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20 pmol g-' h-l for embryos with an average wet weight of 254 mg. Differences in embryonic and maternal blood oxygen affinity may also be important in facilitating maternal-embryonic gas exchange in viviparous fishes. Ingermann et al. (1984) reported that in the embiotocid E. lateralis, oxygen affinity of whole blood is higher in embryos than in adults and that embryonic blood oxygen affinity decreases from midgestation to term. , 1984), although differences in the concentration of erythrocyte hemoglobin and organic phosphate have also been implicated (Ingermann and Terwilliger, 1981b, 1982).

Ingermann et al. (1984) suggested that re- 22 JOHN P. W O W S ET U . placement of embryonic hemoglobin with adult hemoglobin may account for the decrease in blood oxygen affinity during the last half of gestation in E. lateralis. Biochemical and functional differences between embryonic and adult hemoglobins also have been identified in other viviparous fishes. Manwell (1958, 1963) demonstrated that embryonic hemoglobin from Squalus suckleyi has a higher oxygen affinity than adult hemoglobin. Electrophoretic patterns of proteolytic digests of embryonic and adult hemoglobins also differed, indicating biochemical differences.

Demand for additional nutrients has to be met after the yolk reserves have been absorbed completely. The second phase occurs “when the respiratory requirements exceed the capacity of the unspecialized exchange surfaces” (Webb and Brett, 1972a). The subject of respiration and gas exchange in viviparous fishes has been reviewed by Gulidov (1963) and Soin (1971). Most of the available information is contained in anatomical and morphological studies in which function is deduced from structure. It is fortunate that these deductions are probably valid, because only a handful of experimental studies have been carried out to test them.

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A color atlas of Complete Denture Fabrication

by Robert

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