Is maturity index an efficient tool to assess the effects of the physical disturbance on the marine nematode assemblages?-A critical interpretation of disturbance-induced maturity successions in some study cases in Maldives

SEMPRUCCI F.; COLANTONI P.; BALSAMO M.

doi:10.1007/s13131-016-0832-y

Volume 35 Issue 4

Turn off MathJax

Article Contents

Abstract

References

Article Navigation > Acta Oceanologica Sinica > 2016 > 35(4): 89-98

SEMPRUCCI F., COLANTONI P., BALSAMO M.. Is maturity index an efficient tool to assess the effects of the physical disturbance on the marine nematode assemblages?-A critical interpretation of disturbance-induced maturity successions in some study cases in Maldives[J]. Acta Oceanologica Sinica, 2016, 35(4): 89-98. doi: 10.1007/s13131-016-0832-y

Citation:

SEMPRUCCI F., COLANTONI P., BALSAMO M.. Is maturity index an efficient tool to assess the effects of the physical disturbance on the marine nematode assemblages?-A critical interpretation of disturbance-induced maturity successions in some study cases in Maldives[J]. Acta Oceanologica Sinica, 2016, 35(4): 89-98. doi: 10.1007/s13131-016-0832-y

Citation:

SEMPRUCCI F., COLANTONI P., BALSAMO M.. Is maturity index an efficient tool to assess the effects of the physical disturbance on the marine nematode assemblages?-A critical interpretation of disturbance-induced maturity successions in some study cases in Maldives[J]. Acta Oceanologica Sinica, 2016, 35(4): 89-98. doi: 10.1007/s13131-016-0832-y

PDF( 2112 KB)

Is maturity index an efficient tool to assess the effects of the physical disturbance on the marine nematode assemblages?-A critical interpretation of disturbance-induced maturity successions in some study cases in Maldives

doi: 10.1007/s13131-016-0832-y

Dipartimento di Scienze Biomolecolari(DiSB), Università di Urbino, loc. Crocicchia, Urbino 61029, Italy

Received Date: 2014-11-27
Rev Recd Date: 2015-11-25

Abstract

Abstract

Maturity index(MI), based on nematode life strategies, has been proposed in 1990 to assess the possible variations of the terrestrial and freshwater nematode assemblages induced by anthropogenic activities. It was subsequently applied also to marine ecosystems and, even if comparatively not yet very popular, it offers a good method to assess the ecological quality in relation to a wide range of anthropogenic drivers. However, few data are available on its response to physical stress, a key factor especially in the coastal areas. In this study, marine nematode genera from two study cases carried out in Maldives are used to test both MI and life strategy traits(i.e., c-p classes) for detecting the effects of physical disturbance. The results confirm that nematodes are well adapted to physical stress showing a general high rate of recovery. C-p scaling and MI did not seem to be appropriate for revealing this disturbance type probably because there are no empirical evidences on the life strategy of several genera, and a possible differential response to various disturbance types may be hypothesized.
- marine nematodes,
- bioindicators,
- maturity index,
- hydrodynamism,
- tsunami,
- Maldives

FullText(HTML)

References(59)

References

Altaff K, Sugumaran J, Naveed M S. 2005. Impact of tsunami on meiofauna of Marina beach, Chennai, India. Curr Sci, 89(1):34-38

Balsamo M, Albertelli G, Ceccherelli V U, et al. 2010. Meiofauna of the Adriatic Sea:current state of knowledge and future perspect-ives. Chem Ecol, 26(1):45-63

Balsamo M, Semprucci F, Frontalini F, et al. 2012. Chapter 4:Meiofauna as a tool for marine ecosystem biomonitoring. In:Cruzado A, ed. Marine Ecosystems. Rijeka:InTech Publisher, 77-104

Bongers T. 1990. The maturity index:an ecological measure of envir-onmental disturbance based on nematode species composi-tion. Oecologia, 83(1):14-19

Bongers T, Alkemade R, Yeates G W. 1991. Interpretation of disturb-ance-induced maturity decrease in marine nematode as-semblages by means of the Maturity Index. Mar Ecol Prog Ser, 76(2):135-142

Bongers T, Ferris H. 1999. Nematode community structure as a bioin-dicator in environmental monitoring. Trends in Ecology & Evolution, 14(6):224-228

Boufahja F, Semprucci F. 2015. Stress-induced selection of a single species from an entire meiobenthic nematode assemblage:is this possible using iron enrichment and does pre-exposure af-fect the ease of the process?. Environ Sci Pollut Res, 22(3):1979-1998

Buchanan J B. 1984. Sediment analysis. In:Holme N A, McIntyre A D, eds. Methods for the Study of Marine Benthos. 2nd ed. Oxford Boston:Blackwell Scientific Publications, 41-65

Clarke K R, Gorley R N. 2001. PRIMER v5:User Manual/Tutorial. Ply-mouth Marine Laboratory. Plymouth, UK:Primer-E Limited

Clarke K R, Warwick R M. 2001. Change in marine communities:an approach to statistical analysis and interpretation. 2nd ed. Ply-mouth Marine Laboratory, Plymouth, UK:Primer-E Limited

Essink K, Keidel H. 1998. Changes in estuarine nematode communit-ies following a decrease of organic pollution. Aquat Ecol, 32(3):195-202

Folk L R, Ward W C. 1957. Brazos river bar[Texas]; a study in the sig-nificance of grain size parameters. J Sediment Res, 27(1):3-26

Fonsêca-Genevois V, Somerfield P J, Neves M H B, et al. 2006. Colon-ization and early succession on artificial hard substrata by meiofauna. Mar Biol, 148(5):1039-1050

Fraschetti S, Gambi C, Giangrande A, et al. 2006. Structural and func-tional response of meiofauna rocky assemblages to sewage pol-lution. Mar Pollut Bull, 52(5):540-548

Gingold R, Ibarra-Obando S E, Rocha-Olivares A. 2011. Spatial ag-gregation patterns of free-living marine nematodes in contrast-ing sandy beach micro-habitats. J Mar Biol Assoc UK, 91(3):615-622

Grzelak K, Kotwicki L, Szczuciński W. 2009. Monitoring of sandy beach meiofaunal assemblages and sediments after the 2004 tsunami in Thailand. Pol J Environ St, 18(1):43-51

Grzelak K, Szczuciński W, Kotwicki L, et al. 2014. Ecological status of sandy beaches after tsunami events:insights from meiofauna investigations after the 2011 Tohoku-oki Tsunami, Sendai Bay, Japan. In:Kontar Y A, Santiago-Fandi.o V, Takahashi T, eds. Tsunami Events and Lessons Learned-Environmental and So-cietal Significance. Advances in Natural and Technological Hazards Research. Netherlands:Springer, 177-191

Kench P S, Brander R W, Parnell K E, et al. 2006. Wave energy gradi-ents across a Maldivian atoll:implications for island geomor-phology. Geomorphology, 81(1-2):1-17

Kendall M A, Aryuthaka C, Chimonides J, et al. 2009. Post-tsunami re-covery of shallow water biota and habitats on Thailand's Anda-man coast. Pol J Environ St, 18(1):69-75

Kotwicki L, Szczuciński W. 2006. Meiofauna assemblages and sedi-ment characteristic of sandy beaches on the west coast of Thail-and after the 2004 tsunami event. Phuket Mar Biol Cent Res Bull, 67:39-47

Lee H J, Vanhove S, Peck L S, et al. 2001. Recolonisation of meiofauna after catastrophic iceberg scouring in shallow Antarctic sedi-ments. Polar Biol, 24(12):918-925

Losi V, Montefalcone M, Moreno M, et al. 2012. Nematodes as indic-ators of environmental quality in seagrass(Posidonia oceanica) meadows of the NW Mediterranean Sea. Adv Oceanogra Limn-ol, 3(1):69-91

Mirto S, La Rosa T, Gambi C, et al. 2002. Nematode community re-sponse to fish-farm impact in the western Mediterranean. En-viron Pollut, 116(2):203-214

Moreno M, Semprucci F, Vezzulli L, et al. 2011. The use of nemat-odes in assessing ecological quality status in the Mediter-ranean coastal ecosystems. Ecol Indic, 11(2):328-336

Moreno M, Vezzulli L, Marin V, et al. 2008. The use of meiofauna di-versity as an indicator of pollution in harbours. ICES J Mar Sci, 65(8):1428-1435

Netto S A, Attrill M J, Warwick R M. 1999. The effect of a natural wa-ter-movement related disturbance on the structure of meiofauna and macrofauna communities in the intertidal sand flat of Rocas Atoll(NE, Brazil). J Sea Res, 42(4):291-302

Nicholas W L, Hodda M. 1999. The free-living nematodes of a tem-perate, high energy, sandy beach:faunal composition and vari-ation over space and time. Hydrobiologia, 394:113-127

Perry C T, Kench P S, Smithers S G, et al. 2013. Time scales and modes of reef lagoon infilling in the Maldives and controls on the onset of reef island formation. Geology, 41(10):1111-1114

Pfannkuche O, Thiel H. 1988. Sample processing. In:Higgins R P, Thiel H, eds. Introduction to the Study of Meiofauna. Washing-ton:Smithsonian Inst, 134-145

Platt H M, Warwick R M. 1983. Free Living Marine Nematodes. Part I. British Enoplids. Synopses of the British Fauna(New Series) No. 28. Cambridge:Cambridge University Press

Platt H M, Warwick R M. 1988. Free living marine nematodes. Part Ⅱ. British Chromadorids. Synopses of the British Fauna(New Series) No. 38. Leiden, Netherlands:E J Brill/W Backhuys

Raes M, De Troch M, Ndaro S G M, et al. 2007. The structuring role of microhabitat type in coral degradation zones:a case study with marine nematodes from Kenya and Zanzibar. Coral Reefs, 26(1):113-126

Raes M, Vanreusel A. 2006. Microhabitat type determines the com-position of nematode communities associated with sediment-clogged cold-water coral framework in the Porcupine Seabight(NE Atlantic). Deep Sea Research Part I, 53(12):1880-1894

Sandulli R, Semprucci F, Balsamo M. 2014. Taxonomic and function-al biodiversity variations of meiobenthic and nematode as-semblages across an extreme environment:a study case in a Blue Hole cave. Ital J Zool, 81(4):508-516

Schratzberger M, Bolam S G, Whomersley P, et al. 2004a. Develop-ment of a meiobenthic nematode community following the in-tertidal placement of various types of sediment. J Exp Mar Biol Ecol, 303(1):79-96

Schratzberger M, Bolam S, Whomersley P, et al. 2006. Differential re-sponse o nematode colonist communities to the intertidal placement of dredged material. J Exp Mar Biol Ecol, 334(2):244-255

Schratzberger M, Lampadariou N, Somerfield P J, et al. 2009. The im-pact of seabed disturbance on nematode communities:linking field and laboratory observations. Mar Biol, 156(4):709-724

Schratzberger M, Rees H L, Boyd S E. 2000. Effects of simulated de-position of dredged material on structure of nematode as-semblages-the role of burial. Mar Biol, 136(3):519-530

Schratzberger M, Whomersley P, Warr K, et al. 2004b. Colonisation of various types of sediment by estuarine nematodes via lateral in-faunal migration:a laboratory study. Mar Biol, 145(1):69-78

Seinhorst J W. 1959. A rapid method for the transfer of nematodes from fixative to anhydrous glycerin. Nematologica, 4(1):67-69

Semprucci F, Balsamo M, Frontalini F. 2014a. The nematode as-semblage of a coastal lagoon(Lake Varano, Southern Italy):ecology and biodiversity patterns. Sci Mar, 78(4):579-588

Semprucci F, Boi P, Manti A, et al. 2010a. Benthic communities along a littoral of the Central Adriatic Sea(Italy). Helgol Mar Res, 64(2):101-115

Semprucci F, Colantoni P, Baldelli G, et al. 2010b. The distribution of meiofauna on back-reef sandy platforms in the Maldives(Indi-an Ocean). Mar Ecol, 31(4):592-607

Semprucci F, Colantoni P, Baldelli G, et al. 2013a. Meiofauna associ-ated with coral sediments in the Maldivian subtidal habitats(Indian Ocean). Mar Biodiv, 43(3):189-198

Semprucci F, Colantoni P, Sbrocca C, et al. 2011. Meiofauna in sandy back-reef platforms differently exposed to the monsoons in the Maldives(Indian Ocean). J Mar Syst, 87(3-4):208-215

Semprucci F, Colantoni P, Sbrocca C, et al. 2014b. Spatial patterns of distribution of meiofaunal and nematode assemblages in the Huvadhoo lagoon(Maldives, Indian Ocean). J Mar Biol Assoc UK, 94(7):1377-1385

Semprucci F, Frontalini F, Sbrocca C, et al. 2015a. Meiobenthos and free-living nematodes as tools for biomonitoring environments affected by riverine impact. Environ Monit Assess, 187:251

Semprucci F, Losi V, Moreno M. 2015b. A review of Italian research on free-living marine nematodes and the future perspectives in their use as Ecological Indicators(EcoInd). Medit Mar Sci, 16(2):352-365

Semprucci F, Moreno M, Sbrocca S. et al. 2013b. The nematode as-semblage as a tool for the assessment of marine ecological quality status:a case-study in the Central Adriatic Sea. Medit Mar Sci, 14(1):48-57

Soetaert K E R, Muthumbi A, Heip C H R. 2002. Size and shape of ocean margin nematodes:morphological diversity and depth-related patterns. Mar Ecol Prog Ser, 242:179-193

Somerfield P J, Dashfield S L, Warwick R M. 2007. Three-dimensional spatial structure:nematodes in a sandy tidal flat. Mar Ecol Prog Ser, 336:177-186

Stoddart D R, Steers J A. 1977. The nature and origin of coral reef is-lands. In:Jones O A, Endean R, eds. Biology and Geology of Coral Reefs, vol 4. New York:Academic Press, 59-105

UNEP. 2005. After the tsunami:rapid environmental assessment. Nairobi:UNEP

Vanaverbeke J, Soetaert K, Vincx M. 2004. Changes in morphometric characteristics of nematode communities during a spring phytoplankton bloom deposition. Mar Ecol Prog Ser, 273:139-146

Vanaverbeke J, Bezerra T N, Braeckman U, et al. 2015. NeMys:World Database of Free-Living Marine Nematodes. http://nemys. ugent.beon[2015-09-01]

Vanhove S, Vermeeren H, Vanreusel A. 2004. Meiofauna towards the South Sandwich Trench(750-6300 m), focus on nematodes. Deep Sea Research Part Ⅱ, 51(14-16):1665-1687

Vanreusel A, Fonseca G, Danovaro R, et al. 2010. The contribution of deep-sea macrohabitat heterogeneity to global nematode di-versity. Mar Ecol, 31(1):6-20

Warwick R M, Platt H M, Somerfield P J. 1998. Free-living Marine Nematodes:Monhysterids Part Ⅲ(Synopses of the British Fauna),(New Series) No. 53. Shrewsbury, UK:Field Studies Council

Woodroffe C D, McLean R F, Smithers S G, et al. 1999. Atoll reef-is-land formation and response to sea-level change:West Island, Cocos(Keeling) Islands. Mar Geol, 160(1-2):85-104

Relative Articles

Relative Articles

Supplements(0)

Cited By

Cited by

Periodical cited type(10)

1.	Tom Moens, Kasia Sroczynska, Helena Adão. Meiofauna in a changing world. Ecological Indicators, 2022, 138: 108769. doi:10.1016/j.ecolind.2022.108769
2.	Wei-Ling Ng, Cheng-Ann Chen, Saleem Mustafa, et al. Free-living marine nematodes community structure in the conservation area (Chaojing Park) and its adjacent area of Keelung, Taiwan. PLOS ONE, 2022, 17(5): e0268691. doi:10.1371/journal.pone.0268691
3.	André Morgado Esteves, Tarciane Pires Souza, Visnu da Cunha Sarmento, et al. Effects of the ocean acidification on the functional structure of coral reef nematodes. Coral Reefs, 2022. doi:10.1007/s00338-022-02296-x
4.	Eleonora Grassi, Monica Montefalcone, Lucia Cesaroni, et al. Taxonomic and functional nematode diversity in Maldivian coral degradation zones: patterns across reef typologies and depths. PeerJ, 2022, 10: e13644. doi:10.7717/peerj.13644
5.	Thai Thanh Tran, Nguyen Thi My Yen, Ngo Xuan Quang, et al. Maturity Index of Nematode Communities and its Potential use for Measuring Environmental Disturbances with Special Emphasis on Effects of Organic Enrichment in Mangrove Ecosystems. Thalassas: An International Journal of Marine Sciences, 2022, 38(1): 355. doi:10.1007/s41208-021-00387-0
6.	Aaron Ridall, Jeroen Ingels. Suitability of Free-Living Marine Nematodes as Bioindicators: Status and Future Considerations. Frontiers in Marine Science, 2021, 8 doi:10.3389/fmars.2021.685327
7.	Kasia Sroczyńska, Anxo Conde, Paula Chainho, et al. How nematode morphometric attributes integrate with taxonomy-based measures along an estuarine gradient. Ecological Indicators, 2021, 124: 107384. doi:10.1016/j.ecolind.2021.107384
8.	Villares Gabriela, de Ward Catalina Pastor. Increased biomass of free-living marine nematodes may be indicative of disturbances in the ecosystem of the San Antonio bay. Open Journal of Environmental Biology, 2020, 5(1): 001. doi:10.17352/ojeb.000014
9.	Nilvea Ramalho Oliveira, Tom Moens, Gustavo Fonseca, et al. Response of life-history traits of estuarine nematodes to the surfactant sodium dodecyl sulfate. Aquatic Toxicology, 2020, 227: 105609. doi:10.1016/j.aquatox.2020.105609
10.	Olav Giere. Perspectives in Meiobenthology. SpringerBriefs in Biology, doi:10.1007/978-3-030-13966-7_4