Radiocarbon Dating: Fictitious Results with Mollusk Shells

Evidence is presented to show that modern mollusk shells from rivers can have anomalous radiocarbon ages, owing mainly to incorporation of inactive (carbon-14-deficient) carbon from humus, probably through the food web, as well as by the pathway of carbon dioxide from humus decay. The resultant effect, in addition to the variable contributions of atmospheric carbon dioxide, fermentative carbon dioxide from bottom muds, and, locally, of carbonate carbon from dissolving limestones, makes the initial carbon-14-activity of ancient fresh-water shell indeterminate, but within limits. Consequent errors of shell radiocarbon dates may be as large as several thousand years for river shells.     

Controlling and coordinating development in vector-transmitted parasites

Vector-borne parasites cause major human diseases of the developing world, including malaria, human African trypanosomiasis, Chagas disease, leishmaniasis, filariasis, and schistosomiasis. Although the life cycles of these parasites were defined over 100 years ago, the strategies they use to optimize their successful transmission are only now being understood in molecular terms. Parasites are now known to monitor their environment in both their host and vector and in response to other parasites. This allows them to adapt their developmental cycles and to counteract any unfavorable conditions they encounter. Here, I review the interactions that parasites engage in with their hosts and vectors to maximize their survival and spread.     

The catalytic cross-coupling of unactivated arenes

The industrially important coupling of aromatic compounds has generally required differential prefunctionalization of the arene coupling partners with a halide and an electropositive group. Here we report that palladium, in conjunction with a copper oxidant, can catalyze the cross-coupling of N-acetylindoles and benzenes in high yield and high regioselectivity across a range of indoles without recourse to activating groups. These reactions are completely selective for arene cross-coupling, with no products arising from indole or benzene homo-coupling detected by spectroscopic analysis. This efficient reactivity should be useful in the design of other oxidative arene cross-couplings as well.