Connell. 2000. Floating Pontoons Create Novel Habitats for Subtidal Epibiota

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L Journal of Experimental Marine Biology and Ecology

247 (2000) 183–194

www.elsevier.nl/locate/jembe

Floating pontoons create novel habitats for subtidal epibiota

*Sean D. Connell

Centre for Research on Ecological Impacts of Coastal Cities, Marine Ecology Laboratories A11,

University of Sydney, Sydney, NSW 2006, Australia

Received 2 August 1999; received in revised form 14 December 1999; accepted 18 December 1999

Abstract

Urban structures in the form of pontoons and pilings represent major coastal habitats for marine

organisms and understanding the factors causing abundances of organisms to differ between these

and natural habitat has been neglected in the study of coastal ecology. It has been proposed that

composition of substrata explain differences previously described between subtidal assemblages of

epibiota on rocky reef (sandstone) and pontoons (concrete) in Sydney Harbour, Australia. This

study tested the hypothesis that differences in the composition of substratum (sandstone vs.

concrete) independent of type of habitat (rocky reef vs. pontoon) affects the development of

epibiotic assemblages. This was tested by experimentally providing substratum of the two types in

both habitats. Epibiotic assemblages were unaffected by the composition of substratum but

strongly affected by the type of habitat; demonstrating that pontoons constitute novel habitats for

epibiota. This result highlights a need for determining how current ecological understanding of

subtidal epibiota, which is heavily based on studies of urban structures (pilings and pontoons),

relates to natural reef. Future tests of hypotheses about the nature of these differences will not only

contribute to better ecological understanding of epibiota and their use of urban structures as

habitats, but also to better predictions of future changes to the ecology of coastal habitats.

© 2000 Elsevier Science B.V. All rights reserved.

Keywords: Artificial habitats; Disturbance; Fouling; Sessile; Man made

1. Introduction

Urbanisation (sensu McDonnell and Pickett, 1990) of coastal areas is set to continue

with more than half (67%) of the global population living on the coast (Hammond,

*Present address: Department of Environmental Biology, University of Adelaide, South Australia 5005,

Australia. Tel.: 161-8-8303-6125; fax: 1 61-8-8303-4364.

E -mail address: [email protected] (S.D. Connell)

0022-0981/00/$ – see front matter © 2000 Elsevier Science B.V. All rights reserved.

P I I : S 0 0 2 2 - 0 9 8 1 ( 0 0 ) 0 0 1 4 7 - 7



184 S . D. Connell / J . Exp. Mar . Biol. Ecol. 247 (2000) 183 –194

1992), doubling within 30 years (Norse, 1995). Considerable change to the ecology of

coastal habitats is anticipated as natural habitat continues to be destroyed and replaced

by urban structures such as pilings, pontoons and rock walls (Glasby and Connell,

1999). Urban structures are often built over rocky reef, the predominant habitat for someof the world’s most diverse sets of sessile plants and animals (epibiota) that attach to

hard substrata (Moore and Seed, 1986; Womersley, 1987, Shepherd and Davies, 1997).

The urban structures that replace rocky reef support a large subset of these epibiotic

species (Connell and Glasby, 1999) and, therefore, represent a major coastal habitat

occupying thousands of hectares.

Despite this apparent surrogacy for rocky reef there is concern that urban structures

may not substitute natural reef (Glasby and Connell, 1999). Urban structures support

different epibiotic assemblages to those on natural reef (Butler and Connolly, 1996;

Connell and Glasby, 1999; Glasby, 1999a), and may act as different habitats for epibiota.

Such heterogeneity of habitat is one of the most important features influencing theprocesses that affect patterns of abundance (Kolasa and Pickett, 1991). Consequently,

urban structures may cause considerable change to the identity and abundances of

epibiotic species within an area.

Understanding urban structures as marine habitats and how to improve their surrogacy

for natural reef is an area of urgent need in coastal ecology. An immediate priority is the

identification of factors that cause taxa to differ in abundance between urban structures

and reef. Even though a substantial amount of our ecological understanding of subtidal

epibiota is based on studies done on urban structures (primarily pilings and pontoons),

they have been treated as convenient habitats, rather than the basis for hypotheses about

their effects on epibiota (e.g. Osman, 1977; Sutherland and Karlson, 1977; Dean and

Hurd, 1980; Keough, 1984; Butler, 1991; Osman and Whitlach, 1995; Brown and

Swearingen, 1998). Consequently, there is little understanding of the effects of urban

structures on epibiota, and even less on how our current understanding of their ecology

relates to natural reef.

Composition of substratum appears an obvious factor that may explain differences in

abundances of taxa between urban structures and rocky reef. Urban structures are made

of materials naturally foreign to the marine environment (e.g. concrete) and are quite

different to rocky reef. Previous work has shown composition of substratum to affect the

recruitment and development of epibiota on settlement plates (e.g. Crisp and Ryland,1960; Harlin and Lindbergh, 1977; McGuinness, 1989; Anderson and Underwood,

1994). Recent comparisons of rocky reef to several urban structures show the

abundances of epibiota to be more similar among surfaces made of the same material

(concrete pilings and concrete pontoons), and these most different to those on sandstone

reef (Connell and Glasby, 1999). Although differences in composition of substratum

correlate with differences in epibiotic assemblages, this is also true of several other

factors (e.g. age: introduced structures vs. seasoned reef) (Connell and Glasby, 1999).

In this study, the effect of substratum on the development of assemblages of epibiota

was analysed experimentally to assess whether known differences in composition of

substrata (concrete vs. sandstone) explained observed differences in structure of epibioticassemblages between rocky reef and urban structures. Compared to rocky reef, pontoons

support the most distinct assemblages of epibiota (Connell and Glasby, 1999) and would



S . D. Connell / J . Exp. Mar . Biol. Ecol. 247 (2000) 183 –194 185

constitute novel habitats unless substratum explains this dissimilarity. I tested the

hypothesis, therefore, that the development of epibiotic assemblages is affected by

differences in the type of substratum (sandstone vs. concrete) independent of type of

habitat (rocky reef vs. pontoon).

2. Methods

2.1. Study area and experimental treatments

The study was done from June (winter) 1998 to January (summer) 1999 in Middle

Harbour, the northern part of Sydney Harbour, Australia (338489 S, 1518149 E, Fig. 1).

Rocky reefs in Middle Harbour extend about 5 m from the shore and reach a depth of

| 4 m. Pontoons are typically moored 5–10 m from the shore and | 5 m above thesandy bottom. The effects of substrata and habitat were tested by experimentally

providing new substrata (same age) of the two kinds (sandstone and concrete) on the two

habitats (reef and pontoons) at each of four sites |150 m apart.

Experimental plates (153 15 cm) made of either sandstone or concrete were fastened

to pontoons and reef so that they were orientated vertically. Sandstone plates were cut

from sandstone rock and had a grain size and texture ostensibly the same as cleared

areas of subtidal rock. Concrete plates were cut from prefabricated sheets of concrete

and had a smooth texture similar to that of concrete pontoons.

Experimental plates were attached to the outer edges on two sides of a pontoon (3 3 4

m) at a depth of approximately 25 cm. Plates were attached to a beam of PVC pipe that

Fig. 1. Map showing location of sites of study within Sydney Harbour. Location of Sydney Harbour is

indicated on insert of map of Australia.




was strapped to a bottom edge of a pontoon. Experimental plates on the reef were

supported by beams of aluminium 908 angle (1.6 m long) that were bolted to the reef

with stainless steel screws so they were at a depth of approximately 1.5 m below low

water spring tide and 15 cm from the substratum. PVC brackets were glued on to thebacks of plates and these were bolted onto the PVC pipes and beams. Five replicate

plates of each type were attached to each habitat (reef and pontoons) so that they were

1–5 m apart in a haphazard order.

After 7 months, each panel was collected and taken to the laboratory for examination

under a dissecting microscope in which the abundances of benthic invertebrates were

estimated. Primary cover (organisms attached directly to the plate) and secondary cover

(organisms attached to primary cover) were estimated for sessile organisms on the front

of plates using 64 regularly spaced points within a 13 3 13-cm grid (i.e. a 1-cm boarder

around each plate was not sampled to avoid ‘edge effects’). Taxa on the front of plates,

but not under a point were assigned a cover of 0.5%.

2.2. Analytical methods

Abundance data were standardised by converting raw data to percentage data before

summing the primary and secondary covers for all multivariate and univariate tests.

Observations of secondary cover were rare. Multivariate analyses were done using the

41 taxa identified and bare space. Data were fourth-root transformed and the Bray–

Curtis measure (Bray and Curtis, 1957) was used to calculate dissimilarities among

replicates. To visualise multivariate patterns, non-metric multi-dimensional scaling

(nMDS) ordinations were done on the centroids (averages of replicate plates for each

habitat and site, n 5 5). One-way analyses of similarities (ANOSIM) were done (Clarke,

1993) on all replicates to test for differences between substrata and habitats. The

significance level was adjusted for multiple comparisons associated with pairwise tests

(Bonferroni procedure; Rice, 1989).

Univariate analyses were done using three-way ANOVAs (e.g. Underwood, 1997) in

which all factors (substrate, habitat, site) were crossed, ‘substrate’ and ‘habitat’ were

treated as fixed and ‘site’ as random. Data were Arc-sine transformed and significance

was judged at 5 0.05 unless Cochran’s C -test detected heterogeneous variances. Data

with heterogenous variances were judged at the more conservative probability of 0.01.

3. Results

Assemblages on plates were composed primarily of bivalves ( Mytilus edulis,

Crassostrea gigas), encrusting bryozoans (Watersipora arcuata, W . subtorquata,

Cryptosula pallasiana, Schizoporella errata, Beania magellanica, Fenestrulina

mutabilis, Conopeum seurati, Celleporaria sp., Microporella spp.), arborescent

bryozoans ( Bugula neritina, B. stolonifera, Tricellaria inopinata), barnacles ( Balanus

variegatus and B. trigonus), calcareous tubeworms (spirorbids and serpulids), solitaryascidians (Styela pilcata), colonial ascidians ( Diplosoma listerianum, Didemnum sp.),

five taxa of sponges, green algae (Cladophorales, Enteromorpha, Ulvales, Codium), red




algae (Ceramiales, Laurencia, Hypnea, Rhodymenia), brown algae (Feldmania,

Sphacelaria, Dictyotalean spp. Dictyota), and coral (Culicia sp.).

Prior to the experiment, I predicted that the development of epibiotic assemblages is

affected by differences in the type of substratum (sandstone vs. concrete) independent of type of habitat (rocky reef vs. pontoon). The two-factor nMDS plot indicated that the

multivariate differences in the structure of assemblages were greater between habitats

than between substrata (Fig. 2). That is, centroids representing assemblages revealed

greater separation between plates attached to pontoons and reef than between plates

made of concrete and sandstone. Correspondingly, measures of dissimilarity indicated

that assemblages were most different between pontoons and reef, and that assemblages

were most similar between plates made of sandstone and concrete in the same habitat

(Table 1).

Most differences in abundance of individual taxa occurred between pontoons and reef

rather than between plates made of sandstone and concrete (Figs. 3 and 4, Tables 2 and3). All but one of the 12 taxa tested (serpulids) differed in abundance between habitats.

The abundance of only three taxa differed between types of substrata (spirorbids,

concrete. sandstone; red and green algae, concrete, sandstone).

Cover was consistently greater on pontoons than reef for three taxa (abhoresent

bryozoans, colonial ascidians and the mussel, Mytilus edulis ) , although the magnitude of

Fig. 2. Two-factor nMDS ordination comparing centroids of epibiotic assemblages on plates made of

sandstone (grey letters) and concrete plates (black letters) that were attached to rocky reef (R) and pontoons

(P). The structure of assemblages differed between reef and pontoons despite being on plates of the same

substrata; concrete (ANOSIM: R50.83, P,0.05) and sandstone (ANOSIM: R5 0.92, P,0.05). Similarly,

tests did not detect significant differences between plates made of concrete and sandstone attached to pontoons

(ANOSIM: R5 0.04 P.0.05) and reef (ANOSIM: R5 0.08, P.0.05).




Table 1

Bray–Curtis measures of dissimilarities between habitats and surfaces ( the larger the value the more dissimilar

the assemblage)

Treatment Measure of dissimilarityPontoon concrete Pontoon sandstone Reef concrete

Pontoon concrete – – –

Pontoon sandstone 35.8 – –

Reef concrete 56.4 57.3 –

Reef sandstone 57.8 58.2 40.2

the differences varied among sites (Fig. 3, Table 2; SNK tests on Habitat3Site

interaction). The opposite pattern occurred for the tiny calcareous tubeworms (species of

spirorbids), which had one of the most extensive coverage of any taxa (Fig. 4a, Table 3a;

SNK tests on Habitat3Site interaction).

The abundances of several taxa differed between pontoons and reef at all but one site

(i.e. solitary ascidians, pontoons. reef; barnacles, pontoons. reef; red algae,

pontoons, reef) or two sites (sponges, pontoons. reef). No particular site was

associated with the failure to detect differences between habitats (Fig. 3, Table 2; SNK

on Habitat3Site interaction). The remaining taxa (except sepulids) also differed

between pontoons and reef, but these differences varied inconsistently among sites (i.e.

encrusting bryozoans, green and brown algae) (Fig. 4; Table 3; SNK on Habitat3Site

interaction).

4. Discussion

Marine ecologists have a history of taking models developed by terrestrial ecologists

and applying them to the marine environment. This practise is often inappropriate

(Underwood and Denley, 1984), and this is particularly true for understanding the

ecology of urban habitats in the sea. Unlike terrestrial environments, urban structures in

Fig. 3. Percentage cover of taxa (per 153 15 cm6S.E.) on pontoons (pontoon) and rocky reef (reef) for

concrete (unshaded bars) and sandstone plates (shaded bars) at each of four sites (n5 5). The first four bars of

each type of plate (shaded/unshaded bars) in each habitat (pontoon/reef) represent sites 1–4, respectively.




Fig. 4. Percentage cover of taxa (per 153 15 cm6S.E.) on pontoons (pontoon) and rocky reef (reef) for

concrete (unshaded bars) and sandstone (shaded bars) at each of four sites (n 55). The first four bars of each

type of plate (shaded/unshaded bars) in each habitat (pontoon/reef) represent sites 1–4, respectively.

marine environments provide substrate for an abundant and diverse set of plants and

animals (Sutherland and Karlson, 1977; Butler, 1991; Glasby and Connell, 1999). As

such they create new habitat over the natural habitat they replace influencing epibiotic

assemblages in ways we are yet to unravel.

The critical finding of this study was that epibiotic assemblages were affected by

habitat (pontoons vs. reef) rather than by the material these were made from. This is an

important result because it was proposed that the composition of substratum (i.e.

sandstone vs. concrete) explained differences previously described between taxa onrocky reef and pontoons (Connell and Glasby, 1999). Factors other than the composition

of the substratum, therefore, appear important determinants of spatial heterogeneity of




Table 2

Analysis of variance comparing the percentage cover of selected taxa between habitats (pontoon vs. reef) anda

substratum (sandstone and concrete)

Source df (a) Abhoresent bryozoans (b) Colonial ascidians (c) Mytilus edulis

MS F P MS F P MS F P

Habitat 1 1612.32 23.02 . 0.05 4265.91 17.31 . 0.01 6417.42 6.55 . 0.05

Substratum 1 0.18 0.02 . 0.25 23.81 0.48 . 0.25 19.71 0.63 . 0.25

Site 3 80.20 6.86 – 95.15 3.79 – 979.56 24.51 –

H3S 1 43.02 1.37 . 0.25 1.97 0.03 . 0.25 19.71 0.63 . 0.25^ ^

H3Site 3 70.03 5.99 246.45 9.83 979.56 24.51 ***

S3Site 3 10.17 0.87 . 0.25 49.85 1.99 . 0.10 31.36 0.78 . 0.25

H3S3Site 3 31.42 2.69 . 0.05 61.27 2.44 . 0.05 31.36 0.78 . 0.25

Residual 64 11.68 25.08 39.96

a

The comparison of sites was not relevant for testing the hypothesis. * P , 0.05, ** P , 0.01, *** P ,^

0.001, where significance was judged at a 50.01 because variances were heterogeneous (Cochran’s C -test,

P, 0.05).

epibiotic assemblages among urban structures and rocky reef. If pontoons were made of

the same material as natural reef (sandstone), they would not act as surrogate habitats for

epibiotic assemblages that occur on adjacent reef. Whilst the composition of substratum

can influence the abundances of taxa (e.g. Crisp and Ryland, 1960; Harlin and

Lindbergh, 1977; McGuinness, 1989; Anderson and Underwood, 1994), it is becoming

increasingly clear that is not always the primary determinant of spatial variation

(Pomerat and Weiss, 1946; Crisp and Ryland, 1960; Caffey, 1982; Anderson and

Underwood, 1994).

Pontoons are intrinsically different from natural reef and the uniqueness of these

structures as habitats may be better explained by differences in their shapes, sizes and

spatial arrangement. Pontoons provide discrete habitats in the form of new space. Such

isolated pieces of substratum are known as habitat-islands (Simberloff and Abele, 1982)

or type II patches (sensu Sousa, 1985). Variation in the shape, size and arrangement of

these patches affects the colonisation of epibiotic assemblages (Kay and Keough, 1981;

Keough, 1984). Some insight into the response of epibiotic assemblages to patchiness

comes from studies that create space (Connell and Keough, 1985). In most of thesestudies, the shape, size and spatial arrangement of experimental patches are based on

logistical and statistical convenience, rather than on specific hypotheses about observed

patchiness of habitat and known aspects of the biology of organisms studied.

The dual effects of habitat patchiness and differences in the ecology of taxa appear to

have some obvious consequences for their abundances among urban structures and rocky

reef. For example, urban structures occupy different positions in the water column

(vertical distance from reef) and the abundance of a large suite of taxa is strongly

affected by proximity to the seafloor (Withers and Thorp, 1977; Glasby, 1999b). In

particular, spirorbid polychaetes occur in greater abundance close to the seafloor

(Osman, 1977; Glasby, 1999b) and in this study they occurred in greater abundance onthe reef than on pontoons that float above the reef. This pattern appears to reflect

patterns of recruitment, larvae of many tubiculous polychaetes become more demersal as




Table 3

Analysis of variance comparing the percentage cover of selected taxa between habitats (pontoon vs. reef) anda

substratum (sandstone and concrete)

Source df MS F P MS F P MS F P

(a) Spirorbids (b) Solitary ascidians (c) Barnacles

^Habitat 1 16 482.65 99.54 1420.01 10.20 * 7178.42 6.68 . 0.05

Substratum 1 629.69 36.66 . 0.01 68.82 1.69 . 0.25 55.25 4.42 . 0.10

Site 3 245.69 7.43 – 127.42 2.76 – 63.98 1.17 –

H3S 1 307.55 6.51 . 0.05 0.77 0.01 . 0.25 63.83 1.16 . 0.25^

H3Site 3 165.59 5.70 139.28 3.02 * 1074.95 19.70 ***

S3Site 3 17.18 0.59 . 0.25 40.76 0.88 . 0.25 12.49 0.23 . 0.25

H3S3Site 3 47.22 1.63 . 0.10 68.31 1.48 . 0.10 55.24 1.01 . 0.25

Residual 64 29.04 46.14 55.57

(d) Red algae (e) Sponges (f) Encrusting bryozoans

Habitat 1 1556.72 4.20 . 0.10 303.91 2.57 . 0.10 110.53 0.34 . 0.25

Substratum 1 217.53 11.25 * 14.99 0.36 . 0.25 285.47 4.57 . 0.10

Site 3 460.21 7.31 – 59.39 2.88 – 579.28 8.67 –

H3S 1 278.27 5.12 . 0.10 18.61 0.72 . 0.25 3.79 0.20 . 0.25^

H3Site 3 370.29 5.88 ** 118.34 5.74 320.99 4.80 *

S3Site 3 19.33 0.31 . 0.25 42.02 2.04 . 0.10 62.48 0.94 . 0.25

H3S3Site 3 54.35 0.86 . 0.25 25.98 1.26 . 0.25 19.16 0.29 . 0.25

Residual 64 62.94 20.61 66.8

(g) Brown algae (h) Green algae (i) Serpulids

Habitat 1 417.79 5.08 . 0.10 31.32 0.10 . 0.25 274.98 4.78 . 0.10^Substratum 1 183.28 0.59 . 0.25 728.07 65.11 49.22 2.27 . 0.10

Site 3 116.32 2.95 – 17.92 0.75 – 234.14 9.93 –

H3S 1 119.24 5.21 . 0.10 85.28 2.53 . 0.25 8.32 0.80 . 0.25

H3Site 3 82.26 2.08 . 0.11 304.95 12.70 . 0.10 57.51 2.44 . 0.05^ ^

S3Site 3 312.59 7.92 11.18 0.47 21.68 0.92 . 0.25

H3S3Site 3 22.87 0.58 . 0.25 33.67 1.40 . 0.25 10.42 0.44 . 0.25

Residual 64 39.48 24.01 . 0.25 23.58

a

See Table 2 for details.

they develop (Scheltema, 1986). Oppositely, experimental tests have revealed Styela plicata to be most abundant at shallow depths, but in positions away from the seafloor

(Glasby, 1999b) where pontoons are moored. This could explain why in the present

study solitary ascidians (primary Styela plicata) were many times more abundant on

pontoons than on the reef.

Understanding the ecology of urban structures is not just about solving ecological

riddles. Epibiotic assemblages are food and shelter for many types of organisms (e.g.

Bell and Pollard, 1989; Connell and Anderson, 1999; Minchinton and Ross, 1999) and

are important components of the biogenic structure of coastal habitats (Underwood et al.,

1991). These habitats are being rapidly destroyed and urbanised with little appraisal of

the ecological consequences. While it has been relatively simple to record and documentloss of coastal habitats (Gray, 1997), little is known about the consequences of

introducing new habitats as urban structures (Glasby and Connell, 1999).




Interpreting and managing urbanisation not only requires understanding the conse-

quences of destroying natural habitat, but also that of creating new habitat, particularly

in the form of urban structures. Ultimately, this knowledge may aid programmes of

restoration or rehabilitation of damaged habitats. Estuaries pose particular problemsglobally since there is conflict between the interests of industrial development, shipping,

harbour development, fishing, recreation and the needs for conservation (Gray, 1997).

Solutions to some of these competing demands require an understanding of the factors

that enhance the conservation value of structures that continue to result from these

activities.

In conclusion, these results demonstrate that pontoons constitute novel habitats for

epibiota. This highlights a need for determining how current understanding of the

ecology of epibiota, which is primarily based on studies of urban structures (pilings and

pontoons), relates to natural reef. Fundamental differences in the ecology of different

taxa appear to have important consequences for their relative abundances on pontoonsand rocky reef. Future tests of hypotheses about the nature of these differences will not

only contribute to better ecological understanding of epibiota and their use of urban

structures as habitats, but also to better predictions of future changes to the ecology of

coastal habitats.

Acknowledgements

This study was supported by funds from the Centre for Research on EcologicalImpacts of Coastal Cities and a University Research Grant to SDC. I gratefully

acknowledge assistance in the field and laboratory from T. Glasby, S. Heislers, G.

Housefield, and J. People. This paper was improved by T. Glasby and benefited from

discussions with G. Chapman and A. Underwood. [AU]

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Documents

Connell. 2000. Floating Pontoons Create Novel Habitats for Subtidal Epibiota