Some anthropometric studies of the femur of the male West Malaysian Chinese

Measurements and indices were made on 120 male West Malaysian Chinese femora. The findings are compared with appropriate ones from some Eastern and Western series. The Chinese femur is smaller than all the other groups listed except for the Japanese femur. There is a high degree of significance between the maximum and bicondylar lengths of the Chinese femur against those of the Australian aborigine, Maori and White American. The head of the femur is greater in the Maori and White American than the Chinese. The platymeric index is nearly as high as the White American. The difference in the robusticity index of the femur between the Australian aborigine, Maori, White American and the present series is small. The collodiaphyseal angle of the Chinese femur is large being greater than the Australian aborigine, Finn and White American. The angle of torsion of 11.8° is within the range for Westerners with a high incidence of retroversion unlike the Australian aborigine and Maori where no retroversion is seen. Although most of the means of the measurements and indices of the femur show a highly significant difference between the present series and some of the other groups listed there is a wide overlap for measurements of the Chinese femur to be used for racial identification.     

Allozyme variation in rye,Secale cereale L.

Summary Eleven samples of eight European commercial varieties of winter rye were examined at eight polymorphic enzyme loci. Genotype frequencies fitted Hardy-Weinberg expectations at all loci in all samples studied. Of the total genetic diversity recorded at the 8 loci, only 7% was expressed between varieties. Allele frequency differences between varieties were, however, sufficient to allow a characterization of each variety by a specific set of allele frequencies. Using subsets of the original data, it could be demonstrated that all pairs of varieties but one still showed significant allozyme differences, when only 4 loci were screened in samples half the original size of 200 individuals. Even when only one locus was analyzed, all varieties but two were distinguishable, but this diagnostic locus was not identical in all pairwise comparisons.     

Experimental taxonomy of Bulinus (Gastropoda: Planorbidae): the West and North African species reconsidered, based upon an electrophoretic study of several enzymes per individual

Horizontal starch gel electrophoresis was used to score mobilities of seven different enzymes in species of Bulinus from North and West Africa. An account of the intra- and inter-population variation observed was given. Based on the data obtained it was suggested that enzymic data should be used as taxonomic characters in parallel with morphological and anatomical characters. It is suggested that enzymic characters could be used to place taxa into synonymy if the data are collected in such a way that one can write up an enzyme profile for the single individual. The nine taxa of Bulinus known to occur in North and West Africa were revised, the taxon B. jousseaumei was synonymized with B. globosus , and the two taxa B. guernei and B. rohlfsi were synonymized with B. truncatus. As a result of the revision only six species could be recognized as valid from the area, these being B. forskalii, B. globosus, B. senegalensis, B. truncatus, B. ugandae and B. umbilicatus. Finally, some enzymic characters are suggested that may be used for a reliable identification of these morphologically very difficult taxa.     

Effect of herbicides butachlor, 2,4-D and oxyfluorfen on enzyme activities and CO2 evolution in submerged paddy field soil

Summary Identification ofRhizobium trifolii strains using intrinsic antibiotic resistance and serology was performed. Unknown strains, generated by mixing known strains in a common broth, always reacted with only one antiserum but showed variable intrinsic antibiotic resistance patterns. All unknowns were rapidly and unambiguously identified by the immunological double diffusion technique, while 33% of the unknowns were either unidentifiable or identified incorrectly when resistance to various antibiotics was measured. It is concluded that serology is less variable than instrinsic antibiotic resistance when strains ofR. trifolii are identified.     

Biology of long slender land planarians (Turbellaria) in Tokyo and environs

The common short-bodied species of Bipalium does not fragment, but individuals of two newly discovered long-bodied species — B. nobile Kawakatsu & Makino, 1982, and B. multilineatum Makino & Shirasawa, 1983 — do regularly fission, usually behind the mouth or genital pore. Some experimental regenerates of these species form rings by adhesion of the anterior with the posterior cut surface. We found two other forms of Bipalium, perhaps representing a further two species, in Hino City, Tokyo, in 1983; and we have preliminarily arranged the forms of Bipalium known in the region into four groups distinguished on the basis of body coloring, position of the mouth, and structure of the copulatory organ.     

Detection and speciation of common cell culture mycoplasmas by an enzyme-linked immunosorbent assay with biotin-avidin amplification and microporous membrane solid phase

Summary An enzyme-linked immunosorbent assay (ELISA) was developed in order to serve in detecting and speciating mycoplasmas isolated from cell cultures. Its main features included a biotin-streptavidin amplification step and a solid phase consisting of a microporous membrane. Cell samples in the form of suspensions were applied to nitrocellulose or ion exchange membranes immobilized in commerciallyavailable microtiter, multiwell manifolds. The blocking buffer contained 1% purified α-casein. The primary antibodies were monoclonal and the polyclonal secondary antibody was biotinylated. The enzyme utilized was streptavidin-horseradish peroxidase. The substrate-dye complex consisted of either 4-chloro-1-naphthol and hydrogen peroxide or ortho phenylene diamine (OPD) and hydrogen peroxide. The presence of homologous antiserum in the reaction sequence gave clearly visible, colored reactions on the membrane when 50 ul with approximately 10⁵ or more cfu/ml were present. This new biotin-avidin microporous membrane (BAMM-ELISA) test can be used both to detect mycoplasmas and to speciate them. The BAMM-ELISA is simple, rapid, sensitive, specific and economical. As such, it has potential for aiding in the control of mycoplasma contamination in cell culture, and could prove useful in clinical diagnostic applications as well. This study was supported in part by Bionique Laboratories, Inc., and research grants awarded by the National Institutes of Health (SBIR Phase II from NIEHS, R44ES03705) and the New York State Science and Technology Foundation (SSF 84-1). Valuable technical assistance and counsel were provided by Dr. Steven Geary, Angela Alongi and Alexandria Siy. Photography was done through the courtesy of Marina LaDuke of the W. Alton Jones Cell Science Center.     

Multiple forms of peroxidase from Narcissus pseudonarcissus

Multiple forms of peroxidase from Narcissus pseudonarcissus were identified and separated by polyacrylamide gel electrophoresis. The enzyme forms were found to be particulate but could be solubilized in buffers of high ionic strength and high pH. Bulbs at different stages (dormant, early growth, flowering and post-flowering) were investigated and both the number and distribution of peroxidase forms were found to differ. The major peroxidase form in dormant bulbs was purified and displayed a number of notable properties including a MW of at least 10⁵, a high isoelectric point and the apparent absence of a heme prosthetic group.     

Alkanes of four related moth species,Helicoverpa and Heliothis

Comparison of the presence and quantities of cuticular hydrocarbons has been used successfully for identifying sibling species and races of several groups of insects. This approach has been extended to four species of moths previously regarded as belonging to the same genus, Heliothis. Gas chromatography was used to quantify the numerous high-molecular weight alkanes found on the cuticle of two pairs of closely related species: Helicoverpa zea and Helicoverpa armigera, and Heliothis virescens and Heliothis subflexa. Both sexes of H. zea and H. armigera contained different quantities of several alkanes that could be used for unambiguous identification. Similar comparisons of H. subflexa and H. virescens showed four peak ratios that were different for each species. Sexual dimorphism was minor in H. subflexa and H. virescens.     

DNA probes for species identification of mosquitoes in the Anopheles gambiae complex

Abstract. Identification of species within the Anopheles gambiae Giles species complex is essential for the correct evaluation of malaria vector ecology studies and control programmes. The development of DNA probes to distinguish species of the An.gambiae complex is described. Genomic libraries were prepared for four members of the An.gambiae complex. These were screened using radiolabeled DNA from different species of An. gambiae sensu lato and a number of clones selected on the basis of their species specificity. These clones could be divided into two groups, each containing homologous sequences. Sequences homologous to group 1 inserts are highly reiterated in the genomes of Anopheles arabiensis Patton and Anopheles merus Dönitz, present in low copy number in Anopheles melas Theobald, but were not detected in Anopheles gambiae sensu stricto. Studies on the organization of this sequence in the genome of An.arabiensis show that homologous sequences are male specific and interspersed within the chromatin. Sequences homologous to group 2 inserts are highly repeated in the genomes of An.merus and An.melas, but present in low copy number in An.gambiae s.s. and An.arabiensis. Group 2 homologous sequences are not sex-specific in the species tested and appear to be tandemly repeated. When used as hybridization probes, these sequences provide a sensitive means for the identification of species within the Anopheles gambiae complex.