PINE OIL: AN OVIPOSITION DETERRENT FOR THE ONION MAGGOT, DELIA ANTIQUA (MEIGEN) (DIPTERA: ANTHOMYIIDAE)

1987 ◽  
Vol 119 (7-8) ◽  
pp. 605-609 ◽  
Author(s):  
A. Javer ◽  
A.D. Wynne ◽  
J.H. Borden ◽  
G.J.R. Judd

AbstractPine oil (Norpine-65, Northwest Petrochemicals) was assessed as an oviposition deterrent for gravid female onion maggots, Delia antiqua (Meigen), in two types of laboratory experiments. When given a choice for 24 h between a control onion half treated with hexane and an onion half treated with pine oil in hexane, the females oviposited preferentially on or around the control onion half. In a no-choice experiment the females laid over three times as many eggs on or around solvent control onions as on or around onions treated with 1.0% pine oil. The DC50 (deterrent concentration50) was calculated to be 0.09%. The results suggest that pine oil (or its constituents) may have potential as an oviposition deterrent under field conditions.

1996 ◽  
Vol 128 (2) ◽  
pp. 351-352 ◽  
Author(s):  
Yaw A. Ntiamoah ◽  
John H. Borden

The cabbage maggot, Delia radicum (L.), is a major root-infesting pest of cruciferous crops (Davidson and Lyon 1979). Current control methods include soil drenches with fensulfothion, carbofuran, and chlopyrifos (Matthews-Geringer and Hough-Goldstein 1988). Partial deterrency of oviposition by cabbage maggots was achieved using turpentinesoaked stakes (Havukkala 1982), and 3,5-dimethoxy-4-hydroxycinnamica cid, produced in the frass of a lepidopteran pest of cabbage (Jones et al. 1988). A blend of three monoterpenes (3-carene, limonene, and p-cymene) was found by Ntiamoah et al. (1996) to be the major oviposition deterrent for the onion maggot, Delia antiqua (Meigen), in a commercial pine oil, Norpine 65 (Northwest Petrochemicals, Annacortes, Washington). Our objectives were to evaluate this blend, and a more complex blend containing three additional constituents, as oviposition deterrents in the laboratory for the cabbage maggot.


Behaviour ◽  
2011 ◽  
Vol 148 (2) ◽  
pp. 247-264 ◽  
Author(s):  
Masanori Kohda ◽  
Nobuhiro Ohnishi ◽  
Noboru Okuda ◽  
Tomohiro Takeyama ◽  
Omar Myint

AbstractFilial cannibalism, eating one's own viable offspring, is accepted as an adaptive response to trade-offs between current and future reproduction. Theoretical models predict that high mate availability may induce more filial cannibalism, but this prediction is rarely tested. To examine this prediction, we performed laboratory experiments using the nest breeding goby Rhinogobius flumineus. Subject males were allowed to mate with a gravid female and care for the broods. A separate gravid female housed in a small cage (stimulus-female) was shown to the subject males at one of three different points during the brood cycle: prior to spawning, within 1 day after spawning and 1 week after spawning. Empty cages were shown as a control. Males that were shown the stimulus-female before spawning cannibalised more eggs than control males. In contrast, males that were shown the stimulus-females after spawning cannibalised as few eggs as control males did. Additionally, males that were shown the stimulus-female prior to spawning did not court females more intensively than other males. Thus, we suggest that the presence of an additional mate, rather than energy expenditure associated with courtship directed toward an additional mate, can facilitate males to cannibalise their eggs.


BMB Reports ◽  
2006 ◽  
Vol 39 (6) ◽  
pp. 749-758 ◽  
Author(s):  
Bin Chen ◽  
Takumi Kayukawa ◽  
Antonia Monteiro ◽  
Yukio Ishikawa

Gene ◽  
2005 ◽  
Vol 347 (1) ◽  
pp. 115-123 ◽  
Author(s):  
Bin Chen ◽  
Takumi Kayukawa ◽  
Haobo Jiang ◽  
Antónia Monteiro ◽  
Sugihiko Hoshizaki ◽  
...  

Weed Science ◽  
1988 ◽  
Vol 36 (6) ◽  
pp. 818-823 ◽  
Author(s):  
Vicki W. McCusker ◽  
Horace D. Skipper ◽  
Joseph P. Zublena ◽  
Dewitt T. Gooden

Laboratory experiments were conducted to evaluate the biodegradation of14C-labeled butylate, cycloate, EPTC, pebulate, and vernolate in three butylate-history soils that had received three to eight applications of butylate under field conditions. After 20 days, biodegradation of butylate and EPTC was accelerated and had no lag phase in all three butylate-history soils. Butylate-adapted microorganisms were cross-adapted for EPTC and degraded EPTC as readily as butylate. Biodegradation of butylate and EPTC in Dothan soil without a butylate history exhibited a lag phase of 6 days after which14CO2was evolved at an exponential rate. This indicated that enhanced biodegradation was induced after one application of butylate or EPTC. Butylate-adapted microorganisms were cross-adapted for vernolate and pebulate in Dothan and pebulate in Wagram soils with a butylate history. Biodegradation of vernolate and pebulate was not enhanced in Varina butylate-history soil. After 20 days, there was no cross-adaptation for cycloate in any soil. These findings indicated that biodegradation of carbamothioates was influenced by soil type and previous carbamothioate use and that caution should be exercised in use of EPTC on fields of previous butylate use.


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