The Effect of Sulphur Dioxide on the Development of Pine Needle Blight Caused byRhizosphaera kalkhoffii Bubák (I). Die Wirkung von Schwefeldioxyd auf die Entwicklung vonRhizosphaera kalkhoffii Bubák an Kiefernnadeln (I)

1970 ◽  
Vol 43 (10) ◽  
pp. 159-159
Author(s):  
O. Chiba ◽  
K. Tanaka
IMA Fungus ◽  
2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Ariska van der Nest ◽  
Michael J. Wingfield ◽  
Paulo C. Ortiz ◽  
Irene Barnes

2016 ◽  
Vol 46 (5) ◽  
pp. 497-506 ◽  
Author(s):  
V. I. Siziba ◽  
M. J. Wingfield ◽  
D. Sadiković ◽  
M. S. Mullett ◽  
B. Piškur ◽  
...  

1960 ◽  
Vol 38 (2) ◽  
pp. 153-161 ◽  
Author(s):  
S. N. Linzon

Needle blight of eastern white pine (Pinus strobus L.) is characterized by an orange-red discoloration of the distal portions of current year needles. At Chalk River, Ontario, 600 seedlings and saplings of white pine were examined repeatedly throughout the 1957 and 1958 growing seasons for the appearance and development of needle blight symptoms. The first of these were faint pinkish spots on the stomata-bearing faces of needles in semimature (about four-week-old) tissue. These developed rapidly into orange-red bands which within a few days spread to the needle tips. Mature tissue was not susceptible to attack, so lesions which developed subsequently were always proximal, on younger tissues derived from basal meristems. Attacks which occurred in the early summer killed only limited areas at the tips of needles, whereas those that occurred when the needles were nearly full-grown involved most of their length. Needle blight incidence was confined to a few major outbreaks during one season and in each of these many trees developed typical symptoms at essentially the same time. Each of these major outbreaks of the disease occurred after 1 or more days of wet weather which was followed suddenly by a continuous sunny period. No microorganisms were isolated from tissues displaying the initial needle blight symptoms.The data with respect to the nature and occurrence of needle blight are believed to suggest that susceptibility to the unfavorable conditions which incite it is inherent in the individual and that differences in response among members of a local population depend on variations in susceptibility, rather than on a varying local predisposition among uniformly susceptible individuals. The blight is initiated in semimature leaf tissues only but then spreads distally throughout adjacent, more mature tissues with a similar pattern of breakdown.


Author(s):  
C. S. Millar

Abstract A description is provided for Lophodermella conjuncta. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Pinus mugo, P. nigra var. maritima, P. sylvestris. DISEASE: Pine needle blight leading to premature needle cast in plantations. No common name. GEOGRAPHICAL DISTRIBUTION: Europe (Estonian SSR, Finland, Great Britain, Sweden, Switzerland).


Author(s):  
D. W. Minter

Abstract A description is provided for Davisomycella ampla. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Pinus banksiana, P. contorta, P. strobus, P. pinaster, P. radiata. DISEASE: Jack pine needle blight. GEOGRAPHICAL DISTRIBUTION: North America (USA, Canada); South America (Brazil); New Zealand. TRANSMISSION: By air-borne ascospores.


1964 ◽  
Vol 96 (10) ◽  
pp. 1313-1322 ◽  
Author(s):  
W. H. Kearby ◽  
D. M. Benjamin

AbstractOutbreaks of Thecodiplosis piniresinosae Kearby apparently have occurred in North America since 1932 on Pinus resinosa (Ait.). Serious losses of new needles and some mortality of shoots resulted since 1957 in central Wisconsin. Fall browning caused by the midge is distinguished from needle blight and needle droop.Three larval stages and the pupa are described. Adults emerged in late May and oviposited on elongating shoots. Eggs hatched within a week and larvae mined into the bases of the fascicles, where they fed until early October. In October, mature larvae left the fascicles, dropped to the litter, and entered the soil to overwinter. Pupation and transformation to the adult occurred in the spring.One larva usually was present per fascicle during periods of low populations, but during outbreaks up to 11 larvae infested a single fascicle. A monothalmous or polythalmous gall-like enlargement was noticeable during the outbreak. Infested needles formed an abscission layer prematurely and dropped during the winter, 3 to 5 years before normal abscission. Stand conditions, age and spacing conducive to the buildup of midge outbreaks are discussed.


1996 ◽  
Vol 26 (3) ◽  
pp. 402-407 ◽  
Author(s):  
Gregory A. Carter ◽  
William G. Cibula ◽  
Tommy R. Dell

A field study determined an optimal approach for the remote sensing of a pine needle blight of unknown cause that occurs frequently in the southeastern United States. Needle spectral reflectance was measured in five pairs of slash pines (Pinuselliottii Engelm. var. elliottii), each comprising a blighted and a nonblighted tree. Reflectance of blighted needles generally was greater within the 400–700 nm wavelength range and less in the 720–850 nm range compared with nonblighted needles (p ≤ 0.050). The relative change in reflectance, or reflectance sensitivity to the blight, was greatest near 680 nm. As predicted by the reflectance sensitivity, a black and white digital image at 680 ± 5 nm revealed strong contrast of a blighted compared with a nonblighted tree; the blighted canopy was nearly white in the image, while the nonblighted canopy was dark grey. Contrasts were much less at 560 ± 5, 694 ± 3, and 700 ± 5 nm, in the panchromatic visible spectrum (410–740 nm), and at 760 ± 5 nm. Remote sensing of southeastern pine forests at 680 ± 5 nm ultimately could provide regional estimates of blight occurrence and distribution, and thus contribute to determining its cause.


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