Why do decapod crustaceans prefer small-sized molluscan prey?

1992 ◽  
Vol 87 ◽  
pp. 239-249 ◽  
Author(s):  
F Juanes
Keyword(s):  
Decapod Crustaceans

Actin filaments in two spermatozoa of crustacea decapoda

1990 ◽  
Vol 48 (3) ◽  
pp. 70-71
Author(s):  
E. Dupré ◽  
G. Schatten
Keyword(s):  
Electron Microscopy ◽  
Actin Filaments ◽  
Low Voltage ◽  
Active Role ◽  
Main Body ◽  
Robinson Crusoe ◽  
Decapod Crustaceans ◽  
Actual Participation ◽  
Voltage Scanning ◽  
Scanning Electron

Sperm of decapod crustaceans are formed by a round or cup-shaped body, a complex acrosome and one a few appendages emerging from the main body. Although this sperm does not have motility, it has some components of the cytoskeleton like microtubules, which are found inside the appendages. Actin filaments have been found in the spike of penaeidae sperms. The actual participation of the crustacean decapod sperm cytoskeleton during fertilization is not well understood. Actin is supposed to play an active role in drawing the penaeidae shrimp sperm closer to the egg after bending of the spike. The present study was aimed at the localization of actin filaments in sperm of the Robinson Crusoe island lobster, Jasus frontalis and in the crayfish Orconectes propincus, by fluorescent probes and low voltage scanning electron microscopy.

scholarly journals Humane Slaughter of Edible Decapod Crustaceans

Animals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 1089
Author(s):  
Francesca Conte ◽  
Eva Voslarova ◽  
Vladimir Vecerek ◽  
Robert William Elwood ◽  
Paolo Coluccio ◽  
...  
Keyword(s):  
Cognitive Capacity ◽  
Decapod Crustaceans ◽  
The Public ◽  
Large Numbers ◽  
Increasing Demand

Vast numbers of crustaceans are produced by aquaculture and caught in fisheries to meet the increasing demand for seafood and freshwater crustaceans. Simultaneously, the public is increasingly concerned about current methods employed in their handling and killing. Recent evidence has shown that decapod crustaceans probably have the capacity to suffer because they show responses consistent with pain and have a relatively complex cognitive capacity. For these reasons, they should receive protection. Despite the large numbers of crustaceans transported and slaughtered, legislation protecting their welfare, by using agreed, standardized methods, is lacking. We review various stunning and killing systems proposed for crustaceans, and assess welfare concerns. We suggest the use of methods least likely to cause suffering and call for the implementation of welfare guidelines covering the slaughter of these economically important animals.

Neritoptyx hogansoninew species (Gastropoda, Mollusca) from the Upper Cretaceous Fox Hills Formation on the Dakota Isthmus, western United States

2018 ◽  
Vol 93 (2) ◽  
pp. 278-290
Author(s):  
J. Mark Erickson
Keyword(s):  
Heat Transfer ◽  
United States ◽  
New Species ◽  
North America ◽  
Upper Cretaceous ◽  
Gulf Coast ◽  
Western United States ◽  
Western Interior Seaway ◽  
Decapod Crustaceans ◽  
Upper Maastrichtian

AbstractIn midcontinent North America, the Fox Hills Formation (Upper Cretaceous, upper Maastrichtian) preserves the last marine faunas in the central Western Interior Seaway (WIS).Neritoptyx hogansoninew species, a small littoral snail, exhibited allometric change from smooth to corded ornament and rounded to shouldered shape during growth. Specimens preserve a zig-zag pigment pattern that changes to an axial pattern during growth.Neritoptyx hogansoninew species was preyed on by decapod crustaceans, and spent shells were occupied by pagurid crabs. Dead mollusk shells, particularly those ofCrassostrea subtrigonalis(Evans and Shumard, 1857), provided a hard substrate to which they adhered on the Fox Hills tidal flats. This new neritimorph gastropod establishes a paleogeographic and chronostratigraphic proxy for intertidal conditions on the Dakota Isthmus during the late Maastrichtian. Presence of a neritid extends the marine tropical/temperate boundary in the WIS northward to ~44° late Maastrichtian paleolatitude. Late Maastrichtian closure of the isthmus subsequently altered marine heat transfer by interrupting northward flow of tropical currents from the Gulf Coast by as much as 1 to 1.5 million years before the Cretaceous ended.UUID:http://zoobank.org/3ba56c07-fcca-4925-a2f0-df663fc3a06b

Dynamics of hyperacetylated histone H4 (H4Kac) during spermatogenesis in four decapod crustaceans

2021 ◽  
pp. 101594
Author(s):  
Tingrong Chen ◽  
Shumei Mu ◽  
Mingshen Guo ◽  
Zhaohui Zhang ◽  
Xianjiang Kang
Keyword(s):  
Histone H4 ◽  
Decapod Crustaceans

Transmembrane Activity Gradients of K and cl in the Muscle Fibres of Osmoconforming Marine Decapod Crustaceans

1978 ◽  
Vol 72 (1) ◽  
pp. 127-140
Author(s):  
ROBERT W. FREEL
Keyword(s):  
Sea Water ◽  
Membrane Potentials ◽  
Resting Potential ◽  
Muscle Fibres ◽  
Salinity Adaptation ◽  
Decapod Crustaceans ◽  
Marine Crustaceans ◽  
Equilibrium Distributions

1. The resting membrane potentials (Em) and the transmembrane activity gradients for K and Cl were measured in the muscle fibres of osmoconforming (Callianassa and Cancer) and weakly osmoregulating (Pachygrapsus) marine crustaceans acclimated to various osmotic conditions. 2. The muscle membranes of sea water acclimated crabs behave as good K electrodes. However, a slight contribution of Na to the resting potential was demonstrated in all species. The ratio PNa/PK was about 0.01. Equilibrium potentials (measured with ion-selective microelectrodes) for Cl were equal to Em, while EK was always more negative than Em as a result of the slight Na contribution. 3. Acclimation to dilute or concentrated sea water had little effect on the K electrode properties or Na permeabilities of these fibres. The muscle fibres were depolarized in crabs acclimated to concentrated sea water and were hyperpolarized in crabs adapted to dilute sea water. These changes resulted solely from alterations in (aK)i/ (aK)O which were in turn brought about by changes in cellular and haemolymph hydration. 4. Since the Na contribution to Em was so small in all conditions, it was concluded that the distributions of K and Cl are best considered in terms of Donnan equilibria, and that the cellular K and Cl adjustments observed during salinity adaptation reflect the passive re-establishment of new equilibrium distributions for these ions.

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