Schischcatella (Fenestrata,Bryozoa) from the Devonian of the Rhenish Massif,Germany

Abstract: The Devonian fenestrate bryozoan, Schischcatella Waschurova, 1964 , possessed colonies in the form of low, erect bifoliate fronds that grew from an encrusting sheet‐like base with autozooecia arranged in biserial, bifurcating rows. This growth habit is unique in fenestrates, which normally had unilaminate arborescent colonies. Originally, Schischcatella was described from the Lower Devonian of Tajikistan. This article describes a new species, S. heinorum sp. nov., from the Middle Devonian of the Eifel (western Rhenish Massif, Germany) with additional material from the Lower Devonian of the Kellerwald (eastern Rhenish Massif, Germany). External and internal morphologies of this bryozoan have been studied using abundant material. The growth habit of Schischcatella suggests a completely different pattern of feeding currents than that in the normal fenestrate colony. The outflow of the filtered water occurred only on edges of colonies between rami. In the absence of chimneys (areas of vertical water expelling), such a functional morphology may have restricted extension of the colony in a distal direction. The evolution of Schischcatella is apparently an example of paedomorphosis, the genus evolved from an unknown semicosciniid species by the early ontogenetic interruption of colony development and further changes in the mode of growth.     

Development of Eimeria alabamensis from Cattle in Mammalian Cell Cultures*

SYNOPSIS. Monolayer primary cultures of cells from bovine embryonic intestine (BEInt), kidney (BEK), spleen (BES), and thyroid (BETy) and cell line cultures of embryonic bovine trachea (EBTr) and synovium (BESy) as well as established cell line cultures of bovine kidney (Madin-Darby, MDBK), human intestine (Int 407) and Syrian hamster kidney (BHK) were inoculated with freshly excysted sporozoites of Eimeria alabamensis and observed for 4–5 days. Sporozoites penetrated all cell types; during the 1st 24 hr, intracellular sporozoites, trophozoites and binucleate schizonts were seen in all cell cultures. Mature schizonts were more numerous in BES and MDBK cells than in the others. Large schizonts, 14.2 (11–18.5) by 10.2 μ (8.5–11), with 6–14 short, stubby merozoites (each with 2 refractile bodies) occurred at 2 and 3 days in all cells except BESy, Int 407, and BHK. Small schizonts, 9.7 (5.5–13) by 6 μ (5–8.5), with 6–10 long, slender merozoites (each with 2 refractile bodies) were found 3 days after inoculation in all cell types. At 4 days, some intracytoplasmic merozoites and a few intranuclear 2nd generation trophozoites were found. After 4 days post-inoculation, intracellular parasites were rarely seen and these were apparently degenerate. Development within the host cell nucleus, the normal site of development in the host animal, was observed infrequently in cell cultures. Intranuclear sporozoites, found no earlier than 2 days after inoculation, developed similarly to those in the cytoplasm, and small intranuclear schizonts with 6–10 merozoites (each with 2 refractile bodies) occurred after 3 days in culture.     

Eimeria balphae n. sp. from the Ord Kangaroo Rat Dipodomys ordii*

SYNOPSIS. Eimeria balphae n. sp. is described from the Ord kangaroo rat Dipodomys ordii. The sporulated oocysts are broadly ellipsoidal to ovoid, averaging 16.7 by 14.3 μ. A single, large, homogenous body represents the oocyst residuum. A polar granule is present. There is no micropyle. The ovoid sporocysts average 8.7 by 5.9 μ. The sporocyst residuum is composed of 7–14 round, clear granules. This species of Eimeria was found in 1 of 82 D. ordii in northwestern Utah.     

Alterations of Adrenal Cortex and Thyroid in Mice with Congenital Absence of the Thymus

THE possible role of endocrine factors in the thymus and their control by hormones of the adenohypophysis or its target glands has been investigated extensively in animal models. These include mice whose pituitary function has been inhibited or blocked by anti-pituitary serum^1–3 or anti-growth-hormone serum^4–6, neonatally thymectomized mice^1,3,7–9 and the genetically hypopituitary dwarf mice with thymus atrophy^10–12. Further opportunities have been offered by the observation that genetically hairless “nude” mice (genetic symbol: nu)¹³ have no thymus^14,15.