The Secondary Blood Vessel System of Segmental Arteries and Dorsal Aorta in Blennius pavo and Zosterisessor ophiocephalus. Histology, Fine Structure and SEM of Vascular Corrosion Casts.

The secondary blood vessel system of the segmental arteries and of the dorsal aorta of the teleost fish Blennius pavo and Zosterisessor ophiocephalus are examined by light microscopy, transmission electron microscopy and by scanning electron microscopy of appropriately processed tissue and of vascular corrosion casts. Dorsal, lateral and ventral segmental arteries and the caudal portions of the dorsal aorta have a secondary vessel system. The secondary vessels are formed by capillaries which arise from the proximal portions of the segmental arteries and from the caudal parts of the dorsal aorta. In Z. ophiocephalus these capillaries are strongly dilated at their origin, in B. pavo they are less dilated, but more intensively coiled. The secondary vessels establish veins which run parallel to the corresponding primary arteries. At the ultrastructural level the secondary vessels consist of a thin endothelium and a longitudinal and a transversal orientated layer of collagen fibres. Secondary veins lack a basal membrane. A possible function of the secondary vessel system of B. pavo and Z. ophiocephalus as a modified drainage system is discussed

Vascularization of Male Gonads in Blennius pavo (Teleostei, Blenniidae) as Revealed by Scanning Electron Microscopy of Vascular Corrosion Casts

The vascular architecture of male gonads of Blennius pavo is studied by scanning electron microscopy of vascular corrosion casts. Arterial supply to the gonads is by a branch of the first ventral segmental artery of the tail. From the surface of the gonads, this vessel gives rise to branches which supply testes, spermatic ducts, testicular glands, blind pouches, urogenital sinus and urogenital papilla. The testis has a rope-ladder-like capillary network around the seminiferous tubules, while in the testicular gland the capillary network is irregular in form. The spermatic ducts are found to have an exterior capillary network located in the compact connective tissue layer and an interior one, lying subepithelially. Urogenital sinus and urogenital papilla show a multilayered capillary network. Angioarchitecture in mature and immature gonads does not differ

Sperm motility in fish: technical applications and perspectives through CASA systems

[EN] Although a relatively high number of sperm quality biomarkers have been reported over the years in several fish species, sperm motility is nowadays considered the best biomarker for fish spermatozoa. The first scientific reports focusing on fish sperm motility date from a century ago, but the objective assessment allowed by computer-aided sperm analysis (CASA-Mot) systems was not applied to fish species until the mid-1980s. Since then, a high number of sperm kinetic parameters from more than 170 fish species have been reported in more than 700 scientific articles, covering a wide range of topics, such as sperm physiology, sperm storage, broodstock management, the phenomenon of sperm competition, ecotoxicology and understanding the life cycle of the species. The sperm kinetic parameters provided by CASA-Mot systems can serve as powerful and useful tools for aquaculture and ecological purposes, and this review provides an overview of the major research areas in which fish sperm motility assessment by a CASA-Mot system has been used successfully.This writing of this manuscript as received funding from the European Union's Horizon 2020 Research and Innovation program under the Marie Sklodowska-Curie Grant Agreement No. 642893 (ETN IMPRESS). V. Gallego has a postdoctoral grant from the Universitat Politecnica de Valencia (PAID-10-16).Gallego Albiach, V.; Asturiano Nemesio, JF. (2018). Sperm motility in fish: technical applications and perspectives through CASA systems. Reproduction Fertility and Development. 30(6):820-832. https://doi.org/10.1071/RD17460S82083230

Comparison of two techniques for the morphometry study on gilthead seabream (Sparus aurata) spermatozoa and evaluation of changes induced by cryopreservation

[EN] The development of powerful software has made possible spermatozoa morphology studies. However, some problems have emerged in relation to protocol standardization to compare results from different laboratories. This study was carried out to compare two techniques commonly used (staining vs phase contrast technique) for the morphometry study of gilthead sea bream spermatozoa using an integrated sperm analysis system (ISAS). Spermatozoa morphometry values were significantly affected by the technique used, and phase contrast technique was found to be the more accurate method, showing lower coefficients of variation on spermatozoa morphometry parameters measurements. Moreover, it has been shown that cryopreservation process produces damage in gilthead sea bream spermatozoa, causing negative effects in sperm parameters as spermatozoa morphometry (a decrease in cell volume), motility (from 95 to 68% motile cells) and viability (from 95 to 87% of live cells), being the addition of freezing medium containing cryoprotectant (DMSO) an important factor that caused the morphometry changes. (C) 2012 Elsevier Inc. All rights reserved.This work was financed by the Spanish Ministry of Science and Innovation (MICINN; AGL2007-64040-C03-00, Project SELECTBREAM). V. Gallego and I. Mazzeo were supported by predoctoral scholarships financed by the Spanish MICINN and Generalitat Valenciana, respectively. D.S. Penaranda had a postdoctoral grant from UPV.Gallego Albiach, V.; Peñaranda, D.; Marco Jiménez, F.; Mazzeo, I.; Pérez Igualada, LM.; Asturiano Nemesio, JF. (2012). Comparison of two techniques for the morphometry study on gilthead seabream (Sparus aurata) spermatozoa and evaluation of changes induced by cryopreservation. Theriogenology. 77(6):1078-1087. https://doi.org/10.1016/j.theriogenology.2011.10.010S1078108777

Motilidade espermática, fertilização dos ovócitos e eclosão dos ovos de Jundiá em água contaminada por cádmio

Este estudo foi realizado para avaliar o efeito da contaminação da água por cádmio sobre a taxa de fertilização dos ovócitos e de eclosão dos ovos e a duração da motilidade espermática em jundiá (Rhamdia quelen). Foram realizados dois ensaios: no ensaio 1, foi avaliado o efeito do cádmio sobre a fertilização artificial dos ovócitos e a eclosão dos ovos e, no ensaio 2, o efeito do cádmio sobre a duração da motilidade espermática. Em ambos os ensaios, adotou-se o delineamento experimental inteiramente casualizado com cinco níveis de cádmio na água (0; 20; 50; 80 e 110 mg L-1), avaliados com quatro (ensaio 1) ou três repetições (ensaio 2). As taxas de fertilização e eclosão tiveram resposta linear, mantendo-se constantes até os níveis de 28,6 e 40,4 mg L-1, respectivamente. A partir desses níveis, ocorreu um efeito linear inversamente proporcional entre as taxas de fertilização e eclosão e o aumento dos níveis de cádmio. O aumento do nível de cádmio na água teve efeito linear inverso na duração da motilidade espermática, proporcionando redução de 21,8s em água limpa para 10,6s em água contaminada contendo 110 mg-1. Níveis a partir de 20,0 e 28,6 mg L-1 influenciam espermatozoides e ovócitos de jundiá, respectivamente.The objective of this work was to evaluate the effect of water contaminated by cadmium on the rates of oocyte fertilization and egg hatching, and sperm motility duration on jundiá catfish (Rhamdia quelen). Two trials were performed: in trial 1, it was evaluated the effect of cadmium on the artificial fertilization of oocytes and egg hatching and in trial 2, the effects of cadmium on the sperm motility duration were evaluated. In both trials, it was used a completely randomized experimental design with five levels of cadmium in the water (0; 20; 50; 80 and 110 mg L-1) evaluated with four (trial 1) or three replicates (trial 2). Fertilization and hatching rates showed linear response, remaining constant up to the levels of 28.6 and 40.4 mg L-1, respectively. From these levels, a linear effect inversely proportional between the fertilization and hatching rates and an increase in the levels of cadmium occurred. The increase on the level of cadium in the water had an inverse linear effect of sperm motility duration providing a reduction from 21.8s in clean water to 10.6s in contaminated water containing 110 mg L-1. Levels from 20.0 to 28.6 mg L-1 influence sperm and oocytes of jundiá catfish, respectively