Abstract
Annual shell growth was determined by mark and recapture in the limpet Nacella concinna (Strebel 1908) at two contrasting sites in Antarctica. At Signy Island, 60°S, growth was moderately fast, comparable with some limpets in more temperate areas. The fluorescent calcium marker calcein was used to validate the results from the mark/recapture study, and fine-scale growth increments showed that shell growth was seasonal. Further south at Rothera Point, 67°S, mean annual growth over a 3-year period was significantly slower than at Signy, and in 1 year was the slowest yet reported for a limpet. Comparison with an earlier mark/recapture study at Arthur Harbour, Palmer Station (64°S) revealed a cline of decreasing growth performance with increasing latitude along the Antarctic Peninsula. It is not clear whether the slower annual growth rate at higher latitude was caused by physiological constraints, a reduced length of growing season, or a combination of both. Limpets show a global cline in growth performance, which decreases towards higher latitudes.
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Acknowledgements
Mark/recapture work on free-living marine animals is very labour intensive. We thank all those base members at Signy (1994–1995) and Rothera (1997–2000) for help with diving, but especially Simon Brockington, Keiron Fraser, Rob Wood, Hugh Brown, Lesley Thomson and Craig Barnes. We also thank Ken Robinson for the electron microscopy, Inigo Everson for helpful advice on the estimation of growth rates from field data and George Branch for provision of limpet growth data.
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Appendix
Appendix
Growth performance data for patellacean limpets. Data arranged by latitude to ease comparison with Fig. 7 (negative latitudes are southern hemisphere). In some cases values of K and L ∞ are provided in the original literature cited; in others (*) these have been derived from data or plots in the paper. These studies involve a wide range of techniques and sample numbers, and not all studies were concerned primarily with the determination of growth rate; the data must therefore be regarded as indicative rather than definitive in many cases
Species | Latitude | K | L ∞ | Ø | Location | Reference |
---|---|---|---|---|---|---|
Nacella concinna | −67.0 | 0.059 | 38.5 | 4.47 | Rothera Point (1997/8) | This paper |
N. concinna | −67.0 | 0.129 | 57.6 | 6.06 | Rothera Point (1998/9) | This paper |
N. concinna | −67.0 | 0.068 | 50.2 | 5.14 | Rothera Point (1999/2000) | This paper |
N. concinna | −64.0 | 0.109 | 40.6 | 5.19 | Palmer Station | Shabica (1976) |
N. concinna | −63.0 | 0.080 | 46.0 | 5.13 | Hope Bay | Brêthes et al. (1994) |
N. concinna | −61.0 | 0.323 | 34.5 | 5.95 | Signy Island | This paper |
N. concinna | −61.0 | 0.062 | 41.0 | 4.65 | Signy Island | Picken 1980 |
Nacella magellanica | −52.5 | 0.191* | 54.0* | 6.32 | Straits of Magellan | Gunzman and Rios (1987) |
N. magellanica | −52.5 | 0.147* | 55.0* | 6.10 | Straits of Magellan | Gunzman and Rios (1987) |
N. magellanica | −52.5 | 0.127* | 67.0* | 6.35 | Straits of Magellan | Gunzman and Rios (1987) |
N. magellanica | −52.5 | 0.110* | 61.0* | 6.01 | Straits of Magellan | Gunzman and Rios (1987) |
N. magellanica | −52.5 | 0.079* | 61.0* | 5.69 | Straits of Magellan | Gunzman and Rios (1987) |
N. magellanica | −52.5 | 0.026* | 120.0* | 5.94 | Straits of Magellan | Gunzman and Rios (1987) |
N. delesserti | −47.0 | 0.971 | 61.8 | 8.22 | Marion Island | Blankley and Branch (1985) |
Cellana ornata | −42.5 | 0.536 | 39.7 | 6.74 | First Bay; Kaikura, NZ | Dunmore and Schiel (2003) |
C. ornata | −42.5 | 0.400 | 26.3 | 5.62 | Blue Duck; Kaikura, NZ | Dunmore and Schiel (2003) |
Scutellastra cochlear | −34.3 | 0.334 | 49.0 | 6.69 | Kommetjie, South Africa | Branch (1974) |
S. cochlear | −34.3 | 0.117 | 47.0 | 5.56 | Kommetjie, South Africa | Branch (1974) |
Cymbula granatina | −34.3 | 0.509 | 94.0 | 8.41 | Kommetjie, South Africa | Branch (1974) |
Scutellastra granularis | −34.3 | 0.556 | 40.0 | 6.79 | Kommetjie, South Africa | Branch (1974) |
S. granularis | −34.3 | 0.754 | 53.0 | 7.66 | Elands Bay, South Africa | Branch (1974) |
Cymbula oculus | −34.3 | 1.020 | 65.5 | 8.38 | Dwesa, South Africa | Branch and Odendaal (2003) |
S. cochlear | −34.2 | 0.209 | 60.0 | 6.62 | Kalk Bay, South Africa | Branch (1974) |
S. cochlear | −34.2 | 0.137 | 50.0 | 5.84 | Kalk Bay, South Africa | Branch (1974) |
S. granularis | −34.2 | 0.671 | 38.0 | 6.88 | Kalk Bay, South Africa | Branch (1974) |
Scutellastra longicosta | −34.2 | 0.300 | 68.0 | 7.23 | Kalk Bay, South Africa | Branch (1974) |
C. oculus | −34.2 | 0.582 | 79.0 | 8.20 | Kalk Bay, South Africa | Branch (1974) |
Cellana tramoserica | −34.0 | 0.832* | 39.7* | 7.18 | Cape Banks, Botany Bay, NSW | Fletcher (1984) |
C. tramoserica | −34.0 | 1.661* | 47.8* | 8.24 | Cape Banks, Botany Bay, NSW | Fletcher (1984) |
Patelloida latistrigata | −34.0 | 1.232* | 13.0* | 5.34 | Botany Bay, NSW | Creese (1981) |
Patelloida alticostata | −34.0 | 0.226* | 30.5* | 5.35 | Botany Bay, NSW | Creese (1981) |
Notacmaea petterdi | −34.0 | 0.255* | 23.7* | 4.96 | Botany Bay, NSW | Creese 1981 |
Cymbola granatina | −30.8 | 0.270 | 67.9 | 7.13 | Groenrivier, South Africa | Branch (1974) |
Scutellastra argenvillei | −30.8 | 0.210 | 82.0 | 7.25 | Groenrivier, South Africa | Eekhout et al. (1992) |
Fissurella crassa | −20.0 | 0.159* | 94.5* | 7.26 | Huayquique, Chile | Bretos (1980) |
Cellana grata | 22.2 | 1.014* | 36.2* | 7.19 | Cape d’Aguilar, Hong Kong | Liu (1994) |
Cellana eucosmia | 29.5 | 0.689* | 44.1* | 7.20 | Gulf of Suez | Saad (1997) |
Acmaea digitalis | 43.5 | 0.530* | 24.0* | 5.72 | Coos Bay, Oregon | Frank (1965) |
Acmaea paradigitalis | 43.5 | 0.791 | 13.2 | 4.92 | Coos Bay, Oregon | Frank (1965) |
Acmaea persona | 44.0 | 0.256* | 41.6* | 6.09 | Newport, Oregon | Kenny (1968) |
A. digitalis | ND | 0.583 | 25.8 | 5.96 | California | Choat and Black (1979) |
A. digitalis | ND | 0.624 | 20.4 | 5.56 | California | Choat and Black (1979) |
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Clarke, A., Prothero-Thomas, E., Beaumont, J.C. et al. Growth in the limpet Nacella concinna from contrasting sites in Antarctica. Polar Biol 28, 62–71 (2004). https://doi.org/10.1007/s00300-004-0647-8
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DOI: https://doi.org/10.1007/s00300-004-0647-8