Large‐scale fuzzy rule‐based prediction for suitable chestnut ink disease sites: a case study in north‐east Italy

In the past few decades, economic interest in the cultivation of chestnuts for both timber and nut production has resurfaced in the Mediterranean area. However, chestnut cultivation has suffered in recent years from the spread of exotic pests, such as the gall wasp Dryocosmus kuriphilus, and from the resurgence of previously present diseases, most likely due to anomalous climate dynamics. This is the case with chestnut ink disease, caused by the soilborne pathogens Phytophthora cinnamomi and P. cambivora. Scientific and technical support in monitoring and management, that utilizes new forecasting approaches incorporating related environmental variables, is therefore essential. The main aim of this study was to develop a mathematical model assessing the potential for the establishment of chestnut ink disease at a large scale. Towards this goal, fuzzy rule‐based theory was applied to the environmental variables associated with host presence, pathogens' ecological niches and ink disease symptoms expression. The effectiveness of the rule‐based modelling outcomes, provided with uncertainty maps to facilitate their correct interpretation, was confirmed by detailed field data collected from a large chestnut‐growing area where ink disease has been increasing in recent years. The final model gave consistent predictions for disease presence. For this reason, it represents a flexible and valuable decision‐support tool to forecast which sites are at risk from CID.     

Variation in pathogenicity among the three subspecies of Phytophthora alni on detached leaves,twigs and branches of Alnus glutinosa

Pathogenicity tests were carried out on leaves, twigs and branches of Alnus glutinosa using several isolates of Phytophthora alni ssp. alni, P. alni ssp. multiformis and P. alni ssp. uniformis in vitro. Healthy fresh leaves were collected from disease‐free areas and inoculated with mycelium on agar discs or by dipping in zoospore suspensions. In addition, twigs and branches were collected from both disease‐free and disease‐affected areas, inoculated with mycelium on agar discs and incubated at four temperatures (15, 20, 25, 30°C). All subspecies tested were pathogenic but with varied level of virulence. In inoculation tests on foliage, wounding was a key factor in causing infections: lesions on inoculated wounded leaves were larger than on non‐wounded leaves. In the twig and branch inoculation tests, no differences in virulence were observed among the P. alni subspecies in terms of sampling locations, but lesions differed in size according to incubation temperature, with the largest lesions occurring on tissues incubated at 25°C. The work is the first to report foliar necrosis caused by P. alni on A. glutinosa. P. alni ssp. uniformis was the least virulent of the subspecies in branch inoculations. These findings demonstrate that various tissues of A. glutinosa could act as sources of pathogen inoculum and may disseminate alder Phytophthora in natural ecosystems.     

First definite report of natural infection of Fraxinus ornus by Hymenoscyphus fraxineus

Hymenoscyphus fraxineus was isolated from four leaf rachises with necrotic lesions of flowering ash (Fraxinus ornus) seedlings, which had been planted on a forest site in Austria where they were exposed to a massive natural infection pressure. This represents the first definite report of natural infection of this ash species by the ash dieback pathogen.     

Identification of ‘Candidatus phytoplasma ziziphi’ associated with persimmon (Diospyros kaki Thunb.) fasciation in China

Persimmon (Diospyros kaki Thunb.) trees, with fasciation symptoms (PF), were observed in an orchard located in suburban Tai'an, Shandong Province, China. A specific fragment of the phytoplasma 16S rRNA gene, approximately 1.2 kb in length, was amplified from two symptomatic plants via nested polymerase chain reaction, while no fragment was obtained from healthy controls. The two samples (PF1 and PF2) resulted with 99.5% nucleotide sequence identity. Phylogenetic and restriction fragment length polymorphism (RFLP) analysis of 16S rRNA gene sequences revealed that PF1 was a member of ribosomal subgroup B of the elm yellows group (16SrV), and PF2 may represent a novel subgroup within the 16SrV group, designed as 16SrV‐I. This is the first report of phytoplasmas of the 16SrV group associated with persimmon fasciation disease.