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Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

Spatial and temporal variation of meiofauna community structure in soft-sediment pools around Moreton Bay, Australia

Craig A. Chargulaf A B and Ian R. Tibbetts A
+ Author Affiliations
- Author Affiliations

A School of Biological Sciences, The University of Queensland, St Lucia, Qld 4072, Australia.

B Corresponding author. Email: craig.chargulaf@gmail.com

Australian Journal of Zoology 63(3) 204-213 https://doi.org/10.1071/ZO14063
Submitted: 11 August 2014  Accepted: 20 July 2015   Published: 11 August 2015

Abstract

In eastern Australia, small ephemeral soft-sediment pools are common on sheltered sand- and mudflats, and are occupied by the juveniles of fishes of economic and ecological importance. To address the question of whether these pools are merely refugia or whether they constitute a hitherto unrecognised nursery feeding habitat for small obligate meiobenthivorous fishes, we surveyed the meiofaunal communities of ephemeral soft-sediment pools within three intertidal shores of Moreton Bay, Australia. Highest mean meiofaunal abundances occurred at Godwin Beach and differed significantly throughout the year. Nematodes and copepods were the most abundant taxa while all other taxa contributed to <10% of the total meiofaunal abundance. Pool characteristics (i.e. volume and surface area) did not correlate with the abundance of benthic faunal assemblages. Overall, ephemeral soft-sediment pools of Moreton Bay support meiofaunal communities that are likely to provide prey resources for juvenile and small fish that use them as nurseries at low tide.

Additional keywords: community composition, ephemeral soft-sediment pools, meiobenthivorous fish.


References

Aarnio, K., Bonsdorff, E., and Rosenback, N. (1996). Food and feeding habits of juvenile flounder Platichthys flesus (L), and turbot Scophthalmus maximus (L) in the Aland archipelago northern Baltic Sea. Journal of Sea Research 36, 311–320.
Food and feeding habits of juvenile flounder Platichthys flesus (L), and turbot Scophthalmus maximus (L) in the Aland archipelago northern Baltic Sea.Crossref | GoogleScholarGoogle Scholar |

Alongi, D. M. (1985). Effect of physical disturbance on population dynamics and trophic interactions among microbes and meiofauna. Journal of Marine Research 43, 351–364.
Effect of physical disturbance on population dynamics and trophic interactions among microbes and meiofauna.Crossref | GoogleScholarGoogle Scholar |

Anderson, M. J. (2001). A new method for non-parametric multivariate analysis of variance. Aquatic Ecology 26, 32–46.

Anderson, M. J., Gorley, R. N., and Clarke, K. R. (2008). ‘PERMANOVA+ for PRIMER: Guide to Software and Statistical Methods.’ (PRIMER-E: Plymouth, UK.)

Armenteros, M., Martin, I., Williams, J. P., Creagh, B., Gonzalez-Sanson, G., and Capetillo, N. (2006). Spatial and temporal variations of meiofaunal communities from the western sector of the Gulf of Batabano, Cuba. I. Mangrove systems. Estuaries and Coasts 29, 124–132.
Spatial and temporal variations of meiofaunal communities from the western sector of the Gulf of Batabano, Cuba. I. Mangrove systems.Crossref | GoogleScholarGoogle Scholar |

Armonies, W. (1989). Meiofaunal emergence from intertidal sediment measured in the field: significant contribution to nocturnal plantonic biomass in shallow waters. Helgoland Marine Research 43, 29–43.

Bell, S. S., and Sherman, K. M. (1980). A field investigation of meiofaunal dispersal: tidal resuspension and implications. Marine Ecology Progress Series 3, 245–249.
A field investigation of meiofaunal dispersal: tidal resuspension and implications.Crossref | GoogleScholarGoogle Scholar |

Boeckner, M. J., Sharma, J., and Proctor, H. C. (2009). Revisiting the meiofauna paradox: dispersal and colonization of nematodes and other meiofaunal organisms in low- and high-energy environments. Hydrobiologia 624, 91–106.
Revisiting the meiofauna paradox: dispersal and colonization of nematodes and other meiofaunal organisms in low- and high-energy environments.Crossref | GoogleScholarGoogle Scholar |

Castellanos-Galindo, G. A., and Giraldo, A. (2008). Food resource use in a tropical eastern Pacific tidepool fish assemblage. Marine Biology 153, 1023–1035.
Food resource use in a tropical eastern Pacific tidepool fish assemblage.Crossref | GoogleScholarGoogle Scholar |

Chargulaf, C. A., Townsend, K. A., and Tibbetts, I. R. (2011). Community structure of soft sediment pool fishes in Moreton Bay, Australia. Journal of Fish Biology 78, 479–494.
Community structure of soft sediment pool fishes in Moreton Bay, Australia.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M7mtFegtQ%3D%3D&md5=64dc0b603c57cd3a0736588ab9015f18CAS | 21284630PubMed |

Clarke, K. R., and Warwick, R. M. (2001). ‘Change in Marine Communities: an Approach to Statistical Analysis and Interpretation.’ 2nd edn. (PRIMER-E: Plymouth, UK.)

Coull, B. C. (1985). Long-term variability of estuarine meiobenthos: an 11 year study. Marine Ecology Progress Series 24, 205–218.
Long-term variability of estuarine meiobenthos: an 11 year study.Crossref | GoogleScholarGoogle Scholar |

Coull, B. C. (1999). Role of meiofauna in estuarine soft-bottom habitats. Australian Journal of Ecology 24, 327–343.
Role of meiofauna in estuarine soft-bottom habitats.Crossref | GoogleScholarGoogle Scholar |

Coull, B. C., Greenwood, J. G., Fielder, D. R., and Coull, B. A. (1995). Subtropical Australian juvenile fish eat meiofauna – experiments with winter whiting Sillago maculata and observations on other species. Marine Ecology Progress Series 125, 13–19.
Subtropical Australian juvenile fish eat meiofauna – experiments with winter whiting Sillago maculata and observations on other species.Crossref | GoogleScholarGoogle Scholar |

Cross, R. E., and Curran, M. C. (2004). Recovery of meiofauna in intertidal feeding pits created by rays. Southeastern Naturalist 3, 219–230.
Recovery of meiofauna in intertidal feeding pits created by rays.Crossref | GoogleScholarGoogle Scholar |

Danovaro, R., Scopa, M., Gambi, C., and Fraschetti, S. (2007). Trophic importance of subtidal metazoan meiofauna: evidence from in situ exclusion experiments on soft and rocky substrates. Marine Biology 152, 339–350.
Trophic importance of subtidal metazoan meiofauna: evidence from in situ exclusion experiments on soft and rocky substrates.Crossref | GoogleScholarGoogle Scholar |

Davie, P., and Hislop, I. (1998). Moreton Bay, in ‘Wild Guide to Moreton Bay Wildlife and Habitats of a Beautiful Australian Coast – Noosa to the Tweed’. (Ed. M. Ryan.) pp. xiii–xxiv. (Queensland Museum: Brisbane.)

de Morais, L. T., and Bodiou, J. Y. (1984). Predation on meiofauna by juvenile fish in western Mediterranean flatfish nursery ground. Marine Biology 82, 209–215.
Predation on meiofauna by juvenile fish in western Mediterranean flatfish nursery ground.Crossref | GoogleScholarGoogle Scholar |

Delgado, J. D., Riera, R., Monterroso, O., and Nunez, J. (2009). Distribution and abundance of meiofauna in intertidal sand substrata around Iceland. Aquatic Ecology 43, 221–233.
Distribution and abundance of meiofauna in intertidal sand substrata around Iceland.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXkvFeqsLs%3D&md5=9c7d3585c57598c57b6b67306a095367CAS |

Drolet, D., and Barbeau, M. A. (2009). Differential emigration causes aggregation of the amphipod Corophium volutator (Pallas) in tide pools on mudflats of the upper Bay of Fundy, Canada. Journal of Experimental Marine Biology and Ecology 370, 41–47.
Differential emigration causes aggregation of the amphipod Corophium volutator (Pallas) in tide pools on mudflats of the upper Bay of Fundy, Canada.Crossref | GoogleScholarGoogle Scholar |

Fleeger, J. W., Chandler, G. T., Fitzhugh, G. R., and Phillips, F. E. (1984). Effects of tidal currents on meiofauna densities in vegetated salt marsh sediments. Marine Ecology Progress Series 19, 49–53.
Effects of tidal currents on meiofauna densities in vegetated salt marsh sediments.Crossref | GoogleScholarGoogle Scholar |

Gee, J. M. (1989). An ecological and economic review of meiofauna as food for fish. Zoological Journal of the Linnean Society 96, 243–261.
An ecological and economic review of meiofauna as food for fish.Crossref | GoogleScholarGoogle Scholar |

Gning, N., Vidy, G., and Thiaw, O. T. (2008). Feeding ecology and ontogenetic diet shifts of juvenile fish species in an inverse estuary: the Sine-Saloum, Senegal. Estuarine, Coastal and Shelf Science 76, 395–403.
Feeding ecology and ontogenetic diet shifts of juvenile fish species in an inverse estuary: the Sine-Saloum, Senegal.Crossref | GoogleScholarGoogle Scholar |

Heip, C., Huys, R., Vincx, M., Vanreusel, A., Smol, N., Herman, R., and Herman, P. M. J. (1990). Composition, distribution, biomass and production of North Sea meiofauna. Netherlands Journal of Sea Research 26, 333–342.
Composition, distribution, biomass and production of North Sea meiofauna.Crossref | GoogleScholarGoogle Scholar |

Islam, M. S., Hibino, M., Nakayama, K., and Tanaka, M. (2006). Condition of larval and early juvenile Japanese temperate bass Lateolabrax japonicus related to spatial distribution and feeding in the Chikugo estuarine nursery ground in the Ariake Bay, Japan. Journal of Sea Research 55, 141–155.
Condition of larval and early juvenile Japanese temperate bass Lateolabrax japonicus related to spatial distribution and feeding in the Chikugo estuarine nursery ground in the Ariake Bay, Japan.Crossref | GoogleScholarGoogle Scholar |

Kolasinski, J., Frouin, P., Sallon, A., Rogers, K., Bruggemann, H. J., and Potier, M. (2009). Feeding ecology and ontogenetic dietary shift of yellowstripe goatfish Mulloidichthys flavolineatus (Mullidae) at Reunion Island, SW Indian Ocean. Marine Ecology Progress Series 386, 181–195.
Feeding ecology and ontogenetic dietary shift of yellowstripe goatfish Mulloidichthys flavolineatus (Mullidae) at Reunion Island, SW Indian Ocean.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtVClu7bL&md5=f09bff5a0e6b94a59ab2b8808c4bba0aCAS |

Krück, N. C., Chargulaf, C. A., Saint-Paul, U., and Tibbetts, I. R. (2009). Early post-settlement habitat and diet shifts and the nursery function of tidepools during Sillago spp. recruitment in Moreton Bay, Australia. Marine Ecology Progress Series 384, 207–219.
Early post-settlement habitat and diet shifts and the nursery function of tidepools during Sillago spp. recruitment in Moreton Bay, Australia.Crossref | GoogleScholarGoogle Scholar |

La Mesa, M., Borme, D., Tirelli, V., Di Poi, E., Legovini, S., and Umani, S. F. (2008). Feeding ecology of the transparent goby Aphia minuta (Pisces : Gobiidae) in the northwestern Adriatic Sea. Scientia Marina 72, 99–108.

Leduc, D., Probert, P. K., and Duncan, A. (2009). A multi-method approach for identifying meiofaunal trophic connections. Marine Ecology Progress Series 383, 95–111.
A multi-method approach for identifying meiofaunal trophic connections.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXotFSjurg%3D&md5=958066cdb7a4f1a84634f51bbee537fbCAS |

Li, J., Vincx, M., and Herman, P. M. J. (1997). Carbon flows through meiobenthic nematodes in the Westerschelde Estuary. Fundamental and Applied Nematology 20, 487–494.
| 1:STN:280:DC%2BD3s%2Fmt12huw%3D%3D&md5=66d3de5f485e8b1a96d79bc960f81d2eCAS |

Logan, D., Townsend, K. A., Townsend, K., and Tibbetts, I. R. (2008). Meiofauna sediment relations in leeward slope turf algae of Heron Island reef. Hydrobiologia 610, 269–276.
Meiofauna sediment relations in leeward slope turf algae of Heron Island reef.Crossref | GoogleScholarGoogle Scholar |

McCall, J. N., and Fleeger, J. W. (1993). Recognition and utilization of prey aggregations by juvenile spot (Leiostomus xanthurus Lacepede). Journal of Experimental Marine Biology and Ecology 174, 121–134.
Recognition and utilization of prey aggregations by juvenile spot (Leiostomus xanthurus Lacepede).Crossref | GoogleScholarGoogle Scholar |

Meager, J. J., Williamson, I., and King, C. R. (2005). Factors affecting the distribution, abundance and diversity of fishes of small, soft-substrata tidal pools within Moreton Bay, Australia. Hydrobiologia 537, 71–80.
Factors affecting the distribution, abundance and diversity of fishes of small, soft-substrata tidal pools within Moreton Bay, Australia.Crossref | GoogleScholarGoogle Scholar |

Metaxas, A., and Scheibling, R. E. (1993). Community structure and organization of tidepools. Marine Ecology Progress Series 98, 187–198.
Community structure and organization of tidepools.Crossref | GoogleScholarGoogle Scholar |

Metaxas, A., and Scheibling, R. E. (1994). Spatial and temporal variability of tidepool hyperbenthos on a rocky shore in Nova Scotia, Canada. Marine Ecology Progress Series 108, 175–184.
Spatial and temporal variability of tidepool hyperbenthos on a rocky shore in Nova Scotia, Canada.Crossref | GoogleScholarGoogle Scholar |

Muñoz, A. A., and Ojeda, F. P. (1998). Guild structure of carnivorous intertidal fishes of the Chilean coast: implications of ontogenetic dietary shifts. Oecologia 114, 563–573.
Guild structure of carnivorous intertidal fishes of the Chilean coast: implications of ontogenetic dietary shifts.Crossref | GoogleScholarGoogle Scholar |

Muschiol, D., Markovic, M., Threis, I., and Traunspurger, W. (2008). Predator–prey relationship between the cyclopoid copepod Diacyclops bicuspidatus and a free-living bacterivorous nematode. Nematology 10, 55–62.
Predator–prey relationship between the cyclopoid copepod Diacyclops bicuspidatus and a free-living bacterivorous nematode.Crossref | GoogleScholarGoogle Scholar |

Nozais, C., Perissinotto, R., and Tita, G. (2005). Seasonal dynamics of meiofauna in a South African temporarily open/closed estuary (Mdloti Estuary, Indian Ocean). Estuarine, Coastal and Shelf Science 62, 325–338.
Seasonal dynamics of meiofauna in a South African temporarily open/closed estuary (Mdloti Estuary, Indian Ocean).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVKmtb%2FP&md5=fbfd046a16ad2fee5958cf71e3ef7ca2CAS |

Palmer, M. (1988). Dispersal of marine meiofauna: a review and conceptual model explaining passive transport and active emergence with implications for recruitment. Marine Ecology Progress Series 48, 81–91.
Dispersal of marine meiofauna: a review and conceptual model explaining passive transport and active emergence with implications for recruitment.Crossref | GoogleScholarGoogle Scholar |

Pinckney, J. L., Carman, K. R., Lumsden, S. E., and Hymel, S. N. (2003). Microalgal-meiofaunal trophic relationships in muddy intertidal estuarine sediments. Aquatic Microbial Ecology 31, 99–108.
Microalgal-meiofaunal trophic relationships in muddy intertidal estuarine sediments.Crossref | GoogleScholarGoogle Scholar |

Sajan, S., Joydas, T. V., and Damodaran, R. (2010). Meiofauna of the western continental shelf of India, Arabian Sea. Estuarine, Coastal and Shelf Science 86, 665–674.
Meiofauna of the western continental shelf of India, Arabian Sea.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsVSqsrw%3D&md5=9971988eb92624053dd92933c57182abCAS |

Schmid-Araya, J. M., Hildrew, A. G., Robertson, A., Schmid, P. E., and Winterbottom, J. (2002). The importance of meiofauna in food webs: evidence from an acid stream. Ecology 83, 1271–1285.
The importance of meiofauna in food webs: evidence from an acid stream.Crossref | GoogleScholarGoogle Scholar |

Sherman, K. M., and Coull, B. C. (1980). The response of meiofauna to sediment disturbance. Journal of Experimental Marine Biology and Ecology 46, 59–71.
The response of meiofauna to sediment disturbance.Crossref | GoogleScholarGoogle Scholar |

Teasdale, M., Vopel, K., and Thistle, D. (2004). The timing of benthic copepod emergence. Limnology and Oceanography 49, 884–889.
The timing of benthic copepod emergence.Crossref | GoogleScholarGoogle Scholar |

Tita, G., Desrosiers, G., Vincx, M., and Nozais, C. (2000). Predation and sediment disturbance effects of the intertidal polychaete Nereis virens (Sars) on associated meiofaunal assemblages. Journal of Experimental Marine Biology and Ecology 243, 261–282.
Predation and sediment disturbance effects of the intertidal polychaete Nereis virens (Sars) on associated meiofaunal assemblages.Crossref | GoogleScholarGoogle Scholar |

Urban-Malinga, B., and Moens, T. (2006). Fate of organic matter in Arctic intertidal sediments: is utilization by meiofauna important? Journal of Sea Research 56, 239–248.
Fate of organic matter in Arctic intertidal sediments: is utilization by meiofauna important?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xps1GisL4%3D&md5=8898d75f06be328e7d885737fc67d5d4CAS |

Veit-Köhler, G., Laudien, J., Knott, J., Velez, J., and Sahade, R. (2008). Meiobenthic colonization of soft sediments in arctic glacial Kongsfjorden (Svalbard). Journal of Experimental Marine Biology and Ecology 363, 58–65.
Meiobenthic colonization of soft sediments in arctic glacial Kongsfjorden (Svalbard).Crossref | GoogleScholarGoogle Scholar |