Ecology and SocietyEcology and Society
 E&S Home > Vol. 26, No. 4 > Art. 43
The following is the established format for referencing this article:
Weinberger, F., S. Sundt, N. Staerck, C. Merk, R. Karez, and K. Rehdanz. 2021. Shifting beach wrack composition in the SW Baltic Sea and its effect on beach use. Ecology and Society 26(4):43.
https://doi.org/10.5751/ES-12759-260443
Research

Shifting beach wrack composition in the SW Baltic Sea and its effect on beach use

1GEOMAR Helmholtz Centre for Ocean Research, Marine Ecology Division, Kiel, Germany, 2Kiel University, Department of Economics, Kiel, Germany, 3Kiel Institute for the World Economy, Kiel, Germany, 4State Agency for Agriculture, Environment and Rural Areas Schleswig-Holstein, Flintbek, Germany

ABSTRACT

Beach visitors rate beach quality in large part by its appearance. Removal of natural beach litter (called beach wrack) has, therefore, high priority for beach managers in coastal areas dependent on revenues from tourism. Focusing on the German Baltic Sea coast, the amount of beach wrack has increased by a factor of approximately 3.4 between 1977 and 2012/2013. At the same time, the composition of macrophyte communities underwent a severe change from late successional stages (eelgrass and bladder wrack) toward more ephemeral communities. Correspondingly, the contribution of bladder wrack to seaweed litter alone dropped from 75% in 1977 to 18.1% today, while the contribution of ephemeral and nutrient-opportunistic seaweeds increased by a factor larger than 6.2 to approximately 44%. Such seaweed opportunists could have a higher potential for olfactorial nuisance than late successional macrophytes. To test this hypothesis, odors extracted from equal amounts of nutrient-opportunistic and non-opportunistic species that had been partially degraded under equal conditions were compared in a public survey. Participants graded the smell of opportunistic species, in particular Ceramium tenuicorne, consistently as more intense and less pleasant than the odor of non-opportunistic species. The particularly high potential of Ceramium litter and the relatively lower potential of eelgrass litter for deterrence were confirmed in field experiments. We conclude that the documented compositional shift in macrophyte communities at German Baltic Sea coasts since the onset of eutrophication has caused a shift of beach wrack composition toward species with a higher potential for olfactorial deterrence, which could explain recent concerns of beach managers about beach wrack despite the limited increase of biomass in the study area.
Key words: beach management; beach user behavior; beach wrack; coastal eutrophication; nuisance seaweed; seaweed odor

INTRODUCTION

In the Baltic Sea region, as worldwide, coastal tourism and beach recreation provide important employment opportunities and income (Haller et al. 2011; Pendleton 2007). In general, the perception of beach quality by the public is based upon appearance of the water and presence of litter pollution (Vaz et al. 2009, Williams and Barugh 2014). Beach management, therefore, usually gives high priority to the removal of any debris of anthropogenic or natural origin, typically by mechanical grooming, that causes considerable costs. For example, authorities in seaside resorts on the German Baltic Sea coast annually remove 269 kg litter per m of beach, which on average costs 38 € per m (Mossbauer et al. 2012). The annual removal of estimated 100,000 m³ of litter from beaches in Brittany, France, costs between 10 and 150 US$ per m³ (Charlier et al. 2008).[1]

Natural beach litter, also referred to as beach wrack, mostly consists of seaweed and sea grass in different stages of decay. Such beach wrack plays a key role in Baltic Sea shoreline ecosystems, providing important resources to organisms (Malm et al. 2004) and stabilizing soft bottom substrates. Frequent removal of such beach wrack by grooming reduces species richness and ecological diversity of sandy coasts and increases the risk of beach erosion (Defeo et al. 2009, Gilburn 2012, Malm et al. 2004, Vanhooren et al. 2011). There are, thus, good arguments for removing beach wrack less frequently.

However, accumulations of drifting macrophytes increasingly cause problems in beach environments worldwide and there is often compelling evidence for a direct connection between this increase and anthropogenic nutrient supply (Schramm and Nienhuis 1996, Smetacek and Zingone 2013, Valiela et al. 1997). Seaweed communities typically respond to eutrophication with shifts toward more nutrient-opportunistic components (Troell et al. 2005), which may result in an increased nuisance potential of beach wrack. Significant changes of macroalgal communities after eutrophication have also been observed and documented at the 402 km long Baltic Sea coast of Schleswig-Holstein (Schramm and Nienhuis 1996, Voigt and Schramm 1991, Weinberger et al. 2020), where 34.8 million of overnight stays and 58.5 million of day visitors generated revenues of 4200 million € in 2019, providing 83,130 persons with a primary income (Ostsee-Holstein-Tourismus e.V. 2020).

Since beach wrack removal is relatively costly and has a significant negative effect on shoreline ecosystems, information on the nuisance potential of beach wrack (and the necessity of its removal) is relevant for sustainable beach management. The aim of this paper is to provide such information, building on three different approaches. First, we investigate if beach wrack in the area underwent significant compositional change toward more ephemeral and nutrient-opportunistic components. Historical records of beach wrack in the Baltic Sea area are very scarce. A first quantitative study was conducted in August 1977 (Grave and Moeller 1982). It was based upon aerial black-and-white photography and detected 900 kg of dry biomass per km of Schleswig-Holstein's Baltic Sea beaches. A repetition of this study in 2012, using exactly the same approach, found 2 833 kg km-1, corresponding to an increase by a factor of 3.15 (Weinberger et al. 2020). An increase in this order of magnitude alone is unlikely to explain repeated media coverage and scientific publications (Mossbauer et al. 2012, Weinberger et al. 2020). However, compositional changes of beach wrack probably also occurred in the area, reflecting the documented change in species compositions of macroalgal habitats. We here report the results of an analysis of the recent beach wrack composition on Baltic Sea shores of Schleswig-Holstein and we describe changes since 1977. Second, we extract olfactorial compounds from different types of beach wrack and, monitoring their perception in a public survey, we test the hypothesis that nutrient-opportunistic macrophytes have a higher potential for olfactorial nuisance than those of later successional stages when they are present at similar density. Degrading beached biomass may release intensely odorous volatile compounds, and anoxic decomposition may even result in the production of toxic volatiles, such as hydrogen sulfide (H2S), at detrimental concentrations (Tauziède et al. 2009). In addition, repeated coverage by the media (Die Welt 2009, Lübecker Nachrichten 2013, Ostsee-Zeitung 2013, 2015, Schleswiger Zeitung 2015, DeutschlandfunkKultur 2018) suggests that the odor emitted by beach wrack constitutes an important component of its nuisance potential toward beach visitors. Third, we report results of an observational field study of beach visitors' behavior in response to different beach wrack which we had distributed at the beach.

METHODS

Analysis of beach wrack composition

To determine the quantity and composition of beach wrack along the Baltic Sea coast of the German state Schleswig-Holstein 13 sites were visited in 2012 and 2013 (Table 1). All selected sites were neither subject to beach cleaning, nor protected from waves by artificial infrastructures. Further, they represented the full salinity gradient and were characterized by various types of substratum composition and different main wind exposure directions. All sites were sampled in late summer (all but one in August, Table 1), to allow for a direct comparison with historical data obtained in August 1977 (Grave and Moeller 1982).

For samplings a point in the middle of the drift line marked by presence of beach wrack was selected randomly at each visited site. Two additional points in the drift line were marked in the exact distance of 10 m to the left and the right of the first point. At each of the three points, the width of the drift line was measured with a measuring tape. Furthermore, the ground cover of beach wrack within a sampling frame (size: 40 cm x 40 cm) was estimated at each point and its thickness was measured at five different positions within the frame. All beach wrack that fell within each frame was collected in plastic bags, transported to the lab, and stored in a freezer. For analysis, all samples were thawed, rinsed with seawater to remove sand, and sorted into phylogenetic groups (Fucus, other Phaeophyta, Zostera, Ulva, other Chlorophyta, Rhodophyta). The sorted material was dried at 70°C to weight constancy and weighed. The biomass density per m of coastline at the sampling sites was calculated by multiplication of biomass present within the frame, 2.5 to extrapolate from the frame size of 0.4 m to 1 m, and the drift line width. To calculate mean densities and compositions of beach wrack at the sampling sites, data obtained at the three sampling points were averaged.

We compared wind intensities and directions in our sampling area in 2012 and 2013 - as well as in the reference period 1977, as wind must be expected to drive wave action and thereby the accumulation of marine biomass on beaches (Fig. S1). Within the two months during and preceding the sampling periods (1st of July and 31st of August) the main wind directions were W and SE in 2012, and W and ENE in 2013 (Fig. S1a). During the same two months in 1977 less wind from W and considerably more wind from N, NE and E was recorded (Fig. S1a). The average wind speed was 6.0 m s-1 in 1977, but only 5.4 m s-1 in 2012 and 5.5 m s-1 in 2013. In particular, wind coming from SW, SE and N to E had higher average speeds in the reference period 1977 than in 2012 and 2013 (Fig. S1b). As a consequence, more air coming from sea (N to E) and less air coming from land (WNW to WSW) crossed the area in 1977 than in the latter two years (Fig. S1c, compare Fig. 2). This probably resulted in more wave impact on surveyed beaches during and immediately prior to the sampling period in 1977 than in 2012/2013.

Sampling of odorants from beach wrack

Six different macrophytes that are relatively frequent components of macroalgal blooms and beach wrack at the 13 sites were selected for extraction of odorous compounds. They represent the three main phylogenetic groups of marine macrophytes, namely Phaeophyta (Fucus vesiculosus and Dictyosiphon foeniculaceus), Chlorophyta (Zostera marina and Ulva compressa) and Rhodophyta (Agarophyton vermiculophyllum and Ceramium tenuicorne). These three groups are known to differ fundamentally in their biochemical composition (van den Hoek et al. 1995) and thereby potentially in their smell nuisance potential. Within each pair of species belonging to the same phylogenetic group, the second ones (D. foeniculaceus, U. compressa and C. tenuicorne) are relatively ephemeral, and short-lived. In contrast, the first ones (F. vesiculosus, Z. marina and A. vermiculophyllum) all have perennial life strategies. Of them, Z. marina and F. vesiculosus are the main components of late successional macrophyte communities in the study area (see introduction), while A. vermiculophyllum was relatively recently introduced (Weinberger et al. 2008).

Of each species visibly healthy and fresh material, free of other species and of epiphytized specimens, was collected, transported to the lab, and dried in a salad spinner. To obtain comparable degradation conditions portions of 400 g were placed into separate sealed ziplock bags and incubated together for 7 d at 22.6°C (variability: 20.9-25.9°C) in darkness. After this incubation, all macrophytes were dead and partially degraded. For extraction of odorants they were placed on gauze (mesh size: 1 mm) into a funnel and doused with 200 ml of 1,2-propandiol (BASF, Ludwigshafen/Germany). Solvent dripping from the biomass was collected for 4 min, loaded into Sniffin'Sticks (Burghart Messtechnik, Wedel/Germany) (Hummel et al. 1997) and stored at -20°C. For control purposes, additional Sniffin'Sticks were loaded with 50% butanol (Carl Roth, Karlsruhe/Germany) in water (Denzer et al. 2014).

Assessment of public perception of beach wrack odors

To test our hypothesis that nutrient-opportunistic macrophytes have a higher nuisance potential than those of later successional stages we designed a public survey. The survey consisted of two parts. In the first part, respondents were asked face-to-face about their perception of four different Sniffin'Sticks. Fig. 1 illustrates the test sequence with the four Sniffin'Sticks. All participants started by sniffing the same control stick and were asked to rate its intensity and pleasantness. We used a six-item scale for intensity (1 = no smell to 6 = very strong odor) and a seven-item scale for pleasantness (-3 = very unpleasant to +3 = very pleasant). Subsequently, participants were presented a Sniffin'Stick with odor extracted from brown, green or red seaweed and asked to rate its intensity and pleasantness. After using the control stick again to neutralize any odor, they were presented another Sniffin'Stick with odor extracted from a seaweed of the same phylogenetic group as the first but with an opponent life strategy and again asked to rate intensity and pleasantness. Except for the control stick, participants never received the same Sniffin'Stick twice. Fifty percent of the participants first received odor from an opportunist and vice versa for the remaining 50%. We distributed the different sequences of the sticks equally across genders. In the second part of the survey, respondents received a clipboard and had to fill out the remaining questions of the survey on their own. This second part of the survey included questions on socio-demographic characteristics.

We conducted the survey in summer 2016 in three places at the German Baltic Sea coast (Kiel, Eckernförde and Schönberg). In Kiel, we approached visitors at a major public festival ("Kiel Week") and asked them to participate. In Eckernförde and Schönberg, two popular seaside resorts, we asked beach visitors. Table S4 in the appendix provides descriptive statistics of our sample of respondents. Since we found no significant difference between the subsamples in terms of socio-demographic characteristics, we analyzed the three samples jointly. In order to control for differences in the respondents' overall ability to perceive odor, we normalized the odor intensity ratings. To do this, the rating of the control stick was subtracted from the ratings of the sticks with beach wrack extracts. The resulting normalized intensity ratings - as well as the pleasantness ratings - were tested for absence of statistically significant differences using repeated measures-2-way-ANOVA on ranks. As each participant rated odors of one nutrient-opportunistic and one non-opportunistic beach wrack species that both belonged to the same phylogenetic group, the group (green plants, brown algae or red algae) was used as between-subjects factor, while the life strategy (nutrient-opportunistic or non-opportunistic) was used as within-subjects factor.

Behavioral responses to beach wrack odor

To verify the different nuisance potentials of selected macrophytes, two experiments were conducted at a seaside resort, Eckernförde, that were based upon the manipulation of beach wrack and the subsequent hidden observation of the behavior of beach visitors. Located at the inner parts of a bay, Eckernförde has 4 km of sand beach that are a major source of income to this town of 22 000 inhabitants.

In experiment 1, two neighboring beach sections of (A) 106 m and (B) 30 m length that extended along the coastline southward and northward of the point 54°27.829'N 9°50.516'E were designated as experimental plots. On 17 August 2016, natural beach wrack already present on the site - consisting almost exclusively of eelgrass - was equally distributed with rakes along the drift line of both plots. This resulted in a 20-30 cm broad line of loose lying beach wrack with a mean fresh weight density of 333 g per m. In addition, plot B received 200 g per m of partially degraded Ceramium tenuicorne (for the resulting aspect see Fig. S1). This material originated from a macroalgal bloom at 54°25.397'N 10°23.832'E. It had been collected on 8 August 2016 with dip nets and stored for 9 d without water in light-tight plastic bags at ambient temperature (16°C, range 10°C to 20°C). The preparation of both plots was terminated at 11 am and the behavior of beach visitors was recorded from noon to 5 pm. The total number of persons present either on the beach or in the water was counted on each plot in time intervals of 30 min. In addition, the number of people stepping over the beach wrack, mostly swimmers leaving or entering the water, was also counted, as well as the number of persons staying for more than 30 s in a distance of less than 1 m of the beach wrack. Observations made within the same time interval on both plots were treated as connected samples and differences in these observations were tested for statistical significance using the t-test or alternatively the Wilcoxon signed ranks test if the assumption of data normal distribution was not fulfilled.

Natural beaching of drifting macrophytes was not observed during experiment 1, because the Baltic Sea is atidal and wind conditions were extremely calm (bf 1-2, coming from variable directions). In contrast, experiment 2, conducted on 18 and 19 August 2016, was realized with onshore wind on the first day (bf 2 to 5). This caused a steady accumulation of beach wrack (still nearly exclusively eelgrass, see Fig. S3 in appendix) on the shore, except for some sections that were protected by groynes. For this experiment, six new beach sections (33 m to 130 m long) were designated as experimental plots between the positions 54°28.038'N 9°50.446'E and 54°27.599'N 9°50.670'E. Two of these were mechanically cleaned on the morning of day 2 and remained free of beach wrack the entire day. On day 1 between 11:30 am and 4:30 pm and on day 2 between 10:30 am and 3:30 pm the behavior of beach visitors was recorded in intervals of 30 min as described above for experiment 1. In addition, the biomass present in all six plots was repeatedly recorded in intervals of approximately 2 h on both days. To do this the length and breadth of beach wrack present on the plot was measured and all biomass present on three randomly selected beach sections of 50 cm was collected, weighed with a spring scale and put back. The minimum and maximum biomass densities that were observed on single plots were 0 g per m and 15.6 kg per m (Fig. S3 in appendix). Their change in 30 min time intervals was estimated based upon differences between subsequent measurements. Best fitting linear functions were adapted to data distributions, using the Prism6 software (Graphpad, Golden/Co.). The t-test or in case of non-normal data distribution the U-test was used to compare behavior of beach users in absence of beach wrack and in presence of high concentrations of beach wrack.

RESULTS

Beach wrack composition

The sampling conducted on Schleswig-Holstein's Baltic Sea coast in late summer 2012 and late summer 2013 indicates that the composition of beach wrack is geographically highly diverse (Fig. 2, for the detailed data set see Tables S1 to S3 in appendix). However, similar species compositions were often found in both years within the same site. Sea grass and bladder wrack dominated beaches in the Northwestern coastal sections of the study area in both years, while various algal opportunists dominated in the Southeastern part of the coast. Filamentous red algae (primarily of the genus Ceramium, sometimes together with Vertebrata fucoides) and filamentous green algae (primarily of the genus Cladophora) contributed the overwhelming quantity of beach wrack in the South East, while the green algal genus Ulva (represented by Ulva compressa) dominated only one site located in the Kiel Fjord (Mönkeberg). Brown filamentous algae of the genera Pylaiella or Ectocarpus were the dominant beach wrack component at the most southern site (Brodtener Ufer) in 2012, but not in 2013. Additional components representing a wide spectrum of red seaweeds (genera Agarophyton, Delesseria, Coccotylus, Ahnfeltia, Furcellaria), brown seaweeds (Chorda, Dictyosiphon) and green seaweeds (Chaetomorpha) were occasionally detected at various sites, but not particularly abundant. The mean quantity of dried beach wrack along the coastline at the 13 visited sites was estimated to be approximately 4.0 kg m-1 in 2012 (Table S1 in appendix) and 2.4 kg m-1 in 2013 (Table S2 in appendix), the average of both years was 3.2 kg m-1 (Table S3 in appendix). Compared to 1977 (Grave and Möller 1982) the mean relative contribution of Fucus to beach wrack was significantly reduced in 2012 and 2013 (Fig. 3).

Perception of beach wrack odor nuisance potential

Survey respondents (Fig. 4A, Table S5) perceived the odor intensity of surface extracts generated from equal amounts of degrading macrophytes differently. They rated the odors of all three nutrient-opportunistic seaweeds as significantly more intense than odors of the corresponding non-opportunistic seaweeds of the same phylogenetic group. The mean rank difference between opportunists and non-opportunists was 1.03 on a scale ranging from 0 to 3. The odors of the opportunistic species Ceramium tenuicorne and Dictyosiphon foeniculaceus were rated as particularly intense, while extracts of the two non-opportunists Fucus vesiculosus and Zostera marina were rated as the least intense odors. The maximal rank difference (Ceramium vs. Zostera) was 1.66. The intensity also differed significantly between all three phylogenetic groups. The smell of red seaweeds was rated as the most intense and odors emitted by green macrophytes as the least intense. In addition, the pleasantness of odors emitted by opportunistic and non-opportunistic degrading macrophytes was perceived differently: the opportunists' smell was perceived as significantly less pleasant (Fig. 4B, Table S6). Moreover, the two red seaweeds, Ceramium tenuicorne and Agarophyton vermiculophyllum, emitted more deterrent odors than the two brown seaweeds or the two green macrophytes. On average, odor emitted by the two late successional species Fucus vesiculosus and Zostera marina was rated as neutral (close to zero), but the smell of the opportunistic C. tenuicorne clearly as unpleasant (close to -1).

Experimental verification of nuisance potential

Avoidance of a whole beach section treated with C. tenuicorne at a density of 200 g m-1 in addition to eelgrass at 333 g m-1 was not observed and the contaminated section was even visited by significantly more persons than the neighboring uncontaminated section, which only harbored 333 g m-1 of eelgrass (paired t-test: p = 0.0122; see Fig. 5A). Moreover, the willingness of beach visitors to step over the beach wrack was not significantly reduced when Ceramium was present (Wilcoxon matched pairs signed ranks test: p = 0.8457; Fig. 5B). However, three beach visitors in the section with Ceramium contamination were overheard complaining to each other about the smell of the beach wrack and the readiness of persons to stay in the close vicinity of this beach wrack was significantly reduced (paired t-test: p = 0.0276; Fig. 5C).

In contrast, presence of eelgrass alone had relatively little influence on the behavior of beach visitors (Fig. S4 in appendix). Their readiness to cross this beach wrack even at the highest densities of 2.2 to 15.6 kg m-1 was not lower than their readiness to cross a drift line without any biomass (Mann-Whitney test: p = 0.6009, Fig. 6A, see also Fig. S3 in appendix). Only the readiness to stay in the close vicinity of beached eelgrass at such high densities decreased significantly (t-test: p = 0.0071, Fig. 6B), suggesting that C. tenuicorne beach wrack raised avoidance behavior in beach users at a lower concentration than Z. marina beach wrack.

DISCUSSION

Beach wrack producing macrophytes have been abundant habitat formers in Baltic Sea environments even before the onset of industrialization. Eelgrass (Zostera marina) typically formed extended meadows in close vicinity to the shore (Lehmann 1814) and one eelgrass shoot litters 6 to 30 leaves per year (Mateo et al. 2007). Correspondingly, large accumulations of eelgrass litter have already been observed 200 years ago in the region (Lehmann 1814). Another important component of beach litter in Baltic Sea environments is bladder wrack (Fucus vesiculosus), which is buoyant and drifts after detachment over long distances before it finally accumulates onshore (Rothäusler et al. 2015). In 1977 F. vesiculosus contributed 75% of the beach wrack on Schleswig-Holstein's Baltic Sea coast (Grave and Möller 1982).

Increasing amounts of drifting seaweeds are typically observed in coastal regions that are subject to particularly severe eutrophication, such as Brittany (Charlier et al. 2008) or northern central China (Zhou et al. 2015). Furthermore, in many cases the long-term temporal dynamics of macroalgal blooms reflect increases (Schramm and Nienhuis 1996) and decreases (Beusekom et al. 2009) in eutrophication. However, not all marine macrophytes benefit equally from nutrient supply. Ephemeral nutrient-opportunistic species that are capable of rapid nutrient uptake and rapid growth, but largely devoid of stored nutrient resources are typically limited by external nutrient supply. In contrast, slow-growing and long-living perennial macrophytes, such as Zostera or Fucus, that form the late successional stages of macrophyte habitats benefit much less from eutrophication (Bokn et al. 2003, Pedersen and Borum 1997, Pedersen et al. 2010).

This has also been observed and documented at the Baltic Sea coasts, where massive increases of nitrogen and phosphorous input occurred between 1965 and 1985, followed by only partial reductions (Fleming-Lehtinen et al. 2008, Lennartz et al. 2014). Subsequently, the typical late successional vegetation of shallow water was severely reduced in this area, due to increased competition with fast-growing nutrient opportunists: The standing stock of bladder wrack (Fucus vesiculosus) was reduced by 95% (Vogt and Schramm 1991) and local decreases were also reported for eelgrass (Zostera marina) (Messner and von Oertzen 1991). At the same time, various nutrient-opportunistic seaweeds became more abundant and the total standing stock of macrophytes rather increased (Schramm and Nienhuis 1996).

The data presented here hint at considerable variability in the distribution of beach wrack along the Baltic Sea coasts of Schleswig-Holstein, which was already detected in 1977 (Grave and Möller 1982). However, the average beach wrack quantity detected in late summer in 2012 and 2013 (3.2 kg m-1) corresponds with an increase by a factor of approximately 3.4 since 1977 (0.9375 kg m-1, Grave and Moeller 1982). Our estimate, based upon dry matter determination, is approximately in the same order of magnitude as the estimated increase by a factor of 3.1 that was observed earlier based on aerial photography (Weinberger et al. 2020).

Grave and Möller (1982) provided no information about exact sampling dates and it is for this reason impossible to precisely compare the impact of wind speed and wind direction on quantities of beached biomass in 1977 and 2012/2013. However, altogether a stronger exposure of the studied coastal sections to northerly onshore winds was observed in July/August 1977 than in July/August 2012/2013 (Fig. S1) and this difference is reflected in a particularly high beach wrack density in coastal sections exposed toward north in 1977 (Grave and Möller 1982), but not in 2012 and 2013 (Fig. 2). These observations confirm that air exposure in July and August correlates to some degree with beach wrack accumulation in August. The higher detected amounts of biomass in 2012/2013 may then not simply be explained with higher coastal wind exposure during these years, given that this exposure was overall higher in 1977 (Fig. S1), and other causes must have brought about the difference.

Evidence for these causes can be found in the fact that the composition of beach wrack in our study area changed much more than the total amount. (Fig. 3, see also Tabs. S1 to S3 in appendix): In 1977 Fucus contributed on average 75% of the beach wrack at 10 sites between Flensburg and Neustadt that were investigated (Grave and Möller 1982), while its contribution in 2012 and 2013 was reduced to 21% and 14%, respectively. As eutrophication has caused a reduction in the depth distribution of Fucus by approximately 50% since 1976/1978 (Schories et al. 2009; Vogt and Schramm 1991), the standing stock of the species has declined drastically (Schories et al. 2009; Vogt and Schramm 1991), and this is clearly reflected in beach wrack compositions. However, although a similar decline in the standing stock has been observed for eelgrass (Schories et al. 2009) this is not reflected in the quantities that are beached in Schleswig-Holstein. Instead, they rather increased by a factor of at least 4 to 5 (1977: less than 0.23 kg per m, 2012: 1.45 kg per m, 2013: 0.96 kg per m). It currently remains unclear whether this reflects (i) a recovery of the standing stock; (ii) a higher turnover rate (e.g., more production and littering of leaves) than in 1977; or rather (iii) an upward movement of eelgrass within the depth gradient due to increased light limitation (Schramm and Nienhuis 1996), which could bring it into the closer vicinity of beaches. Similar to eelgrass, all other macrophytes except of Fucus also increased. As Grave and Möller (1982) did not distinguish between eelgrass and other algae than Fucus, we have no exact information on the relative contribution of both groups in 1977. In 2012/2013, the group of "other algae" was mainly composed of ephemeral and nutrient-opportunistic red and green filamentous macrophytes of the genera Ceramium, Vertebrata and Cladophora. Each of the two groups (red and green filamentous algae) contributed approximately 20% to the total amount of beach wrack (Tabs. S1 to S3 in appendix), which confirms earlier reports of increasing standing stocks of Ceramium tenuicorne in the area (Schramm and Nienhuis 1996). Interestingly, the genus Ulva was much less abundant, although it is by far the most abundant nuisance seaweed on a global scale (Smetacek and Zingone 2013) and ecological impact of Ulva blooms in the region has been observed on a local scale (Steinhagen et al. 2018). Taken together, the total amount of "other algae", consisting primarily of ephemeral species today, increased from less than 0.225 kg per m in 1977 (Grave and Moeller 1982) to 1.4 kg per m in 2012/2013 (Tab S3 in appendix). This hints at an increase by a factor of at least 6.2. However, given that the value observed in 1977 also, and probably mainly, included eelgrass the true increase of opportunistic seaweeds in the region was probably much more drastic.

To test our hypothesis that nutrient-opportunistic macrophytes have a higher nuisance potential than those of later successional stages when they are present at similar density, we extracted the olfactorial compounds of three nutrient-opportunistic and three non-opportunistic species that had been partially degraded under equal conditions. In a survey, we found that people consistently rated the smell of equal amounts of nutrient-opportunistic species, in particular Ceramium tenuicorne, as more intense and less pleasant than the odor of non-opportunistic species. In particular, odors extracted from the two native perennial species F. vesiculosus and Z. marina, that have already contributed large amounts of beach wrack in the area prior to the onset of eutrophication (Lehmann 1814), were mostly perceived as smelling rather faint and as neutral in pleasantness. The decomposition rate of beach-cast seaweeds is species-specific (Mews et al. 2007). Nutrient-opportunists in the Baltic Sea are generally characterized by larger surface/volume-ratios than non-opportunists (Wallentinus 1984) and they can for this reason be expected to degrade more rapidly, which may explain their higher potential for olfactorial nuisance.

The particularly high potential of Ceramium litter and the relatively lower potential of eelgrass litter for deterrence was confirmed in field experiments, observing beach visitors' behavior toward beach wrack of known composition and quantity. In these experiments, we measured the combined effect of beach wrack odor and appearance. Eelgrass alone generated a reduced willingness of beach visitors to linger at the water line only when it was present at relatively high concentrations above 2.2 kg per m. In contrast, only 0.2 kg per m of Ceramium litter mixed with 0.3 kg per m of eelgrass litter was sufficient to cause the same effect. Further, beach visitors were only heard complaining about beach wrack in general and about its odor in particular when Ceramium was present. Based on these observations, and because the odor of Ceramium litter was rated as particularly intense and unpleasant in our survey, we conclude that odor is an important determinant of deterrence by beach wrack, and potentially more important than its appearance.

SPECULATION

Our comparison of beach wrack composition at German Baltic Sea coasts today with the reference study from 1977 suggests a shift toward more nutrient opportunistic species. Such a change would be expected in principle and appears credible despite the limited availability of historical data, because corresponding changes in the composition of algal habitats in the study area are well documented. At the same time our study of olfactorial perception hints at a higher olfactorial nuisance potential of nutrient opportunistic drift seaweed. Thus, the eutrophication of German Baltic Sea coasts has caused a shift of beach wrack composition toward species with a higher potential for olfactorial deterrence, which could explain recent concerns of local coastal managers despite the limited increase of beached biomass in the study area. A significant reduction of Baltic Sea nutrient levels in the years to come might reverse this trend. However, given that eelgrass litter alone had a deterrent effect when it was present at elevated concentrations its removal from beaches may still be necessary even in a less eutrophicated Baltic Sea environment, despite its importance for the ecosystem. Our study was conducted with selected species from the German Baltic Sea coast. Most other sea areas offer different environmental conditions and harbor different algal species inventories. As a consequence, the specific nuisance potential of SW Baltic Sea beach wrack may not be identical to beach wrack in other areas. However, we predict a more or less general validity of our observation that beach wrack composed of nutrient opportunistic algal species has a relatively higher nuisance potential than beach wrack composed of late successional macrophytes.

__________
[1] The removed material generally ends up in landfills. To reduce costs for removal opportunities to use the material for energy production, as fertilizer or bio-based compost are discussed (see, e.g., Chubarenko et al. 2021 or Kupczyk et al. 2021).

RESPONSES TO THIS ARTICLE

Responses to this article are invited. If accepted for publication, your response will be hyperlinked to the article. To submit a response, follow this link. To read responses already accepted, follow this link.

ACKNOWLEDGMENTS

The authors are thankful to the cities of Eckernförde and Schönberg for permissions and support with the survey. In particular, Stefan Borgmann (Tourism Management Eckernförde) was extremely supportive, as he also permitted and facilitated the field study. Further, we thank three reviewers for their helpful comments on an earlier version of the paper. This study was supported by the DFG cluster of excellence "Future Ocean" at Kiel (grant number CP1515).

DATA AVAILABILITY

The data that support the findings of the olfactorial survey described in this study are available on request from the corresponding author, F. W. These data are not publicly available because they contain information that could compromise the privacy of research participants. All other data are included in the paper and its annex. The ethical responsibility of this study - in particular with regard to the handling of personal data - was affirmed by the Central Ethics Committee of Kiel University.

LITERATURE CITED

Bokn, T., C. M. Duarte, M.F. Pedersen, N. Marbà, F. Moy, C. Barrón, B. Bjerkeng, J. Borum, H. Christie, S. Engelbert, F. L. Fotel, E. E. Hoell, R. Karez, K. Kersting, P. Kraufvelin, C. Lindblad, M. Olsen, K. A. Sanderud, U. Sommer, and K. Sörensen. 2003. The response of experimental rocky shore communities to nutrient addition. Ecosystems 6:577-594. https://doi.org/10.1007/s10021-002-0108-6

Charlier, R.H., P. Morand, and C.W. Finkl. 2008. How Brittany and Florida coasts cope with green tides. International Journal of Environmental Studies 65:191-208. https://doi.org/10.1080/00207230701791448

Chubarenko B., Woelfel J., Hofmann J., Aldag S., Beldowski J., Burlakovs J., Garrels T., Gorbunova J., Guizani S., Kupczyk A., Kotwicki L., Domnin D., Gajewska M., Hogland W., Kołecka K., Nielsen J., and Schubert H. Converting beach wrack into a resource as a challenge for the Baltic Sea (an overview). 2021 Ocean & Coastal Management. Vol. 200. 105413. https://doi.org/10.1016/j.ocecoaman.2020.105413

Defeo, O., A. Mclachlan, D.S. Schoeman, T. A. Schlacher, J. Dugan, A. Jones, M. Lastra, and F. Scapini. 2009. Threats to sandy beach ecosystems: A review. Estuarine, Coastal and Shelf Science 81:1-12. https://doi.org/10.1016/j.ecss.2008.09.022

Denzer, M. Y., S. Gailer, D. W. Kern, L.P. Schumm, N. Thuerauf, J. Kornhuber, A. Buettner, and J. Beauchamp. 2014. Quantitative Validation of the n-Butanol Sniffin'Sticks Threshold Pens. Chemosensory Perception 7:91-101. https://doi.org/10.1007/s12078-014-9168-1

DeutschlandfunkKultur. 2018. Treibsel als natürliche Ressource - Wie Seegras und Algen zu Kissen und Dünger werden. Broadcasted 24.7.2018. https://www.deutschlandfunkkultur.de/treibsel-als-natuerliche-ressource-wie-seegras-und-algen-zu.976.de.html?dram:article_id=423689

Die Welt. 2009. Wege aus der stinkenden Algenplage an der Ostsee. Edition from 20.2.2009. https://www.welt.de/wissenschaft/article3240109/Wege-aus-der-stinkenden-Algenplage-an-der-Ostsee.html. Accessed 30 June 2019

Fleming-Lehtinen, V., M. Laamanen, H. Kuosa, H. Haahti, and R. Olsonen. 2008. Long-term development of inorganic nutrients and chlorophyll alpha in the open Northern Baltic Sea. Ambio 37:86-92. https://doi.org/10.1579/0044-7447(2008)37[86:ldoina]2.0.co;2

Gilburn, A.S. 2012. Mechanical grooming and beach award status are associated with low strandline biodiversity in Scotland. Estuarine, Coastal and Shelf Science 107:81-88. https://doi.org/10.1016/j.ecss.2012.05.004

Grave, H., and H. Moeller. 1982. Quantification of dead marine plant biomass along the Baltic Sea coast of Western Germany. Helgoländer Meeresuntersuchungen 35:517-519. https://doi.org/10.1007/BF01999139

Haller, I., N. Stybel, S. Schumacher, and M. Mossbauer. 2011. Will Beaches be enough? Future Changes for Coastal Tourism at the German Baltic Sea. Journal of Coastal Research Special Issue: 70-80. https://doi.org/10.2112/SI61-001.68

Hummel, T., B. Sekinger, S.R. Wolf, E. Pauli, and G. Kobal. 1997. 'Sniffin'sticks': olfactory performance assessed by the combined testing of odor identification, odor discrimination and olfactory threshold. Chemical Senses 22:39-52. https://doi.org/10.1093/chemse/22.1.39

Kupczyk, A., Kołecka K., Gajewska M. 2019. Solving the beach wrack problems by on-site treatment with reed beds towards fertilizer amendments. Journal of Ecological Engineering. Vol. 20(8):252-261. https://doi.org/10.12911/22998993/111717

Lehmann, M.S.S. 1814. Der entdeckte Nutzen des Seegrases zum Füllen der Küssen und Polster. Sehnbothe, Kopenhagen, 28 pp.

Lennartz, S.T., A. Lehmann, J. Herrford, F. Malien, H.P. Hansen, H. Biester, and H.W. Bange. 2014. Long-term trends at the Boknis Eck time series station (Baltic Sea), 1957-2013: does climate change counteract the decline in eutrophication? Biogeosciences 11:6323-6339. https://doi.org/10.5194/bg-11-6323-2014

Lübecker Nachrichten. 2013. Seegras: Natur pur oder stinkender Unrat? Edition from 5.8.2013. https://www.ln-online.de/Lokales/Nordwestmecklenburg/Seegras-Natur-pur-oder-stinkender-Unrat Accessed 30 June 2019

Malm, T., S. Raberg, S. Fell, and P. Carlsson. 2004. Effects of beach-cast cleaning on beach quality, microbial food web, and littoral macrofaunal biodiversity. Estuarine Coastal and Shelf Science 60: 339-347. https://doi.org/10.1016/j.ecss.2004.01.008

Mateo, M.A., J. Cebri�n, K. Dunton, and T. Mutchler. 2007. Carbon flux in seagrass ecosystems. In Seagrasses: Biology, Ecology and Conservation. (ed. by A.W.D. Larkum, R.J. Orth, and C. Duarte), pp. 158-192.

Messner, U., and J.A. Von Oertzen. 1991. Long-term changes in the vertical distribution of macrophytobenthic communities in the Greifswalder Bodden. Acta Ichthyologica et Piscatoria 21:135-143. https://doi.org/10.3750/AIP1991.21.S.14

Mews, M., M. Zimmer, and D. E. Jelinski. 2007. Species-specific decomposition rates of beach-cast wrack in Barkley Sound, British Columbia, Canada. Marine Ecology Progress Series 328:155-160. https://doi.org/10.3354/meps328155

Mossbauer, M., I. Haller, S. Dahlke, and G. Schernewski. 2012. Management of stranded eelgrass and macroalgae along the German Baltic coastline. Ocean & Coastal Management 57:1-9. https://doi.org/10.1016/j.ocecoaman.2011.10.012

Ostsee-Holstein-Tourismus e.V. 2020. Erfolgreiche Ostsee: Erhebliche Zuwächse in den letzten fünf Jahren an der Ostsee Schleswig-Holsteins. https://www.presseportal.de/pm/59512/4731046 Accessed 27 June 2021

Ostsee-Zeitung. 2013. Algen-Plage: Urlauber ekeln sich. Edition from 24.7.2013. https://www.ostsee-zeitung.de/Mecklenburg/Rostock/Algen-Plage-Urlauber-ekeln-sich. Accessed 30 June 2019

Ostsee-Zeitung. 2015. Stinkende Algen werden zum Problem. Edition from 9.6.2015. https://www.ostsee-zeitung.de/Vorpommern/Ruegen/Stinkende-Algen-werden-zum-Problem. Accessed 30 June 2019

Pedersen, M.F. and J. Borum. 1997. Nutrient control of estuarine macroalgae: growth strategy and the balance between nitrogen requirements and uptake. Marine Ecology-Progress Series 161:155-163. https://doi.org/10.3354/meps161155

Pendleton, L.H. 2007. The Economic and Market Value of Coasts and Estuaries: What's At Stake? Restore Americas Estuaries, Arlington, VA. 175 pp.

Rothäusler E, H. Corell, and V. Jormalainen. 2015. Abundance and dispersal trajectories of floating Fucus vesiculosus in the Northern Baltic Sea. Limnology and Oceanography 60:2173-2184 https://doi.org/10.1002/lno.10195

Schleswiger Nachrichten. 2015. Stinkendes Seegras an der Ostsee nervt Touristen. Edition from 31.7.2015. https://www.shz.de/10344831. Accessed 30 June 2019

Schories, D., C. Pehlke, and U. Selig. 2009. Depth distributions of Fucus vesiculosus L. and Zostera marina L. as classification parameters for implementing the European Water Framework Directive on the German Baltic coast. Ecological Indicators 9:670-680. https://doi.org/10.1016/j.ecolind.2008.08.010

Schramm, W., and P.H. Nienhuis. 1996. Marine benthic vegetation. Recent changes and the effects of eutrophication. In: Marine benthic vegetation. Recent changes and the effects of eutrophication. Springer-Verlag, Berlin (Germany), 470 pp. https://doi.org/10.1007/978-3-642-61398-2

Smetacek, V. and A. Zingone. 2013. Green and golden seaweed tides on the rise. Nature 504:84-88. https://doi.org/10.1038/nature12860

Steinhagen, S., F. Weinberger, and R. Karez. 2018. Molecular analysis of Ulva compressa (Chlorophyta, Ulvales) reveals its morphological plasticity, distribution and potential invasiveness on German North Sea and Baltic Sea coasts. European Journal of Phycology 54:102-114. https://doi.org/10.1080/09670262.2018.1513167

Tauziède, C., A. Morin, H. Biaudet, A. Hervé, N. Chatellier, C. Villey, Y. Dupuis, and K. Adam. 2009. Résultats des mesures ponctuelles des émissions d'hydrogène sulfuré et autres composés gazeux potentiellement toxiques issues de la fermentation d'algues vertes (ulves). INERIS document nr. DRC-09-108407-10226A, 15pp.

Troell, M., L. Pihl, P. Rönnbäck, H. Wennhage, T. Söderqvist and N. Kautsky. 2005. Regime shifts and ecosystem services in Swedish coastal soft bottom habitats: when resilience is undesirable. Ecology and Society 10(1):30. http://www.ecologyandsociety.org/vol10/iss1/art30/ https://doi.org/10.5751/ES-01374-100130

Valiela, I., J. Mcclelland, J. Hauxwell, P.J. Behr, D. Hersh and K. Foreman. 1997. Macroalgal blooms in shallow estuaries:Controls and ecophysiological and ecosystem consequences. Limnology and Oceanography 42:1105-1118. https://doi.org/10.4319/lo.1997.42.5_part_2.1105

van Beusekom, J.E.E., P.V.M. Bot, J. Carstensen, J.H.M. Goebel, H. Lenhart, J. P�tsch, T. Petenati, T. Raabe, K. Reise, and B. Wetsteijn. (2009) Eutrophication.Thematic Report No. 6. Common Wadden Sea Secretariat, Trilateral Monitoring and Assessment Group, Wilhelmshaven 22 pp.

van den Hoek C., D. G. Mann, H.M. Jahns. 1995. Algae: An Introduction to Phycology. Cambridge University Press, 623 pp.

Vanhooren, S., H. Maelfait and K. Belpaeme. 2011. Moving Towards an Ecological Management of the Beaches. Journal of Coastal Research SI61:81-86. https://doi.org/10.2112/SI61-001.70

Vaz, B., A. T. Williams, C.P. Da Silva and M. Phillips. 2009. The importance of user's perception for beach management. Journal of Coastal Research: 1164-1168.

Vogt, H., and W. Schramm. 1991. Conspicuous decline of Fucus in Kiel Bay (Western Baltic): what are the causes? Marine Ecology-Progress Series 69:189-194. https://doi.org/10.3354/meps069189

Wallentinus I. 1984. Comparisons of nutrient uptake rates for Baltic macroalgae with different thallus morphologies Marine Biology 80:215-225. https://doi.org/10.1007/BF02180189

Weinberger, F., B. Buchholz, R. Karez and M. Wahl. 2008. The invasive red alga Gracilaria vermiculophylla in the Baltic Sea: adaptation to brackish water may compensate for light limitation. Aquatic Biology 3: 251-264. https://doi.org/10.3354/ab00083

Weinberger, F., T. Paalme, and S.A. Wikström. 2020. Seaweed resources of the Baltic Sea, Kattegatt and German and Danish North Sea coasts. Botanica Marina 63:61-72. https://doi.org/10.1515/bot-2019-0019

Williams, A. T., and A. Barugh. 2014. Beach user perceptions at the eastern Yucatan peninsula, Mexico Journal of Coastal Research 70:426-430. https://doi.org/doi:10.2112/si70-072.1

Zhou, Y. P., L. J. Tan, Q. T. Pang, F. Li and J. T. Wang. 2015. Influence of nutrients pollution on the growth and organic matter output of Ulva prolifera in the southern Yellow Sea, China Marine Pollution Bulletin 95:107-114. https://doi.org/10.1016/j.marpolbul.2015.04.034

Correspondent author:
Florian Weinberger
fweinberger@geomar.de
Jump to top
Table1  | Figure1  | Figure2  | Figure3  | Figure4  | Figure5  | Figure6  | Appendix1