scholarly journals Dothistroma Needle Blight, Caused by Dothistroma septospora, of Pinus spp. in Vermont

Plant Disease ◽  
2000 ◽  
Vol 84 (6) ◽  
pp. 706-706 ◽  
Author(s):  
S. E. Pfister ◽  
S. Halik ◽  
D. R. Bergdahl

Dothistroma needle blight, caused by Dothistroma septospora (teleo-morph Mycosphaerella pini), is a serious foliage disease of pine species throughout the world. In the northeastern United States, the fungus has been reported from Pennsylvania, but not New York, New Jersey, or any of the New England states. It has been reported from the eastern provinces of Canada (Newfoundland, Quebec). During 1994 to 1998, stromatic conidomata consistent with descriptions of D. septospora were associated with needle blight symptoms on mature landscape pines at four locations (Jericho, Montpelier, Williamstown, Williston) and one Christmas tree farm (Barre) in Vermont. Pinus nigra was affected at four locations; P. mugo and P. ponderosa were affected at one location each. Severe foliar blight and defoliation occurred during successive years on P. nigra and P. mugo. Collections from each location and host were examined microscopically. Mean lengths and widths of 20 or more conidia from each of three collections of P. nigra (Barre, Montpelier, and Williston) were 2.3 × 25, 2.7 × 20, and 2.6 × 24 μm, respectively. Corresponding values for collections from P. mugo and P. ponderosa were 2.4 × 26 and 3.6 × 31 μm, respectively. All collections conformed to descriptions and illustrations of D. septospora (1). No ascigerous state was observed from 1994 to 1998. This is the first report of D. septospora in New England. Reference: (1) H. C. Evans. 1984. The Genus Mycosphaerella and Its Anamorphs Cercoseptoria, Dothistroma and Lecanosticta on Pines. Commonwealth Mycological Institute, Kew, England.

2010 ◽  
Vol 86 (4) ◽  
pp. 412-422 ◽  
Author(s):  
Alex J. Woods ◽  
Don Heppner ◽  
Harry H. Kope ◽  
Jennifer Burleigh ◽  
Lorraine Maclauchlan

BC’s forests have already faced two simultaneous, globally significant, epidemics linked to climate change; the Dothistroma needle blight epidemic in NW BC and the massive mountain pine beetle epidemic throughout the BC Interior. Building on these experiences, we have compiled our best estimates of how we believe other forest health agents may behave as climate change continues to influence our forests. We have drawn on literature from around the world but have focused on the situation in BC. We have made management recommendations based on what we have seen so far and what we expect to come.Key words: climate change, forest health, forest insects, forest pathogens, forest management, British Columbia


2010 ◽  
Vol 40 (8) ◽  
pp. 1653-1660 ◽  
Author(s):  
Miloš Ivković ◽  
Brian Baltunis ◽  
Washington Gapare ◽  
Jo Sasse ◽  
Gregory Dutkowski ◽  
...  

Pine needle blight, caused by Dothistroma septosporum (Dorog.) M. Morelet, is one of the most serious foliar diseases of Pinus spp. in Australia and New Zealand. In 16 Pinus radiata (D.Don.) progeny trials in northeastern Victoria, Australia, Dothistroma-caused defoliation varied widely among trials and assessment years, ranging from 5% to 65%. The estimated narrow sense heritability ranged from nonsignificant to as high as 0.69 with a median of 0.36. Spatial autocorrelation of residuals accounted for a significant proportion of residual variance, and that increased heritability estimates. Genetic correlation between defoliation scores at an early age and growth at a later age was negative with a median value of –0.39. Phenotypic correlation between defoliation and survival was low and negative with a median value of –0.11. Economic analyses indicated that at sites with a high risk of infection, the effect of reducing defoliation on profitability was comparable with that of increasing growth at sites free from infection. The genetic parameters and economic impacts of Dothistroma were used to derive selection indices and include resistance to defoliation into the current breeding objective for radiata pine.


Author(s):  
Peter A. Kopp

Hops, the cone of a climbing plant by the same name, are a key ingredient in beer. Brewers use hops to impart flavors and aroma in their malted concoctions, and they value the ingredient’s preservative properties. This chapter explains the global origins and botanical characteristics of the common hop, Humulus lupulus l., used in brewing. It then describes how brewing, and hop agriculture along with it, spread from Europe to temperate regions across the world. Hop growing reached North America along with the early English colonies and fared quite well. By 1800, New York and New England emerged as producers for the global economy.


2012 ◽  
Vol 50 (No. 7) ◽  
pp. 319-326 ◽  
Author(s):  
L. Jankovský ◽  
M. Bednářová ◽  
D. Palovčíková

Dothistroma needle blight caused by Mycosphaerella pini E. Rostrup was observed for the first time in the Czech Republic on an imported Pinus nigra Arnold in 1999. In 2000, it was also found in the open planting. During three years, it became an important pathogen of pines in the Czech Republic. Its occurrence was noticed in more than 50 localities, above all in the region of Moravia and Silesia and eastern Bohemia. In total, it was found on 10 species of pine (P. nigra Arnold, P.&nbsp;banksiana Lamb., <br />P. contorta Loudon, P. mugo Turra, P.&nbsp;leucodermis Ant., P. sylvestris L., P. cembra L., P. aristata Engelm., P.&nbsp;ponderosa P. et C.&nbsp;Lawson and P. jeffreyi Grev. et Balf.). Also Picea pungens &nbsp;Engelm. was noticed as a host species. In the Czech Republic, Pinus nigra is the most frequent host species of M. pini (80% localities) followed by Pinus mugo (27% localities). On Scots pine P. sylvestris, M. pini was noticed at two localities. The critical period for infection is in the Czech Republic from the second half of May until the end of June. The incubation period lasts about 2&ndash;4 months depending on climatic conditions. The first symptoms on the needles infected in the current year appear in August being clearly expressed from September to November.In the CR, Dothistroma needle blight spread probably with infected planting stock obtained from import at the end of the 80s and at the beginning of the 90s.


2012 ◽  
Vol 52 (No. 1) ◽  
pp. 30-36 ◽  
Author(s):  
M. Bednářová ◽  
D. Palovčíková ◽  
L. Jankovský

Dothistroma needle blight Mycosphaerella pini E. Rostrup and its anamorphic stage Dothistroma septospora (Dorog.) Morelet was detected for the first time in the territory of the Czech Republic in a consignment of imported plants of Austrian pine Pinus nigra Arnold in 1999. In 2000, it was also found on Pinus nigra in an open planting in a plantation of Christmas trees by the village of Jedovnice near Brno in South Moravia. In the Czech Republic, Dothi-stroma needle blight was identified on 13 species of pine. Pinus nigra Arnold and Pinus mugo Turra are the most frequent hosts. In addition to these species, Dothistroma needle blight was observed on Pinus ponderosa Douglas ex Lawson, Pinus jeffreyi Grev. et Balf, Pinus banksiana Lamb., Pinus contorta Douglas, Pinus rotundata Link, Pinus leucodermis Ant. and Pinus sylvestris L. Finds on Pinus aristata Engelm., Pinus rigida Mill., Pinus heldreichii H. Christ. and Pinus cembra L. var. sibirica (Du Tour) G. Don. are a certain rarity. These species are not mentioned anywhere as potential hosts of Dothistroma needle blight. As for the species of other genera Picea pungens Engelm., Picea abies L. Karst. and last but not least Picea schrenkiana Fisch. &amp; C. A. Mey were also observed as hosts. The host range of Dothistroma needle blight recorded in papers is noted as well.


Author(s):  
David Everett

I once took a graduate course, from a well-published and finely educated writer, on the topic of voice. In the first moments of the class, several of us audaciously asked the instructor to define the term. A few minutes into her answer, I sensed confusion in the classroom. After 10 more minutes of wandering discussion, it became clear that our teacher couldn't handle this most basic query. She knew it when she read it, she said to our amazement, but who could hope to define voice or its literary twin, style? Today, after years of teaching voice myself—and of continuing my own writing—I finally understand my instructor's confusion. While all writers crave an individual style, and while we yearn for a distinctive voice for ourselves or the subjects we profile, those goals remain among our greatest challenges, and even experienced practitioners can retreat into debates over their mystery. Many science writers also must contend with journalistic precepts that subjugate or even eliminate individual style. In this chapter I review the complications and examine the tools of voice and style, concluding with exercises that should help writers identify and hone their own. When writers for the New York Times or the Modern Language Association or the New England Journal of Medicine talk of style, they often mean the strict rules of spelling, punctuation, abbreviation, and other usage as set forth in hallowed style manuals. Style is also used, more colloquially, to describe writing according to purpose or profession: academic, scientific, journalistic, digital, bureaucratic, literary, postmodern, and so forth. For academics, style has classical roots in Aristotle, Cicero, and that granddaddy of Rhetoric, Hermogenes, who rated style as grand, middle, or plain. Writer Ben Yagoda, in his The Sound on the Page: Style and Voice in Writing (2004), defines style as how a writer “uses language to forge or reflect an attitude toward the world.” For the purpose of this chapter, let's define voice as a writer's personality on the page. Style is the personality imposed on our writing by outside rules and/or our own techniques and mindset. Voice is an individual writing personality, whether distinctively our own, one we recount or create, or, sometimes inescapably, both.


Forests ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 983
Author(s):  
Chiara Aglietti ◽  
Alessandra Benigno ◽  
Edoardo Scali ◽  
Paolo Capretti ◽  
Luisa Ghelardini ◽  
...  

In this work, we rechecked, using species-specific Loop mediated isothermal AMPlification (LAMP) diagnostic assays followed by sequencing of fungal isolates at the beta-2-tubulin (tub2) gene region, a historical and never confirmed report of Dothistroma needle blight (DNB) in the introduced Monterey pine (Pinus radiata D. Don) in the mountains in the extreme tip of southern Italy. The report dates back to the mid-1970s, and predates the molecular-based taxonomic revision of the genus Dothistroma that defined the species accepted today. In the fall of 2019, symptomatic needles of Monterey pine and Corsican pine (Pinus nigra subsp. laricio (Poir.) Palib. ex Maire) were sampled in the area of the first finding. The applied diagnostic methods revealed the presence of Dothistroma septosporum (Dorogin) M. Morelet on both pine species. In this way, we: (i) confirmed the presence of the disease; (ii) clarified the taxonomic identity of the causal agent now occurring at that site; (iii) validated the species-specific LAMP diagnostic protocol we recently developed for Dothistroma for use on a portable field instrument, and (iv) showed that the pathogen now also attacks the native P. nigra subsp. laricio, a species particularly susceptible to the disease, indigenous to the mountains of Calabria, which is one of the very few areas where the species’ genetic resources are conserved. Comparative genetic analysis of the rare populations of D. septosporum found in the central Mediterranean region and in the native range of P. nigra subsp. laricio could help to clarify the history of the spread of the pathogen in southern Europe and better evaluate the risk it poses to the conservation of native pine species.


Plant Disease ◽  
2014 ◽  
Vol 98 (6) ◽  
pp. 841-841 ◽  
Author(s):  
D. Piou ◽  
R. Ioos

Dothistroma needle blight (DNB), also known as red band needle blight, is an important fungal disease of Pinus spp. that occurs worldwide. On the basis of molecular and morphological studies of the anamorphic stage, Barnes et al. (1) showed that two closely related species were involved in DNB: Dothistroma septosporum (Dorog.) Morelet and D. pini Hulbary. D. septosporum (teleomorph: Mycosphaerella pini Rostr.) has a worldwide distribution and is reported as the species that caused past epidemics of DNB. This species is reported on more than 80 different pine species, and Pinus radiata D. Don (Monterey pine) is classified as a highly or moderately susceptible species, depending on the published sources (4). D. pini (telemorph: unknown) was initially found on needles of P. nigra J. F. Arnold collected from 1964 to 2001 in the north central United States (Minnesota, Nebraska, and Michigan). It was subsequently found in Ukraine and southwestern Russia, where it has been associated with the emergence of DNB on P. nigra subsp. pallasiana (Lamb.) Holmboe, in Hungary on P. nigra, and in Russia on P. mugo Turra (1). In France, D. pini was reported for the first time on P. nigra, and was sometimes found in association with D. septosporum on the same needles (3). Later on, a more intensive survey of DNB was launched in France and 216 stands of Pinus sp. were studied. D. septosporum and D. pini were detected in 133 and 123 stands, respectively. Both species co-occurred in 40 stands but D. pini was only found on P. nigra (subsp. laricio and austriaca) (2). Up to now, D. pini was therefore only reported on European pine species, mainly on the different allopatric subspecies belonging to the black pine complex and on one occasion on P. mugo, which belongs to the same section and subsection as P. nigra. In March 2011, typical symptoms of DNB (needles with orangey-red brown distal ends, dark red bands, and green bases; small and black fruit bodies within the bands) were observed in a 50- to 60-year old P. radiata stand of ~3 ha located in Pyrénées Atlantiques close to the Spanish border (1°36′08″ W, 43°19′51″ N). The density of pine was relatively low and patches of natural regeneration were present. Although nearly all of the trees showed DNB symptoms, less than 50% of their needles were affected by the disease. In this stand, needles showing typical DNB symptoms were randomly taken from four pines and mixed together to form a single sample for analysis. Total DNA was extracted from symptomatic needle pieces. The presence of D. pini was confirmed by a specific multiplex real-time PCR analysis using the D. pini-specific primers/probe combination DPtef-F1-/R1/-P1 (3), and by sequencing a D. pini-specific amplicon generated by another conventional PCR (3) using DPtef-F/DPtef-R primers (GenBank Accession KC853059) (3). D. septosporum was not detected in the sample. To our knowledge, this is the first report worldwide of D. pini on P. radiata, a pine species largely planted in Spain and in the Southern Hemisphere. This is also the first report of this pathogen on a non-European pine species. The original native range and the host range of D. pini remain unknown and there is currently no data about host preferences or aggressiveness on different pine species. References: (1) I. Barnes et al. For. Pathol. 41:361, 2011. (2) B. Fabre et al. Phytopathology 102:47, 2012. (3) R. Ioos et al. Phytopathology 100:105, 2010. (4) M. Watt et al. For. Ecol. Manage. 257:1505, 2009.


HortScience ◽  
1993 ◽  
Vol 28 (4) ◽  
pp. 254D-254
Author(s):  
Duane W. Greene ◽  
Wesley R. Autio

There is a general increase in interest in planting new apple cultivars. The loss of daminozide has provided an additional stimulus for growers in New England to find an alternative to McIntosh. Promising new apple cultivars have been identified from around the world and from breeding programs in Arkansas, British Columbia, New York, New Jersey and the PRI Program. Trees were propagated and planted in a cultivar evaluation block at the University of Massachusetts Horticultural Research Center. In 1992 we evaluated over 80 new cultivars. Fruit assessment consisted of laboratory analysis and visual and sensory evaluation. All cultivar were given an overall rating, and several were identified as being worthy of further evaluation. These apple cultivars include: Arlet, BC 9P 14-32, BC 8M 15-10, BC 17-30, Ginger Gold, Honeycrisp, Kinsei, NJ 55, NY 75414-1, and Sansa.


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