Primitive recursion on higher types

Author(s):  
Stanislaw Ambroszkiewicz
1966 ◽  
Vol 167 (1) ◽  
pp. 53-55 ◽  
Author(s):  
Paul Axt
Keyword(s):  

1999 ◽  
pp. 273-300 ◽  
Author(s):  
W. G. Handley ◽  
S. S. Wainer
Keyword(s):  

1942 ◽  
Vol s2-83 (331) ◽  
pp. 299-316
Author(s):  
T. KERR

1. A general description is given of the pituitary of the perch (Perca fluviatilis L.), and histological details of its various parts. The subdivisions of the glandular component are confluent with each other but distinguished by their different cell types. The nervous lobe makes contact with all three of the subdivisions, but is separated from them by a layer of connective tissue, incomplete in particular areas. 2. The anterior glandular region (anterior lobe) has an anterior chromophil and a posterior chromophobe zone. The middle glandular region (transitional lobe) possesses brightly staining acidophils and basophils as well as chromophobes. The acidophils form a dorsal sheet, deeply indented by processes of the nervous lobe, the basophils lie ventrally and posteriorly, and chromophobes are common towards the extremities of the indentations. The posterior glandular region (intermediate lobe) is elaborately penetrated by nervous lobe processes; the cells are small and consist of amphiphils, dull basophils, and occasional dull acidophils. The possible homologies of these regions to the lobes of higher types are discussed. The nervous lobe is of loose glial tissue with many nuclei and blood vessels and some reticular and collagenous fibres. 3. Strongly acidophil spheres of various sizes and in various numbers occur in the middle glandular region. They originate in ‘sphere cells’ resembling eosinophil leucocytes and after enlarging become free in the tissues of the region. Later they appear to pass into the posterior processes of the nervous lobe to be the larger bodies of the Herring material. Finally these larger elements appear to break down to form a fine granulation, whose further fate could not be followed.


An endeavour is made to trace the evolution of mammals from Cotylosaurian ancestors through the carnivorous Therapsida. In Upper Carboniferous times the line probably passed through some primitive generalised Pelycosaurs; in Lower Permian through primitive, probably Therocephalian, Therapsids. In Middle and Upper Permian the line passed through the Gorgonopsia. In Triassic times the mammalian ancestors were small generalised Cynodonts. In Lower Jurassic the mammals are so Cynodont-like, and the Cynodonts so mammal-like, that in no single case are we absolutely certain which is which. In the Therocephalia, the Gorgonopsia, and the Cynodontia, the skull is very mammal-like. The zygomatic arch is, as in mammals, formed by the jugal and the squamosal. The teeth are divided into incisors, canines and molars. In the later Gorgonopsians there is an imperfect secondary palate; in Cynodonts a complete secondary palate as in mammals. In Permian Therapsids there is a single occipital condyle; in the Triassic Cynodonts there may he a single condyle slightly divided or two exoccipital condyles. There is, on passing from earlier to later types, a steady increase in the size of the dentary and decrease in the size of the other elements of the jaw. The quadrate also becomes much reduced in the higher types. In Gorgonopsians and probably all earlier types the arch of the atlas is a pair of bones; in Cynodonts, as in mammals, there is a single arch.


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