Memoirs: A Contribution to the Morphology of the Teleostean Head Skeleton, based upon a Study of the Developing Skull of the Three-spined Stickleback (Gasterosteus aculeatus)

1902 ◽  
Vol s2-45 (180) ◽  
pp. 503-593
Author(s):  
H. H. SWINNERTON

1. The cranial flexure, together with other features in the shape of the embryonic head skeleton in Teleosts, is probably a mechanical effect due to differences in the degree of distensibility between the dorsal and ventral surfaces of the brain, and to the presence of skeletal structures in close association with the latter (pp. 507-509). 2. The presence of an epiphysial bar, with consequent division of the large dorsal, cranial fontanelle into an anterior and a posterior portion, is a common feature among Teleosts during development (pp. 516, 517). 3. The Ostariophysi differ from all other Teleosts in the retention of this early developmental condition of the cranial roof in the adult (pp. 525, 526). 4. The intra-cranial notochord, so far from undergoing reduction, never at any stage ceases to grow (pp. 513, 516, 523). 5. In Gasterosteus, during embryonic life, those skeletal elements immediately concerned in the support of the jaws and operculum, and in the attachment of associated muscles, seem to undergo a considerable acceleration in the rate of development as compared with the rest of the head skeleton (pp. 534, 535). 6. Among Teleosts and the immediately related Ganoids, three types of palato-ethmoidal relationship exist (pp. 538, 539, 551-557). (a) The Panartete, in which the paratine cartilage or its derivatives is attached to the ventral surface of the ethmoid for the whole length of this, from the parethmoid to the pre-ethmoid cornua, e.g. Amia, probably presented also by many Malacopterygii (Isospondyli). (b) The Disartete, in which the attachment is at the pavethmoid and pre-ethmoid cornua, but not at any intermediate point, e.g. Esox, also presented by the Salmonidæ, Cyprinodontidæ, Acanthopterygii, and probably some Malacopterygii (Isospondyli). (c) The Acrartete, in which the attachment is confined solely to the pre-ethmoid cornua, e.g. Gasterosteus, and also presented by the Thoracostei, Scomberesoces, Plectognathi, Zanclidæ, Acronuridæ, and in a modified form by Lepidosteus. 7. The study of the adult anatomy and comparative ontogeny of the head skeleton in Elasmobranchs and Teleostomes seems to point to a common ancestral stock for these two great divergent branches of fishes. It presented among other features the following: A short embryonic life; weak cranial flexure; trabeculæ united to the extreme anterior end of the parachordals. A wholly cartilaginous cranium, possessing trabecular, parachordal, and occipital portions (pp. 560-562). A cranium having a large dorsal fontanelle, which may or may not have been divided by a transverse epiphysial bar. Also two lateral fontanelles for the passage of the optic, and possibly also the trigeminal and facial nerves. Also a ventral or pituitary fontanelle. Also a large opening between the cavum cranii and auditory capsule (pp. 562-568). A quadrate cartilage supporting a lower moveable jaw, formed by the union of two cartilages in the middle line, and bearing dorsally two, possibly three processes; an anterior one, parallel to its fellow, and not united with it, but with the ethmoid plate, so that a moveable upper jaw did not exist; a middle one articulating with the trabeculæ, in the region lying between the optic and trigeminal nerves; a posterior one articulating with the auditory capsule (pp. 568-573). A branchial apparatus consisting of at least five arches, already segmented into four parts. Balfour's term Prolognathostomata (81, p. 271) would be sufficiently expressive of such a type. 8. The manner of mandibular suspension in Teleosts is insufficiently described by the term Hyostylic (pp. 569, 570). 9. The Lophobranchii and Hemibranchii should no longer be kept in separate orders, for they together constitute a natural group, which may be designated the Thoracostei (pp. 575-579). 10. The Scomberesoces, through the Gasterosteoidei, approach more closely to the Thoracostei than do any other living Physoclisti, and seem to form with them a compact series, which may be provisionally spoken of as the Scomberesocine series (pp. 580, 581). 11. As judged by the study of the ethmoid and suspensorial regions, the Zanclidæ and Acronuridæ are closely allied to the Plectognathi, but the affinities of these forms must not be sought amongst living Physoclisti (pp. 582, 583).

2014 ◽  
Vol 88 (1) ◽  
pp. 68-91 ◽  
Author(s):  
Allison C. Daley ◽  
Gregory D. Edgecombe

Recent description of the oral cone of Anomalocaris canadensis from the Burgess Shale (Cambrian Series 3, Stage 5) highlighted significant differences from published accounts of this iconic species, and prompts a new evaluation of its morphology as a whole. All known specimens of A. canadensis, including previously unpublished material, were examined with the aim of providing a cohesive morphological description of this stem lineage arthropod. In contrast to previous descriptions, the dorsal surface of the head is shown to be covered by a small, oval carapace in close association with paired stalked eyes, and the ventral surface bears only the triradial oral cone, with no evidence of a hypostome or an anterior sclerite. The frontal appendages reveal new details of the arthrodial membranes and a narrower cross-section in dorsal view than previously reconstructed. The posterior body region reveals a complex suite of digestive, respiratory, and locomotory characters that include a differentiated foregut and hindgut, a midgut with paired glands, gill-like setal blades, and evidence of muscle bundles and struts that presumably supported the swimming movement of the body flaps. The tail fan includes a central blade in addition to the previously described three pairs of lateral blades. Some of these structures have not been identified in other anomalocaridids, making Anomalocaris critical for understanding the functional morphology of the group as a whole and corroborating its arthropod affinities.


1913 ◽  
Vol s2-58 (231) ◽  
pp. 411-446
Author(s):  
F. A. POTTS

In several species of Trypanosyllis the stolons are produced from a cushion of proliferating tissue at the posterior end of the stock in successive transverse rows of seven or eight, the number produced by a single individual being between one and two hundred. New rows are established at the anterior end pushing those already formed backwards so that the oldest stolons are most posterior. Ectoderm and mesoderm alone take part in the formation of the stolons so that they are without an alimentary canal. Two slightly varying types of the phenomenon have been distinguished in the two species here studied. The following divisions correspond roughly to the stages observed in the growth of stolons. In no example was it possible to examine the early formation of the proliferating cushion. (1) The aggregation of leucocytes in the posterior segments, which invade the mesoblast of the proliferating cushion. (2) The appearance of centres of proliferation in the epiblast, which cause the formation of stolons. The mesoblast advances and fills the hollow processes formed by the ectoblast. It lies at first in close association with the ventral surface of the stolon. (3) The mesoblast of the stolon proliferates and segments. The first appearance of segmentation is the formation of septa. (4) The invasion of the stolon by two bundles of muscle-fibres in direct continuation with those of the stock, and a single ventral nerve-cord, also an outgrowth of the corresponding structure in the stock. (5) The segmentation of the epiblast of the stolon and the formation of the structures derived from it (setæ, etc.). The gonads are formed as lateral outgrowths from the central mesoblastic mass. With the growth of the stolons the proliferating cushion is gradually absorbed.


2019 ◽  
Author(s):  
S.G. Seamone ◽  
D.A. Syme

ABSTRACTParticle image velocimetry and video analysis were employed to discern and describe the mechanism used by the stingray Potamotrygon motoro to bury into the substrate. P. motoro repeatedly and rapidly pumped the body up and down while folding the posterior portion of the pectoral fins up and over, drawing water in and suspending sediment beneath the pectoral disc. As the fins folded up and over, vortices of fluidized sediment travelled along the ventral surface of the fins toward the fin tips, and were then directed onto the dorsal surface of the fins and towards the dorsal midline of the fish, where they dissipated and the sediment settled over the dorsal surface of the ray. As displacement and speed of the body pumping and finbeat motions increased, the speed of the sediment translating across the dorsal surface increased, and accordingly, sediment coverage of the dorsal surface increased. Mean sediment coverage was 82.5% ± 3.0 S.E.M, and appeared to be selectively controlled, whereby the pectoral fins tended to bury more than the body, head and tail, and the body more than the head and the tail. In the most vigorous burying events, vortices of sediment shed from each fin collided at the midline and annihilated, reorienting the sediment flow and sending jets of sediment towards the head and the tail, covering these locations with sediment. Hence, this study demonstrates that the mechanism of burying employed by P. motoro permits effective control of sediment vortices and flows to modulate the extent of burying.


1956 ◽  
Vol s3-97 (38) ◽  
pp. 235-249
Author(s):  
R. B. CLARK

The four longitudinal vessels of the circulatory system of Nephtys californiensis are dorsal, sub-intestinal, and neural, the latter being paired. There is a complete longitudinal circulation; the dorsal vessel communicates with the sub-intestinal by way of the proboscidial circulation and with the neural by way of the circum-oral vessels. In each middle and posterior segment segmental vessels from each of the longitudinal trunks carry blood to and from the parapodia and body-wall. The segmental circulation is completed by a circum-intestinal vessel connecting the dorsal and subintestinal vessels in each segment and an intersegmental branch connecting the dorsal and sub-intestinal segmental vessels. A trans-septal branch of the neural segmental vessel communicates with the sub-intestinal segmental vessel. This arrangement is modified in anterior segments which house the muscular, eversible pharynx, and no blood-vessels cross the coelom except by running through the body-wall. On anatomical grounds and by comparison with other polychaetes it seems likely that segmental is subordinate to longitudinal circulation. There are no endothelial capillaries such as have been described in some other polychaetes; instead there are numerous blindending vessels the walls of which are composed of the same three layers as other vessels and which are probably contractile. The dorsal vessel, where it is in contact with the ventral surface of the supra-oesophageal ganglion, forms a plexus in close association with a modified part of the brain capsule and a special axonal tract within the ganglion. It is thought that by way of this ‘cerebro-vascular complex’, hormones produced in the neurosecretory cells of the brain pass into the blood-stream.


1964 ◽  
Vol 12 (1) ◽  
pp. 42 ◽  
Author(s):  
RL Hughes

A study of 24 male Tasmanian rat-kangaroos, Potorous tridactylus (Kerr), gave no evidence of either seasonal change in testis size or interruption to spermatogenesis during the 9 months when captures were made. One captive male (weight 1028 g) attained sexual maturity within a year and only a few epididymal sperm were found in a wild animal weighing 639 g. The spermatozoon head is of unusual shape. It is bluntly pointed anteriorly and broadens towards the centre. The posterior portion of the head is flattened dorsoventrally and a depression situated in its posterior ventral half gives it a forked appearance in the rear. The acrosome is almost entirely embedded in the anterior dorsal surface of the head. The nucleus possesses two basal granules and occupies most of the head volume. The flagellum is composed of a finely pointed neck, a middle piece with mitochondria1 helix, and a tail body which possesses no distinguishable end-piece. The flagellum is attached to the mid-ventral surface of the head by the extremely slender anterior portion of the neck. The axial filament complex passes throughout the entire length of the flagellum and is composed of at least four fibrils.


2017 ◽  
Author(s):  
Lucie Grécias ◽  
Julie Valentin ◽  
Nadia Aubin-Horth

ABSTRACTMany parasites with complex life cycles modify their intermediate host’s behaviour, which has been proposed to increase transmission to their definitive host. This behavioural change could result from the parasite actively manipulating its host, but could also be explained by a mechanical effect, where the parasite’s physical presence affects host behaviour. We created an artificial internal parasite using silicone injections in the body cavity to test this mechanical effect hypothesis. We used the Schistocephalus solidus - threespine stickleback (Gasterosteus aculeatus) system, as this cestode can reach up to 92% of its fish host mass. Our results suggest that the mass burden brought by this macroparasite alone is not sufficient to cause behavioural changes in its host. Furthermore, our results show that wall-hugging (thigmotaxis), a measure of anxiety in vertebrates, is significantly reduced in Schistocephalus-infected sticklebacks, unveiling a new altered component of behaviour that may result from manipulation by this macroparasite.


1984 ◽  
Vol 62 (6) ◽  
pp. 999-1004 ◽  
Author(s):  
William J. Rowland

A method was devised, using several independent judges, to estimate the degree of nuptial coloration of male three-spined sticklebacks, Gasterosteus aculeatus. Using the color-state scores that resulted from this technique, territorial males were compared with respect to their coloration level and with respect to their responsiveness to live and dummy stimulus fish. These comparisons reveal a positive association between color state and responsiveness: brightly colored males tend to court (zigzag) and attack (bite) stimulus fish more vigorously than duller colored males do. Therefore, the degree to which a male three-spined stickleback's nuptial coloration is developed can be used to some extent to predict its responsiveness, with the particular category of response (courtship or aggression) dependent on the stimulus presented. A close association between zigzag and bite frequencies was also found, responsive males showing higher levels of both courtship and aggression than less responsive ones. These results are consistent with evidence pertaining to the hormonal control of nuptial coloration, courtship, and aggression and to the signal value of nuptial coloration in G. aculeatus.


1937 ◽  
Vol s2-79 (316) ◽  
pp. 507-557
Author(s):  
DATUS M. HAMMOND

1. The neuromotor system of Euplotes patella Ehrenberg was studied in different stages of the life-cycle, including the adult, and asexual and sexual reproduction. 2. In the adult the basal granules of all the cirri are arranged in straight primary and secondary rows. The fibrils from the bases of the cirri are in general parallel with either the primary or secondary rows of basal granules of the cirri to which they are attached. This is interpreted as an indication of the evolution of the organism from an ancestor with a simple neuromotor system in which the cilia were uniformly distributed over the surface of the body in longitudinal, slightly spiral rows. 3. The basal apparatus of a bristle consists of a basal granule at the bottom of a depression in the ectoplasm which is surrounded by a group of rodlets and ends at the surface in a ring connected with the polygonal system. The polygonal or silverline system is pellicular in position. 4. During asexual reproduction the entire set of cirri is resorbed and replaced by two new sets of cirri, one for each daughter. One frontal cirrus for the anterior daughter develops in the old peristomial field of the parent, while the corresponding cirrus for the posterior daughter develops in the new peristome. The right marginal cirri arise on the dorsal surface along the rows of bristles and later move to the ventral surface. The fibrils develop outward from the bases of the cirri. 5. During binary fission a new peristome arises in a depression in the ectoplasm independently of the old peristome. The old peristome remains in the anterior daughter without at the time undergoing any visible change in structure. 6. The multiplication of the bristles is limited to a zone on either side of the future plane of constriction. Multiplication occurs by a series of fissions of the basal granules in this area. Dedifferentiation of bristles was not seen. 7. The polygonal system is replaced over the entire surface of the body with the exception of the old peristomial field. The new system originates in many separate loci in connexion with the bristles on the dorsal surface, and with the rudiments (Anlagen) of the cirri and peristome on the ventral surface. 8. During conjugation there are two successive reorganizations of the neuromotor system, that of the ‘gamete’ (conjugant) and that of the zygote. 9. The first reorganization, that of the gamete, begins during the maturation divisions preparatory to fertilization. During this reorganization the posterior portion of the peristome is resorbed and the remaining anterior portion is later replaced. The eighteen cirri are replaced by a set containing only seventeen cirri. 10. The second reorganization, that of the zygote, occurs during the differentiation of the nuclei in the exconjugants. It involves the completion of the peristome by differentiation of the missing posterior portion, and the replacement of the set of seventeen cirri by a complete set of eighteen cirri. 11. These protoplasmic reorganizations, invariably associated with both asexual and sexual reproduction, involve a structural and presumably a physiological rejuvenation resulting in the possibility of an indefinitely continued existence of the individual in the Protozoa. It may be that sexual reproduction is not necessary to bring about this result, but further work on the relationship of endomixis to the problem is needed.


Author(s):  
T. Shirahama ◽  
M. Skinner ◽  
A.S. Cohen

A1thought the mechanisms of amyloidogenesis have not been entirely clarified, proteolysis of the parent proteins may be one of the important steps in the amyloid fibril formation. Recently, we reported that "dense fibrillar inclusions" (DFI), which had the characteristics of lysosomes and contained organized fibrillar profiles as well, were observed in the reticuloendothelial cells in close association with the foci of new amyloid deposits. We considered the findings as evidence for the involvement of lysosomal system in amyloid fibril formation (l). In the present study, we attempted to determine the identity of the contents of the DFI by the use of antisera against the amyloid protein (AA) and an immuno-electron microscopic technique.Amyloidosis was induced in CBA/J mice by daily injections of casein (l). AA was isolated from amyloid-laden spleens by gel filtration and antibody to it was produced in rabbits (2). For immunocytochemistry, the unlabeled antibody enzyme method (3) was employed.


Author(s):  
Awtar Krishan

Earle's L-929 fibroblasts treated with mitosis-arresting but sub-lethal doses of vinblastine sulfate (VLB) show hypertrophy of the granular endoplasmic reticulum and annulate lamellae. Exposure of the cells to heavier doses of vincristine sulfate (VCR), a VLB-related drug, leads to the accumulation of large amounts of helical polyribosomes, Golgi membranes and crystals in the cytoplasm. In many of these cells a large number of helical polyribosomes are arranged in prominent linear rows, some of which may be up to 5 micrometers in length. Figure 1 shows a large array of helical polyribosomes near a crystalline mass (CRS) in an Earle's L-929 fibroblast exposed to VCR (5ϒ/ml.) for 3 hours At a higher magnification, as seen in figure 2, the helical polyribosomes are seen arranged in parallel rows. In favorably cut sections, a prominent backbone like "stalk" of finely granular material, measuring approximately 300Å in width is seen in close association with the linear rows of helical polyribosomes.


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