First Report of Lymphocystis in the Family Gerreidae: Caitipa MojarrasDiapterus rhombeusfrom La Parguera, Puerto Rico

1996 ◽  
Vol 8 (2) ◽  
pp. 176-179 ◽  
Author(s):  
Lucy Bunkley-Williams ◽  
John M. Grizzle ◽  
Ernest H. Williams
2009 ◽  
Vol 45 (2-3) ◽  
pp. 151-167 ◽  
Author(s):  
K. Ryan-Mishkin ◽  
J. P. Walsh ◽  
D. R. Corbett ◽  
M. B. Dail ◽  
J. A. Nittrouer
Keyword(s):  

Author(s):  
M. Rodríguez

Abstract A description is provided for Meliola mangiferae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: Meliola mangiferae, as with the family Meliolaceae in general, is found on living leaves parasitizing the epidermis and sometimes deeper tissues, but without production of obvious disease symptoms. HOSTS: Mangifera indica, M. rigida and Mangifera sp. (Hansford, 1961). GEOGRAPHICAL DISTRIBUTION: Brazil, British Guiana, Costa Rica, Cuba, India, Indonesia (Java), Jamaica, Malaysia, Panama, Philippines, Puerto Rico, Surinam, Trinidad & Tobago, Venezuela. Meliola mangiferae is found in practically all areas of mango cultivation, with the exception of Africa and Australia (Hansford, 1961). TRANSMISSION: By air-borne ascospores.


2017 ◽  
Vol 18 (1) ◽  
pp. 17-18 ◽  
Author(s):  
Consuelo Estévez de Jensen ◽  
Ismael E. Badillo-Vargas ◽  
Galen Frantz ◽  
H. Charles Mellinger ◽  
William W. Turechek ◽  
...  

Tomato chlorotic spot virus (TCSV) has recently been detected in tomato, bell pepper, jimsonweed, and lettuce in Puerto Rico. Observations of weeds and additional crops in 2015 and 2016 revealed TCSV-like symptoms. Testing of these symptomatic plants identified three new hosts of TCSV in Puerto Rico: erect spiderling (Boerhavia erecta); Asian spiderflower (Cleome viscosa); and sweet chili pepper (Capsicum chinense).


2016 ◽  
Vol 37 (2) ◽  
pp. 729
Author(s):  
Rodrigo Vieira da Silva ◽  
Dalila Sêni de Jesus ◽  
Brenda Ventura de Lima e Silva ◽  
Bruno Eduardo Cardozo de Miranda ◽  
João Pedro Elias Gondim

Miconia albicans (Melastomataceae), whose common name is canela-de-velha, is a native plant of the tropical region that is abundant in the Cerrado biome. A nematode species was found parasitizing M. albicans, causing severe deformation and gall-like structures on the infected leaves and inflorescences. Morphological, morphometric and molecular characterizations identified the nematode as Ditylenchus gallaeformans. This nematode has great potential as a biocontrol agent of plants in the family Melastomataceae, which are invasive weeds in ecosystems of the Pacific Islands. This is the first report of D. gallaeformans parasitizing M. albicans in the Cerrado of the state of Goiás.


2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Reem M. Hassan ◽  
Dina M. Bassiouny ◽  
Yomna Matar

Kocuria kristinae is opportunistic Gram-positive cocci from the family Micrococcaceae. It is usually considered part of the normal flora that rarely is isolated from clinical specimens. Here, we report a case of Kocuria kristinae bacteremia; to the best of our knowledge, this is the first report from Egypt.


Plant Disease ◽  
2009 ◽  
Vol 93 (4) ◽  
pp. 425-425 ◽  
Author(s):  
W.-L. Rao ◽  
Z.-K. Zhang ◽  
R. Li

Plants in the genus Prunus of the family Rosaceae are important fruit and ornamental trees in China. In June of 2007, sweet cherry (Prunus avium) trees with mottling and mosaic symptoms were observed in a private garden near Kunming, Yunnan Province. Twenty-four samples, six each from sweet cherry, sour cherry (P. cerasus), flowering cherry (P. serrulata), and peach (P. persica) were collected from trees in private and community gardens in the area. The peach and sour and flowering cherry trees did not show any symptoms. Total nucleic acids were extracted using a cetyltrimethylammoniumbromide (CTAB) extraction method, and the extracts were tested for the following eight viruses by reverse transcription (RT)-PCR: American plum line pattern virus, Apple chlorotic leaf spot virus, Cherry green ring mottle virus, Cherry necrotic rusty mottle virus, Cherry virus A (CVA), Little cherry virus 1, Prune dwarf virus, and Prunus necrotic ringspot virus. Only CVA was detected in two symptomatic sweet cherry trees by RT-PCR with forward (5′-GTGGCATTCAACTAGCACCTAT-3′) and reverse (5′-TCAGCTGCCTCAGCTTGGC-3′) primers specific to an 873-bp fragment of the CVA replicase gene (2). The CVA infection of the two trees was confirmed by RT-PCR using primers CVA-7097U and CVA-7383L that amplified a 287-bp fragment from the 3′-untranslated region (UTR) of the virus (1). Amplicons from both amplifications were cloned and sequenced. Analysis of the predicted amino acid sequences of the 873-bp fragments (GenBank Accession Nos. EU862278 and EU862279) showed that they were 98% identical with each other and 97 to 98% with the type isolate of CVA from Germany (GenBank Accession No. NC_003689). The 286-bp sequences of the 3′-UTR (GenBank Accession Nos. FJ608982 and FJ608983) were 93% identical with each other and 93 to 98% with the type isolate. The sequence indicated that the three isolates were very similar and should be considered to be the same strain. CVA is a member of the genus Capillovirus in the family Flexiviridae and has been previously reported in Europe, North America, and Japan. The contribution of CVA to the symptoms observed and its distribution in China remain to be evaluated. To our knowledge, this is the first report of CVA in sweet cherry in China. References: (1) M. Isogai et al. J. Gen. Plant Pathol. 70:288. (2) W. Jelkmann. J. Gen. Virol. 76:2015, 1995.


Plant Disease ◽  
2004 ◽  
Vol 88 (6) ◽  
pp. 681-681
Author(s):  
A. Garibaldi ◽  
D. Bertetti ◽  
M. L. Gullino

Aquilegia flabellata Sieb. and Zucc. (columbine) is a perennial garden species belonging to the family Ranunculaceae. During the summer of 2003, a severe outbreak of a previously unknown powdery mildew was observed in several gardens near Biella (northern Italy). Upper surfaces of leaves were covered with a white mycelium and conidia, and as the disease progressed infected leaves turned yellow and died. Foot cell was cylindric and appressorium lobed. Conidia were hyaline, ellipsoid, and measured 31.2 to 47.5 × 14.4 to 33 μm (average 38.6 × 21.6 μm). Fibrosin bodies were not present. Cleistothecia were globose, brown, had simple appendages, ranged from 82 to 127 (average 105) μm in diameter, and contained one to two asci. Ascocarp appendages measured five to eight times the ascocarp diameter. Asci were cylindrical (ovoidal) and measured 45.3 to 58.2 × 30.4 to 40.2 μm. Ascospores (three to four per ascus) were ellipsoid or cylindrical and measured 28.3 to 31.0 × 14.0 to 15.0 μ;m. On the basis of its morphology, the pathogen was identified as Erysiphe aquilegiae var. aquilegiae (1). Pathogenicity was confirmed by gently pressing diseased leaves onto leaves of five, healthy A. flabellata plants. Five noninoculated plants served as controls. Inoculated and noninoculated plants were maintained in a garden where temperatures ranged between 20 and 30°C. After 10 days, typical powdery mildew symptoms developed on inoculated plants. Noninoculated plants did not show symptoms. To our knowledge, this is the first report of the presence of powdery mildew on Aquilegia flabellata in Italy. E. communis (Wallr.) Link and E. polygoni DC. were reported on several species of Aquilegia in the United States (2), while E. aquilegiae var. aquilegiae was previously observed on A. flabellata in Japan and the former Union of Soviet Socialist Republics (3). Specimens of this disease are available at the DIVAPRA Collection at the University of Torino. References: (1) U. Braun. Nova Hedwigia, 89:700, 1987. (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) K. Hirata. Host Range and Geographical Distribution of the Powdery Mildews. Faculty of Agriculture, Niigata University, 1966.


2018 ◽  
Vol 18 (2) ◽  
pp. 78-80
Author(s):  
Lalawmawia Sailo ◽  
Lawmsangzuala Chhangte ◽  
Rochamliana Aineh ◽  
H. Lalthanzara

In this paper we report the first confirmed sighting of chestnut-flanked white-eye Zosterops erythropleurus (Swinhoe, 1863) from Mizoram and first photographic report from India. chestnut-flanked white-eye belongs to the family Zosteropidae and is a resident of Cambodia, China, Hongkong, Korea, Democratic People’s Republic of Korea, Laos, Myanmar, Russia, Thailand and Vietnam. In the Indian Sub-continent this is the only sighting report for this species and details of sightings and habitat are discussed.


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