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The aim of the present study was to better understand the cortical structures and neuronal processes involved in aversive differential trace conditioning in healthy subjects. According to previous findings in literature, we tested whether the stimulus preceding negativity (SPN) in an emotional trace-conditioning paradigm shows a frontocentral maximum reflecting affective anticipation, e.g. in the anterior cingulate, or a centroparietal maximum reflecting time estimation and sensory anticipation. Two distinct SPN intervals were analyzed, one during the presentation of the CS (comparable to delay conditioning) and another one after CS offset (trace conditioning). In the CS+ condition, where subjects anticipated the onset of an aversive electrical stimulus after CS+ offset, a significantly larger negativity than in the unpaired (CS-) condition was present. SPN revealed a sustained midcentral and posterior parietal negativity during both SPN intervals. Differences between the two analyzed SPN intervals pointed towards occipital activity being found in the first interval (delay), but not in the second (trace). Aversive conditioning paradigms with longer trace intervals seem to rely upon a similar activation pattern as cognitive stimulus anticipation.

Eight recombination-deficient (Rec(-)) mutants of Escherichia coli were studied. Progeny lines were obtained on solid media, by means of micromanipulation, and the colony-forming ability of individual cells was analyzed. Cells of all eight strains gave rise to colony-forming as well as non-colony-forming descendants ("lethal sectoring"). Lethal sectors, i.e., groups of non-colony-forming cells which originate from a common ancestor, appeared with frequencies per generation ranging between 4 and 20% in Rec(-) strains, whereas lethal sectors were rare in Rec(+) strains (less than 1%). A strain carrying a mutation (uvrA6) in one of the genes involved in pyrimidine dimer excision from deoxyribonucleic acid (DNA) showed twice as many lethal sectors per generation as a strain with the genotype uvrA(+). Similarly, a double mutant (AB2480, uvrA6, recA13) showed twice as much spontaneous lethal sectoring as the corresponding Rec(-) strain (uvrA(+), recA13). The kinetics of growth curves obtained in nutrient broth and the frequency of non-colony-forming units in stationary-phase broth cultures indicate clearly that lethal sectors occur in liquid cultures too. The causes for spontaneous lethal sectoring are unknown at present. It seems reasonable to assume that gene uvrA and the rec genes are somehow involved in the repair of spontaneously occurring DNA lesions, since a deficiency in this type of repair may cause lethal sectors. The extent to which spontaneous lethal sectoring (observed in all Rec(-) strains of E. coli studied) may contribute indirectly to the failure to form recombinants is discussed.