Gametogenesis

Gametogenesis is the origin and development of germ cells.

Figure 1. Gonadal follicles in marine mussels (10X).

Gonadal development in Bivalves

In bivalves, the reproductive cycle involves a period of gametogenesis that ends with one or more spawning events, which is the release of cells for fertilization. After spawning, the gonad goes through a period of tissue repair by specialized cells (e.g. amoebocytes), and a new gonadal cycle begins. Gametogenesis takes place within the follicles of the gonadal tissue (Fig. 1).

During spermatogenesis, the spermatogonia go through various stages until they become flagellated spermatozoa that reach sizes of up to 60 μm in length (Franco et al. 2008, Oyarzún et al. 2014 - Fig. 2). On the other hand, oogenesis follows a similar pattern to spermatogenesis in that primary oogonia are transformed by mitosis into secondary oogonia which are arrested at the prophase stage of meiosis I. The remaining meiotic stages are completed at fertilization (extracted from Gosling 2015). The oocytes then go through a period of vitellogenesis, which involves the accumulation of lipids and glycogen, important nutrients during embryogenesis (Chung 2007). During this period, the size of the oocytes increases (Fig. 3), a characteristic that fluctuates between species (e.g. ~70 μm in the Chilean mussel Mytilus chilensis or ~130 μm in the chorito maico, Perumytilus purpuratus - Oyarzún et al. 2011, 2018). At the end of vitellogenesis some oocytes can be lysed, those are called atresic oocytes. Atresia provides metabolic substrates for energy production at a time when energy stores are in short supply (Beninger & Le Pennec 2006).

Figure 2. Scanning electron micrographs of the mature sperm of a) Mytilus chilensis, and b) Mytilus galloprovincialis. a: acrosome, n: nucleus, f: flagellum, ep: end piece or tail. Oyarzún et al. (2014).

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Figure 3. Photomicrographs of sections of female’s gonads of Mytilus chilensis. a) In development, b) mature, c) spawned, d) post spawned. OG: oogonies. OP: pre-vitellogenic oocyte. OV: vitellogenic oocyte. OM: mature oocyte. LM: follicular lumen. TI: Inter-follicular tissue. PF: follicular wall. AM: amebocytes. RC: cellular debris. Oyarzún et al. (2011).

Gonadal maturation is conditioned by exogenous factors such as temperature, salinity and food (quantity and quality). However, endogenous factors, such as the genetic pool and hormonal load, are also important (see Gosling 2015). Oyarzun et al. (2018) indicated that latitude does not have an effect on the development stage, but it does on the spawning date. However, there is a relationship between the reproductive cycles and temperature fluctuations. The decrease in temperature reduces the rate of development stages and, therefore, increases the reproductive cycles from semi-annual to annual, as evidenced in bivalve samples from Taltal, along a semi-decadal period (2007–2012) (see Fig. 4).

Figure 4. Time series in the Taltal station (Chilean coast) between 2003 and 2012. Monthly SST anomalies. Semi-annual cycle extracted from Oyarzún et al. (2010); Annual cycle data from Oyarzún et al. 2018.

Understanding the gametogenic cycles allows making predictions about recruitment, about the time of collection of seeds for aquaculture, for the establishment of fishing ban, and for the determination of minimum catch sizes (Oyarzún et al. 2011). For this reason, reproductive information is essential for fisheries management.

Reference

Beninger PG & Le Pennec M (2006) Structure and function in scallops. In: Scallops: Biology, Ecology and Aquaculture (eds SE Shumway & GJ Parson), 2nd edn. pp. 123–127. Elsevier Science, Boston.

Chung E‐Y. (2007) Oogenesis and sexual maturation in Meretrix lusoria (Röding 1798) (Bivalvia: Veneridae) in western Korea. Journal of Shellfish Research 26: 71–80.

Franco C, Berthelin H, Goux D, Sourdaine P. & Mathieu M (2008) Fine structure of the early stages of spermatogenesis in the Pacific oyster, Crassostrea gigas (Mollusca, Bivalvia). Tissue and Cell 40: 251–260.

Gosling E (2015) “Reproduction, settlement and recruitment,” in Marine Bivalve Molluscs, ed. E. Gosling (Hoboken, NJ: John Wiley & Sons, Ltd), 157–202.

Oyarzún PA, Toro JE, Jaramillo R, Guiñez R, Briones C & M. Astorga (2010) Análisis comparativo del ciclo gametogénico de Perumytilus purpuratus (Bivalvia: Mytilidae), en las localidades de Taltal y Huasco, Norte de Chile. Revista de Biología Marina y Oceanografía, 45: 43-58.

Oyarzún PA, Toro JE, Jaramillo R, Guiñez R, Briones C & M. Astorga (2011) Gonadal cycle from mussel Mytilus chilensis (Bivalvia: Mytilidae) at two localities in southern Chile. Latin American Journal of Aquatic Research. 39:512-525.

Oyarzún, PA., Toro, J.E., Garrido, O., Briones, C. & Guiñez, R. (2014) Differences in sperm ultrastructure between Mytilus chilensis and Mytilus galloprovincialis (Bivalvia, Mytilidae): could be used as a taxonomic trait? Latin American Journal of Aquatic Research 42(1):172-179

Oyarzún PA, Toro JE, Garcés-Vargas J, Alvarado C, Guiñez R, Jaramillo J, Briones C, Campos B (2018) Reproductive patterns of mussels Perumytilus purpuratus (Bivalvia: Mytilidae), along the Chilean coast: effects caused by climate change? Journal of the Marine Biological Association of the United Kingdom 98:375-385.