Consumption rates and prey preference of the invasive gastropod Rapana venosa in the Northern Adriatic Sea
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The alien Asian gastropod Rapana venosa (Valenciennes 1846) was first recorded in 1973 along the Italian coast of the Northern Adriatic Sea. Recently, this predator of bivalves has been spreading all around the world oceans, probably helped by ship traffic and aquaculture trade. A caging experiment in natural environment was performed during the summer of 2002 in Cesenatico (Emilia-Romagna, Italy) in order to estimate consumption rates and prey preference of R. venosa. The prey items chosen were the Mediterranean mussel Mytilus galloprovincialis (Lamarck 1819), the introduced carpet clam Tapes philippinarum (Adams and Reeve 1850), both supporting the local fisheries, and the Indo-Pacific invasive clam Anadara (Scapharca) inaequivalvis (Bruguière 1789). Results showed an average consumption of about 1 bivalve prey per day (or 1.2 g wet weight per day). Predation was species and size selective towards small specimens of A. inaequivalvis; consumption of the two commercial species was lower. These results might reduce the concern about the economical impact on the local bivalve fishery due to the presence of the predatory gastropod. On the other hand, selective predation might probably alter local community structure, influencing competition amongst filter feeder/suspension feeder bivalve species and causing long-term ecological impact. The large availability of food resource and the habitat characteristics of the Emilia-Romagna littoral makes this area an important breeding ground for R. venosa in the Mediterranean Sea, thus worthy of consideration in order to understand the bioinvasion ecology of this species and to control its likely further dispersal.
KeywordsRapanavenosa Gastropod Introduced species Predation Northern Adriatic Sea
The Asian whelk Rapana venosa (Valenciennes 1846) was unintentionally introduced along the Northern Adriatic littoral in the 1970s (Ghisotti 1974). This gastropod is a successful invader of marine coastal/brackish ecosystems, being tolerant to wide variations in temperature, salinity and oxygen concentration (Zolotarev 1996; Mann and Harding 2003). Moreover, throughout spring and summer this dioecious species produces a large number of planktonic veliger larvae which persist in the water column for a minimum of 14 to a maximum of 80 days prior settlement on the sea bottom (ICES 2004), thus granting high dispersal opportunity (Savini and Occhipinti Ambrogi 2004). Its native distribution includes the Sea of Japan, Yellow Sea, Bohai Sea and the East China Sea to Taiwan (Lai and Pan 1980; Tsi et al. 1983). The whelk has been spreading very fast in the last century when it colonised the Black Sea since 1947 (Drapkin 1953), the Adriatic Sea since 1973 (Ghisotti 1974), the Aegean Sea since 1990 (Koutsoubas and Voultsiadou-Koukoura 1991), the American Atlantic Sea/ Chesapeake Bay since 1998 (Harding and Mann 1999), and the South Atlantic/Bahia Samborombon, Uruguay and Argentina since 1999 (Pastorino et al. 2000). Few live specimens were reported also for the Tyrrhenian Sea (Terreni 1980; Paolini 1987) and the Northern Atlantic coasts of France/Quiberon Bay (Goulletquer 2000). Ballast water transport was claimed as the main vector of introduction for the species (ICES 2004), although trade of bivalve stocks and spat could represent an additional important dissemination route (Goulletquer 2002).
This large (up to 160 mm shell length) predatory gastropod is considered a pest; it has been causing the depletion of large stocks of commercial bivalves (oysters, mussels, and clams) in the Black Sea since the 1950s (Drapkin 1963; Ciuhcin 1984; Zolotarev 1996). So far, no similar threats to the ecosystem were reported in the other localities of introduction, but the international scientific community agrees in considering R. venosa a dangerous alien species for which study efforts should be prioritised (ICES 2004).
Since 2001, our research group is conducting baseline investigations in order to understand R. venosa distribution, population structure, and ecology in Italian waters. The aim of our study is the preparation of a risk assessment protocol for managing R. venosa bioinvasion, foreseeing further spreading, defining risk levels and thresholds of risk acceptability.
A very important step forward in defining the protocol is represented by understanding the complexity of biotic interactions, such as predation and competition, between the invasive gastropod and the benthic community; these interactions need to be quantified for a reliable evaluation of the ecological impact of the gastropod in the recipient ecosystem.
Investigations conducted by Harding and Mann (1999) in the Chesapeake Bay showed that R. venosa occupies an important position as a secondary consumer in the native food web of coastal ecosystem, preying on native filter feeders and suspension feeders bivalves. It was shown experimentally that, differing from other muricids, this gastropod preys only on live specimens avoiding carrions; an adult specimen of 140 mm length is capable of consuming an 80 mm shell length clam in less than 1 h. Feeding experiments showed preferences for local hard clams (Mercenaria mercenaria) while other bivalves such as Crassostrea virginica, Mya arenaria and Mytilus edulis were eaten only when M. mercenaria were unavailable. Large R. venosa (101–160 mm shell length) were able to consume on average 1.5 g of M. mercenaria (wet weight) per day at a water temperature of approximately 26°C (Savini et al. 2002).
According to the optimal foraging theory (Hughes 1980), R. venosa could behave as a “pursuer” that searches for specific prey, thus maximizing its net rate of energy intake spending much time in handling a specific prey than searching for general prey species. The introduction of a new predator would cause complex structural changes in the community, directly influencing population density, distribution and growth of the preferred prey and indirectly modifying interspecific relationships amongst local prey species. It is largely recognised that when an alien species finds optimal conditions for its growth and reproduction (i.e. large availability of food and a suitable habitat for reproduction), the lack of an efficient control on it by competitors/predators could determine a collapse of the entire trophic web; well-known examples of such situations are the bioinvasion of the comb jelly Memniopsis leidyi in the Black Sea/Caspian Sea (Shiganova et al. 2001; Shiganova et al. 2003) or of the European green crab Carcinus maenas along the coasts of United States and Australia (Grosholz and Ruiz 1995; Walton et al. 2002).
In this paper, we present the results of an experimental investigation aiming at quantifying R. venosa consumption rates and prey preferences in Cesenatico (Emilia-Romagna, Italy), a locality in the Northern Adriatic Sea, where the gastropod has been showing a constant increase in population density (Savini et al. 2004; Savini and Occhipinti Ambrogi, unpublished data). Our hypotheses is that R. venosa could act as a pursuer also in our study area, where, due to the local abundance of different potential bivalve prey, food availability is not a limiting factor. This preliminary investigation on the dietary requirement of R. venosa would represent a starting point for understanding the potential ecological impact of this species in the Northern Adriatic Sea.
Materials and methods
The hard bottom community living on the artificial limestone reefs is characterised in larger proportion by the Mediterranean mussel Mytilus galloprovincialis, and in lower proportion by the flat oyster Ostrea edulis and the introduced Pacific oyster Crassostrea gigas (Savini and Occhipinti Ambrogi unpublished data).
T. philippinarum: 10 ind. SC1 = 15–30 mm SL; 10 ind. SC2 = 31–45 mm SL
A. inaequivalvis: 10 ind. SC1 = 15–30 mm SL; 10 ind. SC2 = 31–45 mm SL
M. galloprovincialis: 5 ind. SC1 = 20–60 mm SL; 5 ind. SC2 = 61–90 mm SL
Starting from May 1st 2002, for an experimental period of 44 days, enclosures were examined two-three times a week by scuba diving, removing and measuring (calliper: 0.1 mm) the empty shells of all prey eaten. In the same occasions, bivalves consumed were replaced with prey of similar dimensions thus maintaining constant prey/size availability. Water temperature (mercury thermometer) and salinity (portable refractometer) values were recorded in the experimental cages at each control.
A size range of 50 bivalve specimens for each prey species was collected by scuba diving both on sandy bottom (A. inaequivalvis: 17–57 mm SL; T. philippinarum: 22–37 mm SL) and rocky reefs (M. galloprovincialis: 20–65 mm SL). Samples were individually measured (shell length, mm) and weighed prior the removal of the soft tissue; soft tissue was weighted (wet weight, g) to the nearest 0.1 g. Data were utilised for elaborating prey size/weight relationships.
Prey density at the study site was estimated by random quadrate sampling. T. philippinarum and A. inaequivalvis population densities were computed digging out and counting the number of bivalves collected in square frame (side: 50 cm) randomly flung on the sea bottom at low tide per 35 spatial replicates. M. galloprovincialis density was assessed by scuba diving along the limestone reefs of Cesenatico, scraping a 15 × 15 surface (in 24 replicates) of the mussel community in a steel sampling net (0.5 mm mesh).
Data analysis was performed utilizing the multivariate techniques described by Roa (1992) for multiple-choice feeding-preference experiments. An analogous of Quade’s (1979) statistic test, the Friedman test (Conover 1999) was applied to the data set using the software StatsDirect Version 2.4.5. Linear regression analysis between linear and non-linear parameters (i.e. length/weight relationships) were performed using the software Minitab 12.0 Student Edition; data were log10 transformed in order to normalise/homogenise variances; significance levels for all statistical tests were established at P = 0.05 a priori.
Prey preferences and consumption rates
A clear preference for A. inaequivalvis was observed; this species was consumed during the entire period, whereas T. philippinarum and were consumed mainly in the first and M. galloprovincialis in the last weeks of the experiment. The average consumption rate of A. inaequivalvis (±standard deviation) per cage was 25±10 ind.; T. philippinarum, 6±3 ind.; M. galloprovincialis, 5±4 ind. Friedman test confirmed significant differences between the number of individuals eaten of the three prey species (T 2 (F) = 16.7, df = 2, P<0.05); whereas A. inaequivalvis was consumed more than the other two prey species (P<0.05), no significant differences in consumption rates between T. philippinarum and M. galloprovincialis (P>0.05) were found.
Prey biomass and consumption rates
Log10 wet weight (wwt, g)/log10 shell length (SL, mm) linear relationships for the three species of bivalve prey utilized in the feeding experiments
A. inaequivalvis (N.50)
M. galloprovincialis (N.50)
T. philippinarum (N.50)
log wwt = −4.29+3.10 log SL
log wwt = −5.00 + 3.21 log SL
log wwt = −4.47 + 3.20 log SL
R 2 = 95.4%; F = 789.8 P<0.05
R 2 = 97.3%; F = 1705.7 P<0.05
R 2 = 97.1%; F = 1588.1 P<0.05
A Rapana specimen of 104.5±9.9 average shell length (wet weight = 70.8±24.3 g) ate daily ~ 0.5 g wwt. d−1 A. inaequivalvis, ~ 0.1 g wwt. d−1 T. philippinarum, ~ 0.6 g wwt. d−1 M. galloprovincialis; the total daily food requirement being ~ 1.2 g wwt. d−1.
Prey size selection
Prey size selection. N. eaten total number of prey eaten. SC1 eaten number of small size class prey eaten. SC2 eaten number of large size class prey eaten
F = 48.3; P<0.05*
F = 31.4; P<0.05
F = 1.5; P>0.05
F = 1.1; P>0.05
F = 1.4; P>0.05
Discussion and conclusion
In the Northern Adriatic Sea, R. venosa feeding rates were consistent with results of previous investigations in Chesapeake Bay (Savini et al. 2002); regardless prey species, the estimated average food requirement for an individual of 10 –14 cm shell length was 1.2 (Northern Adriatic) to 1.5 (Chesapeake) g wwt. day−1.
Results of the experiment confirmed the hypothesis that R. venosa behaves as a “pursuer” also in the Northern Adriatic sea, where a clear preference for the invasive Indo-Pacific species A. inaequivalvis was shown. Moreover, a size selective predation towards small size prey was observed. Food preference could be explained by adopting a foraging behaviour which maximise the net rate of energy intake (Hughes 1980), i.e. choosing a prey which can be handled and consumed faster than other prey species. Although R. venosa presents the typical anatomical characters of a shell boring gastropod, such as the presence of an Accessory Boring Organ (ABO) (Carriker 1981), drilling behaviour has been observed only in the early life stage (Kingsley-Smith et al. 2003). Adult whelks hold their prey into the shell aperture rasping the shell margins or suffocating the bivalve, covering it with abundant mucus till it gasps (Savini et al. 2002). The prolapse of the valves might be facilitated by the presence of biotoxins in the mucus as suggested by Cesari and Mizzan (1993) as the hypobranchial gland of different muricid and thaidid gastropods produces toxins (urocanilcoline, diihydromurexine, and senecioilcoline) impairing neuro-muscular transmission (Ghiretti and Cariello 1984). Biochemical tests on R. venosa mucus would be important to understand the gastropod foraging strategy and justify the observed preferences, as a higher sensibility of a prey species to toxins would minimise prey handling time, maximizing energy profit.
In the ecological context of the study area, high feeding rates on a non-indigenous bivalve species with no commercial interest, such as A. inaequivalvis, could have the positive effect of limiting the distribution of this alien bivalve along the Northern Adriatic coasts. On the other hand, a wide availability of this food resource helps maintenance and further spreading of its predator R. venosa. Anadara (Scapharca) inaequivalvis is present along the Adriatic shores since 1969 (Ghisotti 1972). In a few years, this species became dominant in the SFBC biocoenosis (sensu Pérès and Picard 1964) outcompeting the native bivalve Chamelea gallina and other native (e.g. Tapes decussatus, Cerastoderma glaucum) and non native (e.g. Tapes philippinarum) bivalves (Ghisotti and Rinaldi 1976; Taviani et al. 1985).
Density of A. inaequivalvis at the study site was estimated in about 600 ind.100 m−2 (the correspondent density of R. venosa being of 4 ind. 100 m−2 (Savini et al. 2004). If every month and a half (44 days experimental period) a gastropod eats on average 25 Anadara, the bivalve population would be reduced by ~17%: Feeding rate (25) × Rapana density (4)/Anadara density (600) * 100 = % density reduction (16.7%).
Complex synergistic interactions between introduced species and the recipient community usually occur, in some cases accelerating impacts on native ecosystems, the so-called invasional ‘meltdown’ process (Simberloff and Von Holle 1999); in the case of R. venosa introduction, selective predation on A. inaequivalvis might, at the contrary, weaken the competitive pressure of this alien on other local bivalve species. This could both support the re-colonisation of the habitat by native species, such as C. gallina, and help the diffusion of other well established non-indigenous species, such as T. philippinarum. These considerations are highly speculative but they could represent a basis for future experimental investigations, such as the evaluation in mesocosms (i.e. experimental ecosystems) of community structural changes and biodiversity alteration occurring in presence of the predatory gastropod; for the moment, there are not enough available information to foresee the effects of the removal of the competitive pressure of A. ineaquivalvis on the structural complexity of the infaunal community.
The lower consumption rates observed for T. philippinarum (6 ± 3 ind. in 44 days; average population density=2,200±1,400 ind. 100 m−2), which constitutes the most important bivalve fishery resource in the area, reduce the concern about the potential economical threat to bivalve fishery due to Rapana predation. Also, M. galloprovincialis (consumption rates: 5±4 ind. in 44 days; average population density = 14,000 ± 5,000 ind. 100 m−2) do not seem in danger of depletion, especially because they are locally harvested on suspended ropes locally called “reste”, which do not reach the sea bottom, thus preventing the predatory gastropod to reach them. Large natural mussel stocks are present on the artificial rocky reefs of Cesenatico and are consumed all year round by Rapana (author’s personal observation), but this population is not commercially exploited, since collection is forbidden due to the risk of algal blooms and toxin infections (DSP, PSP) (Ade et al. 2003).
In summary, the experimental results obtained do not support the hypothesis of an economical threat posed by the gastropod in the study area, whereas a selective predation towards another non-indigenous species (A. inaequivalvis) might play an important role in regulating the local introduced population of the bivalve and altering the benthic community structure.
R. venosa has found optimal conditions for its development along the Northern Adriatic coast, and particularly in Emilia-Romagna, where an almost continuous belt (~ 31 km) of rocky artificial reefs offers a large area for reproduction (Savini and Occhipinti Ambrogi 2004) and the surrounding sandy bottom provides a vast quantity of food resources. Taking the above into consideration, the area represents a breeding ground for R. venosa in the Mediterranean Sea, thus it is a relevant study place where further investigations aimed at the understanding of the bioinvasion ecology of this species should take place.
We thank the Regional Agency for the Protection of the Environment (ARPA-Emilia-Romagna) and its Oceanographic Structure “Daphne” for the logistic support. We also thank Tino Zanoli, Mauro Favruzzo and Michela Castellazzi for field work assistance. The methods used in this experiment comply with the current laws in Italy. The authors acknowledge the support by the MARBEF Network of Excellence “Marine Biodiversity and Ecosystem Functioning” which is funded in the Community’s Sixth Framework Programme (Contract no. GOCE-CT-2003-505446). This publication is contribution number MPS-060011 of MarBEF.
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