A new pelagic marine rotifer from the southern Benguela,Synchaeta hutchingsi,n. sp., with notes on its temperature and salinity tolerance and methods of culture

A new species of marine rotifer is described from the S.E. Atlantic off Cape Town. Synchaeta hutchingsi n. sp. is unique among the approximately 36 recognized Synchaeta species in exhibiting the following combination of characters: single sharply pointed toe; slender bristle along ventral midline of foot: single lateral antenna on left side near foot base; spur on dorsal side of foot used to carry egg; total length 165–200 µm. Salinity tolerance experiments showed the new species to be obligate brackwater/marine; a temperature of 35 °C could be tolerated for a short period of time. The new species has been mass-cultured for use as an experimental live food for rearing marine fish larvae.     

A Comprehensive Genetic Map of Murine Chromosome 11 Reveals Extensive Linkage Conservation between Mouse and Human

Interspecific backcross animals from a cross between C57BL/6J and Mus spretus mice were used to generate a comprehensive linkage map of mouse chromosome 11. The relative map positions of genes previously assigned to mouse chromosome 11 by somatic cell hybrid or genetic backcross analysis were determined (Erbb, Rel, 11-3, Csfgm, Trp53-1, Evi-2, Erba, Erbb-2, Csfg, Myhs, Cola-1, Myla, Hox-2 and Pkca). We also analyzed genes that we suspected would map to chromosome 11 by virtue of their location in human chromosomes and the known linkage homologies that exist between murine chromosome 11 and human chromosomes (Mpo, Ngfr, Pdgfr and Fms). Two of the latter genes, Mpo and Ngfr, mapped to mouse chromosome 11. Both genes also mapped to human chromosome 17, extending the degree of linkage conservation observed between human chromosome 17 and mouse chromosome 11. Pdgfr and Fms, which are closely linked to II-3 and Csfgm in humans on chromosome 5, mapped to mouse chromosome 18 rather than mouse chromosome 11, thereby defining yet another conserved linkage group between human and mouse chromosomes. The mouse chromosome 11 linkage map generated in these studies substantially extends the framework for identifying homologous genes in the mouse that are involved in human disease, for elucidating the genes responsible for several mouse mutations, and for gaining insights into chromosome evolution and genome organization.     

A Monte Carlo investigation of the dosimetric properties of monoenergetic neutron beams for neutron capture therapy

A Monte Carlo simulation study has been carried out to investigate the suitability of neutron beams of various energies for therapeutic efficacy in boron neutron capture therapy. The dosimetric properties of unidirectional, monoenergetic neutron beams of varying diameters in two different phantoms (a right-circular cylinder and an ellipsoid) made of brain-equivalent material were examined. The source diameter was varied from 0.0 to 20.0 cm; neutron energies ranged from 0.025 eV up to 800 keV, the maximum neutron energy generated by a tandem cascade accelerator using 2.5-MeV protons in a 7Li(p,n)7Be reaction. Such a device is currently under investigation for use as a neutron source for boron neutron capture therapy. The simulation studies indicate that the maximum effective treatment depth (advantage depth) in the brain is 10.0 cm and is obtainable with a 10-keV neutron beam. A useful range of energies, defined as those neutron energies capable of effectively treating to a depth of 7 cm in brain tissue, is found to be 4.0 eV to 40.0 keV. Beam size is shown not to affect advantage depth as long as the entire phantom volume is used in determining this depth. Dose distribution in directions parallel to and perpendicular to the beam direction are shown to illustrate this phenomenon graphically as well as to illustrate the differences in advantage depth and advantage ratio and the contribution of individual dose components to tumor dose caused by the geometric differences in phantom shape.     

Calcium regulation of inositol 1,4,5-trisphosphate receptors

Ca2+ exerts both a stimulatory and inhibitory effect on type-I IP3R channel activity. However, the structural determinants of Ca2+ sensing in IP3Rs are not fully understood. Previous studies by others have identified eight domains of the type-I IP3R that bind 45Ca2+ when expressed as GST-fusion proteins. We have mutated six highly conserved acidic residues within the second of these domains (aa378-450) in the full-length IP3R and measured the Ca2+ regulation of IP3-mediated Ca2+ release in COS-7 cells. 45Ca2+ flux assays measured with a maximal [IP3] (1 microM) indicate that one of the mutants retained a Ca2+ sensitivity that was not significantly different from control (E411Q), three of the mutants show an enhanced Ca2+ inhibition (D426N, E428Q and E439Q) and two of the mutants were relatively insensitive to Ca2+ inhibition (D442N and D444N). IP3 dose-response relationships indicated that the sensitivity to Ca2+ inhibition and affinity for IP3 were correlated for three of the constructs. Other mutants with enhanced IP3 sensitivity (e.g. R441Q and a type-II/I IP3R chimera) were also less sensitive to Ca2+ inhibition. We conclude that the acidic residues within the aa378-450 segment are unlikely to represent a single functional Ca2+ binding domain and do not contribute to Ca2+ activation of the receptor. The different effects of the mutations may be related to their location within two clusters of acidic residues identified in the crystal structure of the ligand-binding domain [I. Bosanac, J.R. Alattia, T.K. Mal, et al., Structure of the inositol 1,4,5-trisphosphate receptor binding core in complex with its ligand, Nature 420 (2002) 696-700]. The data support the view that all IP3R isoforms may display a range of Ca2+ sensitivities that are determined by multiple sites within the protein and markedly influenced by the affinity of the receptor for IP3.     

Water quality requirements for first-feeding in marine fish larvae. II. pH,oxygen, and carbon dioxide

Previously unfed larvae representing eight species of marine teleosts (a soleid, Heteromycteris capensis Kaup; a cynoglossid. Trulla capensis Kaup; a gadid, Gaidropsarus capensis (Kaup); a congiopodid, Congiopodus spinifer (Smith); three sparids, Diplodus sargus (L.), Pachymetopon blochi (Val.), and an unidentified species; and a centracanthid, Pterosmaris axillaris (Boulenger)) were exposed for 24 h to various pH's and concentrations of dissolved oxygen and carbon dioxide and then tested for their ability to first-feed. Mortalities recorded during the 24-h exposure went into the fitting of response curves and the calculation of the LC₅₀ and LC₁₀. The incidence of successful first-feeding during the subsequent 4-h exposure to food yielded values for the EC₅₀ and EC₁₀. The exposure to sub-optimal conditions continued during the 4-h feeding test. The sensitivity of first-feeding larvae to high pH and dissolved oxygen may pose hazards for the marine fish culturist; low pH appears to be harmful (at least in the short term) only at levels below about pH 6.0; carbon dioxide poisoning is of doubtful importance in practical fish culture. There were only minor interspecific differences in calculated 24-h first-feeding EC₅₀'s, which suggests general applicability of the results to a wide variety of first-feeding marine fish larvae.