A major facilitator superfamily transporter in Colletotrichum fructicola (CfMfs1) is required for sugar transport,appressorial turgor pressure,conidiation and pathogenicity

The major facilitator superfamily (MFS) is one of the largest membrane‐protein families. To investigate the role of MFS proteins in the fungal plant anthracnose pathogen Colletotrichum fructicola, the CfMFS1 gene was deleted. This resulted in reduced mycelial growth, conidial yield and decreased virulence on tea oil camellia leaves. In addition, ?Cfmfs1 showed increased sensitivity to osmotic stress and to a cell‐wall stressor. Further analysis revealed that CfMfs1 is required for conidial penetration and appressorial turgor pressure, both important for fungal pathogen invasion. Confocal fluorescence microscopy showed that CfMfs1 is localized to membranes of both hyphae and conidia, suggesting that it may be a membrane transporter. Our study provides evidence that CfMfs1 has a role in conidiation, sugar transport, stress response, conidial penetration, appressorial turgor pressure and virulence against tea oil camellia.     

Development and population growth of <Emphasis Type="Italic">Stephanitis pyri</Emphasis> (F.) (Heteroptera: Tingidae) at five temperatures

Pear lace bug, Stephanitis pyri (F.) (Heteroptera: Tingidae) is a pest of apple and pear trees and ornamental Rosaceae plants in Mediterranean countries and palearctic region. The aim of this study is to determine the effects of temperatures on S. pyri in the laboratory. Development and fecundity of S. pyri reared on apple leaves (Pyrus malus L.) were investigated at five constant temperatures (20, 23, 26, 29 and 32 ± 1°C) and a 16L:8D photoperiod. Longevity was determined to be 12.6 days at 32°C and 58.7 days at 20°C for females, and 9.7 and 37.7 days for males. Females laid 186.9 eggs per female with the highest number achieved during 28.5 days of oviposition period at 26°C. Female lifetime fecundity was reduced at 32°C (40.0 eggs per female). While the net reproductive rate (R ₀) was highest at 26°C, the intrinsic rate of natural increase (r _m ) was highest at both 26 and 32°C. The mean generation time (G) was estimated to be 27.2–78.4 days at 20 and 32°C, respectively. The longest development times for egg and total nymph stages were obtained as 22.0 and 24.9 days, respectively, at 20°C. S. pyri developed fastest from egg to egg in 24.3 days at 32°C. The lower developmental threshold (T ₀) was 9.7°C and the thermal constant (K) was 517.3 degree-days for S. pyri. Thus, S. pyri is calculated to have 3.8 theoretical generations in Tekirdag. The optimum developmental temperature for S. pyri was 26°C.     

Identification of Colletotrichum species associated with anthracnose of Spondias spp. in Brazil

Plants of the genus Spondias are commonly cultivated in northern and north‐eastern Brazil for fruit production. Severe leaf anthracnose, caused by Colletotrichum spp., is frequently observed in several species of Spondias. The objectives of this study were to identify and characterize Colletotrichum species associated with anthracnose in species of Spondias by using the concept of morphological and phylogenetic analyses. Leaves with symptoms of anthracnose were collected from orchards in the state of Piauí, Brazil. Morphological identification; sequencing analysis of ACT, ITS and GS gene regions; and a pathogenicity test confirmed three Colletotrichum spp. (C. dianesei, C. siamense and C. brevisporum) were able to cause the disease. This is the first record of these species of Colletotrichum causing anthracnose in Spondias spp. in Brazil.     

Enhancing resistance in Pinus radiata seedlings to terminal crook (Colletotrichum acutatum) using methyl jasmonate and ultraviolet‐C radiation

Colletotrichum acutatum is a fungal pathogen that causes terminal crook disease in radiata pine (Pinus radiata) seedlings in New Zealand forest nurseries. Symptoms of infection include malformation or death of the growing tip and a stiffening and thickening of the stem. Although the disease can be managed effectively using fungicides, the New Zealand forest industry is interested in alternative control options such as induced resistance. The aim of this study was to evaluate spray application of chitosan (1.4 g/l) or 2.25 mm methyl jasmonate (MeJA) and irradiation with UV‐C (2.16 kJ/m²) for their potential to induce resistance to terminal crook. The treatments were applied to 4‐month‐old seedlings at 1 week before pathogen inoculation. By the end of the experimental period (42 days after inoculation), there was 80% disease incidence in the controls, with 48% of seedlings exhibiting severe terminal crook symptoms. The most effective treatment (p < 0.05) was MeJA with 16% disease incidence and none with severe symptoms. UV‐C also significantly (p < 0.05) reduced infection with 52% incidence and 20% of seedlings exhibiting severe symptoms. Chitosan did not reduce disease incidence (72%) compared with the control (80%) but did significantly reduce (p < 0.05) disease severity with 28% exhibiting severe symptoms. MeJA was the only treatment that significantly (p < 0.05) reduced the detrimental effects of infection on seedling apical growth and stem diameter. To our knowledge, this is the first report demonstrating the potential for MeJA and UV‐C to control terminal crook in radiata pine.     

Incidence of dieback disease following fungal inoculations of sexually and asexually propagated shisham (Dalbergia sissoo)

Shisham (Dalbergia sissoo) is an important multipurpose tree with great economic importance, but this tree has been devastated by dieback disease. Seedlings and asexually propagated (cuttings) plants were artificially inoculated with four fungi (Fusarium solani, Botryodiplodia theobromae, Curvularia lunata and Ganoderma lucidum) to evaluate the potential role of these fungi in shisham dieback disease. Results at 2 years revealed that highest disease was caused by inoculation of F. solani (31.39%), followed by B. theobromae (19.042%) and C. lunata (12.22%), but no dieback disease was caused by G. lucidum. During both years, seedlings exhibited greater susceptibility to disease (17.24%) compared to cuttings (7.83%). In particular, F. solani caused more disease in seedlings (46.18%) compared to cuttings (16.61%). With the F. solani inoculations, maximum disease rate was observed at 8 weeks post‐inoculation both in seedlings (77%) and in cuttings (31%), but the maximum disease increase was observed at 4–5 weeks post‐inoculation. Analysis of variance showed significant differences among the different fungi and also between seedlings and cuttings. F. solani can be considered as a major fungal pathogen contributing to dieback disease of shisham, and asexual propagation can reduce the severity of dieback.     

Screening of Metrosideros polymorpha (‘ōhi‘a) varieties for resistance to Ceratocystis lukuohia

Stands of the landscape‐dominant tree, Metrosideros polymorpha (‘ōhi‘a) on the Island of Hawai‘i, HI., USA, are dying from a phenomenon known as rapid ‘ōhi‘a death (ROD). Approximately 180,000 acres of forest have already been impacted by the disease, the majority of which is attributed to C. lukuohia, the more aggressive of the two Ceratocystis species responsible for ROD. Three isolates of C. lukuohia were compared for differences in aggressiveness. Mean disease severity and mean number of days to death did not differ among the three isolates of C. lukuohia. A single isolate was selected for use in a resistance screening of 128 plants across four varieties of M. polymorpha occurring on Hawai‘i Island: incana, glaberrima, polymorpha and newellii. Disease severity was lower in early‐successional var. incana (38.84%) and riparian var. newellii (36.11%) compared to late‐successional var. glaberrima (61.27%) and high‐elevation var. polymorpha (70.27%). Var. incana and var. newellii also had the lowest mortality (63% and 77%, respectively) while var. glaberrima (86%) and var. polymorpha (100%) had the highest mortality. Eighty‐five per cent of the plants that died did so within 49 days post‐inoculation and mean number of days to death was significantly higher for var. glaberrima (46) compared to var. polymorpha (31). The results of this preliminary study suggest that some form of resistance might be present in natural populations of at least one variety of M. polymorpha on Hawai‘i Island and should be investigated more intensively.     

Biochemical responses associated with induced resistance to Colletotrichum acutatum in Pinus radiata seedlings treated with methyl jasmonate and Trichoderma spp.

The effect of Trichoderma (T. atrobrunneumFCC320 and T. atrovirideLU633) and/or methyl jasmonate (MJ) on resistance to terminal crook (Colletotrichum acutatum) and on seedling biochemistry was investigated in radiata pine (Pinus radiata) seedlings. Seedlings were germinated and grown in Trichoderma‐amended or non‐amended media for 3 months and then sprayed with 2.25 mM MJ 1 week before inoculation with C. acutatum. The incidence and severity of terminal crook in the seedlings treated with MJ and Trichoderma+MJ were lower than in Trichoderma‐treated and Trichoderma‐untreated seedlings. The MJ‐induced resistance response was concomitant with an increase in the concentrations of the monoterpenes α‐pinene, β‐pinene, β‐phellandrene, camphene and myrcene in needles, and also α‐pinene, β‐pinene and camphene in stems. The concentrations of α‐pinene, β‐pinene and camphene were elevated from at least 1 week until 4 weeks after MJ application, compared with those in non‐MJ counterparts. Trichoderma alone did not affect monoterpenes, but the concentrations of α‐pinene, β‐pinene and camphene were greater in needles of Trichoderma+MJ than in MJ‐treated seedlings after 28 days. Total phenolic concentration in needles and peroxidase activity in stems were twofold greater in MJ‐treated seedlings than in non‐MJ seedlings over the same period. None of the treatments affected the activity of peroxidase in needles. It is proposed that the accumulation of monoterpene and phenolics and the induction of peroxidases contribute, in part, to MJ‐induced resistance to terminal crook in radiata pine seedlings.     

Physiological and morphological responses of young mahogany (Swietenia macrophylla King) plants to drought

Young mahogany (Swietenia macrophylla King) plants were grown under either well-watered (pre-dawn leaf water potential, Ψ_pd, ca. −0.40 MPa) or drought (Ψ_pd, ca. −3.52 MPa) conditions to examine some physiological strategies that allow the maintenance of leaf turgor. In well-watered plants, stomatal conductance (g_s) was nearly constant (440 mmol m⁻² s⁻¹) between 7:00 and 13:00 h. This was accomplished by significant increases in transpiration (E) and apparent total hydraulic conductance (K_T), in which averages were higher at 13:00 h. From 13:00 to 17:00 h, g_s, E, and K_T decreased sharply, reaching their lower values at 17:00 h. In these plants, significant increases in height (116%), stem diameter (50%) and leaf area (200%) were registered over the experimental period (20 days). Analyses of linear regression between g_s or E and leaf-to-air vapor pressure deficit (Δ_w) were not significant. In water-stressed plants, g_s and E were higher at 7:00 h and lower from 9:00 to 17:00 h, while K_T was higher in early morning (7:00 h) and in late afternoon (17:00 h) than between 9:00 and 15:00 h. Moreover, both g_s and E decreased potentially (P < 0.001) with the diurnal increases on Δ_w. Drought also decreased leaf and leaflet numbers and reduced total leaf area, but had no effect on stem height and diameter. Leaf proline was higher (ca. 400%, between 13:00 and 15:00 h) in water-stressed plants, suggesting osmotic adjustment under drought. Twelve hours after resumption of irrigation, Ψ_pd was similar (P > 0.05) between well-watered and drought-stressed plants, suggesting an ability of plants to recover turgor after stress cessation. Altogether, our data support the hypothesis that young mahogany plants have the ability to satisfactorily tolerate or postpone drought.     

Chitosan as a biocontrol agent against the pinewood nematode (Bursaphelenchus xylophilus)

The pine wilt disease (PWD) is caused by Bursaphelenchus xylophilus and poses great environmental and economic challenges. Thus, the development of sustainable techniques for the control of this epidemic disease is of major importance. This work aimed at evaluating if the application of different molecular weight (MW) chitosans as a soil amendment could be used to control the PWD in maritime pine (Pinus pinaster, very susceptible to the disease) and stone pine (Pinus pinea, less susceptible). At the end of the experimental period (24 days after inoculation), P. pinaster and P. pinea untreated plants presented ca. 3825 ± 100 and 70 ± 47 nematodes, respectively. In P. pinaster, the high‐MW chitosan prompted the most drastic results, inducing a 21.9‐fold reduction in nematodes numbers, whereas in P. pinea, the most effective was the low MW chitosan, which reduced nematodes numbers up to 7‐fold, compared with untreated plants. P. pinea seems to be highly resistant to the disease, presenting nematode numbers up to 54.6‐fold lower than P. pinaster and less severe chlorophyll loss (ca. 2‐fold).     

Leaves from grafted Meliaceae species affect survival and performance of <Emphasis Type="Italic">Hypsipyla grandella</Emphasis> (Zeller) (Lepidoptera: Pyralidae) larvae

In order to determine their effects on growth and mortality of instar II Hypsipyla grandella (Zeller), larvae were fed with leaf disks taken from shoots of susceptible species (Cedrela odorata L. and Swietenia macrophylla King) scions grafted onto resistant ones (Khaya senegalensis Desr. A. Juss and Toona ciliata M. Roem.), from their reciprocal grafts, and from both intact and autografted plants. In addition, crude leaf extracts from the susceptible and resistant plants, as well as from C. odorata grafted onto T. ciliata plants, were tested on C. odorata leaf disks. Mortality was evaluated 2, 10, and 25 days after starting the bioassay. Leaf area consumed and weight gain per larva were assessed 2 days after starting bioassay. Time to reach pupation, pupal weight and length 1 day after pupation, and time to adult stage and appearance of wings were determined at the end of the bioassay. Plant species significantly affected mortality (P ≤ 0.04) throughout the test. Eighty to 100% of larvae fed leaf disks from intact T. ciliata and its autograft, or C. odorata onto T. ciliata and its reciprocal graft died in the first 2 days of evaluation. All other factors measured, except pupal weight and length, were also affected (P ≤ 0.01) by the leaf disks. Intact resistant plants and reciprocal grafted plants reduced leaf consumption and caused larval weight loss. Larvae fed on K. senegalensis grafted onto S. macrophylla extended by 8 days the time to pupa and to adult stages and induced abnormal wing formation compared to larvae fed intact leaves of C. odorata. Crude extracts from resistant plants equally affected larval survival and performance compared to crude extract from C. odorata grafted onto T. ciliata plants, and these extracts were more detrimental to larvae than those from susceptible species. This study demonstrated that grafting borer-susceptible species on resistant rootstocks can affect the survival and performance of instar II H. grandella larvae.     

Identification and pathogenicity of Alternaria alternata causing leaf spot and blight disease of Ailanthus excelsa in India

Alternaria leaf spot of Ailanthus excelsa is generally considered as minor disease in India. Recently, severe disease outbreaks were recorded in the nursery of the Forest Research Institute, Dehradun, progeny trial at Jhumpa, Haryana, and in a nearby farm field. Leaf symptoms included small circular, brown, necrotic spots with a chlorotic halo. With severe infections, leaf spots coalesced and resulted in leaf blight. A small‐spored Alternaria with concatenated conidia was isolated consistently from the leaf samples with spot symptoms. Sequence analyses of the internal transcribed spacer (ITS) region of ribosomal DNA (rDNA) and the translation elongation factor 1‐alpha (tef‐1α) gene region of two fungal isolates confirmed the species as A. alternata. In detached leaf assays, both isolates produced symptoms similar to those observed on the nursery/field‐grown plants. To validate the detached leaf assay result, pathogenicity was also demonstrated on whole plants in a glasshouse. Koch's postulates were fulfilled by re‐isolating A. alternata from the inoculated leaves. This work is the first to confirm that A. alternata is associated with leaf spot and blight disease of A. excelsa in India.     

Impacts of inoculation with Herpotrichia pinetorum,Gremmenia infestans and Gremmeniella abietina on Pinus nigra subsp. pallasiana and Cedrus libani seedlings in the field

Herpotrichia pinetorum, Gremmenia infestans and Gremmeniella abietina were inoculated onto 2‐year‐old Anatolian black pine (Pinus nigra subsp. pallasiana) and Taurus cedar (Cedrus libani) seedlings planted in a high mountain forest (1800 m a.s.l) in south‐western Turkey, to determine the effects of these fungi during winter. In June, 8 months after inoculation, 39.9% of experimental plants were dead and 20.4% of the surviving plants failed to flush. Gremmeniella abietina and H. pinetorum caused the most fatalities. Prevention of new shoot formation on surviving plants, however, was mainly an effect of G. abietina infections, although many surviving plants inoculated with G. infestans or H. pinetorum also failed to flush. All three pathogens had the potential to severely damage young plants of P. nigra subsp. pallasiana and C. libani growing at high elevations near to forests with heavy inoculum loads. The implications of this finding for P. nigra afforestations at high altitudes in Turkey are discussed. This study is also the first to report that G. infestans can infect and cause disease on young C. libani plants.     

Volatile organic compounds (VOC) as biomarkers for detection of Ceratocystis platani

Ceratocystis platani causes canker stain of plane trees, and it represents a serious disease of Platanus spp. both in the United States and Europe. Current chemical or biological controls do not effectively manage C. platani, so new preventive methods need to be developed in order to limit this pathogen spreading. In this work, we have characterized the main volatile organic compounds (VOC) emitted in vitro from pure cultures of C. platani and other common pathogenic fungal species of hosts plants growing in the same ecosystems as plane trees. We found that C. platani emitted a similar blend of VOC compared with phylogenetically similar species C. populicola. In particular, C. platani was characterized by emission of isoamyl acetate and isobutyl acetate while C. populicola by ethyl acetate and isobutyl acetate, which were not released by any of the other out‐group fungal species grown on the same medium. Moreover, following a targeted approach based on the main VOC found in vitro, we have successfully validated in vivo that VOC uniquely emitted by C. platani (i.e. isobutyl acetate along with isoamyl alcohol) were released from the bark of plane trees following C. platani inoculation. Our results highlight the possibility to exploit VOC emitted specifically by C. platani as biomarkers to recognize Platanus x acerifolia plants infected by this pathogen.     

Effect of host plants on development and reproduction of <Emphasis Type="Italic">Rhynchophorus ferrugineus</Emphasis> (Olivier) (Coleoptera: Curculionidae)

The development, survivorship and reproduction of red palm weevil Rhynchophorus ferrugineus, reared on five ornamental palm slices, were studied in the laboratory at constant temperature of 26°C. The developmental time of R. ferrugineus was 68.8 days on Washington palm (Washingtonia filifera), 74.1 days on Canary Island date palm (Phoenix canariensis), 82.1 days on Chusan palm (Trachycarpus fortunei), 85.4 days on pindo palm (Butia capitata) and 90.6 days on silver date palm (Phoenix sylvestris), respectively, and the developmental time on silver date palm was significantly longer than that on the other plants. The survival of immature R. ferrugineus ranged from 25.0 to 38.3%. Most mature larvae began to pupate at eighth-instar on Canary Island date palm and Washington palm, while on Chusan palm, Pindo palm and silver date palm, most of them began to pupate at ninth-instar. The mean lifetime fecundity of R. ferrugineus on Canary Island date palm, Chusan palm, Pindo palm, Washington palm and silver date palm was 267.8, 134.0, 109.8, 216.0, and 131.4 eggs, respectively, and lifetime fecundity on Canary Island date palm and Washington palm was significantly greater than that on the other plants. The intrinsic rate of natural increase (r _m ), net reproductive rate (R ₀) and mean generation time (T) were 0.038, 78.3 and 115.0 days on Canary Island date palm, 0.028, 33.1 and 125.5 days on Chusan palm, 0.029, 40.9 and 128.2 days on Pindo palm, 0.041, 64.0, 101.4 days on Washington palm, and 0.025, 30.6, 135.6 days on silver date palm, respectively. Based on population growth parameters, it is concluded that Canary Island date palm and Washington palm were the more suitable host plants and silver date palm was the least suitable host plant for R. ferrugineus.     

Modeling leaf maximum net photosynthetic rate of <Emphasis Type="Italic">Festuca pallescens</Emphasis>, the dominant perennial grass of Patagonian pine-based silvopastoral systems

The integrated relationship in a simple mechanistic model between the critical environmental factors controlling leaf photosynthesis of understory species would be a useful tool to optimize the management of the silvopastoral systems. Individual effect of leaf temperature, water stress and light environment over net maximum photosynthetic rate (Pmax) was evaluated on Festuca pallescens leaves grown in a silvopastoral system of two Pinus ponderosa canopy covers (350 and 500 trees ha⁻¹) and natural grassland. The aim was to integrate individual functions for Pmax against these environmental factors into a multiplicative model. We measured pre-dawn water potential (ψ _pd), leaf temperature and net photosynthetic rate (Pn), stomatal conductance (gs) and intercellular CO₂ concentration (Ci) as a function of photosynthetic photon flux density (PPFD). The highest Pmax under non-limiting conditions was 20.4 μmol CO₂ m⁻² s⁻¹ and was defined as standardized dimensionless Pmax _s  = 1 for comparison of environmental factors. The leaf temperature function showed an optimum range between 20.2 and 21.8°C where Pmax _s  = 1. Then, Pmax _s declined by an average 1 μmol CO₂ m⁻² s⁻¹ C⁻¹ from the optimum to 4.7 and 38.5°C. Pmax _s decreased at a rate of 9.49 μmol CO₂ m⁻² s⁻¹ MPa⁻¹ as water potential reaches −1.9 MPa and showed a lower slope as water potential decreased down to −4.3 MPa. The light environment was estimated from hemispherical photograph analysis. Pmax _s was 20% higher in leaves of open control plants than under the maximum tree canopy cover. The simple multiplicative model accounted for 0.82 of the variation in Pmax. Such a simple mechanistic model is the first step towards a more effective decision support tool.     

Molecular characterization of a phytoplasma associated with Euonymus bungeanus witches’ broom in China

Euonymus bungeanus plants exhibiting symptoms of abnormal branches, small leaves and phyllody, which is indicative of E. bungeanus witches’ broom (EbWB) disease, have recently been found in Beijing, China. A phytoplasma from symptomatic E. bungeanus plants was identified by 16S rRNA polymerase chain reaction (PCR) using the phytoplasma‐specific universal primer pair R16mF2/R16mR1. Inoculation of healthy E. bungeanus plants by grafting with diseased scions was also performed. The rp and secY genes of the EbWB phytoplasma were cloned and sequenced as was the 16S rRNA gene. Sequence and phylogenetic analyses of 16S rRNA, rp and secY genes indicated that the phytoplasma associated with E. bungeanus belongs to the 16SrV‐B, rpV‐C and secY‐C subgroup, the same subgroup as the jujube witches’ broom (JWB) phytoplasma that is widely distributed among jujube trees in China. Comparative analyses based on virtual restriction fragment length polymorphism (RFLP) showed that the EbWB phytoplasma is more closely related to another 16SrV‐B subgroup strain: RPWB (Robinia pseudoacacia witches’ broom). To the best of our knowledge, this is the first report of a witches’ broom phytoplasma in E. bungeanus in China, and the findings add a new cultivated plant species to the already broad natural host range of 16SrV‐B subgroup phytoplasmas.     

Wilt and die‐back of Eucalyptus spp. caused by Erwinia psidii in Brazil

A new disease of unknown bacterial aetiology has been observed in eucalyptus stands since 2009. It is characterized by die‐back, wilting and lesions on the branches, petiole and midrib in association with macroscopic and microscopic bacterial ooze. To date, this disease has been observed in stands of clonal Eucalyptus saligna, E. grandis and E. urophylla x E. grandis hybrids and in E. dunnii seedling plantations in the states of São Paulo, Rio Grande do Sul and Mato Grosso do Sul. Considering the economic importance of eucalyptus plantations and the potential losses caused by this disease, this study aimed to identify and characterize the causal agent. Thirty‐four strains were obtained from infected plants, which were collected in the field from four locations. The inoculation of detached leaves and intact rooted cuttings supported pathogenicity in eucalyptus. The phylogenetic analysis of four housekeeping genes (16S rDNA, gapA, recA and rpoB) as well as biochemical tests confirmed the identity of strains belonging to the species Erwinia psidii. This is the first report of E. psidii as the cause of wilt and die‐back in Eucalyptus spp. in Brazil.     

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.     

Genetic diversity of the myrtle rust pathogen (Austropuccinia psidii) in the Americas and Hawaii: Global implications for invasive threat assessments

Since the myrtle rust pathogen (Austropuccinia psidii) was first reported (as Puccinia psidii) in Brazil on guava (Psidium guajava) in 1884, it has been found infecting diverse myrtaceous species. Because A. psidii has recently spread rapidly worldwide with an extensive host range, genetic and genotypic diversities were evaluated within and among A. psidii populations in its putative native range and other areas of myrtle rust emergence in the Americas and Hawaii. Microsatellite markers revealed several unique multilocus genotypes (MLGs), which grouped isolates into nine distinct genetic clusters [C1–C9 comprising C1: from diverse hosts from Costa Rica, Jamaica, Mexico, Puerto Rico, and USA‐Hawaii, and USA‐California; C2: from eucalypts (Eucalyptus spp.) in Brazil/Uruguay and rose apple (Syzygium jambos) in Brazil; C3: from eucalypts in Brazil; C4: from diverse hosts in USA‐Florida; C5: from Java plum (Syzygium cumini) in Brazil; C6: from guava and Brazilian guava (Psidium guineense) in Brazil; C7: from pitanga (Eugenia uniflora) in Brazil; C8: from allspice (Pimenta dioica) in Jamaica and sweet flower (Myrrhinium atropurpureum) in Uruguay; C9: from jabuticaba (Myrciaria cauliflora) in Brazil]. The C1 cluster, which included a single MLG infecting diverse host in many geographic regions, and the closely related C4 cluster are considered as a “Pandemic biotype,” associated with myrtle rust emergence in Central America, the Caribbean, USA‐Florida, USA‐Hawaii, Australia, China‐Hainan, New Caledonia, Indonesia and Colombia. Based on 19 bioclimatic variables and documented occurrences of A. psidii contrasted with reduced sets of specific genetic clusters (subnetworks, considered as biotypes), maximum entropy bioclimatic modelling was used to predict geographic locations with suitable climate for A. psidii which are at risk from invasion. The genetic diversity of A. psidii throughout the Americas and Hawaii demonstrates the importance of recognizing biotypes when assessing the invasive threats posed by A. psidii around the globe.     

Effect of ivermectin on larval mortality and reproductive potential of <Emphasis Type="Italic">Albizia</Emphasis> foliage feeder, <Emphasis Type="Italic">Spirama retorta</Emphasis> Cramer (Lepidoptera: Noctuidae)

Toxicity of ivermectin (Ivecop-12), a derivative of avermectin B, produced by a soil actinomycete, Streptomyces avermitilis, was evaluated in laboratory against the larvae of Spirama retorta Cramer (Lepidoptera: Noctuidae), a major stenophagous insect defoliator of Albizia spp. (family Leguminosae) in nurseries and young plantations. The study was conducted with eight treatment concentrations of lethal and sub-lethal doses. Results revealed that ivermectin is highly toxic and induce larval mortality when applied separately on host plant leaves and larvae, and on leaves and larvae of the insect pest together. The nature of treatment affects the larval mortality. Treatment of host plant leaves alone as well as leaves together with larvae showed 100% mortality by the treatment of 0.075% concentration whereas only 95% larval mortality was recorded due to larval treatment by the concentration of 1.2%. The LC₅₀ value of the tested product was worked out to be 0.014, 0.170 and 0.012% for leaf and larval treatments separately and leaf and larval treatments together, respectively, against the insect pest. This clearly shows that ivermectin is more effective in larval killing when ingested through food. Further, the adults developed from treatments of sub-lethal concentrations and subsequently, when mated laid significantly (P < 0.05–0.01) less number of eggs and also showed significant (P < 0.05–0.01) reduction in hatching percentage compared to control. These observations suggest that the tested bioproduct, ivermectin, interfere physiological programming of larvae thereby causing alteration in fecundity and fertility of the target insect pest.