyl ester have been determined by spectrophotometric titration in various buffer systems. Information on the basicity of uroporphyrin I and mesoporphyrin IX is also included. N -Methyl coproporphyrin has been prepared. The relationship of these p K' a values to the thermodynamic dissociation constants is discussed. Comparison of the p K' values obtained has led to certain conclusions regarding the effect on its basicity of some substituents of the tetrapyrrolic ring, and possible structures for the free bases and cations are considered in the light of these findings.


2002 ◽  
Vol 20 (5) ◽  
pp. 441-452 ◽  
Author(s):  
Joanna Kapica ◽  
Robert Pełech ◽  
Jacek Przepiórski ◽  
Antoni W. Morawski

The kinetics of the adsorption of Cu2+ and Pb2+ ions from aqueous solution on to WD-ekstra activated carbon was studied by batch methods. Such adsorption processes proceeded in two stages: an initial rapid stage followed by a slower one. The Bangham equation was used to describe the kinetics of both adsorption processes. Measurements were carried out for solutions containing only one type of metal ion and also for binary systems containing both Cu2+ and Pb2+ ions. A considerable influence of Pb2+ ions on the adsorption of Cu2+ ions was observed in the binary system. It was found that the equilibrium isotherms could be analyzed using the Langmuir, Freundlich–Langmuir and Freundlich methods.


1991 ◽  
Vol 277 (1) ◽  
pp. 213-221 ◽  
Author(s):  
M D Skudlarek ◽  
M C Orgebin-Crist ◽  
D R P Tulsiani

Previous studies from this laboratory using p-nitrophenyl alpha-D-mannoside (p-NPM) as substrate provided no evidence for the presence of mannosidase II in the rat epididymis [Skudlarek & Orgebin-Crist (1988) J. Reprod. Fertil. 84, 611-617]. However, rat epididymal epithelial cells cultured in the presence of swainsonine, an inhibitor of mannosidase II, produce abnormally processed N-linked glycoproteins containing hybrid-type oligosaccharides instead of complex-type [Tulsiani, Skudlarek & Orgebin-Crist (1990) Biol. Reprod. 43, 130-138], a result providing indirect evidence for the presence of mannosidase II-like enzyme in rat epididymis. In the studies described here, we present evidence for the occurrence of this processing enzyme in rat epididymal Golgi membranes. This enzyme is an integral Golgi membrane component. Like liver mannosidase II, the epididymal enzyme cleaves alpha 1,3- and alpha 1,6-linked mannosyl residues from GlcNAcMan5GlcNAc. However, unlike liver mannosidase II, the epididymal enzyme shows no activity towards the synthetic substrate, p-NPM. The epididymal mannosidase cross-reacts with liver anti-(mannosidase II) antibody, a result suggesting that the two enzymes share a common antigenic site(s). Immunoblotting studies following resolution of liver and epididymal Golgi membranes on SDS/PAGE show that, whereas the liver mannosidase II was resolved as a doublet of Mr 120,000 and 122,000, only the Mr 120,000 band was observed in the epididymal Golgi membranes. Immunoblotting of the Golgi-rich fractions, resolved under non-denaturing conditions, showed different patterns of charge and/or size isomers from the two tissues. These studies demonstrate tissue-specific differences in processing enzymes with similar function.


HortScience ◽  
2006 ◽  
Vol 41 (4) ◽  
pp. 1017B-1017
Author(s):  
Jiwon Jeong ◽  
James Lee ◽  
Donald J. Huber

This study was performed to characterize the physiological responses of tomato (Lycopersicon esculentum L.) fruit harvested at either 10% to 30% or 30% to 60% color change and treated with two forms of 1-methylcyclopropene (1-MCP). Tomato fruit were treated either by submersion for 1 min in 1-MCP aqueous solution at the ambient temperature or by exposure for 12 h at 20 °C in air with 1-MCP gas, then stored at 20 °C. The concentrations (1.0, 5.0, or 10.0 μL·L-1) in 1-MCP aqueous solution were achieved through addition of 0.5, 2.5, or 5.0 g of AFxRD-300 powder (2.0% formulation, Agro-Fresh, Inc.) to 10 L of the de-ionized water, following manufacturer's instructions. 1-MCP (0.5 μL·L-1) gas in a 174-L container was achieved through addition of 0.22 g of SmartFresh® powder (0.14% formulation, Agro-Fresh, Inc.) to 100 mL of tap water. Both forms of 1-MCP significantly delayed ripening of fruit at the two initial ripeness stages, as noted by a significant delay in fruit softening and peel color change. The firmness of 30% to 60% color change tomatoes was significantly retained in response to gaseous or aqueous 1-MCP. Control fruit softened rapidly and reached the minimum marketable firmness value (about 5 N) within 8 days of storage at 20 °C, whereas fruit treated with gaseous 1-MCP (0.5 μL·L-1) or aqueous 1-MCP (1.0 or 5.0 μL·L-1) reached the same stage after 16, 20, or 24 days, respectively. Firmness retention was also highly significant for 10% to 30% color change tomatoes treated with both forms of 1-MCP. The highest concentration of aqueous 1-MCP (10.0 μL·L-1) did not result in a further delay in ripening compared with treatment at 5.0 or 1.0 μL·L-1 1-MCP.


1952 ◽  
Vol 140 (898) ◽  
pp. 143-144

Porphyrins have been shown to be stronger bases than previously supposed, two protons being added in two stages to the nitrogen atom s in the conjugated tetrapyrrolic ring as the pH of an aqueous solution is decreased from pH 12 to 0. The existence of mono-cations of certain porphyrins in aqueous solution with characteristic visible and ultra-violet absorption spectra has been established, p K ' a values for the two more basic ring nitrogen atoms of coproporphyrin I, deuteroporphyrin IX dimethyl ester disulphonic acid, N -methyl coproporphyrin I free acid and its tetram ethyl ester have been determ ined by spectrophotom etric titratio n in various buffer systems. Inform ation on the basicity of uroporphyrin I and mesoporphyrin IX is also included. N -Methyl coproporphyrin has been prepared. The relationship of these p K ' a values to the therm odynamic dissociation constants is discussed. Comparison of the p K ' values obtained has led to certain conclusions regarding the effect on its basicity of some substituents of the tetrapyrrolic ring, and possible structures for the free bases and cations are considered in the light of these findings.


In a preliminary paper one of us, in conjunction with Prof. Heilbron and Prof. Barker, described some observations on the action of ultra-violet light on pure aqueous solutions of carbonic acid. It was found that traces of formaldehyde were present in these solutions after insolation, provided that a stream of the gas were passed through the water during the exposure to the light. These results differed from those which had previously been recorded by Moore and Webster, who had stated that the presence of a catalyst such as colloidal ferric or uranium hydroxide was necessary. The observation by Moore and Webster that formaldehyde in aqueous solution is converted by ultra-violet light into reducing sugars was fully confirmed, and the view was put forward that the mechanism of the photosynthesis of carbohydrates from carbonic acid consisted of two stages, first, the formation of formaldehyde, and, second, the conversion of this substance into hexoses.


2020 ◽  
Author(s):  
Raphaël Laurenceau ◽  
Nicolas Raho ◽  
Zev Cariani ◽  
Christina Bliem ◽  
Mohammed A. M. Osman ◽  
...  

ABSTRACTLanthipeptides are a family of ribosomally synthesized, post-translationally modified peptides that are widespread among bacteria, typically functioning as antibacterials. The marine picocyanobacteria Prochlorococcus and Synechococcus produce an unusual and diverse set of lanthipeptides of unknown function called prochlorosins. While well-studied model bacteria produce one or two different molecules of this type, a single picocyanobacterium can produce as many as 80; the community of picocyanobacteria in a single milliliter of seawater can collectively encode up to 10,000 prochlorosins. The molecular events that led to this expansion and diversification of the lanthipeptide repertoire in picocyanobacteria – the numerically dominant photosynthesizers in the oceans – is unknown.We present evidence for an unusual association between prochlorosin genes with a single-stranded DNA transposase belonging to the TnpAREP family. The genes co-occur and co-localize across the phylogeny of marine picocyanobacteria forming a distinct association pattern within genomes, most likely resulting from the transposase activity. Given the role of TnpAREP homologs in other bacteria, we propose - based on genomic structures - that they contribute to the creation of the prochlorosin structural diversity through a diversifying recombination mechanism.IMPORTANCEOnly a few mechanisms have been described that promote the diversification of a targeted gene region in bacteria. We present indirect evidence that the TnpAREP transposases associated with prochlorosins in picocyanobacteria could represent a novel such mechanism, and explain the extreme expansion and diversification of prochlorosins in this abundant marine microbe.


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