Relationship between oocyte morphology and reproductive strategy in loricariid catfishes of the Paraná River , Brazil

Relationships between ovarian structure, oocyte structure/development, and parental care/life history strategies of six loricariid catfishes common in the upper Paraná River, Brazil were examined with analysis of catch data, relative gonad weight, histology, and microscopy. Three life history strategies were observed. Loricariichthys platymetopon, Loricariichthys sp. and Loricaria sp. produce several small clutches of large eggs over a protracted spawning period. Males of these species guard their eggs and larvae, which are transported as a mass on the ventral surface of the male’s body. Hypostomus ternetzi and Megalancistrus aculeatus produce the largest mature eggs and the smallest clutches relative to adult mass. The spawning periods of these species are short, and males guard their broods in excavations. Rhinelepis aspera has high fecundity, high relative mass of mature gonads (both sexes), small mature eggs, and broadcast spawning with no parental care. This species migrates to spawn over firm substrates in channel areas during a contracted period. Mature oocytes of external bearers had the thickest zona radiata, followed by the egg scatterer, and cavity nesters. The thickness of the zona radiata probably is an adaptation to protect the developing egg from injury from abrasion. The zona granulosa appeared to be associated with production of secretions responsible for egg adhesion, and this layer was thickest in mature oocytes of the cavity nesting species, followed by the external bearers. All six species have wide distributions in the Paraná River, tributaries, floodplain lagoons, and the Itaipu Reservoir, but brood guarders tended to be most common in lentic habitats. 2000 The Fisheries Society of the British Isles

[1]  H. P. Godinho,et al.  Induced reproduction and reproductive characteristics of Rhinelepis aspera Agassiz, 1829 (osteichthyes: Siluriformes, Loricariidae) , 1998 .

[2]  R. Mazzoni,et al.  Observations on the reproductive biology of female Hypostomus luetkeni Lacèpéde 1803 , 1997 .

[3]  Â. A. Agostinho,et al.  Colonização ictiofaunística do Reservatório de Itaipu e áreas adjacentes , 1997 .

[4]  A. Agostinho,et al.  The catfish, Rhinelepis aspera (Teleostei; Loricariidae), in the Guaíra region of the Paraná River: an example of population estimation from catch-effort and tagging data when emigration and immigration are high , 1995 .

[5]  É. P. Caramaschi,et al.  Caracteristicas reprodutivas de hypostomus grupo h. Punctatus no rio ubatiba , marica , rj ( osteichthyes , siluriformes ) , 1994 .

[6]  K. Rose,et al.  Patterns of Life-History Diversification in North American Fishes: implications for Population Regulation , 1992 .

[7]  K. Winemiller Life-history strategies and the effectiveness of sexual selection , 1992 .

[8]  W. Burgess An Atlas of Freshwater and Marine Catfishes: A Preliminary Survey of the Siluriformes , 1989 .

[9]  S. Schaefer Osteology of Hypostomus plecostomus (Linnaeus), with a phylogenetic analysis of the loricariid subfamilies (Pisces: Siluroidei) , 1987, Contributions in science.

[10]  A. Adebisi The relationships between the fecundities, gonado­ somatic indices and egg sizes of some fishes of Ogun River, Nigeria , 1987, Archiv für Hydrobiologie.

[11]  M. Gross,et al.  The evolution of male and female parental care in fishes , 1985 .

[12]  Jeffrey N. Taylor Field Observations on the Reproductive Ecology of Three Species of Armored Catfishes (Loricariidae: Loricariinae) in Paraguay , 1983 .

[13]  Â. A. Agostinho,et al.  Morfologia dos ovarios de Plecostomus commersonii (Valenciennes, 1840) Osteichthyes - Loricariidae : desenvolvimento dos ovocitos e escala de maturidade , 1982 .

[14]  C. Breder,et al.  Modes of Reproduction in Fishes , 1967 .

[15]  G. Nikolsky Ecology of Fishes , 1963 .