Parasites of the laboratory woodchuck (Marmota monax)

The parasite burden of captive and colony-born woodchucks maintained in laboratory animal facilities was determined and compared to woodchucks recently trapped. Microfilariae of Ackertia marmotae in blood or dermis were most commonly observed in trapped woodchucks. There was a linear decrease in woodchucks positive for microfilariae after introduction in the laboratory colony, but even after 39 months, 53% were positive. Microfilaremia or microfilariderma were never observed in colony born woodchucks. Eggs or oocysts of Obeliscoides cuniculi, Citellina triradiata and Eimeria sp. were found by fecal flotation. The O. cuniculi population declined exponentially in captive woodchucks following colony entry, and this nematode was never found in colony-born woodchucks. However, low rates of infection with Citellina and Eimeria sp. were found in the colony-born group. Ixodes cookei, Oropsylla sp., and Androlaelaps sp. ectoparasites were observed commonly in recently trapped woodchucks, but were not present in any woodchucks maintained in the colony. Clinical disease associated with parasitic infection was not observed.     

Optimal systems: I. The vascular system

An approach to quantitative work on optimal systems is considered. Desired optimal principles are utilized in constructing a hypothetical system similar to the organ system considered. A comparison of this constructed system with the anatomical system then gives an indication of the importance of the optimal principles in the form or function of the organ system considered. These ideas are applied to the mammalian vascular system, and limiting values are obtained for some of its important component parts. The constructed system gives good agreement with anatomical data for vessel radii, lengths, and hydrodynamic resistance to flow.     

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Ohne Zusammenfassung     

STUDIES IN THE PHYSICAL CHEMISTRY OF THE PROTEINS : VI. THE ACTIVITY COEFFICIENTS OF THE IONS IN CERTAIN OXYHEMOGLOBIN SOLUTIONS.

1. The solvent action of a neutral salt upon a protein, oxyhemoglobin, has been found identical to the solvent action of a neutral salt upon a bi-bivalent or uni-quadrivalent compound. 2. The solubility of oxyhemoglobin in phosphate solutions of varying ionic strength has been defined by the equation: log See PDF for Equation in which µ is the ionic strength, and S ₀ is the solubility in the absence of salt. 3. The values of S ₀ have been calculated to be 12.2, 11.2, and 13.1 gm. per liter respectively at pH 6.4, 6.6, and 6.8. 4. The relatively great solubility of oxyhemoglobin in water has been ascribed to the strong affinity constants for acid and base of certain groups in oxyhemoglobin. 5. The small change in the solubility of oxyhemoglobin effected by neutral salts suggests that but few such groups are dissociated in oxyhemoglobin in the state in which it crystallizes near its isoelectric point. 6. Certain of the other properties of oxyhemoglobin, such as its low viscosity, are considered in the light of its molecular weight and its valence type.