No abstract

Fluorous biphasic chemistry enables the recovery of homogeneous catalysts but presents engineering challenges because of issues concerning phase contacting and solvent loss. The addition of gaseous CO2 to fluorous−organic biphasic systems results in a single homogeneous liquid phase at temperatures well below the upper critical solution temperature of the binary liquid mixture. This phenomenon is due to the high solubility of CO2 in both organic liquids and fluorocarbons, and it facilitates reactions and can also reduce fluorous solvent losses. We demonstrate two homogeneously catalyzed reactions, a hydrogenation and an epoxidation, which result in an enhancement in the turnover frequency of 70% and 50%, respectively, for the CO2-merged phase relative to the fluorous biphasic system. This creates new opportunities for the use of fluorous-sequestered catalysts.

Tunable solvents such as gas-expanded liquids offer unique opportunities as benign and economic reaction media. We have improved the turnover frequency of a water-soluble catalyst system by a factor of 85 for the hydroformylation of 1-octene by using a tunable solvent system, which also increases substrate solubility. In our approach, the reaction is run homogeneously in a miscible water-organic solution, and after reaction, CO 2 is used as a "miscibility switch" for efficient product and catalyst recovery. Two water-soluble ligands, TPPTS (tris(3-sulfophenyl)phosphine) and TPPMS ((3-sulfophenyl)diphenylphosphine), were compared to triphenylphosphine for hydroformylation activity of their rhodium complexes. The catalyst was recycled three times with no loss of activity.

Many species defend themselves against enemies using repellent chemicals. An important but unanswered question is why investment in chemical defence is often variable within prey populations. One explanation is that some prey benefit by cheating, paying no costs of defence, but gaining a reduced attack rate because of the presence of defended conspecifics. Two important assumptions about predator behaviour must be met to explain cheating as a stable strategy: first, predators increase attack rates as cheats increase in frequency; second, defended prey survive attacks better than non‐defended conspecifics. We lack data from wild predators that evaluate these hypotheses. Here, we examine how changes in the frequency of non‐defended ‘cheats’ affect predation by wild birds on a group of otherwise defended prey. We presented mealworm larvae that were either edible (‘cheats’) or unpalatable (bitter tasting), and varied the proportion of cheats from 0 to 1 by increments of 0.25. We found strong frequency‐dependent effects on the birds' foraging behaviour, with the proportion of prey attacked increasing nonlinearly with the frequency of cheats. We did not, however, observe that birds taste‐rejected defended prey at the site of capture. One explanation is that wild birds may not assess prey palatability at the site of capture, but do this elsewhere. If so, defended and undefended prey may pay high costs of initial attack and relocation away from ecologically favourable locations. Alternatively, defended prey may not be taste‐rejected because with acute time constraints, wild birds do not have time to make fine‐grained decisions during feeding. We discuss the data in relation to the evolutionary ecology of prey defences.

Aposematism is a well-known strategy in which prey defend themselves from predation by pairing defenses such as toxins, with warning signals that are often visually conspicuous color patterns. Here, we examine the possibility that aposematism can be induced in a host by colonies of infectious parasites in order to protect the parasites from the consequences of attacks on the host. Earlier studies show that avian predators are reluctant to feed on carcasses of host prey that are infected with the entomopathogenic nematode, Heterorhabditis bacteriophora. As the age of infection increases, the parasites kill and preserve the host and subsequently cause its color to change, becoming bright pink then red. Nematode colonies in dead hosts may also be vulnerable, however, to nocturnally active foragers that do not use vision in prey detection. Here, then we test a novel hypothesis that the nematode parasites also produce a warning odor, which functions to repel nocturnally active predators (in this case, the beetle Pterostichus madidus). We show that beetles decrease their feeding on infected insect prey as the age of infection increases and that olfactory cues associated with the infections are effective mechanisms for deterring beetle predation, even at very early stages of infection. We propose that "parasite-induced aposematism" from the nematodes serves to replace the antipredator defenses of the recently killed host. Because sessile carcasses are exposed to a greater range of predators than the live hosts, several alternative defense mechanisms are required to protect the colony, hence aposematic signals are likely diverse in such "parasite-induced aposematism."