What is a lunar standstill III?

Prehistoric monument alignments on lunar standstills are currently understood for horizon range, perturbation event, crossover event, eclipse prediction, solstice full Moon and the solarisation of the dark Moon. The first five models are found to fail the criteria of archaeoastronomy field methods. The final model of lunar-solar conflation draws upon all the observed components of lunar standstills – solarised reverse phased sidereal Moons culminating in solstice dark Moons in a roughly nine-year alternating cycle between major and minor standstills. This lunar-solar conflation model is a syncretic overlay upon an antecedent Palaeolithic template for lunar scheduled rituals and amenable to transformation.

What is a Superhero?

The essay argues that Marvel's Civil War is an interesting narrative concerning the superhero metacode at work. After a brief overview of the crossover event, its allegorical qualities will be discussed followed by a supplemental reading focusing on how superheroes, as agents of pretend play, come to be socialized, coded, and distributed across shared social networks.

Transformation of the Lyme Disease Spirochete Borrelia burgdorferi with Heterologous DNA

ABSTRACT Studies of the spirochete Borrelia burgdorferi have been hindered by the scarcity of genetic tools that can be used in these bacteria. For the first time, a method has been developed by which heterologous DNA (DNA without a naturally occurring B. burgdorferi homolog) can be introduced into and persistently maintained by B. burgdorferi. This technique uses integration of circular DNA into the bacterial genome via a single-crossover event. The ability to transform B. burgdorferi with heterologous DNA will now permit a wide range of experiments on the biology of these bacteria and their involvement in the many facets of Lyme disease.

Monoclonal antibody characterization of a unique immune response control locus between H-2S and D.

The primary in vitro antibody response to the type 2 antigen, trinitrophenyl (TNP)-Ficoll, is controlled by two complementing loci in the H-2 region of the mouse major histocompatibility complex (MHC). High responder alleles at both loci are necessary for a high responder phenotype. Previous studies mapped one locus of control to the I-A subregion. In this report we demonstrate by recombinant analysis that the second locus of control is located between the H-2S and D regions. A comparison of responses in the B10.BAR6, B10.BAR10, and B10.BAR11 strains defined a locus controlling the response to TNP-Ficoll in a single haplotype, bounded on the left by the crossover event in the B10.BAR10 and on the right by the crossover event in the B10.BAR6 strain. A monoclonal antibody directed against this right-hand region of control has been produced (48.21.7) that blocks the response to TNP-Ficoll at the level of the antigen-presenting cell. The monoclonal antibody 48-21.7 is specific for the high responder b allele at the right-hand locus and did not inhibit responses to other protein antigens tested. The immune response to TNP-Ficoll was not inhibited by monoclonal antibodies that react with H-2Db or Qa-2 specificities, suggesting that the TNP-Ficoll response is controlled by a unique locus located between H-2S and D. Finally, 48-21.7 recognizes and precipitates a unique product of approximately 40,000 mol wt that is distinct from the H-2D region product recognized by the monoclonal antibody B22/249.

The detection of a recessive visible gene in finite populations

Robertson, 1978, addressed the interesting problem of ascertaining the distribution of the time to detection of a recessive homozygote in a finite population. He was motivated in part by breeding and artificial selection practices. The same problem arises in the context of evolutionary processes and medical genetics since it refers to the time of first appearance as a homozygote of a new crossover event or a mutant gene.

THE RELATIONSHIP BETWEEN SYNAPTINEMAL COMPLEXES, RECOMBINATION NODULES AND CROSSING OVER IN NEUROSPORA CRASSA BIVALENTS AND TRANSLOCATION QUADRIVALENTS

ABSTRACT Reconstruction of serially sectioned zygotene and pachytene nuclei has allowed the estimation of both the number and position of central component recombination nodules in the synaptinemal complexes of two chromosomally different strains of Neurospora crussa. In both strains the number of nodules is that expected if each nodule represents one crossover event (50 map units). The distribution of nodules within the arms of bivalents shows evidence of centromeric repulsion and telomeric localizatioa. Nodules appear quite early in the zygotene before pairing of chromosomes is complete. Evidence was found of size differences in nodules, and multiple nodules were occasionally seen. Chromosome lengths and nuclear sizes increased from early zygotene to late pachytene. The three quadrivalents present in the alcoy translocation heterozygotes were readily distinguishable in reconstructions, and their cytological dimensions were in agreement with predictions from linkage map distances.