13 results on '"Abascal FJ"'
Search Results
2. Biodegradable DFADs: Current Status and Prospects
- Author
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Zudaire, I, Moreno, G, Murua, J, Murua, H, Tolotti, Mt, Roman, M, Hall, M, Lopez, J, Grande, M, Merino, G, Escalle, L, Hamer, P, Basurko, Oc, Capello, Manuela, Dagorn, Laurent, Ramos, Ml, Abascal, Fj, Baez, Jc, Pascual-alayon, Pj, Deniz, S, Santiago, J, Zudaire, I, Moreno, G, Murua, J, Murua, H, Tolotti, Mt, Roman, M, Hall, M, Lopez, J, Grande, M, Merino, G, Escalle, L, Hamer, P, Basurko, Oc, Capello, Manuela, Dagorn, Laurent, Ramos, Ml, Abascal, Fj, Baez, Jc, Pascual-alayon, Pj, Deniz, S, and Santiago, J
- Abstract
Until recently, dFAD structure, materials and designs have remained quite rudimentary and virtually the same since their discovery, characterized by the increase of the dimensions and prevailing heavy use of plastic components. Biodegradable materials are called to be an important part of the solution, as they can faster degrade in the environment, free of toxins and heavy metals, reducing their lifespan, and preventing them from accumulating in sensitive areas once they are abandoned, lost or discarded. During last decades, regulatory measures at tRFMOs have advanced in the gradual implementation of biodegradable materials in dFAD constructions together with other measures limiting the number of active dFADs and the use of netting materials. However, more clarity is needed starting with a standardised definition of biodegradable dFADs among tRFMOs, to provide operational guidance. Research with those natural and synthetic materials is required, along with updated data collection for monitoring standards, as well as alternative and complementary actions need to be explored to contribute to minimising dFAD adverse effects on environment. Acknowledging the current difficulties for the implementation of fully biodegradable dFADs a stepwise process towards the implementation of fully biodegradable dFADs should be considered.
- Published
- 2021
3. Reply to: Shark mortality cannot be assessed by fishery overlap alone
- Author
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Queiroz, N, Humphries, NE, Couto, A, Vedor, M, da Costa, I, Sequeira, AMM, Mucientes, G, Santos, AM, Abascal, FJ, Abercrombie, DL, Abrantes, K, Acuña-Marrero, D, Afonso, AS, Afonso, P, Anders, D, Araujo, G, Arauz, R, Bach, P, Barnett, A, Bernal, D, Berumen, ML, Lion, SB, Bezerra, NPA, Blaison, AV, Block, BA, Bond, ME, Bonfil, R, Bradford, RW, Braun, CD, Brooks, EJ, Brooks, A, Brown, J, Bruce, BD, Byrne, ME, Campana, SE, Carlisle, AB, Chapman, DD, Chapple, TK, Chisholm, J, Clarke, CR, Clua, EG, Cochran, JEM, Crochelet, EC, Dagorn, L, Daly, R, Cortés, DD, Doyle, TK, Drew, M, Duffy, CAJ, Erikson, T, Espinoza, E, Ferreira, LC, Ferretti, F, Filmalter, JD, Fischer, GC, Fitzpatrick, R, Fontes, J, Forget, F, Fowler, M, Francis, MP, Gallagher, AJ, Gennari, E, Goldsworthy, SD, Gollock, MJ, Green, JR, Gustafson, JA, Guttridge, TL, Guzman, HM, Hammerschlag, N, Harman, L, Hazin, FHV, Heard, M, Hearn, AR, Holdsworth, JC, Holmes, BJ, Howey, LA, Hoyos, M, Hueter, RE, Hussey, NE, Huveneers, C, Irion, DT, Jacoby, DMP, Jewell, OJD, Johnson, R, Jordan, LKB, Joyce, W, Keating Daly, CA, Ketchum, JT, Klimley, AP, Kock, AA, Koen, P, Ladino, F, Lana, FO, Lea, JSE, Llewellyn, F, Lyon, WS, MacDonnell, A, Macena, BCL, Marshall, H, McAllister, JD, Queiroz, N, Humphries, NE, Couto, A, Vedor, M, da Costa, I, Sequeira, AMM, Mucientes, G, Santos, AM, Abascal, FJ, Abercrombie, DL, Abrantes, K, Acuña-Marrero, D, Afonso, AS, Afonso, P, Anders, D, Araujo, G, Arauz, R, Bach, P, Barnett, A, Bernal, D, Berumen, ML, Lion, SB, Bezerra, NPA, Blaison, AV, Block, BA, Bond, ME, Bonfil, R, Bradford, RW, Braun, CD, Brooks, EJ, Brooks, A, Brown, J, Bruce, BD, Byrne, ME, Campana, SE, Carlisle, AB, Chapman, DD, Chapple, TK, Chisholm, J, Clarke, CR, Clua, EG, Cochran, JEM, Crochelet, EC, Dagorn, L, Daly, R, Cortés, DD, Doyle, TK, Drew, M, Duffy, CAJ, Erikson, T, Espinoza, E, Ferreira, LC, Ferretti, F, Filmalter, JD, Fischer, GC, Fitzpatrick, R, Fontes, J, Forget, F, Fowler, M, Francis, MP, Gallagher, AJ, Gennari, E, Goldsworthy, SD, Gollock, MJ, Green, JR, Gustafson, JA, Guttridge, TL, Guzman, HM, Hammerschlag, N, Harman, L, Hazin, FHV, Heard, M, Hearn, AR, Holdsworth, JC, Holmes, BJ, Howey, LA, Hoyos, M, Hueter, RE, Hussey, NE, Huveneers, C, Irion, DT, Jacoby, DMP, Jewell, OJD, Johnson, R, Jordan, LKB, Joyce, W, Keating Daly, CA, Ketchum, JT, Klimley, AP, Kock, AA, Koen, P, Ladino, F, Lana, FO, Lea, JSE, Llewellyn, F, Lyon, WS, MacDonnell, A, Macena, BCL, Marshall, H, and McAllister, JD
- Published
- 2021
4. Influence of sampling gear in assessment of reproductive parameters for bluefin tuna in the western Mediterranean
- Author
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Medina, A, primary, Abascal, FJ, additional, Aragón, L, additional, Mourente, G, additional, Aranda, G, additional, Galaz, T, additional, Belmonte, A, additional, de la Serna, JM, additional, and García, S, additional
- Published
- 2007
- Full Text
- View/download PDF
5. Body size and isotopic profiles enable discrimination between long-term resident and highly migrant contingents of Atlantic bluefin tuna.
- Author
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Medina A, Magro A, Abascal FJ, and Varela JL
- Subjects
- Animals, Atlantic Ocean, Mediterranean Sea, Population Dynamics, Carbon Isotopes analysis, Nitrogen Isotopes analysis, Environmental Monitoring, Tuna, Animal Migration, Body Size
- Abstract
The Atlantic bluefin tuna (ABFT) population ranges throughout the Atlantic Ocean and Mediterranean Sea, and consists of multiple contingents that use diverse habitats and show different movement patterns over the life cycle. Based on body size, elemental and isotopic data of C and N in muscle and liver, we analysed eastern-stock ABFT by comparing mid-sized individuals caught by hook-and-line gears with larger individuals harvested from traps in the Strait of Gibraltar (SoG). Our results show that trophic-related chemical markers have potential for separating temporarily sympatric contingents throughout the ABFT population range, reflecting size-dependent spatial distribution and differential patterns of residency and migration. We present evidence of long-term residency of ABFT in the SoG that persists until the estimated age of ∼5 years (size of ∼140 cm in straight fork length). This age apparently marks a turning point in the life history, where there occurs an ontogenetic switch in the migratory behaviour and distributional pattern. This study contributes new insight into our knowledge about size structure and residency-movement patterns in eastern ABFT. It shows distinct size-dependent migratory and spatial dynamics. The present results encourage further investigation on poorly studied ABFT contingents for a better understanding of the population dynamics towards more comprehensive management plans., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2024
- Full Text
- View/download PDF
6. Reply to: Caution over the use of ecological big data for conservation.
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Queiroz N, Humphries NE, Couto A, Vedor M, da Costa I, Sequeira AMM, Mucientes G, Santos AM, Abascal FJ, Abercrombie DL, Abrantes K, Acuña-Marrero D, Afonso AS, Afonso P, Anders D, Araujo G, Arauz R, Bach P, Barnett A, Bernal D, Berumen ML, Lion SB, Bezerra NPA, Blaison AV, Block BA, Bond ME, Bonfil R, Braun CD, Brooks EJ, Brooks A, Brown J, Byrne ME, Campana SE, Carlisle AB, Chapman DD, Chapple TK, Chisholm J, Clarke CR, Clua EG, Cochran JEM, Crochelet EC, Dagorn L, Daly R, Cortés DD, Doyle TK, Drew M, Duffy CAJ, Erikson T, Espinoza E, Ferreira LC, Ferretti F, Filmalter JD, Fischer GC, Fitzpatrick R, Fontes J, Forget F, Fowler M, Francis MP, Gallagher AJ, Gennari E, Goldsworthy SD, Gollock MJ, Green JR, Gustafson JA, Guttridge TL, Guzman HM, Hammerschlag N, Harman L, Hazin FHV, Heard M, Hearn AR, Holdsworth JC, Holmes BJ, Howey LA, Hoyos M, Hueter RE, Hussey NE, Huveneers C, Irion DT, Jacoby DMP, Jewell OJD, Johnson R, Jordan LKB, Joyce W, Keating Daly CA, Ketchum JT, Klimley AP, Kock AA, Koen P, Ladino F, Lana FO, Lea JSE, Llewellyn F, Lyon WS, MacDonnell A, Macena BCL, Marshall H, McAllister JD, Meÿer MA, Morris JJ, Nelson ER, Papastamatiou YP, Peñaherrera-Palma C, Pierce SJ, Poisson F, Quintero LM, Richardson AJ, Rogers PJ, Rohner CA, Rowat DRL, Samoilys M, Semmens JM, Sheaves M, Shillinger G, Shivji M, Singh S, Skomal GB, Smale MJ, Snyders LB, Soler G, Soria M, Stehfest KM, Thorrold SR, Tolotti MT, Towner A, Travassos P, Tyminski JP, Vandeperre F, Vaudo JJ, Watanabe YY, Weber SB, Wetherbee BM, White TD, Williams S, Zárate PM, Harcourt R, Hays GC, Meekan MG, Thums M, Irigoien X, Eguiluz VM, Duarte CM, Sousa LL, Simpson SJ, Southall EJ, and Sims DW
- Subjects
- Conservation of Natural Resources, Big Data, Ecology
- Published
- 2021
- Full Text
- View/download PDF
7. Reply to: Shark mortality cannot be assessed by fishery overlap alone.
- Author
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Queiroz N, Humphries NE, Couto A, Vedor M, da Costa I, Sequeira AMM, Mucientes G, Santos AM, Abascal FJ, Abercrombie DL, Abrantes K, Acuña-Marrero D, Afonso AS, Afonso P, Anders D, Araujo G, Arauz R, Bach P, Barnett A, Bernal D, Berumen ML, Lion SB, Bezerra NPA, Blaison AV, Block BA, Bond ME, Bonfil R, Bradford RW, Braun CD, Brooks EJ, Brooks A, Brown J, Bruce BD, Byrne ME, Campana SE, Carlisle AB, Chapman DD, Chapple TK, Chisholm J, Clarke CR, Clua EG, Cochran JEM, Crochelet EC, Dagorn L, Daly R, Cortés DD, Doyle TK, Drew M, Duffy CAJ, Erikson T, Espinoza E, Ferreira LC, Ferretti F, Filmalter JD, Fischer GC, Fitzpatrick R, Fontes J, Forget F, Fowler M, Francis MP, Gallagher AJ, Gennari E, Goldsworthy SD, Gollock MJ, Green JR, Gustafson JA, Guttridge TL, Guzman HM, Hammerschlag N, Harman L, Hazin FHV, Heard M, Hearn AR, Holdsworth JC, Holmes BJ, Howey LA, Hoyos M, Hueter RE, Hussey NE, Huveneers C, Irion DT, Jacoby DMP, Jewell OJD, Johnson R, Jordan LKB, Joyce W, Keating Daly CA, Ketchum JT, Klimley AP, Kock AA, Koen P, Ladino F, Lana FO, Lea JSE, Llewellyn F, Lyon WS, MacDonnell A, Macena BCL, Marshall H, McAllister JD, Meÿer MA, Morris JJ, Nelson ER, Papastamatiou YP, Peñaherrera-Palma C, Pierce SJ, Poisson F, Quintero LM, Richardson AJ, Rogers PJ, Rohner CA, Rowat DRL, Samoilys M, Semmens JM, Sheaves M, Shillinger G, Shivji M, Singh S, Skomal GB, Smale MJ, Snyders LB, Soler G, Soria M, Stehfest KM, Thorrold SR, Tolotti MT, Towner A, Travassos P, Tyminski JP, Vandeperre F, Vaudo JJ, Watanabe YY, Weber SB, Wetherbee BM, White TD, Williams S, Zárate PM, Harcourt R, Hays GC, Meekan MG, Thums M, Irigoien X, Eguiluz VM, Duarte CM, Sousa LL, Simpson SJ, Southall EJ, and Sims DW
- Subjects
- Animals, Conservation of Natural Resources, Seafood, Fisheries, Sharks
- Published
- 2021
- Full Text
- View/download PDF
8. Common dolphinfish, Coryphaena hippurus, spawn at their easternmost Atlantic range adjacent to the Mediterranean Sea.
- Author
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Medina A, Abascal FJ, and Varela JL
- Subjects
- Animals, Atlantic Ocean, Female, Male, Mediterranean Sea, Seasons, Spain, Perciformes physiology, Reproduction, Sexual Behavior, Animal physiology
- Abstract
This study provides sound evidence of the spawning activity of common dolphinfish (Coryphaena hippurus) in the Gulf of Cadiz (southwest Spain) during summer months. Along with waters off Côte d'Ivoire, this area adjacent to the Mediterranean Sea is the easternmost Atlantic spawning ground documented for the species. All the fish analysed (5 males and 15 females) were at spawning stage, except the smallest female (61.5 cm in fork length), which might not have yet reached sexual maturation. The oceanographic conditions during the samplings were similar to those occurring during the peak spawning season in the Gulf of Mexico. The study results are consistent with recent genetic studies indicating differentiation between Mediterranean and Atlantic dolphinfish populations, with the Strait of Gibraltar representing a boundary between two distinct reproductive units. The present results may contribute to improve the understanding of the dynamics of dolphinfish population and the management of eastern Atlantic and Mediterranean stocks., (© 2020 The Fisheries Society of the British Isles.)
- Published
- 2020
- Full Text
- View/download PDF
9. Global spatial risk assessment of sharks under the footprint of fisheries.
- Author
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Queiroz N, Humphries NE, Couto A, Vedor M, da Costa I, Sequeira AMM, Mucientes G, Santos AM, Abascal FJ, Abercrombie DL, Abrantes K, Acuña-Marrero D, Afonso AS, Afonso P, Anders D, Araujo G, Arauz R, Bach P, Barnett A, Bernal D, Berumen ML, Bessudo Lion S, Bezerra NPA, Blaison AV, Block BA, Bond ME, Bonfil R, Bradford RW, Braun CD, Brooks EJ, Brooks A, Brown J, Bruce BD, Byrne ME, Campana SE, Carlisle AB, Chapman DD, Chapple TK, Chisholm J, Clarke CR, Clua EG, Cochran JEM, Crochelet EC, Dagorn L, Daly R, Cortés DD, Doyle TK, Drew M, Duffy CAJ, Erikson T, Espinoza E, Ferreira LC, Ferretti F, Filmalter JD, Fischer GC, Fitzpatrick R, Fontes J, Forget F, Fowler M, Francis MP, Gallagher AJ, Gennari E, Goldsworthy SD, Gollock MJ, Green JR, Gustafson JA, Guttridge TL, Guzman HM, Hammerschlag N, Harman L, Hazin FHV, Heard M, Hearn AR, Holdsworth JC, Holmes BJ, Howey LA, Hoyos M, Hueter RE, Hussey NE, Huveneers C, Irion DT, Jacoby DMP, Jewell OJD, Johnson R, Jordan LKB, Jorgensen SJ, Joyce W, Keating Daly CA, Ketchum JT, Klimley AP, Kock AA, Koen P, Ladino F, Lana FO, Lea JSE, Llewellyn F, Lyon WS, MacDonnell A, Macena BCL, Marshall H, McAllister JD, McAuley R, Meÿer MA, Morris JJ, Nelson ER, Papastamatiou YP, Patterson TA, Peñaherrera-Palma C, Pepperell JG, Pierce SJ, Poisson F, Quintero LM, Richardson AJ, Rogers PJ, Rohner CA, Rowat DRL, Samoilys M, Semmens JM, Sheaves M, Shillinger G, Shivji M, Singh S, Skomal GB, Smale MJ, Snyders LB, Soler G, Soria M, Stehfest KM, Stevens JD, Thorrold SR, Tolotti MT, Towner A, Travassos P, Tyminski JP, Vandeperre F, Vaudo JJ, Watanabe YY, Weber SB, Wetherbee BM, White TD, Williams S, Zárate PM, Harcourt R, Hays GC, Meekan MG, Thums M, Irigoien X, Eguiluz VM, Duarte CM, Sousa LL, Simpson SJ, Southall EJ, and Sims DW
- Subjects
- Animals, Population Density, Risk Assessment, Sharks classification, Ships, Time Factors, Animal Migration, Fisheries statistics & numerical data, Geographic Mapping, Oceans and Seas, Sharks physiology, Spatio-Temporal Analysis
- Abstract
Effective ocean management and the conservation of highly migratory species depend on resolving the overlap between animal movements and distributions, and fishing effort. However, this information is lacking at a global scale. Here we show, using a big-data approach that combines satellite-tracked movements of pelagic sharks and global fishing fleets, that 24% of the mean monthly space used by sharks falls under the footprint of pelagic longline fisheries. Space-use hotspots of commercially valuable sharks and of internationally protected species had the highest overlap with longlines (up to 76% and 64%, respectively), and were also associated with significant increases in fishing effort. We conclude that pelagic sharks have limited spatial refuge from current levels of fishing effort in marine areas beyond national jurisdictions (the high seas). Our results demonstrate an urgent need for conservation and management measures at high-seas hotspots of shark space use, and highlight the potential of simultaneous satellite surveillance of megafauna and fishers as a tool for near-real-time, dynamic management.
- Published
- 2019
- Full Text
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10. Atlantic bluefin tuna spawn at suboptimal temperatures for their offspring.
- Author
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Reglero P, Ortega A, Balbín R, Abascal FJ, Medina A, Blanco E, de la Gándara F, Alvarez-Berastegui D, Hidalgo M, Rasmuson L, Alemany F, and Fiksen Ø
- Subjects
- Animals, Atlantic Ocean, Chlorophyll, Female, Larva growth & development, Ovum growth & development, Seasons, Time Factors, Zooplankton, Animal Migration physiology, Global Warming, Reproduction physiology, Temperature, Tuna physiology
- Abstract
Life-history traits such as spawning migrations and timing of reproduction are adaptations to specific environmental constraints and seasonal cycles in many organisms' annual routines. In this study we analyse how offspring fitness constrains spawning phenology in a large migratory apex predator, the Atlantic bluefin tuna. The reproductive schedule of Atlantic bluefin tuna varies between spawning sites, suggesting plasticity to local environmental conditions. Generally, temperature is considered to be the main constraint on tuna spawning phenology. We combine evidence from long-term field data, temperature-controlled rearing experiments on eggs and larvae, and a model of egg fitness, and show that Atlantic bluefin tuna do not spawn to optimize egg and larval temperature exposure. The timing of spawning leads to temperature exposure considerably lower than optimal at all spawning grounds across the Atlantic Ocean. The early spawning is constrained by thermal inhibition of egg hatching and larval growth rates, but some other factors must prevent later spawning. Matching offspring with ocean productivity and the prey peak might be an important driver for bluefin tuna spawning phenology. This finding is important for predictions of reproductive timing in future climate warming scenarios for bluefin tuna., (© 2018 The Author(s).)
- Published
- 2018
- Full Text
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11. Spawning behaviour and post-spawning migration patterns of atlantic bluefin tuna (Thunnus thynnus) ascertained from satellite archival tags.
- Author
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Aranda G, Abascal FJ, Varela JL, and Medina A
- Subjects
- Animals, Atlantic Ocean, Environment, Female, Male, Satellite Communications, Seasons, Spain, Animal Migration, Behavior, Animal, Remote Sensing Technology, Tuna physiology
- Abstract
Spawning behaviour of Atlantic bluefin tuna (Thunnus thynnus) was investigated using electronic satellite tags deployed in the western Mediterranean spawning ground, around the Balearic Islands (years 2009-2011). All the fish were tagged underwater and released within schools. In general, the fish tagged in the same year/school displayed common migratory trends. Following extended residency around the Balearic Islands, most tagged tuna crossed the Strait of Gibraltar heading for the North Atlantic. Discrepancies between the migratory tracks reconstructed from this and previous electronic tagging studies suggest that the bluefin tuna Mediterranean population may comprise distinct units exhibiting differing migratory behaviours. The diving behaviour varied between oceanic regions throughout the migratory pathways, the shallowest distribution taking place in the spawning ground and the deepest at the Strait of Gibraltar. A unique diving pattern was found on the majority of nights while the fish stayed at the spawning ground; it consisted of frequent and brief oscillatory movements up and down through the mixed layer, resulting in thermal profiles characterized by oscillations about the thermocline. Such a pattern is believed to reflect recent courtship and spawning activity. Reproductive parameters inferred from the analysis of vertical profiles are consistent with those estimated in previous studies based on biological samples.
- Published
- 2013
- Full Text
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12. Ultrastructure of oogenesis in the bluefin tuna, Thunnus thynnus.
- Author
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Abascal FJ and Medina A
- Subjects
- Animals, Female, Tuna physiology, Oocytes growth & development, Oocytes ultrastructure, Oogenesis physiology, Tuna anatomy & histology, Tuna growth & development
- Abstract
Ovarian ultrastructure of the Atlantic bluefin tuna (Thunnus thynnus) was investigated during the reproductive season with the aim of improving our understanding of the reproductive biology in this species. The bluefin, like the other tunas, has an asynchronous mode of ovarian development; therefore, all developmental stages of the oocyte can be found in mature ovaries. The process of oocyte development can be divided into five distinct stages (formation of oocytes from oogonia, primary growth, lipid stage, vitellogenesis, and maturation). Although histological and ultrastructural features of most these stages are similar among all studied teleosts, the transitional period between primary growth and vitellogenesis exhibits interspecific morphological differences that depend on the egg physiology. Although the most remarkable feature of this stage in many teleosts is the occurrence of cortical alveoli, in the bluefin tuna, as is common in marine fishes, the predominant cytoplasmic inclusions are lipid droplets. Nests of early meiotic oocytes derive from the germinal epithelium that borders the ovarian lumen. Each oocyte in the nest becomes surrounded by extensions of prefollicle cells derived from somatic epithelial cells and these form the follicle that is located in the stromal tissue. The primary growth stage is characterized by intense RNA synthesis and the differentiation of the vitelline envelope. Secondary growth commences with the accumulation of lipid droplets in the oocyte cytoplasm (lipid stage), which is then followed by massive uptake and processing of proteins into yolk platelets (vitellogenic stage). During the maturation stage the lipid inclusions coalesce into a single oil droplet, and hydrolysis of the yolk platelets leads to the formation of a homogeneous mass of fluid yolk in mature eggs., (2004 Wiley-Liss, Inc.)
- Published
- 2005
- Full Text
- View/download PDF
13. The spermatozoon morphology of Solea senegalensis (Kaup, 1858) (Teleostei, Pleuronectiformes).
- Author
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Medina A, Megina C, Abascal FJ, and Calzada A
- Subjects
- Animals, Centrioles ultrastructure, Flatfishes classification, Male, Microscopy, Electron, Species Specificity, Sperm Head ultrastructure, Sperm Tail ultrastructure, Flatfishes anatomy & histology, Spermatozoa ultrastructure
- Abstract
The spermatozoon of Solea senegalensis (Kaup, 1858) consists of an acrosome-less ovoid head, a short midpiece containing several irregular mitochondria embedded in the cytoplamic mass, and a long tail with two lateral fins and a conventional 9 + 2 axoneme. The centrioles are housed in a deep nuclear fossa and are both orientated in the same longitudinal axis of the spermatozoon. The overall structure of this spermatozoon conforms to the sperm type considered to be plesiomorphic in the neopterigians (type I sperm). The likely apomorphic (coaxial) orientation of the centrioles defines the spermatozoal morphology of the Soleidae investigated thus far and separates them from the other known pleuronectiform spermatozoa.
- Published
- 2000
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