https://doi.org/10.4081/jlimnol.2020.1971
Cladocera resting egg banks in temporary and permanent wetlands
Submitted: 14 June 2020
Accepted: 7 October 2020
Published: 28 October 2020
Accepted: 7 October 2020
Abstract Views: 2134
PDF: 446
HTML: 41
HTML: 41
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Cladocerans are important filter-feeders transferring energy up the food web to different invertebrate and vertebrate predators. Along the flood period, cladocerans are one of the primary food sources for juvenile fish in floodplain. Resting egg banks allow cladoceran populations to overcome the environmental stress, related to several limnological changes, including complete drying of temporary wetlands. After drought, resting egg banks influence cladoceran community attributes during the cyclic and successional processes driven by episodic flood events. In this study we compared the taxonomic richness of active (from the water column) and dormant (from the sediment) Cladocera assemblages and analyzed the structure of resting egg banks, comparing the diversity, abundance and apparent viability/unviability of the eggs, between six temporary and six permanent wetlands, located along the Ovens River Floodplain, Victoria, Australia. The qualitative analysis shows higher taxonomic richness in active assemblages from temporary (24 taxa) than permanent (13 taxa) wetlands compared to dormant assemblages present in resting egg banks (9 taxa) from temporary and permanent wetlands. However, richness was influenced by taxonomic level of identification, with the majority of resting eggs only being identified to the taxonomic level of family (i.e. Chydoridae). Total taxa richness within egg banks was similar between wetland types, however, on average higher Shannon’s diversity of resting eggs was found within permanent (1.53) than temporary (0.82) wetlands. This is likely to be due to more stable wetlands not providing appropriate cues to trigger dormancy induction or breakage for specific populations, leading to higher values of evenness in permanent than temporary wetlands. Comparing permanent and temporary wetlands, higher abundance of resting eggs (more than four times) consisting of higher abundance of unviable eggs and similar viable egg abundance to permanent wetlands, was found within temporary wetlands, suggesting that the increased resting egg abundance in temporary wetlands is balanced by the losses due to factors such as predation, parasitism or other physical damage, during the terrestrial phase. Despite resistant outer shell structure, this study highlights that the damage to egg integrity is intensified in wetlands that undergo dry phases. Cladoceran resting egg banks represent the potential assemblage to recover after disturbance events such as drying, and information about these is important to ensure appropriate management and conservation of floodplain biodiversity.
Alekseev VR, 2007. Diapause in crustaceans: peculiarities of induction, p. 29-63. In: V.R. Alekseev, B.T. De Stasio and J.J. Gilber (eds.), Diapause in aquatic invertebrates: theory and human use. Dordrecht: Springer.
DOI: https://doi.org/10.1007/978-1-4020-5680-2_3
Amsinck SL, Jeppesen E, Verschuren D, 2007. Use of cladoceran resting eggs to trace climate-driven and anthropogenic changes in aquatic ecosystems, p. 135-157. In: V.R. Alekseev, B.T. De Stasio and J.J. Gilber (eds.), Diapause in aquatic invertebrates: theory and human use. Dordrecht: Springer.
DOI: https://doi.org/10.1007/978-1-4020-5680-2_8
Bachmann R, Hoyer M, Canfield D, 2018. Possible sediment mixing and the disparity between field measurements and paleolimnological inferences in shallow Iowa lakes in the Midwestern United States. Geosciences 8:40.
DOI: https://doi.org/10.3390/geosciences8020040
Benzie JAH, 1998. The systematics of Australian Daphnia (Cladocera: Daphniidae). Multivariate morphometrics. Hydrobiologia 166:163-182.
DOI: https://doi.org/10.1007/BF00028633
Boulton AJ, Lloyd, L, 1992. Flooding frequency and invertebrate emergence from dry floodplain sediments of the River Murray, Australia. Regul. River. 7:137-151.
DOI: https://doi.org/10.1002/rrr.3450070203
Brendonck L, De Meester L, 2003. Egg banks in freshwater zooplankton: evolutionary and ecological archives in the sediment. Hydrobiologia 49:65-84.
DOI: https://doi.org/10.1023/A:1024454905119
Brendonck L, Pincel T, Ortells R, 2017. Dormancy and dispersal as mediators of zooplankton population and community dynamics along a hydrological disturbance gradient in inland temporary pools. Hydrobiologia 796:201-222.
DOI: https://doi.org/10.1007/s10750-016-3006-1
Brock MA, Nielsen DL, Shiel RJ, Green JD, Langley JD, 2003. Drought and aquatic community resilience: the role of eggs and seeds in sediments of temporary wetlands. Freshwater Biol. 48:1207-1218.
DOI: https://doi.org/10.1046/j.1365-2427.2003.01083.x
Cáceres CE, Tessier AJ, 2003. How long to rest: the ecology of optimal dormancy and environmental constraint. Ecology 84:1189-1198.
DOI: https://doi.org/10.1890/0012-9658(2003)084[1189:HLTRTE]2.0.CO;2
Coronel JS, Aguilera X, Decleck S, Brendock L, 2009. Resting egg bank reveals high cladoceran species richness in high-altitude temporary peat land pools. Rev. Bol. Ecol. Amb. 25:51–67.
Davies P, Lawrence S, Turnbull J, Rutherfurd I, Grove J, Silvester E, Baldwin D, Macklin M, 2018. Reconstruction of historical riverine sediment production on the goldfields of Victoria, Australia. Anthropocene 21:1-15.
DOI: https://doi.org/10.1016/j.ancene.2017.11.005
De Bernardi R, Giussani G, Manca M, 1987. Cladocera: Predators and prey. Hydrobiologia 145:225-243.
DOI: https://doi.org/10.1007/BF02530284
De Stasio BT, Jr, 1989. The seedbank of a freshwater crustacean: copepodology for the plant ecologist. Ecology 70:1377-1389.
DOI: https://doi.org/10.2307/1938197
Eskinazi-Sant’Anna EM, Pace, ML, 2018. The potential of the zooplankton resting-stage bank to restore communities in permanent and temporary waterbodies. J. Plankton Res. 40:458-470.
DOI: https://doi.org/10.1093/plankt/fby023
Gehard M, Iglesias C, Clemente JM, Goyenola G, Meerhoff M, Pacheco JP, Mello FT, Mazzeo N, 2017. What can resting egg bank tell about cladoceran diversity in a shallow subtropical lake? Hydrobiologia 798:75-86.
DOI: https://doi.org/10.1007/s10750-016-2654-5
Gell PA, 2019. Restoring Murray River floodplain wetlands: Does the sediment record inform on watering regime? River Res. Appl. 36:1-10.
DOI: https://doi.org/10.1002/rra.3439
Gilchrist BM, 1978. Scanning electron microscope studies of the eggshell in some Anostraca (Crustacea: Branchiopoda). Cell Tissue Res. 193:337-351.
DOI: https://doi.org/10.1007/BF00209045
Guerrero-Jiménez G, Ramos-Rodríguez E, Silva-Briano M, Adabache-Ortiz A, Conde-Porcuna JN, 2020. Analysis of the morphological structure of diapausing propagules as a potential tool for the identification of rotifer and cladoceran species. Hydrobiologia 847:243-266.
DOI: https://doi.org/10.1007/s10750-019-04085-0
Gyllström M, Hansson L, 2004. Dormancy in freshwater zooplankton: Induction, termination and the importance of benthic-pelagic coupling. Aquat. Sci. 66:274-295.
DOI: https://doi.org/10.1007/s00027-004-0712-y
Hairston NGJ, Van Brunt RA, Kearns CM, 1995. Age and survivorship of diapausing eggs in a sediment egg bank. Ecology 76:1706-1711.
DOI: https://doi.org/10.2307/1940704
Humphries P, King AJ, Koehn J, 1999. Fish, flows and flood plains: links between freshwater fishes and their environment in the Murray-Darling River system, Australia. Environ. Biol. Fish. 56:129-151.
DOI: https://doi.org/10.1023/A:1007536009916
Iglesias C, Bonecker C, Brandão L, Crispim C, Eskinazi-Santanna EM, Gerhard M, Portinho J, Maia-Barbosa PM, Panarelli EA, Santangelo J, 2016. Current knowledge of South American cladoceran diapause: A brief review. Int. Rev. Hydrobiol. 101:1-14.
DOI: https://doi.org/10.1002/iroh.201501825
Jenkins LM, Boulton J, 2003. Connectivity in a dryland river: short-term aquatic microinvertebrate recruitment following floodplain inundation. Ecology 84:2708-2723.
DOI: https://doi.org/10.1890/02-0326
Jenkins LM, Boulton J, 2007. Detecting impacts and setting restoration targets in arid-zone rivers: aquatic micro-invertebrate responses to reduced floodplain inundation. J. Appl. Ecol. 44:823-832.
DOI: https://doi.org/10.1111/j.1365-2664.2007.01298.x
Junk W, Bayley PB, Sparks RE, 1989. The flood pulse concept in river-floodplain systems. In: D.P Dodge (ed.), Proc. International Large River Symp. Can. Spec. Publ. Fish. Aquat. Sci. 110-127.
King A, Humphries P, Lake PS, 2003. Fish recruitment on floodplains: the roles of patterns of flooding and live history characteristics. Can. J. Fish. Aquat. Sci. 60:773-786.
DOI: https://doi.org/10.1139/f03-057
Kingsford RT, 1995. Ecological effects of river management in New South Wales, p. 144-161. In: R.A. Bradstock, T.D. Auld, D.A. Keith, R.T. Kingsford, D. Lunney and D.P. Sivertsen (eds.), Conserving biodiversity: threats and solutions. Surrey Beatty & Sons: Chipping Norton.
Kingsford RT, 2000. Ecological impacts of dams, water diversions and river management on floodplain wetlands in Australia. Austral Ecol. 25:109-127.
DOI: https://doi.org/10.1046/j.1442-9993.2000.01036.x
Marren PM, Woods KL, 2011. Inundation of anabranching river floodplain wetlands: the Ovens River, Victoria, Australia, p. 229-234. In: C. Abesser, G. Nützmann, M.C. Hill, G. Blöschl and E. Lakshmanan (eds.), Conceptual and modelling studies of integrated groundwater, surface water and ecological systems. International Association of Hydrological Sciences.
May L, 1986. Rotifer sampling - a complete species list from one visit? Hydrobiologia 134:117-120.
DOI: https://doi.org/10.1007/BF00006735
MDBA - Murray-Darling Basin Authority, 2018. Discover the Basin: Ovens. Accessed 28 July 2018. Available from: https://www.mdba.gov.au/discover-basin/catchments/ovens
Ning NSP, Nielsen DL, 2011. Community structure and composition of macrofaunal egg bank assemblages in riverine and floodplain sediments. Hydrobiologia 661:211-221.
DOI: https://doi.org/10.1007/s10750-010-0525-z
Nielsen DL, Smith FJ, Hillman TJ, Shiel RJ, 2000. Impact of water regime and fish predation on zooplankton resting egg production and emergence. J Plankton Res 22:433-446
DOI: https://doi.org/10.1093/plankt/22.3.433
Nielsen DL, Hillman TJ, Smith FJ, Shiel RJ, 2002. The influence of seasonality and duration of flooding on zooplankton in experimental billabongs. River. Res. Appl. 18:227-237.
DOI: https://doi.org/10.1002/rra.641
Nielsen DL, Brock MA, 2009. Modified water regime and salinity as a consequence of climate change: prospects for wetlands of Southern Australia. Climatic Change 95:523-533.
DOI: https://doi.org/10.1007/s10584-009-9564-8
Nielsen DL, Podnar K, Watts RJ, Wilson AL, 2013. Empirical evidence linking increased hydrologic stability with decreased biotic diversity within wetlands. Hydrobiologia 708:81-96.
DOI: https://doi.org/10.1007/s10750-011-0989-5
Nielsen DL, Merrin, LE, Pollino, CA, Karim F, Stratford D, O’Sullivan J 2020. Climate change and dam development: Effects on wetland connectivity and ecological habitat in tropical wetlands. Ecohydrology 13:e2228.
DOI: https://doi.org/10.1002/eco.2228
Orlova-Bienkowskaja MY, 2001. Cladocera: Anomopoda - Daphniidae: genus Simocephalus. Guides to the identification of the Microinvertebrates of Continental waters of the world. Leyden, Backhuys Publishers: 130 pp.
Pallazo F, Bonecker CC, Fernandes AP, 2008. Resting cladoceran eggs and their contribution to zooplankton diversity in a lagoon of the Upper Paraná River floodplain. Lake Reserv. Manage. 13:207-214.
DOI: https://doi.org/10.1111/j.1440-1770.2008.00370.x
Panarelli EA, Kawamura HA, Elmoor-Loureiro LMA, Sousa FDR, Corgosinho PHC, Previatelli D, Rocha CEF, 2019. Life history of Karualona muelleri (Richard, 1897) (Chydoridae, Aloninae). J. Limnol. 78:1848.
DOI: https://doi.org/10.4081/jlimnol.2019.1848
Petts GE, Amoros C, 1996. Fluvial hydrosystems. London, Chapman & Hall: 322 pp.
DOI: https://doi.org/10.1007/978-94-009-1491-9
Piscia R, Guilizzoni P, Fontaneto D, Vignati DA, Appleby PG, Manca M, 2012. Dynamics of rotifer and cladoceran resting stages during copper pollution and recovery in a subalpine lake. Ann. Limnol. - Int. J. Lim. 48:151-160.
DOI: https://doi.org/10.1051/limn/2012006
Porter KG, Pace ML, Battey JL, 1979. Ciliate protozoans as links in freshwater zooplanktonic food chains. Nature 277:563-565.
DOI: https://doi.org/10.1038/277563a0
Quinn GP, Hillman TJ, Cook R, 2000. The response of macroinvertebrates to inundation in floodplain wetlands: a possible effect of river regulation? Regul. River. 16:469-477.
DOI: https://doi.org/10.1002/1099-1646(200009/10)16:5<469::AID-RRR598>3.0.CO;2-1
Radzikowski J, 2013. Resistance of dormant stages of planktonic invertebrates to adverse environmental conditions. J. Plankton Res. 35:707-723.
DOI: https://doi.org/10.1093/plankt/fbt032
Radzikowski J, Krupinska K, Slusarczyk M, 2018. Different thermal stimuli initiate hatching of Daphnia diapausing eggs originating from lakes and temporary waters. Limnology 19:81-88.
DOI: https://doi.org/10.1007/s10201-017-0520-4
R Development Core Team, 2015, R: A Language and Environment for Statistical Computing. Vienna, R Foundation for Statistical Computing. Available from: http://www.R-project.org/
Redfield G, Vincent W, 1979. Stages of infection and ecological effects of a fungal epidemic on the eggs of a limnetic copepod. Freshwater Biol. 9:503-510.
DOI: https://doi.org/10.1111/j.1365-2427.1979.tb01534.x
Santangelo JM, Lopes PM, Nascimento MO, Fernandes APC, Baartole S, Figueiredo-Barros MP, Leal JJF, Esteves FA, Farjalla VF, Bonecker CC, Bozelli RL, 2015. Community structure of resting egg banks and concordance patterns between dormant and active zooplankters in tropical lakes. Hydrobiologia 758:183-195.
DOI: https://doi.org/10.1007/s10750-015-2289-y
Sinev AY, 2016. Key for identification of Cladocera of the subfamily Aloninae (Anomopoda: Chydoridae) from South-East Asia. Zootaxa 4200:451-486.
DOI: https://doi.org/10.11646/zootaxa.4200.4.1
Smirnov NN, 1996. Cladocera: the Chydorinae and Sayciinae (Chydoridae) of the world. Guides to the identification of the Microinvertebrates of Continental waters of the world. Amsterdam, SPB Academic Publishing: 197 pp.
Smirnov NN, 2013. Nutrition, p. 33-74. In: N. Smirnov (ed.), Physiology of the Cladocera. Amsterdam, Academic Press.
DOI: https://doi.org/10.1016/B978-0-12-396953-8.00004-5
Smirnov NN, Timms BV, 1983. A revision of the Australian Cladocera (Crustacea). Sydney, Records of the Australian Museum: 132 pp.
DOI: https://doi.org/10.3853/j.0812-7387.1.1983.103
Thoms M, 1995. The impact of catchment development on a semiarid wetland complex: the Barmah Forest, Australia. IAHS Publications-Series of Proceedings and Reports-Intern Assoc. Hydrol. Sci. 230:121–130.
Thoms M, Ogden R, Reid M, 1999. Establishing the condition of lowland floodplain rivers: a palaeo‐ecological approach. Freshwater Biol. 41:407-423.
DOI: https://doi.org/10.1046/j.1365-2427.1999.00439.x
Van Damme K, Dumont HJ, 2008. Further division of Alona Baird, 1843: separation and position of Colonatella Dybowski & Grochowski and Ovalona gen. n. (Crustacea: Cladocera). Zootaxa 1960:1-44.
DOI: https://doi.org/10.11646/zootaxa.1960.1.1
Vandekerkhove J, Declerck S, Vanhove M, Brendonck L, Jeppesen E, Conde Porcuna JM, De Meester L, 2004. Use of ephippial morphology to assess richness of anomopods: potentials and pitfalls. J. Limnol. 63:s1.75.
DOI: https://doi.org/10.4081/jlimnol.2004.s1.75
Vargas AL, Santangelo JM, Bozelli RL, 2019. Recovery from drought: viability and hatching patterns of hydrated and desiccated zooplankton resting eggs. Int. Rev. Hydrobiol. 104:26-33.
DOI: https://doi.org/10.1002/iroh.201801977
Ward JV, 1989. The four-dimensional nature of lotic ecosystems. J. N. Am. Benthol. Soc. 8:2-8.
DOI: https://doi.org/10.2307/1467397
Ward JV, 1998. Riverine landscapes: biodiversity patterns, disturbance regimes, and aquatic conservation. Biol. Conserv. 83:269-278.
DOI: https://doi.org/10.1016/S0006-3207(97)00083-9
Edited by
Giampaolo Rossetti, Dept. of Bioscences, University of Parma, ItalySupporting Agencies
the Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)How to Cite
Panarelli, Eliana A., Daryl Nielsen, and Aleicia Holland. 2020. “Cladocera Resting Egg Banks in Temporary and Permanent Wetlands”. Journal of Limnology 80 (1). https://doi.org/10.4081/jlimnol.2020.1971.
Copyright (c) 2020 The Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Similar Articles
- Angela Boggero, Lyudmila Kamburska, Silvia Zaupa, Marzia Ciampittiello, Michela Rogora, Tiziana Di Lorenzo, Synoptic results on the potential impacts of the Lake Maggiore water management strategy on freshwater littoral ecosystems and invertebrate biocoenosis (NW, Italy) , Journal of Limnology: Vol. 81 No. s2 (2022): Effects of water level management on lake littorals and downstream river areas
- Csaba Vadadi-Fülöp, Levente Hufnagel, Climate change and plankton phenology in freshwater: current trends and future commitments , Journal of Limnology: Vol. 73 No. 1 (2014)
- Vittoria Ferrari, Arianna Gualdi, Isabella Bertani, Diego Fontaneto, Lyudmila Kamburska, Karimullah Karimullah, Federico Marrone, Ulrike Obertegger, Giampaolo Rossetti, Rocco Tiberti, Tommaso Cancellario, A georeferenced dataset of Italian occurrence records of the phylum Rotifera , Journal of Limnology: Vol. 82 No. s1 (2023): Georeferenced freshwater biodiversity data
- Valeria Rossi, Catia Maurone, Giorgio Benassi, Silvia Marková, Petr Kotlík, Nicolò Bellin, Ireneo Ferrari, Phenology of Daphnia in a Northern Italy pond during the weather anomalous 2014 , Journal of Limnology: Vol. 74 No. 3 (2015)
- Cleber C. Figueredo, Ricardo M. Pinto-Coelho, Ana Maria M.B. Lopes, Pedro H.O. Lima, Björn Gücker, Alessandra Giani, From intermittent to persistent cyanobacterial blooms: identifying the main drivers in an urban tropical reservoir , Journal of Limnology: Vol. 75 No. 3 (2016)
- Jérôme Kaiser, Bora Ön, Helge W. Arz, Sena Akçer-Ön, Sedimentary lipid biomarkers in the magnesium rich and highly alkaline Lake Salda (south-western Anatolia) , Journal of Limnology: Vol. 75 No. 3 (2016)
- Angela Boggero, Elzbieta Dumnicka, Riccardo Fornaroli, Daniele Paganelli, Silvia Zaupa, Geotargeting spatial and temporal data of Italian freshwater high-altitude macroinvertebrates , Journal of Limnology: Vol. 82 No. s1 (2023): Georeferenced freshwater biodiversity data
- Luciana Avigliano, Alicia Vinocour, Griselda Chaparro, Guillermo Tell, Luz Allende, Influence of re-flooding on phytoplankton assemblages in a temperate wetland following prolonged drought , Journal of Limnology: Vol. 73 No. 2 (2014)
- Pol Tarrats, Miguel Cañedo-Argüelles, Maria Rieradevall, Narcís Prat, Chironomid communities as indicators of local and global changes in an oligotrophic high mountain lake (Enol Lake, Northwestern Spain) , Journal of Limnology: Vol. 76 No. 2 (2017)
- Enlou Zhang, Yanmin Cao, Peter Langdon, Qian Wang, Ji Shen, Xiangdong Yang, Within-lake variability of subfossil chironomid assemblage in a large, deep subtropical lake (Lugu lake, southwest China) , Journal of Limnology: Vol. 72 No. 1 (2013)
<< < 8 9 10 11 12 13 14 15 16 17 > >>
You may also start an advanced similarity search for this article.
List of Cited By :
