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Upper thermal tolerance in red and blue king crab: sublethal and lethal effects

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Abstract

Red and blue king crab (Paralithodes camtschaticus and P. platypus) are both important fisheries species in Alaska. Despite the threat of climate change, the upper thermal tolerance of these species has been little studied. In this paper, we determine the lethal and sub-lethal thermal responses of year-0 juvenile red and blue king crab. Crab were exposed to a range of temperatures for 24 h to determine the lethal temperature at which mortality was 50% (LT50). Feeding rations were determined at sub-lethal temperatures for both species. Finally, crab were held for 45 days at sub-lethal temperatures and growth and long-term mortality rates were measured. The LT50s of red and blue king crab were 24.3 and 21.3 °C, respectively. Feeding ration peaked between 12 and 17 °C for red king crab and between 5 and 10 °C for blue king crab. The growth rate of red king crab decreased at temperatures above 12 °C, while blue king crab exhibited very low growth rates at temperatures 12 °C and above. Increased mortality in the 45-day experiment occurred for red king crab at 20 °C and blue king crab at 17 °C. This study suggests that, within their current distribution, the juveniles of both species could withstand warming of several degrees and not be thermally stressed; however, more research into the effect of increased temperature variability and other response variables, such as resting and active respiration, is needed. In addition, increased temperature could affect other life-history stages differently or have indirect effects, such as altered species interactions and food availability.

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References

  • Armstrong DA, Armstrong JL, Palacios R, Williams G, Jensen GC, Pearson W (1985) Early life history of juvenile blue king crab, Paralithodes platypus, around the Pribilof Islands. In: Davis SK, Gaffney F, McCrary J, Paul AJ, Otto RS (eds) Proceedings of the International King Crab Symposium. Alaska Sea Grant College Program, University of Alaska Fairbanks, Anchorage, pp 211–229

  • Bopp L, Resplandy L, Orr JC, Doney SC, Dunne JP, Gehlen M, Halloran P, Heinze C, Ilyina T, Seferian R (2013) Multiple stressors of ocean ecosystems in the 21st century: projections with CMIP5 models. Biogeosciences 10:6225–6245. doi:10.5194/bg-10-6225-2013

    Article  Google Scholar 

  • Breitburg DL, Salisbury J, Bernhard JM, Cai W-J, Dupont S, Doney SC, Kroeker KJ, Levin LA, Long WC, Milke LM (2015) And on top of all that… Coping with ocean acidification in the midst of many stressors. Oceanography 28:48–61. doi:10.5670/oceanog.2015.31

    Article  Google Scholar 

  • Brett JR (1971) Energetic responses of salmon to temperature. A study of some thermal relations in the physiology and freshwater ecology of sockeye salmon (Oncorhynchus nerka). Am Zool 11:99–113

    Article  Google Scholar 

  • Brylawski BJ, Miller TJ (2006) Temperature-dependent growth of the blue crab (Callinectes sapidus): a molt process approach. Can J Fish Aquat Sci 63:1298–1308

    Article  Google Scholar 

  • Chang ES (1995) Physiological and biochemical changes during the molt cycle in decapod crustaceans: an overview. J Exp Mar Biol Ecol 193:1–14

    Article  CAS  Google Scholar 

  • Chilton EA, Foy RJ, Armistead CE (2010) Temperature effects on assessment of red king crab in Bristol Bay, Alaska. In: Kruse GH, Eckert GL, Foy RJ, Lipcius RN, Sainte-Marie B, Stram DL, Woodby D (eds) Biology and management of exploited crab populations under climate change. University of Alaska Fairbanks, Alaska Sea Grant, pp 249–263

    Google Scholar 

  • Chittleborough R (1975) Environmental factors affecting growth and survival of juvenile western rock lobsters Panulirus longipes (Milne-Edwards). Mar Freshw Res 26:177–196

    Article  Google Scholar 

  • Christiansen JS, Sparboe M, Saether BS, Siikavuopio SI (2015) Thermal behaviour and the prospect spread of an invasive benthic top predator onto the Euro-Arctic shelves. Divers Distrib 21:1004–1013. doi:10.1111/ddi.12321

    Article  Google Scholar 

  • Clarke A, Johnston NM (1999) Scaling of metabolic rate with body mass and temperature in teleost fish. J Anim Ecol 68:893–905

    Article  Google Scholar 

  • Daly B, Long WC (2014) Inter-cohort cannibalism of early benthic phase blue king crabs (Paralithodes platypus): alternate foraging strategies in different habitats lead to different functional responses. PLoS ONE 9:e88694. doi:10.1371/journal.pone.0088694

    Article  Google Scholar 

  • Daly B, Swingle JS, Eckert GL (2012) Increasing hatchery production of juvenile red king crabs (Paralithodes camtschaticus) through size grading. Aquaculture 364–365:206–211. doi:10.1016/j.aquaculture.2012.08.034

    Article  Google Scholar 

  • Dew CB (1990) Behavioral ecology of podding red king crab, Paralithodes camtschatica. Can J Fish Aquat Sci 47:1944–1958

    Article  Google Scholar 

  • Gillooly JF, Brown JH, West GB, Savage VM, Charnov EL (2001) Effects of size and temperature on metabolic rate. Science 293:2248–2251

    Article  CAS  Google Scholar 

  • Gish R (2010) The 2008 Pribilof district king crab survey. Alaska Department of Fish and Game, Anchorage

    Google Scholar 

  • Gish R, Vanek V, Pengilly D (2012) Results of the 2010 triennial St. Matthew Island blue king crab pot survey and 2010/11 tagging study. Alaska Department of Fish and Game, Anchorage

    Google Scholar 

  • Grant WS, Cheng W (2012) Incorporating deep and shallow components of genetic structure into the management of Alaskan red king crab. Evol Appl 5:820–837. doi:10.1111/j.1752-4571.2012.00260.x

    Article  Google Scholar 

  • Jensen GC, Armstrong DA (1989) Biennial reproductive cycle of blue king crab, Paralithodes platypus, at the Pribilof Islands, Alaska and comparison to a congener, P. camtschatica. Can J Fish Aquat Sci 46:932–940

    Article  Google Scholar 

  • Kurata H (1960) Studies on the larvae and postlarvae of Paralithodes camtschatica III. The influence of temperature and salinity on the survival and growth of the larvae. Bull Hokkaido Region Fish Res Lab 21:9–14

    Google Scholar 

  • Long WC (2016) A new quantitative model of multiple transitions between discrete stages, applied to the development of crustacean larvae. Fish Bull, US 114:58–66. doi:10.7755/FB.114.1.5

    Article  Google Scholar 

  • Long WC, Whitefleet-Smith L (2013) Cannibalism in red king crab: habitat, ontogeny, and the predator functional response. J Exp Mar Biol Ecol 449:142–148

    Article  Google Scholar 

  • Long WC, Popp J, Swiney KM, Van Sant SB (2012) Cannibalism in red king crab, Paralithodes camtschaticus (Tilesius, 1815): effects of habitat type and predator density on predator functional response. J Exp Mar Biol Ecol 422–423:101–106. doi:10.1016/j.jembe.2012.04.019

    Article  Google Scholar 

  • Long WC, Swiney KM, Foy RJ (2013a) Effects of ocean acidification on the embryos and larvae of red king crab, Paralithodes camtschaticus. Mar Pollut Bull 69:38–47. doi:10.1016/j.marpolbul.2013.01.011

    Article  Google Scholar 

  • Long WC, Swiney KM, Harris C, Page HN, Foy RJ (2013b) Effects of ocean acidification on juvenile red king crab (Paralithodes camtschaticus) and Tanner crab (Chionoecetes bairdi) growth, condition, calcification, and survival. PLoS ONE 8:e60959. doi:10.1371/journal.pone.0060959

    Article  CAS  Google Scholar 

  • Long WC, Van Sant SB, Swiney KM, Foy R (2017) Survival, growth, and morphology of blue king crabs: effect of ocean acidification decreases with exposure time. ICES J Mar Sci 74:1033–1041. doi:10.1093/icesjms/fsw197

    Google Scholar 

  • Mangum CP, McMahon BR, deFur PL, Wheatly MG (1985) Gas exchange, acid-base balance, and the oxygen supply to the tissues during a molt of the blue crab Callinectes sapidus. J Crust Biol 5:188–206. doi:10.2307/1547866

    Article  Google Scholar 

  • McGaw IJ, Whiteley NM (2012) Effects of acclimation and acute temperature change on specific dynamic action and gastric processing in the green shore crab, Carcinus maenas. J Therm Biol 37:570–578

    Article  Google Scholar 

  • McLeese D (1956) Effects of temperature, salinity and oxygen on the survival of the American lobster. J Fish B Can 13:247–272

    Article  Google Scholar 

  • Miller NA, Paganini AW, Stillman JH (2013) Differential thermal tolerance and energetic trajectories during ontogeny in porcelain crabs, genus Petrolisthes. J Therm Biol 38:79–85

    Article  Google Scholar 

  • Morley S, Martin S, Bates A, Clark M, Ericson J, Lamare M, Peck L (2012) Spatial and temporal variation in the heat tolerance limits of two abundant Southern Ocean invertebrates. Mar Ecol Prog Ser 450:81–92

    Article  Google Scholar 

  • Morley SA, Lai C-H, Clarke A, Tan KS, Thorne MA, Peck LS (2014) Limpet feeding rate and the consistency of physiological response to temperature. J Comp Physiol B 184:563–570

    Article  Google Scholar 

  • Morley S, Bates A, Lamare M, Richard J, Nguyen K, Brown J, Peck L (2016) Rates of warming and the global sensitivity of shallow water marine invertebrates to elevated temperature. J Mar Biol Assoc UK 96:159–165

    Article  Google Scholar 

  • Nakanishi T (1987) Rearing condition of eggs, larvae and post-larvae of king crab. Bull Japan Sea Reg Fish Res Lab 37:57–161

    Google Scholar 

  • National Centers for Environmental Information (2016) Water temperature table of all coastal regions. National Oceanic and Atmospheric Administration, https://www.nodc.noaa.gov/dsdt/cwtg/all_meanT.html, Accessed 8 Aug, 2016

  • National Weather Service (2017) NOAA Online Weather Data, http://w2.weather.gov/climate/xmacis.php?wfo=pafc, Accessed June 19, 2017

  • Nguyen KDT, Morley SA, Lai C-H, Clark MS, Tan KS, Bates AE, Peck LS (2011) Upper temperature limits of tropical marine ectotherms: global warming implications. PLoS ONE 6:e29340

    Article  CAS  Google Scholar 

  • Peck LS, Clark MS, Morley SA, Massey A, Rossetti H (2009) Animal temperature limits and ecological relevance: effects of size, activity and rates of change. Funct Ecol 23:248–256

    Article  Google Scholar 

  • Pörtner H-O (2002) Climate variations and the physiological basis of temperature dependent biogeography: systemic to molecular hierarchy of thermal tolerance in animals. Comp Biochem Physiol A: Mol Integr Physiol 132:739–761

    Article  Google Scholar 

  • Pörtner H-O, Farrell AP (2008) Physiology and climate change. Science 322:690–692

    Article  Google Scholar 

  • Pörtner HO, Peck L, Somero G (2007) Thermal limits and adaptation in marine Antarctic ectotherms: an integrative view. Philo Trans R Soc Lond B: Biol Sci 362:2233–2258

    Article  Google Scholar 

  • Rice SD, Brodersen C, Arasmith PJ (1985) Feeding rates, molting success, and survival of juvenile red king crabs at different temperatures. In: Davis SK, Gaffney F, McCrary J, Paul AJ, Otto RS (eds) Proceedings of the International King Crab Symposium. Alaska Sea Grant College Program, University of Alaska Fairbanks, Anchorage, AK, pp 187–191

  • Richard J, Morley SA, Thorne MA, Peck LS (2012) Estimating long-term survival temperatures at the assemblage level in the marine environment: towards macrophysiology. PLoS ONE 7:e34655

    Article  CAS  Google Scholar 

  • Roberts JL (1957) Thermal acclimation of metabolism in the crab Pachygrapsus crassipes Randall. I. The influence of body size, starvation, and molting. Physiol Zool 30:232–242

    Article  Google Scholar 

  • Ryer CH, Long WC, Spencer ML, Iseri P (2015) Depth distribution, habitat associations, and differential growth of newly settled southern Tanner crab (Chionoecetes bairdi) in embayments around Kodiak Island, Alaska. Fish Bull, US 113:256–269. doi:10.7755/FB.113.3.3

    Article  Google Scholar 

  • Shirley SM, Shirley TC (1989a) Interannual variability in density, timing and survival of Alaskan red king crab Paralithodes camtschatica larvae. Mar Ecol Prog Ser 54:51–59

    Article  Google Scholar 

  • Shirley T, Shirley S (1989b) Temperature and salinity tolerances and preferences of red king crab larvae. Marine Behaviour and Physiology 16:19–30

    Article  Google Scholar 

  • Shirley TC, Shirley SM, Korn S (1990) Incubation period, molting and growth of female red king crabs: effects of temperature. In: Melteff B (ed) Proceedings of the International Symposium on king and Tanner crabs Lowell Wakefield Symposia. Alaska Sea Grant Report 90-04, pp 51–63

  • Stevens BG (1990) Temperature-dependent growth of juvenile red king crab (Paralithodes camtschatica) and its effects on size-at-age and subsequent recruitment in the eastern Bering Sea. Can J Fish Aquat Sci 47:1307–1317

    Article  Google Scholar 

  • Stevens BG, Swiney KM (2007) Hatch timing, incubation period, and reproductive cycle for captive primiparous and multiparous red king crab, Paralithodes camtschaticus. J Crust Biol 27:37–48

    Article  Google Scholar 

  • Stevens BG, Persselin S, Matweyou J (2008) Survival of blue king crab Paralithodes platypus Brandt, 1850, larvae in cultivation: effects of diet, temperature and rearing density. Aquacult Res 39:390–397. doi:10.1111/j.1365-2109.2007.01798.x

    Article  Google Scholar 

  • Stillman JH, Somero GN (2000) A comparative analysis of the upper thermal tolerance limits of eastern Pacific porcelain crabs, genus Petrolisthes: influences of latitude, vertical zonation, acclimation, and phylogeny. Physiol Biochem Zool 73:200–208

    Article  CAS  Google Scholar 

  • Stoner AW (2009) Habitat-mediated survival of newly settled red king crab in the presence of a predatory fish: role of habitat complexity and heterogeneity. J Exp Mar Biol Ecol 382:54–60

    Article  Google Scholar 

  • Stoner AW, Ottmar ML, Haines SA (2010) Temperature and habitat complexity mediate cannibalism in red king crab: observations on activity, feeding, and prey defense mechanisms. J Shellfish Res 29:1005–1012

    Article  Google Scholar 

  • Stoner AW, Copeman LA, Ottmar ML (2013) Molting, growth, and energetics of newly-settled blue king crab: effects of temperature and comparisons with red king crab. J Exp Mar Biol Ecol 442:10–21. doi:10.1016/j.jembe.2013.02.002

    Article  Google Scholar 

  • Storch D, Fernández M, Navarrete SA, Pörtner H-O (2011) Thermal tolerance of larval stages of the Chilean kelp crab Taliepus dentatus. Mar Ecol Prog Ser 429:157–167

    Article  Google Scholar 

  • Sulkin S, Mojica E, McKeen G (1996) Elevated summer temperature effects on megalopal and early juvenile development in the Dungeness crab, Cancer magister. Can J Fish Aquat Sci 53:2076–2079

    Google Scholar 

  • Sunday JM, Bates AE, Dulvy NK (2011) Global analysis of thermal tolerance and latitude in ectotherms. Proc R Soc Lond B Biol Sci 278:1823–1830

    Article  Google Scholar 

  • Sundberg K, Clausen D (1977) Post-larval king crab (Paralithodes camtschatica) distribution and abundance in Kachemak Bay Lower Cook Inlet, Alaska, 1976. Alaska Department of Fish and Game, Anchorage

    Google Scholar 

  • Swiney KM, Long WC, Persselin SL (2013) The effects of holding space on juvenile red king crab (Paralithodes camtschaticus) growth and survival. Aquacult Res 44:1007–1016. doi:10.1111/j.1365-2109.2012.03105.x

    Article  Google Scholar 

  • Swiney KM, Long WC, Foy RJ (2017) Decreased pH and increased temperatures affect young-of-the-year red king crab (Paralithodes camtschaticus). ICES J Mar Sci 74:1191–1200. doi:10.1093/icesjms/fsw251

    Google Scholar 

  • Swingle JS, Daly B, Hetrick J (2013) Temperature effects on larval survival, larval period, and health of hatchery-reared red king crab, Paralithodes camtschaticus. Aquaculture 384–387:13–18. doi:10.1016/j.aquaculture.2012.12.015

    Article  Google Scholar 

  • Wainwright TC, Armstrong DA, Andersen H, Dinnel PA, Herren D, Jensen GC, Orensanz JM, Shaffer JA (1992) Port Moller king crab studies. University of Washington, Seattle

    Google Scholar 

  • Walther K, Crickenberger SE, Marchant S, Marko PB, Moran AL (2013) Thermal tolerance of larvae of Pollicipes elegans, a marine species with an antitropical distribution. Mar Biol 160:2723–2732

    Article  Google Scholar 

  • Westphal MJ, Eckert GL, Tamone SL (2014) Comparison of first year growth among field, hatchery- and laboratory-raised juvenile red king crab, Paralithodes camtschaticus (Tilesius, 1815), in Alaska. J Crust Biol 34:319–325

    Article  Google Scholar 

  • Wyban J, Walsh WA, Godin DM (1995) Temperature effects on growth, feeding rate and feed conversion of the Pacific white shrimp (Penaeus vannamei). Aquaculture 138:267–279

    Article  Google Scholar 

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Acknowledgements

We thank the staff of the Kodiak Laboratory, particularly K. Swiney, A. Emley, S. Van Sant, R. Fields, and S. Dresdow, and the Alutiiq Pride Shellfish Hatchery for assistance in rearing the juvenile crab, and N. Gabriel for help performing the experiments. Previous versions of this paper were improved by comments from K. Swiney and J. Long. The findings and conclusions in the paper are those of the authors and do not necessarily represent the views of the National Marine Fisheries Service, NOAA. Reference to trade names or commercial firms does not imply endorsement by the National Marine Fisheries Service, NOAA.

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Long, W.C., Daly, B. Upper thermal tolerance in red and blue king crab: sublethal and lethal effects. Mar Biol 164, 162 (2017). https://doi.org/10.1007/s00227-017-3190-1

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