OCHROPLEURA IMPLECTA (LEPIDOPTERA: NOCTUIDAE), A NEW CUTWORM PEST OF CRANBERRIES

2000 ◽  
Vol 132 (3) ◽  
pp. 365-367
Author(s):  
Sheila M. Fitzpatrick ◽  
James T. Troubridge ◽  
Deborah Henderson

In 1997, larvae of the cutworm moth, Ochropleura implecta Lafontaine, caused economic damage to cranberries (Vaccinium macrocarpon Aiton; Ericaceae) on several neighbouring farms in Richmond (49° 10′N, 123°07′W), British Columbia, Canada. This is the first report of O. implecta on cranberries. Published host records for O. implecta include willow and a variety of herbaceous plants, such as clover and endive (Crumb 1956; Lafontaine 1998), but there are no reports of pest status on any crop. On the affected cranberry farms, larvae partially consumed unripe and ripe berries in July and August. On one farm, damaged fruit was downgraded from fresh fruit sales to the juice market, resulting in an estimated loss of $40 000 Can.

Author(s):  
D. W. Minter

Abstract A description is provided for Lophodermium oxycocci. Information is included on the disease, cranberry twig blight, caused by the organism, that can cause serious economic damage to commercial cranberry crops in Oregon and Washington. Some information on cultural and chemical control is given, along with details of its transmission, geographical distribution (Canada (British Columbia), USA (Alaska, Maine, Massachusetts, Michigan, New Jersey, Oregon and Washington), Russia, Czech Republic, Finland, France, Germany, UK, Poland, Sweden and Ukraine) and hosts (Vaccinium macrocarpon, Vaccinium sp. and V. oxycoccus).


2017 ◽  
Vol 24 (2) ◽  
pp. 31
Author(s):  
K. B. Simoglou ◽  
A. I. Anastasiades ◽  
J. Baixeras ◽  
E. Roditakis

In June 2015, infestations of sunflower crops by the bordered straw Heliothis peltigera (Lepidoptera: Noctuidae) were recorded in rural areas of the Regional Unit of Drama, N. Greece. Larval feeding-damage symptoms were observed on leaves and buds of sunflower plants, mostly at pre-flowering growth stages. Infestations were recorded in approximately 80% of the inspected sunflower fields, the infestation levels, however, were low (<5%) apparently resulting in no economic damage. The presence of H. peltigera has been reported in Southern and Central Europe, Canada, the Middle East and Africa, infesting several hosts. Infestations of sunflower crops have been reported in India, Pakistan and Sudan. To our knowledge, this is the first report of H. peltigera infestations on sunflower crops in Greece and possibly in Europe.


2010 ◽  
Vol 142 (2) ◽  
pp. 135-142 ◽  
Author(s):  
Peter J. Landolt ◽  
D. Thomas Lowery ◽  
Lawrence C. Wright ◽  
Constance Smithhisler ◽  
Christelle Gúedot ◽  
...  

AbstractLarvae of Abagrotis orbis (Grote) (Lepidoptera: Noctuidae) are climbing cutworms and can damage grapevines, Vitis vinifera L. (Vitaceae), in early spring by consuming expanding buds. A sex attractant would be useful for monitoring this insect in commercial vineyards. (Z)-7-Tetradecenyl acetate and (Z)-11-hexadecenyl acetate were found in extracts of female abdominal tips. In multiple field experiments, male A. orbis were captured in traps baited with a combination of these two chemicals but not in traps baited with either chemical alone. Males were trapped from mid-September to early October in south-central Washington and south-central British Columbia. Other noctuid moths (Mamestra configurata Walker, Xestia c-nigrum (L.), and Feltia jaculifera (Guenée)) were also captured in traps baited with the A. orbis pheromone and may complicate the use of this lure to monitor A. orbis. Abagrotis discoidalis (Grote) was captured in traps baited with (Z)-7-tetradecenyl acetate but not in traps baited with the two chemicals together.


Plant Disease ◽  
2014 ◽  
Vol 98 (5) ◽  
pp. 691-691 ◽  
Author(s):  
Y. H. Jeon ◽  
W. Cheon

Worldwide, Japanese yew (Taxus cuspidata Sieb. & Zucc.) is a popular garden tree, with large trees also being used for timber. In July 2012, leaf blight was observed on 10% of Japanese yew seedling leaves planted in a 500-m2 field in Andong, Gyeongsangbuk-do Province, South Korea. Typical symptoms included small, brown lesions that were first visible on the leaf margin, which enlarged and coalesced into the leaf becoming brown and blighted. To isolate potential pathogens from infected leaves, small sections of leaf tissue (5 to 10 mm2) were excised from lesion margins. Eight fungi were isolated from eight symptomatic trees, respectively. These fungi were hyphal tipped twice and transferred to potato dextrose agar (PDA) plates for incubation at 25°C. After 7 days, the fungi produced circular mats of white aerial mycelia. After 12 days, black acervuli containing slimy spore masses formed over the mycelial mats. Two representative isolates were further characterized. Their conidia were straight or slightly curved, fusiform to clavate, five-celled with constrictions at the septa, and 17.4 to 28.5 × 5.8 to 7.1 μm. Two to four 19.8- to 30.7-μm-long hyaline filamentous appendages (mostly three appendages) were attached to each apical cell, whereas one 3.7- to 7.1-μm-long hyaline appendage was attached to each basal cell, matching the description for Pestalotiopsis microspora (2). The pathogenicity of the two isolates was tested using 2-year-old plants (T. cuspidata var. nana Rehder; three plants per isolate) in 30-cm-diameter pots filled with soil under greenhouse conditions. The plants were inoculated by spraying the leaves with an atomizer with a conidial suspension (105 conidia/ml; ~50 ml on each plant) cultured for 10 days on PDA. As a control, three plants were inoculated with sterilized water. The plants were covered with plastic bags for 72 h to maintain high relative humidity (24 to 28°C). At 20 days after inoculation, small dark lesions enlarged into brown blight similar to that observed on naturally infected leaves. P. microspora was isolated from all inoculated plants, but not the controls. The fungus was confirmed by molecular analysis of the 5.8S subunit and flanking internal transcribed spaces (ITS1 and ITS2) of rDNA amplified from DNA extracted from single-spore cultures, and amplified with the ITS1/ITS4 primers and sequenced as previously described (4). Sequences were compared with other DNA sequences in GenBank using a BLASTN search. The P. microspora isolates were 99% homologous to other P. microspora (DQ456865, EU279435, FJ459951, and FJ459950). The morphological characteristics, pathogenicity, and molecular data assimilated in this study corresponded with the fungus P. microspora (2). This fungus has been previously reported as the causal agent of scab disease of Psidium guajava in Hawaii, the decline of Torreya taxifolia in Florida, and the leaf blight of Reineckea carnea in China (1,3). Therefore, this study presents the first report of P. microspora as a pathogen on T. cuspidata in Korea. The degree of pathogenicity of P. microspora to the Korean garden evergreen T. cuspidata requires quantification to determine its potential economic damage and to establish effective management practices. References: (1) D. F. Farr and A. Y. Rossman, Fungal Databases, Syst. Mycol. Microbiol. Lab. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ (2) L. M. Keith et al. Plant Dis. 90:16, 2006. (3) S. S. N. Maharachchikumbura. Fungal Diversity 50:167, 2011. (4) T. J. White et al. PCR Protocols. Academic Press, San Diego, CA, 1990.


Plant Disease ◽  
2005 ◽  
Vol 89 (6) ◽  
pp. 685-685 ◽  
Author(s):  
S. F. Shamoun ◽  
S. Zhao

Salal (Gaultheria shallon Pursh.) is an ericaceous, evergreen, and rhizomatous shrub that competes for nutrients and moisture with young conifers in low elevation, coastal British Columbia (BC). A survey was conducted on southern Vancouver Island, BC during the summer of 1999 to find fungal pathogens of salal that might serve as biocontrol organisms (3). Phoma exigua Desmaz. (isolate PFC2705) near Parksville, BC proved to be pathogenic on salal. Identification of PFC2705 at the Centraalbureau voor Schimmelcultures was based on morphology and ITS sequences (GenBank Accession No. AY927784). Pathogenicity was determined with 24 salal seedlings (3-month-old) by inoculating with mycelial suspensions (20% v/v) or conidial suspensions (1 × 106 conidia per ml in 0.5% potato dextrose broth). Inoculated seedlings were placed in plastic bags and incubated in a greenhouse (16 to 23°C with natural light). Plastic bags were removed after 2 days. Initial disease symptoms were observed 2 days after inoculation. Brown, sunken lesions appeared on the surface of young leaves and stems and extended quickly. All seedlings were killed within 14 days. Twelve control plants showed no disease symptoms. With diseased salal leaves incubated at 23°C with 12-h fluorescent light/dark and 100% relative humidity, pycnidia appeared on leaf surfaces within 5 days. Conidia were hyaline, ellipsoid, one-celled, sometimes two- to three-celled, 2.5 to 3.8 × 5 to 12.5 μm, with a rounded base; the colony was gray or dark gray on potato dextrose agar after 5 to 7 days. Reisolation from the inoculated diseased leaves produced a mycelial colony that shared the same growth and morphological characteristics as the initial isolate. Phyllosticta gaultheriae Ellis & Everh., a widely reported foliar pathogen of salal, is distinct morphologically from P. exigua (1). To our knowledge, this is the first report of P. exigua as a pathogen of salal in Canada (2). A voucher specimen has been deposited at the Pacific Forestry Center Herbarium (DAVFP No. 28735). References: (1) J. Bissett and S. J. Darbyshire. No. 275 in: Fungi Canadenses, 1984. (2) D. F. Farr et al. Fungi on Plants and Plant Products in the United States. The American Phytopathological Society. St. Paul. MN, 1989. (3) S. F. Shamoun et al. Can. J. Plant Pathol. 22:192, 2000.


1959 ◽  
Vol 39 (1) ◽  
pp. 34-44 ◽  
Author(s):  
R. Glendenning

Coast moles were studied and trapped from 1935 to 1945 at Agassiz, British Columbia. They cause economic damage in the lower Fraser Valley by injuring growing crops and by covering up to 15 per cent of the surface of a field with their hills.The moles ate almost any arthropod, annelid, or molluscan that they captured, but earthworms comprised 93 per cent of the stomach contents. Adults ate nearly twice their weight in earthworms daily, or 100–150 grams, representing more than 100 worms. The populations of moles apparently varied in proportion to those of the earthworms.The moles mated from January to early March. The young were born in March or April. Yearling females had two embryos; 2-year-old females had three; and mature females had four. Of 940 trapped during the winters, 45 per cent were over 1, and 6 per cent were over 3 years old. The average weight of mature 74 males was 74.3 ± 5.6 grams; the average weight of 30 mature females was 69.8 ± 4.1 grams.Natural control was ineffective. The disastrous Fraser River flood of 1948 lowered the numbers significantly, but recovery was rapid.Artificial controls tested included: poisons, caustic irritants, explosives, flooding, earthworm poisons, combinations of chemical fertilizers and irrigations, mechanical and chemical barriers, commercial mole destroyers, poison gases, deterrents, and traps. Only the last two were of value; crude flake naphthalene was a deterrent, and the scissors type was the most effective trap. In heavy infestations as many as three moles per man-hour were trapped. Naphthalene was expensive but protected small plots for up to 6 weeks. For economic control by trapping an area of 300 to 500 acres should be trapped in one season. Smaller areas are quickly reinfested, since the moles travel up to 1 mile.


Plant Disease ◽  
2012 ◽  
Vol 96 (3) ◽  
pp. 454-454 ◽  
Author(s):  
J. E. Munyaneza ◽  
V. G. Sengoda ◽  
L. Sundheim ◽  
R. Meadow

Carrot (Daucus carota) plants with symptoms resembling those associated with the carrot psyllid Trioza apicalis and the bacterium “Candidatus Liberibacter solanacearum” (1–4) were observed in 70 to 80% of commercial fields and experimental plots in southeastern Norway from late July to mid-September of 2011; all cultivars grown were affected with approximately 10 to 100% symptomatic plants per field. T. apicalis, a pest of carrot in northern and central Europe, including Norway, can cause as much as 100% crop loss and is associated with “Ca. L. solanacearum” (1–4). Symptoms on affected plants include leaf curling, yellow and purple discoloration of leaves, stunted growth of shoots and roots, and proliferation of secondary roots. Carrot plant samples were collected from five T. apicalis-infested fields in Ostfold, Vestfold, Oppland, and Hedmark counties. Total DNA was extracted from petiole and root tissues of 54 plants, including 27 symptomatic plants and 27 asymptomatic plants from four cultivars (Namdal, Panther, Romance, and Yukon) with the cetyltrimethylammonium bromide (CTAB) buffer extraction method (2,3). DNA samples were tested by PCR assay using primer pairs OA2/OI2c and CL514F/R to amplify a portion of 16S rDNA and rplJ/rplL ribosomal protein genes, respectively, of “Ca. L. solanacearum” (2,3). A 1,168-bp 16S rDNA fragment was detected in the DNA from 22 (81.5%) symptomatic plants and a 668-bp rplJ/rplL fragment was amplified from the DNA of 26 (96.3%) symptomatic and 5 (18.5%) asymptomatic plants, indicating the presence of liberibacter. No liberibacter was detected in the asymptomatic carrot plants with the primer pair OA2/OI2c. Amplicons from the DNA of four carrot root samples with each primer pair were cloned (pCR2.1-TOPO; Invitrogen, Carlsbad, CA) and three clones of each of the eight amplicons were sequenced (MCLAB, San Francisco, CA). BLAST analysis of the 16S rDNA consensus sequence from the carrot root tissues (GenBank Accession No. JN863097) showed 100% identity to those of “Ca. L. solanacearum” previously amplified from carrot (GU373048 and GU373049) and T. apicalis (GU477254 and GU477255) in Finland (2,3). The rplJ/rplL consensus sequence from the carrots (GenBank Accession No. JN863098) was 99% identical to the sequences of rplJ/rplL “Ca. L. solanacearum” ribosomal protein gene from carrots in Finland (GU373050 and GU373051). To our knowledge, this is the first report of “Ca. L. solanacearum” associated with carrot in Norway. This bacterial species has caused millions of dollars in losses to potato and several other solanaceous crops in North and Central America and New Zealand (1). This plant pathogen has also been reported from carrots and T. apicalis in Finland, where it has caused significant economic damage to carrot crops (2–4). References: (1) J. E. Munyaneza. Southwest. Entomol. 35:471, 2010. (2) J. E. Munyaneza et al. Plant Dis. 94:639, 2010. (3) J. E. Munyaneza et al. J. Econ. Entomol. 103:1060, 2010. (4) A. Nissinen et al. Entomol. Exp. Appl. 125:277, 2007.


Sign in / Sign up

Export Citation Format

Share Document