Maximal species richness in Conus: diversity, diet and habitat on reefs of northeast Papua New Guinea

The gastropod genus Conus is shown to be among many marine taxa that attain maximal known diversity along the northeast coast of Papua New Guinea. Thirty-six species co-occurred on the reef platform fringing Laing Island in Hansa Bay, 33% more than previously documented on any single reef. Near Madang, 32 species occurred on four small reefs. Maximal density at both sites was 3/m², with overall density 0.1-0.2/m². Species richness, diversity, and general patterns of microhabitat use were similar at both, but composition differed markedly. Only 23 species were found at both sites, and proportional similarity was 44%. The most common species at each site were uncommon at the other. The diets of 34 species were determined; 26, including the most abundant, preyed exclusively on polychaetes. As on other Indo-Pacific reefs, species partitioned prey types more finely than substrate types. Among vermivores, a different polychaete dominated the diet of each predator. Other species specialized on an enteropneust, other gastropods, and fishes. Most prey were herbivores or deposit feeders, indicating that the major trophic role of Conus species in the reef community is as primary carnivores. The results suggest that species are not more specialized than where fewer congeners co-occur, but rather overlap somewhat more in resource use.     

Sequence-selective topoisomerase II inhibition by anthracycline derivatives in SV40 DNA: relationship with DNA binding affinity and cytotoxicity

Topoisomerase II mediated double-strand breaks produced by anthracycline analogues were studied in SV40 DNA. The compounds included doxorubicin, daunorubicin, two doxorubicin stereoisomers (4'-epimer and beta-anomer), and five chromophore-modified derivatives, with a wide range of cytotoxic activity and DNA binding affinity. Cleavage of 32P-end-labeled DNA fragments was visualized by autoradiography of agarose and polyacrylamide gels. Structure-activity relationships indicated that alterations in the chromophore structure greatly affected drug action on topoisomerase II. In particular, removal of substituents on position 4 of the D ring resulted in more active inducers of cleavage with lower DNA binding affinity. The stereochemistry between the sugar and the chromophore was also essential for activity. All the active anthracyclines induced a single region of prominent cleavage in the entire SV40 DNA, which resulted from a cluster of sites between nucleotides 4237 and 4294. DNA cleavage intensity patterns exhibited differences among analogues and were also dependent upon drug concentration. Intensity at a given site depended on both stimulatory and suppressive effects depending upon drug concentration and DNA sequence. A good correlation was found between cytotoxicity and intensity of topoisomerase II mediated DNA breakage.     

Mechanism of activation of Sepharose and Sephadex by cyanogen bromide

The mechanism of CNBr activation of polysaccharide resins like Sepharose and Sephadex has been elucidated using recently published analytical procedures for the determination of cyanate esters and imido carbonates. It was found that on agarose-based resins coupling of ligand occurs predominantly via cyanate esters, and not via imidocarbonates as in the case of Sephadex. This explains the different behaviours of Sepharose and Sephadex during CNBr activation.