No description available.

A Molecular Approach to Assessing Meiofauna Diversity in Marine Sediments Heather C. Hamilton Abstract The purpose of this study was to determine if a molecular approach could be applied to calculating the diversity of meiofauna in marine sediments from two sites in Tampa Bay, FL, similar to the approach of McCaig et al, 1999 in calculating the diversity of microbes in pastureland soils. The approach includes extracting total DNA directly from the sediment and amplifying the 18S rRNA gene by PCR. Clone libraries from the 18S gene would be created for each site and 300 sequences from each clone library would be obtained. These sequences would then be phylogenetically analyzed and assigned to an OTU, from which diversity indices can be calculated. The phylogenetic analysis of the sequences from the two sites revealed that of the 102 OTUs assigned from the sequences, only 7 OTUs included sequences from both sites, while 93 OTUs contained sequences from one site or from the other. Thus the sites were phylogenetically different from each other. Shannon diversity indices calculated for each site showed a difference between the two sites and paralleled diversity indices for macrofauna data for each site collected by the Hillsborough County Environmental Protection Commission. Sequences from 30 OTUs were completely sequenced and identified by phylogenetic comparison with a metazoan reference alignment. A discrepancy between the sequence data and data collected from preserved samples taken at each site was evident upon analysis: roughly 60% of each preserved sample consisted of nematodes and 10% consisted of copepods, while roughly 30% of the identified OTUs consisted of copepods and 10% consisted of nematodes. This discrepancy could be explained if the OTUs that were not identified consisted of nematode sequences or if a primer bias were present in the PCR amplification such that the regions flanking the primer site in the nematode sequences inhibited primer annealing.

No description available.

Le jujubier (ou Ziziphus mauritiana Lam.) est une espèce à usages multiples (fruits, fourrage, bois de service) prioritaire pour le reboisement et l’arboriculture fruitière dans le Sahel. Dans ce contexte où les sols sont souvent dégradés et pauvres en minéraux (P en particulier), la mycorhization et la fertilisation phosphatée pourraient jouer un rôle important dans l’amélioration de la croissance et de la productivité des jujubiers.L’objectif principal de ce travail était d’améliorer la croissance et la production fruitière de Z. mauritiana par l’inoculation mycorhizienne dans deux vergers au Sénégal. Il avait pour objectifs spécifiques (i) d’évaluer les réponses à l’inoculation avec des CMAs de différentes espèces de Ziziphus et de provenances de Z. mauritiana en serre, (ii) d’évaluer l’impact de l’inoculation avec R. irregularis IR27 sur la croissance, la survie et la production fruitière de Z. mauritiana, (iii) d’évaluer l’impact de l’inoculation sur la diversité des communautés de CMAs associés à Z. mauritiana en plantation et (iv) de déterminer la persistance de R. irregularis IR27 dans les racines de Z. mauritiana en plantation. Le champignon R. irregularis IR27 s’est avéré le plus efficace parmi les CMAs testés dans ce travail. Le couple Z. mauritiana /R. irregularis IR27 a donc été choisi comme modèle pour étudier l’impact de l’inoculation sur la production fruitière de deux provenances, Gola (variété indienne sélectionnée pour ses fruits de grosse taille) et Tasset (provenance locale à fruits de petite taille) dans deux sites contrastés (Amally et Keur Mangari). Nos résultats ont montré un effet positif de l’inoculation sur la croissance, la survie et le taux de mycorhization de Z. mauritiana à 13 et 24 mois respectivement à Amally et à Keur Mangari. L’inoculation a également augmenté la production fruitière des jujubiers à 18 et 30 mois de plantation à Keur Mangari. Ces résultats montrent la grande capacité de R. irregularis IR27 à compétir face aux CMAs indigènes. Le séquençage Illumina MiSeq du gène 18S a permis de révéler un impact négatif de l’inoculation sur la diversité et la richesse des communautés de CMAs natifs à Amally contrairement à Keur Mangari où l’inoculation n’a pas eu d’impact ni sur la diversité ni sur la richesse des CMAs. Le gène RPB1 s’est révélé pertinent comme marqueur pour détecter R. irregularis IR27 dans les racines de Z. mauritiana inoculés et évaluer par qPCR l’intensité de la colonisation racinaire des jujubiers par R. irregularis IR27 qui a représenté 11 à 13% à 13 mois de plantation à Amally et 12 à 15% à 24 mois de plantation à Keur Mangari. Cependant, il s’avère important d’évaluer à plus long terme l’impact de R. irregularis IR27 et son devenir dans les racines de Z. mauritiana en plantation dans une large gamme de conditions environnementales. / The jujube (or Ziziphus mauritiana Lam.) is an important multipurpose species (e.g. fruits, fodder, wood) for reforestation and fruit farming in the Sahel. In this context where soils are often degraded and deficient in P, mycorrhization and phosphorus fertilization could play a major role on improvement of jujube growth and productivity. The main objective of this work was to improve growth and fruit production of Z. mauritiana by mycorrhizal inoculation in two orchards at Senegal. This work aims (i) to evaluate the responses of different species of Ziziphus and provenances of Z. mauritiana to inoculation with AMF in greenhouse conditions, (ii) to assess the impact of inoculation with R. irregularis IR27 on growth, survival and fruit production of Z. mauritiana, (iii) to assess the impact of inoculation on diversity of native AMF communities associated to Z. mauritiana after planting and (iv) to determinate the persistence of R. irregularis IR27 in roots of Z. mauritiana after planting.The fungus R. irregularis IR27 proved to be the most effective AMF tested in this work. The pair Z. mauritiana /R. irregularis IR27 has been chosen as model to study the impact of inoculation on fruit production of two provenances, Gola (Indian variety selected for its large size fruits) and Tasset (local cultivar with small-sized fruits) in two sites with contrasting rainfall (Amally and Keur Mangari). Our results showed a positive effect of inoculation on growth, survival and mycorrhizal colonization of Z. mauritiana plants at 13 and 24 months after planting at Amally and Keur Mangari respectively. Inoculation increased also fruit production of jujubes at 18 and 30 months after planting at Keur Mangari. These results indicated the high ability of R. irregularis to compete with indigenous AMF. The MiSeq Illumina sequencing of 18S rRNA gene revealed a negative impact of inoculation on AMF richness and diversity at Amally, unlike at Keur Mangari where inoculation had no impact on AMF richness and diversity. The RPB1 gene proved to be an appropriate marker to detect of R. irregularis IR27 in inoculated Z. mauritiana roots and to evaluate by qPCR the root colonization of R. irregularis IR27 which accounted for 11 to 13% at 13 months after planting at Amally and 12 to 15% at 24 months after planting at Keur Mangari. Therefore, it is important to assess at long-term the impact of R. irregularis IR27 and its persistence in inoculated Z. mauritiana roots in large environmental conditions.