Aug 14, 2014 - We will improve the description of CO2SYS in the revised manuscript, mentioning that it is written in QBasic, not DOS. Thank you for this catching this glitch. As authors of the original version of CO2SYS, upon which most of the other
We welcome contri- butions to identify research needs, deliver research to answer key questions and bring new evidence back into practice to strengthen public health research in the UK for the future. ... been enthusiastic with the arrival of two car
Mar 10, 2011 - The distinction between CPL and CTRL (control) namelists ... namics:" This is of course not true as the offline fields simply replace the online ...
50:5246â5254. Applegate, T., G. Schatzmayr, K. Prickel, C. Troche, and Z. Jiang. 2009. Effect of aflatoxin culture on intestinal function and nutri- ent loss in laying hens. Poult. Sci. 88:1235â1241. Awad, W. A., J. R. Aschenbach, F. M. C. S. Set
the effect of day length, sex, and genotype (Ross Ã. Ross 308 and 708) on mortality causes, bird mobility, footpad health, and ocular size, with 4 trials within the experiment. Four graded day lengths were chosen to allow the study of relationship b
ETH ZURICH for the degree of. DOCTOR OF SCIENCES. Presented by. SABRINA SCHMIDT. Diplom biologist, TU Braunschweig. Born on May 23, 1982. Citizen of Germany ... CHAPTER 2: EXPERIMENTAL PROCEDURES. .... production were measured after the addition of m
FB1 was also observed in turkey lymphocytes (Dombrink-. Kurtzman et al., 1994). ... soybean meal basal diet. Diets were ... Whole blood samples were serially diluted with sterile PBS, and 100. ÂµL of each dilution at each time point was plated onto.
al., 2003). In this study, we investigated a number of diets with high energy content, different macronutrient composi- tion, and low crude fiber content, which can be ..... 174 Â± 2.9. 37. 164 Â± 3.7. No. 117. 201 Â± 2.7. 80. 180 Â± 2.8. 38. 176 Â±
DAVID A. BRAKE, GEORGE STRANG,1 JANET E. LINEBERGER,2 CAROLYN H. FEDOR,3. ROBERT CLARE,4 TODD A. BANAS,5 and TIMOTHY MILLER6. Animal Health Biological Discovery, Pfizer Central Research Division, Pfizer Inc.,. Eastern Point Road, Groton, Connecticut
Molecular Genetics Questions in Poultry ... ABSTRACT The ability to answer some of the questions .... 2, and immunoglobulin lambda light chain genes, were.
2001 Poultry Science 80:1710â1717. INTRODUCTION. Threonine may be the third limiting amino acid, after. Met and Lys in diets, composed primarily of ground yel- low corn and soybean meal (SBM), for broiler chickens. (Han et al., 1992; Fernandez et a
ABSTRACT This study was undertaken to describe the growth pattern of the pearl gray Guinea fowl. Using BW data from hatch to 22 wk, 3 nonlinear mathematical func- tions (Richards, Gompertz, and logistic) were used to estimate growth patterns of the p
Embryonating specific pathogen-free (SPF) chicken eggs (10 d; Guangdong Dahuanong Animal Health. Products Co. Ltd., Yunfu ... South China Agricultural University, Guangzhou 510642, China; and. â State Key Laboratory of Biocontrol, College of Life S
... of Food. Biotechnology, University of Agriculture, 29-Listopada Avenue, 46; 31-425 Krakow, Poland. ABSTRACT A study was conducted to determine the efficacy of phytase, an enzymic cocktail, and a waste. Aspergillus niger mycelium to hydrolyze phyt
Apr 25, 2013 - Downloaded from. Author manuscripts have been peer reviewed ...... Milone MC, Fish JD, Carpenito C, Carroll RG, Binder GK, Teachey D, et al.
Serum protein fractions were examined by electrophoresis and urinalysis with standard methods on autoanalyzer together with microsco- pic examination of urine sediment. Erythrocyte sedimentation rate, blood culture and urine culture tests were perfor
the Childhood Autism Rating Scale (CARS; Schopler, Reichler, & Rocher Renner,. 1988) classified 15 children as mild-moderately autistic, and 11 children as severely autistic. To comply with the inclusion criteria, all participants scored within the a
Feb 14, 2015 - the patients with Diamond-Blackfan anemia (DBA) developed CMMT. When we compared the three categories with the largest numbers of patients, DBA, FA and SDS, the difference in risk of developing CMMT by 18 years of age was significant (
Dec 22, 2011 - inguinal hernia; LIH, Left inguinal hernia; PCP, phencyclidine. .... ASA, American Society of Anesthesiologist: SAP, baseline systolic arterial ...
you have obtained prior permission, you may not download an entire issue ... theory underlying these theoretical predictions is rejected, as less than 50% ..... 3 the revenue difference is significantly different from zero at better than the 1% level
Feb 5, 2008 - Detection of alpha-thalassemia-1 Southeast Asian type using ... Faculty of Associated Medical Sciences, Chiang-Mai University, Chiang-Mai, ...
method to treat the end-stage liver disease. In China, ... cases of hepatolenticular degeneration. All selected patients were ... preservation liquid were perfused at suspensory ligament of duodenum by intubating to portal vein through superior ...
Nov 19, 2001 - ... 1999-2005, 20 pages.*. Young-II Choi et ai, "An Integrated Data Model and a Query .... tion," Advanced Information Systems Center, The MITRE Corpo- ration (1997). Merlino et al. ...... Rei nux'\: :!bu.UI that. ""'ilh help o( this .
Response to Reviews “Long-term bioerosion” by Färber et al. Dear Professor Kitazato, We would like to thank you, Mr. William Kiene, and the anonymous reviewer for the very detailed and careful reviews. Please find attached our reply to your and the reviewers’ comments that were followed in most instances. Some minor corrections were also made during proofreading. Sincerely yours, Claudia Färber and coauthors
Editor Comments 1) You used micritic limestones and marbles. Does all the experimental blocks originate from Rhodes Island? Response: According to Bromley et al. 1990 the blocks were surplus material of the Greek building industry and their provenance is unknown. However, in the present context we do not consider this to be disadvantageous or relevant for the experimental design. 2) You found ecological succession of microboring by sponges. These sponge groups all live in Rhodes Island? If not, how many percentages of local sponges are repopulated on experimental blocks. Response: According to the editor’s comment we added information regarding the abundance of boring sponges at Rhodes and the Eastern Mediterranean Sea: Page 9, Line 17-21: “We distinguished C. cf. viridis, C. schmidtii, C. cf. celata morphospecies 1 and 2, and C. rhodensis as main producers of the observed bioerosion traces. When ignoring our second morphospecies of C. celata, the retrieved species represented 36 % of the diversity of the locally reported Clionaidae, or 50 % of the reported Cliona spp. for the Eastern Mediterranean (e.g. Evcen and Çinar, 2015; Vacelet et al., 2008). Apart from these, we assume that other sponges bioeroded the blocks as well, as evidenced by further rare spicules and by few traces that may have differed from the above, but from which no spicules could be extracted. This possibly includes Cliothosa hancocki (Topsent, 1888), which was reported together with C. viridis and C. rhodensis to be one of the most abundant sponges at Rhodes (Rützler and Bromley, 1981).”
Review 1 (William Kiene) 1) Experimental design: It is not clear what the original sizes of the experimental blocks were. Surface area of the blocks is said to be 11 x 11 cm or more. Blocks have three dimensions. How were they deployed on the sea floor? The different lithologies of the blocks and variations in their deployment and size likely had significant influences on the results (such as the lack of colonization in the 4-year collection but 2 and 3 year blocks were colonized). This is referred to on Page 10, Lines 1-2, but some 1
indication of these variations would be helpful in the methods. On Page 11, Line 26, it is indicated that the blocks came from a previous study by Bromley. Please refer to this in the methods. Response: We noticed that both reviews expressed confusion about the experimental design. In order to clarify this, we added a brief summary of the original description of the experiment in Bromley et al., 1990, addressing questions about the size of the blocks, the deployment, and the preparation for micro-CT analysis. With respect to the lithology of the blocks, we agree with the reviewers that differences in lithology could be a source of bias for the succession of bioeroders. We used marble blocks throughout with the only exception of two micritic limestone blocks (one 4- and the 5-year block). The lithology of the blocks was examined in thin sections and is described in Table 1. We agree with reviewer 1 that the lack of bioerosion in the 4-year blocks is striking and might be an effect the micritic lithology of one of them. However, the other 4-year block (marble) shows no indication of macrobioerosion either, while in the micritic 5-year block intensive bioerosion was recorded. Hence, while we cannot entirely rule out an effect of the different lithologies, such an effect cannot be confirmed with the present data. According to the reviewers’ comments we modified chapters 2.1 and 2.2 of the Methods section as follows and added a short comment on lithological differences in the Discussion: 2.1 Experimental design (page 3, line 3-16): “The settlement experiment was carried out in the vicinity of four limestone cliffs (...) The original description of the experiment is provided in Bromley et al., 1990 and is summarised here as follows: Between 1982 and 1989, experimental blocks were deployed in water depths between 3 and 17 m. The blocks were of marble and micritic limestone, and respective lithologies were confirmed by petrographic thin sections (Table 1). Initially, smaller blocks (1-3 kg) were placed directly on the sea floor, but many of these were lost during winter storms in the first year. Accordingly, larger blocks were laid out (5-30 kg) and smaller blocks were tied securely to iron or plastic frames to increase their stability. However, except in the most turbulent sites, anchoring of blocks was avoided to simulate natural conditions as closely as possible. Between 1982 and 1996 each year some blocks were retrieved, all by skin diving and using floatation devices. Recovered blocks were rinsed in fresh water, and soft epiliths were removed. The blocks were subsequently photographed and dried.” 2.2 Micro-computed tomography (page 3, line 18-21): “Internal bioerosion in the blocks was investigated by micro-computed tomographic analysis (micro-CT). From the whole inventory of 46 recovered blocks, twelve were chosen from different depths (3 to 17 m) and exposure times (1 to 14 years), all with a surface area of 11 x 11 cm or larger. Most of the blocks showed no evidence for having been dislocated during the experiment, however, some had slightly moved and for some blocks the information about the recovery date and/or water depth was incomplete (Table 1). This was reviewed case by case, and ultimately these blocks were included in the study. In order to yield a spatial resolution of about 70 µm, the chosen blocks were cut with a rock saw to a uniform surface area of 10 x 10 cm. The thickness of these blocks varied between 2 to 5 cm, but to keep mechanical destruction as small as possible, adjusting the thickness was avoided at this stage. The 7-year block was cut into three such blocks as replicates to obtain an impression of the spatial variability of bioerosion within a single block. From blocks that were large enough to be cut into several subsamples, replicates were randomly chosen. In this way, a total of 14 samples were produced for micro-CT analysis. Micro-CT scanning was carried out (...)” 2
4.2 The macrobioeroder community (page 10, line 3): “In addition to environmental parameters, sponge bioerosion is sensitive to substrate characteristics such as lithology, density, porosity, crystal size, and the presence of siliciclastic fragments (e.g., Calcinai et al., 2007). During the experiment mostly marble blocks were used, but also two micritic limestone blocks: one 4-year block that showed no indication of macrobioerosion (Fig. 2E), and the 5-year block that was intensely bioeroded (Fig. 3A). Based on the present material, substrate effects cannot be ruled out, but are difficult to identify and distinguish from environmental effects.” 2) Page 3, Line 21: What are “the following called blocks”? Response: This was meant to address that subsequently the cut samples were used for micro-CT analysis and no longer represented the original-sized “blocks”. However, we recognise that this is unnecessary and omitted it. 3) Page 4, Line 3: Blocks were digitally cropped for analysis. Were these the dimensions used to quantify area for rates of bioerosion indicated in Line 14, or was the cut size of the blocks used? The physical cutting and digital cropping does not consider the original surface area on which the bioeroders established. This may not be too important though, since the characterization and volume of borings are the main result, and the bioerosion rates calculated are not critical to the conclusions. Response: Bioerosion rates were calculated in relation to the surface of the digitally cropped blocks. The first step, the mechanical cutting of the blocks with a rock saw was predominantly required to reduce the sample size for higher spatial resolution. As mentioned by the reviewer, based on this method we could not refer to the original surface area on which the bioeroders established (cf. page 9, line 9-15). This would have been, of course, more precise and would also have allowed including the grazer impact, but would have required scanning the blocks before deployment as reference. This will be, of course, realised in future experiments. 4) Page 4, Line 24: Were the fragmented blocks the same ones that were also digitally scanned? Response: Yes. In order to clarify this, we added “For the identification of the trace makers of Entobia cavity networks, sponge spicule preparations were made from dry sponge tissue preserved in the scanned blocks” 5) Page 8, Line 31: Suggest changing “closely mingle” to “live closely together” or cohabitate, if this is what you mean. Are you suggesting that different sponge species can occupy the same gallery? Response: “Closely mingled” was meant to address that different specimens of boring sponges were closely inhabiting one substrate and almost merging. According to the reviewer’s comment we modified the sentence as follows: “that were produced by species or individuals living closely together“. 6) Page 10, Line 11: Hutchings et al didn’t use image analysis, but quantified erosion on sections cut through experimental blocks and point-counting erosion areas under a microscope. Response: According to the reviewer’s comment we specified the applied methods: “(...), because these experiments were based on coral substrates and different quantification methods such as point-counting of sections (Kiene and Hutchings, 1992, 1994) and image analysis of sections (Carreiro-Silva and McClanahan, 2012; Osorno et al., 2005; Pari et al., 1998, 2002). 3
7) Page 10, Line 17: Remove the “,” after “This is” Response: Was changed accordingly. 8) Page 11, Line 30: Does a “stable bioeroding community” establish if the surface of a bored substrate is eroded by grazing or other action? If a surface is eroded by grazing, new uncolonized substrate would be continually exposed. The intensity of this grazing and subsequent exposure could also vary substantially in space and time. Such factors would need to be isolated to conclude what a “stable” community of borers or rate of bioerosion looks like. Response: We consider “a stable bioeroding community” to reflect conditions when all ambient bioeroders – generally said microborers, grazers, macroborers – are present on/in the experimental substrates and the bioeroder assemblage does not significantly change anymore. As outlined by the reviewer, continuously fresh substrate becomes exposed and colonised, resulting in constant bioerosion rates. We added a short explanation in the text accordingly: “mature bioeroding community (i.e. a fully developed bioeroding community of microborers, macroborers, and grazers also present in the ambient environment, with relatively stable bioerosion rates) has established.” 9) Table 1: Explain how the three replicates of the 7-year sample were made Response: Was added accordingly: “*The 7-year block was cut into three replicates to obtain an impression of the spatial variability of bioerosion within a single block”.
Review 2 (Anonymous Referee) 1) Page 3 line 3. 46 blocks of marble and limestone were used for the experiment and placed on the sea floor. You chose 20 blocks for your analysis. Could you detail the lithology of the chosen blocks? Response: We noticed that both reviews requested more detail in the description of the experimental design. Please see our response to comment 1 of review 1. 2) Page 3 line 13, page 8 line 17. You cut blocks to a size of 10x10 cm. What is their thickness? What is the size of the blocks used for micro-CT? is it 90x90x18 mm as reported in the legends? How did you choose the parts of the blocks for micro-CT analysis? Response: Please see again our response to comment 1 and 3 of review 1. 3) Page 6 line 23- Cliona schmidti. See comments for the legend of figure 3. line 24 and followings. When you quote the figure 6 with the spicules of the sponges, please quote also the corresponding figs of the bioerosion traces got with m-CT. Response: A summary of the observed bioerosion traces and referred producers is provided in Table 2 and referenced at the beginning of chapter 3.2. In order to keep the information concise and clear, this comment was not implemented. 4) Discussion page 8. Could you consider if the lithology of the blocks affect the results of the erosion rates? Response: Please see our response to comment 1 of review 1. 4
5) Page 9 lines 15-18. Please add comments about the dominance of sponges in the excavated blocks, discussing the succession phase of bioeroders. Sponges may precede worms and bivalves in colonisation (e.g. Hutchings, 1986). This could be true only for tropical waters, and moreover, these data about successional phases refer to shorter time gaps. But in temperate areas bioerosion rates are slow (for Teredinidae is demonstrated). Is it for this reason that worms are scarce? Moreover, these blocks are small (10x10 cm). Likely, they moved and rolled on the bottom. Worms (with singles openings) could have been smothered by mud, and the vacant holes occupied by sponges. Response: Thank you very much for this valuable comment. We added information to the Discussion. The total absence of bioeroding bivalves and low occurrence of polychaetes during our experiment appears to be highly remarkable, but we assume that this is an effect of the high spatial variability of macrobioeroders. Because most of the deployed blocks were large enough to be stable under turbulent conditions, and smaller ones were anchored where necessary (please see comment 1 of review 1), movement of the blocks affecting the settlement of bioeroders is rather unlikely. We assume that the succession of bioeroder guilds in the Mediterranean Sea is very similar to that in the tropics with polychaetes being present after a few months, while sponges and molluscs may need several years to develop. However, the detection of organism succession would have required a more extended experimental design. Content changes (page 10, line 3): Although on the surrounding sea floor (...) Other long-term experiments in the tropics indicated a distinct succession of macroborers with polychaetes being present after a few months, while sponges and molluscs needed several years to establish (CarreiroSilva and McClanahan, 2012; Kiene and Hutchings, 1992, 1994; Osorno et al., 2005; Pari et al., 1998, 2002; Peyrot-Clausade et al., 1995). We assume that the dominance of sponges during the present study is (...) 6) Page 10 line 20-25. Is it your case? the different lithology of the blocks could have influenced also the erosion traces? Response: Please see our response to comment 1 of review 1. 7) Figure 1. Show the Mediterranean sea and where Rhodes is. Response: Figure changed accordingly. Figure 3. Could be possible that in B two distinct traces are presents? Apart E. ovula, there are other cylindrical chambers arranged in chains, very similar to fig. 2C (E. cateriformis). In fact, the erosion traces in 2C are attributed to C. schmidti, and the traces in figure. 3B to two distinct species: Cliona viridis and C. schmidti. The chambers arranged in chains in Fig. 3C could belong to C. schmidti and the others, globose-ovoid to C. viridis. So the sentence “ Cliona schmidtii (Ridley, 1881) was recognised as the trace maker of E. cateniformis and E. ovula “ should be reconsidered. Response: Thank you very much for this valuable comment. We agree that the cylindrical chambers crossing the main trace show a high resemblance to an early phase Entobia cateniformis. However, according to the original diagnosis in Bromley & D’Alessandro (1984), in its early phase E. ovula is similarly described to show “chambers that are separated from neighbours by a very short intercameral canal, usually reduced to a construction, which are arranged in straight strings”. 5
According to this we consider the gallery to represent the earliest part of the E. ovula cluster, which was filled with the characteristic ovoid chambers in its later stage.
Additional minor changes: Replaced “&” by “and” throughout. Table 2, corrected missing value. Figure 6: Abbreviation of Cliona after first account. Supplement Table S1: Correction wrong assignment label Fig. 6 G and H in column B. Supplement Table S2: Correction of automatic-correction errors in column “unassignable macroborings”. References: Updated reference Baum and Titschack, subm. (Page 4, Line 2/Page 13, Line 4): Baum, D. and Titschack, J.: Cavity and pore segmentation in 3D images with ambient occlusion, in: Eurographics Conference on Visualization, Groningen, Netherlands, 6-10 June 2016, in press. Added references: Page 14, Line 13: Calcinai et al., 2007: Calcinai, B., Azzini, F., Bavestrello, G., Gaggero, L., and Cerrano, C.: Excavating rates and boring pattern of Cliona albimarginata (Porifera: Clionaidae) in different substrata, in: Porifera Research: Biodiversity, Innovation & Sustainability, Proceedings of the 7th International Sponge Symposium, Búzios, Rio de Janeiro, 7-13 May 2006, 203-210, 2007. Page 15, Line 16: Evcen, A., and Çinar, M. E.: Bioeroding sponge species (Porifera) in the Aegean Sea (Eastern Mediterranean), J. Black Sea/Mediterranean Environment, 21, 285-306, 2015. Page 2, Line 26/Page 19, Line 10: Silbiger, N. J., Guadayol, Ò., Thomas, F. I. M., and Donahue, M. J.: A novel μCT analysis reveals different responses of bioerosion and secondary accretion to environmental variability, PLoS ONE, 11, e0153058, 2016. Page 20, Line 1: Vacelet, J., Bitar, G., Dailianis, T., Zibrowius, H., and Perez, T.: A large encrusting clionaid sponge in the Eastern Mediterranean Sea, Mar. Ecol, 29, 237-246, 2008.
Long-term macrobioerosion in the Mediterranean Sea assessed by micro-computed tomography C. Färber1, J. Titschack1,2, C.H.L. Schönberg3, 4, K. Ehrig5, K. Boos2, D. Baum6, B. Illerhaus5, U. Asgaard7, R.G. Bromley7, A. Freiwald1, M. Wisshak1 5
Senckenberg am Meer, Abteilung Meeresforschung, Südstrand 40, 26382 Wilhelmshaven, Germany MARUM, Center for Marine Environmental Sciences, Leobener Straße, 28359 Bremen, Germany 3 Oceans Institute, The University of Western Australia, Crawley, WA 6009, Australia 4 Western Australian Museum, Welshpool, WA 6106, Australia 5 Bundesanstalt für Materialforschung und –prüfung (BAM), Unter den Eichen 87, 12205 Berlin, Germany 6 ZIB, Zuse Institute Berlin, Takustraße 7, 14195 Berlin, Germany 7 Rønnevej 97, DK-3720 Aakirkeby, Denmark 2
Correspondence to: Claudia Färber ([email protected]) Abstract. Biological erosion is a key process for the recycling of carbonate and the formation of calcareous sediments in the oceans. Experimental studies showed that bioerosion is subject to distinct temporal variability, but previous long-term 15
studies were restricted to tropical waters. Here, we present results from a 14 year bioerosion experiment that was carried out along the rocky limestone coast of the island of Rhodes, Greece, in the Eastern Mediterranean Sea, in order to monitor the pace at which bioerosion affects carbonate substrate and the sequence of colonisation by bioeroding organisms. Internal macrobioerosion was visualised and quantified by micro-computed tomography and computer-algorithm based segmentation procedures. Analysis of internal macrobioerosion traces revealed a dominance of bioeroding sponges producing eight types
of characteristic Entobia cavity networks, which were matched to five different clionaid sponges by spicule identification in extracted tissue. The morphology of the entobians strongly varied depending on the species of the producing sponge, its ontogenetic stage, available space, and competition by other bioeroders. An early community developed during the first 5 years of exposure with initially very low macrobioerosion rates and was followed by an intermediate stage when sponges formed large and more diverse entobians and bioerosion rates increased. After 14 years, 30 % of the block volumes were
occupied by boring sponges, yielding maximum bioerosion rates of 900 g m-2 yr-1. A high spatial variability in macrobioerosion prohibited clear conclusions about the onset of macrobioerosion equilibrium conditions. This highlights the necessity of even longer experimental exposures and higher replication at various factor levels in order to better understand and quantify temporal patterns of macrobioerosion in marine carbonate environments.
1 Introduction Bioerosion, the erosion of hard substrate by living organisms (Neumann, 1966), generally comprises (i) internal microbioerosion by boring cyanobacteria, algae, and fungi, (ii) internal macrobioerosion by boring sponges, worms, and bivalves, and (iii) external bioerosion by grazing gastropods, echinoids, and fish (e.g., Glynn, 1997; Tribollet et al., 2011). 1
Experimental studies showed that the succession of bioerosion agents is subject to distinct temporal variability: Under favourable conditions, microborers can reach stable communities within 1 year of exposure (Grange et al., 2015; Tribollet and Golubic, 2005), whereas establishment of mature communities of macrobioeroders may take several years to form mature communities (e.g., Chazottes et al., 2002; Kiene and Hutchings, 1992, 1994; Pari et al., 1998, 2002; Tribollet and 5
Golubic, 2005). Most bioerosion experiments were conducted over a period of only 1-2 years, giving a detailed picture on microbioerosion in different geographical settings (e.g., Kiene, 1988; Vogel et al., 1996, 2000; Wisshak, 2006; Wisshak et al., 2010, 2011). Experimental studies on the succession of macrobioeroders were previously limited to tropical coral reef systems and commonly lasted about 4-8 years (Carreiro-Silva and McClanahan, 2012; Kiene and Hutchings, 1992, 1994; Pari et al., 2002). The longest experiments have been conducted over 12 years at the Great Barrier Reef (Kiene and
Hutchings, 1992) and 13 years at Jamaica (Scott et al., 1988). To date, no experimental data on long-term bioerosion from non-tropical settings are available, but would constitute important information for evaluating global patterns of bioerosion and for modelling future impacts of bioerosion. This is particularly relevant since bioerosion is considered to increase with ongoing ocean acidification (Tribollet et al., 2009), a trend that is especially true for bioeroding sponges (e.g., Fang et al., 2013; Wisshak et al., 2012, 2013, 2014), with potentially detrimental effects on carbonate-dominated ecosystems (Kennedy
et al., 2013). In the Mediterranean Sea, bioerosion affects sensitive ecosystems such as limestone coasts, deposits of coralline algae, and cold-water coral reefs, as well as molluscs in aquaculture, submerged man-made materials, and artefacts (see Schönberg and Wisshak, 2014 for a review). Experimental data on Mediterranean bioerosion are only available in form of short-term observations on microendoliths (Färber et al., 2015; Le Campion-Alsumard, 1979). Here, we present results from a long-
term bioerosion experiment that was carried out over 14 years along the limestone rocky shore of Rhodes (Greece) in order to analyse the succession of bioeroders in the Eastern Mediterranean Sea. A preliminary summary on macroscopic observations during the first 6 years was provided by Bromley et al. (1990). For the visualisation of internal macrobioerosion traces and quantification of macrobioerosion rates, micro-computed tomographic analysis was chosen as a non-destructive approach. Computed tomography is increasingly used to visualise bioerosion traces in three dimensions (Beuck et al., 2007,
2008; Bromley et al., 2008; Schönberg and Shields, 2008), but quantitative approaches are still scarce and comparatively new (Crook et al., 2013; DeCarlo et al., 2015; Silbiger et al., 2014, 2016). Aim of this paper is (i) to introduce a novel approach to visualise and quantify internal bioerosion using computer-algorithm based segmentation procedures, (ii) to provide an inventory of macrobioerosion traces, (iii) to identify trace making boring sponges through spicule analysis, and (iv) to assess the long-term development of bioerosion rates and ontogenetic development of sponge borings in terms of a
possible onset of macrobioerosion equilibrium conditions.
2 Material and Methods 2.1 Experimental design The settlement experiment was carried outExperimental blocks were deployed in the vicinity of four limestone cliffs at the east and west coast of the island of Rhodes, Greece (Fig. 1): (i) at the south and east edge of Ladiko Bay (36°19’5”N, 5
28°12’17”E; 36°19’10”N, 28°12’29”E), (ii) south of Kolimbia (36°14’26”N, 28°9’44”E; 36°14’21”N, 28°9’47”E), (iii) north of St. Paul’s Bay near Lindos (36°5’17”N, 28°5’20”E), and (iv) in Pyrgos (36°10’10”N, 27°43’55”E). All localities were characterised by limestone rock ground or boulder fields, and were free from local pollution. Annual monitoring in October showed no indication of interference of the experiment by human activities. The original description of the experiment is provided in Bromley et al., 1990 and is summarised here as follows: Between
1982 and 1989, experimental blocks were deployed in water depths between 3 and 17 m. The blocks were of marble and micritic limestone, and respective lithologies were confirmed by petrographic thin sections (Table 1). Initially, smaller blocks (1-3 kg) were placed directly on the sea floor, but many of these were lost during winter storms in the first year. Accordingly, larger blocks were laid out (5-30 kg) and smaller blocks were tied securely to iron or plastic frames to increase their stability. However, except in the most turbulent sites, anchoring of blocks was avoided to simulate natural conditions as
closely as possible. Between 1982 and 1989 each year some blocks were retrieved, all by skin diving and using floatation devices. Recovered blocks were rinsed in fresh water and soft epiliths were removed. The blocks were subsequently photographed and dried. 46 blocks were placed directly on the sea floor, in water depths between 3 and 17 m, and until 1996 each year some blocks were retrieved, all by skin diving and using floatation devices. Recovered blocks were rinsed in fresh water and soft epiliths
were removed. The blocks were subsequently photographed and dried.The blocks were of pure calcium carbonate (marble and limestone), and respective lithology was confirmed by petrographic thin sections. From all retrieved blocks, for the present approach twelve were chosen from different depths (3 to 17 m) and exposure times (1 to 14 years), all with a surface area of 11 x 11 cm or more. Most of these showed no evidence for having been dislocated during the experiment, however, some blocks had slightly moved and for some the information about recovery date and/or water depth was incomplete (Table
1). This was reviewed case by case, and ultimately the latter blocks were included in the study. 2.2 Micro-computed tomography Internal bioerosion in the blocks was investigated by micro-computed tomographic analysis (micro-CT). The blocks were of pure calcium carbonate (marble and limestone), and respective lithology was confirmed by petrographic thin sections.From the whole inventory of 46 recovered blocks, twelve were chosen from different depths (3 to 17 m) and exposure times (1 to
14 years), all with a surface area of 11 x 11 cm or more. Most of the blocks showed no evidence for having been dislocated during the experiment, however, some had slightly moved and for some blocks the information about recovery date and/or 3
water depth was incomplete (Table 1). This was reviewed case by case, and ultimately the latter blocks were included in the study. In order to yield a spatial resolution of about 70 µm, the chosen blocks were cut with a rock saw to a uniform surface area of 10 x 10 cm. The thickness of these blocks varied between 2 to 5 cm, but to keep mechanical destruction as small as possible, adjusting the thickness was avoided at this stage. The 7-year block was cut into three such replicates to obtain an 5
impression of the spatial variability of bioerosion within a single block. From blocks that were large enough to be cut into several subsamples, replicates were randomly chosen. The 7-year block was cut into three such replicates to obtain an impression of the spatial variability of bioerosion within a single block. In this way, a total of 14 samples (in the following called blocks) were selectedproduced for micro-CT analysis. In order to yield spatial resolutions of about 70 µm, blocks
Micro-CT scanning was carried out at the Bundesanstalt für Materialforschung und –prüfung (BAM), Berlin, Germany, using the 225 kV system (Badde and Illerhaus, 2008). An X-ray source voltage of 210 kV, a current of 90 µA, and a prefilter of 1 mm copper was applied. Attenuation images were taken at smallest possible resolution due to specimen size. To achieve the best signal-to-noise-ratio, 2400 projections over 360 degrees with a total measuring time of 16 h were taken. Images were reconstructed using BAM software generated from the original Feldkamp algorithm (Feldkamp et al., 1984).
The resulting voxel size was 72 µm. Post-processing of micro-CT data was conducted using the Amira software edition from the Zuse Institute Berlin, ZIBAmira version 2014.51 (Stalling et al., 2005). In an initial segmentation step all encrusting epiliths on the surface of the blocks were excluded from the dataset using the Segmentation Editor. Limestone substrate was distinguished from the surrounding air and organic tissue (borings were partially filled by air and organic remains of the sponges) using the marker-based
Watershed segmentation module. Segmentation of the borings from the space surrounding the block was carried out with the AmbientOcclusionField module (Baum and& Titschack, in presssubm.). Resulting micro-CT images of the blocks were cropped to uniform sizes of 90 x 90 x 18 mm with the CropEditor to obtain comparable volumes. The respective volumes of substrate and bioerosion per block were quantified with the MaterialStatistics module using the results from the latter segmentation. To quantify the total surface area of each block, bioerosion and substrate were selected together and the
surface was calculated using the SurfaceGen module. After removing all other surfaces except the upper surface with the SurfaceEditor, this surface area was quantified with the SurfaceStatistics module. To further evaluate the bioerosion constituents, a third segmentation step was performed based on a DistanceMap of the segmented bioerosion traces employing the ContourTreeSegmentation module to gain an automatic separation of different bioerosion traces in the blocks (threshold: 0, persistence value: 0.05; see Titschack et al., 2015). Subsequently, each trace was parameterised with the
ShapeAnalysis module. The maximum trace extent defined microbioerosion patterns as < 1 mm and macrobioerosion patterns as > 1 mm, following the definition by Wisshak (2012). Bioerosion rates (including micro- and macrobioerosion; g m-2 yr-1) were calculated by multiplying the volume of bioerosion (cm3) with the mean density of limestone/marble of 2.7 g cm-3 (Schön, 2011) and expressing the result per surface area (m2) per duration of exposure (years). These rates include the
residual internal micro- and macrobioerosion, since the volume of substrate removed by grazers (potentially also including micro- and macrobioerosion) was impossible to quantify without a reference to the original substrate surface. 2.3 Bioerosion inventory Bioerosion ichnotaxa were identified following descriptions of Bromley (1970) and Bromley and D'Alessandro (1983, 1984, 5
1989). Ontogenetic stages of sponge borings were classified into putative growth phases A-E according to characterisations in Bromley and D'Alessandro (1984). 2.4 Sponge spicule analysis and species identification For the identification of the trace makers of Entobia cavity networks, sponge spicule preparations were made from dry sponge tissue preserved in the scanned blocks. To extract the tissue from the equivalent positions as in micro-CT
reconstruction, the blocks were fragmented with hammer and chisel, and tissue was carefully removed with a dissecting needle. For spicule preparations sponge tissue was digested in 68 % concentrated nitric acid in test tubes in a heated sand bath (60-70°C) for about 2 h, then leaving the solutions in place over night without heat application. On the next day, acidcleaned spicules were washed three times in distilled water and dehydrated three times in laboratory-grade ethanol, each wash occurring after centrifugation and pipetting off the supernatant, taking care not to accidentally remove spicules.
Spicules were then mounted for scanning electron microscopy (SEM) by drying aliquots of re-suspended spicules directly on SEM stubs, followed by sputter-coating with gold, and analysis with the SEM (VEGA3, TESCAN). In some cases, colour of the dry tissue helped with classification efforts (e.g., Christomanos and Norton, 1974), but in most cases species identification had to rely exclusively on spicules. We mostly referred to descriptions of Mediterranean bioeroding sponges by Rosell and Uriz (2002). Tylostyle measurements were obtained from 20 spicules per specimen. Spirasters and
amphiasters were scarce and often broken, so that only five microscleres were measured where possible. Measurements were carried out using ImageJ v.1.48 (Rasband, 1997-2015).
3 Results 3.1 Bioerosion traces 25
Analysis of bioerosion patterns in the experimental blocks revealed ten different ichnotaxa, eight of which were attributed to the activity of excavating sponges and two to polychaete worms (Table 2). In respect to general patterns, the boring intensity distinctly increased with exposure time (Fig. 2-5). In blocks deployed for 2 to 5 years, superficial cavity networks were observed (Fig. 2-3). From 7 years onward, extensive three-dimensional networks had developed (Fig. 4-5). Diversity increased over time as well, with blocks containing more than one ichnospecies after 5 years (Table 2). 5
In the two blocks deployed for 1 year no macroborings were detected (Fig. 2A-B). The first distinct sponge boring was observed in the 2-year block (Fig. 2C). The trace was characterised by cylindrical chambers (about 1.4-5.1 mm in length, 0.7-1.3 mm in width) that were arranged in long, sublinear chains that coalesced in cross-, T- or L-shape, which is characteristic for Entobia cateniformis Bromley and& D’Alessandro, 1984 in the late ontogenetic growth phase C. This 5
system formed one tier in about 0.1-0.2 mm depth in the block parallel to the external surface, extending through the entire block. In the 3-year block, an early-stage of Entobia megastoma (Fischer, 1868) was found. It was composed of a sublinear gallery (about 50 x 4 mm in size) with hand-like extensions (phase A-B; Fig. 2D). In the two 4-year blocks no assignable macrobioerosion patterns occurred (Fig. 2E-F).
In the 5-year block, a well-developed Entobia geometrica Bromley and& D’Alessandro, 1984 cavity network was detected (Fig. 3A). The trace consisted of subrectangular to subtriangular flattened chambers with rounded corners (about 3.5-9.9 mm in diameter) that were aligned in weakly developed rows (phase D). The system extended in one tier throughout the entire surface of the block, parallel to the substrate surface in about 0.2-0.5 mm depth. In addition, one early-stage and two welldeveloped specimens of the polychaete bioerosion traces Caulostrepsis isp. penetrated from the upper surface into the block
(Fig. 3A1-3). In the 6-year block, a well-developed network of Entobia cf. ovula Bromley and& D’Alessandro, 1984 occurred (Fig. 3B). The trace was characterised by globose-ovoid to sub-prismatic chambers (about 0.7-1.5 mm in diameter) that were arranged in a crowded boxwork pattern (phase D). The entire system had a diameter of 40-50 mm and was arranged in one tier parallel to the external substrate surface in about 0.2-0.6 mm depth.
In the 7-year block, the bioerosion intensity strongly varied within the three subsamples (Fig. 4A-C). In the first subsample only an early-stage sponge boring was found that resembled Entobia mammilata Bromley and& D’Alessandro, 1984 in growth phase A-B (Fig. 4A). In the second subsample, two separate specimens of E. megastoma and one of E. mammilata occurred (Fig. 4B). The first specimen of E. megastoma was composed of subcylindrical galleries that formed a threedimensional system (30 x 40 mm) and penetrated about 1.5 cm into the substrate (phase B-C; Fig. 4B1). The second
specimen of E. megastoma was connected with E. mammilata (Fig. 4B2). This specimen of E. megastoma appeared to be an earlier growth stage than the other specimens in the same block (phase B). Entobia mammilata formed chains of turnipshaped chambers (about 1.3-1.7 mm; in phase B). The galleries extended over an area of about 42 x 40 mm and were arranged in two tiers in about 10 mm depth of the block. The third subsample was crowded with bioerosion traces that were identified as two entobian ichnospecies (Fig. 4C). Here, a well-developed network of E. mammilata was composed of
clusters of tubercle-like chambers in about 1.2-1.4 mm of the block (phase D; Fig. 4C1). The network extended over an area of 30 x 90 mm and had penetrated the entire depth of the block (18 mm). In addition, several juvenile specimens of E. megastoma occurred. The largest specimen was 25 x 50 mm in size and had a subcylindrical gallery of about 3 mm in diameter with long-exploratory threads (phase B; Fig. 4C2).
The 8-year block showed a dense network of shallow bioerosion (Fig. 5A), which was composed of three different entobians, dominated by a large network of E. cf. ovula clusters that were interconnected by long galleries in growth phase D. The largest cluster was about 25 x 40 mm in size and extended in about 0.2-0.6 mm depth of the block in one tier parallel to the external substrate surface (Fig. 5A1). In addition, four large chambers of about 6 mm in diameter being connected by 5
numerous exploratory threads were found that resembled E. magna Bromley and& D’Alessandro, 1989 in phase B (Fig. 5A2). The third entobian was a specimen of Entobia cf. parva Bromley and& D’Alessandro, 1989, which was identified through its compact boxwork of densely distributed, inflated chambers of about 0.2-0.6 mm that were arranged in a 15 x 40 mm tier in about 10 mm depth of the block (phase D; Fig. 5A3). In the 8- to 9-year block, an advanced network of E. megastoma and several scattered early-stage galleries co-occurred (Fig.
5B). The 1-4 mm, subcylindrical galleries of the advanced specimen extended over an area of about 50 x 90 mm and were distributed in parallel to the block surface (phase B). The smaller specimens were about 10-15 mm in size and formed characteristic hand-like cavities (phase A). The 14-year block was extensively bioeroded and entobians difficult to separate (Fig. 5C). Several specimens of Entobia cf. cretacea Bromley, 1970 exhibited large polygonal chambers of about 1.3-4.2 mm in diameter, being connected by numerous
canals, and with the entobians extending through the entire depth of the block (18 mm; Fig. 5C1-2). Bromley (1970) did not define distinct phases for E. cretacea, but we considered the detected traces to reflect phase C-D. Apart from entobians, three galleries of the worm boring Trypanites isp. extended as slim sack-like cavities into the blocks (Fig. 5C3-5). The software initially attributed these to the surrounding E. cretacea cavity network and the worm borings were afterwards separated manually from the sponge borings.
3.2 Identification of boring sponges We recognised spicules of five clionaid bioeroding sponge species that could be assigned as trace makers of eight different entobians (Fig. 6, Table 2, Table S1). However, not from every cavity network spicules could be extracted, and other, rare, broken or non-diagnostic spicules occurred that could not conclusively be matched to smaller entobians or used to identify bioeroding sponges at species level (these possibly included spicules from the genera Pione, Cliothosa, Spirastrella,
Siphonodictyon, and Thoosa). Cliona schmidtii (Ridley, 1881) was recognised as the trace maker of E. cateniformis and E. ovula in the 2-year and the 8year blocks (Fig. 6A-B, Table 2). Even when dry, the sponge tissue retained its characteristic purple colour that was an immediate indicator for C. schmidtii. Tylostyles were 170-275 µm in length and 3-8 µm in thickness, and had a slightly bent shaft. A spectrum of spiraster sizes was observed: We distinguished (i) relatively thin and long spirasters with small spines
distributed along the convex sides of the helical shaft (axis 57-84 µm in length and 1-3 µm in thickness), (ii) relatively short and thick spirasters with conical spines (axis 25-52 µm in length and 2-3 µm in thickness), and (iii) short, thick amphiasterlike spirasters (axis 17-21 µm in length and 3-7 µm in thickness). 7
Two morphospecies of Cliona cf. celata Grant, 1826 were distinguished as trace makers of two different entobians. Cliona cf. celata 1 was trace maker of E. geometrica in the 5- year block (Fig. 6C, Table 2), and Cliona cf. celata 2 was matched to E. megastoma in the 7-year block (Fig. 6D-F, Table 2). Both morphospecies had brown dry sponge tissue and exclusively tylostyles. Tylostyles of C. cf. celata 1 were 243-373 µm in length and 6-13 µm in thickness, were comparatively robust 5
with well-formed tyles that were occasionally subterminal, and had mostly straight or subtly bent shafts. Tylostyles of C. cf. celata 2 were comparatively slim, often with subterminal, occasionally multiple tyles, and tyles could be strongly displaced or weakly pronounced, and occasional near-stylar modifications occurred. The tylostyle shafts of C. cf. celata 2 were occasionally flexuous, being on 208-369 µm in length, but only about 3-9 µm in thickness. Based on scarce spirasters Cliona cf. viridis (Schmidt, 1862) was tentatively identified as trace maker of E. ovula and E.
mammilata in the 6- and 7-year blocks (Fig. 6G-H, Table 2). The colour of the dry sponge tissue was brown. Tylostyles were 217-394 µm in length and about 3-9 µm in thickness, fusiform, slightly bent and had round, oval or subterminal tyles. Two types of spirasters were distinguished: (i) straight, 20-44 µm in length and 1-2 µm in thickness, with relatively long spines that were mainly clustered at the ends of the shaft and (ii) helical, 18 µm in length and 1 µm in thickness, with small spines. Cliona rhodensis Rützler and& Bromley, 1981 was identified as trace maker of E. magna in the 8-year block (Fig. 6I, Table
2). The colour of the dry sponge tissue was brown. Tylostyles were near straight and fusiform, 245-356 µm in length and about 6-10 µm in thickness, and had distinct tyles. Only one complete, undamaged spiraster was found, which was 23 µm in length and 1 µm in thickness, and had discrete, relatively long spines slightly recurving at their tips. 3.3 Bioerosion intensity and rates Quantification of bioerosion in the experimental blocks revealed that in blocks deployed for 1 to 4 years only small volumes
of substrate were removed by bioerosion (<1 %; Fig. 7A, Table S2). In the 5- to 8-year blocks, the volume of bioerosion increased to 4-9 %. The highest bioerosion intensity was measured in the block that was deployed for 14 years (30 %). With respect to the proportional contribution of the different groups of bioeroding organisms to total bioerosion, the largest part of bioerosion in the 1- and 4-year blocks was represented by microbioerosion and unassignable macrobioerosion patterns (Fig. 7B). In all other blocks, bioerosion was predominantly produced by boring sponges. Only in the 5- and 14-year
blocks complementary worm bioerosion was observed, but it contributed less than 1 % to the total volume of bioerosion. Analogous to the gradual increase in total volume of bioerosion, total bioerosion rates (i.e. residual micro- and macrobioerosion) increased with exposure time (Fig. 7C, Table S3). Lowest values were found in the 1- to 4-year blocks (1.5-85 g m-2 yr-1), except in the 2-year block, where bioerosion rates tallied with 224 g m-2 yr-1. In the 5- to 7-year blocks bioerosion was elevated compared to blocks retrieved after shorter periods and reached values of 308-648 g m-2 yr-1.
However, in 7- and 8 to 9-year blocks lower values of 53 and 62 g m-2 yr-1 were observed. Highest bioerosion rates were measured in the 14-year block, resulting in a maximum value of 900 g m-2 yr-1. Overall, observed bioerosion patterns suggest that not only the bioerosion intensity, i.e. the absolute volume removed by bioerosion, but also the bioerosion rates, i.e. 8
bioerosion normalised to a time span of one year, increased with time of exposure. An additional statistical evaluation was not considered feasible, however, due to the limited amount of available blocks suitable for micro-CT analysis.
4.1 Micro-CT as a tool for the visualisation and quantification of internal macrobioerosion Methods used in this study represent a new approach and perspective for precise and automatic differentiation and quantification of internal structures of bioerosion, and they can be employed for similar aspects in biogeoscience research. Previously, evaluation of internal bioerosion by tomographic analysis was restricted to two-dimensional image analysis of consecutive layers (e.g., Becker and Reaka-Kudla, 1997; Hassan, 1998; Sammarco and Risk, 1990; Schönberg, 2001), and
only recently included also three-dimensional measurement tools (Crook et al., 2013). Above methods are suitable for comparatively simple bioerosion structures, but show clear limitations in the differentiation of complex cavity networks. In our study we took advantage of program algorithms that help to distinguish different traces. This function needs to be manually revised, however, as it does not automatically identify ichnotaxa according to morphological differences. This becomes especially clear where morphological distinct traces were identified as fused to one connected cavity network (Fig.
4B2, 5A), an effect likely caused by insufficient separation of traces due to different generations of endoliths overprinting earlier borings or galleries of bioeroding sponges that were produced by can closely mingle with other species or individuals living closely together (unlike observations in Bromley and Tendal, 1973). Another restriction of micro-CT analysis is the correlation of sample size and spatial resolution. Based on the sample dimensions of 10 x 10 cm spatial resolutions of 72 µm were possible, which allowed preserving large cavity networks, as
well as capturing thin exploratory threads of the sponges. However, where connecting galleries were near or below this resolution, occasionally different units of the same trace were split into apparently different specimens (Fig. 4C). Neither was the present resolution high enough to capture smaller microborings. Subsequent manual separation or joining of specimens needs to be assessed case-by-case. That is comparatively easy and feasible for cylindrical borings such as Trypanites isp. (Fig. 5C3-5), but for complex cavity networks, such as sponge borings, this can potentially become very
time-consuming. Apart from microborings and thin exploratory threads, a small proportion of deeper borings was also neglected due to the digital cropping of the blocks. In addition, some proportion of bioerosion became unavailable for quantification when grazers simultaneously removed surface layers and micro- as well as macrobioerosion traces within them. This substrate loss cannot be quantified without a reference that indicates the original thickness of the experimental blocks. What was actually
measured, hence, is the residual internal bioerosion. Particularly in those blocks that were exposed long-term, bioerosion rates thus were somewhat underestimated, in turn implying that the observed increase in bioerosion rates can be expected to be even more pronounced for total bioerosion. 9
4.2 The macrobioeroder community We distinguished C. cf. viridis, C. schmidtii, C. cf. celata morphospecies 1 and 2, and C. rhodensis as main producers of the observed bioerosion traces. When ignoring our second morphospecies of C. celata, the retrieved species represented 36 % of the diversity of the locally reported Clionaidae, or 50 % of the reported Cliona spp. for the Eastern Mediterranean (e.g. 5
Evcen and Çinar, 2015; Vacelet et al., 2008). Apart from these, we assume that other sponges bioeroded the blocks as well, as evidenced by further rare spicules and by few traces that may have differed from the above, but from which no spicules could be extracted. This possibly includes the locally common boring sponges Cliothosa hancocki (Topsent, 1888), which
was reported together with C. viridis and C. rhodensis to be one of the most abundant sponges at Rhodes (Rützler and
Formatiert: Schriftart: Kursiv
Bromley, 1981)Pione vastifica (Hancock, 1849), and Cliothosa hancocki (Topsent, 1888), which Rützler and Bromley
Formatiert: Schriftart: Kursiv
(1981) and Bromley et al. (1990) reported from Rhodes. Bioeroding sponge distributions and abundances, as well as their bioerosion rates, are dependent on environmental parameters such as water flow, nutrients, salinity, temperature, and light (see Schönberg, 2008 for a review). Especially C. viridis and C. celata are very characteristic for the Mediterranean and known to be among the most abundant and destructive sponges in the Mediterranean Sea (e.g., Calcinai et al., 2011; Rosell et al., 1999). Both species, however, are difficult to
identify and are members of species complexes that encompass very similar, but taxonomically different species, which means that earlier accounts on their biology may refer to more than one species (e.g., Leal et al., 2015; Xavier et al., 2010). This may also be the case for C. schmidtii, because specimens from different sample sites can have somewhat different spicule morphologies (Schönberg, pers. obs.). However, C. schmidtii and C. rhodensis were the presently best confirmed species, but little is known about their ecological requirements: Both can be found in light and shade, and occur in
moderately clear water and may avoid sedimentation (Rützler and Bromley, 1981; Carballo et al., 1994; Corriero et al., 2000), but it is not known what else characterises their ecological niches. To draw conclusions about environmental conditions from our data is difficult, because blocks were from different depths and current regimes, and the lack of replication prevented us from matching species distributions with environmental conditions.
In addition to environmental parameters, sponge bioerosion is sensitive to substrate characteristics such as lithology, density, porosity, crystal size, and the presence of siliclastic fragments (e.g., Calcinai et al., 2007). During the experiment mostly marble blocks were used, but also two micritic limestone blocks: one 4-year block that showed no indication of macrobioerosion (Fig. 2E), and the 5-year block that was intensely bioeroded (Fig. 3A). Based on the present material, substrate effects cannot be ruled out, but are difficult to identify and distinguish from environmental effects.
Although on the surrounding sea floor also boring bivalves and worms (sipunculans, polychaetes) were reported to be very common, our experimental blocks were dominated by boring sponges. Other long-term experiments in the tropics indicated a distinct succession of macroborers with polychaetes being present after a few months, while sponges and molluscs needed several years to establish (Carreiro-Silva and McClanahan, 2012; Kiene and Hutchings, 1992, 1994; Osorno et al., 2005; Pari 10
et al., 1998, 2002; Peyrot-Clausade et al., 1995). We assume that theis dominance of sponges during the present study is an effect of the high spatial variability of macroborers and that locally sponges were most prevalent and determined the predominant larval supply. This assumption is in good agreement with results from other long-term experiments in the tropics, where macrobioerosion strongly varied with water depth and nutrient supply (Carreiro-Silva and McClanahan, 2012; 5
Kiene and Hutchings, 1992, 1994; Osorno et al., 2005; Pari et al., 1998, 2002; Peyrot-Clausade et al., 1995). The low occurrence of polychaete borings in the blocks may be also explained by the fact that polychaetes have comparatively short life spans and that their vacant burrows became inhabited and overprinted by newly settled larvae of other boring species (Hutchings et al., 1992). To draw a direct comparison between bioerosion rates from these studies and our experiment, however, is difficult, because these experiments were based on coral substrates and different quantification methods such as
point-counting of sections (Kiene and Hutchings, 1992, 1994) and image analysis of sections (Carreiro-Silva and McClanahan, 2012; Osorno et al., 2005; Pari et al., 1998, 2002).assessed via image analysis. 4.3 Palaeoenvironmental implications In the fossil record, sponge borings are preserved as trace fossils in calcareous hard substrates such as rocky shores, hardgrounds, or shells providing important information about palaeoenvironmental conditions (Wilson, 2007). Whereas
recent boring sponges can be identified by their spicules or other morphological and molecular characters, the description of fossil entobians mostly relies on the morphological characterisation of their bioerosion traces. This is, because the preservation potential of the boring is much higher than that of the siliceous spicules, which are only rarely preserved within the borings (e.g., Blissett et al., 2006; Bromley and Schönberg, 2008; Reitner and Keupp, 1991). Thus, in order to allow conclusions about past environmental conditions drawn in an actualistic approach from the ecophysiology studied in extant
sponges, traces of recent sponges need to be matched with the sponge spicule record, so that deductions about fossil trace makers can be made where a close morphological resemblance is found between fossil and recent traces. This study is one of the few that allowed matching sponge borings (bioerosion traces) and boring sponges (trace makers) by combining micro-CT with spicule analysis, providing respective information for five species of recent sponges. This information furthers an earlier detailed inventory of Mediterranean sponge borings and boring sponges by Bromley and
D'Alessandro (1989). These authors were also able to obtain some clear matches between sponge species and ichnospecies, but in accordance with our results they also showed that one sponge species can produce different traces. Especially C. celata was described several times as producing traces that vary morphologically (Bromley and D'Alessandro, 1989; De Groot, 1977), E. geometrica and E. megastoma, even in the same type of substrate. However, as mentioned above, C. celata is not a single species, but a species complex of several morphologically indistinct species, and a proper separation of
species presently relies on molecular taxonomy (De Paula et al., 2012; Xavier et al., 2010). While spicular morphology can be variable with different environmental conditions (Bavestrello et al., 1993; Hoeksema, 1983; Rosell and Uriz, 1991), we recognised subtle but consistent differences in spicule morphology between C. cf. celata 1 (producing E. geometrica) and C. 11
cf. celata 2 (producing E. megastoma), and in this case different traces may in fact represent different trace makers. A similar situation may be the case for the two borings found in the other difficult species, C. cf. viridis (E. ovula and E. mammilata), but as present samples were not preserved for molecular analysis, we cannot confirm or reject this assumption. In contrast to C. celata, we distinguished two different entobians for C. schmidtii: E. cateniformis and E. cf. ovula. Bromley 5
and D'Alessandro (1989) also identified C. schmidtii as trace maker of E. ovula, but in their study E. cateniformis was produced by P. vastifica (formerly C. vastifica). We furthermore identified C. cf. viridis as trace maker for E. ovula and E. mammilata, which led to the conclusion that not only the same species can produce different traces, but the same trace can be produced by different species – which is not a surprise but in accordance to basic ichnological principles (e.g., Bromley and Fürsich, 1980). Our results thus also agree with the assumption of Bromley and D'Alessandro (1984) that the
morphology of entobians can strongly vary with the nature and structure of the substrate, the quality of the surrounding environment, the proximity of other endoliths, the species of the boring sponge, and the ontogeny of the borer. However, we lack comparative data as all presently available research on the correlation of sponge borings and boring sponges was carried out in Mediterranean Sea. Further studies are needed in order to ascertain whether the observed correlations also apply to different biogeographic realms, and to better understand the application and limitations of sponge bioerosion traces as
palaeoenvironmental indicators. 4.4 Long-term succession of boring sponges: Are 14 years long enough to develop equilibrium communities in a warm-temperate environment? This study provides one of the longest records for a bioerosion experiment, and is one of the few available from the Mediterranean. It included quantitative analyses and observations on succession dynamics of macrobioeroders, all of which
represents vital information to assess the impact of macrobioerosion on marine carbonate environments. Using the approach of micro-CT in combination with sponge spicule analysis revealed that during the experiment the blocks were predominantly bioeroded by sponges. The present study from a warm-temperate habitat confirms findings from tropical coral reefs that sponges require a few years to colonise newly available substrates and may only form larger infestations after more than 7 years (e.g., Kiene and Hutchings, 1992, 1994). Based on the present results and taking earlier macroscopic observations of
the same blocks into account (Bromley et al., 1990), we recognised two developmental phases during our experiment: (1) an early community stage with initial sponge bioerosion and comparatively low macrobioerosion rates between years 1 and 5 and (2) an intermediate stage starting in year 6 or 7 when boring sponges become firmly established and bioerosion rates increase. Especially in the latter phase, our material displayed much variability, which we expect to decrease at later stages, when a stable bioeroding community (i.e. a fully developed bioeroding community of microborers, macroborers, and grazers
also present in the ambient environment, with relatively stable bioerosion rates) has established. Across the early and intermediate stages, bioerosion rates increased over time, but can be expected to slow down to a relatively stable rate when equilibrium conditions are eventually reached. Based on the present dataset, a sound prediction about the onset of these 12
equilibrium conditions is not feasible, and would require even longer exposures combined with a higher number of replicates, and such experiments would be necessary to determine whether bioerosion rates peak at an equilibrium plateau, or, more likely, that highest bioerosion rates are reached in the intermediate stage of colonisation, when substrate is not yet limited and competition not yet restricting further growth. 5
The analysis of ontogenetic stages of the observed entobians, nevertheless, suggests a distinct development of sponge bioerosion over time. Having settled down on suitable substrates and finding ample space, boring sponges can rapidly mature, preferentially by lateral extension. With more specimens colonising the blocks, boring sponges formed increasingly three-dimensional patterns, but less developed ontogenetic stages. This is in good agreement with observations by Rützler (1975), who showed that with sufficient space and little competition, sponge borings mostly spread laterally and
progressively bore vertically when the substrate edges are reached or lateral spreading is compromised by neighbouring competitors or other limitations. The presence of an increasing number of vertical borings during the intermediate stage in our experiment could indicate the gradual onset of a saturation phase. Similar observations with macrobioerosion rates proceeding at lower rates when free substrates became scarce and crowded with borings were demonstrated during long-term studies from the tropical realm (Carreiro-Silva and McClanahan, 2012; Kiene and Hutchings, 1994; Lescinsky et al., 2008).
At present, however, we cannot conclude how much time is needed in warm-temperate environments to reach equilibrium phases. This again underlines the necessity for further long-term studies, especially outside the tropical realm.
5 Conclusions This study presents the first record on long-term bioerosion from the warm-temperate realm and showcases the use of micro20
CT to study internal bioerosion. In contrast to previous studies, experimental blocks were almost exclusively colonised by boring sponges, while only few worm and no bivalve borings were observed. Analyses of bioerosion traces and rates suggested an early community development stage during the first 5 years of exposure, where first boring sponges settle, but yield low rates of macrobioerosion, and an intermediate stage commencing in years 6 to 7 when boring sponges matured and bioerosion rates increase. After 14 years, 30 % of the block volumes were occupied by boring sponges. Analysis of
ontogenetic stages of sponge borings suggested that successful settlement of boring sponges is strongly dependent on the availability of space and on competition by other bioeroders. A high spatial variability in macrobioerosion prohibited clear conclusions about the onset of macrobioerosion equilibrium conditions. More long-term experiments are needed in order to identify equilibrium conditions and to assess the impact of macrobioerosion in different biogeographic realms.
Acknowledgements We thank Nicol Mahnken (Senckenberg am Meer) for technical support and Ines Pyko (Erlangen) for her help in inventorying the experimental blocks. This study was funded by the Deutsche Forschungsgemeinschaft (DFG Wi 3754/2-1). The editor Hiroshi Kitazato, William Kiene and an anonymous referee are acknowledged for valuable comments on the 13
Formatiert: Englisch (USA)
manuscript. This paper is published with the permission of the Director of the Institute of Geology and Mineral Exploration, Athens, Greece.
References Badde, A. and Illerhaus, B.: Three dimensional computerized microtomography in the analysis of sculpture, Scanning, 30, 16-26, 2008. Baum, D. and Titschack, J.: Cavity and pore segmentation in 3D images with ambient occlusion, in: Eurographics 5
Conference on Visualization (EuroVis), Cagliari, Italy, 25-29 May 2015, submitted.Baum, D. and Titschack, J.: Cavity and pore segmentation in 3D images with ambient occlusion, in: Eurographics Conference on Visualization, Groningen, Netherlands, 6-10 June 2016, in press. Bavestrello, G., Bonito, M., and Sarà, M.: Influence of depth on the size of sponge spicules, Sci. Mar., 57, 415-420, 1993. Becker, L. C. and Reaka-Kudla, M. L.: The use of tomography in assessing bioerosion in corals, in: Proceedings of the 8th
International Coral Reef Symposium Vol. 2, Smithsonian Tropical Research Institute, Panama, 24-29 June 1996, 1819-1824, 1997. Beuck, L., Vertino, A., Stepina, E., Karolczak, M., and Pfannkuche, O.: Skeletal response of Lophelia pertusa (Scleractinia) to bioeroding sponge infestation visualised with micro-computed tomography, Facies, 53, 157-176, 2007. Beuck, L., Wisshak, M., Munnecke, A., and Freiwald, A.: A giant boring in a Silurian stromatoporoid analysed by computer
tomography, Acta Palaeontol. Pol., 53, 149-160, 2008. Blissett, D. J., Pickerill, R. K., and Rigby, J. K.: A new species of boring sponge from the White Limestone Group, Jamaica, Caribb. J. Sci., 42, 247-251, 2006. Bromley, R. G.: Borings as trace fossils and Entobia cretacea Portlock, as an example. Geol. J., Spec. Iss. 3, 49-90, 1970. Bromley, R. G. and D'Alessandro, A.: Bioerosion in the Pleistocene of southern Italy: ichnogenera Caulostrepsis and
Maeandropolydora, Riv. Ital. Paleontol. S., 89, 283-309, 1983. Bromley, R. G. and D'Alessandro, A.: The ichnogenus Entobia from the Miocene, Pliocene and Pleistocene of southern Italy, Riv. Ital. Paleontol. S., 90, 227-296, 1984.
Bromley, R. G. and D'Alessandro, A.: Ichnological study of shallow marine endolithic sponges from the Italian coast, Riv. Ital. Paleontol. S., 95, 279-314, 1989. Bromley, R. G. and Fürsich, F. T.: Comments on the proposed amendments to the International Code of Zoological Nomenclature regarding ichnotaxa. Z.N. (S.) 1973, B. Zool. Nomencl., 37, 6-10, 1980. 5
Bromley, R. G. and Schönberg, C. H.: Borings, bodies and ghosts: spicules of the endolithic sponge Aka akis sp. nov. within the boring Entobia cretacea, Cretaceous, England, in: Current Developments in Bioerosion, Wisshak, M. and Tapanila, L. (Eds.), Springer, Berlin, 235-248, 2008. Bromley, R. G., Hanken, N.-M., and Asgaard, U.: Shallow marine bioerosion: preliminary results of an experimental study, B. Geol. Soc. Denmark, 38, 85-99, 1990.
Bromley, R. G. and Tendal, O. S.: Example of substrate competition and phobotropism between two clionid sponges. J. Zool. Lond, 169, 151-155, 1973. Bromley, R. G., Beuck, L., and Ruggiero, E. T.: Endolithic sponge versus terebratulid brachiopod, Pleistocene, Italy: accidental symbiosis, bioclaustration and deformity, in: Current Developments in Bioerosion, Wisshak, M. and Tapanila, L. (Eds.), Springer, Berlin, 361-368, 2008.
Calcinai, B., Azzini, F., Bavestrello, G., Gaggero, L., and Cerrano, C.: Excavating rates and boring pattern of Cliona
Formatiert: Schriftart: Kursiv
albimarginata (Porifera: Clionaidae) in different substrata, in: Porifera Research: Biodiversity, Innovation & Sustainability,
Formatiert: Nicht Hervorheben
Proceedings of the 7 International Sponge Symposium, Búzios, Rio de Janeiro, 7-13 May 2006, 203-210, 2007. Calcinai, B., Bavestrello, G., Cuttone, G., and Cerrano, C.: Excavating sponges from the Adriatic Sea: description of Cliona adriatica sp. nov. (Demospongiae: Clionaidae) and estimation of its boring activity, J. Mar. Biol. Assoc. U.K., 91, 339-346, 20
2011. Carballo, J. L., Sanchez-Moyano, J.E., and García-Gómez, J. C.: Taxonomic and ecological remarks on boring sponges (Clionidae) from the Straits of Gibraltar (southern Spain): tentative bioindicators?, Zool. J. Linnean Soc., 112, 407-424, 1994. 16
Carreiro-Silva, M. and McClanahan, T. R.: Macrobioerosion of dead branching Porites, 4 and 6 years after coral mass mortality, Mar. Ecol. Prog. Ser., 458, 103-122, 2012. Chazottes, V., Le Campion-Alsumard, T., Peyrot-Clausade, M., and Cuet, P.: The effects of eutrophication-related alterations to coral reef communities on agents and rates of bioerosion (Reunion Island, Indian Ocean), Coral Reefs, 21, 3755
390, 2002. Christomanos, A. A. and Norton, A. B.: Beiträge zur Kenntnis der Pigmente der Schwämme Aplysina aerophoba und Clione schmidtii, Folia Bioch. et Biol. Graeca, 11, 10-20, 1974. Corriero, G., Scalera Liaci, L., Ruggiero, D., and Pansini, M.: The sponge community of a semi-submerged Mediterranean cave, Mar. Ecol., 21, 85-96, 2000.
Crook, E. D., Cohen, A. L., Rebolledo-Vieyra, M., Hernandez, L., and Paytan, A.: Reduced calcification and lack of acclimatization by coral colonies growing in areas of persistent natural acidification, PNAS, 110, 11044-11049, 2013. DeCarlo, T. M., Cohen, A. L., Barkley, H. C., Cobban, Q., Young, C., Shamberger, K. E., Brainard, R. E., and Golbuu, Y.: Coral macrobioerosion is accelerated by ocean acidification and nutrients, Geology, 43, 7-10, 2015. De Groot, R. A.: Boring sponges (Clinoidae) and their trace fossils from the coast near Rovinj (Yugoslavia), Geol.
Mijnbouw, 56, 168-181, 1977. De Paula, T. S., Zilberberg, C., Hajdu, E., and Lôbo-Hajdu, G.: Morphology and molecules on opposite sides of the diversity gradient: four cryptic species of the Cliona celata (Porifera, Demospongiae) complex in South America revealed by mitochondrial and nuclear markers, Mol. Phylogenet. Evol., 62, 529-541, 2012. EMODnet Portal for Bathymetry, available at: http://www.emodnet-bathymetry.eu, 2015.
Evcen, A., and Çinar, M. E.: Bioeroding sponge species (Porifera) in the Aegean Sea (Eastern Mediterranean), J. Black Sea/Mediterranean Environment, 21, 285-306, 2015. Fang, J. K. H., Mello-Athayde, M. A., Schönberg, C. H. L., Kline, D. I., Hoegh-Guldberg, O., and Dove, S.: Sponge biomass and bioerosion rates increase under ocean warming and acidification, Glob. Change Biol., 19, 3581-3591, 2013. 17
Färber, C., Wisshak, M., Pyko, I., Bellou, N., and Freiwald, A.: Effects of water depth, seasonal exposure, and substrate orientation on microbial bioerosion in the Ionian Sea (Eastern Mediterranean), PLoS ONE, 10, e0126495, 2015. Feldkamp, L. A., Davis, L. C., and Kress, J. W.: Practical cone-beam algorithm, J. Opt. Soc. Am. A, 1, 612-619, 1984. Fischer, P. M.: Recherches sur les éponges perforantes fossiles, Nouv. Arch. Mus. Hist. Nat. Paris, 4, 117-173, 1868. 5
Glynn, P. W.: Bioerosion and coral reef growth: a dynamic balance, in: Life and Death of Coral Reefs, Birkeland, C. (Ed.), Chapman and Hall, New York, 68-95, 1997. Grange, J. S., Rybarczyk, H., and Tribollet, A.: The three steps of the carbonate biogenic dissolution process by microborers in coral reefs (New Caledonia), Environ. Sci. Pollut. Res. Int., 22, 13625-13637, 2015. Grant, R. E.: Notice of a new zoophyte (Cliona celata, Gr.) from the Firth of Forth, Edinburgh New Phil. J., 1, 78-81, 1826.
Hancock, A.: On the excavating powers of certain sponges belonging to the genus Cliona; with descriptions of several new species, and an allied generic form. Ann. Mag. Nat. Hist., Ser. 2, 3, 321-348, 1849. Hassan, M.: Modification of carbonate substrata by bioerosion and bioaccretion on coral reefs of the Red Sea, Shaker Verlag, Aachen, 1998. Hoeksema, B. W.: Excavation patterns and spiculae dimensions of the boring sponge Cliona celata from the SW
Netherlands, Senckenbergiana Marit., 15, 55-85, 1983. Hutchings, P. A., Kiene, W. E., Cunningham, R. B., and Donnelly, C.: Spatial and temporal patterns of non-colonial boring organisms (polychaetes, sipunculans and bivalve molluscs) in Porites at Lizard Island, Great Barrier Reef, Coral Reefs, 11, 23-31, 1992. Kennedy, E. V., Perry, C. T., Halloran, P. R., Iglesias-Prieto, R., Schönberg, C. H. L., Wisshak, M., Form, A. U., Carricart-
Ganivet, J. P., Fine, M., Eakin, C. M., and Mumby, P. J.: Avoiding coral reef functional collapse requires local and global action, Curr. Biol., 23, 912-918, 2013. Kiene, W. E.: A model of bioerosion on the Great Barrier Reef, Proceedings of the 6th International Coral Reef Symposium Vol. 3, Townsville, Australia, 8-12 August 1988, 449-454, 1988. 18
Kiene, W. E. and Hutchings, P. A.: Long-term bioerosion of experimental coral substrates from Lizard Island, Great Barrier Reef, Proceedings of the 7th International Coral Reef Symposium Vol. 1, UOG Station, Guam, 22-27 June 1992, 397-403, 1992. Kiene, W. E. and Hutchings, P. A.: Bioerosion experiments at Lizard Island, Great Barrier Reef, Coral Reefs, 13, 91-98, 5
1994. Le Campion-Alsumard, T.: Les cyanophycées endolithes marines. Systématique, ultrastructure, écologie et biodestruction, Oceanol. Acta, 2, 143-156, 1979. Leal, C. V., De Paula, T. S., Lôbo-Hajdu, G., Schönberg, C. H. L., and Esteves, E. L.: Morphological and molecular systematics of the ‘Cliona viridis complex’ from south-eastern Brazil, J. Mar. Biol. Assoc. U.K., doi:
10.1017/S0025315415001642, 2015. Lescinsky, H. L., Hill, M., and Hoedt, B. A.: Results of long-term bioerosion study: Belize patch reefs, Proceedings of the 11th International Coral Reef Symposium, Ft. Lauderdale, Florida, 7-11 July 2008, 26-30, 2008. Neumann, A. C.: Observations on coastal erosion in Bermuda and measurements of the boring rate of the sponge, Cliona lampa, Limnol. Oceanogr., 11, 92-108, 1966.
Osorno, A., Peyrot-Clausade, M., and Hutchings, P. A.: Patterns and rates of erosion in dead Porites across the Great Barrier Reef (Australia) after 2 years and 4 years of exposure, Coral Reefs, 24, 292-303, 2005. Pari, N., Peyrot-Clausade, M., Le Campion-Alsumard, T., Hutchings, P., Chazottes, V., Golubic, S., Le Campion, J., and Fontaine, M. F.: Bioerosion of experimental substrates on high islands and on atoll lagoons (French Polynesia) after two years of exposure, Mar. Ecol. Prog. Ser., 166, 119-130, 1998.
Pari, N., Peyrot-Clausade, M., and Hutchings, P. A.: Bioerosion of experimental substrates on high islands and atoll lagoons (French Polynesia) during 5 years of exposure, J. Exp. Mar. Bio. Ecol., 276, 109-127, 2002.
Peyrot-Clausade, M., Le Campion-Alsumard, T., Hutchings, P., LeCampion, J., Payri, C., and Fontaine, M.-F.: Initial bioerosion and bioaccretion on experimental substrates in high island and atoll lagoons (French Polynesia), Oceanol. Acta, 18, 531-541, 1995. Rasband, W. S.: ImageJ. U. S. National Institutes of Health, Bethesda, Maryland, USA, http://imagej.nih.gov/ij/, 1997-2015. 5
Reitner, J. and Keupp, H.: The fossil record of the haplosclerid excavating sponge Aka de Laubenfels. In: Fossil and Recent Sponges, Reitner, J. and Keupp, H. (Eds.), Springer, Berlin, 102-120, 1991. Ridley, S. O.: Account of the zoological collections made during the surveys of the H. M. S. “Alert” in the Strait of Magellan and on the coast of Patagonia. Spongida, Proc. Zool. Soc., London, 107-139, 1881. Rosell, D. and Uriz, M.-J.: Cliona viridis (Schmidt, 1862) and Cliona nigricans (Schmidt, 1862) (Porifera, Hadromerida):
evidence which shows they are the same species, Ophelia, 33, 45-53, 1991. Rosell, D. and Uriz, M.-J.: Excavating and endolithic sponge species (Porifera) from the Mediterranean: species descriptions and identification key, Org. Divers. Evol., 2, 55-86, 2002. Rosell, D., Uriz, M.-J., and Martin, D.: Infestation by excavating sponges on the oyster (Ostrea edulis) populations of the Blanes littoral zone (north-western Mediterranean Sea), J. Mar. Biol. Assoc. U.K., 79, 409-413, 1999.
Rützler, K.: The burrowing sponges of Bermuda, Smithson. Contr. Zool., 165, 1-32, 1974. Rützler, K.: The role of burrowing sponges in bioerosion, Oecologia, 19, 203-216, 1975. Rützler, K. and Bromley, R. G.: Cliona rhodensis, new species (Porifera: Hadromerida) from the Mediterranean, Proc. Biol. Soc. Wash., 94, 1219-1225, 1981. Sammarco, P. W. and Risk, M. J.: Large-scale patterns in internal bioerosion of Porites: cross continental shelf trends on the
Great Barrier Reef, Mar. Ecol. Prog. Ser., 59, 145-156, 1990. Schmidt, O: Die Spongien des adriatischen Meeres, Engelmann, Leipzig, 1862.
Schön, J.: Physical properties of rocks: a workbook, Handbook of Petroleum Exploration and Production, 8, Elsevier, Amsterdam, 2011. Schönberg, C. H. L.: Estimating the extent of endolithic tissue of a Great Barrier Reef clionid sponge. Senckenbergiana marit., 31, 29-19, 2001. 5
Schönberg, C. H. L.: A history of sponge erosion: from past myths and hypotheses to recent approaches, in: Current Developments in Bioerosion, Wisshak, M. and Tapanila, L. (Eds.), Springer, Berlin, 165-202, 2008. Schönberg, C. H. L. and Shields, G.: Micro-computed tomography for studies on Entobia: transparent substrate versus modern technology, in: Current Developments in Bioerosion, Wisshak, M. and Tapanila, L. (Eds.), Springer, Berlin, 147164, 2008.
Schönberg, C. H. L. and Wisshak, M.: Marine bioerosion, in: The Mediterranean Sea, Goffredo, S. and Dubinsky, Z. (Eds.), Springer, Netherlands, 49-68, 2014. Scott, P. J. B., Moser, K. A., and Risk, M. J.: Bioerosion of concrete and limestone by marine organisms: A 13 year experiment from Jamaica, Mar. Pollut. Bull., 19, 219-222, 1988. Silbiger, N. J., Guadayol, Ò., Thomas, F. I. M., and Donahue, M. J.: Reefs shift from net accretion to net erosion along a
natural environmental gradient, Mar. Ecol. Prog. Ser., 515, 33-44, 2014. Silbiger, N. J., Guadayol, Ò., Thomas, F. I. M., and Donahue, M. J.: A novel μCT analysis reveals different responses of bioerosion and secondary accretion to environmental variability, PLoS ONE, 11, e0153058, 2016. Stalling, D., Westerhof, M., and Hege, H.-C.: Amira: a highly interactive system for visual data analysis, in: The Visualization Handbook, Hansen, C. D. and Johnson, C. R. (Eds.), Elsevier Butterworth-Heinemann, Burlington, 749-767,
2005. Titschack, J., Baum, D., De Pol-Holz, R., López Correa, M., Forster, N., Flögel, S., Hebbeln, D., and Freiwald, A.: Aggradation and carbonate accumulation of Holocene Norwegian cold-water coral reefs, Sedimentology, 62, 1873-1898, 2015. 21
Topsent, E.: Contribution à l’étude des Clionides. Arch. Zool. Exper. Gén., Ser. 2, 5, 1-165, 1888. Tribollet, A. and Golubic, S.: Cross-shelf differences in the pattern and pace of bioerosion of experimental carbonate substrates exposed for 3 years on the northern Great Barrier Reef, Australia, Coral Reefs, 24, 422-434, 2005. Tribollet, A., Godinot, C., Atkinson, M., and Langdon, C.: Effects of elevated pCO2 on dissolution of coral carbonates by 5
microbial euendoliths, Global Biogeochem. Cy., 23, GB3008, 2009. Tribollet, A., Radtke, G., and Golubic, S.: Bioerosion, in: Encyclopedia of Geobiology, Reitner, J. and Thiel, V. (Eds.), Springer, Dordrecht, 117-134, 2011. Vacelet, J., Bitar, G., Dailianis, T., Zibrowius, H., and Perez, T.: A large encrusting clionaid sponge in the Eastern Mediterranean Sea, Mar. Ecol, 29, 237-246, 2008.
Vogel, K., Kiene, W. E., Gektidis, M., and Radtke, G.: Scientific results from investigation of microbial borers and bioerosion in reef environments, Göttinger Arb. Geol. Pal., Sb 2, 139-143, 1996. Vogel, K., Gektidis, M., Golubic, S., Kiene, W. E., and Radtke, G.: Experimental studies on microbial bioerosion at Lee Stocking Island, Bahamas and One Tree Island, Great Barrier Reef, Australia: implications for paleoecological reconstructions, Lethaia, 33, 190-204, 2000.
Wilson, M.: Macroborings and the evolution of marine bioerosion, In: Trace fossils: Concepts, Problems, Prospects, Milller III, W. (Ed.), Elsevier, Amsterdam, 356-367, 2007. Wisshak, M.: High-latitude bioerosion: The Kosterfjord experiment, Springer, Berlin Heidelberg, 2006. Wisshak, M.: Microbioerosion, in: Trace Fossils as Indicators of Sedimentary Environments, Knaust, D. and Bromley, R. G. (Eds.), Elsevier, Amsterdam, 213-243, 2012.
Wisshak, M., Form, A., Jakobsen, J., and Freiwald, A.: Temperate carbonate cycling and water mass properties from intertidal to bathyal depths (Azores), Biogeosciences, 7, 2379-2396, 2010. Wisshak, M., Tribollet, A., Golubic, S., Jakobsen, J., and Freiwald, A.: Temperate bioerosion: ichnodiversity and biodiversity from intertidal to bathyal depths (Azores), Geobiology, 9, 492-520, 2011. 22
Wisshak, M., Schönberg, C. H. L., Form, A., and Freiwald, A.: Ocean acidification accelerates reef bioerosion, PLoS ONE, 7, e45124, 2012. Wisshak, M., Schönberg, C. H. L., Form, A., and Freiwald, A.: Effects of ocean acidification and global warming on reef bioerosion–lessons from a clionaid sponge, Aquatic Biol., 19, 111-127, 2013. 5
Wisshak, M., Schönberg, C. H. L., Form, A., and Freiwald, A.: Sponge bioerosion accelerated by ocean acidification across species and latitudes?, Helgol. Mar. Res., 68, 253-262, 2014. Xavier, J. R., Rachello-Dolmen, P. G., Parra-Velandia, F., Schönberg, C. H. L., Breeuwer, J. A., and van Soest, R. W.: Molecular evidence of cryptic speciation in the “cosmopolitan” excavating sponge Cliona celata (Porifera, Clionaidae), Mol. Phylogenet. Evol., 56, 13-20, 2010.
Table 1. Metadata of experimental blocks deployed during the experiment and analysed via micro-computed tomography (E = east, W = west, Ma = marble, Mi = micritic limestone). Exposure Site Coast Water depth Deployment Recovery Block (yrs) (m) lithology 1 Lindos E 3-8 21.10.1982 25 October 1983 Ma 1 Pyrgos W 3-6 20.10.1982 26 October 1983 Ma 2 Pyrgos W 8 26.10.1983 15 October 1985 Ma 3 Ladiko E 3-4 28.10.1983 22 October 1986 Ma 4 Lindos E 16-17 19.10.1982 19 October 1986 Mi 4 Ladiko E 3.5 28.10.1983 October 1987 Ma 5 Ladiko E 3 28.10.1983 14 October 1988 Mi 6 Lindos E 12 18.10.1985 18 October 1991 Ma 7* Kolimbia E 3 17.10.1982 13 October 1989 Ma 8 Lindos E 12 18.10.1985 1993 Ma 8-9 Pyrgos W 3 or 8 m 20.10.1982/83 16 October 1991 Ma 14 Pyrgos W 7 20.10.1982 1996 Ma * The 7-year block was cut into three such replicates to obtain an impression of the spatial variability of bioerosion within a 5
single block.three replicates scanned
Table 2. Inventory of bioerosion traces. Sponge borings (trace = Entobia ispp.) and boring sponges (trace maker = Cliona spp.) in the scanned experimental blocks were assigned via spicule analysis. Ontogenetic phases of sponge boring traces were determined according to Bromley and D'Alessandro (1984) with most mature stages in brackets. Measurements of sponge spicules are given as ranges, with length before widths, and means in parenthesis. Number of tylostyles n = 20, number of spirasters n = 5, unless otherwise indicated in square brackets. Exposure Boring Phase Producer Tylostyles Spiraster (yrs) (µm) (µm) 2 Entobia cateniformis Fig. 2C C (D) Cliona Fig. 6A 170-247 (198) x a) 57-71 (66) x schmidtii 3-8 (5) 2-3 (2)
Entobia megastoma Entobia geometrica
Fig. 2D Fig. 3A
A-B (D) D (D)
Caulostrepsis isp. Entobia cf. ovula
Fig. 3A1-3 Fig. 3B
Entobia cf. mammilata Entobia megastoma
Entobia mammilata Entobia mammilata
Fig. 4B2 Fig. 4C1
B (E) D (E)
Entobia cf. ovula
Entobia cf. magna
Entobia cf. parva Entobia megastoma Entobia cf. cretacea Trypanites isp.
218-369 (316) x 4-8 (6) 208-339 (283) x 3-9 (6) 234-394 (324) x 4-9 (7)
Cliona cf. celata 2 Cliona cf. schmidtii
Cliona rhodensis Sponge Sponge Sponge Worm
Fig. 6E Fig. 6G
235-358 (321) x 5-9 (7) 179-275 (220) x 3-6 (5)
245-356 (289) x 6-10 (8) -
a) 30-44 (35) x 1-2 (1) b) 18 x 1  a) 58-84 (75) x 1-2 (2) b) 25-46 (35) x 2 (2) c) 21 x 7  23 x 1  -
Figure 1. Location of the long-term experiment at Rhodes, Greece, in the Eastern Mediterranean Sea. Between 1982 and 5
1996, experimental blocks were deployed at four sites on the east and west coast of Rhodes in 3 to 17 m water depth. Bathymetric data were derived from the EMODnet Portal for Bathymetry (EMODnet, 2015).
Figure 2. Micro-computed tomographic visualisation of bioerosion traces in experimental blocks deployed for 1-4 years. (AB) 1-year blocks showed no macrobioerosion traces. First bioerosion traces were observed (C) in the 2-year block with 5
Entobia cateniformis and (D) in the 3-year block with E. megastoma. (E-F) The 4-year blocks showed no distinct macrobioerosion traces (size of blocks = 90 x 90 x 18 mm).
Figure 3. Micro-computed tomographic visualisation of bioerosion traces in experimental blocks deployed for 5-6 years. (A) The 5-year block showed a network of Entobia geometrica and specimens of Caulostrepsis isp. (A1-A3). (B) The 6-year 5
block showed a cluster of E. cf. ovula (scales A1-A3 = 2 mm, size of blocks = 90 x 90 x 18 mm).
Figure 4. Micro-computed tomographic visualisation of bioerosion traces in three subsamples of the 7-year block. (A) First subsample of the block with Entobia cf. mammilata, B) second subsample of the block showing two specimens of E. 5
megastoma (B1 and large chambers B2) and E. mammilata (small chambers B2), and C) third subsample of the block with E. mammilata (C1) and E. megastoma (C2) (scales = 10 mm, size of blocks = 90 x 90 x 18 mm).
Figure 5. Micro-computed tomographic visualisation of bioerosion traces in experimental blocks deployed for 8-14 years. (A) 8-year block with Entobia cf. ovula (A1), E. magna (A2), and E. cf. parva (A3), B) 8-9-year block with E. megastoma, 5
and C) 14-year block with E. cf. cretacea (C1-C2) and Trypanites isp. (C3-C5) (scales A1-A3, C1-C2 = 5 mm, scales C3-C5 = 1 mm, size of blocks = 90 x 90 x 18 mm).
Figure 6. Spicules of boring sponges extracted from sponge tissue preserved in cavity networks in the scanned blocks. (A-B) Tylostyles and spirasters of Cliona schmidtii, (C) tylostyles of C.liona cf. celata 1, (D-F) tylostyles of Cliona C. cf. celata 2, 5
(G-H) tylostyles and spirasters of Cliona C. cf. viridis, (I) tylostyles and spirasters of Cliona C. rhodensis (Fig. 5A2) (scales: tylostyles = 50 µm, spirasters = 20 µm).
Figure 7. (A) Proportion of retained substrate vs. internal bioerosion in the scanned blocks, (B) proportional contribution of the different groups of boring organisms to the internal bioerosion in A, and (C) internal bioerosion rates (g m-2-² yr-1) 5
measured in experimental substrates during the experiment.