Skip to main content

Advertisement

Log in

Assessing environmental response of gastropod species in karst springs: what species response curves say us about niche characteristic and extinction risk?

  • Original Paper
  • Published:
Biodiversity and Conservation Aims and scope Submit manuscript

Abstract

Spring ecosystems are exceptionally threatened and their conservation is often emphasized due to high levels of endemism among the groups inhabiting these ecosystems. This study includes gastropod assemblages of 36 springs situated in the northwestern part of Bosnia and Herzegovina. The aims of this paper were: to determine key factors for distribution of gastropod species on microspatial scale; to define the environmental preferences of gastropod species with respect to the physicochemical properties of water, the hydrological characteristics and the sediment structure; to determine species tolerance ranges and species optimums, with special emphasis on new and endemic species. Moreover the aim was to identify the species with highest extinction risk. The contribution of endangered and rare species to the total density was extremely high (64.6%). Species Response Curves were used to predict the distribution of gastropod species along the environmental gradient in the spring environments for the first time. The most important factors in structuring gastropod spring assemblages were oxygen and temperature. HOF (Huisman–Olff–Fresco) models may determine differences in range of environmental tolerance of species with similar ecological requirements. Our results have shown that two species: Ancylus fluviatilis and A. recurvus may be distinguished by their species response curves. Although there are no data on conservation status of A. recurvus, the extinction risk should be inferred as high, suggesting that IUCN status for this species should be updated to the category Vulnerable. Our study using HOF models revealed the potential gastropod species useful as indicators of karstic springs.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Alonso A, Camargo JA (2003) Short-term toxicity of ammonia, nitrite, and nitrate to aquatic snail Potamopyrgus antipodarum (Hydrobiidae, Mollusca). Bull Environ Contam Toxicol 70:1006–1012

    CAS  PubMed  Google Scholar 

  • Balkovič J, Kollár J, Šimonovič V (2012) Experience with using Ellenberg’s Rindicator values in Slovakia: oligotrophic and mesotrophic submontanebroad-leaved forests. Biologia 67(3):474–482

    Google Scholar 

  • Benavides JC, Vitt DH (2014) Response curves and the environmental limits for peat-forming species in the northern Andes. Plant Ecol 215:937–952

    Google Scholar 

  • Bódis E, Tóth B, Sousa R (2016) Freshwater mollusk assemblages and habitat associations in the Danube River drainage, Hungary. Aquat Conserv 26:319–332

    Google Scholar 

  • Bole J, Velkovrh F (1987) Nove vrste podzemeljskih polzev Jugoslavije (New Species of the subterranean Snails of Yugoslavia). SAZU 28(3):69–83

    Google Scholar 

  • Cadotte MW, Carscadden K, Mirotchnick N (2011) Beyond species: functional diversity and the maintenance of ecological processes and services. J Appl Ecol 48:1079–1087

    Google Scholar 

  • Dmitrović D, Savić A, Pešić V (2016) Discharge, substrate type and a temperature as a factors affecting the gastropod assemblages in springs in North-Western Bosnia and Herzegovina. Arch Biol Sci 68(3):613–621

    Google Scholar 

  • Florescu D, Ioneto RE, Sandru C, Iordache A, Culea M (2011) The influence of pollution monitoring parameters in characterizing the surface water quality from Romanian southern areas. Rom J Phys 56(7–8):1001–1010

    CAS  Google Scholar 

  • Fortunato H (2015) Mollusks: tools in environmental and climate research. Am Malacol Bull 33(2):1–15

    Google Scholar 

  • Glöer P, Pešić V (2010) The freshwater snails of the gennus Bythinella Moquin-Tandon (Gastropoda: Rissooidea: Hydrobiidae) from Montenegro. Arch Biol Sci 62(2):441–447

    Google Scholar 

  • Glöer P, Pešić V (2012) The freshwater snails (Gastropoda) of Iran, with descriptions of two new genera and eight new species. Zookeys 219:11–61

    Google Scholar 

  • Glöer P, Pešić V (2014a) Belgrandiella bozidarcurcici n. sp., a new species from Bosnia and Hercegovina (Gastropoda: Hydrobiidae). Arch Biol Sci 66(2):461–464

    Google Scholar 

  • Glöer P, Pešić V (2014b) Two new species of the genus Bythinella Moquin-Tandon, 1856 (Mollusca: Gastropoda: Hydrobiidae) from the Western Balkan Peninsula. Ecol Monten 1(4):249–255

    Google Scholar 

  • Glöer P, Pešić V (2014c) New subterranean freshwater gastropod of Montenegro (Molusca: Gastropoda: Hydrobiidae), with description of one new genus and two new species. Ecol Monten 1(4):244–248

    Google Scholar 

  • Hahn HJ (2000) Studies on classifying of undisturbed springs in Southwestern Germany by macrobenthic communities. Limnologica 30(3):247–259

    Google Scholar 

  • Hoffsten PO, Malmqvist B (2000) The macroinvertebrate fauna and hydrogeology of springs in central Sweden. Hydrobiologia 436:91–104

    Google Scholar 

  • Huisman J, Olff H, Fresco LFM (1993) A hierarchical set of models for species response analysis. J Veg Sci 4:37–46

    Google Scholar 

  • Jansen F, Oksanen J (2013) How to model species responses along ecological gradients-Huisman-Olff-Fresco models revisited. J Veg Sci 24(6):1108–1117

    Google Scholar 

  • Jenačković DD, Zlatković ID, Lakušić DV, Randjelović V (2016) Macrophytes as bioindicators of the physicochemical charactristic of wetlands and lowland and montain regions of the central Balkan Peninsula. Aquat Bot 134:1–9

    Google Scholar 

  • Książkiewicz-Parulska Z, Ablett JD (2017) Microspatial distribution of molluscs and response of species to litter moisture, water levels and eutrophication in moist, alkaline ecosystems. Belg J Zool 147(1):37–53

    Google Scholar 

  • Lawesson JE, Fosaa AM, Olsen E (2003) Calibration of Ellenberg indicator values for the Faroe Islands. Appl Veg Sci 6:53–62

    Google Scholar 

  • Lydeard C, Cowie RH, Ponder WF, Bogan AE, Bouchet P, Clark SA, Cummings KS, Frest TJ, Gargominy O, Herbrt DG, Hershler R, Perez KE, Roth B, Seddon M, Strong EE, Thompson FG (2004) The global decline of nonmarine mollusks. Bioscience 54(4):321–330

    Google Scholar 

  • Martinez MA, Thome DM (2006) Habitat usage by the Page springsnail, Pyrgulopsis morrisoni (Gastropoda: Hydrobiidae) from central Arizona. Veliger 48(1):8–16

    Google Scholar 

  • Murria C, Bonada N, Prat N (2008) Effects of the invasive species Potamopyrgus antipodarum (Hydrobiidae, Mollusca) on community structure in a small Mediterranean stream. Fund Appl Limnol 171–172:131–143

    Google Scholar 

  • Oksanen J, Minchin PR (2002) Continuum theory revisited: what shape are species responses along ecological gradients? Ecol Modell 157:119–129

    Google Scholar 

  • Oyem HH, Oyem IM, Ezeweali D (2014) Temperature, pH, electrical conductivity, total dissolved solids and chemical oxygen demand of groundwater in Boji-BojiAgbor/Owa area and immediate suburbs. Res J Environ Sci 8:444–450

    Google Scholar 

  • Pennak RW (1989) Fresh-water invertebrates of the United States: Protozoa to Mollusca. Wiley, New York

    Google Scholar 

  • Pešić V, Glöer P (2013a) A new freshwater snail genus (Hydrobiidae, Gastropoda) from Montenegro, with a discussion on gastropod diversity and endemism in Skadar Lake. ZooKeys 281:69–90

    Google Scholar 

  • Pešić V, Glöer P (2013b) Montenegrospeum, a new genus of Hydrobiid snails (Gastropoda: Risooidea) from Montenegro. Acta Zool Bull 64(4):565–566

    Google Scholar 

  • Pešić V, Dmitrović D, Savić A, von Fumetti S (2016) Studies on eucrenal-hypocrenal zonation of springs along the river mainstream: a case study of a karst canyon in Bosnia and Hercegovina. Biologia 71(7):809–817

    Google Scholar 

  • Pešić V, Gligorović B, Savić A, Buczynski P (2017) Ecological patterns of Odonata assemblages in karst springs in central Montenegro. Knowl Mang Aquat Ecosyst 418(3):20. https://doi.org/10.1051/kmae/2016035

    Article  Google Scholar 

  • Pešić V, Dmitrović D, Savić A et al (2019a) Application of macroinvertebrate multimetrics as a measure of the impact of anthropogenic modification of spring habitats. Aquat Conserv 2019:1–12

    Google Scholar 

  • Pešić V, Savić A, Jablonska A, Michonski G, Grabowski M, Bankowska A, Zawal A (2019b) Environmental factors affecting water mite assemblages along eucrenon-hypocrenon gradients in Mediterranean karstic springs. Exp Appl Acarol. https://doi.org/10.1007/S10493-019-00360-w

    Article  PubMed  Google Scholar 

  • Piechocki A, Wawrzyniak-Wydrowska B (2016) Guide to freshwater and marine Mollusca of Poland. Bogucki Wydawnictwo Naukowe, Poznań

    Google Scholar 

  • Régnier C, Fonteine B, Bouchet P (2009) Not knowing, not recording, not listening: numerous unnoticed mollusk extinctions. Conserv Biol 23:1212–1221

    Google Scholar 

  • Reiss H, Cunze S, König K, Neumann H, Kröncke I (2011) Species distribution modelling of marine benthos: a North Sea case study. Mar Ecol Prog Ser 442:71–86

    Google Scholar 

  • Richards DC, Cazier LD, Lester GT (2001) Spatial distribution of three snail species, including the invader Potamopyrgus antipodarum, in a freshwater spring. West N Am Nat 61:375–380

    Google Scholar 

  • Savić A, Dmitrovic D, Pešić V (2017) Ephemeroptera, Plecoptera and Trichoptera assemblages of karst springs in relation to some environmental factors: a case study in central Bosnia and Herzegovina. Turk J Zool 41:119–129

    Google Scholar 

  • Seddon MB (2010) Islamia bosniaca. The IUCN Red List of Threatened Species 2010: e.T155763A4838848. https://doi.org/10.2305/iucn.uk.2010-4.rlts.t155763a4838848.en

  • Sket B, Seddon MB (2010) Marstoniopsis vrbasi. The IUCN Red List of Threatened Species 2010: e.T156040A4896969. https://doi.org/10.2305/iucn.uk.2010-4.rlts.t156040a4896969.en

  • Strong EE, Gargominy O, Ponder WF, Bouchet P (2008) Global diversity of gastropods (Gastropoda; Mollusca) in freshwater. Hydrobiologia 595:149–166

    Google Scholar 

  • Tichý L (2002) JUICE, software for vegetation classification. J Veg 13(3):451–453

    Google Scholar 

  • Uğurlu E, Oldeland J (2012) Species response curves of oak species along climatic gradients in Turkey. Int J Biometeorol 56(1):85–93

    PubMed  Google Scholar 

  • Von Fumetti S, Dmitrović D, Pešić V (2017) The influence of flooding and river connectivity on macroinvertebrate assemblages in rheocrene springs along a third-order river. Fund Appl Limnol 190(3):251–263

    Google Scholar 

  • Wamelink GW, Goedhart PW, Van Dobben HF, Berendse F (2005) Plantspecies as predictors of soil pH: replacing expert judgment with measurements. J Veg Sci 16(4):461–470

    Google Scholar 

  • Webb DW, Wetzel MJ, Reed PC, Philippe LR, Young TC (1998) The macroninvertebrate biodiversity, water quality, and hydrogeology of ten karst springs in the Salem Plateau of Illinois. In: Botosaneanu L (ed) Studies in Crenobiology: the biology of springs and springbrooks. Backhuys Publishers, Leiden, pp 39–48

    Google Scholar 

  • Zawal A, Sulikowska-Drozd A, Stępień E, Jankowiak Ł, Szlauer-Łukaszewska A (2016a) Regeneration of the molluscan fauna of a small lowland river after dredging. Fund Appl Limnol 187:281–293

    Google Scholar 

  • Zawal A, Lewin I, Stępień E, Szlauer-Łukaszewska A, Buczyńska E, Buczyński P, Stryjecki R (2016b) The influence of the landscape structure within buffer zones, catchment land use and instream environmental variables on mollusc communities in a medium-sized lowland river. Ecol Res 31:853–867

    CAS  Google Scholar 

  • Zawal A, Stryjecki R, Stępień E, Buczyńska E, Buczyński P, Czachorowski S, Pakulnicka J, Śmietana P (2017) The influence of environmental factors on water mite assemblages (Acari, Hydrachnidia) in a small lowland river: an analysis at different levels of organization of the environment. Limnology 18:333–343

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ana Savić.

Ethics declarations

Conflict of interest

The authors declare no conflict of interest.

Additional information

Communicated by David Hawksworth.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 37 kb)

Supplementary material 2 (DOCX 49 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Savić, A., Dmitrović, D., Glöer, P. et al. Assessing environmental response of gastropod species in karst springs: what species response curves say us about niche characteristic and extinction risk?. Biodivers Conserv 29, 695–708 (2020). https://doi.org/10.1007/s10531-019-01905-6

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10531-019-01905-6

Keywords

Navigation