Autotomy and regeneration of the visceral mass in feather stars

Zoomorphology ◽  
2020 ◽  
Vol 139 (2) ◽  
pp. 171-187
Author(s):  
Igor Yu. Dolmatov ◽  
Nadezhda V. Kalacheva ◽  
Elena S. Mekhova ◽  
Lidia T. Frolova
Keyword(s):  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Zehua Zheng ◽  
Kazuhiro Kawakami ◽  
Dingkun Zhang ◽  
Lumi Negishi ◽  
Mohamed Abomosallam ◽  
...  

AbstractThe Pacific oyster, Crassostrea gigas, is a traditional food worldwide. The soft body of the oyster can easily accumulate heavy metals such as cadmium (Cd). To clarify the molecular mechanism of Cd accumulation in the viscera of C. gigas, we identified Cd-binding proteins. 5,10,15,20-Tetraphenyl-21H,23H-porphinetetrasulfonic acid, disulfuric acid, tetrahydrate, and Cd-binding competition experiments using immobilized metal ion affinity chromatography revealed the binding of water-soluble high molecular weight proteins to Cd, including C. gigas protein disulfide isomerase (cgPDI). Liquid chromatography–tandem mass spectrometry (LC–MS/MS) analyses revealed two CGHC motifs in cgPDI. The binding between Cd and rcgPDI was confirmed through a Cd-binding experiment using the TPPS method. Isothermal titration calorimetry (ITC) revealed the binding of two Cd ions to one molecule of rcgPDI. Circular dichroism (CD) spectrum and tryptophan fluorescence analyses demonstrated that the rcgPDI bound to Cd. The binding markedly changed the two-dimensional or three-dimensional structures. The activity of rcgPDI measured by a PDI Activity Assay Kit was more affected by the addition of Cd than by human PDI. Immunological analyses indicated that C. gigas contained cgPDI at a concentration of 1.0 nmol/g (viscera wet weight). The combination of ITC and quantification results revealed that Cd-binding to cgPDI accounted for 20% of the total bound Cd in the visceral mass. The findings provide new insights into the defense mechanisms of invertebrates against Cd.


2014 ◽  
Vol 456 (1) ◽  
pp. 195-198 ◽  
Author(s):  
T. V. Tinkova ◽  
A. O. Kasumyan ◽  
P. Y. Dgebuadze ◽  
L. T. K. Oanh ◽  
T. A. Britaev

1964 ◽  
Vol 42 (2) ◽  
pp. 305-321 ◽  
Author(s):  
Austina V. Kennedy ◽  
Helen I. Battle

Cyclic changes in the gonad of Crassostrea virginica (Gmelin), a dioecious, oviparous lamellibranch, are described as they occurred toward the most northerly limit of the range, Malpeque Bay, P.E.I., Canada, during 1961 and 1962. The gonad, composed of right and left gonadal lobes lying immediately beneath the mantle, consists of extensively branched follicles comprising the outer margin of the visceral mass. The follicles open into peripherally located ducts which lead into paired gonoducts terminating in the suprabranchial chamber. During the fall and winter the germinal epithelium is in an indifferent or inactive state. The sex for the current season is distinguishable when proliferation commences in May. Maximum gonadal development occurs in late June or early July as determined by comparison of gonadal width to body width in mid-transverse sections. Primary oocytes are initially distinguishable from oogonia by the presence of a distinct nucleolus, and later by an amphinucleolus consisting of a plasmosome and a karyosome. Seasonal growth of the primary oocyte was followed by a planimetry method using measurements of total area and nuclear area from prepared sections. The spindle for the first meiotic division is established immediately on rupture of the oocyte from the follicular wall. Spermatogenesis and spermiogenesis are completed within the follicle. Following spawning, amoebocytes infiltrate the follicles and interfollicular connective tissue to phagocytize unspawned gametes. By late October the follicles of both male and female consist of a low germinal epithelium and a few unresorbed gametes, and remain inactive until proliferation the following spring.


1994 ◽  
Vol 27 (1) ◽  
pp. 97-101 ◽  
Author(s):  
Alberto E. Minetti ◽  
Giancesare Belli

2005 ◽  
Vol 59 (3-4) ◽  
pp. 463-474 ◽  
Author(s):  
Olgica Dragicevic ◽  
Milan Baltic

The consumption of snail meat goes back to prehistoric times. Different ancient nations had snails on their menu, but Helices culture as a productive activity was born as a Roman culture. Some of the most economically important edible species are: Helix aspersa (Mtiller) Helixpomatia (Linne), Helix iucorum (Linne), Helix aperta (Born), Eobania vermiculata (Miiller). Together with its tasie, snail meat has several advantages over others: quite low lipid rate and calorie values versus rich mineral, essential amino acid and fatty acid content. The composition of snail meat is presented. In addition, the composition of different snail species and the part analyzed (pedal mass and visceral mass) is presented. Also, the differences in composition according to the species (snail meat horse/chicken meat, beef, swine meat, fish meat) are presented. The French are the world's leading consumers of snails. !n France snails come to market in a variety of ways. Estimated consumption of snails in France is around 40 000 tones/year. Total French imports account for 25% of world imports. France is also the leading exporter of prepared snails, mainly sold as preserved snails and prepared dishes. Snail imports have been much higher than exports (65 tones exported in 2002. vs. 2.700 tones imported). Despite the large consumption, only 3% of snails in France come from production (farming). Italy is in second place in the world consumption of snails, and Spain and Germany are in the third and fourth place. The development of snails consumption in Italy is followed with the same amount of production of snails in the whole biological circle. In 2001, from 24,700 tons, 9,350 tons (37.8%) came from production, 6 00 tons (2.4%) came from nature, and 14,750 tons (59.70%) came from imports (frozen, fresh and prepared snails). In Serbia, at the beginning of 2005, we had over 400 registered farms for snail production.


1937 ◽  
Vol s2-79 (315) ◽  
pp. 423-445
Author(s):  
DAPHNE ATKINS

A form of fusion involving only the cuticle has been found in certain Lamellibranchs between the outer demibranchs and the mantle or the visceral mass; between the two inner demibranchs; and, in forms possessing a fourth aperture, between the mantle lobes in the mid-ventral line between this and the pedal aperture. The histological structure of the junction is described, and is especially considered in relation to the condition of the fourth aperture in the Solenidae.


Paleobiology ◽  
2018 ◽  
Vol 44 (3) ◽  
pp. 444-459 ◽  
Author(s):  
Brendan M. Anderson ◽  
Warren D. Allmon

AbstractAlthough generally considered rare in gastropods, septation has long been noted in turritellids, but functional hypotheses do not survive strong scrutiny. Here we outline a methodology for testing spandrel hypotheses and apply it to the problem of turritellid septa. We follow Gould in using “spandrel” as a term for all features that are nonadaptive sequelae of adaptive features of organisms, including those that are structurally necessary, those that are developmentally correlated, and nondeterministic by-products that are correlated to features under selection.In turritellids, septa are constructed in microstructural continuity with secondary internal thickening of the shell, are highly variable features infraspecifically, and are strongly associated with degree of shell thickening. We therefore conclude that rather than being themselves adaptive, turritellid septa are spandrels of shell thickening. Turritellid septa are composed of crossed lamellar aragonite, which appears to be constructed by mantle epithelium over the visceral mass. Septation was also found in 22 of 24 gastropod families examined from a broad phylogenetic distribution. Septa thus appear to be a widespread feature of caenogastropods, in strong contrast to previous assertions that septa are less common in modern or high-spired shells.


1992 ◽  
Vol 6 ◽  
pp. 117-117
Author(s):  
James W. Hagadorn ◽  
George E. Boyajian

The escalation of predator-prey interactions over the Phanerozoic is described as an “arms race” among the Gastropoda. Examples of escalation have been extensively documented on the scale of hundreds of millions of years, however, these patterns are not well documented on shorter time scales. Effective escalation of prey defenses should cause a drop in predatory efficiency. We study the efficiency of Naticid and Muricid predation upon Turritelline gastropods from the Miocene to the Pliocene. These predators leave a well preserved trace of predation in the form of a borehole in the shell of the prey. This study focuses on 18 species of Miocene and Pliocene Turritella from the southeastern United States. Over five thousand individual shells were examined and measured, collected from 13 localities from Maryland to southern Florida.Predatory efficiency is determined by a number of factors: shell thickness at drillhole site, vertical location of drillhole, percent of shells that have multiple drillholes, and percent of shells that contain incomplete drillholes. Shell thickness at drillhole and location of drillhole are measured because predators would benefit by expending less energy drilling into the thinnest part of the shell that is nearest the visceral mass of the prey. Multiple complete boreholes represent at least one failure to obtain food. Incomplete boreholes represent a drilling attempt which has failed to produce food at the cost of metabolic energy.While the intensity of Naticid and Muricid predation of Turritella increases (χ2, α<.01), predators become less efficient from the Miocene to the Pliocene. Decreased predatory efficiency is indicated by an increase in the number of shells with multiple and incomplete drilling sites (χ2, α<.01). Although predators appear to have little radial preference, they indicate strong vertical preference for centrally located drilling sites (t-test, α<.01). Predators appear to be drilling into thicker parts of Turritelline shells and thus expending more energy in drilling -however, this pattern is not statistically significant (χ2, α>.20).We show that the efficiency of Naticid and Muricid predators decreased from the Miocene to Pliocene. Decreased efficiency of predators might result from newly evolved structural changes in prey shells, new prey escape responses or problems in predator recognition of live versus dead prey shells resulting from high densities of both living and dead individuals.It remains to be seen whether predatory efficiency declines over longer time scales. In light of previous studies which have concentrated on evolution in the shell shape and ornamentation of prey in response to predators, a more promising and direct measure of the efficiency of predation may lie in the study of the frequency of multiple and incompletely drilled shells. By this method we might better judge the effectiveness of defense mechanisms and the evolutionary significance of predator-prey escalation.


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