Primary and diagenetic microstructures in trilobites

McAllister, John E. & Brand, Uwe 1989 01 15: Primary and diagenetic microstructures in trilobites. Lethaia , Vol. 22, pp. 101–111. Oslo. ISSN 0024–1164.
Ordovician and Devonian trilobites were studied by scanning electron microscopy (SEM) to define primary and diagenetic microstructures. Primary structures such as Osmólska cavities and hexagonal surface openings are present in samples obtained from both shale and limestone lenses in shales. Generally, samples with primary microstructures are also geochemically well preserved. Diagenetic microstructures were found in samples from shales and limestones, but those from limestones are the most geochemically and microstructurally altered. 'Dendritic' patterns and fused matrices were found in the altered cuticles of trilobites of different species and ages and are therefore considered a normal feature of the diagenetic alteration of cuticular calcite. Primary and diagenetic microstructures of trilobite cuticles are independent of size, species and age of the specimens, but are largely controlled by lithology and thus diagenesis. * Trilobita, primary-, diagenetic microstructures, fossil diagenesis .     

Induced Protein Synthesis during the Adaptation to H2 Production in Chlamydomonas moewusii

Gas production by Chlamydomonas moewusii in the light has been followed by manometric techniques during the adaptation to anaerobiosis. The only detectable gases produced are CO₂ and H₂ CO₂ is produced at a rather constant rate whereas H₂ evolution increase with time. This increase of H₂ evolution during the adaptation period can be inhibited by cycloheximide and by chloral hydrate, two inhibitors of protein synthesis. If the inhibitors are added to already adapted cells there is no effect on H₂ evolution. Adapted cell suspensions are sensitive to oxygen. Incubation under O₂ for 10 min inhibits the H₂ evolution to 100%. After removal of oxygen the capability to evolve H₂ can be restored only by a new adaptation period. This second adaptation to H₂ evolution can also be inhibited by cycloheximide.     

Vipera pontica sp.n., a new viper species in the kaznakovi group (Reptilia, Viperidae) from northeastern Turkey and adjacent Transcaucasia

Vipera pontica sp.n. from northeastern Turkey and Transcaucasia is a member of the Vipera kaznakovi group characterized by partial fragmentation of frontal and parietals, sharp canthus rostralis, and a colour pattern on the head of the Vipera dinnicki type. It differs from all vipers in the Near and Middle East in having an upturned but hornless snout, and in a number of scalation and colour pattern characters. It is most similar to the west European V. aspis, but differs in having a yellow green tail tip, more loreals and fewer subcaudals. The affinities to the latter species as well as to V. barani are discussed.     

An electrophoretic and morphological study of three Ecdyonurus species (Ephemeroptera: Heptageniidae) occurring in the British Isles

Abstract The objective was to investigate the validity of three closely-related British species: Ecdyonurus dispar, E. venosus and E. torrentis . The species were characterized by eleven enzyme-substrates and fifteen different enzyme-loci, comparisons being made not only between species but also between five populations of E.dispar (three from Britain, one from France, one from Switzerland), two populations of E.venosus and two populations of E. torrentis (one from Britain, one from Switzerland for both species).
Four monomorph enzyme-loci (aldolase, mannose phosphate isomerase, arginine phosphokinase, glutamate-oxaloacetate transaminase-2) exhibited interspecific differences in their mobilities and therefore validated the conclusion that E. dispar, E. venosus and E. torrentis are distinct species. There were no monomorph enzyme-loci that were different between populations of the same species. There were, however, some intraspecific differences revealed by the presence of polymorphic enzyme-loci: seven in E.dispar (retinol dehydrogenase, hexokinase-1 and 2, glutamate-oxaloacetate transaminase-!, malate dehydrogenase-1, phospho-glucomutase, indophenol oxidase-2), three in E. venosus (glutamate-oxaloacetate transaminase-1, malate dehydrogenase-1, phospho-glucomutase) and three in E. torrentis (hexokinase-1, glutamate-oxaloacetate transaminase-1, malate dehydrogenase-1).
The morphological characters of larvae and adults were examined and some were used in new keys to larvae and adults.     

Increased Blood Levels of Human S100 in Melanoma Chick Embryo Xenografts’ Circulation

The chorioallantoic membrane (CAM) of the fertilized egg allows grafting of human melanomas for short‐term investigations and offers the opportunity to investigate the behavior of metastasizing cells and the release of S100β into peripheral blood. Tissue from one primary melanoma as well as cutaneous and subcutaneous metastases of 10 melanoma patients with elevated levels of S100 in the peripheral blood before surgery were transplanted onto the CAM of chick embryos at day 5/6 of development. Grafts were nourished by the host blood supply 2 days after transplantation. Histologically, 3 days after grafting, metastasizing melanoma cells could be found near the vessels of the host membrane, penetrating the endothelial layer and entering the blood system. Growth conditions remained stable for 6 days after transplantation. Blood samples were taken from a larger CAM vessel before collecting the xenografts 5 days after grafting. Measurement of human S100 in peripheral blood was performed in a blinded manner. No negative control showed elevated levels of human S100 protein. Samples deriving from melanoma xenografts contained highly elevated levels of S100 protein in 80% of cases. The data strongly support the concept of graft–host interaction concerning adherence of tumors and extravasation of human melanoma cells.     

Linking geochemical processes with microbial community analysis: successional dynamics in an arsenic-rich, acid-sulphate-chloride geothermal spring

The source waters of acid‐sulphate‐chloride (ASC) geothermal springs located in Norris Geyser Basin, Yellowstone National Park contain several reduced chemical species, including H₂, H₂S, As(III), and Fe(II), which may serve as electron donors driving chemolithotrophic metabolism. Microorganisms thriving in these environments must also cope with high temperatures, low pH (～3), and high concentrations of sulphide, As(III), and boron. The goal of the current study was to correlate the temporal and spatial distribution of bacterial and archaeal populations with changes in temperature and geochemical energy gradients occurring throughout a newly formed (redirected) outflow channel of an ASC spring. A suite of complimentary analyses including aqueous geochemistry, microscopy, solid phase identification, and 16S rDNA sequence distribution were used to correlate the appearance of specific microbial populations with biogeochemical processes mediating S, Fe, and As cycling and subsequent biomineralization of As(V)‐rich hydrous ferric oxide (HFO) mats. Rapid As(III) oxidation (maximum first order rate constants ranged from 4 to 5 min^?1, t_1/2 = 0.17 ? 0.14 min) was correlated with the appearance of Hydrogenobaculum and Thiomonas–like populations, whereas the biogenesis of As(V)‐rich HFO microbial mats (mole ratios of As:Fe ～0.7) was correlated with the appearance of Metallosphaera, Acidimicrobium, and Thiomonas–like populations. Several 16S sequences detected near the source were closely related to sequences of chemolithotrophic hyperthermophilic populations including Stygiolobus and Hydrogenobaculum organisms that are known H₂ oxidizers. The use of H₂, reduced S(–II,0), Fe(II) and perhaps As(III) by different organisms represented throughout the outflow channel was supported by thermodynamic calculations, confirming highly exergonic redox couples with these electron donors. Results from this work demonstrated that chemical energy gradients play an important role in establishing distinct community structure as a function of distance from geothermal spring discharge.     

Protein Targeting into Secondary Plastids1

ABSTRACT. Most of the coding capacity of primary plastids is reserved for expressing some central components of the photosynthesis machinery and the translation apparatus. Thus, for the bulk of biochemical and cell biological reactions performed within the primary plastids, many nucleus‐encoded components have to be transported posttranslationally into the organelle. The same is true for plastids surrounded by more than two membranes, where additional cellular compartments have to be supplied with nucleus‐encoded proteins, leading to a corresponding increase in complexity of topogenic signals, transport and sorting machineries. In this review, we summarize recent progress in elucidating protein transport across up to five plastid membranes in plastids evolved in secondary endosymbiosis. Current data indicate that the mechanisms for protein transport across multiple membranes have evolved by altering pre‐existing ones to new requirements in secondary plastids.