Memoirs: The Embryonic Development of the Stick-Insect, Carausius morosus

1936 ◽  
Vol s2-78 (311) ◽  
pp. 487-511
Author(s):  
A. J. THOMAS

1. The maturation of the egg takes place in the ovarian tube, and is immediately followed by the formation of the cleavagenucleus and its division into many nuclei. 2. The entire products of the cleavage-nucleus migrate to the surface to form the blastoderm. Cleavage of the yolk was not observed even in late stages. Yolk-cells are absent when the blastoderm is being formed. 3. Primitive endodermal cells are proliferated from the middle of the germ-band, and form a membrane between the germ-band and the yolk. The membrane is present only in embryonic stages; some of the cells proliferated wander into the yolk and act as vitellophags. 4. Mesoderm is formed by proliferation of cells from the ventral plate. It is preceded by the formation of a shallow gastrular furrow, and from the bottom of this furrow proliferation takes place. The mesoderm becomes arranged in segmental masses. 5. Two masses of cells proliferated at the anterior and posterior ends of the germ-band are shown to be the endodermal rudiments from which the mid-gut epithelium is formed. The invaginations of the stomodaeum and proctodaeum grow against these masses and carry parts of the proliferating areas near their blind ends. It is shown that the various methods of mid-gut formation which have been described could be reconciled with the process described in Carausius. 6. The hinder end of the mid-gut is flanked by two plates of ectoderm which are forward extensions of the proctodaeum. Into these extensions the Malpighian tubules open, and, as their histology is identical with that of these extensions and widely different from that of the mid-gut, these tubules must be ectodermal in nature. 7. The formation of the amnion and serosa are described.

1970 ◽  
Vol 52 (3) ◽  
pp. 653-665 ◽  
Author(s):  
DIANA E. M. PILCHER

1. Urine secretion by isolated Malpighian tubules of Carausius is accelerated by a diuretic hormone which can be extracted from the brain, corpora cardiaca and suboesophageal ganglion. 2. The level of this hormone in the haemolymph varies according to the state of hydration of the insect. 3. The hormone is inactivated by the tubules, and a mechanism is proposed whereby the tubules might be controlled by the hormone in vivo.


1997 ◽  
Vol 29 (3) ◽  
pp. 257-266 ◽  
Author(s):  
A.M. Fausto ◽  
M. Mazzini ◽  
A. Cecchettini ◽  
F. Giorgi

1936 ◽  
Vol s2-78 (311) ◽  
pp. 533-542
Author(s):  
MABEL DRUMMOND

1. The mid-gut epithelium of Ephestia is derived from cephalic and caudal mesendoderm rudiments which are proliferated from the germ-band independently of the stomodaeal and proctodaeal invaginations. 2. The oesophageal valve is formed by the backward growth from the blind end of the stomodaeum of six tubules, which later in a slightly altered form extend into the cavity of the mid-gut to form the valve of the larva. 3. The stomodaeum and proctodaeum are purely ectodermal. 4. The malpighian tubules are ectodermal.


Genetics ◽  
1997 ◽  
Vol 147 (1) ◽  
pp. 243-253 ◽  
Author(s):  
Joseph Jack ◽  
Guy Myette

Abstract The products of two genes, raw and ribbon (rib), are required for the proper morphogenesis of a variety of tissues. Malpighian tubules mutant for raw or rib are wider and shorter than normal tubules, which are only two cells in circumference when they are fully formed. The mutations alter the shape of the tubules beginning early in their formation and block cell rearrangement late in development, which normally lengthens and narrows the tubes. Mutations of both genes affect a number of other tissues as well. Both genes are required for dorsal closure and retraction of the CNS during embryonic development. In addition, rib mutations block head involution, and broaden and shorten other tubular epithelia (salivary glands, tracheae, and hindgut) in much same manner as they alter the shape of the Malpighian tubules. In tissues in which the shape of cells can be observed readily, rib mutations alter cell shape, which probably causes the change in shape of the organs that are affected. In double mutants raw enhances the phenotypes of all the tissues that are affected by rib but unaffected by raw alone, indicating that raw is also active in these tissues.


2007 ◽  
Vol 24 (2) ◽  
pp. 436-441 ◽  
Author(s):  
Rosemary I. Egonmwan

The late stages of embryogenesis in the achatinid land snail Limicolariaflammea (Müller, 1774) were described using light and electron microscopy. Embryos at various stages of development were present in the eggs during the first hour after they were laid, from 4-cell blastulae to morulae and fairly advanced stages. The advanced embryo which was fully developed on the second day bears a long cephalic sac, first to be developed, attached to the embryo and a podocyst which is attached to the foot of the embryo. Both of these structures are reduced in size as embryogenesis progresses until they finally disappear at about the 7th day after the egg was deposited. The embryonic shell was apparent on the second day and spiral coiling was apparent at about day 5. The spiral shell had one whorl when formed and more spirals were added so that at hatching the young snails had three whorls.


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