In Situ Rates of Fertilization Among Broadcast Spawning Gorgonian Corals

In Situ Rates of Fertilization Among Broadcast Spawning Gorgonian Corals

Reference: Biol. Bull. 190: 45-55. (February, 1996) In situ Rates of Fertilization Among Broadcast Spawning Gorgonian Corals HOWARD R. LASKER, DANIEL A. BRAZEAU1, JULIO CALDERON2, MARY ALICE COFFROTH, RAFEL COMA, AND KIHO KIM Department of Biological Sciences, State University of New York at Buffalo, g#z/o,#ew Fort 74260 Abstract. Fertilization rates among marine benthic column as gametes are diluted, spawning behavior of taxa have implicitly been assumed to be uniformly high the gorgonians, and the current regime. Fertilization in most analyses of life history evolution, but in situ rates are often low and may represent a limiting step fertilization rates during natural spawning events are in recruitment during some years. Low fertilization rates rarely measured. Fertilization rates of the Caribbean may also be an important component of the life history gorgonians Plexaura kuna and Pseudoplexaura porosa evolution of these species. were measured at a site in the San Bias Islands, Panama, by collecting eggs downstream of colonies during syn- Introduction chronous spawning events during the summer months in the years 1988-1994. Eggs collected by divers were One of the primary goals of benthic ecology has been incubated, and the proportion of eggs that developed the determination of the factors limiting populations. For was determined. Proportions of eggs developing suggest most of this century, such efforts have been concentrated fertilization rates that vary from 0% to 100%. Monthly on post-recruitment events in the life history of the or- means ranged from 0% to 60.4%. Failure of gametes to ganism (i.e., Connell, 1961, and hundreds of subsequent develop can be attributed to sperm limitation, as eggs studies). Missing from such analyses are the processes that collected during spawning had higher fertilization rates directly or indirectly affect the number of larvae that settle. if incubated with an excess of sperm. Plexaura kuna The importance of such processes was recognized by many fertilization rates were highest during the July spawning authors (e.g., Thorson, 1946), but the difficulties of mea- events. Fertilization of Plexaura kuna eggs was usually suring phenomena such as survival of larvae in the water lower during the first two nights of the 4-6 night spawn- column led to research that virtually ignored larval ecology ing event. The proportion of eggs being fertilized when in favor of the more knowable post-settlement dynamics collected from a given place and time was highly vari- of populations. More recently, larval ecology has been able, with one peak in the frequency distribution at or rediscovered (Young, 1990; Grosberg and Levitan, 1992), below 20% fertilization, and a second group of samples and a wide variety of work has documented the impor- with greater fertilization rates. High variance in fertil- tance of larval dynamics and the circumstances under ization rates is evident at all levels of analysis: between which recruitment may limit populations (Connell, 1985; replicate samples, times within nights, and among Gaines and Roughgarden, 1985; Gaines et ah, 1985; nights and months. This variance can be attributed to Roughgarden et ah, 1988). a combination of the effects of heterogeneity in the water As in the earlier treatments, most studies of larval ecol- ogy have also glossed over a potentially limiting but seem- ingly unknowable component of the life cycle of broadcast- Received 24 April 1995; accepted 3 October 1995. spawning taxa: the proportion of gametes that are fertilized ' Current address: Dept. of Zoology, University of Florida, Gainesville, FL 32611. and that complete early development. This bias reflects 2 Current address: Dept. of Biological Sciences, Universidad Santa the general difficulties of determining the fate of gametes Maria La Antigua, Panama, Republic of Panama. and embryos after they are released into the water column. 45 46 H. R. LASKER ET AL. Thus, most analyses of benthic invertebrate reproductive Table I strategies have focused on fecundity and the subsequent Fertilization rates determined from in situ collections of spawned eggs survival of the larvae as the rate-limiting steps controlling or from incubations of eggs with sea water samples successful recruitment (for instance, Vance, 1973; Strath- mann, 1978, 1985; Strathmann and Strathmann, 1982; Species Fertilization rate Reference Roughgarden, 1989). Assumptions that are implicit in Briareum <0.01-6.5% Brazeau and Lasker, these analyses are that eggs are readily fertilized, that fer- asbestinum 1992 tilization rates are relatively uniform over time and space, (gorgonian) and that the proportion of eggs fertilized is independent Montipora digitata 0.2-49.0% Oliver and Babcock, of reproductive strategy. (coral) 1992 Acanthaster planci 23-83% Babcock and Mundy, The assumption that fertilization is uniformly great may (asteroid) 1992 be incorrect for many species, and a growing body of lit- Actinopyga lecanora 67-78% Babcock et al., 1992 erature suggests that fertilization has the potential to be (holothurian) a limiting step in the life histories of some benthic species. Bohadshia argus 0-96% Babcock et al, 1992 Pennington (1985), Yund (1990), Levitan (1991), Levitan (holothurian) Cucumaria miniata 92 (1-100%) Sewell and Levitan, et al. (1991, 1992), Babcock et al. (1992, 1994), Brazeau (holothurian) 1992 and Lasker (1992), Oliver and Babcock (1992), Benzie et Holuthuria coluber 9-83% Babcock et al, 1992 al. (1994), Benzie and Dixon (1994), Yund and Mc- (holothurian) Cartney (1994), and Levitan (1995) have experimentally Halichoeres 20-100% Petersen, 1991 demonstrated the potential for sperm limitation in the bivittatus (wrasse) fertilization of a variety of benthic species. These mea- Thalassoma 76% (0-100%) Petersen et al, 1992 surements, in concert with the modeling efforts of Denny bifaciatum (1988) and Denny and Shibata (1989), suggest that eggs (wrasse) are often sperm limited. Measurements of fertilization rates from naturally spawning events have yielded rates that are substantially seemingly healthy populations may have little impact on below 100% (Table I). The most extreme of those rates the survival of a species. Petersen and colleagues (Petersen, have been those o{ Briareum asbestinum, which has been 1991; Petersen et al, 1992) reported on fertilization rates observed over multiple years and sites. Observed rates of wrasses, both across reefs and across days, and they were as low as those suggested by experimental data (Bra- identified environmental conditions that may enhance zeau and Lasker, 1992). However, in many cases fertil- fertilization success and explain variance in fertilization ization rates during natural spawning events have been success. These results suggest that fertilization success, by surprisingly great, as among Acanthaster planci (Babcock controlling the relative contribution of individuals, may and Mundy, 1992). Although the rates presented in Table be an important variable in the evolution of the life history I are generally below 100%, most are also well above 0%. of a species. Apparent fertilization rates that are lower than 100% could In this paper we report fertilization rates for the broad- be a function of egg viability or biases introduced by sam- cast spawning Caribbean gorgonians Plexaura kuna and pling techniques. The fertilization rates that have been re- Pseudoplexaura porosa at a site in the San Bias Islands, ported, although consistent with the hypothesis of sperm Panama. We document variation in fertilization rates over limitation, do not demonstrate sperm limitation. Further- spawning events that occurred over 15 months during the more they suggest that sperm limitation may be taxon-, period 1988-1994, and we show that the low fertilization site-, and time-dependent. If these restrictions held, sperm rates can be attributed directly to sperm limitation at this limitation could contribute to the differential success of site. populations and species at differing sites. Most field measurements of fertilization rates have also Materials and Methods been restricted to either single spawning events or sites. Thus both the extent and source of variation in fertiliza- Fertilization success of the gorgonians Plexaura kuna tion rates are unknown for most taxa. Characterization (previously discussed as Plexaura A, Lasker et al, 1996) of this variation, when it has been conducted, has proven and Pseudoplexaura porosa was measured by determining to be extremely interesting. Brazeau and Lasker (1992) the proportion of spawned eggs which initiated develop- examined fertilization rates of Briareum asbestinum at ment. P. kuna is a gonochoric, broadcast spawner that two sites in Panama over two years. They reported 0.0% releases its eggs during 4-6 day spawning events that occur fertilization rates from one of those sites (i.e., complete four days after the full moon during the months of June- reproductive failure), suggesting that some sites with September or May-August depending on the timing of GORGONIAN FERTILIZATION RATES 47 the full moon (Brazeau and Lasker, 1989). In Panama throughout the water in the container. Seawater in the spawning is restricted to a 60-min period starting 0-40 containers was changed at 12 h and when applicable at min after sunset, and most of the spawning occurs during 36 h. The number of developing embryos observed either the middle 30 min of the release period. Pseudoplexaura 12 h (1993, 1994) or 36 h after spawning (1988-1992) porosa is also a gonochoric

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    11 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us