FEEDING BEHAVIOUR OF THE FIRST-INSTAR CHORISTONEURA FUMIFERANA AND CHORISTONEURA PINUS PINUS (LEPIDOPTERA: TORTRICIDAE)

1999 ◽  
Vol 131 (1) ◽  
pp. 79-84 ◽  
Author(s):  
A. Retnakaran ◽  
W.L. Tomkins ◽  
M.J. Primavera ◽  
S.R. Palli
Keyword(s):  
Fluorescent Protein ◽  
Choristoneura Fumiferana ◽  
Glass Tube ◽  
Choristoneura Pinus ◽  
Jack Pine Budworm ◽  
Occlusion Bodies ◽  
Early Instar ◽  
Choristoneura Pinus Pinus ◽  
Green Fluorescent ◽  
Red Dye

AbstractWe have discovered that, contrary to the long-held belief, 1st-instar spruce budworm, Choristoneura fumiferana Clemens, do feed. They display red alimentary tracts if they are provided with diet containing the red dye amaranth. They graze on the surface of balsam fir needles sprayed with rhodamine and ingest the fluorescent material, which can be detected in the frass pellets deposited inside the hibernacula. When emerging 1st instars were allowed to crawl on the inside surface of a glass tube coated with the polyhedral inclusion bodies of a recombinant C. fumiferana virus containing the gene for the green fluorescent protein, the larvae showed the characteristic green fluorescence, indicating that not only had they ingested the occlusion bodies but also the virus had replicated and infected different tissues. Similar results were obtained with the jack pine budworm, Choristoneura pinus pinus Freeman, which has an identical life history. The advantages of early-instar intervention to minimize defoliation by using control agents such as the ecdysteroid agonist, tebufenozide (RH-5992, Mimic® formulation), are discussed.

Association of within-tree jack pine budworm feeding patterns with canopy level and within-needle variation of water, nutrient, and monoterpene concentrations

1998 ◽  
Vol 28 (2) ◽  
pp. 228-233 ◽  
Author(s):  
Kimberly F Wallin ◽  
Kenneth F Raffa
Keyword(s):  
Pinus Banksiana ◽  
Jack Pine ◽  
Larval Feeding ◽  
Feeding Patterns ◽  
Choristoneura Pinus ◽  
Jack Pine Budworm ◽  
Choristoneura Pinus Pinus ◽  
Zinc Levels ◽  
Calcium Iron ◽  
Relative Differences

The possibility that uneven within-tree feeding patterns by jack pine budworm (Choristoneura pinus pinus Freeman) larvae could be related to underlying variation in host jack pine (Pinus banksiana Lamb.) foliar water, nutrient, and monoterpene contents was considered. Choristoneura pinus pinus feeds disproportionately in the upper portion of the canopy and almost exclusively on the basal portions of needles. Within needles, the distribution of water, several nutrients, and monoterpenes varied significantly between the distal and basal sections. Water, nitrogen, sulfur, manganese, and zinc levels occurred in higher concentrations in the distal section of the needle, which would not be predicted based on C. pinus pinus feeding patterns. Phosphorus, potassium, calcium, iron, and copper were significantly higher in the basal section. Although the latter differences might be predicted based on C. pinus pinus feeding patterns, they were not strong (ranging from 7.8% to 36.4% relative differences, as compared with 10.7%-50.0% relative differences in the former group). By contrast, concentrations of foliar monoterpenes were more strongly associated with known feeding patterns of C. pinus pinus. These relative differences ranged from myrcene (26.8%) to limonene (44.79%). Thus, foliar differences affecting within-needle feeding selection appear more associated with allelochemicals than nutrients or water. In contrast with the within-needle associations between larval feeding and foliar chemistry, no associations between upper and lower canopy foliage were observed. Water, nutrients, and monoterpenes were evenly distributed across the upper and lower canopy locations. Thus, differential feeding between canopy locations cannot be explained by foliar constituents. Rather, it is more likely explained by other environmental factors, such as proximity to and density of reproductive and vegetative shoots.

Infection of the Jack Pine Budworm, Choristoneura pinus Freeman, with a Nuclear Polyhidrosis Virus of the Spruce Budworm, Choristoneura fumiferana (Clemens), (Lepidoptera: Tortricidae)

1960 ◽  
Vol 92 (12) ◽  
pp. 906-908 ◽  
Author(s):  
G. R. Stairs
Keyword(s):  
Nuclear Polyhedrosis Virus ◽  
Choristoneura Fumiferana ◽  
Spruce Budworm ◽  
Jack Pine ◽  
Choristoneura Pinus ◽  
Jack Pine Budworm ◽  
Polyhedrosis Virus ◽  
Nuclear Polyhedrosis

A nuclear polyhedrosis virus has been isolated from the spruce budworm, Choristoneura fumiferana (Clemens) (Bergold, 1949; Bird, 1949; Bergold, 1951; Bird and Whalen, 1954; Bird, 1959), but no similar virus has been recovered from the jack pine budworm, Choristoneura pinus Freeman. Since these two species are very closely related (Smith, 1953) it was of interest to determine if C. pinus is susceptible to the C. fumiferana virus.

scholarly journals The ecological interaction of the mountain pine beetle and jack pine budworm in the boreal forest

2010 ◽  
Vol 86 (6) ◽  
pp. 766-774 ◽  
Author(s):  
Lindsay J. Colgan ◽  
Nadir Erbilgin
Keyword(s):  
Climate Change ◽  
Boreal Forest ◽  
Mountain Pine Beetle ◽  
Dendroctonus Ponderosae ◽  
Jack Pine ◽  
Mountain Pine ◽  
Choristoneura Pinus ◽  
Pine Beetle ◽  
Jack Pine Budworm ◽  
Choristoneura Pinus Pinus

As climate change facilitates the range and host expansion of insect species into new ecosystems, the development of newstrategies for managing and preventing biological invasion is receiving considerable interest. In recent years, the range ofthe mountain pine beetle (Dendroctonus ponderosae Hopkins) has expanded from lodgepole pine-dominated forests eastof the Rocky Mountains into lodgepole x jack pine hybrid forest of western Alberta, and may soon invade jack pine forestsof the boreal. Our understanding of factors contributing colonization of jack pine by mountain pine beetle is far fromcomplete and several factors may limit its spread in these forests, including tree resistance and competitors. Among these,the jack pine budworm (Choristoneura pinus pinus Freeman) is one of the most important insect enemies of jack pine andan outbreak defoliator that potentially weakens jack pine trees, which may make them more susceptible to MPB attacks.To develop effective management strategies in the face of the short-run impacts of climate change, we need an in-depthunderstanding of factors influencing establishment and survival of the beetle in jack pine forests.Key words: Choristoneura pinus pinus, Dendroctonus ponderosae, jack pine, range expansion, invasion biology, climatechange in the boreal forest, conifer-mediated interactions, tree induced defences, tripartite interactions

scholarly journals Autographa californica multiple nucleopolyhedrovirus ORF 23 null mutant produces occlusion-derived virions with fewer nucleocapsids

2009 ◽  
Vol 90 (6) ◽  
pp. 1499-1504 ◽  
Author(s):  
Ian-Ling Yu ◽  
Doug Bray ◽  
Ying-Chu Lin ◽  
Oliver Lung
Keyword(s):  
Fluorescent Protein ◽  
Autographa Californica ◽  
Dapi Staining ◽  
Recombinant Viruses ◽  
Multiple Nucleopolyhedrovirus ◽  
Gfp Fluorescence ◽  
Occlusion Bodies ◽  
Green Fluorescent ◽  
And Control ◽  
Autographa Californica Multiple Nucleopolyhedrovirus

Two envelope fusion protein gene homologues have been identified in the baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV). AcMNPV GP64 protein is fusogenic and essential for propagation and pathogenicity. The F homologue (Ac23) is not essential, is fusion-incompetent in standard assays, but contributes to faster host death. Here, we show that occlusion bodies (OBs) from Ac23null mutants and control viruses do not differ significantly in size and the number of occlusion-derived virions (ODVs) contained; however, Ac23null OBs had a much higher percentage of ODVs with a single nucleocapsid (44.6 %) than the near-isogenic control (11.3 %). Infection of Sf9 cells with Ac23–green fluorescent protein (gfp)-expressing recombinant viruses showed Ac23–gfp fluorescence overlapping perinuclear DAPI staining at later times, a pattern not observed with GP64. These results suggest that F proteins have evolved functions beyond envelope fusion and play a different role from that of GP64 in viruses that contain both proteins.

PARASITISM IN SUSTAINED AND COLLAPSING POPULATIONS OF THE JACK PINE BUDWORM, CHORISTONEURA PINUS PINUS FREE. (LEPIDOPTERA: TORTRICIDAE), IN ONTARIO, 1985–1987

1991 ◽  
Vol 123 (5) ◽  
pp. 1065-1075 ◽  
Author(s):  
V.G. Nealis
Keyword(s):  
Population Studies ◽  
Spruce Budworm ◽  
Jack Pine ◽  
Larval Stages ◽  
Northwestern Ontario ◽  
Choristoneura Pinus ◽  
Jack Pine Budworm ◽  
Choristoneura Pinus Pinus

AbstractSixteen species of parasitoids were found attacking outbreak and collapsing populations of the jack pine budworm, Choristoneura pinus pinus Free. (Lepidoptera: Tortricidae), in several plots in northeastern and northwestern Ontario. The patterns of parasitism were similar among widely separated plots with only a few species consistently dominating the parasitoid fauna. The greatest difference in the pattern of parasitism was between sustained and collapsing infestations. Collapsing populations of jack pine bud-worm were associated with relatively high levels of parasitism by Meteorus trachynotus Vier. (Hymenoptera: Braconidae) and Lypha setifacies (West.) (Diptera: Tachinidae) which attacked the late larval stages of the budworm. The results are discussed in comparison with other jack pine budworm studies and with spruce budworm population studies.

NUCLEOPOLYHEDROVIRUS PATHOLOGY IN SPRUCE BUDWORM LARVAE

2000 ◽  
Vol 132 (5) ◽  
pp. 581-590 ◽  
Author(s):  
J.W. Barrett ◽  
T.R. Ladd ◽  
M.J. Primavera ◽  
A. Retnakaran ◽  
S.S. Sohi ◽  
...  
Keyword(s):  
Fluorescent Protein ◽  
Fat Body ◽  
Choristoneura Fumiferana ◽  
Spruce Budworm ◽  
Temporal And Spatial Distribution ◽  
Tracheal System ◽  
Tracheal Epithelial Cells ◽  
Multiple Nucleopolyhedrovirus ◽  
Temporal And Spatial ◽  
Green Fluorescent

AbstractChoristoneura fumiferana (Clemens) (Lepidoptera: Tortricidae) multiple nucleopolyhedrovirus (CfMNPV) expressing green fluorescent protein was used to study aspects of nucleopolyhedrovirus infection in the spruce budworm. The temporal and spatial distribution of fluorescence indicated that the virus infected the midgut, entered the tracheal system, and traveled to the epidermis, fat body, and muscles. In contrast to Autographa californica (Speyer) (Lepidoptera: Noctuidae) multiple nucleopolyhedrovirus (AcMNPV) infection, hemocytes from infected C. fumiferana did not exhibit fluorescence until after CfMNPV had passed from the midgut into the tracheae. Therefore the role of hemocytes may be limited during CfMNPV infection. Also the fluorescence pattern spread from the tracheolar cells to tracheal epithelial cells throughout the tracheal system. Our results indicate that the temporal and spatial events involved in CfMNPV infection of C. fumiferana larvae are consistent with those observed in other lepidopteran hosts infected with AcMNPV Minor deviations between these two systems may be attributed to differences in virulence, infection rate, and possibly host range of the virus.

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