Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Fueling of a marine-terrestrial ecosystem by a major seabird colony


Seabirds redistribute nutrients between different ecosystem compartments and over vast geographical areas. This nutrient transfer may impact both local ecosystems on seabird breeding islands and regional biogeochemical cycling, but these processes are seldom considered in local conservation plans or biogeochemical models. The island of Stora Karlsö in the Baltic Sea hosts the largest concentration of piscivorous seabirds in the region, and also hosts a large colony of insectivorous House martins Delichon urbicum adjacent to the breeding seabirds. We show that a previously reported unusually high insectivore abundance was explained by large amounts of chironomids—highly enriched in δ15N—that feed on seabird residues as larvae along rocky shores to eventually emerge as flying adults. Benthic ammonium and phosphate fluxes were up to 163% and 153% higher close to the colony (1,300 m distance) than further away (2,700 m) and the estimated nutrient release from the seabirds at were in the same order of magnitude as the loads from the largest waste-water treatment plants in the region. The trophic cascade impacting insectivorous passerines and the substantial redistribution of nutrients suggest that seabird nutrient transfer should be increasingly considered in local conservation plans and regional nutrient cycling models.


Animals can act as powerful biological pumps and transfer nutrients, trace elements and environmental contaminants between ecosystems1,2,3,4,5. Seabirds are arguably the most pertinent present-day vectors of compounds from marine to terrestrial ecosystems6,7 and have been demonstrated to enhance production and alter dynamics of local ecosystems adjacent to breeding colonies8,9,10. This general marine-terrestrial ecosystem coupling can have a number of cascade effects on biological communities. For example, seabird derived nutrients have been shown to result in complex changes on spiders and insects, and general productivity increases in terrestrial plants10,11,12,13. Other trophic cascades involving terrestrial-marine linkages are insectivorous passerines benefitting from salmon runs in Canadian rivers14, and the introduction on foxes which has diminished seabird populations and thereby changed plant communities on the Aleutian islands15. The diversity of pathways and often surprising effects in the above-mention studies calls for further empirical research, with a future goal of a general understanding of the role of seabirds in local ecological cascade effects and regional nutrient cycling.

The ecological significance of seabird driven nutrient fluxes have often been studied in nutrient poor terrestrial ecosystems where the addition of marine nitrogen (N) and phosphorus (P) have led to increases in productivity and diversity in plant communities10,11,16. The majority of the global population of seabirds breed in areas with low terrestrial productivity, and nutrient driven productivity increases have hence been interpreted to have positive effects on nutrient-limited terrestrial ecosystems10,11. Less focus has been given to areas where nutrients may leak to surrounding coastal ecosystems17,18 and especially in systems where the point sources of seabirds may aggravate already existing problems with eutrophication. Eutrophication is a widespread global problem in lakes and semi-enclosed seas19, and many areas affected by coastal eutrophication problems also have important seabird colonies, such as Japan and the countries around the Baltic Sea and North Sea7. Combatting eutrophication is an issue high on the political agenda in many areas in the world, and effective measures require a solid scientific background on bio-geochemical dynamics including the role of seabirds as nutrient vectors19,20.

Feather samples from juvenile piscivorous seabirds (Common murres, Uria aalge) and insectivorous passerines (House martins, Delichon urbica) collected in the largest seabird colony in the Baltic Sea, the island of Stora Karlsö have previously been shown to have a striking similarity in their δ13C isotopic ratio, suggesting a common (marine) provenance of nutrients21. The density of House martins on the island is also one of the highest recorded throughout the species’ distribution—and the suggested pathway for the high density has been hyperabundance of chironomids21. Chironomids, or non-biting midges, are insects whose larvae live in the aquatic environment and feed on microalgae, detritus and organic matter (such as seabird excrements), eventually emerging as flying adults and thus becoming available as food to insectivorous birds22. In this study, we clarify the ecological and bio-geochemical pathways contributing to the trophic cascade from seabirds to insectivores, by asking the following questions:

- What is the pathway by which seabird excrements feed the terrestrial foodweb?

- How does seabird excrements affect nutrient fluxes in soft bottom sediments?

- How does seabird N and P loading to the pelagic ecosystem compare to other point sources in the region?

We hypothesized that seabird nutrients would be traceble in both near-shore rocky and deep-water soft-bottom habitats, that chironomid larvae are growing up in both habitats, and that nutrient redistributed by seabirds are comparable to anthropogenic nutrient point sources in the region. The study contributes to the knowledge on ecosystem effects of seabird colonies by: (1) Exploring biological and biogeochemical pathways in which nutrient release can lead to cascade effects on terrestrial ecosystem, and (2) Describing and quantifying effects of seabird colony nutrient release in the context of an ecosystem suffering from eutrophication.

Material and methods

Study site

The study was performed on the island of Stora Karlsö (57°17′N, 17°58′E) (Fig. 1), which is the largest seabird colony in the Baltic Sea23. The two most abundant seabird species on Stora Karlsö are Common Murre Uria aalge (15,700 breeding pairs) and Razorbill Alca torda (12,000 breeding pairs)23 of which approximately 9,000 pairs breed along a 300 m long narrow cliff edge indicated as V1 in Fig. 1c. The two species forage on sprat Sprattus sprattus and herring Clupea harengus and have a foraging range during the breeding period of approximately 2,000 km224. The breeding period is from mid-April to early August and takes place on limestone cliffs 5–40 m above sea level 0–15 m from the shoreline. House martins breed on the lighthouse building on Stora Karlsö, 20 m from the cliff edge under which the seabird ledges are distributed. The number of breeding pairs in recent years have been around 150, which is one of the largest colonies in Europe of this declining species21.

Figure 1
figure 1

Study area. (a) Baltic Sea, (b) Island of Gotland, with Stora Karlsö indicated as a green rectangle, and sites for reference samples indicated as blue asterisks, (c) Island of Stora Karlsö with sediment sampling stations S1–S4 and rocky shore sampling stations V1 and V2. Guano samples were collected on the cliffs just above the V1 station.

Water and sediment samples

Water and sediment samples were taken from onboard R/V Electra, a 24 m research vessel from Stockholm University, in April 2017. To locate suitable areas for sediment samples, two scientific echo-sounders were used, a multibeam Kongsberg EM2040, 0.4° × 0.7°, 200–400 kHz and a Kongsberg Topas PS40, 24 channels, parametric (35–45 kHz/1–10 kHz). The bottom substrate around the colony mainly consisted of hard bottom (sedimentary rocky and gravelly shores) with smaller hollows where soft sediment could accumulate. Such soft sediment areas were in the size range of 5,000 and 25,000 m2 and located at 1,300–2,700 m distance from the main seabird colony, and at depths of 65–69 m, and sediment sampling stations (S1–S4, Fig. 1) were located within these areas. CTD cast was performed at S1–S4 to record oxygen concentrations, temperature and salinity in the whole water column including the bottom water in situ.

Collection and preparation of biological samples

Guano samples were taken from active breeding ledges of Common Murres in May 2017 in the Karlsö Auk lab (a man-made breeding facility for Murres and Razorbills)25, by scraping off material using a spatula, and then frozen to − 18 °C until preparation for isotopic analysis.

Efforts to sample macrofauna in the soft bottom sediments were performed in April 2017 on stations S1–S4. One van Veen grab (0.1 m2) was taken at each station and sieved through two fractions of 1 mm sieves following the European standard (ISO 16665:2014). No macrofauna was found in the samples.

Samples from the rocky shore habitat (Stations V1 and V2, Fig. 1c) were collected in April 2017 and samples at three reference sites (Fig. 1b) were collected in July and September 2018. Samples were collected by a snorkeler that scraped macroalgae into a bag (mesh size < 0.5 mm) taking 6–14 subsamples from each station and preserving the contents in 90% ethanol. The major macroalgae taxa were Fucus vesiculosus and Cladophora glomerata. Chironomid larvae was sorted out from the macroalgae subsamples in the laboratory for isotopic analyses, where the isotopic signal of each subsample was analysed separately to obtain averages by station. Stations V1 and V2 were at a distance of 10 and 500 m from the main seabird colony, respectively, whereas the distance to the reference stations all exceeded 15,000 m. All samples were collected at a distance from shore of 2 – 10 m. The Baltic Sea has no tide.

Sediment coring procedures

Sediments at S1–S4 were sampled by means of a Kajak corer (tube length: 50 cm, internal diameter: 8 cm), which provided nearly undisturbed sediment surface. At each station, one bottom water sample was taken from the Kajak core and the sediment was then immediately sliced at the following resolution: 1 cm slices for the first 4 cm, and then 2 cm slices from 4 to 10 cm. Each sediment slice was transferred into a 50 mL Falcon tube and centrifuged at 670×g (2,500 rpm) for 15 min to extract porewater. The bottom water and porewater samples were collected with a clean plastic syringe and filtered (0.45 μm polyethersulfone filter) into a 10 mL polypropylene tube. The tubes were stored at − 20 °C until later analyses of dissolved ammonium (NH4+), phosphate (PO43−) and nitrate plus nitrite (NO3 + NO2). At each station, a second Kajak core was sliced with resolution of 1 cm slices for the first 4 cm and samples were stored at -20 °C for later determination of organic geochemistry parameters (org C, N, δ13C, δ15N signatures and sediment porosity).

Isotopic ratio (δ13C and δ15N) analyses of biological and sediment samples

Sediment and biological (bird faeces and chironomid larvae) samples were freeze dried, ground, homogenized and weighed in tin capsules. Analyses on biological samples were performed with a PDZ Europa ANCA-GSL elemental analyzer (1,000 °C combustion) connected to a PDZ Europa 20-20 isotope ratio mass spectrometer (IRMS, Sercon Ltd.), while sediment samples were analyzed on an Elementar Vario EL Cube elemental analyzer (Elementar Analysensysteme GmbH) (1,080 °C combustion) connected to the same IRMS system. Isotopic compositions were reported using the conventional δ notation26, which reports the isotopic composition of a sample as the ‰ deviation of a sample relative to Vienna Peedee belemnite (VPDB) for δ13C and to atmospheric N2 for δ15N. Samples were regularly interspersed with two different laboratory standards, which were previously calibrated against NIST Standard Reference Materials (IAEA-600, USGS-40, USGS-41, USGS-42, USGS-43, USGS-61, USGS-64 and USGS-65). Based on the analyses of these standards the analytical precision was ± 0.2 ‰ for δ13C and ± 0.3 ‰ for δ15N.

Porewater analyses and diffusive flux calculations

Porewater samples were thawed, diluted 1:10 and NH4+, NOx (= NO3 + NO2) and PO43− were analyzed on a segmented flow autoanalyzer system (ALPKEM, Flow Solution IV) following the standard methods for seawater analyses27. Precision was ± 0.036 µmol L−1 for NH4+,  ± 0.014 µmol L−1 for NOx and ± 0.016 µmol L−1 for PO43−. As there was no macrofauna in the sediment, porewater profile shapes could be easily modeled to calculate diffusive fluxes of NH4+ and PO43−, while NOx profiles did not show any generalizable trend and were not modeled. Profiles were modeled with the numerical interpretation by Berg et al.28, which provides the best fit to a measured concentration profile assuming steady state conditions and returns diffusive fluxes between the sediment–water interface (SWI) as a function of depth. We assumed that biological diffusivity (movement of solutes due to bioturbation) was zero as macrofauna was absent, so that diffusive sediment–water fluxes (J) could be calculated according to Fick’s First Law of diffusion:

$$J=-\varphi Ds\frac{\delta C}{\delta x}$$

where φ is sediment porosity, Ds is molecular diffusivity in sediment, C is the solute concentration determined analytically and x is sediment depth. Porosity was estimated from sediment water content, which was calculated by measuring the wet and dry weight of 5 mL sediment aliquots after drying them at 105 °C. Ds was calculated according to the equations reported by Iversen and Jørgensen29.

Quantification of total nutrient emissions

We compiled literature values on guano production as well as nitrogen and phosphorus concentration in guano to calculate the nitrogen and phosphorus emissions from the colony:

$${\text{Em}}_{i} = {\text{Pop}}*{\text{DG}}*{\text{PC}}*{\text{Conc}}_{i}$$

where Em is the total emissions of nutrient i (nitrogen and phosphorus) [g], Pop is the population size of the two seabird species, DG is the Daily guano output per individual and day [g day−1 dry mass], PC is the time each seabird individual spent in the colony, and Conc is the concentration of nutrient i in bird faeces. Population sizes were taken from a recent census23 and time spent in the colony was estimated from observation studies of adult birds feeding chicks30. Daily guano production was taken from previously reported data on Thick-billed murre, a closely related species of the same breeding ecology and size as Common murre31. Nutrient content in guano was taken from a number of published studies on seabirds (Table S1) where we used the median, 5th and 95th percentiles to calculated confidence intervals for the daily seabird nutrient emissions.


Seabird impacts on chironomid abundance

The samples of macroalgae near the seabird colony included large numbers of Chironomidae larvae which were highly enriched in δ15N (Fig. 2a). Also the δ13C signal was seen as a gradient with increasing values at increasing distance from the colony (Fig. 2b). The deep-water soft bottom sediments did not host any living macrofauna at all. We observed no effect of distance to the bird colony on the δ15N signal in the sediments (Fig. 2c) whereas the δ13C signal was seen as a gradient with decreasing values at incresing distance from the colony (Fig. 2d). Although the oxygen concentrations measured would not prevent the presence of typical Baltic Sea macrofauna in the sediments, monthly data on dissolved oxygen from a nearby oceanographic sampling station (57.116 N, 17.667 E) revealed anoxic events in early 2016 and possibly also in mid 2016, i.e. 1–1.5 year prior to the benthic sampling in this study (Fig. S1).

Figure 2
figure 2

Stable isotopes as a function of distance to the seabird colony. (a) δ15N in chironomids (rocky shore habitat), (b) δ13C in chironomids (rocky shore habitat), (c) δ15N in sediments, and (d) δ13C in sediments. “Source” refers to seabird guano sampled inside the colony. “Ref.” refers to reference samples (island of Gotland, Fig. 1b). Black triangles indicate raw data at different stations and red circles denote mean by station. For station description see Fig. 1c. All δ values are given as ‰.

Porewater nutrient profiles and fluxes in soft-bottom sediments

Porewater NH4+ and PO43− concentrations increased with depth in the sediment and were highly elevated at the sediment station closest to the seabird colony (S1) reaching ca. 300 and 80 µmol L−1 at 9 cm depth, respectively (Fig. 3). Concentrations of the two solutes were on a lower level at the three other stations (S2‒S4), where they did not exceed 170 and 40 µmol L−1 at 9 cm depth, respectively (Fig. 3). Porewater NOx concentrations were negligible and even in the top oxidized layer (0.5 cm layer) they were < 1.5 µmol L−1 (data not shown). Bottom waters at all sediment stations were low in oxygen (1.7–2.4 ml L−1) but not anoxic. The four stations had similar salinity (8.1–8.2‰) and water temperature (5.0–5.1 °C).

Figure 3
figure 3

Nutrient concentrations in sediments at different sediment depths. (a) NH4+ and (b) PO43−. − 0.5 cm (top data value) refers to bottom water.

The diffusive fluxes of both NH4+ and PO43− were higher at S1 compared to the other three stations (S2‒S4) (Fig. 4), suggesting a stronger release of nutrients in proximity of the colony compared to the more offshore stations.

Figure 4
figure 4

Modelled fluxes in soft-bottom sediments. (a) NH4+, and (b) PO43−.

Nutrient release from seabirds

Daily release from seabirds in the colony were estimated at 393 kg N day−1, 95% C.I. [166–483], and 37 kg P day−1 95% C.I. [8–69] (Fig. 5). The wide confidence intervals are caused by the large variation in the estimations of N and P concentrations of seabird guano (Table S1). Nevertheless, the numbers indicate that the order of magnitude of the seabirds’ P emissions are similar to those of the largest waste water treatment plants and N emissions are in the same magnitude as a number of mid size treatment plants in the Baltic Sea (Fig. 5).

Figure 5
figure 5

Estimated daily nutrient release from the Stora Karlsö seabird colony compared to other major Baltic Sea point sources (Waste-water treatment plants, WWTP). (a) nitrogen, and (b) phosphorus. WWTP data were obtained from32. Abbreviations in x-labels: SE = Sweden, PL = Poland, LT = Lithuania, DE = Germany.


Seabirds can act as powerful biological pumps by moving chemical compounds across wide distances and are thereby significant drivers of biogeochemical cycling7 and biovectors of environmental contaminants6. We show that N and P release from a seabird colony in the eutrophic Baltic Sea is in the same order of magnitude as waste water treatment plants32, and thereby a driver of regional nutrient cycling. These significant releases have constrasting effects in two habitats. Along rocky shores, the release lead to high production of chironomid larvae, and thereby enhanced food supply to insectivorous House martins breeding on the island that feed on adult (flying) chironomids21. In deep-water sediments surrounding the colony, nutrient release did not support macrofaunal production, probably because of seasonal anoxia, and these sediments acted as sources of dissolved N and P to the water column. These contrasting effects on different ecosystem compartments arise from dynamics at different spatial and temporal scales that interact in a complex manner (Fig. 6).

Figure 6
figure 6

Conceptual visualization of the main processes investigated in this paper. The Stora Karlsö lighthouse with house martin nests are shown at the top right, with the seabird colony located at the cliff edges at the shoreside. Illustration by Fredrik Saarkoppel / Kobolt Media AB.

How do seabirds support increased insect production?

This study was originally conceived based on an observation of the unusually large colony of House martins (i.e., insectivorous passerines) on the lighthouse adjacent to the seabird colony (Fig. 6), something that later was linked to the seabirds via isotopic analysis of feather samples21. Here we expand on these findings by investigating the pathways by which the seabird derived nutrients affect the surrounding terrestrial and marine ecosystems. We found that the nutrients can be traced both along rocky shores and in deep-water sediments, but it was only along the rocky shores that the nutrients supported chironomid production. The isotopic signature of N (δ15N) in chironomids in the rocky shores show a decreasing trend with distance from the colony, which indicates seabird derived nutrients in the chironomid production. Our visual observations from the island suggest extremely high concentrations of flying chironomids during spring months, which is probably supporting not only House martins but insectivore bird species on the island in general. The seabirds are thus increasing the availability of nutrients in support of local biological production in the near-shore marine habitats, which cascades back to the terrestrial (island) ecosystem. Our results reinforce earlier studies that have shown strong and sometimes unexpected effects of seabirds in local flora and fauna10,11,12,13. We believe that such seabird mediated cross-scale ecosystem interactions are often overlooked, and should be considered more generally, e.g., in constructing management plans of protected areas33,34,35.

Seabird effects on sediment fluxes

The deep-water sediments near the seabird colony were strongly enriched in nutrients but did not support any macrofaunal production. Although our measured oxygen concentrations would not prevent the presence of typical Baltic Sea macrofauna, regularly returning anoxic events preceeding the sampling was the probable reason behind the lack of macrofauna in this habitat. Since we sieved the sediments with 1.0 mm sieves, we cannot exclude that smaller invertebrates (e.g., meiofauna, larval stages of macrofaunal organisms, etc.) were actually living in these sediments, but it is not the focus of this study as they cannot explain the link between the marine habitat and terrestrial birds. Another potential explanation for the lack of chironomids in the sediments would be that larval growth occurs later in the season, however, chironomids are known to have extended growing seasons with overlapping generation and are thus expected to be detected throughout the year36, and the emergence of adults in the Baltic Sea occurs in May and June37 which means that larvae, if present in the habitat, would be detected in April.

The nutrient data alone cannot say whether there was a direct fertilization effect by the birds or if the enrichment was due to some indirect effects. However, the δ13C signals in the guano were very similar to those in the sediment samples close to the station, which strongly indicate a direct C fertilization effect. The observed gradient with decreasing δ13C at increasing distance from the colony could theoretically be an effect of decreasing input of terrestrial dissolved organic matter (DOM) 38,39. However, the type of benthic ecosystem at our offshore study site is thought to be much more affected by benthic-pelagic coupling than by terrestrial DOM input40 by which we can be relatively certain that the δ13C is a function of colony distance rather than general DOM input variability.

The δ15N signals in the sediments (ca. + 3 ‰) were lower than those from Baltic coastal settings affected by human sewage discharge (+ 7‒8‰) as reported by Bonaglia et al.41. The low values of the present study are likely supported by high contribution of surface N2-fixing cyanobacterial blooms and subsequent deposition of this biomass. There is a strong link between hypoxia and cyanobacterial blooms in the Baltic Sea42. Altogether, this suggests that N fertilization from bird guano was not reflected in N burial, but was rather supporting N recycling, which exacerbates hypoxia and cyanobacteria blooms.

Our nutrient data indicate that the near-colony sediments were acting as stronger sources of both nitrogen and phosphorus to the water mass than sediments further away. This was due to the combination of high ammonium and phosphate concentrations in the porewater environment, and low oxygen. With more oxygen, the essential nutrients such as phosphate would remain in the sediments and possibly lead to biological production including chironomid larvae, i.e. a strengthened link between the seabirds and the surrounding benthic and terrestrial ecosystem compartments43. With even less oxygen than under present conditions, there would be more phosphate and ammonium present both in the sediment porewater and in the water column as these compounds would be prevented from precipitating (PO43−), oxidizing (NH4+) or binding to sediment particles (NH4+), and they would tend to leave even more from the sediment to the water phase than under present conditions44. In Baltic Sea sediments affected by hypoxia, NH4+ is generally produced at high rates in the sediment and efficiently exchanged to the water column because of high rates of dissimilatory reduction to ammonium (DNRA), anaerobic mineralization of organic matter and ammonification41. In these conditions, additionally, NH4+ adsorption to sediment particles is generally limited since water content is extremely high and the sites of NH4+ exchange likely saturated45 . In hypoxic Baltic sediments, phosphate desorption from iron oxyhydroxides leads to high sediment–water fluxes of PO43− and generally high PO43− concentrations in the bottom water42.

Seabird fertilization in relation to regional nutrient cycling

The majority of studies on seabird colony nutrient enrichment has been performed in nutrient poor ecosystems10,11,16. We study a strongly eutrophic system, an offshore area in the Baltic Sea, where under normal circumstances a high proportion of the biological production in the pelagic ecosystem sinks to the bottom40, and contributes to oxygen consumption at depths of 60‒70 m and below46. Seabirds’ foraging movements thus release the effect of eutrophication from their foraging areas by removing pelagic fish biomass and at the same time contributing to eutrophication around the colony (Fig. 6). The estimated daily release from the seabird colony of 393 kg N and 37 kg P day−1 assumes that all the N and P excreted as guano by the birds ends up in the Baltic Sea. However, a part of these nutrients, especially the very reactive N, will be lost via volatilization of ammonia and especially by denitrification in the anoxic, deposited faeces on the island7. In case of significant denitrification happening in the guano, the N content should be < 10% according to a study from cave guano47. However, the N% of our guano samples and especially the average value (11.2%) was above that threshold. We thus conclude that overall decomposition and N loss were negligible if compared to the quantity of N leaking into the Baltic Sea.

The total emission from the colony is in the same order of magnitude as the major anthropogenic point sources in the Baltic Sea, keeping in mind that the birds do not add nutrients to the system but concentrate them to small and distinct areas. Nevertheless, internal nutrient fluxes in the Baltic Sea are of similar magnitude or even larger than external inputs48. Thus, our findings suggest the need for considering previously overlooked dynamics between nutrient cycling such as seabird foraging especially when studying processes on smaller (< 10,000 km2) spatial scales.


Colonial seabirds forage over vast geographic areas but release the majority of their excrements at their colonies, leading in our case to local nutrient release in the order of magnitude as major point sources considered in management plans to mitigate eutrophication. We can track the effect of this nutrient release in two completely different habitats adjacent to the colony (macroalgae growing along rocky shores and muddy deep-water sediments), where they lead to contrasting effects on biological production. The magnitude of the seabird nutrient transfer and local enrichment motivates increased consideration of these processes in regional biogeochemical modelling. Furthermore, our results suggest that the success of terrestrial biodiversity conservation on seabird islands may be conditioned by the supply of marine derived nutrients, which calls for a better integration between marine and terrestrial management and conservation plans. Modelling studies suggest that seabird’s nutrients transfers are globally significant, but the ramifications of these cross-scale ecosystem linkages for terrestrial ecosystem management and conservation are yet to be described and quantified.

Data availability

The datasets generated from this study are available in the Mendeley data repository, and


  1. Blais, J. M. et al. Arctic seabirds transport marine-derived contaminants. Science  309, 445 (2005).

    CAS  PubMed  Article  Google Scholar 

  2. Qin, X. et al. From sea to land: assessment of the bio-transport of phosphorus by penguins in Antarctica. Chin. J. Oceanol. Limnol. 32, 148–154 (2014).

    ADS  CAS  Article  Google Scholar 

  3. Nicol, S. et al. Southern Ocean iron fertilization by baleen whales and Antarctic krill. Fish Fish. 11, 203–209 (2010).

    Article  Google Scholar 

  4. Doughty, C. E. et al. Global nutrient transport in a world of giants. Proc. Natl. Acad. Sci. 113, 868–873 (2016).

    ADS  CAS  PubMed  Article  Google Scholar 

  5. Macavoy, S. E., Garman, G. C. & Macko, S. A. Anadromous fish as marine nutrient vectors. Fish. Bull. 107, 165–174 (2009).

    Google Scholar 

  6. Michelutti, N. et al. Seabird-driven shifts in Arctic pond ecosystems. Proc. R. Soc. B Biol. Sci. 276, 591–596 (2009).

    Article  Google Scholar 

  7. Otero, X. L., De La Peña-Lastra, S., Pérez-Alberti, A., Ferreira, T. O. & Huerta-Diaz, M. A. Seabird colonies as important global drivers in the nitrogen and phosphorus cycles. Nat. Commun. 9, 246 (2018).

  8. Ellis, J. R., Fariña, J. M. & Witman, J. D. Nutrient transfer from sea to land: the case of gulls and cormorants in the Gulf of Maine. J. Anim. Ecol. 75, 565–574 (2006).

    PubMed  Article  Google Scholar 

  9. Kolb, G. S., Ekholm, J. & Hambäck, P. A. Effects of seabird nesting colonies on algae and aquatic invertebrates in coastal waters. Mar. Ecol. Prog. Ser. 417, 287–300 (2010).

    ADS  Article  Google Scholar 

  10. Anderson, W. & Polis, G. Nutrient fluxes from water to land: seabirds affect plant nutrient status on Gulf of California islands. Oecologia 118, 324–332 (1999).

    ADS  PubMed  Article  Google Scholar 

  11. Zwolicki, A., Zmudczyńska-Skarbek, K. M., Iliszko, L. & Stempniewicz, L. Guano deposition and nutrient enrichment in the vicinity of planktivorous and piscivorous seabird colonies in Spitsbergen. Polar Biol. 36, 363–372 (2013).

    Article  Google Scholar 

  12. Duda, M. P. et al. Long-term changes in terrestrial vegetation linked to shifts in a colonial seabird population. Ecosystems (2020).

    Article  Google Scholar 

  13. Kolb, G. S., Jerling, L. & Hambäck, P. A. The impact of cormorants on plant-arthropod food webs on their nesting Islands. Ecosystems 13, 353–366 (2010).

    CAS  Article  Google Scholar 

  14. Christie, K. S., Hocking, M. D. & Reimchen, T. E. Tracing salmon nutrients in riparian food webs: isotopic evidence in a ground-foraging passerine. Can. J. Zool. 86, 1317–1323 (2008).

    CAS  Article  Google Scholar 

  15. Maron, J. L. et al. An introduced predator alters Aleutian Island plant communities by thwarting nutrient subsidies. Ecol. Monogr. 76, 3–24 (2006).

    Article  Google Scholar 

  16. Wainright, S. C., Haney, J. C., Kerr, C., Golovkin, A. N. & Flint, M. V. Utilization of nitrogen derived from seabird guano by terrestrial and marine plants at St. Paul, Pribilof Islands, Bering Sea, Alaska. Mar. Biol. 131, 63–71 (1998).

    CAS  Article  Google Scholar 

  17. Lorrain, A. et al. Seabirds supply nitrogen to reef-building corals on remote Pacific islets. Sci. Rep. 7, 1–11 (2017).

    CAS  Article  Google Scholar 

  18. Gagnon, K., Rothäusler, E., Syrjänen, A., Yli-Renko, M. & Jormalainen, V. Seabird guano fertilizes Baltic Sea littoral food webs. PLoS ONE 8, e61284 (2013).

    ADS  CAS  PubMed  PubMed Central  Article  Google Scholar 

  19. Diaz, R. J. & Rosenberg, R. Spreading dead zones and consequences for marine ecosystems. Science 321, 926–929 (2008).

    ADS  CAS  Article  PubMed  Google Scholar 

  20. Gustafsson, B. et al. Reconstructing the development of Baltic sea eutrophication 1850–2006. Ambio 41, 534–548 (2012).

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  21. Cross, A. D. P., Hentati-Sundberg, J., Österblom, H., McGill, R. A. R. & Furness, R. W. Isotopic analysis of island House Martins Delichon urbica indicates marine provenance of nutrients. Ibis 156, 676–681 (2014).

    PubMed  Article  Google Scholar 

  22. Armitage, P. D., Cranston, P. S. & Pinder, L. C. V. The Chironomidae. Biology and Ecology of Non-biting Midges (Springer, New York, 1995).

    Google Scholar 

  23. Olsson, O. & Hentati-Sundberg, J. Population trends and status of four seabird species (Uria aalge, Alca torda, Larus fuscus, Larus argentatus) at Stora Karlsö in the Baltic Sea. Ornis Svecica 27, 64–93 (2017).

    Article  Google Scholar 

  24. Hentati-Sundberg, J. et al. Fish and seabird spatial distribution and abundance around the largest seabird colony in the baltic sea. Mar. Ornithol. 46, 61–68 (2018).

    Google Scholar 

  25. Hentati-Sundberg, J., Österblom, H., Kadin, M., Jansson, Å & Olsson, O. The Karlsö Murre lab methodology can stimulate innovative seabird research. Mar. Ornithol. 40, 11–16 (2012).

    Google Scholar 

  26. Bond, A. L. & Hobson, K. A. Reporting stable-isotope ratios in ecology: recommended terminology, guidelines and best practices. Waterbirds 35, 324–331 (2012).

    Article  Google Scholar 

  27. Grasshoff, K., Kremling, K. & Ehrhardt, M. Methods of Seawater Analysis. Wiley, Hoboken. (2009).

    Article  Google Scholar 

  28. Berg, P., Risgaard-Petersen, N. & Rysgaard, S. Interpretation of measured concentration profiles in sediment pore water. Limnol. Oceanogr. 43, 1500–1510 (1998).

    ADS  CAS  Article  Google Scholar 

  29. Iversen, N. & Jørgensen, B. B. Diffusion coefficients of sulfate and methane in marine sediments: Influence of porosity. Geochim. Cosmochim. Acta 57, 571–578 (1993).

    ADS  CAS  Article  Google Scholar 

  30. Berglund, P. A. Evaluating ten years of ecological seabird research in the Baltic Sea. (MSc thesis, Stockholm University, 2016).

  31. Brekke, B. & Gabrielsen, G. W. Assimilation efficiency of adult Kittiwakes and Brünnich’s Guillemots fed Capelin and Arctic Cod. Polar Biol. 14, 279–284 (1994).

    Article  Google Scholar 

  32. HELCOM. Sources and pathways of nutrients to the Baltic Sea. Balt. Sea Environ. Proc. 153, 48 (2018).

    Google Scholar 

  33. Lescroël, A. et al. Seeing the ocean through the eyes of seabirds: a new path for marine conservation?. Mar. Policy 68, 212–220 (2016).

    Article  Google Scholar 

  34. Yorio, P. Marine protected areas, spatial scales, and governance: implications for the conservation of breeding seabirds. Conserv. Lett. 2, 171–178 (2009).

    Article  Google Scholar 

  35. Länsstyrelsen Gotlands Län. Bevarandeplan för Natura 2000-området SE0340023 Stora Karlsö. (2018).

  36. Pinder, L. C. V. Biology of freshwater chironomidae. Annu. Rev. Entomol. 31, 1–23 (1986).

    Article  Google Scholar 

  37. Hirvenoja, M., Palmén, E. & Hirvenoja, E. The emergence of Halocladius variabilis (Staeger) (Diptera: Chironomidae) in the surroundings of the Tvärminne Biological Station in the northern Baltic Sea. Entomol. Fenn. 17, 87–89 (2006).

    Article  Google Scholar 

  38. Voss, M., Larsen, B., Leivuori, M. & Vallius, H. Stable isotope signals of eutrophication in Baltic Sea sediments. J. Mar. Syst. 25, 287–298 (2000).

    Article  Google Scholar 

  39. Deutsch, B., Alling, V., Humborg, C., Korth, F. & Mörth, C. M. Tracing inputs of terrestrial high molecular weight dissolved organic matter within the Baltic Sea ecosystem. Biogeosciences 9, 4465–4475 (2012).

    ADS  CAS  Article  Google Scholar 

  40. Griffiths, J. R. et al. The importance of benthic-pelagic coupling for marine ecosystem functioning in a changing world. Glob. Chang. Biol. 23, 2179–2196 (2017).

    ADS  PubMed  Article  Google Scholar 

  41. Bonaglia, S., Deutsch, B., Bartoli, M., Marchant, H. K. & Brchert, V. Seasonal oxygen, nitrogen and phosphorus benthic cycling along an impacted Baltic Sea estuary: regulation and spatial patterns. Biogeochemistry 119, 139–160 (2014).

    CAS  Article  Google Scholar 

  42. Bianchi, T. S. et al. Cyanobacterial blooms in the Baltic Sea: Natural or human-induced?. Limnol. Oceanogr. 45, 716–726 (2000).

    ADS  CAS  Article  Google Scholar 

  43. Gunnars, A. & Blomqvist, S. Phosphate exchange across the sediment-water interface when shifting from anoxic to oxic conditions: an experimental comparison of freshwater and brackish-marine systems. Biogeochemistry 37, 203–226 (1997).

    CAS  Article  Google Scholar 

  44. Brook, B. W., Ellis, E. C., Perring, M. P., Mackay, A. W. & Blomqvist, L. Does the terrestrial biosphere have planetary tipping points?. Trends Ecol. Evol. 28, 396–401 (2013).

    PubMed  Article  Google Scholar 

  45. Mackin, J. E. & Aller, R. C. Ammonium adsorption in marine sediments. Limnol. Oceanogr. 29, 250–257 (1984).

    ADS  CAS  Article  Google Scholar 

  46. Carstensen, J., Andersen, J. H., Gustafsson, B. & Conley, D. J. Deoxygenation of the Baltic Sea during the last century. Proc. Natl. Acad. Sci. 111, 5628–5633 (2014).

    ADS  CAS  PubMed  Article  PubMed Central  Google Scholar 

  47. Cleary, D. M., Onac, B. P., Forray, F. L. & Wynn, J. G. Effect of diet, anthropogenic activity, and climate on δ15N values of cave bat guano. Palaeogeogr. Palaeoclimatol. Palaeoecol. 461, 87–97 (2016).

    Article  Google Scholar 

  48. Vahtera, E. et al. Internal ecosystem feedbacks enhance nitrogen-fixing cyanobacteria blooms and complicate management in the Baltic Sea. Ambio 36, 186–194 (2007).

    CAS  PubMed  Article  Google Scholar 

Download references


The authors would like to thank the crew onboard R/V Electra for support during field work. Reference biological samples were collected by Susanne Qvarfordt at DEEP, Stockholm University for the Swedish National Monitoring Program funded by the Swedish Agency for Marine and Water Management, and Aron Hejdström. Karlsö Jagt- och Djurskyddsförenings AB supported field work. Field sampling within the Nature Reserve Stora Karlsö was regulated through a decision by the Gotland County Administrative Board, diary number 521-3763-2017. The abiotic data in Fig. S1 originate from the publicly available Swedish Oceanographic Archive (SHARK) database hosted by the Swedish Agency for Marine and Water Management and the Swedish Meteorological and Hydrological Institute (, data accessed 2020-03-25.


Funding was provided by the Stockholm University Baltic Sea Science Centre through the project “Baltic Ecosystem Adaptive Management” (BEAM). S.B. was supported by funding from the Swedish Research Council Formas (Grant No. 2017-01513). Open access funding provided by Swedish University of Agricultural Sciences.

Author information

Authors and Affiliations



Conceived of or designed study (J.H.S., C.R., S.B.); Performed research (J.H.S., C.R., M.S., O.S., S.B.); Analyzed data (C.R., O.S., S.B.); Wrote the paper (J.H.S., C.R., M.S., O.S., B.G., S.B.).

Corresponding author

Correspondence to J. Hentati-Sundberg.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher's note

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

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Hentati-Sundberg, J., Raymond, C., Sköld, M. et al. Fueling of a marine-terrestrial ecosystem by a major seabird colony. Sci Rep 10, 15455 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing