Fróðskaparrit - 01.07.2004, Qupperneq 35

Fróðskaparrit - 01.07.2004, Qupperneq 35
VAL AV LÍVØKI HJÁ ARBUSKULSOPPUM í FØROYUM SAMMETT VIÐ AÐRASTAÐNI 33 recombinant DNA molecule was trans- ferred into competent E. coli cells (DH5a from Gibco BRL Life Technologies). All steps strictly followed the manufacturers’ manual. The competent cells were grown on solid medium, forming colonies of iden- tical clones. At least 16 clones were used for each sample, giving a total of 244 clones. RLFP The clones were grouped by using the en- zymes Hinfl and Hsp92U (Promega) main- ly to distinguish between the glomalian types, while Stul and Hpall were used to detect amplified ascomycetes. Hpall did also distinguish between some acaulospora types. When all the ascomycetes were omitted, only 127 clones were left. T-RLFP The results where an English site (Sour- hope) is compared with Faroese sites are obtained by T-RLFP (Liu et al., 1997). The PCR products were digested with Hinfl and then run on a Beckman Coulter CEQ8000. The fragment length was analysed with Beckman Coulter CEQ8000 software (from Beckman Coulter). Sequencing Representatives for each main glomalean group were sent for sequencing at the Tech- nology Facility, University of York, UK. Only one strand was sequenced. The se- quencing was done on a Beckman Coulter CEQ8000 analyser. Statistics ClustalX (Thompson et al., 1997) was used for multiple alignment and neighbour-join- ing phylogenetic analysis (Saitou and Nei, 1987), using Corallochytrium limacispo- rum, a putative choanozoan (Cavalier- Smith and Allsopp, 1996) as the outgroup. The phylogenetic tree is drawn in TreeView (Page, 1996). All other statistical analyses were carried out using SPSS version 11.01. Results 5 main types of AM fungi were found in Agrostis capillaris roots (Table 1). A fur- ther 10 types were found which only oc- curred once or twice in total. Two of the main types were mainly found at high alti- tude, and two other were only found at low altitude. In total 16 types were found, although not all of them are sequenced, and therefore there might still be some ascomycetes in the group. The unsequenced clones are 12 in total, so their importance is low com- pared with the main group. To avoid a high Shannon index due to undetected as- comycetes, all the unsequenced clones were omitted from the calculations, result- ing in a Shannon index ranging from 0 to 1.19 (Table 1). However, if we remove the altitude factor and only consider the aspect, then the Shannon index is 1.63 on north- facing slopes, 0.45 on south-facing (Table 2). The very low diversity at south-facing high altitude arises because only one of the main types is found. This is “Glo3” which seems to be a very competetive colonisator, present in all studies mentioned in this
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