Communities of arbuscular mycorrhizal fungi (AMF) in five agricultural field sites of different management intensities were studied. Variable regions of the ribosomal RNA genes were used to detect and identify AMF directly within colonized roots. Roots from a continuous maize monoculture showed low AMF diversity, in agreement with previous reports on molecular diversity of AMF in agricultural soils. In contrast, a substantially higher diversity of AMF was found throughout the long term 'DOK' field experiment, where organic and conventional agricultural practices have been compared side by side since 1978. In this experiment, a 7-year crop rotation is performed under lower levels of inorganic fertilizer input and chemical pest control. These results are in good agreement with analyses of the spore community previously conducted in these field sites. In a third site, an organically managed leek field with soil of very high phosphate content reflecting the highly intensive conventional field history and intensive tillage, we detected a low-diversity community comparable to the maize monoculture. In addition to fungi from Glomus group A, which have previously been reported to dominate arable soils, we regularly found members of the genera Scutellospora, Paraglomus and Acaulospora. The genus Acaulospora was shown to occur more frequently early in the growing season, suggesting that the life history strategy of AMF may influence the active community at a given time. These data show that the diversity of AMF is not always low in arable soils. Furthermore, low-input agriculture involving crop rotation may provide better conditions to preserve AMF diversity, by preventing the selection for the few AMF taxa tolerating high nutrient levels.
ReuseUnless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version -refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher's website. TakedownIf you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing eprints@whiterose.ac.uk including the URL of the record and the reason for the withdrawal request.toxicity is due to the diatom culture conditions in the laboratory or that cases of toxicity are exceptions, owing to the species or strains maintained in laboratory cultures being unrepresentative of natural field populations.However, any explanation for the discrepancy between the laboratory and field results does not affect our conclusion. The range of areas and copepod and diatom species considered in this study provide strong evidence that, under natural environmental conditions, there is no negative effect of diatoms on copepod hatching success. We conclude that there is no need to revise existing conceptual models of energy transfer from phytoplankton, through copepods, to fish in diatom-dominated systems.A Methods Hatching successEggs for the hatching success measurements were obtained from females incubated in filtered or natural sea water (depending on the species, some copepods stop spawning in filtered sea water) during the first 12-24 h after capture 18 . The intention was to minimise the effect of the incubation conditions to obtain hatching rates representative of the field values. From the egg production experiments 30-100 eggs were selected randomly and gently transferred to 60-ml tubes filled with filtered sea water. The samples were incubated, at sea surface temperature, for periods ranging from 48 to 96 h (depending on the temperature). After the incubation period, the samples were examined microscopically to determine the number of nauplii and unhatched eggs. Microplankton identification and biomassWater samples for identification of microplankton (.2 mm, nanoplankton plus microplankton) species and carbon estimation were collected generally at the chlorophyll maximum depth and preserved with 1% final concentration of Lugol's iodine solution 19 . Subsamples (100 ml) were settled (Utermöhl technique) and counted with an inverted microscope. Phytoplankton carbon biomass was estimated from cell volume 20 and using a factor of 0.21 pg C mm 23 (ref. 21) for ciliates. Heterotrophic dinoflagellates were separated from autotrophic forms according to taxonomic considerations 22 .
Molecular identification methods are about to revolutionize studies on ecology of arbuscular mycorrhiza. These techniques offer the unique opportunity to investigate communities of arbuscular mycorrhizal fungi (AMF) within roots. Recent technical advances are reviewed, discussing their drawbacks and advantages. An experimental approach to analyze AMF communities within roots using a molecular identification method is presented. Sample results from the analysis of trap cultures from a current project are shown.
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