scholarly journals A New Cane Dieback Disease of Northern Highbush Blueberry in the United States Caused by Lasiodiplodia mediterranea

Plant Disease ◽  
2017 ◽  
Vol 101 (7) ◽  
pp. 1317-1317 ◽  
Author(s):  
M. S. Wiseman ◽  
M. Serdani ◽  
M. L. Putnam
Plant Disease ◽  
2005 ◽  
Vol 89 (9) ◽  
pp. 920-925 ◽  
Author(s):  
C. L. Xiao ◽  
R. J. Boal

Winter pears (Pyrus communis) in the United States are produced primarily in the Pacific Northwest. Potebniamyces pyri (anamorph Phacidiopycnis piri) is the causal agent of Phacidiopycnis rot, a recently reported postharvest disease on pears in the United States. Infection of fruit by P. pyri occurs in the orchard, and symptoms develop during storage. P. pyri was observed to be associated with cankers, dead bark, and twig dieback of pear trees. P. pyri was isolated from 40 to 50% of the twig samples exhibiting dieback symptoms from three commercial d'Anjou pear orchards, and 35% of dying bark samples from one orchard. However, little information is available regarding pathogenicity of P. pyri on pear trees. To determine the distribution of P. pyri, dying and dead bark samples were collected from pear orchards in various pear-producing areas in Oregon and Washington, and examined for presence of fruiting bodies (pycnidia or apothecia) of P. pyri. In the orchard, 2-year-old twigs were wounded using a sterile cork borer with or without spraying with a commercial aerosol tissue-freezing product at the wound sites. Wounds were then inoculated with either mycelial plugs from an agar medium or conidial suspensions of P. pyri. In a separate experiment, freshly made pruning wounds were inoculated with conidial suspensions of P. pyri. Canker development was monitored approximately monthly for up to 6 months after inoculation, at which time reisolation of P. pyri was attempted. P. pyri was found to be widespread in the Pacific Northwest. Incidence of trees infected by P. pyri based on presence of viable pycnidia in pear orchards ranged from 0 to 100%. Monthly tree inoculations in the orchard indicated that P. pyri in general did not cause cankers on non-cold-injured, wound-inoculated twigs, but apparently became established on cold-injured, wound-inoculated twigs and caused small cankers. Minor dieback developed on twigs inoculated at pruning wounds. At 6 months after inoculation, P. pyri was recovered from the majority of inoculated twigs. Thus, P. pyri appears to be a weak canker-causing pathogen on pear trees.


EDIS ◽  
2019 ◽  
Vol 2019 (2) ◽  
Author(s):  
Oscar E. Liburd ◽  
Douglas A. Phillips

Blueberry gall midge is a small fly native to North America that feeds on blueberries and cranberries. It can be found throughout the United States, including Florida, where its larvae feed on southern highbush blueberry and rabbiteye floral and vegetative buds. Reports of blueberry gall midge damage on southern highbush blueberry in Florida have become more common in recent years, in some cases significantly impacting yield where there was severe feeding damage to floral buds. This 3-page fact sheet written by Oscar Liburd and Doug Phillips and published by the UF/IFAS Department of Entomology and Nematology will inform growers how to scout for, identify, and control blueberry gall midge. http://edis.ifas.ufl.edu/in1239


Plant Disease ◽  
2011 ◽  
Vol 95 (2) ◽  
pp. 227-227 ◽  
Author(s):  
I. Y. Choi

This study was conducted to identify the causal organism of bark dieback disease of highbush blueberry (Vaccinium corymbosum L.) observed in Korea. Blueberry, a woody plant that is native to North America, belongs to the family Ericaceae and genus Vaccinium. Of the 400 species of blueberry in the world, most are distributed in the tropics of Malaysia and Southeast Asia. Highbush blueberry is abundantly grown in Canada and the United States and has become a popular commercial crop in Korea for products such as jam, wine, and sauce. Bark dieback disease of blueberry was found in Sunchang (<5% incidence), Jeollabuk-do, Korea in July 2009. Typical symptoms of the disease were blight and dieback on the stems with lesions extending along entire branches. Morphological examination revealed that the perithecia were of the globose type with a nipple, 155 to 490 (374.6) μm, and brown on the dead bark. Asci were bitunicate and clavate or cylindrical with dimensions of 63 to 125 × 16 to 20 μm and containing eight ascospores. Ascospores were of the long ovoid type with dimensions of 13.2 to 23.7 (17.98) × 25.4 to 41.1 (33.21) μm. From extracted genomic DNA, the internal transcribed spacer (ITS)-5.8S ribosomal DNA region was amplified with universal primers ITS1 (5′-TCCGTAGGTGAACCTGCGG-3′) and ITS4 (5′-TCCTCCGCTTATTGATATGC-3′). A BLAST search of GenBank with the ITS sequence revealed that the Sunchang isolate (GenBank Accession No. HQ384217) had 99 to 100% sequence identity with the following Botryosphaeria dothidea accessions: FJ517657, AJ938005, FJ478129, FJ171723, and AJ938004. Phylogenetic analysis with the Sunchang isolate, B. dothidea strains, and related species revealed that the B. dothidea isolate and strains comprised a monophyletic group distinguished from other Botryosphaeria spp. including B. ribis, B. parva, B. protearum, B. lutea, B. australis, B. rhodina, B. obtuse, and B. stevensii (2). On the basis of morphological and molecular results, the isolate was identified as B. dothidea (Moug.) Ces. & De Not. A culture of B. dothidea isolate was grown on potato dextrose agar (PDA) for 10 days. A 5-mm plug was inoculated into stem wounds created with a No. 2 cork borer in 20 2-year-old disease-free blueberry plants grown in a greenhouse. Six plants inoculated with only PDA plugs served as noninoculated controls. The wounds were covered with Parafilm. After 3 months, the Parafilm was removed and black lesions were observed at the fungal inoculation sites, while no lesion was observed on the control plants. To complete Koch's postulates, the fungus was reisolated from the lesions and confirmed to be B. Dothidea (1). There is an urgent need to determine the spread of this disease in Korea, estimate the losses, and develop methods for reducing damage through biological and eco-friendly cultural control methods. References: (1) D. Jurc et al. Plant Pathol. 55:299, 2006. (2) B. Slippers et al. Mycologia 96:83, 2004.


Author(s):  
A. Hakam ◽  
J.T. Gau ◽  
M.L. Grove ◽  
B.A. Evans ◽  
M. Shuman ◽  
...  

Prostate adenocarcinoma is the most common malignant tumor of men in the United States and is the third leading cause of death in men. Despite attempts at early detection, there will be 244,000 new cases and 44,000 deaths from the disease in the United States in 1995. Therapeutic progress against this disease is hindered by an incomplete understanding of prostate epithelial cell biology, the availability of human tissues for in vitro experimentation, slow dissemination of information between prostate cancer research teams and the increasing pressure to “ stretch” research dollars at the same time staff reductions are occurring.To meet these challenges, we have used the correlative microscopy (CM) and client/server (C/S) computing to increase productivity while decreasing costs. Critical elements of our program are as follows:1) Establishing the Western Pennsylvania Genitourinary (GU) Tissue Bank which includes >100 prostates from patients with prostate adenocarcinoma as well as >20 normal prostates from transplant organ donors.


Author(s):  
Vinod K. Berry ◽  
Xiao Zhang

In recent years it became apparent that we needed to improve productivity and efficiency in the Microscopy Laboratories in GE Plastics. It was realized that digital image acquisition, archiving, processing, analysis, and transmission over a network would be the best way to achieve this goal. Also, the capabilities of quantitative image analysis, image transmission etc. available with this approach would help us to increase our efficiency. Although the advantages of digital image acquisition, processing, archiving, etc. have been described and are being practiced in many SEM, laboratories, they have not been generally applied in microscopy laboratories (TEM, Optical, SEM and others) and impact on increased productivity has not been yet exploited as well.In order to attain our objective we have acquired a SEMICAPS imaging workstation for each of the GE Plastic sites in the United States. We have integrated the workstation with the microscopes and their peripherals as shown in Figure 1.


2001 ◽  
Vol 15 (01) ◽  
pp. 53-87 ◽  
Author(s):  
Andrew Rehfeld

Every ten years, the United States “constructs” itself politically. On a decennial basis, U.S. Congressional districts are quite literally drawn, physically constructing political representation in the House of Representatives on the basis of where one lives. Why does the United States do it this way? What justifies domicile as the sole criteria of constituency construction? These are the questions raised in this article. Contrary to many contemporary understandings of representation at the founding, I argue that there were no principled reasons for using domicile as the method of organizing for political representation. Even in 1787, the Congressional district was expected to be far too large to map onto existing communities of interest. Instead, territory should be understood as forming a habit of mind for the founders, even while it was necessary to achieve other democratic aims of representative government.


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