Access the full text.
Sign up today, get DeepDyve free for 14 days.
L. Schroeder (2001)
Tree Mortality by the Bark Beetle Ips typographus (L.) in storm-disturbed standsIntegrated Pest Management Reviews, 6
P. Price, P. Barbosa, J. Schultz (1987)
Chapter 12 – The Role of Natural Enemies in Insect Populations
B. Aukema, K. Raffa (2004)
Does aggregation benefit bark beetles by diluting predation? Links between a group‐colonisation strategy and the absence of emergent multiple predator effectsEcological Entomology, 29
J. Schultz, I. Baldwin (1982)
Oak Leaf Quality Declines in Response to Defoliation by Gypsy Moth LarvaeScience, 217
E. Christiansen (2009)
Ips/Ceratocystis-infection of Norway spruce: what is a deadly dosage?1Journal of Applied Entomology, 99
Christiansen Christiansen (1985)
Ips / Ceratocystis ‐infection of Norway spruce: what is a deadly dosage?Zeitschrift für Angewandte Entomologie, 99
O. Anderbrant, F. Schlyter, G. Birgersson (1985)
Intraspecific competition affecting parents and offspring in the bark beetle ips typographusOikos, 45
E. Christiansen, R. Waring, A. Berryman (1987)
Resistance of conifers to bark beetle attack: Searching for general relationshipsForest Ecology and Management, 22
T. Tscharntke, A. Gathmann, I. Steffan‐Dewenter (1998)
Bioindication using trap‐nesting bees and wasps and their natural enemies: community structure and interactionsJournal of Applied Ecology, 35
L. Schroeder (1999)
Population levels and flight phenology of bark beetle predators in stands with and without previous infestations of the bark beetle Tomicus piniperdaForest Ecology and Management, 123
E. Forsse (1989)
Migration in bark beetles with special reference to the spruce bark beetle Ips typographus.
E. Forsse, C. Solbreck (2009)
Migration in the bark beetle Ips typographus L.: duration, timing and height of flightJournal of Applied Entomology, 100
P. Brodmann, C. Wilcox, S. Harrison (1997)
Mobile parasitoids may restrict the spatial spread of an insect outbreakJournal of Animal Ecology, 66
Maron Maron, Harrison Harrison, Greaves Greaves (2001)
Origin of an insect outbreak: escape in space or time from natural enemiesOecologia, 126
A. Kruess, T. Tscharntke (1994)
Habitat Fragmentation, Species Loss, and Biological ControlScience, 264
O. Anderbrant (1990)
Gallery construction and oviposition of the bark beetle Ips typographus (Coleoptera: Scolytidae) at different breeding densitiesEcological Entomology, 15
(1995)
Catalogus Coleopterum Sueciae . Naturhistoriska riksmuseet
J. Cronin, J. Reeve, R. Wilkens, P. Turchin (2000)
The pattern and range of movement of a checkered beetle predator relative to its bark beetle preyOikos, 90
(1975)
Windthrow in forests – it ’ s causes and effect of forestry measures
Peter Mulock, E. Christiansen (1986)
The threshold of successful attack by Ips typographus on Picea abies: a field experimentForest Ecology and Management, 14
H. Godfray (1993)
Parasitoids: Behavioral and Evolutionary Ecology
Kung-Sik Chan, H. Tong, R. Boonstra, S. Boutin, C. Krebs, E. Post, M. O’Donoghue, N. Yoccoz, M. Forchhammer, J. Hurrell
Dynamical Role of Predators in Population Cycles of a Forest Insect : An Experimental Test
(2001)
Origin of an insect
J. Weslien (1992)
The arthropod complex associated with Ips typograpfius (L.) (Coleoptera, Scolytidae): species composition, phenology, and impact on bark beetle productivityEntomologica Fennica, 3
L. Schroeder (1999)
Prolonged development time of the bark beetle predator Thanasimus formicarius (Col.: Cleridae) in relation to its prey species Tomicus piniperda (L.) and Ips typographus (L.) (Col.: Scolytidae)Agricultural and Forest Entomology, 1
(1971)
Sex ratio in Ips typographus L . ( Col . , Scolytidae )
Erik Göthlin, L. Schroeder, Å. Lindelöw (2000)
Attacks by Ips typographus and Pityogenes chalcographus on Windthrown Spruces (Picea abies) During the Two Years Following a Storm FellingScandinavian Journal of Forest Research, 15
P. Hedgren, L. Schroeder (2004)
Reproductive success of the spruce bark beetle Ips typographus (L.) and occurrence of associated spe
E. Christiansen, A. Bakke (1988)
The Spruce Bark Beetle of Eurasia
M. Kenis, B. Wermelinger, J. Grégoire (2007)
Research on Parasitoids and Predators of Scolytidae – A Review
D. Strong, J. Lawton, S. Southwood (1987)
INSECTS ON PLANTS. COMMUNITY PATTERNS AND MECHANISMS.
S. Nouhuys, I. Hanski (2002)
Colonization rates and distances of a host butterfly and two specific parasitoids in a fragmented landscapeJournal of Animal Ecology, 71
J. Weslien, E. Annila, A. Bakke, B. Bejer, H. Eidmann, K. Narvestad, A. Nikula, H. Ravn (1989)
Estimating risks for spruce bark beetle (Ips typographus (L.)) damage using pheromone‐baited traps and treesScandinavian Journal of Forest Research, 4
K. Ryall, L. Fahrig (2005)
Habitat loss decreases predator/prey ratios in a pine-bark beetle systemOikos, 110
A. Kruess, T. Tscharntke (2000)
Species richness and parasitism in a fragmented landscape: experiments and field studies with insects on Vicia sepiumOecologia, 122
Peter Turchin, Andrew Taylor, John Reeve (1999)
Dynamical role of predators in population cycles of a forest insect: An experimental testScience, 285 5430
J. Weslien, L. Schroeder (1999)
Population levels of bark beetles and associated insects in managed and unmanaged spruce standsForest Ecology and Management, 115
M. Rossiter (1992)
2 – The Impact of Resource Variation on Population Quality in Herbivorous Insects: A Critical Aspect of Population Dynamics
L. Schroeder (2003)
Differences in responses to α-pinene and ethanol, and flight periods between the bark beetle predators Thanasimus femoralis and T. formicarius (Col.: Cleridae)Forest Ecology and Management, 177
B. Wermelinger (2002)
Development and distribution of predators and parasitoids during two consecutive years of an Ips typographus (Col., Scolytidae) infestationJournal of Applied Entomology, 126
L. Schroeder, Å. Lindelöw (2002)
Attacks on living spruce trees by the bark beetle Ips typographus (Col. Scolytidae) following a storm‐felling: a comparison between stands with and without removal of wind‐felled treesAgricultural and Forest Entomology, 4
F. Menalled, Richard Smith (2009)
Plant-Provided Food for Carnivorous Insects: a Protective Mutualism and Its Applications, 35
Hedgren Hedgren, Schroeder Schroeder (2004)
Reproductive success of the spruce bark beetle. Ips typographus (L.) and occurrence of associated insects: a comparison between standing beetle‐killed trees and cut treesForest Ecology and Management, 203
B. Wermelinger (2004)
Ecology and management of the spruce bark beetle Ips typographus—a review of recent researchForest Ecology and Management, 202
Forsse Forsse, Solbreck Solbreck (1985)
Migration in the bark beetle Ips typographus L. duration, timing and height of flightZeitschrift für Angewandte Entomologie, 100
C. Bouget, P. Duelli (2004)
The effects of windthrow on forest insect communities: a literature reviewBiological Conservation, 118
F. Lieutier, K. Day, A. Battisti, J. Grégoire, H. Evans (2004)
Bark and Wood Boring Insects in Living Trees in Europe, a Synthesis
(2001)
Vejledning I styrkelse af stormfasthed og sundhed i Nåletraebevoksninger [Guidelines for the degree of storm vulnerability and vitality in coniferous stands
1 Populations of the spruce bark beetle, Ips typographus (L.), are known to grow rapidly in storm‐disturbed stands as a result of relaxation from intraspecific competition. In the present study, it was tested whether a second mechanism, escape in space from natural enemies, also contributes to the rapid population increase. 2 The experiment was conducted during the initiation phase of five local outbreaks of I. typographus triggered by a storm‐disturbance in November 1995 in southern Sweden. 3 The impact of natural enemies on the ratio of increase (number of daughters per mother) of I. typographus was compared pairwise between disturbed stands with high numbers of storm‐felled trees and undisturbed stands without wind‐felled trees. 4 Enemy impact was assessed by comparing the ratio of increase in uncaged (exposed to enemies) and caged (protected from enemies) bolts colonized by I. typographus prior to being placed in the stands. The experiment was conducted in the second and third summers after the storm‐felling. 5 Enemy impact was about twice as high in stands without wind‐felled trees compared with in stands with wind‐felled trees in the second summer whereas there was no significant difference between the stand types in the third summer. 6 The result demonstrates that spatial escape from enemies contributes to the rapid population growth of I. typographus after storm‐disturbances.
Agricultural and Forest Entomology – Wiley
Published: May 1, 2007
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.