Polar Biology

, Volume 36, Issue 8, pp 1205–1214 | Cite as

Lack of recovery from disturbance in high-arctic boulder communities

Original Paper

Abstract

High-arctic boulder communities that are impacted by anthropogenic and natural influences can result in the removal or scouring of sessile organisms leaving either open space or damaged organisms. This project asks how sessile communities recover after disturbances by determining (1) timing of recolonization, (2) grazer effects on recolonization, and (3) vegetative regrowth rates for encrusting sponges and corallines. Cleared boulders were monitored over 7 years to determine recolonization timing and grazer impacts. Vegetative regrowth rates were determined by monitoring partial clearings for 4 years. This study found that recolonization was slow with less than 10 % of the boulder surfaces being colonized after 7 years. Recolonization was so slow that it was difficult to ascertain grazer impacts, although it appeared there were no impacts. Lastly, this study showed that vegetative regrowth of sponges and encrusting coralline algae was fast. Sponges averaged 100 % regrowth after 2 years and corallines averaged 40 % after 4 years. Coralline regrowth was slower when exposed to higher sedimentation. This study showed that community recovery from disturbances is very slow in the Beaufort Sea, especially if entire organisms are removed. However, if removal is partial, recovery can be quicker, particularly in low sediment areas. Complete community recovery in this system after a disturbance may take a decade or more.

Keywords

Disturbance Recovery Recolonization Arctic Grazing 

References

  1. Aguilera MA, Navarrete SA (2007) Effects of Chiton granosus (Frembly, 1827) and other molluscan grazers on algal succession in wave exposed mid-intertidal rocky shores of central Chile. J Exp Mar Biol Ecol 349:84–98CrossRefGoogle Scholar
  2. Airoldi L (2000) Response of algae with different life histories to temporal and spatial variability of disturbance in subtidal reefs. Mar Ecol Prog Ser 195:81–92CrossRefGoogle Scholar
  3. Airoldi L (2003) The effects of sedimentation on rocky coast assemblages. Oceanogr Mar Biol 41:161–236Google Scholar
  4. Airoldi L, Cinelli F (1997) Effects of sedimentation on subtidal macroalgal assemblages: an experimental study from a Mediterranean rocky shore. J Exp Mar Biol Ecol 215:269–288CrossRefGoogle Scholar
  5. Atalah J, Crowe TP (2010) Combined effects of nutrient enrichment, sedimentation and grazer loss on rock pool assemblages. J Exp Mar Biol Ecol 388:51–57CrossRefGoogle Scholar
  6. Aumack CF, Dunton KH, Burd AB, Funk DW, Maffione RA (2007) Linking light attenuation and suspended sediment loading to benthic productivity within an arctic kelp bed community. J Phycol 43:853–863CrossRefGoogle Scholar
  7. Barnes DKA, Kuklinski P (2005) Low colonization of artificial substrate in arctic Spitsbergen. Polar Biol 29:65–69CrossRefGoogle Scholar
  8. Bell JJ (2008) Sponges as agents of biological disturbance. Mar Ecol Prog Ser 368:127–135CrossRefGoogle Scholar
  9. Bertness MD (1984) Habitat and community modification by an introduced herbivorous snail. Ecology 65:370–381CrossRefGoogle Scholar
  10. Bertness MD, Trussell GC, Ewanchuk PJ, Silliman BR, Crain CM (2004) Consumer controlled community states on Gulf of Maine rocky shores. Ecology 85:1321–1331CrossRefGoogle Scholar
  11. Beuchel F, Gulliksen B (2008) Temporal patterns of benthic community development in an Arctic fjord (Kongsfjorden, Svalbard): results of a 24-year manipulative study. Polar Biol 31:913–924CrossRefGoogle Scholar
  12. Caffey HM (1982) No effect of naturally-occurring rock types on settlement or survival in the intertidal barnacle, Tesseropora rosea (Krauss). J Exp Mar Biol Ecol 63:119–132CrossRefGoogle Scholar
  13. Campana GL, Zacher K, Fricke A, Molis M, Wulff A, Quartina ML, Wiencke C (2009) Drivers of colonization and succession in polar benthic macro- and microalgal communities. Bot Mar 52:655–667CrossRefGoogle Scholar
  14. Carmack EC, MacDonald RW (2002) Oceanography of the Canadian shelf of the Beaufort Sea: a setting for marine life. Arctic 55:29–45Google Scholar
  15. Connell JH (1978) Diversity in tropical rain forests and coral reefs. Science 199:1302–1310PubMedCrossRefGoogle Scholar
  16. Cowen RK, Lwiza KMM, Sponaugle S, Paris CB, Olson DB (2000) Connectivity of marine populations: open or closed? Science 287:857–859PubMedCrossRefGoogle Scholar
  17. Cross WE, Wilce RT, Fabijan MF (1987) Effects of experimental releases of oil and dispersed oil on Arctic nearshore macrobenthos. III. Macroalgae. Arctic 40:211–219Google Scholar
  18. Davis AR (2006) The role of mineral, living, and artificial substrata in the development of subtidal assemblages. In: Wahl M (ed) Marine hard bottom communities, ecological studies vol 201. Springer, New York, pp 19–38Google Scholar
  19. Dayton PK (1989) Interdecadal variation in an Antarctic sponge and its predators from oceanographic climate shifts. Science 245:1484–1486PubMedCrossRefGoogle Scholar
  20. Debenham C (2005) Multiple stable isotopic analyses of the Boulder Patch, a high arctic kelp community: trophic and temporal perspectives. Masters Thesis. University of Alaska FairbanksGoogle Scholar
  21. Deiman MR, Iken K, Konar B (2012) Susceptibility of Nereocystis luetkeana (Laminariales, Ochrophyta) and Eualaria fistulosa (Laminariales, Ochrophyta) spores to sedimentation. Algae 27:115–123CrossRefGoogle Scholar
  22. Diaz-Pulido G, McCook LJ (2003) Relative roles of herbivory and nutrients in the recruitment of coral-reef seaweeds. Ecology 84:2026–2033CrossRefGoogle Scholar
  23. Duggins DO, Eckman JE, Sewell AT (1990) Ecology of understory kelp environments II. Effects of kelps on recruitment of benthic invertebrates. J Exp Mar Biol Ecol 143:27–45CrossRefGoogle Scholar
  24. Dunton KH, Schell DM (1986) Seasonal carbon budget and growth of Laminaria solidungula in the Alaskan High Arctic. Mar Ecol Prog Ser 31:57–66CrossRefGoogle Scholar
  25. Dunton KH, Schonberg SV (2000) The benthic faunal assemblage of the Boulder Patch kelp community, Chapter 18. In: Johnson SR, Truett JC (eds) The natural history of an Arctic oil field. Academic, San Diego, pp 371–397CrossRefGoogle Scholar
  26. Dunton KH, Reimnitz E, Schonberg S (1982) An Arctic kelp community in the Alaskan Beaufort Sea. Arctic 35:465–484Google Scholar
  27. Eckman JE (1983) Hydrodynamic processes affecting benthic recruitment. Limnol Oceanogr 28:241–257CrossRefGoogle Scholar
  28. Gaylord B, Reed DC, Raimondi PT, Washburn L, McLean SR (2002) A physically based model of macroalgal spore dispersal in the wave and current-dominated nearshore. Ecology 83:1239–1251CrossRefGoogle Scholar
  29. Gaylord B, Reed DC, Raimondi PT, Washburn L (2006) Macroalgal spore dispersal in coastal environments: mechanistic insights revealed by theory and experiment. Ecol Monogr 76:481–502CrossRefGoogle Scholar
  30. Grime JP (1977) Evidence for the existence of three primary strategies in plants and its relevance to ecological and evolutionary theory. Am Nat 111:1169–1194CrossRefGoogle Scholar
  31. Gutt J (2011) On the direct impact of ice on marine benthic communities, a review. Polar Biol 24:553–564CrossRefGoogle Scholar
  32. Hop H, Pearson T, Hegseth EN, Kovacs KM, Wiencke C, Kwasniewski S, Eiane K, Mehlum F, Gulliksen B, Wlodarska-Kowalczuk M, Lydersen C, Weslawski JM, Cochrane S, Gabrielsen GW, Leakey RJG, Lønne OJ, Zajaczkowski M, Falk-Petersen S, Kendall M, Wangberg SA, Bischof K, Voronkov AY, Kovaltchouk NA, Wiktor J, Poltermann M, diPrisco G, Papucci C, Gerland S (2002) The marine ecosystem of Kongsfjorden, Svalbard. Polar Res 21:167–208CrossRefGoogle Scholar
  33. Huang YM, McClintock JB, Amsler CD, Peters KJ, Baker BJ (2006) Feeding rates of common Antarctic gammarid amphipods on ecologically important sympatric macroalgae. J Exp Mar Biol Ecol 329:55–65CrossRefGoogle Scholar
  34. Huston MA (1979) A general hypothesis of species diversity. Am Nat 113:81–101CrossRefGoogle Scholar
  35. Iken K (1999) Feeding ecology of the Antarctic herbivorous gastropod Laevilacunaria antarctica Martens. J Exp Mar Biol Ecol 236:133–148CrossRefGoogle Scholar
  36. Jackson JBC (1979) Overgrowth competition between encrusting ectoprocts in a Jamaican cryptic reef environment. J Anim Ecol 48:805–824CrossRefGoogle Scholar
  37. Kedra M, Wlodarska-Kowalczuk M, Weslawski JM (2010) Decadal change in a macrobenthic soft bottom community structure in a high Arctic fjord (Kongsfjorden, Svalbard). Polar Biol 33:1–11CrossRefGoogle Scholar
  38. Keough MJ (1984) Effects of patch size on the abundance of sessile marine invertebrates. Ecology 65:423–437CrossRefGoogle Scholar
  39. Kinlan BP, Gaines SD, Lester SE (2005) Propagule dispersal and the scales of marine community processes. Divers Distrib 11:139–148CrossRefGoogle Scholar
  40. Konar B (2007) Recolonization of a high latitude hard-bottom nearshore community. Polar Biol 30:663–667CrossRefGoogle Scholar
  41. Konar B, Estes JA (2003) The stability of boundary regions between kelp beds and deforested areas. Ecology 84:174–185CrossRefGoogle Scholar
  42. Konar B, Foster MS (1992) Distribution and recruitment of subtidal geniculate coralline algae. J Phycol 28:273–280CrossRefGoogle Scholar
  43. Konar B, Iken K (2005) Competitive dominance among sessile marine organisms in a high Arctic boulder community. Polar Biol 29:61–64CrossRefGoogle Scholar
  44. Konar B, Roberts C (1996) Large scale landslide effects on two exposed rocky subtidal areas in California. Bot Mar 39:517-524Google Scholar
  45. Kuklinski P, Berge J, McFadden L, Dmoch K, Zajaczkowski M, Nygard H, Piwosz K, Tatarek A (2013) Seasonality of occurrence and recruitment of Arctic marine benthic invertebrate larvae in relation to environmental variables. Polar Biol 36:549–560CrossRefGoogle Scholar
  46. Markham JW (1968) Studies on the haptera of Laminaria sinclairii (Harvey) Farlow, Anderson et Eaton. Syesis 1:125–131Google Scholar
  47. McCook LJ, Chapman ARO (1992) Vegetative regeneration of Fucus rockweed canopy as a mechanism of secondary succession on an exposed rocky shore. Bot Mar 35:35–46CrossRefGoogle Scholar
  48. McGuinness KA (1987a) Disturbance and organisms on boulders I. Patterns in the environment and the community. Oecologia 71:409–419CrossRefGoogle Scholar
  49. McGuinness KA (1987b) Disturbance and organisms on boulders II. Causes of patterns in diversity and abundance. Oecologia 71:420–430CrossRefGoogle Scholar
  50. Milazzo M, Badalamenti F, Riggio S, Chemello R (2004) Patterns of algal recovery and small-scale effects of canopy removal as a result of human trampling on a Mediterranean rocky shallow community. Biol Conserv 117:191–202CrossRefGoogle Scholar
  51. Minchinton TA, Scheibling RE, Hunt HL (1997) Recovery of an intertidal assemblage following a rare occurrence of scouring by sea ice in Nova Scotia, Canada. Bot Mar 40:139–148CrossRefGoogle Scholar
  52. Mumby PJ, Harborne AR, Williams J, Kappel CV, Brumbaugh DR, Micheli F, Holmes KE, Dahlgren CP, Paris CB, Blackwell PG (2007) Trophic cascade facilitates coral recruitment in a marine reserve. PNAS 104:8362–8367PubMedCrossRefGoogle Scholar
  53. O’Connor MI, Bruno JF, Gaines SD, Halpern BS, Lester SE, Kinlan BP, Weiss JM (2007) Temperature control of larval dispersal and the implications for marine ecology, evolution, and conservation. PNAS 104:1266–1271PubMedCrossRefGoogle Scholar
  54. Pearse VB, Pearse JS (1991) Year-long settling plate study yields no Antarctic placozoans and surprisingly little else. Antarct J US 26:149–150Google Scholar
  55. Pineda J, Reyns NB, Starczak VR (2009) Complexity and simplification in understanding recruitment n benthic populations. Popul Ecol 51:17–32CrossRefGoogle Scholar
  56. Poore AGB, Fagerström T (2001) A general model for selection among modules in haplodiploid life histories. Oikos 92:256–264CrossRefGoogle Scholar
  57. Rogers C (1990) Responses of coral reefs and reef organisms to sedimentation. Mar Ecol Prog Ser 62:185–202CrossRefGoogle Scholar
  58. Santelices B (1990) Patterns of reproduction, dispersal and recruitment in seaweeds. Oceanogr Mar Biol 28:177–276Google Scholar
  59. Schiel DR, Foster MS (2006) The population biology of large brown seaweeds: ecological consequences of multiphase life histories in dynamic coastal environments. Ann Rev Ecol Evol Syst 37:343–372CrossRefGoogle Scholar
  60. Schiel DR, Wood SA, Dunmore RA, Taylor DI (2006) Sediment on rocky intertidal reefs: effects on early post-settlement stages of habitat-forming seaweeds. J Exp Mar Biol Ecol 331:158–172CrossRefGoogle Scholar
  61. Slattery M, McClintock JB, Heine JN (1995) Chemical defenses in Antarctic soft corals: evidence for antifouling compounds. J Exp Mar Biol Ecol 190:61–77CrossRefGoogle Scholar
  62. Smith JE, Smith CM, Hunter CL (2001) An experimental analysis of the effects of herbivory and nutrient enrichment on benthic community dynamics on a Hawaiian reef. Coral Reefs 19:332–342Google Scholar
  63. Sousa WP (1979) Experimental investigations of disturbance and ecological succession in a rocky intertidal algal community. Ecol Monogr 49:227–254CrossRefGoogle Scholar
  64. Sousa WP (1980) The responses of a community to disturbance: the importance of successional age and species’ life histories. Oecologia 45:72–81CrossRefGoogle Scholar
  65. Stanwell-Smith D, Barnes DKA (1997) Benthic community development in Antarctica: recruitment and growth on settlement panels at Signy Island. Ecology 212:61–79Google Scholar
  66. Stocker LJ (1986) Artifactual effects of caging on the recruitment and survivorship of a subtidal colonial invertebrate. Mar Ecol Prog Ser 34:305–307CrossRefGoogle Scholar
  67. Sussmann AV, DeWreede RE (2007) Relative contribution of vegetative propagation and sexual reproduction in the maintenance of Acrosiphonia (Chlorophyta) populations. Phycologia 46:79–85CrossRefGoogle Scholar
  68. Todd CD (1998) Larval supply and recruitment of benthic invertebrates: do larvae always disperse as much as we believe? Hydrobiologia 375(376):1–21CrossRefGoogle Scholar
  69. Trefry JH, Rember RD, Trocine RP, Savoie M (2004) ANIMIDA Task 4: sources, concentrations and dispersion pathways for suspended sediment in the coastal Beaufort Sea. Final report, U.S. Department of Interior Minerals Management Service, OCS Study MMS 2004-032, p 97Google Scholar
  70. vanTamelen PG (1987) Early successional mechanisms in the rocky intertidal: the role of direct and indirect interaction. J Exp Mar Biol Ecol 112:39–48CrossRefGoogle Scholar
  71. Vaselli S, Bertocci I, Maggi E, Benedetti-Cecchi L (2008) Effects of mean intensity and temporal variance of sediment scouring events on assemblages of rocky shores. Mar Ecol Prog Ser 364:57–66CrossRefGoogle Scholar
  72. Węsławski JM, Kendall MA, Włodarska-Kowalczuk M, Iken K, Kędra M, Legezynska J, Sejr M (2011) Climate change effects on Arctic fjord and coastal macrobenthic diversity—observations and predictions. Mar Biodiv 41:71–85CrossRefGoogle Scholar
  73. Wessels H, Hagen W, Molis M, Wiencke C, Karsten W (2006) Intra- and interspecific differences in palatability of Arctic macroalgae from Kongsfjorden (Spitzbergen) for two benthic sympatric invertebrates. J Exp Mar Biol Ecol 329:20–33CrossRefGoogle Scholar
  74. Włodarska-Kowalczuk M, Pearson T, Kendall MA (2005) Benthic response to chronic natural physical disturbance by glacial sedimentation in an Arctic fjord. Mar Ecol Prog Ser 303:31–41CrossRefGoogle Scholar
  75. Wulff A, Iken K, Quartino ML, Al-Handal A, Wiencke C, Clayton MN (2009) Biodiversity, biogeography and zonation of marine benthic micro- and macroalgae in the Arctic and Antarctic. Bot Mar 52:491–507CrossRefGoogle Scholar
  76. Zacher K, Wulff A, Molis M, Hanelt D, Wiencke C (2007) Ultraviolet radiation and consumer effects on a field-grown intertidal macroalgal assemblage in Antarctica. Glob Change Biol 13:1201–1215Google Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2013

Authors and Affiliations

  1. 1.School of Fisheries and Ocean SciencesUniversity of Alaska FairbanksFairbanksUSA

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