The ecological basis of boll weevil (Anthonomus grandis Boheman) management

The boll weevil (Anthonomus grandis Boheman), generally considered to be native to Mexico or Central America, spread into the southern United States of America in the late 1800s and seriously threatened the cotton industry. As there were no effective alternatives, pest control specialists studied the insect's ecology and advocated cultural practices that would disrupt its environment and maximize the benefits of natural biological and environmental controls. An ecologically orientated pest management scheme founded on cultural practices emerged well before suitable chemical control technology became available and allowed farmers to live with the weevil problem.Despite the ingenuity of the early management scheme, it frequently did not provide satisfactory boll weevil control gauged by present standards. Control of the pest thus shifted largely from an ecological to a chemical approach as effective synthetic organic insecticides became available after World War II. The chemical approach was successful for a number of years, but problems of insecticide-resistant strains of pests, secondary pest outbreaks, environmental quality, and increased costs of the insecticides have forced pest control specialists to re-emphasize the nonchemical techniques used widely against the boll weevil before World War II and to revive the ecological approach to weevil management.This article examines boll weevil ecology as related to management of the insect and reviews the status and prospects of ecologically-based weevil management techniques in the United States.     

Insektenpheromone

Pheromones — semiochemicals used by insects for intraspecific chemical communication — can be isolated and with special analytical techniques their chemical structure elucidated. With stereoselective synthesis methods, presented by the preparation of sex attractants and aggregating pheromones of moths and beetles, respectively, a synthetic access to compounds is given which can be used for behavior manipulation of insects. Aside the importance of these compounds for investigations of the sensoric process the possibility of their application in an integrated and biological pest control is discussed.     

Prenatal diagnosis of mosaic 4p – in a fetus with trisomy 21

Mosaicism for the Wolf-Hirschhorn syndrome, del(4)(p16), is extremely rare and has not been reported in association with a numerical chromosome abnormality. We report the prenatal diagnosis of mosaic del(4)(p16) and non-mosaic trisomy 21 in a 16-week female fetus. The pregnancy ended in spontaneous abortion at 34 weeks secondary to fetal demise. The fetus had features of both 4p – and trisomy 21.     

Prenatal diagnosis of herlitz junctional epidermolysis bullosa by amniocentesis

Herlitz junctional epidermolysis bullosa (HJEB) is a severe blistering disorder which usually results in death during infancy. We have previously shown that the anchoring filament protein laminin-5 (kalinin/nicein), which mediates keratinocyte attachment and dermal–epidermal cohesion, is abnormally expressed in individuals with HJEB. Laminin-5 was detected by Western blot analysis in amniotic fluid from 44 consecutive normal secondtrimester control pregnancies, but was undetectable in second-trimester amniotic fluid from four pregnancies with fetuses affected by HJEB. In one case of severe non-Herlitz JEB, laminin-5 was detected in both amniotic fluid and skin. In human amniotic fluid, the laminin-5 a3 subunit was processed to a major 165 kD species and a minor 145 kD species and the β2 subunit was partially processed to 105 kD. Although laminin-5 was covalently associated with laminin-6 (K-laminin) in amniotic membrane, no covalent interaction was detected in amniotic fluid. Laminin-5 from amniotic fluid strongly supported keratinocyte attachment. These results suggest that Western blot analysis of second-trimester amniotic fluid is useful in determining the prenatal diagnosis of HJEB and that laminin-5 may serve a physiologically important function in amniotic fluid.     

Prenatal exclusion of stickler syndrome

Stickler syndrome is an autosomal dominant disorder of the connective tissue which includes ocular and systemic manifestations. We report on a large kindred in which we were able to demonstrate very tight linkage between the disease and the type II collagen gene (COL2A1) (LOD score 3·91 at θ=0). In a family in which the father and one of his daughters were severely affected, DNA analysis from a chorionic villus sample demonstrated that the fetus possessed the normal allele of COL2A1. Thereafter a normal child was born.