1967
DOI: 10.1111/j.1570-7458.1967.tb02457.x
|View full text |Cite
|
Sign up to set email alerts
|

The Ecology of Cold Hardiness in Different Populations of the Black Currant Gall Mite, Cecidophyopsis Ribis

Abstract: Population samples of C. ribis from eastern Norway, western Norway, and England, and cuttings of 5 black currant varieties were exposed for different periods to — 18.5° ± 0.5° C and mites also to 6°. Mite mortality, mite emigration, egg production at 6°, and bud burst of the cuttings, were observed. Marked differences were found between the mite populations both in their ability to produce eggs at 6°, and in cold hardiness at — 18.5°. Mortality during cold treatment was inversely related to mite density in dif… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
3
0
1

Year Published

1971
1971
2019
2019

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(4 citation statements)
references
References 6 publications
0
3
0
1
Order By: Relevance
“…The existence of geographical temperature races in insects and other organisms is well known and manifested in many ways (Andrewartha & Birch 1954;Mayr 1963;Bateman 1967;Taksdal 1967;Krebs 1972;Prosser 1973). Differences in the innate capacity for increase r^^, sometimes linked with measurements of temperature tolerance, have been used successfully by several authors to demonstrate the existence of temperature races in insects (Birch et al 1963;Lewontin & Birch 1966;Bateman 1967 Both S. oryzae dind S. granarius are regarded as species of oriental origin although the former is now typically a pest of sub-tropical to warm temperate regions and the latter a pest of temperate regions (Champ & Dyte 1976).…”
Section: The Development Of Cold-tolerancementioning
confidence: 99%
“…The existence of geographical temperature races in insects and other organisms is well known and manifested in many ways (Andrewartha & Birch 1954;Mayr 1963;Bateman 1967;Taksdal 1967;Krebs 1972;Prosser 1973). Differences in the innate capacity for increase r^^, sometimes linked with measurements of temperature tolerance, have been used successfully by several authors to demonstrate the existence of temperature races in insects (Birch et al 1963;Lewontin & Birch 1966;Bateman 1967 Both S. oryzae dind S. granarius are regarded as species of oriental origin although the former is now typically a pest of sub-tropical to warm temperate regions and the latter a pest of temperate regions (Champ & Dyte 1976).…”
Section: The Development Of Cold-tolerancementioning
confidence: 99%
“…There is much information available on the life cycle of the mite (Massee 1928;Behrens 1964;Taksdal 1967;Gajek 1997;Apenite et al 2012), the annual cycle of egg (Collingwood & Brock 1959;Csapo 1992) and mite content of galls (Smith 1960a(Smith , b, 1961Mitchell et al 2011), and the migration of mites from galls in spring in order to colonize new buds (Łabanowska & Gajek 1999;Cross & Ridout 2001). Although, it has been long recognized that the timing of the migration of the gall mite is not closely associated with a particular growth stage of the plant, commercial acaricide applications are still timed according to plant growth stage (Apenite et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…Lifecycle and biology. The lifecycle of the mite has been extensively studied by Massee (1928), Collingwood and Brock (1959), Smith (1960a, 1961) and Taksdal (1967) (Fig. 6).…”
mentioning
confidence: 99%