Reduced alarm response by peach-potato aphids, Myzus persicae (Hemiptera : Aphididae), with knock-down resistance to insecticides (kdr) may impose a fitness cost through increased vulnerability to natural enemies

Termites were sampled using randomized soil pits in 64 cropping plots, each 25 x 25 m, forming an experimental agrisilvicultural system in both a 6- and an 18-year-old Terminalia ivorensis plantation, in which canopy cover, crop, cropping system and land preparation were the principal treatment variables. The treatments were established in April 1995 and sampling was carried out in November 1995, February 1996 and July 1996. A total of 82 termite species were found, of which 67 were soil-feeders. Overall termite abundance and the abundance of soil-feeders increased between November 1995 and July 1996, reaching a mean of nearly 6000 m -2 . Pooling termite data from these sampling dates, in the old plantation, the high canopy cover treatment (192 stems ha -1 ) had a greater abundance of termites, compared with the low canopy cover treatment (64 stems ha -1 ) and this effect was independent of crop type (plantain or cocoyam), cropping system (single stands or mixed crops) and land preparation (mulch retained or burned, plantain only). The young tree plantation (same tree densities as in the old plantation) showed no significant difference in termite abundance between high and low canopy (levels of tree foliage) densities, though the high canopy sheltered a greater number of termites. Analysis of covariance showed that crop yield (both plantain and cocoyam) was not directly linked to the abundance of all termite populations, but that the cocoyam yield was positively correlated with the abundance of soil-feeding termites (the majority in the assemblage) in the young plantation. This may be due to the beneficial conditioning of soil resulting from the foraging and construction activities of soil-feeders.

[1]  A. Devonshire,et al.  A sodium channel point mutation is associated with resistance to DDT and pyrethroid insecticides in the peach‐potato aphid, Myzus persicae (Sulzer) (Hemiptera: Aphididae) , 1999, Insect molecular biology.

[2]  A. Devonshire,et al.  Intensification of insecticide resistance in UK field populations of the peach-potato aphid, Myzus persicae (Hemiptera: Aphididae) in 1996 , 1998 .

[3]  M. Mugglestone,et al.  Evidence for a possible fitness trade-off between insecticide resistance and the low temperature movement that is essential for survival of UK populations of Myzus persicae (Hemiptera: Aphididae) , 1997 .

[4]  A. Devonshire,et al.  Use of biochemical and DNA diagnostics for characterising multiple mechanisms of insecticide resistance in the peach-potato aphid, Myzus persicae (Sulzer). , 1997 .

[5]  P. Usherwood,et al.  Functional analysis of a rat sodium channel carrying a mutation for insect knock‐down resistance (kdr) to pyrethroids , 1997, FEBS letters.

[6]  Christine M. Woodcock,et al.  Climate change may increase vulnerability of aphids to natural enemies , 1997 .

[7]  M. Kenward,et al.  Comparative survival of insecticide-susceptible and resistant peach-potato aphids, Myzus persicae (Sulzer) (Hemiptera: Aphididae), in low temperature field trials , 1996 .

[8]  J. Houghton,et al.  Climate change 1995: the science of climate change. , 1996 .

[9]  A. Devonshire,et al.  Insecticide-insensitive acetylcholinesterase can enhance esterase-based resistance in Myzus persicae and Myzus nicotianae , 1994 .

[10]  J. Carlson,et al.  Evidence that the Drosophila olfactory mutant smellblind defines a novel class of sodium channel mutation. , 1994, Genetics.

[11]  Christine Woodcock,et al.  The Chemical Ecology of Aphids , 1992 .

[12]  A. Devonshire,et al.  Seasonal variation of susceptible and resistant variants of Myzus persicae. , 1990 .

[13]  R. ffrench-Constant,et al.  Resistance Detection and Documentation: The Relative Roles of Pesticidal and Biochemical Assays , 1990 .

[14]  B. Tabashnik,et al.  Pesticide Resistance in Arthropods , 1990, Springer US.

[15]  R. ffrench-Constant,et al.  Changes in DNA methylation are associated with loss of insecticide resistance in the peach‐potato aphid Myzus persicae (Sulz.) , 1989 .

[16]  A. Devonshire,et al.  Molecular evidence that insecticide resistance in peach-potato aphids (Myzus persicae Sulz.) results from amplification of an esterase gene. , 1988, The Biochemical journal.

[17]  R. ffrench-Constant,et al.  Detection of insecticide resistance by immunological estimation of carboxylesterase activity in Myzus persicae (Sulzer) and cross reaction of the antiserum with Phorodon humuli (Schrank) (Hemiptera: Aphididae) , 1986 .

[18]  A. Devonshire,et al.  A carboxylesterase with broad substrate specificity causes organophosphorus, carbamate and pyrethroid resistance in peach-potato aphids (Myzus persicae) , 1982 .

[19]  D. A. Williams,et al.  Extra‐Binomial Variation in Logistic Linear Models , 1982 .

[20]  R. Blackman Variation in the photoperiodic response within natural populations of Myzus persicae (Sulz.). , 1971, Bulletin of entomological research.

[21]  S. Maddrell Secretion by the Malpighian Tubules of Rhodnius. The Movements of Ions and Water , 1969 .