Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-27T11:39:26.949Z Has data issue: false hasContentIssue false
  • English
  • Français

Dynamics of helminth fauna of black-legged kittiwake in the Russian Arctic in the context of climate changes

Published online by Cambridge University Press:  26 May 2022

Vadim V. Kuklin Open the ORCID record for Vadim V. Kuklin [Opens in a new window]  and
Marina M. Kuklina Open the ORCID record for Marina M. Kuklina [Opens in a new window]
Vadim V. Kuklin*
Affiliation:
Laboratory of Ornithology and Parasitology, Murmansk Marine Biological Institute, Russian Academy of Sciences, 183010 Murmansk, Russia
Marina M. Kuklina
Affiliation:
Laboratory of Ornithology and Parasitology, Murmansk Marine Biological Institute, Russian Academy of Sciences, 183010 Murmansk, Russia
*
Author for correspondence: Vadim V. Kuklin, E-mail: vv_kuklin@mail.ru
Get access Rights & Permissions [Opens in a new window]

Abstract

We present the results of our studies of the helminth fauna and the diet of the black-legged kittiwake (Rissa tridactyla Linnaeus, 1758) in the Gorodetskiy bird colonies on the Rybachiy Peninsula (Murman coast of the Barents Sea) carried out in 2006–2008 and in 2018–2020. We did not find any noticeable changes in the species diversity of the helminth fauna of the kittiwakes, the proportion of the dominant parasite species and the values of most quantitative infection indices between the two study periods. At the same time, there was a marked decrease in the mean abundance of the dominant cestode species (Alcataenia larina Krabbe, 1869 and Tetrabothrius erostris Loennberg, 1889) in 2018–2020 as compared to 2006–2008. The changes in parasitology of birds found in our study appear to be largely determined by fluctuations of abiotic conditions (increased water and air temperature) and the state of the food supply (size structure of the zooplankton) in the study area.

Keywords

Barents SeakittiwakeRissa tridactylaclimate changeshelminths
Type
Research Paper
Information
Journal of Helminthology , Volume 96 , 2022 , e36
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Anker-Nilssen, T, Barrett, RT, Christensen-Dalsgaard, S, et al. (2018) Key-site monitoring in Norway 2017, including Svalbard and Jan Mayen. SEAPOP Short Report 1. Available at https://seapop.no/wp-content/uploads/2021/03/seapop-short-report-1-2018.pdf (accessed 15 December 2020).Google Scholar
Årthun, M, Eldevik, T, Smedsrud, LH, Skagseth, Ø and Ingvaldsen, RB (2012) Quantifying the influence of Atlantic heat on the Barents Sea ice variability and retreat. Journal of Climate 25(13), 4736–4743.CrossRefGoogle Scholar
Ashford, RW (1971) Blood parasites and migratory fat at Lake Chad. Ibis 113(1), 100–101.CrossRefGoogle Scholar
Balazy, K, Trudnowska, E, Wichorowski, M and Blachowiak-Samolyk, K (2018) Large versus small zooplankton in relation to temperature in the Arctic shelf region. Polar Research 37, 1427409.CrossRefGoogle Scholar
Barus, V, Sergeeva, TP, Sonin, MD and Ryzhikov, KM (1978) Helminths of fish-eating birds of the palearctic region I. Nematoda. Prague, Publ. House Academia. p. 319.CrossRefGoogle Scholar
Box, JE, Colgan, WT, Christensen, TR, et al. (2019) Key indicators of Arctic climate change: 1971–2017. Environmental Research Letters 14, 045010.CrossRefGoogle Scholar
Bryant, DM and Furness, RW (1995) Basal metabolic rates of North Atlantic seabirds. Ibis 137(2), 219–226.CrossRefGoogle Scholar
Burthe, S, Daunt, F, Butler, A, Elston, DA, Frederiksen, M, Johns, D, Newell, MA, Thackeray, SJ and Wanless, S (2012) Phenological trends and trophic mismatch across multiple levels of a North Sea pelagic food web. Marine Ecology Progress Series 454, 119–133.CrossRefGoogle Scholar
Carroll, MJ, Butler, A, Owen, E, et al. (2015) Effect of sea temperature and stratification changes on seabird breeding success. Climate Research 66, 75–89.CrossRefGoogle Scholar
Dalpadado, P, Arrigo, KR, van Dijken, GL, Skjoldal, HR, Bagøien, E, Dolgov, AV, Prokopchuk, IP and Sperfeld, E (2020) Climate effect on temporal and spatial dynamics of phytoplankton and zooplankton in the Barents Sea. Progress in Oceanography 185, 102320.CrossRefGoogle Scholar
Descamps, S, Anker-Nilssen, T, Barrett, RT, et al. (2017) Circumpolar dynamics of a marine top-predator track ocean warming rates. Global Change Biology 23(9), 3770–3780.CrossRefGoogle ScholarPubMed
Eriksen, E, Skjoldal, HR, Dolgov, AV, Dalpadado, P, Orlova, EL and Prozorkevich, DV (2016) The Barents Sea euphausiids: methodological aspects of monitoring and estimation of abundance and biomass. ICES Journal of Marine Science 73(6), 1533–1544.CrossRefGoogle Scholar
Ezhov, A (2019) Murman kittiwake (Rissa tridactyla) and guillemot (Uria aalge & U. Lomvia) reaction on the long-term instability of food availability in the Barents Sea. Herald of the Tver State University Series: Biology and Ecology 53, 72–82 (in Russian).CrossRefGoogle Scholar
Fauchald, P, Anker-Nilssen, T, Barrett, RT, et al. (2015) The status and trends of seabirds breeding in Norway and Svalbard. NINA Report 1151. 84 p. Available at https://www.miljodirektoratet.no/globalassets/publikasjoner/M396/M396.pdf (accessed 17 December 2020).Google Scholar
Fossheim, M, Primicerio, R, Johannesen, E, Ingvaldsen, RB, Aschan, MM and Dolgov, AV (2015) Recent warming leads to a rapid borealization of fish communities in the Arctic. Nature Climate Change 5(7), 673–677.CrossRefGoogle Scholar
Gabrielsen, GW, Mehlum, F and Karlsen, HE (1988) Thermoregulation in four species of Arctic seabirds. Journal of Comparative Physiology B 157(6), 703–708.CrossRefGoogle Scholar
Galaktionov, KV (1996) Life cycles and distribution of seabird helminths in Arctic and subarctic regions. Bulletin of the Scandinavian Society for Parasitology 6(2), 31–49.Google Scholar
Galaktionov, KV (2017) Patterns and processes influencing helminth parasites of Arctic coastal communities during climate change. Journal of Helminthology 91(4), 387–408.CrossRefGoogle ScholarPubMed
Gaston, AJ and Elliot, K (2013) Effects of climate induced changes in parasitism, predation and predator-predator interactions on reproduction and survival of on Arctic marine birds. Arctic 66(1), 43–51.CrossRefGoogle Scholar
Gaston, AJ, Gilchrist, HG, Mallory, ML and Smith, PA (2009) Changes in seasonal events, peak food availability, and consequent breeding adjustment in a marine bird: a case of progressive mismatching. Condor 111(1), 111–119.CrossRefGoogle Scholar
Goert, HF, Garton, EO and Poe, AJ (2018) Effects of climate change and environmental variability on the carrying capacity of Alaskan seabird populations. The Auk 135(4), 975–991.CrossRefGoogle Scholar
Gremillet, D, Fort, J, Amelineau, F, Zakharova, E, Le Bot, T, Sala, E and Gavrilo, M (2015) Arctic warming: nonlinear impacts of sea-ice and glacier melt on seabird foraging. Global Change Biology 21(3), 1116–1123.CrossRefGoogle ScholarPubMed
Hemmingsen, W, Lombardo, I and Mackenzie, K (1991) Parasites as biological tags for cod, Gadus morhua L., in the northern Norway: a pilot study. Fisheries Research 12(4), 365–373.CrossRefGoogle Scholar
Hilton, GM, Ruxton, GD, Furness, RW and Houston, DC (2000) Optimal digestion strategies in seabirds: a modeling approach. Evolutionary Ecology Research 2(2), 207–330.Google Scholar
Hoberg, EP (1987) Recognition of larvae of the Tetrabothriidae (Eucestoda): implications for the origin of tapeworms in marine homeothermes. Canadian Journal of Zoology 65(4), 997–1000.CrossRefGoogle Scholar
Hoberg, EP, Kutz, SJ, Cook, JA, Galaktionov, K, Haukisalmi, V, Henttonen, H, Laaksonen, S, Makarikov, A and Marcogliese, DJ (2013) Parasites in terrestrial, freshwater and marine systems. pp. 476–505 In Meltofte, H (Ed.) Arctic biodiversity assessment—Status and trends in Arctic biodiversity. Akureyi, Iceland, Conservation of Arctic Flora and Fauna, Arctic Council.Google Scholar
Conservation of Arctic Flora and Fauna (2020) International black-legged kittiwake conservation strategy and action plan, circumpolar seabird expert group. Akureyri, Iceland, Conservation of Arctic Flora and Fauna.Google Scholar
Karasev, AB (2003) The catalogue of parasites of the Barents Sea fishes. Murmansk, PINRO Press (in Russian). p. 150.Google Scholar
Kortsch, S, Primicerio, R, Fossheim, M, Dolgov, AV and Aschan, M (2015) Climate change alters the structure of Arctic marine food-webs due to poleward shifts of boreal generalists. Proceedings of the Royal Society B: Biological Sciences 282, 20151546.CrossRefGoogle ScholarPubMed
Krasnov, YV and Ezhov, AV (2020) The status of sea bird populations and factors determining their development in the Barents Sea. Transactions of the Kola Science Centre, ser. 7 – Oceanology 4, 225–244 (in Russian).Google Scholar
Kristoffersen, R (1992) Occurrence of the digenean Cryptocotyle lingua in a farmer Arctic charr Salvenius alpinus and periwinkles Littorina littorea sampled close to charr farms in the northern Norway. Diseases of Aquatic Organisms 12(1), 59–65.CrossRefGoogle Scholar
Landrum, L and Holland, MM (2020) Extremes become routine in an emerging new Arctic. Nature Climate Change 10(12), 1108–1115.CrossRefGoogle Scholar
Lind, S and Ingvaldsen, RB (2012) Variability and impact of Atlantic water entering the Barents Sea from the north. Deep-Sea Research. Part I: Oceanographic Research Papers 62(1), 70–88.CrossRefGoogle Scholar
Lind, S, Ingvaldsen, RB and Furevik, T (2018) Arctic warming hotspot in the northern Barents Sea linked to declining sea-ice import. Nature Climate Change 8(7), 634–639.CrossRefGoogle Scholar
Marcogliese, DJ (2008) The impact of climate change on the parasites and infection diseases of aquatic animals. Revue Scientifique et Technique (International Office of Epizootics) 27(2), 467–484.Google Scholar
Mitchell, I, Daunt, F, Fredriksen, M and Wade, K (2020) Impacts of climate change on seabirds, relevant to coastal and marine environment around the UK. MCCIP Science Review, 382–399.Google Scholar
Muzaffar, SB (2009) Helminths of murres (Alcida: Uria spp.): markers of ecological change in the marine environment. Journal of Wildlife Diseases 45(3), 672–683.CrossRefGoogle Scholar
Muzaffar, SB, Hoberg, EP and Jones, IL (2005) Possible recent expansion of Alcataenia longicervica (Eucestoda: Dilepididae) parasitic in murres Uria spp. (Alcida) into the North Atlantic. Marine Ornithology 33(1), 189–191.Google Scholar
NOAA NCEP EMC CMB GLOBAL Reyn_SmithOIv2 monthly. Climate Modeling Branch, National Centers for Environmental Prediction, National Oceanic and Atmospheric Administration. Available at http://iridl.ldeo.columbia.edu (accessed 1 February 2022).Google Scholar
Oil Spill Prevention, Administration and Response: Marine Bird Abundance. Intermediate Assessment (2017a). Available at https://oap.ospar.org/en/ospar-assessments/intermediate-assessment-2017/biodiversity-status/marine-birds/bird-abundance/ (accessed 5 June 2021).Google Scholar
Oil Spill Prevention, Administration and Response: Marine Bird Breeding Success/Failure. Intermediate Assessment (2017b). Available at https://oap.ospar.org/en/ospar-assessments/intermediate-assessment-2017/biodiversity-status/marine-birds/marine-bird-breeding-success-failure/ (accessed 5 June 2021).Google Scholar
Orlova, EL, Dolgov, AV, Renaud, PE, Boitsov, VD, Prokopchuk, IP and Zashihina, MV (2013) Structure of the macroplankton–pelagic fish–cod trophic complex in a warmer Barents Sea. Marine Biology Research 9(9), 851–866.CrossRefGoogle Scholar
Oswald, SA and Arnold, JM (2012) Direct impacts of climatic warming on heat stress of endothermic species: seabirds as bioindicators of changing thermoregulatory constrains. Integrative Zoology 7(2), 121–136.CrossRefGoogle Scholar
Oswald, SA, Bearshop, S, Furness, RW, Huntley, B and Hamer, KC (2008) Heat stress in a high latitude seabird: effect of temperature and food supply on bathing and nest attendance of great skuas Catharacta skua. Journal of Avian Biology 39(2), 163–169.CrossRefGoogle Scholar
Richardson, AJ and Schoeman, DS (2004) Climate impact on plankton ecosystems in the northeast Atlantic. Science 305(5690), 1609–1612.CrossRefGoogle ScholarPubMed
Rozsa, L, Reiczigel, J and Majoros, G (2000) Quantifying parasites in samples of hosts. Parasitology 86(2), 228–232.CrossRefGoogle ScholarPubMed
Ryzhikov, KM, Rusavy, B, Khokhlova, IG, Tolkatchova, LM and Kornyuchin, VV (1985) Helminths of fish-eating birds of the palaearctic region. Part II. Prague, Academia. p. 412.Google Scholar
Shimazu, T (1975) Some cestodes and acanthocephalan larvae from euphasiid crustaceans collected in northern North Pacific Ocean. Bulletin of the Japanese Society of Science and Fisheries 41(8), 813–821.CrossRefGoogle Scholar
Sonin, MD (1986) Keys to trematodes of fish-eating birds of the Palaearctic (opisthorchids, renicolides, strigeids). Moscow, Nauka. p. 256.Google Scholar
Temirova, SI and Skrjabin, AS (1978) Tetrabothriidata and Mesocestoidata – tapeworms of birds and marine mammals. Moscow, Nauka Press (in Russian). p. 117.Google Scholar
Tolonen, A and Karlsbakk, E (2003) The parasite fauna of the Norwegian spring spawning herring (Clupea harengus L. ICES Journal of Marine Science 60(1), 77–84.CrossRefGoogle Scholar
Walsh, JE, Overland, JE, Groisman, PY and Rudolf, B (2011) Ongoing climate change in the Arctic. AMBIO: A Journal of the Human Environment 40(1), 6–16.CrossRefGoogle Scholar
Weather archive in Tsypnavolok. Available at http://rp5.md/archive.php?wmo_id=22012&lang=ru (accessed 30 December 2021).Google Scholar
Wingfield, JC, Suydam, R and Hunt, K (1994) The adrenocortical responses to stress in snow buntings (Plectrophenax nivalis) and Lanland longspurs (Calcarius lapponicus) at Barrow, Alaska. Comparative Biochemistry and Physiology 108(3), 299–306.Google Scholar
Zabolotskikh, EV and Myasoedov, AG (2017) Spatial and temporal variability of the Barents Sea ice retrieved from satellite passive microwave radiometer data. Current Problems in Remote Sensing of the Earth From Space 14(1), 195–208.Google Scholar