Braconidae (Hymenoptera) associated with forest and ornamental trees and shrubs in Israel

Data are presented on the occurrence of Braconidae (Hymenoptera parasitica) parasitizing insects associated with forest and ornamental trees and shrubs in Israel. Fifty-five genera of plants are listed, the richest in braconid fauna being tamarisk (9 species); acacia, pistachio and poplar (8 species each); carob and oak (7 species each). Of the 95 species of insect hosts mentioned, 53 are Lepidoptera, mostly Gelechiidae (7 species), Pyralidae (6 species), Noctuidae (5 species), Gracillariidae, Tortricidae, Geometridae, Lymantriidae and Lycaenidae (3 species each); 44 are Coleoptera, mostly Cerambycidae (13 species), Scolytidae (12 species), and Bostrichidae (9 species); three are Diptera. Of the 92 species of braconids listed, of which only 65 have been fully named, 56 develop in Lepidoptera, mostly Noctuidae (15 species), Gelechiidae (11 species) and Pyralidae (9 species); 33 species develop in Coleoptera, mostly Cerambycidae (12 species, Bostrichidae (10 species) and Scolytidae (5 species); and three species develop in Diptera. Thirty-eight species are new to the fauna of Israel; at least three of them are new to science,viz., Gnaptodon, Gildoria andDendrosotinus titubatus Papp.     

Arthropod fauna and main insect pests of plane trees in Israel

Fifty-four insect and four mite species are included in a list of the entomofauna of plane trees in Israel. Only two species are monophagous:Phyllonorycter platani (Stgr.) (Lepidoptera: Gracillariidae) andEdwardsiana iranicola Zachv. (Heteroptera: Cicadellidae). Four species are noxious:P. platani, the main insect pest of the plane trees in Israel;Zeuzera pyrina L. (Lepidoptera: Cossidae);Kalotermes flavicollis F. (Isoptera: Kalotermitidae); andE. iranicola. Of much lesser importance areTargionia vitis Sign. (Homoptera: Diaspididae),Heliothrips haemorrhoidalis Bché. andRetithrips syriacus May. (Thysanoptera: Thripidae). About half of the listed species are natural enemies and many are parasites ofP. platani. Details are given on the noxious species, together with recommendations for prevention and control.     

Effect of Cotton leaf curl virus infected plants on the biology of the whitefly,Bemisia tabaci (Hemiptera: Aleyrodidae): Vector–virus mutualism

Cotton leaf curl virus (CLCuV) (Geminiviridae : Begomovirus), the causative agent of leaf curl disease in cotton plants (Gossypium hirsutum), is exclusively transmitted by whitefly species Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). CLCuV transmission occurs in Sriganganagar (Rajasthan), an area endemic with cotton leaf curl disease. The relationships between plant viruses, their herbivore vectors and host plants can be beneficial, neutral, or antagonistic, depending on the species involved. To further understand these relationships, fecundity and life history parameters of an indigenous non- b (Asia II genetic group) biotype whitefly, B. tabaci, were compared on 10, 25, and 40 days post-inoculation (DPI), in CLCuV-infected and healthy cotton plants to determine the effect of virus on its vector. The development time of the immature stages of whiteflies was significantly reduced on CLCuV-infected plants. The development time of the immature stages did not change with severity of symptoms at 25 and 40 DPI (45- and 60-d-old plants). Cotton leaf curl virus infection increased percent egg viability of B. tabaci. Whiteflies deposited significantly fewer eggs on virus-infected plants than on healthy plants. Whiteflies had better egg viability on younger plants than older plants, whereas plant age did not affect the fecundity. Male and female whiteflies had shorter longevity on CLCuV-infected plants than on healthy plants.     

Alien scale insects (Hemiptera Coccoidea) in European and Mediterranean countries: the fate of new and old introductions

This contribution focuses on recent interceptions and introductions of alien scale insects and their current distribution in European and Mediterranean countries. Data and collections were gathered in markets, nurseries, and botanical gardens, mostly in Italy, either indoors or outdoors. New or recent records of the following alien species are presented: Exallomochlus hispidus (Morrison); Ferrisia virgata (Cockerell) (Pseudococcidae); Coccus viridis (Green); Milviscutulus mangiferae (Green) (Coccidae); Aonidiella orientalis (Newstead); Aspidiotus destructor Signoret; Aulacaspis tubercularis Newstead; Fiorinia fioriniae Targioni Tozzetti; Lepidosaphes pinnaeformis (Bouché); Pseudaulacaspis brimblecombei Williams (Diaspididae). New data and pest status of Phoenicococcus marlatti Cockerell (Phoenicococcidae) and Trabutina mannipara (Hemprich & Ehrenberg) (Pseudococcidae) are also reported. The possible repeated introductions of the latter from North Africa to south Italy by trans-Mediterranean winds, is hypothesized.     

Development of conventional and real-time PCR protocols for specific and sensitive detection of Colletotrichum capsici in chilli (Capsicum annuum L.)

Anthracnose, caused by Colletotrichum capsici, is a major disease of chilli (Capsicum annuum L.) affecting both fruit and seed quality. The pathogen is both internally and externally seedborne. However, a rapid and sensitive method for detection of this pathogen in seeds is currently limited. In this study, a polymerase chain reaction (PCR) method based on sequence characterized amplified region (SCAR) marker was developed for specific and sensitive detection of C. capsici in chilli seeds and fruits. The developed SCAR primers were highly specific to C. capsici and resulted in the amplification of an expected 250-bp fragment from genomic DNA of all seven of the C. capsici isolates tested. No amplification occurred when the SCAR primers were tested with genomic DNA from three other fungal isolates and four other Colletotrichum species. The SCAR primers successfully amplified similar sized fragments from DNA derived from C. capsici-infected chilli fruits. The molecular detection sensitivity of C. capsici was 1 pg of purified C. capsici DNA template and 25 ng of DNA from C. capsici-infected chilli fruits. A real-time PCR assay was also developed using SYBR Green chemistry for detection of C. capsici in chilli fruits and seeds. The standard curve obtained showed a linear correlation between copy number of the cloned target DNA sequence of C. capsici and cycle threshold (Ct) values, with R² of 0.98. These PCR-based assays may be highly useful in detection of this important pathogen in chilli seeds and fruits in plant quarantine laboratories.     

Analysis of genetic and virulence variability of Stemphylium lycopersici associated with leaf spot of vegetable crops

Stemphylium lycopersici (Enjoji) W. Yamam was initially described from tomato and has been reported to infect different hosts worldwide. Sequence analyses of the internal transcribed spacer (ITS) regions 1 and 2, including 5.8S rDNA (ITS-5.8S rDNA) and glyceraldehyde-3-phosphate dehydrogenase (gpd) gene, random amplified polymorphic DNA (RAPD) and inter-simple sequence repeat (ISSR), as well as virulence studies were conducted to analyze 46?S. lycopersici isolates. Stemphylium lycopersici isolates used in this study were obtained from diseased tomato (Solanum lycopersicum L.), eggplant (Solanum melongena L.), pepper (Capsicum annuum L.) and lettuce (Lactuca sativa L.) from major vegetable growing regions of Malaysia, including the three states of Pahang, Johor and Selangor between 2011 and 2012. Phylogenetic analysis of a combined dataset of the ITS-5.8S rDNA and gpd regions indicated that all isolates were clustered in the sub-cluster that comprised S. lycopersici, and were distinguished from other Stemphylium species. Cluster analyses using the UPGMA method for both RAPD and ISSR markers grouped S. lycopersici isolates into three main clusters with similarity index values of 67 and 68 %. The genetic diversity data confirmed that isolates of S. lycopersici are in concordance to host plants, and not geographical origin of the isolates. All S. lycopersici isolates were pathogenic on their original host plants and showed leaf spot symptoms; however, virulence variability was observed among the isolates. In cross-inoculation assays, the representative isolates were able to cause leaf spot symptoms on eggplant, pepper, lettuce and tomato, but not on cabbage.     

Identification and species status of the mango biotype of Colletotrichum gloeosporioides in Ghana

Research work was carried out to identify and ascertain the species status of the mango biotype of Colletotrichum gloeosporioides infecting mangoes in Ghana. Forty five isolates of Colletotrichum species were collected from 12 districts in Ghana while five each were obtained from mango fruits from Florida, Mexico and Puerto Rico. The entire internal transcribed spacer region, partial beta-tubulin gene and partial glyceraldehyde-3-phosphate dehydrogenase gene of isolates were sequenced and used in phylogenetic studies. The results of the sequence analysis of the first ribosomal transcribed spacer (ITS 1) region showed that 35 % of the isolates from Ghana and all the five isolates from Mexico were the mango biotype of C. gloeosporioides, while the others were not. Phylogenetic studies showed that the mango biotype of the pathogen was Colletotrichum asianum but not C. gloeosporioides as previously thought. However, the other isolates that were not the mango biotype were identified as Colletotrichum siamense and Colletotrichum species which had probably cross-infected mango from other fruit crops in the field.     

The overwintering mode ofBemisia tabaci and its parasitoids in Israel

Wild and cultivated plants in the vicinity of Kibbutz Nahshon and a few additional locations in Israel were sampled for the presence ofBemisia tabaci Genna-dius (Homoptera: Aleyrodidae). The whiteflies, together with their parasites,Eretmocerus mundus andEncarsia lutea, were found to develop on numerous host species throughout the winter. Especially high levels were reached onLan-tana camara, Abutilon grandifolium andIpomoea batatas. During late winter and spring the population on these hosts declined. From April onwards the populations increased on potatoes and sunflowers.     

Plant ferredoxin-like protein enhances resistance to bacterial soft rot disease through PAMP-triggered immunity in Arabidopsis thaliana

The protection of plants against bacterial disease is one of the important issues that need to be studied in agricultural applications. The application of a transgene, such as a gene that encodes plant ferredoxin-like protein (PFLP), to generate resistant plants is one possible strategy. Our previous reports have demonstrated that transgenic plants that express extracellular PFLP (ESF plants) are more resistant to bacterial pathogens. This protein intensifies the hypersensitive response (HR) in plants when they are infiltrated by a pathogen-associated molecular pattern (PAMP), harpin (HrpZ), from Pseudomonas syringae. In addition, this intensified HR is associated with the expression of membrane-bound NADPH oxidase. Thus, we attempted to determine the involvement of PFLP in intensifying PAMP-triggered immunity (PTI) to enhance disease resistance. First, we showed that transgenic Arabidopsis plants with the pflp gene were resistant to bacterial soft rot caused by Pectobacterium carotovorum subsp. carotovorum (Pcc). Then, the fliC gene which encoded flagellin from Pcc was cloned and expressed. The FliC protein was used in the functional study with PFLP in Arabidopsis Col-0 plants. The reactive oxygen species (ROS) generation and HR ratio were induced by the treatment with both PFLP and FliC together, but they were not induced by treatment with PFLP or FliC alone. Similar results were confirmed in ESF plants, where FliC elicited rapid ROS accumulation and callose deposition. Moreover, we demonstrated that the PFLP-intensified ROS generation and HR were related to Ca²⁺ influx and activation of NADPH oxidase. We concluded that the PFLP-intensified disease resistance is associated with the intensification of PAMP-triggered immunity.     

Integrative diagnosis and molecular phylogeny of dagger and needle nematodes of olives and grapevines in the island of Crete,Greece, with description of Xiphinema cretense n. sp. (Nematoda,Longidoridae)

The occurrence and geographic distribution of longidorid nematode species inhabiting the rhizosphere of cultivated and wild olive and grapevine in Crete Island were investigated. Morphological and morphometrical studies identified five Longidorus and six Xiphinema species, with frequencies of prevalence (for wild and cultivated olives and grapevines, respectively) as follows: Longidorus closelongatus (2.0–13.3 %), L. cretensis (1.0–6.7 %), L. moesicus (13.3 % only in grapevines), L. orientalis (3.3 % only in grapevines), L. pseudoelongatus (7.0 % only in olives), Xiphinema cretense n. sp. (3.0 % only in olives), X. index (3.0–23.3 %), X. israeliae (6.3 % only in olives), X. italiae (3.3–10.0 %), X. pachtaicum (26.7–42 %) and X. simile (3.3 % only in grapevines). Xiphinema cretense n. sp. is characterized by a body size 3,872–6,135 μm long, lip region anteriorly rounded, separated from the rest of the body by a depression, odontostyle and odontophore 140.6 and 80.3 μm long respectively, vulva position at 46.0–50.5 %, female tail 31.0–38.0 μm long, nearly hemispherical with curvature essentially dorsal and with a tip completely rounded or presenting a very short bulge, c ratio (119.1–186.9), c’ ratio (0.7–0.8). Molecular characterisation using D2-D3 expansion regions of 28S rRNA, 18S rRNA and ITS1-rRNA was carried out and maximum likelihood and Bayesian inference analysis were used to reconstruct phylogenetic relationships among these species and with other longidorids.     

Pyrethroid synergism and prevention of emergence inTribolium castaneum andMusca domestica vicina by the insect growth regulator RO 13-5223

Ethyl [2-(4-phenoxyphenoxy)ethyl] carbamate (RO 13-5223) at a dietary concentration of 100 mg kg^-1 synergized the toxicity of thetrans- andcis-isomers of permethrin and cypermethrin in inhibiting the growth (measured as gain in larval weight) ofTribolium castaneum andMusca domestica vicina. With both species the synergism factor forcis-cypermethrin with 100 mg kg^-1 synergist was 1.5- to twofold for RO 13-5223 and about fourfold for piperonyl butoxide. Synergism was more pronounced with first instar than with fourth instarT. castaneum larvae. Methoprene was not a pyrethroid synergist withT. castaneum larvae, so the synergistic effect of RO 13-5223 appears to depend on its structural features and not its insect-growth-regulator activity. Joint application of RO 13-5223 and pyrethroids resulted in a dual effect on bothT. castaneum andM. domestica: increased inhibition of larval growth due to pyrethroid synergism, and progeny suppression — expressed by larval and pupal mortality — due to RO 13-5223 juvenilizing activity.     

Detection and partial molecular characterization of Plum pox virus on almond trees in Turkey

Almond (Prunus dulcis) is one of the well known stone fruit species grown for its unripe fruits and delicious seeds in Turkey. In the Trakya region, however, some prevailing virus infections have reduced almond yields and quality. In ten districts of Trakya, 260 leaf samples were collected from affected almond trees in June 2010. DAS–ELISA assays and RT-PCR tests were employed for the identification of viruses. As a result of these detection studies, five of the 260 leaf samples gathered from symptomatic almond trees had Plum pox virus (PPV), 81 of them had Prunus necrotic ringspot virus (PNRSV), and 11 samples contained Prune dwarf virus (PDV). Only four out of 260 samples had a mixture of these viruses. Partial nucleotide sequences of five almond isolates of PPV were determined and compared with 17 other PPV isolates in databases. Computer analysis of obtained and published nucleotide sequences showed identity ranged from 75.72% to 96.87%. Of the five PPV almond isolates obtained, however, there was a close nucleotide identity of 95.82–96.61% to Turkish isolates. Phylogenetic analysis of nucleotides and amino acids showed that five PPV isolates of almond from the Trakya Region of Turkey were clustered in the same subgroup with PPV-T Turkish isolates in GenBank. Therefore we can consider almond isolates of PPV as PPV-T strain, like the two other isolates from apricot trees in Turkey.     

Characterization of Alternaria species associated with leaf blight of sunflower in China

Nine Alternaria species have been reported to be associated with sunflower leaf blight worldwide, and A. helianthi has been recognized as the most prevalent and damaging species. However, the population structure of Alternaria species causing leaf blight of sunflower in China had not been examined thoroughly prior to this study. During 2010 to 2013, a total of 272 Alternaria isolates were obtained from infected sunflower leaves in 11 provinces, autonomous regions, and municipalities of China. Based on morphological traits and sequence analyses of the internal transcribed spacer (ITS) regions of ribosomal DNA (rDNA) and the partial coding sequences of the histone 3 gene, 227 (83.5 %) isolates were identified as belonging to Alternaria tenuissima, the remainder 45 isolates were grouped to A. alternata (16.5 %). Compared with the ITS regions of rDNA, sequence analyses of the partial coding sequences of histone 3 gene displayed a critical role in discrimination of the small-spored Alternaria species. Phylogenetic analysis of the partial coding sequence of histone 3 gene clearly divided the representative Alternaria isolates into two main clades, A. tenuissima and A. alternata. The pathogenicity of A. tenuissima and A. alternata on detached leaves of sunflower cv. Gankui No.2 did not significantly differ between the two species or among isolates from different geographical origins. Our results indicate that the population structure of Alternaria species associated with sunflower leaf blight differed from that reported previously in China since A. helianthi was not found in this study. In addition, this is the first report about A. tenuissima causing leaf blight on sunflower in China.     

Survey on viroids infecting grapevine in Italy: identification and characterization of Australian grapevine viroid and Grapevine yellow speckle viroid 2

Five viroid species have been reported from grapevine. Hop stunt viroid (HSVd) and Grapevine yellow speckle viroid 1 (GYSVd-1) are distributed worldwide, whereas Grapevine yellow speckle viroid 2 (GYSVd-2), Australian grapevine viroid (AGVd) and Citrus exocortis viroid (CEVd) are found only sporadically. However, the presence of AGVd and GYSVd-2 in several countries, including China, Turkey and Tunisia, suggests a wider dissemination, possibly also in Europe, where AGVd has never been found and GYSVd-2 has been occasionally identified in Italy. Taking advantage of a multiplex RT-PCR assay recently developed for detecting simultaneously these five viroids, vines growing in Italy in commercial vineyards and germplasm collections were surveyed. Besides confirming the widespread presence of HSVd and GYSVd-1 in the field, GYSVd-2 and/or AGVd were identified in two grapevine table cultivars (Sultanina Bianca and Red Globe) from germplasm collections. Tests extended to vines cultivated in southern Italy confirmed the presence of both viroids, which were further characterized. No major sequence divergences between the AGVd and GYSVd-2 variants from Italy and those previously described from other countries were observed. Phylogenetic analysis supported the close relationships among AGVd variants from Italy, Tunisia and Australia. To our knowledge this is the first report of AGVd in Europe and the first molecular characterization of GYSVd-2 isolates from a European country.     

Phenotypic and genotypic structure of Phytophthora infestans populations on tomato and potato in the North of Thailand in 2000–2002

A total of 80 single–lesion isolates of Phytophthora infestans were collected from tomatoes and potatoes in several locations in Chiang Mai and Tak provinces in 2000–2002. These isolates were analyzed for mating type, metalaxyl sensitivity, mitochondrial DNA (mtDNA) haplotype RFLP pattern as determined by probe RG57, and for microsatellite markers. All isolates were A1 mating type. Isolates from tomato were usually sensitive to metalaxyl, but isolates from potato were usually resistant to metalaxyl. With one exception, all tomato isolates were related to the US-1 clonal lineage. With two exceptions, all potato isolates were related to two European lineages. In these two provinces, the populations of P. infestans on tomatoes are clearly different from those on potatoes.     

A list of arthropod pests of avocado and pecan trees in Israel

Lists are given of arthropod pests of avocado and pecan trees in Israel. These include ten new pests of avocado and three of pecan. The pests of economic importance on avocado includeBoarmia (Ascotis) selenaria (Schiff.) (Geometridae, Lepidoptera) andHeliothrips haemorrhoidalis (Bouché) (Thrypidae, Thysanoptera). The pests of importance on pecans includeEmpoasca decedens (Paoli) (Jassidae, Homoptera),Zeuzera pyrina L. (Cossidae, Lepidoptera), andMonellia costalis (Fitch) (Aphididae, Homoptera).     

A leaf spot disease of Nymphaea alba in the Netherlands

A destructive leaf spot disease was found onNymphaea alba in the lakes near Kortenhoef, Netherlands. After comparison of fresh material and herbarium specimens the causal agent is namedColletotrichum nymphaeae (Pass.) van der Aa, comb. nov. Synonymy, morphology and cultural characters of the fungus are described and discussed. Some remarks on the relationship with several host plants are given and the provisional conclusion is that the species is a widespread parasite, but that the destructive attack in the Kortenhoef region is probably caused by a combination of various factors.     

Control of phytophthora leaf blight of taro (Colocasia esculenta) by fungicides and roguing

Six fungicides were evaluated under laboratory and field conditions for control of Phytophthora leaf blight of taro,Coloeasia esculenta, incited byPhytophthora colocasiae. Inin vitro tests Deraosan 65W was the most effective in inhibiting the mycelial growth of the test pathogen followed by Difolatan 80W, Fytolan (copper oxychloride), Apron 35F, Topsin-M 50W and Dithane Z-78 75W. Excellent control was obtained with Demosan 65W and Difolatan 80W, good control with Apron 35F, fair control with Fytolan, and poor control with Topsin-M 50W and Dithane Z-78 75W. Results ofin vivo tests were correlated with those of thein vitro tests. Roguing of infected leaves did not eradicate the pathogen but can only delay epiphytotics.     

Effects of variable temperatures on responses ofAphytis melinus andA. lingnanensis to host density

The effects of three variable temperature regimes (18–24, 24–29, and 29–35°C) on the responses of two species of the genusAphytis Howard (Hymenoptera: Aphelinidae), parasitic upon the California red scale, were studied, and a test to analyze parasite behavior was developed.Aphytis lingnanensis Compere was generally more efficient thanA. melinus DeBach; however, whereas a high temperature regime (29–35°C) had a negative effect on the responses ofA. lingnanensis, it improved those ofA. melinus. The two species distributed their eggs in clumps, but were able to respond to increasing host density by reducing the number of eggs laid per encounter. The combined effects of numerical, and functional responses of the two species on host population were considered, with special reference to the mechanism of competitive displacement.     

Involvement of Phytophthora cryptogea in sweet cherry decline in Turkey

Sweet cherry is a major commercial crop in Turkey, the most important producer of the fruit worldwide. Sweet cherry decline was observed in an orchard in Ankara province of Turkey. Affected young trees exhibited reduced tree vigor, yellowing and wilting of leaves, and dieback symptoms resulted in tree death. A Phytophthora sp. was consistently isolated from necroses that appeared on taproots and crowns. The pathogen was identified as Phytophthora cryptogea based on several morphological features and DNA sequence of the internal transcribed spacer (ITS) region. P. cryptogea was pathogenic on excised shoots and 1-year-old cherry rootstocks. This is the first report of P. cryptogea causing disease of sweet cherry in Turkey.