In der vorliegenden Arbeit wurden die Einflüsse der landwirtschaftlichen Nutzung auf die Struktur und Biomasse von Nematoden entlang eines Tiefengradientens und innerhalb zweier Vegetationsperioden an einem Ackerstandort untersucht. Die Freilandanalyse der Nematodengemeinschaft wies auf ein mit Nährstoffen angereichertes und gestörtes Ökosystem, mit einer geringen Diversität, hin. Entlang des Tiefengradienten bildeten die Nematoden Metacommunities, welche Umweltgegebenheiten wie Nahrungsquellen und abiotischen Faktoren widerspiegeln. Signifikant höhere Biomassen wurden unter Weizen im Vergleich zu Mais als Ackerfrucht beobachtet. Die Streuapplikation induzierte einen „bottom-up“ Effekt mit größeren Biomassen in den niedrigen als in den höheren trophischen Stufen. Die Nematoden Biomassen sowie die faunistischen Indizes (Channel Index, Enrichment Index) zeigten, dass der Kohlenstofffluss im Bakterienkanal des Bodens dominierte. Allerdings deckte das 13C Pulse-Labelling Experiment im Feld auf, dass der Kohlenstofffluss durch die Pilzgemeinschaft sowie die pilzfressenden Nematoden wesentlich höhere Umsatzraten aufweist. In einem 14C-Laborexperiment wurde ein vollständiges Budget des Flusses von wurzelbürtigem Kohlenstoff in das Nahrungsnetz der Nematoden bestimmt. Hierbei wiesen die pflanzenparasitären Nematoden die höchsten 14C-Gehalte innerhalb weniger Tage auf, da sie direkt an den Wurzeln fressen und über die Herbivorenkette den Nährstoffzyklus im Boden eröffnen. / The present research considered the effects of agricultural management practice on the nematode community structure and biomass in three different depths and two successive vegetation periods at an arable field site. The resource quality was manipulated by crop plant and organic amendment, to investigate the major soil carbon pathways based on roots, bacteria and fungi. The nematode community analysis pointed to a highly enriched and disturbed ecosystem with low biodiversity. Along the depth gradient the nematodes formed distinct metacommunities, reflecting resource availability and abiotic environmental factors. Wheat supported significantly greater nematode biomass than maize. The litter amendment induced bottom-up effects, with greater biomass allocation at lower than at higher trophic levels. The biomass of nematode families as well as faunal indices (Channel Index, Enrichment Index) revealed a predominance of the bacterial carbon channel in the arable soil. A 13C pulse-labelling experiment investigating the flux of root- derived C into the soil food web revealed high turnover rates in the fungal carbon pathway. This was evident for soil fungi as well as for fungal-feeding nematodes and contradicts general assumptions of a more active bacterial pathway in arable soils. A laboratory experiment with 14C isotope was used to compile a complete budget for the root-derived carbon in the nematode food web. Here plant-feeding nematodes, which feed on living plant roots, thereby opening the root C cycling into the food web, showed highest amounts of 14C allocation within a few days.

第23回名古屋大学年代測定総合研究センターシンポジウム平成22(2010)年度報告

During photosynthesis Plantaginaceae species can produce glucose derivatives such as iridoid glycosides and alcohol sugars that in addition to sucrose can be exported from leaves. Plantago lanceolata transported sorbitol in addition to sucrose especially at warmer leaf temperatures. However, two iridoids, catalpol and aucubin, found in P. lanceolata were not readily labelled from 14CO2 under any conditions examined. In contrast, in two greenhouse, cut-flower cultivars of Antirrhinum majus the iridoids, antirrhinoside and antirrhide, were readily 14C-labelled along with sucrose but little 14C was recovered in alcohol sugars (e.g., mannitol). The amount of 14C-partitioned into antirrhinoside increased at higher temperatures. Exposing leaves of P. lanceolata and A. majus to reduced-photorespiratory conditions (e.g. short-term CO2 enrichment and/or low O2) increased fixation and export. Under low O2 in P. lanceolata sorbitol 14C-labelling increased relative to sucrose and in A. majus 14C-labelling of sucrose increased relative to antirrhinoside. Also 14C-labelling of antirrhide increased more than antirrhinoside. During both short-term and long-term acclimation to high CO2, whole plant NCER, leaf photosynthesis and export increased in A. majus. Taken together the temperature and CO2 enrichment studies show plasticity in Plantaginaceae species to synthesize and transport sucrose and auxiliary glucose esters and alcohol sugars in a species-specific manner (depending on the rate of carboxylation).

名古屋大学年代測定総合研究センターシンポジウム報告

名古屋大学年代測定総合研究センターシンポジウム報告

<p>The Pitted Ware Culture site Korsnäs in Södermanland, Sweden presents a, for the region, unique amount of preserved organic material suitable for chemical analyses. Human and faunal skeletal material has been subjected to stable isotope analysis with the aim of examining whether the diet of the Korsnäs people correlates with the seal-based subsistence of Pitted Ware Culture groups on the Baltic islands. Further, the relationship between the faunal assemblage and the human diet has been studied, and the debated question of whether the Pitted Ware people kept domestic pigs has been addressed. Ten new radiocarbon dates are presented, which place the excavated area of the site in Middle Neolithic A, with a continuity of several hundred years. The results show that the diet of the Korsnäs people was predominantly based on seal, and seal hunting was probably an essential part of the Pitted Ware Culture identity. Based on the dietary pattern of the species, it is argued that the pigs were not domestic. The faunal assemblage, dominated by seal and pig bones, does not correlate with the dietary pattern, and it is suggested that wild boar might have been hunted and sacrificed and/or ritually eaten on certain occasions.</p>

L'objectif de ce travail est l'étude des processus et des changements environnementaux récents (durant les derniers 30000 ans) à travers leurs enregistrement sédimentaire dans la zone Nord-Ouest de la Mer Noire (carottes sédimentaires prélevées à des profondeurs allant de 55 à 2100 m sous la tranche d'eau). Nous avons privilégié des méthodes permettant d'obtenir des informations sur le milieu de dépôt et la chronologie des évènements telles que : analyses des argiles, sédimentologie, magnétisme environnemental, caractéristiques isotopiques de la matière organique totale, 14C AMS. Afin d'obtenir une chronologie la plus fiable possible des évènements nous avons effectué des datations par le 14C de la matière organique et des coquilles fossiles du sédiment. La comparaison des datations obtenues sur les coquilles et la matière organique provenant d'un même niveau sédimentaire nous a montré que l'application des corrections sur les données 14C reste difficile ; cette difficulté provient du fait que le bassin a contenu tantôt de l'eau douce oxygénée, tantôt de l'eau stratifiée. C'est en associant les résultats de l'étude des taux des carbonates le long des carottes aux données 14C que nous avons établi l'échelle chronologique proposée. L'étude des minéraux argileux des sédiments nous a permis de conclure que pour le nord-ouest du bassin, l'origine des sédiments à smectite doit être recherchée au nord, et non au sud du bassin versant de la Mer Noire, comme il est admis dans la littérature. Les données de magnétisme environnemental nous ont permis de mettre en évidence des variations significatives dans les conditions d'oxygénation (aérobie/anaérobie) au sommet du sédiment ou dans la colonne d'eau. Ces données magnétiques, ainsi que celles de matière organique montrent aussi des modifications des conditions de salinité dans le bassin. En conclusion nous proposons une reconstitution des conditions d'environnement au cours des derniers 30000 ans.

La datation absolue des archives climatiques est essentielle pour comprendre les mécanismes du climat. Cette étude a porté sur la fraction fine (<63 μm) riche en aragonite (adaptée à la datation U/Th) et sur les tests de foraminifères planctoniques (>150 μm) d'une carotte de sédiments marins de la Mer des Caraïbes couvrant le dernier million d'années, en utilisant une approche minéralogique et des traceurs géochimiques. Les objectifs sont : 1) évaluer le<br />synchronisme entre le δ18O et les âges absolus de deux fractions de tailles différentes et 2) reconstruire les paléoenvironnements de la zone. La minéralogie de la fraction fine est contrôlée par les changements du niveau marin à l'échelle glaciaire-interglaciaire. Les décalages temporels entre le δ18O et le 14C des deux fractions durant la Terminaison I sont en partie expliqués par un modèle de bioturbation. Les essais de datation U/Th sur la fraction fine des Terminaisons II et V ont montré une contamination par du Th non-radiogénique, nécessitant des développements analytiques. Les reconstitutions des variations de δ18O de l'eau de mer suggèrent une diminution de la salinité de surface à la fin de la Transition Mid-Pléistocène, associée à la position de l'ITCZ au niveau de la Mer des Caraïbes.

<p>This thesis concerns the study of reaction mechanisms by means of kinetic isotope effects (KIEs). Studies of the nucleophilic bimolecular substitution (S_N2) reaction had the dual purpose of improving our fundamental understanding of molecular reactivity and assessing the ability of kinetic isotope effects to serve as mechanistic tools. The transition state of the S_N2 reaction between a cyanide ion and ethyl chloride in tetrahydrofuran was found to be reactant like and only slightly tighter than has been found previously for the same reaction in dimethyl sulphoxide. One conclusion was that the transition-state structure in this reaction was predicted fairly well by the theoretical calculations, even without solvent modelling. The S_N2 reactions between cyanide ions and <i>para</i>-substituted benzyl chlorides were found to have reactant-like transition states, of which the C_α-Cl bond was most influenced by the <i>para</i>-substitution. Theoretical calculations indicated that the chlorine KIEs could be used as probes of the substituent effect on the C_α-Cl bond if bond fission was not too advanced in the transition state. Furthermore, the nucleophile carbon ¹¹C/¹⁴C KIEs were determined for the reactions between cyanide ions and various ethyl substrates in dimethyl sulphoxide.</p><p>Precision conductometry was employed to estimate the aggregation status of tetrabutylammonium cyanide in tetrahydrofuran and in dimethyl sulphoxide, which is of interest as tetrabutylammonium cyanide is frequently used as the nucleophilic reagent in mechanistic investigations and synthetic reactions. The tendency for ion-pair formation was found to be very slight, significant, and very strong in dimethyl sulphoxide, water, and tetrahydrofuran, respectively. </p><p>The nitrogen kinetic isotope effect on monoamine oxidase B catalysed deamination of benzylamine was determined in an attempt to obtain conclusive evidence regarding the mechanism of the oxidation. Monoamine oxidase is an important drug target in connection with the treatment of, for example, depression and Parkinson’s disease, and knowledge on how the enzyme effects catalysis would facilitate the design of highly selective and efficient inhibitors.</p>

This thesis concerns the study of reaction mechanisms by means of kinetic isotope effects (KIEs). Studies of the nucleophilic bimolecular substitution (SN2) reaction had the dual purpose of improving our fundamental understanding of molecular reactivity and assessing the ability of kinetic isotope effects to serve as mechanistic tools. The transition state of the SN2 reaction between a cyanide ion and ethyl chloride in tetrahydrofuran was found to be reactant like and only slightly tighter than has been found previously for the same reaction in dimethyl sulphoxide. One conclusion was that the transition-state structure in this reaction was predicted fairly well by the theoretical calculations, even without solvent modelling. The SN2 reactions between cyanide ions and para-substituted benzyl chlorides were found to have reactant-like transition states, of which the Cα-Cl bond was most influenced by the para-substitution. Theoretical calculations indicated that the chlorine KIEs could be used as probes of the substituent effect on the Cα-Cl bond if bond fission was not too advanced in the transition state. Furthermore, the nucleophile carbon 11C/14C KIEs were determined for the reactions between cyanide ions and various ethyl substrates in dimethyl sulphoxide. Precision conductometry was employed to estimate the aggregation status of tetrabutylammonium cyanide in tetrahydrofuran and in dimethyl sulphoxide, which is of interest as tetrabutylammonium cyanide is frequently used as the nucleophilic reagent in mechanistic investigations and synthetic reactions. The tendency for ion-pair formation was found to be very slight, significant, and very strong in dimethyl sulphoxide, water, and tetrahydrofuran, respectively. The nitrogen kinetic isotope effect on monoamine oxidase B catalysed deamination of benzylamine was determined in an attempt to obtain conclusive evidence regarding the mechanism of the oxidation. Monoamine oxidase is an important drug target in connection with the treatment of, for example, depression and Parkinson’s disease, and knowledge on how the enzyme effects catalysis would facilitate the design of highly selective and efficient inhibitors.