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Effect of sampling location, release technique and time afteractivation on the movement characteristics of scallop (Pecten maximus)sperm

Published online by Cambridge University Press:  08 April 2013

Marc Suquet*
Affiliation:
Ifremer, UMR 6539, Physiologie fonctionnelle des organismes marins, Station expérimentale d’Argenton, Argenton, France
Claudie Quere
Affiliation:
Ifremer, UMR 6539, Physiologie fonctionnelle des organismes marins, Plouzané, France
Christian Mingant
Affiliation:
Ifremer, UMR 6539, Physiologie fonctionnelle des organismes marins, Station expérimentale d’Argenton, Argenton, France
Luc Lebrun
Affiliation:
Ifremer, UMR 6539, Physiologie fonctionnelle des organismes marins, Station expérimentale d’Argenton, Argenton, France
Dominique Ratiskol
Affiliation:
Ifremer, UMR 6539, Physiologie fonctionnelle des organismes marins, Station expérimentale d’Argenton, Argenton, France
Philippe Miner
Affiliation:
Ifremer, UMR 6539, Physiologie fonctionnelle des organismes marins, Plouzané, France
Jacky Cosson
Affiliation:
University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, 38925 Vodnany, Czech Republic
*
a Corresponding author:[email protected]
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Abstract

Sperm characteristics of scallops have not been well described in the scientificliterature. The effects of sperm release technique (thermal shock versus serotonininjection), of sperm collection technique (testis sampling versus serotonin injection), ofsperm sampling location along the genital tract, of in vitro sperm maturation, and of timepost activation on scallop sperm characteristics were assessed in the present work.Whatever sperm release technique used, no significant differences were observed regardingthe percentage of motile spermatozoa and the velocity of the average path (VAP). Comparedto testicular sperm, a higher percentage of motile spermatozoa, VAP and intracellularadenosine triphosphate (ATP) content were observed for sperm shed after serotonininjection. From the distal part of testes up to the gonopore, an increase of thepercentage of motile spermatozoa and VAP was assessed, suggesting a sperm ‘maturationprocess’ along the genital ducts. A higher increase in the percentage of motile sperm wasrecorded during a 5 min incubation of testicular sperm in seawater containing 2 mMserotonin and seawater containing 10 mM caffein compared to seawater (control). Inaddition, a higher VAP was assessed, incubating testicular sperm in caffein, compared tocontrol or serotonin. Then, the percentage of motile spermatozoa, VAP and intracellularATP content exhibited a progressive reduction during the 10 h swimming period. Mean valuesof the percentage of motile spermatozoa, VAP, sperm track linearity (LIN) andintracellular ATP content recorded at the beginning of the movement period for spermsamples collected after intragonadal serotonin injection, were 82 ± 7%,162 ± 15μm s-1, 0.33 ± 0.12 and 212 ± 133 nmol × 10-9 spermatozoa (n = 9 males), respectively. The presentstudy confirms the existence of a sperm “maturation process” along scallop genital ducts.In addition, the cessation of scallop sperm movement can be explained by the exhaustion ofATP content at the end of the movement phase.

Type
Research Article
Copyright
© EDP Sciences, IFREMER, IRD 2013

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