Reef coral reproduction in the eastern Pacific: Costa Rica,Panamá, and Galápagos Islands (Ecuador). III. Agariciidae (Pavona gigantea and Gardineroseris planulata)

The reproductive ecology of Pavona gigantea Verrill and Gardineroseris planulata (Dana) was investigated in the equatorial eastern Pacific region from 1985 to 1994. These zooxanthellate scleractinian corals were adversely affected in this region during the 1982–1983 El Niño warming event. Both species were hermaphroditic, with individual colonies showing sequential cosexual development, thus resulting in dominantly outbreeding reproduction. Sexuality was mixed, with high percentages of gonochoric and hermaphroditic colonies in both species. Approximately 1:1 male-to-female gonad ratios were found in gonochoric and hermaphroditic colonies combined. Broadcast spawning was observed in P. gigantea in the Galápagos Islands, and the sudden disappearance of mature gametes and the presence of spent gonads suggest that G. planulata is also a broadcast spawner. Colonies of both species with 200 cm² (10 cm diam) live tissue were nonreproductive. Estimated ages of the youngest reproductive colonies were 11 yr for P. gigantea and 20 yr for G. planulata. The percentage of all colonies of P. gigantea with gonads at nonupwelling sites (Caño Istand, Costa Rica and Uva Island, Panamá) ranged from 37 to 47%, respectively; colonies with gonads from upwelling environments (Saboga and Taboga Islands, Panamá) ranged from 31 to 39%, respectively, and reproductively active colonies from the thermally variable Galápagos islands comprised 40% of the collections. Compared with P. gigantea, the numbers of sexually active G. planulata colonies were roughly onehalf at nonupwelling Caño Island (20%) and Uva Island (25%) sites, or less (10%) at the upwelling Saboga Island site. Peak reproductive activity in P. gigantea occurred during the rainy season at all study sites. In the nonupwelling Costa Rican (Caño Island) and Panamainan (Uva Island) sites, mean monthly sea-surface temperatures (SSTs) were high (28 to 29°C), but slightly lower than in the dry season (29°C). In the upwelling Gulf of Panamá (Saboga and Taboga Islands), reproduction occurred after mean monthly SSTs increased from 24 to 28–29°C. In the Galápagos Islands, reproductive activity peaked during sea warming, when mean monthly SSTs reached 25°C. Sexually active colonies of G. planulata, present only at the main collection sites of Caño and Uva Islands, were also observed during the wet season. The presence of mature or spawned gonalds in both species mostly around new and full lunar phases suggests that spawning is at least weakly synchronized with moon phase. Fecundity estimates disclosed the following nonsignificant differences between sites for P. gigantea, expressed as egg production cm^-2 colony surface surface yr^-1: Galápagos (10 300 to 30 800), Uva Island (4900 to 9800), Caño Island (1800 to 7400), Saboga Island (600 to 1300) Taboga Island (1200 to 2400). Fecundity estimates for G. planulata were considerably lower: Uva Island (700 to 1400), Caño Island (500 to 1000). The sexual recruitment of P. gigantea into El Niño-Southern Oscillation (ENSO) 1982–1983-disturbed, equatorial eastern Pacific coral communities has been low, with only moderate recovery evident since 1983. G. planulata has revealed no sexual recruitment where seed populations are absent or rare (Caño Island, Galápagos Islands), and only low recruitment (Panamá) in areas with colonies that survived the ENSO disturbance.     

Reef coral reproduction in the equatorial eastern Pacific: Costa Rica, Panamá, and the Galápagos Islands (Ecuador). VII. Siderastreidae, Psammocora stellata and Psammocora profundacella

Two zooxanthellate, scleractinian species present in the equatorial eastern Pacific, Psammocora stellata and Psammocora profundacella, were examined in terms of their reproductive biology and ecology at four study sites, non-upwelling (Ca?o Island, Costa Rica, and Uva Island, Panamá), upwelling (Gulf of Panamá, Panamá), and seasonally varying thermal environments (Galápagos Islands). Both species were gonochoric broadcast spawners lacking zooxanthellae in mature ova. Mature gametes and spawned gonads are present around full moon; however, no spawning was observed naturally or in outdoor aquaria. Mature gametes occurred in P. stellata at Ca?o Island for nearly 6?months, and year round at Uva Island, both non-upwelling sites. Reproductively active colonies occurred mostly in the warmer months in the Gulf of Panamá and Galápagos Islands. In the Galápagos Islands, where collecting effort was greatest for P. profundacella, mature gametes were also most prevalent during the warm season. Annual fecundity was high in both species, 1.3–1.8?×?10⁴?ova?cm^?2?year^?1 in P. stellata and 1.2–2.0?×?10⁴?ova?cm^?2?year^?1 in P. profundacella. Compared to other eastern Pacific corals, P. stellata was relatively resistant to ENSO-related bleaching and mortality, especially populations inhabiting deep (12–20?m) coral communities. Rapid recovery and persistence of Psammocora spp. can be attributed to several factors: (a) relative resistance to bleaching, (b) deep refuge populations, (c) broadcast spawning, (d) protracted seasonal reproduction, (e) high fecundity, and (f) asexual propagation.     

Reef coral reproduction in the eastern Pacific: Costa Rica,Panamá, and the Galápagos Islands (Ecuador). VI. Agariciidae, <Emphasis Type="Italic">Pavona clavus</Emphasis>

The reproductive ecology of the zooxanthellate reef coral Pavona clavus was investigated at several sites in Costa Rica, Panamá, and the Galápagos Islands (Ecuador) over the period 1985–2009. Pavona clavus displayed stable gonochorism as only five hermaphrodites were found in 590 samples. At four of five locations, sex ratios were skewed toward female dominance; however, at Saboga Island (Panamá) male colonies predominated. In Panamá, sexual maturity was observed in an estimated eight-year-old female colony, and several colonies of 10–20 years of age demonstrated gametogenesis. Sexual activity was observed at all study sites, but gamete development occurred in only 14–31% of colonies sampled sporadically. Seasonality of gametogenic activity occurred predominantly during the warm/wet season, June to August, at mainland sites (Caño Island, Costa Rica, and Gulfs of Chiriquí and Panamá, Panamá). This pattern was repeated in the Galápagos Islands, but mainly from March to May when seasonally high sea temperatures and rainfall prevailed there. Histological sampling and field observations indicated that spawning was centered around the full moon, most frequently on lunar day 17, and near sunset (1,800 h). Mean fecundity (mature ova cm^?2 live tissue) estimates were significantly different for two sites and ranged from ~1,780 (Saboga Island, Gulf of Panamá, seasonally upwelling) to ~4,280 (Uva Is, Gulf of Chiriquí, non-upwelling). Assuming three annual spawning events colony^?1 (August, September, October), extrapolation of minimum and maximum fecundities yield 5,340 and 12,840 ova cm^?2 year^?1. Seasonal, lunar, and diel spawning patterns in nine zooxanthellate species at Uva Island indicate asynchronous coral community spawning.     

Reproductive biology and population structure of the sea cucumber <Emphasis Type="Italic">Isostichopus fuscus</Emphasis> (Ludwig, 1875) (Holothuroidea) in Caamaño,Galápagos Islands,Ecuador

Pre-spawning reproductive biology and population structure of the sea cucumber Isostichopus fuscus were analysed at the Caamaño Island, Galápagos Islands, Ecuador on a monthly basis between January 1995 and June 1996. An average of 25 individuals of all sizes were collected each month. Using microscopic characteristics of the gonads three gonadal stages were described: (1) immature; (2) mature, and (3) spent. Mature individuals showed statistically different morphometric characteristics. I. fuscus was continuously sexually mature throughout the year independent of changes in sea water temperature. Mean oocyte diameter indicated planktotrophic larval development. Mean fecundity for this species was 567,884 (±95,528 SE) eggs per gonad. Size at first maturity was between 161.0 and 170.9 g drained weight and the smallest individual found with mature gonads had a drained weight between 121.0 and 130.9 g. The population sampled ranged between 13 and 31 cm (81.0–400.0 g) with less than 10% of the population of individuals ≥25 cm (≥300.0 g). No juveniles were recorded.