Abstract

Abstract. Coral δ18O variations are used as a proxy for changes in sea surface temperature (SST) and seawater isotope composition. Skeletal δ13C of coral is frequently used as a proxy for solar radiation because most of its variability is controlled by an interrelationship between three processes: photosynthesis, respiration, and feeding. Coral growth rate is known to influence the δ18O and δ13C isotope record to a lesser extent than environmental variables. Recent published data show differences in growth parameters between female and male coral in the gonochoric brooding coral Porites panamensis; thus, skeletal δ18O and δ13C are hypothesized to be different in each sex. To test this, this study describes changes in the skeletal δ18O and δ13C record of four female and six male Porites panamensis coral collected in Bahía de La Paz, Mexico, whose growth bands spanned 12 years. The isotopic data were compared to SST, precipitation, photosynthetically active radiation (PAR), chlorophyll a, and skeletal growth parameters. Porites panamensis is a known gonochoric brooder whose growth parameters are different in females and males. Splitting the data by sexes explained 81 and 93 % of the differences of δ18O, and of δ13C, respectively, in the isotope record between colonies. Both isotope records were different between sexes. δ18O was higher in female colonies than in male colonies, with a 0.31 ‰ difference; δ13C was lower in female colonies, with a 0.28 ‰ difference. A difference in the skeletal δ18O could introduce an error in SST estimates of ≈ 1.0 to ≈ 2.6 °C. The δ18O records showed a seasonal pattern that corresponded to SST, with low correlation coefficients (−0.45, −0.32), and gentle slopes (0.09, 0.10 ‰ °C−1) of the δ18O–SST relation. Seasonal variation in coral δ18O represents only 52.37 and 35.66 % of the SST cycle; 29.72 and 38.53 % can be attributed to δ18O variability in seawater. δ13C data did not correlate with any of the environmental variables; therefore, variations in skeletal δ13C appear to be driven mainly by metabolic effects. Our results support the hypothesis of a sex-associated difference in skeletal δ18O and δ13C signal, and suggest that environmental conditions and coral growth parameters affect skeletal isotopic signals differently in each sex. Although these findings relate to one gonochoric brooding species, they may have some implications for the more commonly used gonochoric spawning species such as Porites lutea and Porites lobata.

Highlights

  • Massive hermatypic coral are useful as recorders of oceanic conditions because their growth and skeletal materials incorporated during growth are affected by environmental variables

  • All X-radiographs had a low-density annual growth band in the apex of the slice. This means that P. panamensis form a low-density band in winter

  • Our isotope data showed a significant dependency of skeletal δ18O on sea surface temperature (SST), with a low r (−0.45 in female coral, and −0.28 in male coral), and a gentle slope of the δ18O–SST calibration equations (0.09 ‰ ◦C−1 F; 0.11 ‰ ◦C−1 M; Fig. 5), compared with slopes (> 0.20 ‰ ◦C−1) in Porites spp. in other areas of the Pacific: the Great Barrier Reef (Gagan et al, 1994), Costa Rica (Carriquiry, 1994), Panama (Wellington and Dunbar, 1995), and the Galapagos Archipelago (McConnaughey, 1989)

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Summary

Introduction

Massive hermatypic coral are useful as recorders of oceanic conditions because their growth and skeletal materials incorporated during growth are affected by environmental variables. The calcareous material is deposited in annual density bands that allow for the determination of events over time (Druffel, 1997; Gagan et al, 2000; Grottoli and Eakin, 2007; Lough and Barnes, 2000; Lough and Cooper, 2011). This memory of oceanographic conditions at the time of calcifica-. Cabral-Tena et al.: Sex-associated variations in coral skeletal oxygen and carbon tion records variations at the intra-annual, inter-annual, interdecadal, and sometimes centennial timescale of El Niño–

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