Land-based salmon aquacultures change the quality and bacterial degradation of riverine dissolved organic matter


Aquacultures are of great economic importance worldwide but pollute pristine headwater streams, lakes, and estuaries. However, there are no in-depth studies of the consequences of aquacultures on dissolved organic matter (DOM) composition and structure. We performed a detailed molecular level characterization of aquaculture DOM quality and its bacterial degradation using four salmon aquacultures in Chile. Fluorescence measurements, ultrahigh-resolution mass spectrometry, and nuclear magnetic resonance spectroscopy of the DOM revealed specific and extensive molecular alterations caused by aquacultures. Aquacultures released large quantities of readily bioavailable metabolites (primarily carbohydrates and peptides/proteins, and lipids), causing the organic matter downstream of all the investigated aquacultures to deviate strongly from the highly processed, polydisperse and molecularly heterogeneous DOM found in pristine rivers. However, the upstream individual catchment DOM signatures remained distinguishable at the downstream sites. The benthic algal biovolume decreased and the bacterial biovolume and production increased downstream of the aquacultures, shifting stream ecosystems to a more heterotrophic state and thus impairing the ecosystem health. The bacterial DOM degradation rates explain the attenuation of aquaculture DOM within the subsequent stream reaches. This knowledge may aid the development of improved waste processing facilities and may help to define emission thresholds to protect sensitive stream ecosystems.


Streams and rivers are regarded as global hotspots of organic-matter processing and CO2 evasion1,2. The streambed and its biofilm microbiomes drive fundamental ecosystem processes and biogeochemical cycles2,3,4 through the physical fractionation and chemical processing of organic molecules. Most of the terrestrial organic carbon entering freshwater systems is either respired to CO2 locally or buried in sediments, and only a fraction is discharged into the ocean4,5,6. Inherently complex stream biofilms are hotspots of biodiversity and enzymatic and metabolic activity across all domains of life (including microalgae, bacteria, fungi, protozoans and small metazoans)2. Biofilms co-evolve with their respective streambed environments; land use, rather than spatial factors, such as latitude or elevation, most strongly define the community composition, diversity and capacity to perform critical ecosystem services2.

Many streams and rivers are affected by anthropogenic DOM loads with altered molecular composition, usually due to urban point sources7 or agricultural diffuse sources8. In Chile, pristine streams with otherwise rarely observed intact natural organic CHNO cycles9 occur in spatial proximity to anthropogenically affected streams. Land-based aquaculture has recently been shown to impact streams with high levels of altered DOM in northern Patagonia in Chile10. Chilean salmon production is economically important, contributing ~25% of the worldwide salmon yield (Chile ranks second of the world’s salmon-producing countries11). Salmon farming has continuously increased in recent decades; the annual salmonid production in Chile was 820,000 tons in 2012, representing a value of 4.9 billion USD (32% of the total worldwide value of salmonid production11). Small salmon are reared in land-based aquacultures supplied with stream water, whereas mid-sized fish are grown in cages in lakes and adult fish in cages along the coast. The effluents from land-based aquaculture pollute pristine streams with nutrients, antibiotics and organic carbon, resulting in oxygen depletion12 and negative consequences for the abundance and biodiversity of stream organisms, as well as for critical ecosystem functions, such as stream metabolism13. While aquacultures have recently started to remove suspended matter from waste water using sedimentation basins and rotating drum filters, dissolved components are still discharged untreated.

Nutrients and DOM originating from the leaching of remaining food pellets, fish faeces and fish excretions are major components released by aquacultures. One aquaculture in northern Patagonia was estimated to release DOM amounting to 21% of the carbon applied as feed and 76% of the annual fish production10. However, limited detailed information on the DOM composition associated with fish aquaculture is available. The DOM leached from decaying carcasses after salmon spawning has been characterized by fluorescence measurements14,15, but only two studies have applied this method to assess DOM quality from aquacultures: one study on rainbow trout in Denmark16 and one on salmon in Chile10. The latter study demonstrated that aquaculture DOM was dominated by protein-like fluorescence, which quickly degraded downstream within 2700 m10; however, advanced DOM specification and measurement of bacterial activity were not performed. No in-depth molecular characterization of DOM associated with aquaculture effluent has been conducted using ultrahigh-resolution Fourier transform ion cyclotron mass spectrometry (FTICR MS)17,18,19, nuclear magnetic resonance spectroscopy (NMR)20,21,22, or a combination of these techniques with excitation-emission matrices (EEM)23. Moreover, little is known about the consequences of aquacultures on bacterial abundance and diversity (see review12). An increase in bacterial number, heterotrophic activity, and extracellular enzyme activity was observed in the waters and sediments downstream of aquacultures24,25 in addition to a decline in the phosphatase activity in biofilms26. However, the spatial localization of the main DOM degradation in the stream, i.e., free water or benthic zone, is not clear.

In the present study, we characterized the DOM composition of pristine headwaters with low DOM concentrations and of polluted aquaculture effluents and downstream sites of four land-based aquacultures in northern Patagonia (Molco, Peuco, Huililco, and Niltre). The DOM composition was assessed using fluorescence spectroscopy, ultrahigh-resolution FTICR MS, and NMR. These measurements were complemented by the estimation of the bacterial biomass production of planktonic bacteria in stream water and epilithic biofilms, aiding in the differentiation of organic carbon processing between water and the benthic zone.


DOM bulk characteristics

The dissolved organic carbon (DOC) concentrations in the four investigated streams ranged in the order of control (0.2–0.4 mg C L−1) < downstream (0.4–2.2 mg C L−1) < effluents (1.5–4.2 mg C L−1) (Fig. 1A). The parallel factor analysis (PARAFAC) of the DOM fluorescence spectra identified five components (Table S1). The protein-like fluorescence of EEM was dominated by tryptophan-like (Trp/Trp2)27 and tyrosine-like (Tyr)28,29 components, which were shown to reflect the aquatic production of highly biodegradable DOM30. In addition, two distinct, humic-like fluorescence components, HS and HS231, were also identified. HS, which is associated with terrestrial origins and has a relatively high molecular weight32,33, was more prevalent, whereas HS2, with microbial origin and lower molecular weight31,34, was less abundant. The pattern of the fluorescence intensities (Fmax values) followed that of the DOC concentrations (Fig. 1). Effluents showed a particularly high fluorescence of protein-like DOM. EEM/PARAFAC analysis of aquaculture-induced DOM quality differences showed increased loadings of Trp-like and Tyr-like components by the aquacultures in the order of Molco > Niltre ~ Peuco  Huililco (Fig. 1).

Figure 1

Concentrations of dissolved organic carbon (DOC) of the control sites, effluents and downstream of the aquacultures of the four sampling sites (A). Fluorescence intensities (Fmax values, Raman units) of the parallel factor analysis (PARAFAC) components of the control sites, effluents and downstream of the aquacultures of the four sampling sites (BE; Trp: tryptophan-like, Tyr: tyrosine-like, HS, HS2: humic acid-like).

Ultrahigh-resolution Fourier transform ion cyclotron (FTICR) mass spectrometry of the control sites

The negative electrospray FTICR mass spectra of the DOM isolated from four pristine catchments showed broad, continual mass-peak distributions indicative of highly processed organic matter (Fig. S1; FTICR mass spectra of the control sites, van Krevelen diagrams and mass-edited H/C ratios, inter-sample ranking analysis, counts of the mass peaks, and molecular compositions common to effluents and downstream sites are shown in detail in the Supplementary Information). Overall, the mass peak distribution differed between the four streams, and the most common spacings corresponded to methylene (Δm = 14.0156 Da) and double bond equivalents (DBE: Δm = 2.1057 Da)18. Considerable variance was observed in the average mass at the control sites (Niltre > Peuco > Huililco > Molco) and in the relative proportions of CHNO compounds (Molco > Peuco > Huililco > Niltre), which differed from those of CHOS compounds (Molco > Peuco ≈ Huililco > Niltre; Table S2). Relative unsaturation (expressed as DBE/C) and average oxygenation (expressed as O/C ratio) were aligned (Niltre > Peuco > Huililco ≈ Molco). The van Krevelen diagrams and mass-edited H/C ratios confirmed the similarity of the control sites for Molco and Huililco DOM, as revealed by principal component analysis (PCA; Fig. 2B). FTICR MS-based inter-sample ranking analysis of CHO compounds17 demonstrated that the Niltre River SPE-DOM contained relatively high proportions of oxygen-rich and hydrogen-deficient (tannin-like) CHO compounds (m/z ~ 350–700) compared to all other DOM (Fig. S2). Analogous compounds were least abundant in Huililco DOM. Aliphatic components with H/C > 1.1, particularly those with m/z > 500, were less abundant in Niltre DOM than in the three other rivers. The Molco River had a greater abundance of small molecules with m/z < 500 and H/C > 1.2 than the other three streams. Overall, the large variance in the intensity ranks in all four rivers demonstrated the individuality of DOM quality in pristine waters.

Figure 2

Alterations in the dissolved organic matter (DOM) characteristics as observed by (left) Fourier transform ion cyclotron mass spectrometry (FTICR MS) and (right) 1H nuclear magnetic resonance (NMR) spectroscopy. Top: hierarchical cluster analysis (HCA; A) and principal component analysis (PCA; B) of four pristine control DOM (cf. Figs 4A and S1). Bottom: HCA (C) and PCA (D) of the control, effluent and downstream DOM (cf. Figs S6–S9). Colour code: green, control DOM; red, aquaculture effluent DOM; blue, DOM downstream of the aquaculture.

FTICR MS derived common molecules in the effluent and downstream DOM

Hierarchical cluster analysis (HCA) and PCA of the FTICR mass spectra revealed large compositional differences between pristine and effluent DOM, with intermediate positioning of downstream DOM (Fig. 2). The quality differences between the control and effluent DOM exceeded those of the effluent and downstream samples for Molco, Peuco and Huililco (Fig. 2C, S3). However, the clustering of pristine, effluent and downstream DOM was very dense for Niltre DOM and somewhat more expansive for Huililco DOM, whereas both Peuco and Molco DOM showed large scatter and differences in their trajectories (Fig. 2D). At this level of resolution, the overall chemical diversity of the control, effluent and downstream DOM differed according to catchment in the order of Niltre < Huililco < Peuco ≈ Molco. Peuco and Molco DOM showed extensive and largely different molecular alterations comparing pristine, effluent and downstream DOM (Fig. 2C,D). The parameters calculated from the mass spectra (Table S2) showed a lower average mass for effluent DOM than pristine DOM, with the exception of Huililco, which remained nearly unchanged. The intensity-weighted H/C values increased, whereas the respective O/C values decreased in the order of Molco > Peuco > Niltre > Huililco riverine DOM. All three Huililco DOM values had nearly identical bulk parameters, such as average mass, elemental ratios (H/C and O/C), and DBE/C values. The percentages of CHNO, CHOS and CHNOS compounds in effluent DOM was strongly (Molco and Peuco), moderately (Huililco) and marginally (Niltre) increased; the relative depletion of CHO compounds occurred in the order Molco > Peuco > Huililco > Niltre.

The differential analysis of pairwise FTICR mass spectra showed a clear association of particular molecular changes and the alteration of pristine to effluent DOM. Unique molecular compositions belonging to either pristine or effluent DOM showed highly individual, catchment-specific patterns in the van Krevelen diagrams and mass-edited H/C ratios (Fig. 3). The effluents of Molco and Peuco contained many saturated and oxygen-deficient CHON and CHONS (H/C > 1.2; O/C < 0.5) compounds. Newly formed compounds found in Molco and Peuco effluents also showed some admixture of low mass (m/z < 400 Da), fairly saturated (H/C > 1.4) and oxygen-deficient CHO compounds of lipid origin (Fig. 3). The effluent of Huililco contained a particular series of several dozens of CHOS compounds with intermediate unsaturation (H/C ratio 1.4 ± 0.1), relatively low oxygenation (O/C ratio: 0.3 ± 0.1) and considerable mass (m/z ~ 600–800; Fig. 3). The effluent of Huililco and both effluents of Niltre showed many high-intensity CHO compounds that were less or moderately saturated (H/C < 1.5) and a comparably low number of CHNO and CHNOS compounds.

Figure 3

Fourier transform ion cyclotron mass spectrometry (FTICR MS) derived molecular compositions unique to (A) pristine and (B) effluent dissolved organic matter (DOM); left: van Krevelen diagrams; right: mass-edited H/C ratios. Colour code: blue, CHO; green, CHOS; orange, CHNO; and red, CHNOS molecular series. Circled area reflects the relative mass peak amplitude.

The FTICR MS derived molecular compositions in both the effluent and downstream DOM (and absent from the control) showed distinct patterning in the van Krevelen diagrams and mass-edited H/C ratios for each of the four catchments, which was indicative of specific DOM transformations (Fig. S4). The common presence in the effluent and downstream site was characteristic for CHO/CHNO/CHNOS/CHOS compounds in the Molco River and Peuco River, with highly saturated H/C > 1.4 and O/C < 0.6 (oxygen deficient). In the Peuco River, a group of CHNO compounds with 0.5 < H/C < 1 and 0.4 < O/C < 0.6 was found in the effluent and downstream site. In the Huililco River, a suite of sulfolipids was common to the effluent and downstream site, with 1.3 < H/C < 1.7, 0.2 < O/C < 0.4 and relatively large mass (m > 600 Da). Niltre River had a near-contiguous string of carboxyl-rich alicyclic molecules (CRAM)35 with average H/C and O/C ratios and higher proportions of oxygenated and unsaturated CHO compounds common to the effluent and downstream site (Figs 3 and S4). In general, not all compounds present in the effluents and absent in the controls were found at the downstream sites. On a few occasions, single large-amplitude mass peaks were observed in all catchments (Table 1 and Fig. S5). This limited set of intense mass peaks, considered to be pollutants, was subjected to structure search via software freely available from the internet (, and the key lead structures were categorized.

Table 1

NMR spectroscopy of the control sites

One-dimensional 1H NMR spectra of pristine riverine DOM (control) acquired in CD3OD showed considerable variance, demonstrating the individuality of each river catchment with respect to organic matter composition (Figs 4A and S6–S9; 1H NMR spectra and section integrals, 13C NMR spectra and section integrals, and 2D NMR spectra are shown in detail in the Supplementary Information). However, certain NMR resonance patterns were observed in all samples: the ramp-like increase of aromatic 1H NMR resonances from δH ~ 8.5 to 6.6 ppm indicated (poly)phenols (δH ~ 6.6–7.2 ppm); the abundant broadened NMR resonance at δH ~ 1.3 ppm indicated the presence of linear and branched aliphatics. Variable proportions of carboxyl-rich alicyclic materials (CRAM; δH ~ 1.95–3.1 ppm) and other oxygenated aliphatic compounds ( H CO units; δH ~ 3.1–4.9 ppm) were present (Tables S3–S5), but the general NMR lineshape characteristics appeared congruent, suggesting differences in concentration rather than fundamental variance in the chemical diversity of individual pristine river catchment DOM. The control site in Molco showed major NMR aliphatic resonance at δH ~ 1.3 ppm, indicative of abundant linear and branched lipids, with secondary NMR resonances at δH ~ 2.2 ( H Cα), 1.7 ( H Cβ), 1.4 ( H Cγ) and 0.9 (C H3) ppm, representing common C3–5 units connected to carbonyl derivatives (likely carboxylic acids: HOOC-CHα-CHβ-CHγ-Cn-CH3). In contrast, Niltre showed a large proportion of methoxy groups (δH ~ 3.6–4.0 ppm), indicative of lignins, which was further corroborated by the sizable share of phenolic NMR resonances at δH ~ 6.6–7.2 ppm. Consequently, HCA separated Molco and Niltre from Peuco and Huililco, which both contained higher proportions of broad NMR resonances indicative of bulk DOM (Fig. 2). Huililco presented elevated lipid content compared with Peuco, in line with its HCA placement (Fig. 2A,B).

Figure 4

(Top): 1H nuclear magnetic resonance (NMR) spectra (800 MHz, CD3OD) of four DOM derived from “pristine” riverine catchments. (Bottom): Manual overlay difference 1H NMR spectra (800 MHz, CD3OD): effluent (red) minus pristine (green) DOM, with positive/negative amplitude referring to elevated abundance in the effluent/pristine DOM.

NMR spectroscopy of the effluent and downstream sites

Difference NMR spectra [effluent minus pristine (Fig. 4B) and effluent minus downstream (data not shown)] demonstrated an increased abundance of peptide and carbohydrate metabolite signatures in the effluent DOM. 13C NMR spectra acquired exclusively from the Niltre River DOM indicated the prevalence of bulk organic matter signatures with variable proportions of superimposed sharp NMR resonances resulting from abundant small molecules (Fig. S10). Their contributions were marginal in the DOM from the control sites, prominent in the effluent DOM, and attenuated in the downstream DOM. 13C NMR section integrals revealed an increased abundance of XC H units in the effluent DOM, representing primarily CONHCα H units from peptides and proteins and OC H units from carbohydrates (Table S6). Common aliphatic and aromatic chemical environments showed a decreased abundance in effluent DOM (Tables S3–S5). The 2D NMR spectra showed weak cross peak patterning in pristine DOM (with the exception of the JRES NMR spectra, which favour the detection of terminal Cn units in mobile aliphatic chains with slow transverse NMR relaxation)21 and very strong patterning of abundant and intense cross peaks in the COSY, TOCSY, and HSQC NMR spectra of effluent DOM, which remained recognizable in the downstream DOM (Fig. S11). These molecular changes indicated an increased abundance of peptides (proteins) and carbohydrates, as confirmed by homonuclear and heteronuclear 2D NMR spectroscopy, in which many of the newly appearing cross peaks corresponded with those derived from random coil proteins, with a few additional lipid-derived cross peaks (Fig. 5).

Figure 5

(Panel A) Overlay of 1H, 1H COSY (correlated spectroscopy; green cross peaks), 1H, 1H TOCSY (total correlated spectroscopy; coloured cross peaks) and (panel B) 1H, 13C DEPT HSQC (distortionless enhancement by polarization transfer; heteronuclear single quantum coherence) nuclear magnetic resonance (NMR) spectra (colour code: purple, CH123; blue, CH; green, CH2; red, CH3) of the Niltre first effluent DOM (NiEf1) aliphatic section, with cross peaks of proteinaceous amino acids (see attendant single letter code) in proteins following alanine, (A) annotated according to position and carbon multiplicity. (Panel A): upper left half: amino acid-derived COSY cross peaks according to positioning in peptides (blue squares); lower right half: amino acid-derived TOCSY cross peaks according to individual amino acids (individual grey symbols). (Panel B): 1H, 13C DEPT HSQC NMR spectrum; colour code: purple, CH123; blue, CH; green, CH2; red: CH357,58. Orange box denotes the section of OCHn cross peaks59 (cf. Figs 3A and S2). e1: aromatic methyl esters, e2: aliphatic methyl esters, e3: aromatic methyl esters, e4: aliphatic methyl ethers, e5: oxyomethylene OCH2, largely from carbohydrates. The abundance follows: e5 e1 ≈ e2: > e3 e4. Projection 1H NMR spectra on top (F2 dimension) represent the Niltre first effluent DOM NiEf1 (black) and difference 1H NMR spectra (1st effluent minus pristine; NiEf1 – NiCo) Niltre first effluent DOM (cf. Fig. S9), whereas multiplicity edited 13C NMR subspectra (F1 dimension) are shown for panel B (cf. Fig. S10).

Effects on the microbial community

Confocal laser scanning microscopy revealed that the biofilms consisted of EPS-glycoconjugates, eukaryotic algae, cyanobacteria and bacteria (Fig. 6A–D). Many algae and some cyanobacteria were observed at the control sites, whereas at the downstream sites, the gravel stones were covered by a dense bacterial biofilm. This result was confirmed by semi-quantitative biovolume data: the algae biovolumes were higher at the control sites than at the downstream sites, whereas the bacterial biovolumes were higher downstream of the effluents from the aquacultures (Fig. 6A–D). Bacterial production (BP) of planktonic bacteria was very low at Molco, Peuco and Niltre control sites (0.5–1.2 μg C L−1 d−1) and was slightly higher in Huililco (Fig. 6E,F). The planktonic BP downstream of the aquacultures followed a different pattern than the DOC concentrations: BP was either strongly increased (Molco, Niltre) or slightly (Huililco) or strongly (Peuco) decreased compared with the control. The BP of the biofilm bacteria exceeded the BP of the planktonic bacteria per dm2 stream area. In all streams, the BP downstream of the aquacultures was greater than the BP at the control sites upstream of the aquacultures. The BP of stream water bacteria was positively related to the Fmax values of the Trp- and Tyr-like fluorescence components (Trp: r2 = 0.48, p = 0.058; Tyr: r2 = 0.82, p = 0.002). In addition, biofilm BP was positively correlated with the Fmax values of the Trp- and Tyr-like compounds (Trp: r2 = 0.74, p = 0.006; Tyr: r2 = 0.85, p = 0.001; Fig. 6G,H).

Figure 6

Biofilm biovolumes derived from confocal laser scanning microscopy (CLSM) image data (A,C), with two representative maximum intensity projections (B,D). (A,B) Biofilm data from a control location (Rio Niltre) showing the dominance of eukaryotic algae. (C,D) Downstream site of the aquaculture (Rio Niltre) with biofilms dominated by non-phototrophic bacteria. Colour code: blue, autofluorescence of chlorophyll a; purple, cyanobacteria; green, bacteria; red, lectin-specific EPS-glycoconjugates. Bacterial production of planktonic (E) and biofilm bacteria (F) at control sites and downstream of the aquacultures at the four sampling sites. Production of biofilm bacteria as a function of the fluorescence intensities (Fmax values, Raman units) of tryptophan-like (G) and tyrosine-like (H) compounds.


The NMR spectra produced an unbiased depiction of the pristine riverine DOM composition and structure and showed mostly polyphenols from terrestrial input in addition to linear and branched aliphatics (possibly originating from plant waxes and other microbial lipids36). The individual characteristics of the NMR spectra for the control sites reflected differences in land use within the respective catchments. The Niltre River catchment is ~99% covered by natural forest (Table 2), which produces compounds with specific lignin-related features, such as abundant methoxy groups and phenols (Fig. 4A). This is in accordance with the FTICR MS-based, inter-sample ranking analyses of the CHO components17, which indicated higher proportions of hydrogen-deficient and oxygen-rich compounds (i.e., lignins and tannins) in the Niltre River than in the Molco, Peuco and Huililco Rivers (Fig. S2). The EEM fluorescence spectra recorded the largest loading of the humic-like component HS in the Niltre River; the lowest HS and HS2 loadings were found in the Molco River (Fig. 1).

Table 2

The Molco River catchment had the lowest percentage of forest coverage (~65%) but the largest proportion of volcanic soil (~19%; Table 2). NMR and FTICR MS indicated an increased abundance of aliphatic lipids at the expense of aromatic compounds, and the EEM fluorescence spectra showed decreased loadings of humic acids. The 1H NMR spectra of the Molco riverine DOM showed abundant linear and branched aliphatics with depleted bulk DOM molecules, such as CRAM (Tables S3–S5 and Fig. 4A), and a distinct, narrow methoxy resonance (δH ~ 3.6 ppm), likely representing aliphatic methyl esters resulting from the quenching of reactive CHOS compounds by methanol during SPE37. Saturated and unsaturated sulfolipids were more abundant in the Molco DOM than in the DOM of the three other river catchments (Figs 3 and S2). FTICR MS-based inter-sample rankings analyses demonstrated low proportions of lignin (H/C > 1; O/C ~ 0.4–0.5) and tannin (H/C < 1; O/C > 0.5) components (Fig. S2A). The Peuco (which originates from a spring proximate to the aquaculture) and Huililco Rivers contained elevated proportions of bulk DOM, as demonstrated by NMR (Fig. 4A), suggesting highly processed, biogeochemical organic matter with limited contributions from individual metabolite molecules.

The FTICR mass and NMR spectra revealed alteration in DOM quality between pristine, effluent and downstream DOM: in general, the downstream DOM properties were between those of the control and effluent DOM (Fig. 2). Compared with all four pristine DOM, all four effluent DOM featured newly formed, abundant peptide/protein and carbohydrate molecules, which produced unambiguous signatures in the 1H spectra, composing ~35% of the overall NMR integral (Figs 4B and S6–S9), and in the 13C and 2D NMR spectra for the Niltre River (Figs 5 and S10, S11). These molecules remained discernible in the downstream DOM, albeit at decreased abundances (Figs S6–S10). The larger differences in the EEM/PARAFAC analysis for Molco and Niltre compared to the observations for the Peuco and Huililco Rivers reflected changes in unsaturated carbon chemical environments (Fig. 4B), in agreement with the enhanced plankton BP in Molco and Niltre in the downstream sample and the comparably smaller changes in the Peuco and Huililco Rivers.

Due to individual catchment biogeochemistry and aquaculture management practices, the molecular alterations from pristine to effluent and downstream DOM were not unidirectional: variable extents of non-conservative mixing between pristine and effluent DOM were indicated by (difference) NMR and FTICR MS spectra and HCA/PCA of the downstream DOM (Figs 2D, 3 and S3). Intrinsic catchment characteristics were retained throughout the DOM alteration and precluded the unambiguous attribution of effluent and downstream DOM from positioning in the NMR- and FTICR MS-derived HCA and PCA diagrams (Fig. 2). The abundant peptides, carbohydrates and lipids present in the effluent DOM (Fig. 5) were easily available substrates for rapid microbial consumption, as opposed to highly processed, polydisperse pristine DOM, which exhibited greater overall chemo-diversity at low concentrations of individual molecules.

The differences between the four pristine and downstream samples primarily accounted for the downstream pollution potential imposed by aquaculture. The distinct patterning of the FTICR MS-derived molecular compositions present in both effluent and downstream DOM indicated specific processing in each catchment (Fig. 2). The FTICR spectra revealed a large increase in CHNO, CHOS, and CHNOS compounds in the effluents compared to the controls in Molco and Peuco, a moderate increase in Huililco, and a minor increase in Niltre (Table S2). The DOM of both Molco and Peuco was severely impacted, with largely different chemistries in the FTICR MS spectra (Figs 3 and S4), as indicated by the divergent individual trajectories in the PCA analyses (Fig. 2D). Although variable ionization selectivity in the mass spectrometry of these complex, polydisperse mixtures18 could have emphasized the alteration from more conventional pristine to more heteroatom-rich effluent DOM, the 1H NMR spectra also indicated larger differences between pristine and effluent DOM for Peuco and Molco than for Huililco and Niltre (Figs 2D and 4B). In contrast, the effluent of Huililco showed a moderate distinction for the control site (Figs 2C and S3), suggesting a limited effect of that aquaculture due to the small effluent:control discharge ratio (Table 2). The Niltre and Huililco DOM reflected conventional biogeochemistry based on CHO compounds (Fig. 3 and S4); the Molco and in particular the Peuco Rivers showed conspicuous patterning of CHNO, CHOS, and CHNOS compounds, indicative of an anthropogenic origin of downstream DOM.

Several peaks with large amplitudes were found in the four aquacultures in both the effluent and downstream samples, and possible known chemical structures were tested by compositional matching using ChemSpider software (Table 1). Some compounds (shaded boxes) have lead structures for which xenobiotic effects have been proposed. Substances containing oxocholan structures, such as C26H41O6N1S1, may have an effect similar to steroids and can act as juvenoid compounds (insect hormogenic compounds, pro-drug-like agents38). Such substances may have phytochemical effects39. The C21H17O10N1 component likely incorporated pyridinedicarboxylate, which can inhibit enzymes such as the glutamate dehydrogenase found in fungi40. Oxazole amides, a potential substructure of the C27H40O6N4, component, are the chemical building blocks of alkaloids41.

Regarding the microbial community, the low productions of planktonic bacteria at the control sites (0.5–7 μg C L−1 d−1) corresponded with the low DOC concentrations and were in the range of those measured in Amazonian streams42 but were near the minimum values in the Biobio River in Chile43 and in streams in Southern Ontario44. The biofilm BP in the biofilms at the control sites (71–425 μg C dm−2 d−1) corresponded to the values measured for epilithic bacterial production in small streams in Texas45. After calculating the areal planktonic BP using the volumetric values and mean stream depth, the biofilm bacterial production per dm2 was an average of 9–314 times higher than the production in stream water at the control sites and 8–175 times higher downstream of the aquacultures, indicating a clear dominance of benthic over plankton production. The abundance of bacteria in epilithic biofilms increased downstream of the aquacultures in accordance with the observed enhancement of bacterial numbers downstream of other aquacultures24,25. Moreover, we observed a decline in benthic algae and a shift towards heterotrophy12. A reduction in algal biomass and a shift to heterotrophic conditions was also found in periphyton downstream of a fish farm in an Andean stream46. The pattern of planktonic BP did not follow that of the increasing DOM concentration: some streams showed increased bacterial production, similar to that of the heterotrophic activity24, whereas others showed decreased BP. In contrast, the BP of biofilms increased downstream of the aquacultures in all streams, and biofilm production was positively correlated with Trp- and Tyr-like compounds (Fig. 6F–H).

Finally, we compared the observed DOM decline along a reach downstream of the aquaculture in the Molco River10 with the measured rates of DOM degradation (estimated from BP in the present study). A 2700-meter stretch of the Molco River, with a stream width of 5 m and a factor of two for the top and bottom surface areas of gravel stones, resulted in a total biofilm area of 27,000 m2. The BP in the biofilms of the Molco River amounted to 1.5 mg C dm−2 d−1 (Fig. 6F), equivalent to an average bacterial carbon demand of 6 mg C dm−2 d−1 or 25 mg C m−2 h−1 (assuming a bacterial growth efficiency of 25%)47,48. The effluent discharge (200 L s−1)10 and DOM concentration of 2 mg C L−1 (Fig. 1) resulted in an organic carbon load of 1.44 kg C h−1. The degradation of that load at a rate of 25 mg C m−2 h−1 and within two hours (the travel time for the 2700-m reach of the Molco River10) would necessitate a surface area of 28,800 m2, closely matching the computed surface area of stones (27000 m2). However, we measured DOM degradation during base flow conditions only. At higher discharge rates during other seasons (autumn, winter), we would expect a lower concentration of aquaculture DOM in the streams due to higher dilution and a longer distance downstream of the effluent that would be necessary for degradation due to the higher flow velocity. In addition, the lower water temperature during autumn and winter would further decrease bacterial activity.

In conclusion, highly specific molecular and biological changes were found downstream of the aquaculture operations. The DOC concentration and the fluorescence analysis of the DOM were able to distinguish pristine and polluted downstream samples. FTICR MS showed which elemental formula components could be detected as pollution in the downstream samples. The NMR analysis provided the most detailed information on the chemistry of the polluting components. To the best of our knowledge, the present study is the most detailed investigation of riverine DOM quality change due to aquaculture. The observed changes in DOM composition led to an increase in bacteria and a decrease in benthic algae downstream of the aquacultures. This shift in epilithic biofilms from autotrophy to heterotrophy alters the metabolism of the stream ecosystem, strongly impairing ecosystem health49. Biofilm bacterial DOM degradation was stimulated (depending on protein-like DOM compounds), which explained the disappearance of aquaculture DOM within the stream reaches. This knowledge may help to define emission thresholds for DOM to protect sensitive stream ecosystems and to design appropriate reactors for the treatment of aquaculture effluent DOM. The degradation rates measured in this study might be used to calculate the dimensions of percolated biological filters and chains of waste water treatment ponds. In light of climate change50, we expect that increasing temperatures will stimulate bacterial DOM degradation, but lower precipitation and discharge will decrease dilution. Thus, water quality problems will be increased due to high DOM concentrations, bacterial biomass, and oxygen demand. Finally, to build upon the description of the diversity of aquaculture DOM in the present study, further studies should investigate the effect of specific pollutants on stream ecosystems and the duration and river distance necessary for their degradation.


Study site and sampling

The investigations were conducted in the IX. and X. region of Chile (Region de la Araucania) in the vicinity of Lago Villarica (Fig. S12) at four aquaculture sites on the Molco (Mo), Peuco (Pe), Huililco (Hu), and Niltre (Ni; Table 2) rivers. Samples were taken 10–20 m upstream of the aquacultures (control, Co), from their effluents (Ef), and approximately 100–200 m downstream after effluent mixing (Do). Gravel stones were sampled randomly across the respective river sections. Measurements were performed during summer (between 12th and 19th January 2015) under summer base flow conditions (see Table 2 for discharge conditions). The river discharges were determined according to the mid-section velocity area method, for which the average velocity was measured using a WINLAB discharge velocity metre every 0.5 m along the stream width and at 0.6 of the distance from the stream surface to the streambed. The discharge was calculated as the product of the recorded velocity, depth and width of the corresponding river cross-section; the total stream discharge corresponds to the sum of each individual cross-section. There had been no rain since 1st January; the maximum daily temperature on the sampling days ranged between 21 °C and 30 °C (weather station Pichoy Airport, Valdivia).

Measurement of the DOC concentration

For the DOC analysis, water samples were transferred into acid-rinsed and combusted brown glass bottles (I-Chem 100, Merck), kept at 4 °C for a maximum of 24 h, and then filtered through 0.22-μm pore size PES membrane syringe filters (Millex Merck Millipore). DOC concentrations were measured using high-temperature catalytic oxidation (HighTOC, Elementar Systems) with a combustion temperature of 1050 °C and high-purity synthetic air (Alphagaz Airliquide) as the carrier gas, with a detection limit of 0.1 mg C L−1.

Fluorescence measurement of DOM

Fluorescence measurements were conducted with a Varian Cary Eclypse fluorescence spectrometer (Santa Clara, CA, USA)10. Excitation from 240 to 450 nm (5 nm steps) and emission from 300 to 600 nm (2 nm steps), with a slit width of 5 nm, were measured to produce excitation-emission matrices (EEM)28. All samples were measured at room temperature and were corrected to the absorbance spectra recorded in the range of 190 to 800 nm for the instrument baseline. Absorbance was measured in 1-cm cuvettes using a Pharo Spectroquant 200 spectrophotometer for the inner-filter correction of the fluorescence measurements (Darmstadt, Germany). Daily measurements of the area under the Raman peak of MilliQ water were recorded to assess instrument stability51. Primary and secondary inner-filter effects were removed using mathematical inner-filter corrections52. Excitation corrections were normalized by the area under the Raman peak at the 350 nm excitation wavelength51. These corrections were conducted using the FDOMcorr toolbox53 for Matlab (version R2012a, MathWorks, Ismaning, Germany) and allowed the best possible comparability to other DOM fluorescence studies51,53.

High-field FTICR mass spectrometry of SPE-DOM

For DOM enrichment, 10 L of stream water was filtered through GFF and acidified with HCl to pH 2.0–2.5. Bond Elut SPE PPL cartridges (1 g; Agilent Technologies) were rinsed with 5 mL of 100% methanol, 5 mL of pure water and 5 mL of 0.01 N HCl. Pre-filtered stream water (8 L) was filtered through each cartridge. After rinsing with 10 mL of 0.01 N HCl, drying, and eluting with 10 mL of 100% methanol (LCMS grade), samples were stored at −25 °C. High-field Fourier transform ion cyclotron (FTICR) mass spectra were acquired using a 12 Tesla Bruker Solarix mass spectrometer (Bruker Daltonics, Bremen, Germany) hyphenated to an Apollo II electrospray ionization source in negative mode [ESI(−)]23. The SPE-DOM samples were injected into the electrospray source using a microliter pump at a flow rate of 120 μL h−1, a nebulizer gas pressure of 138 kPa, and a drying gas pressure of 103 kPa. A source heater temperature of 200 °C was maintained to ensure rapid desolvation in the ionized droplets. The spectra were acquired with a time domain of four megawords in [ESI(−)], and 500 scans were accumulated for each mass spectrum. All spectra were internally calibrated using appropriate reference mass lists. Data processing was conducted using Compass Data Analysis 4.0 (Bruker, Bremen, Germany). Possible elemental formulas were assigned using our own software (a formula calculator). The generated formulas were validated by setting sensible chemical constraints [signal-to-noise (S/N) > 3, N rule, O/C ratio ≤ 1, H/C ratio ≤ 2n + 2, element counts: C ≤ 100, H ≤ 200, O ≤ 80, N ≤ 6, S ≤ 3 and mass accuracy window (set at ± 500 ppb)], and the final molecular formula assignments were branded into groups containing CHO, CHNO, CHOS or CHNOS molecular compositions, which were used to reconstruct the group-selective mass spectra. The FTICR MS and NMR datasets were processed using Hierarchical Clustering Explore 3.5 after normalizing the data using unit variance scaling. Samples and variables were then clustered by applying average linkage (UPGMA) and Pearson correlation coefficient to analyse the distance measure. SIMCA-P version 9.0 from UNIMETRICS was used for the PCA plots.

NMR spectroscopy of SPE-DOM

Proton-detected NMR spectra of methanolic riverine SPE-DOM extracts were acquired using a Bruker Avance III NMR spectrometer at 800.13 MHz (B0 = 18.7 T) and 283 K from ~3 to 7 mg (cf. Table S7) of solid SPE-DOM obtained by evaporation of the original methanol-h4 solution. Proton NMR spectra were acquired in approximately 170 μL of CD3OD (Merck. 99.95% 2H) solution with a 5-mm z-gradient 1H/13C/15N/31P QCI cryogenic probe (90° excitation pulses: 13C ~ 1H ~ 10 μs) in sealed 3.0-mm Bruker MATCH tubes. 1D 1H NMR spectra were recorded with a spin-echo sequence (10 μs delay) to allow for high-Q probe ringdown, and classical pre-saturation to attenuate the residual water present “noesypr1d”, typically using 512 scans (5 s acquisition time, 5 s relaxation delay, 1 ms mixing time; 1 Hz exponential line broadening). 13C NMR spectra were acquired with a Bruker Avance III NMR spectrometer at 500.13 MHz (B0 = 11.7 T) at 283 K with a 5-mm z-gradient 1H/1H/dual cryogenic probe (90° excitation pulses: 13C ~ 10 μs; 1H ~ 16.5 μs). A Bray-Curtis similarity assessment was performed by cluster analysis of the 800 MHz spectra in the chemical shift range δH = 0.7–8.7 ppm, with the exclusion of the methanol (δH = 3.2–3.4 ppm) and residual water (δH = 4.7–5.2 ppm) NMR resonances by means of AMIX-based bucket analysis (0.001 ppm uniform width, normalized total 1H NMR integral = 100%).

The one-bond coupling constant 1J(CH) used in the 2D 1H,13C DEPT HSQC spectra (hsqcedetgpsisp2.2) was set to 145 Hz; other conditions: 13C 90 deg decoupling pulse, GARP (70 μs); 50 kHz WURST 180 degree 13C inversion pulse (Wideband, Uniform, Rate, and Smooth Truncation; 1.2 ms); F2 (1H): spectral width of 5981 Hz (11.96 ppm); 1.25 s relaxation delay; F1 (13C): SW = 17,607 Hz (140 ppm). HSQC-derived NMR spectra were computed to an 8192 × 1024 matrix. The absolute value JRES, phase-sensitive COSY and echo-antiecho TOCSY spectra (with solvent suppression: jresgpprqf, cosygpph19, dipsi2etgpsi19) used a spectral width of 5498 Hz [JRES (F1) = 50 Hz] and were computed to a 16384 × 2048 matrix [JRES/TOCSY (F1) = 128/4096]. The other NMR acquisition conditions are given in Table S7.

Confocal laser scanning microscopy (CLSM)

Structural analysis of the microbial biofilm community was conducted by CLSM using a TCS SP5 X (Leica)54. Extracellular polymeric substances (EPS) were stained by the lectin AAL (Aleuria aurantia) (Vector Laboratories) conjugated with the fluorochrome Alexa568 (Molecular Probes). Bacteria were stained with the nucleic acid specific fluorochrome Syto9 (Molecular Probes). Excitation was performed at 500 nm (reflection, Syto9), 578 nm (AAL-Alexa568, cyanobacterial autofluorescence) and 633 nm (cyanobacterial and algal autofluorescence). Emission signals were collected sequentially for reflection (495–505 nm), Syto9 (515–560 nm) and chlorophyll A (650–720 nm) in one scan. The emission of AAL-Alexa568 was recorded in a second scan. Three gravel stones per site were used for imaging, and three images were recorded for each, from the top and bottom sides. The digital signals for bacteria, EPS-glycoconjugates, cyanobacteria and chlorophyll autofluorescence were extracted using JImageAnalyser55 software. Semi-quantitative biovolume values were estimated after manual thresholding. The EPS-glycoconjugates and cyanobacteria data, as well as the cyanobacteria and algae present in two channels, were separated using the Imaris ver. 7.7.2 (Bitplane) co-localization tool.

Bacterial biomass production

The production of pelagic bacteria in the stream water and of biofilm bacteria on the gravel stones was measured using the leucine technique54,56. For free-water bacteria, triplicate 5 mL aliquots and one formalin-treated control (3.7%, final concentration) were spiked with 14C-leucine (10.8 MBq mmol−1, Sigma, 50 nM final concentration). Samples were incubated in situ within the stream for 1 h in the dark. Incorporation was stopped using formalin, and 0.6 mL of 50% trichloroacetic acid (TCA) was added. Proteins were extracted for 15 min and filtered through 0.2-μm Nuclepore membranes. Filters were rinsed twice with 1 mL of 5% TCA and once with 80% ethanol. After dissolving the filters in 0.5 mL of Soluene (Packard) and adding 2.5 mL of biodegradable counting scintillant (Amersham) to each scintillation vial, radioactivity was measured using a liquid scintillation analyser (LS 6500, Beckman). The external standard ratio method was used for quenching, and bacterial carbon production was calculated56. The production of biofilm bacteria was also estimated based on leucine incorporation. Gravel stones of approximately 1 cm in length were transferred to scintillation vials and covered with 4 mL of sterile-filtered stream water. Triplicate aliquots and one formalin-treated control (3.7%, final concentration) were spiked with 14C-leucine (5 mM final concentration). After in situ incubation for 1 h and extraction with TCA on ice, the biofilms were removed from the stones by ultrasonication for 1 min (20 kHz, 20%; vibra cell VCX 130, Sonics, USA). Stones were removed and rinsed, and the supernatant was filtered and measured as described above. To estimate the surface area of the rocks, they were wrapped in tin foil, and the weight of the foil was related to the weight of one cm2 foil.

Additional Information

How to cite this article: Kamjunke, N. et al. Land-based salmon aquacultures change the quality and bacterial degradation of riverine dissolved organic matter. Sci. Rep. 7, 43739; doi: 10.1038/srep43739 (2017).

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.


  1. 1

    Raymond, P. A. et al. Global carbon dioxide emissions from inland waters. Nature 503, 355–359 (2013).

    Article  ADS  CAS  PubMed  Google Scholar 

  2. 2

    Battin, T. J., Besemer, K., Bengtsson, M. M., Romani, A. M. & Packman, A. I. The ecology and biogeochemistry of stream biofilms. Nat. Rev. Microbiol. 14, 251–263 (2016).

    Article  CAS  PubMed  Google Scholar 

  3. 3

    Romani, A. M. et al. Biofilm structure and function and possible implications for riverine DOC dynamics. Microb. Ecol. 47, 316–328 (2004).

    Article  CAS  PubMed  Google Scholar 

  4. 4

    Battin, T. J. et al. Biophysical controls on organic carbon fluxes in fluvial networks. Nat. Geosci. 1, 95–100 (2008).

    Article  ADS  CAS  Google Scholar 

  5. 5

    Cole, J. J. et al. Plumbing the global carbon cycle: integrating inland waters into the terrestrial carbon budget. Ecosystems 10, 171–184 (2007).

    Article  CAS  Google Scholar 

  6. 6

    Aufdenkampe, A. K. et al. Riverine coupling of biogeochemical cycles between land, oceans, and atmosphere. Front. Ecol. Environ. 9, 53–60 (2011).

    Article  Google Scholar 

  7. 7

    Gücker, B., Silva, R. C. S., Graeber, D., Monteiro, J. A. F. & Boechat, I. G. Urbanization and agriculture increase exports and differentially alter elemental stoichiometry of dissolved organic matter (DOM) from tropical catchments. Sci. Total Environ. 550, 785–792 (2016).

    Article  ADS  CAS  PubMed  Google Scholar 

  8. 8

    Graeber, D. et al. Global effects of agriculture on fluvial dissolved organic matter. Sci. Rep. 5, 16328 (2015).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  9. 9

    Perakis S. S. & Hedin L. O. Nitrogen loss from unpolluted South American forests mainly via dissolved organic compounds. Nature 415, 416–419 (2002).

    Article  ADS  PubMed  Google Scholar 

  10. 10

    Nimptsch, J. et al. Tracing dissolved organic matter (DOM) from land-based aquaculture systems in North Patagonian streams. Sci. Total Environ. 537, 129–138 (2015).

    Article  ADS  CAS  PubMed  Google Scholar 

  11. 11

    FAO. The state of world Fisheries and Aquaculture. Rome. 223 pp., ( (2014).

  12. 12

    Tello, A., Corner, R. A. & Telfer, T. C. How do land-based salmonid farms affect stream ecology? Environ. Pollut. 158, 1147–1158 (2010).

    Article  CAS  PubMed  Google Scholar 

  13. 13

    Rosa, R. S., Aguiar, A. C. F., Boechat, I. G. & Gücker, B. Impact of fish farm pollution on ecosystem structure and function of tropical headwater streams. Environ. Pollut. 174, 204–213 (2013).

    Article  CAS  Google Scholar 

  14. 14

    Hood, E., Fellman, J. & Edwards, R. T. Salmon influences on dissolved organic matter in a coastal temperate brown-water stream: An application of fluorescence spectroscopy. Limnol. Oceanogr. 52, 1580–1587 (2007).

    Article  ADS  CAS  Google Scholar 

  15. 15

    Fellman, J. B., Hood, E., Edwards, R. T. & D’Amore, D. V. Return of salmon-derived nutrients from the riparian zone to the stream during a storm in southeastern Alaska. Ecosystems 11, 537–544 (2008).

    Article  CAS  Google Scholar 

  16. 16

    Hambly, A. C. et al. Characterizing organic matter in recirculating aquaculture systems with fluorescence EEM spectroscopy. Wat. Res. 83, 112–120 (2015).

    Article  CAS  Google Scholar 

  17. 17

    Herzsprung, P. et al. Variations of DOM quality in inflows of a drinking water reservoir: Linking of van Krevelen diagrams with EEMF spectra by rank correlation. Environ. Sci. Technol. 46, 5511–5518 (2012).

    Article  ADS  CAS  PubMed  Google Scholar 

  18. 18

    Hertkorn, N. et al. Natural organic matter and the event horizon of mass spectrometry. Anal. Chem. 80, 8908–8919 (2008).

    Article  CAS  PubMed  Google Scholar 

  19. 19

    Wagner, S., Jaffe, R., Cawley, K., Dittmar, T. & Stubbins, A. Associations between the molecular and optical properties of dissolved organic matter in the Florida everglades, a model coastal wetland system. Front. Chem. 3, 66 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  20. 20

    Lam, B. et al. Major Structural Components in Freshwater Dissolved Organic Matter. Environ. Sci. Technol. 41, 2840–2847 (2007).

    Article  ADS  CAS  Google Scholar 

  21. 21

    Hertkorn, N., Harir, M., Koch, B. P., Michalke, B. & Schmitt-Kopplin, P. High-field NMR spectroscopy and FTICR mass spectrometry: powerful discovery tools for the molecular level characterization of marine dissolved organic matter. Biogeosciences 10, 1583–1624 (2013).

    Article  ADS  CAS  Google Scholar 

  22. 22

    Bell, N. G. A., Michalchuk, A. A. L., Blackburn, J. W. T., Graham, M. C. & Uhrin, D. Isotope-filtered 4D NMR spectroscopy for structure determination of humic substances. Angew. Chem. Int. Ed. 54, 1–5 (2015).

    Article  CAS  Google Scholar 

  23. 23

    Hertkorn, N., Harir, M., Cawley, K. M., Schmitt-Kopplin, P. & Jaffe, R. Molecular characterization of dissolved organic matter from subtropical wetlands: a comparative study through the analysis of optical properties, NMR and FTICR/MS. Biogeosciences 13, 1–21 (2016).

    Article  CAS  Google Scholar 

  24. 24

    Carr, O. J. & Goulder, R. Fish-farm effluents in rivers - I. Effects on bacterial populations and alkaline phosphatase activity. Wat. Res. 24, 631–638 (1990).

    Article  CAS  Google Scholar 

  25. 25

    Brown, S. E. & Goulder, R. Extracellular-enzyme activity in trout-farm effluents and a recipient river. Aquacult. Res. 27, 895–901 (1996).

    Article  Google Scholar 

  26. 26

    Brown, S. E. & Goulder, R. Change in riverine epilithic extracellular enzyme activity in response to fish farm effluent. Lett. Appl. Microbiol. 29, 385–388 (1999).

    Article  CAS  PubMed  Google Scholar 

  27. 27

    Osburn, C. L., Handsel, L. T., Mikan, M. P., Paerl, H. W. & Montgomery, M. T. Fluorescence tracking of dissolved and particulate organic matter quality in a river-dominated estuary. Environ. Sci. Technol. 46, 8628–8636 (2012).

    Article  ADS  CAS  PubMed  Google Scholar 

  28. 28

    Stedmon, C. A. & Markager, S. Resolving the variability in dissolved organic matter fluorescence in a temperate estuary and its catchment using PARAFAC analysis. Limnol. Oceanogr. 50, 686–697 (2005a).

    Article  ADS  CAS  Google Scholar 

  29. 29

    Stedmon, C. & Markager, S. Tracing the production and degradation of autochthonous fractions of dissolved organic matter by fluorescence analysis. Limnol. Oceanogr. 50, 1415–1426 (2005b).

    Article  ADS  CAS  Google Scholar 

  30. 30

    Fellman, J., Hood, E., D’Amore, D., Edwards, R. & White, D. Seasonal changes in the chemical quality and biodegradability of dissolved organic matter exported from soils to streams in coastal temperate rainforest watersheds. Biogeochemistry 95, 277–293 (2009).

    Article  CAS  Google Scholar 

  31. 31

    Fellman, J., Hood, E. & Spencer, R. Fluorescence spectroscopy opens new windows into dissolved organic matter dynamics in freshwater ecosystems: a review. Limnol. Oceanogr. 55, 2452–2462 (2010).

    Article  ADS  CAS  Google Scholar 

  32. 32

    Stedmon, C. A. et al. Characteristics of dissolved organic matter in Baltic coastal sea ice: allochthonous or autochthonous origins? Environ. Sci. Technol. 41, 7273–7279 (2007).

    Article  ADS  CAS  PubMed  Google Scholar 

  33. 33

    Walker, S. A., Amon, R. M., Stedmon, C., Duan, S. & Louchouarn, P. The use of PARAFAC modeling to trace terrestrial dissolved organic matter and fingerprint water masses in coastal Canadian Arctic surface waters. J. Geophys. Res. Biogeosciences 114, G00F06 (2009).

    Article  ADS  CAS  Google Scholar 

  34. 34

    Osburn, C. L., Wigdahl, C. R., Fritz, S. C. & Saros, J. E. Dissolved organic matter composition and photoreactivity in prairie lakes of the US Great Plains. Limnol. Oceanogr. 56, 2371–2390 (2011).

    Article  ADS  CAS  Google Scholar 

  35. 35

    Hertkorn, N. et al. Characterization of a major refractory component of marine dissolved organic matter. Geochim. Cosmochim. Acta 70, 2990–3010 (2006).

    Article  ADS  CAS  Google Scholar 

  36. 36

    Naafs, D. F. W., Van Bergen, P. F., de Jong, M. A., Oonincx, A. & de Leeuw, J. W. Total lipid extracts from characteristic soil horizons in a podzol profile. Eur. J. Soil Sci. 55, 657–669 (2004).

    Article  CAS  Google Scholar 

  37. 37

    Schmitt-Kopplin, P. et al. Analysis of the unresolved fraction in atmospheric aerosols with ultahigh-resolution mass spectrometry and nuclear magnetic resonance spectroscopy: organosulfates as photochemical smog constituents. Anal. Chem. 82, 8017–8026 (2010).

    Article  CAS  PubMed  Google Scholar 

  38. 38

    Svobodová, H. et al. Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids. Bioorg. Med. Chem. 18, 8194–8203 (2010).

    Article  CAS  PubMed  Google Scholar 

  39. 39

    Wyson, J. W., Deventhiran M., Saravanan, P., Anand, D. & Rajarajan, S. Phtyochemical analysis of leaf extract of Eclipta prostrata (L.) by GC-MS method. Internat. J. Pharmaceut. Sci. Res. 7, 272–278 (2016).

    Google Scholar 

  40. 40

    Jastrzebowska, K. & Gabriel, I. Inhibitors of amino acids biosynthesis as antifungal agents. Amino Acids 47, 227–249 (2015).

    Article  CAS  PubMed  Google Scholar 

  41. 41

    Davyt, D. & Serra, G. Thiazole and oxazole alkaloids: Isolation and synthesis. Mar. Drugs 8, 2755–2780 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. 42

    Farjalla, V. F., Esteves, F. A., Bozelli, R. L. & Roland, F. Nutrient limitation of bacterial production in clear water Amazonian ecosystems. Hydrobiologia 489, 197–205 (2002).

    Article  CAS  Google Scholar 

  43. 43

    Vargas, C. A., Arriagada, L., Sobarzo, M., Contreras, P. Y. & Saldias, G. Bacterial production along a river-to-ocean continuum in central Chile: implications for organic matter cycling. Aquat. Microb. Ecol. 68, 195–213 (2013).

    Article  Google Scholar 

  44. 44

    Williams, C. J., Yamashita, Y., Wilson, H.-F., Jaffe, R. & Xenopoulos, M. A. Unraveling the role of land use and microbial activity in shaping dissolved organic matter characteristics in stream ecosystems. Limnol Oceanogr. 55, 1159–1171 (2010).

    Article  ADS  CAS  Google Scholar 

  45. 45

    Scott, J. T., Back, J. A., Taylor, J. M. & King, R. S. Does nutrient enrichment decouple algal-bacterial production in periphyton? J. N. Am. Benthol. Soc. 27, 332–344 (2008).

    Article  Google Scholar 

  46. 46

    Villanueva, V. D., Queimalinos, C., Modenutti, B. & Ayala, J. Effect of fish farm effluents on the periphyton of an Andean stream. Arch. Fish. Mar. Res. 48, 283–294 (2000).

    Google Scholar 

  47. 47

    Tranvik, L. J. Availability of dissolved organic carbon for planktonic bacteria in oligotrophic lakes of differing humic content. Microb. Ecol. 16, 311–322 (1988).

    Article  CAS  PubMed  Google Scholar 

  48. 48

    Weiss, M. & Simon, M. Consumption of labile dissolved organic matter by limnetic bacterioplankton: the relative significance of amino acids and carbohydrates. Aquat. Microb. Ecol. 17, 1–12 (1999).

    Article  Google Scholar 

  49. 49

    Young, R. G., Matthaei, C. D. & Townsend, C. R. Organic matter breakdown and ecosystem metabolism: functional indicators for assessing river ecosystem health. J. N. Am. Benthol. Soc. 27, 605–625 (2008).

    Article  Google Scholar 

  50. 50

    Magrin, G. O. et al. Central and South America in Climate Change 2014: Impacts, Adaptation, and Vulnerability. Part B: Regional Aspects. Contribution of Working Group II to the Fifth Assessment Report of the Intergovernmental Panel of Climate Change (eds. Barros, V. R. et al.) 1499–1566 (Cambridge University Press, 2014).

  51. 51

    Lawaetz, A. & Stedmon, C. Fluorescence intensity calibration using the Raman scatter peak of water. Appl. Spectrosc. 63, 936–940 (2009).

    Article  ADS  CAS  PubMed  Google Scholar 

  52. 52

    Lakowicz, J. A. Principles of Fluorescence Spectrometry, 3rd ed. Springer, Heidelberg (2006).

  53. 53

    Murphy, K. et al. Measurement of dissolved organic matter fluorescence in aquatic environments: an interlaboratory comparison. Environ. Sci. Technol. 44, 9405–9412 (2010).

    Article  ADS  CAS  PubMed  Google Scholar 

  54. 54

    Kamjunke, N., Herzsprung, P. & Neu, T. R. Quality of dissolved organic matter affects planktonic but not biofilm bacterial production in streams. Sci. Total Environ. 506–507, 353–360 (2015).

    Article  ADS  CAS  PubMed  Google Scholar 

  55. 55

    Staudt, C., Horn, H., Hempel, D. C. & Neu, T. R. Volumetric measurements of bacterial cells and EPS glycoconjugates in biofilms. Biotechnol. Bioengineer. 88, 585–592 (2004).

    Article  CAS  Google Scholar 

  56. 56

    Simon, M. & Azam, F. Protein content and protein synthesis rates of planktonic bacteria. Mar. Ecol. Prog. Ser. 51, 201–213 (1989).

    Article  ADS  CAS  Google Scholar 

  57. 57

    Hertkorn, N. et al. Comparative analysis of partial structures of a peat humic and fulvic acid using one- and two-dimansional nuclear magnetic resonance spectroscopy. J. Environ. Qual. 31, 375–387 (2002)

    Article  CAS  PubMed  Google Scholar 

  58. 58

    Wishart, D. S., Bigman, C. G., Holm, A., Hodges, R. S. & Sykes, B. D. 1H, 13C, and 15N random coil NMR chemical shifts of the common amino acids. I. Investigations of nearest-neighbor effects. J. Biomol. NMR 5, 67–81 (1995).

    Article  CAS  PubMed  Google Scholar 

  59. 59

    Zhang, F. et al. Molecular and structural characterization of dissolved organic matter during and post cyanobacterial bloom in Taihu by combination of NMR spectroscopy and FTICR mass spectrometry. Wat. Res. 57, 280–294 (2014)

    Article  CAS  Google Scholar 

Download references


We thank S. Thaller and I. Locker for the preparation of the samples for NMR and FTICR-MS. The Confocal Laser Scanning Microscopy conducted by U. Kuhlicke was also greatly appreciated. The research was supported by FONDECYT project number 1130132 and German Academic Exchange service (DAAD). D. Graeber was partly supported by a grant from the Danish Centre for Environment – DCE, Aarhus University. Furthermore, we would like to thank Frederic Bartlett and Siobhan Filbey-Schidlack for correcting our English.

Author information




N.K. and J.N. designed the investigation. N.K., J.N., D.G., S.O., J.V., J.C.R. and S.W. did the field sampling, and P.H., M.H., P.S.-K., T.R.N. and N. H. performed subsequent measurements. N.K., J.N., P.H., M.H. and N.H. analysed the data and wrote the paper. All authors discussed the results and commented on the manuscript.

Corresponding author

Correspondence to Norbert Kamjunke.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Kamjunke, N., Nimptsch, J., Harir, M. et al. Land-based salmon aquacultures change the quality and bacterial degradation of riverine dissolved organic matter. Sci Rep 7, 43739 (2017).

Download citation

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.


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