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Romania (Quercus cerris, Q. frainetto, Q. robur) and - EdituraSilvica.ro

Romania (Quercus cerris, Q. frainetto, Q. robur) and - EdituraSilvica.ro

Romania (Quercus cerris, Q. frainetto, Q. robur) and - EdituraSilvica.ro

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Ann. For. Res. 54(1): 57-71, 201166m30m29m28m27m26m25m24m23m22m21m20m19m18m17m16m15m14m13m12m11m10m9m8m7m6m5m4m3m2m10 10 20Figure 2 Frequencies of mycorrhizal morphotypesin <strong>ro</strong>ot samples of Quecus <st<strong>ro</strong>ng>cerris</st<strong>ro</strong>ng>,<st<strong>ro</strong>ng>Quercus</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>frainetto</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>Quercus</st<strong>ro</strong>ng> <st<strong>ro</strong>ng><strong>ro</strong>bur</st<strong>ro</strong>ng>in several locations in Southern <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng>North-Western <st<strong>ro</strong>ng>Romania</st<strong>ro</strong>ng>Research articlesity-dissimilarity matrix was used for clusteringby means of g<strong>ro</strong>up average method. Statisticaltests were performed using KyPlot p<strong>ro</strong>gram.ResultsThere were identied 30 morphotypes of ectomycorrhizae,corresponding to <st<strong>ro</strong>ng>Quercus</st<strong>ro</strong>ng> <st<strong>ro</strong>ng><strong>ro</strong>bur</st<strong>ro</strong>ng>,<st<strong>ro</strong>ng>Quercus</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>cerris</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>Quercus</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>frainetto</st<strong>ro</strong>ng> in Southern,Western <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng> North-Western locations,presented in Table 1. The original descriptions(with the exception of Cenoccocum geophilumdescribed by Agerer in 1987), are presented inTable 2.The investigation of the maximum numbe<strong>ro</strong>f morphotypes active a certain moment in therhizosphere of the host is 14 (Fig. 1) which isthe real instantaneous value of morphotyperichness (Q. <st<strong>ro</strong>ng>cerris</st<strong>ro</strong>ng> at Dobreti).The described morphotypes include only 6cases of identied mycobionts (Amanita maireiFoley, Scle<strong>ro</strong>derma citrinum Pers., Russulaat<strong>ro</strong>purpurea (K<strong>ro</strong>mbh.) Britzelm, Lactariusquietus (Fr.) Fr., Russula virescens (Schaeff.)Fr., Boletus chrysente<strong>ro</strong>n Bull.) based on mycelialcontinuity between mycorrhizal mantle<st<strong>ro</strong>ng>and</st<strong>ro</strong>ng> the mycelium at the base of the carpophores.Easily recognizable Cenoccocumgeophilum Fr. is also included in morphotypedescriptions. Mantles of mycorrhizas with speciesof Lactarius as mycobionts (as examinedon c<strong>ro</strong>ss sections of ne <strong>ro</strong>ots) exhibit characteristiclaticifers <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng> pigments which are alsofound in the structure of the spo<strong>ro</strong>carps. Thoseof Rusulla spp. exhibit distinctive cystidia <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng>sulfovaniline reactive cells (Kernaghan <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng>Currah 1997).The analysis of frequency distribution of thevarious morphotypes (Fig. 2) shows that thedominating type is Cenococcum geophilum(M30) that is present in all locations. Nextmost frequent morphotype is M2 described inQ. <st<strong>ro</strong>ng><strong>ro</strong>bur</st<strong>ro</strong>ng> <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng> Q. <st<strong>ro</strong>ng>cerris</st<strong>ro</strong>ng> at Buteni, Oradea <st<strong>ro</strong>ng>and</st<strong>ro</strong>ng>Slveti but found in almost all locations lessfrequently than C.geophilum.

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