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Species composition and distribution of Alcyonacea (Octocorallia) in the northern Persian Gulf

Published online by Cambridge University Press:  03 August 2021

Shemshad Shahbazi
Affiliation:
Department of Marine Biology, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran
Nasrin Sakhaei*
Affiliation:
Department of Marine Biology, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran
Hossein Zolgharnein
Affiliation:
Department of Marine Biology, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran
Catherine S. McFadden
Affiliation:
Department of Biology, Harvey Mudd College, Claremont, CA, USA
*
Author for correspondence: Nasrin Sakhaei, E-mail: sakhaei@kmsu.ac.ir
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Abstract

Studies concerning octocoral species from the Persian Gulf coral reefs are few. This study documents the diversity and abundance of octocoral communities from three islands in the north Persian Gulf, namely, Larak Island, Hengam Island and Qeshm Island. Belt transects were used to survey the octocoral communities at these islands. We used a rapid ecological assessment technique (REA) to assess the status and abundance of octocorals. Also, K Independent sample analysis was conducted on abundance and Shannon Diversity index data to determine if octocoral abundance and species diversity varied between islands. A total of 22 morphospecies, belonging to seven alcyonacean families, including Plexauridae, Ellisellidae, Alcyoniidae, Nephtheidae, Briareidae, Acanthogorgiidae and Subergorgiidae, were identified in this study. Statistical analysis indicated octocoral abundance and diversity at Larak Island reefs were higher than those around Hengam and Qeshm islands. The primary data presented in this study could serve as the baseline data for long-term biomonitoring programmes to estimate the status of octocorals in the Persian Gulf.

Type
Research Article
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of Marine Biological Association of the United Kingdom

Introduction

Climate change is an important environmental, economic and social issue of our time and these changes are happening fast (IPCC, 2007; Hoegh-Guldberg, Reference Hoegh-Guldberg2011). The rate of change is 2–3 times faster than the rapid changes between glacial and interglacial periods observed over the last 740,000 years (Augustin et al., Reference Augustin, Barbante, Barnes, Barnola, Bigler, Castellano, Cattani, Chappellaz, DahlJensen and Delmonte2004; Hansson et al., Reference Hansson, Hoffmann, Hutterli, Huybrechts, Isaksson, Johnsen, Jouzel, Kaczmarska, Karlin and Kaufmann2006), and there is a lot of evidence to suggest that biological systems around the globe are changing (Walther et al., Reference Walther, Post, Convey, Menzel, Parmesan, Beebee, Fromentin, Hoegh-Guldberg and Bairlein2002). One of these systems is coral reef ecosystems, which play a particularly important role in our understanding of how Earth's ecosystems respond to rapid climate change. They are seriously threatened by current and future changes in the temperature and acidity of the oceans and other factors, and are a good indicator to observe the state of climate change (Hoegh-Guldberg, Reference Hoegh-Guldberg2011). Therefore, the study of coral ecosystems in a specific region such as the Persian Gulf, which is an important natural laboratory, can provide valuable information for planning to protect them in the future.

In general, the Persian Gulf is a very special region for coral reefs. Because it is home to some of the northernmost coral reefs in the western Indian Ocean and is the warmest sea in the world in summer while in winter it is among the coldest with abundant coral growth, this is especially important for scientists in a world that is subject to climate change (Riegl & Purkis, Reference Riegl and Purkis2012). The Persian Gulf today is characterized by a thermal regime comparable to that predicted for other tropical oceans in the years 2090–2099 (IPCC, 2007; Riegl & Purkis, Reference Riegl and Purkis2012). Riegl & Purkis (Reference Riegl and Purkis2012) reported that the Persian Gulf coral reef organisms have adapted to this climate regime for more than 6000 years and that many of the world's most crucial ocean lessons can be learned from study of this system. So, the Iranian reefs in the Persian Gulf are attracting international scientific attention due to their development and persistence in such extreme environmental conditions (Coles & Fadlallah, Reference Coles and Fadlallah1991).

The Persian Gulf is a shallow and semi-enclosed sea located in the tropics of the Indo-Pacific and connected to the Indian Ocean by a narrow waterway called the Strait of Hormuz. There is limited water exchange through this crater of the Persian Gulf (Pous et al., Reference Pous, Carton and Lazure2004) with high salinity, high seasonal fluctuations in sea surface water temperature (14–34°C) (Riegl & Purkis, Reference Riegl and Purkis2012), and very low tides generally leading to extreme conditions in the Persian Gulf (Coles & Fadlallah, Reference Coles and Fadlallah1991; Sheppard & Sheppard, Reference Sheppard and Sheppard1991; Koupaei et al., Reference Koupaei, Mostafavi, Mehrabadi, Fatemi and Dehghani2016). These factors have significant effects on coral reefs, which are one of the most varied and economically valuable ecosystems on the planet, and are mainly found on islands in the northern parts of the Persian Gulf (Rezai et al., Reference Rezai, Samimi, Kabiri, Kamrani, Jalili and Mokhtari2010; Koupaei et al., Reference Koupaei, Mostafavi, Mehrabadi, Fatemi and Dehghani2016). Iran has 17 islands with fringing reefs in the Persian Gulf (Sheppard & Sheppard, Reference Sheppard and Sheppard1991). Among them, Hengam, Larak, Qeshm and Hormuz islands are located in the Strait of Hormuz and are affected by oceanic waters with lower salinity and high nutrient levels originating from the Oman Sea, especially during the monsoon upwelling in summer. As a result, the reefs around these islands have a relatively great variety and richness of species, so these areas are different from the interior of the Persian Gulf (Bauman et al., Reference Bauman, Feary, Heron, Pratchett and Burt2013).

Octocorallia is a unique group with a substantial presence in benthic communities, which is significant due to their beauty, diversity, abundance and associations with other organisms (Williams & Cairns, Reference Williams and Cairns2013; Pérez et al., Reference Pérez, de Moura Neves, Cordeiro, Williams and Cairns2016). Octocorals are distributed in all marine environments and are common on almost all coral reefs, but are generally most common on shallow tropical reefs and in deep sea habitats (Pérez et al., Reference Pérez, de Moura Neves, Cordeiro, Williams and Cairns2016). However, despite their commonness, relatively little has been published on the distribution and ecology of most octocorals. In many cases, identification is done only from sclerites (microscopic skeletal elements) prepared from preserved specimens, and as a result of variation in the appearance of sclerites within species and even in colonies, they are difficult to identify (Bayer, Reference Bayer1961; Lasker & Coffroth, Reference Lasker and Coffroth1983). The rarity of environmental studies of octocorals in the Persian Gulf may be due to the difficulty of identifying species in this area, which makes many researchers not interested in studying them.

To date, most studies of the biodiversity of coral reefs on the Iranian shores of the Persian Gulf have been related to the order Scleractinia (Rezai & Savari, Reference Rezai and Savari2004; Rezai et al., Reference Rezai, Samimi, Kabiri, Kamrani, Jalili and Mokhtari2010; Samiei et al., Reference Samiei, Dab, Ghezellou and Shirvani2013; Salimi et al., Reference Salimi, Mostafavi, Chen, Fatemi and Pichon2018) and other hexacorals (Koupaei et al., Reference Koupaei, Mostafavi, Mehrabadi and Fatemi2014, Reference Koupaei, Mostafavi, Mehrabadi, Fatemi and Dehghani2016; Darvishi et al., Reference Darvishi, Moradinasab, Hosseini, Mohammadnia, Aminikhoei, Nasri and Nabipour2018). However, there have been a few studies on order Alcyonaria (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009; Shahbazi et al., Reference Shahbazi, Sakhaei, Zolgharnein and McFadden2019) that address their taxonomy. More than 19 genera in nine families of Octocorallia (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009, 2012) have been described from the Persian Gulf to date. However, there are few data on the abundance and distribution of octocorals in the Persian Gulf.

The aim of this study was to investigate the distribution, abundance and diversity of octocorals in the three islands of Larak, Hengam and Qeshm in the northern part of the Persian Gulf. Therefore, a list of species and their distribution is provided.

Materials and methods

Study area

Octocoral surveys were conducted at coral reefs located at three northern islands of the Persian Gulf, namely Qeshm, Larak and Hengam Islands, during 2018–2019. These islands were selected based on previous reports (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009, 2012) of the occurrence of octocorals at these reef systems. The sampling sites were determined according to visual habitat characteristics such as occurrence of hard or sandy substrate and water quality. A total of 14 stations were surveyed using scuba (from 1–30 m depth), with five stations at Larak Island, four stations at Hengam Island and five stations at Qeshm Island (Figure 1 and Table 1).

Fig. 1. Map showing the location of the islands and the sampling stations (1–14) in the northern Persian Gulf (Iran).

Table 1. Coordinates of octocoral sampling stations in the north of the Persian Gulf

LI, Larak Island; HI, Hengam Island; QI, Qeshm Island.

Octocorals survey

Data on octocorals were collected by using visual census methods in combination with belt transects (BT) (English et al., Reference English, Wilkinson and Baker1994; Seah et al., Reference Seah, Yap, Tan and Goh2015). A 200 m belt transect was applied at 14 stations (three transects per station), in which observations of octocorals were made within an area 2 m to the left and right sides of the transect. If possible, all octocorals observed in the area were photographed in situ, counted and some specimens were collected for further identification and molecular study (Shahbazi et al., Reference Shahbazi, Sakhaei, Zolgharnein and McFadden2021). Specimens of Viminella sp., Verrucella cf. reticulata (Thomson & Simpson, Reference Thomson and Simpson1909), Acanthogorgia sp., Echinomuricea sp. d and Euplexaura sp. c were collected by a local fisherman (with gillnet) at Hengam Island from 60–70 m depth.

We used a rapid ecological assessment technique (REA) to assess the status of abundance of octocorals (Fabricius & De'ath, Reference Fabricius and De'ath2001; Fabricius et al., Reference Fabricius, Alderslade, Williams, Colin and Golbuu2007). Relative abundances of species were visually estimated on the following rating scale for each island: 0 = absent; 1 = one or few colonies; 2 = uncommon; 3 = common; 4 = abundant; and 5 = dominant (Fabricius & De'ath, Reference Fabricius and De'ath2001).

Octocoral identification

The specimens were identified using morphological characteristics of the colony and sclerites. The overall structure of the colonies was examined by stereomicroscope. To extract the sclerites for identification, first a small piece of tissue from the collected samples was dissolved in 10% sodium hypochlorite (Fabricius & Alderslade, Reference Fabricius and Alderslade2001). Extracted sclerites were viewed under a light microscope at magnifications of 100 × . Dimensions of sclerites were measured and they were photographed with Dino Capture. The latest related references were used to identify the species (Bayer & Grasshoff, Reference Bayer and Grasshoff1994; Grasshoff, Reference Grasshoff2000; Fabricius & Alderslade, Reference Fabricius and Alderslade2001; Kumar et al., Reference Kumar, Raghunathan, Raghuraman, Sreeraj and Venkataraman2014; Williams & Chen, Reference Williams, Chen, Williams and Gosliner2011). The identified species of octocorals were compared with previously published studies from the Persian Gulf such as Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012). The specimens, preserved in 75% ethanol, were deposited temporarily in the Khoramshahr University of Marine Science and Technology (KMSU); they will be transferred to the Museum of the University of Tehran following the completion of ongoing taxonomic studies.

Statistical analysis

The abundance of octocoral species encountered during each transect was calculated for each island. Octocoral diversity for each island surveyed was represented by the Shannon–Wiener index of diversity (Hutcheson, Reference Hutcheson1970). This index of diversity was computed for each island based on species richness and abundance (number of colonies) of octocoral species.

K Independent sample analysis was conducted on the abundance and Shannon Diversity index data to determine if octocoral abundance and species diversity varied between islands. The Kruskal–Wallis test was used to further determine significant differences between islands in terms of species diversity and abundance. Analysis of data was conducted using SPSS 19 (IBM SPSS Statistics 19, released 2010). Excel 2011 (Microsoft Office 2011) was used to draw the charts.

Octocoral community composition at the three islands was assessed using the PRIMER v6 (Plymouth Routines in Multivariate Ecological Research) software package (Clarke & Green, Reference Clarke and Green1988; Clarke, Reference Clarke1993). Bray–Curtis similarity matrices were used for this purpose. The Bray–Curtis similarity results were illustrated using hierarchical clustering with group-average linkage and a non-parametric multi-dimensional scaling (nMDS) ordination plot. Then, one way analysis of similarity (ANOSIM) was used to test for dissimilarity among the octocoral communities at the islands. In cases where the pairwise R value determined for the survey islands was greater than the Global R, it indicated significant dissimilarity in community structure between the islands (P < 0.02).

Results

Octocoral identification

The result of species identification indicates that there are 22 species of octocorals present at the three islands (Table 2). All of the 22 species of the subclass Octocorallia belonged to the order Alcyonacea (soft corals and sea fans). In the Alcyonacea, members of four of the six informal subordinal groups were found, representing seven families and 14 genera (Table 2). The four subordinal groups comprised three genera of Alcyoniina, two Scleraxonia, six Holaxonia and three Calcaxonia. Fifteen taxa were identified to the genus level and only seven taxa to the species level (Table 2). Family Plexauridae was represented by 12 species, followed by Ellisellidae (three species); Alcyoniidae (two species); Nephtheidae (two species); Briareidae (one species); Acanthogorgiidae (one species); and Subergorgiidae (one species).

Table 2. Octocorals species composition at three islands in the northern Persian Gulf

LI, Larak Island; HI, Hengam Island; QI, Qeshm Island.

Abundance according to REA (Fabricius & De'ath, Reference Fabricius and De'ath2001). Morphospecies designations follow Samimi-Namin & Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) and Shahbazi et al. (Reference Shahbazi, Sakhaei, Zolgharnein and McFadden2021).

Abundance and diversity of octocorals

In Larak Island, 17 species of 11 genera were observed, of which the genus Menella (four species) and then Echinogorgia (three species) were the most diverse. Other genera were of low diversity and only one species was observed from each except genus Dendronephthya which had two species. An examination of the abundance of octocorals at Larak Island revealed that Juncella juncea (Ellisellidae) (Figure 2E) is dominant. Sinularia erecta (Figure 2C) (Alcyoniidae) and Subergorgia suberosa (Subergorgiidae) were both abundant; Dendronephthya sp. b (Figure 2D) (Nephtheidae), Menella sp. g (Figure 2I), Echinogorgia sp. b (Figure 2H), Echinogorgia sp. c and Astrogorgia fruticosa (Figure 2G) (Plexauridae) species were common; Dendronephthya sp. a (Nephtheidae), Briareum hamrum (Briareidae), Menella sp. d, Menella sp. e and Echinogorgia sp. a (Figure 2B) (Plexauridae) were uncommon species; while other species that were present were all rare (Table 2).

Fig. 2. Some species identified in this survey. (A) Sarcophyton minusculum Samimi-Namin and Ofwegen, 2009; (B) Echinogorgia sp. a; (C) Sinularia erecta Tixier-Durivault, 1945; (D) Dendronephthya sp. b; (E) Junceella juncea (Pallas, 1766); (F) Verrucella cf. reticulata (Thomson and Simpson, 1909); (G) close up of Astrogorgia fruticosa Samimi-Namin and Ofwegen, 2009; (H) Echinogorgia sp. b; (I) Menella sp. g.

In the waters of Hengam Island, 12 species of 11 genera were observed (five of which were collected by local fishermen). The genus Echinogorgia was the most diverse with two species, and the other genera each had one species. An examination of the abundance of octocorals at this island revealed that J. juncea is abundant; Echinogorgia sp. c and A. fruticosa were both common; S. erecta and Dendronephthya sp. a were uncommon; while two species, B. hamrum and Echinogorgia sp. b, were rare (Table 2).

At Hengam Island five species, i.e. Viminella sp., V. reticulata (Figure 2F) (Ellisellidae), Echinomuricea sp. d, Euplexaura sp. c (Plexauridae) and Acanthogorgia sp. (Acanthogorgiidae), were collected by local fishermen from a depth of ~60–70 m with gillnet. Therefore, since they were collected in a way other than the transect belt and only one colony of each species has been observed, we do not know their abundance status in deep water.

Qeshm Island had the least diversity among these three islands with seven species from six genera. Dendronephthya (Nephtheidae) with two species was more diverse than the other genera, each of which had one species. The survey of the abundance of octocorals in this island determined that J. juncea (Ellisellidae) was common, S. suberosa (Subergorgiidae) and Menella sp. g (Plexauridae) were both uncommon, while other species and genera that were present were all rare (Table 2).

Relative abundance was measured as the percentage of each species with respect to the total number of specimens (Figure 3).

Fig. 3. Per cent composition of octocoral taxa comprising the 22 identified species in the survey. (A) percentages of genera in subordinal groups; (B) percentages of identified octocoral species within Alcyonacea families (rounded to the nearest percentage).

Fourteen stations were surveyed for octocorals. Three stations had no octocorals present (stations 7, 13 and 14). Twenty-two species were recorded from the 11 stations where octocorals were present. The results of octocoral abundance showed that among the studied islands, Larak Island had the highest abundance of octocorals, followed by Hengam and Qeshm islands (Figure 4). K Independent sample analysis of abundance and diversity data indicated significant differences between the three islands. The Kruskal–Wallis test indicated that octocoral abundance at stations 4 and 5 at Larak Island were significantly higher than other stations at Hengam Island and Qeshm Island at P < 0.05 (Figure 4). The Shannon Diversity index was also significantly higher at stations 4 and 5 at Larak Island than at the other stations (Figure 5).

Fig. 4. Mean (± S.E.) abundance (colony number per belt transect) of octocorals at survey stations (n=3 transects per station). Different letters (a, b) indicate significant differences (P < 0.05). (No octocorals found at stations 7, 13 and 14).

Fig. 5. Mean (± S.E.) Shannon-Wiener diversity index (colony number per belt transect) of octocorals at survey stations (n=3 transects per station). Different letters (a, b and c) indicate significant differences (P < 0.05). (No octocorals found at stations 7, 13 and 14.)

nMDS analysis of octocoral communities

The 2D MDS plot indicated that Larak Island octocoral communities were distinct from those at Hengam Island and Qeshm Island (Figure 6). At Larak Island, the difference in community structure between stations 4 and 5 and other stations is clear (Figure 6). Additionally, the Analysis of Similarities (ANOSIM) test results indicated that there were significant dissimilarities in octocoral community structure between Larak Island and the two other islands (Hengam and Qeshm) (P < 0.02; Table 3). Also, ANOSIM results indicated that the octocoral community structures between Hengam Island and Qeshm Island were not significantly dissimilar (P > 0.1; Table 3).

Fig. 6. Two-dimensional MDS configuration of octocoral communities at Larak Island (LI), Hengam Island (HI) and Qeshm Island (QI). A stress value of 0.1 gave a good representation of the data.

Table 3. R statistics derived from pairwise tests using ANOSIM to compare dissimilarities of octocoral communities among the three islands

a Values above the Global R (0.357) indicate significant dissimilarities between islands (P < 0.02).

Discussion

Overall, 22 distinct octocoral morpho-species were identified based on colony morphologies as well as comparison of sclerites (Table 2). Molecular analyses support the distinction of these morphotypes as different species (Shahbazi et al., Reference Shahbazi, Sakhaei, Zolgharnein and McFadden2021). So far, no study has been done on the abundance, diversity and species composition of octocorals in the Persian Gulf, and this study surveyed them for the first time. Accordingly, due to the lack of previous studies, we do not have a comparison point. Almost half of the octocorals identified in the current study had been reported by Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2012) from the Persian Gulf.

In general, Plexauridae had the highest diversity and abundance in the whole study area. This family of gorgonians is one of the richest in genera and species (Bayer, Reference Bayer1981; Lopez-Gonzalez, Reference Lopez-Gonzalez2006), which are well represented in temperate and tropical waters (Grasshoff, Reference Grasshoff2000; Fabricius & Alderslade, Reference Fabricius and Alderslade2001). Among the genera of this family, Menella was most diverse, which was observed in Larak and Qeshm Islands. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) reported this genus as one of the most common genera throughout the Persian Gulf. They reported species of this genus from the islands of Larak, Hengam, Farur, Kish and near the Strait of Hormuz, as well as from Kuwait. Echinogorgia is another of the most common genera in the Persian Gulf. We identified species of this genus from all three islands (Table 2). In previous studies, species of this genus have been reported from Farur and Qeshm Islands and near the Strait of Hormuz (Rezai, Reference Rezai1996; Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009, 2012). Two species of Euplexaura were observed during this study, one in the waters of Larak Island and the other in Hengam Island. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) stated that this genus is one of the most common genera in the Persian Gulf. They reported some species of this genus from different parts of the Persian Gulf. So far, of the genus Astrogorgia, only Astrogorgia fruticosa Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009 has been reported from the Persian Gulf. This species has only been reported from the waters around Hengam Island (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009, 2012), which is also the only location where we found it. Echinomuricea also seems to be a common genus in the Persian Gulf. We identified two species of this genus, one in the waters of Larak Island and the other in Hengam Island. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) reported two different species from those in this study, from Farur, Hengam, Kish and Kharku Islands and Kuwait.

The family Ellisellidae is widely distributed throughout the Indo-Pacific region, the eastern and western Atlantic Ocean, the Red Sea and the Mediterranean Sea (Grasshoff, Reference Grasshoff2000; Cairns, Reference Cairns2007; Fabricius & Alderslade, Reference Fabricius and Alderslade2001; Bilewitch et al., Reference Bilewitch, Ekins, Hooper and Degnan2014). This family is smaller than some other octocoral families, and currently has 10 genera and about 110 species (Bayer & Grasshoff, Reference Bayer and Grasshoff1994; Bilewitch et al., Reference Bilewitch, Ekins, Hooper and Degnan2014). We diagnosed three species of three genera in the Persian Gulf of which Junceella juncea was abundant at all three islands. According to Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2012) this species is widely distributed in the Persian Gulf. The other two species belonging to this family are Verrucella reticulata and Viminella sp. that were collected only in waters between 60–70 m on Hengam Island by local fishermen. We find that these species are rare and are probably distributed in deeper waters of the Persian Gulf. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) stated that V. reticulata is rare throughout the Persian Gulf, and they only recorded this species from Qeshm Island. Viminella sp. previously was reported only from Hengam Island by Shahbazi et al. (Reference Shahbazi, Sakhaei, Zolgharnein and McFadden2019).

Acanthogorgiidae and Subergorgiidae were two other families of gorgonians, each of which had one species observed throughout the study area. They are widely distributed in the Indo-Pacific region (Fabricius & Alderslade, Reference Fabricius and Alderslade2001; Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2012). So far, only two genera including Acanthogorgia (Acanthogorgia spinosa Hiles, Reference Hiles1899, recorded from off Bahrain) and Muricella (Muricella sp., recorded from the south of Hengam Island) have been reported from the Persian Gulf that belonged to family Acanthogorgiidae (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009, 2012). Also, only one species of family Subergorgiidae has been reported from the Persian Gulf. This species is S. suberosa, which has been recorded from Qeshm, Farur and Lesser Tonb Islands. This species was first reported in the Persian Gulf by Rezai et al. (Reference Rezai, Wilson, Claereboudt and Riegl2004) from Lesser Tonb. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) stated that this is not a common species. We identified this species from Larak and Qeshm Islands, where it was an abundant species on Larak Island (Table 2).

Among the non-gorgonian octocorals, we observed the three families Alcyoniidae, Nephtheidae and Briareidae throughout the study area. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2012) reported these three families plus Clavulariidae. These families are widely distributed in the Indo-Pacific region (Fabricius & Alderslade, Reference Fabricius and Alderslade2001). Alcyoniidae is represented by two genera, Sarcophyton and Sinularia, in the Persian Gulf. Sarcophyton was first reported by Rezai (Reference Rezai1996) from Larak and Lesser Tonb islands as Sarcophyton sp. Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009) described and reported Sarcophyton minusculum (Figure 2A) from Larak Island. Sarcophyton has not been reported from any other part of the Persian Gulf. In the present study, S. minusculum was observed only in the waters of Larak Island. Fabricius & Alderslade (Reference Fabricius and Alderslade2001) stated that Sarcophyton is widespread from the Red Sea to Polynesia. Sinularia is also one of the most widespread and common genera of soft corals found in the coral reefs of the Indo-Pacific (McFadden et al., Reference McFadden, van Ofwegen, Beckman, Benayahu and Alderslade2009). They are widely distributed from Africa and the Red Sea to Hawaii (Fabricius & Alderslade, Reference Fabricius and Alderslade2001). So far, this genus has two representatives (Sinularia erecta Tixier-Durivault, Reference Tixier-Durivault1945 and Sinularia polydactyla (Ehrenberg, 1834)) in the Persian Gulf. Both species have previously been reported from the Larak, Hengam and Farur Islands (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2009, 2012). In this study, we observed only S. erecta at Larak, Hengam and Qeshm, where it was more abundant at Larak Island than the other two islands.

According to previous studies, the family Nephtheidae has two genera, Dendronephthya and Umbellulifera, represented in the Persian Gulf. This family is widely distributed in the Indo-Pacific region and also extends from Africa to Micronesia and Polynesia (Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2012). Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2009, 2012) reported two species, Dendronephthya sp. a (only from Hengam Island) and Dendronephthya sp. b, that they stated could be found in most of the Iranian Islands. We observed Dendronephthya sp. a in all three islands of Larak, Hengam and Qeshm, and Dendronephthya sp. b from the two islands of Larak and Hengam. Family Briareidae is widespread in the Indo-Pacific region (Fabricius & Alderslade, Reference Fabricius and Alderslade2001). Only the species Briareum hamrum (Gohar, Reference Gohar1948) has been reported from the Persian Gulf. We have seen this species in the Larak and Hengam Islands. Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2012 recorded this species from Larak, Farur and Kish Islands and stated that it is most likely to occur in other Iranian Islands close to the Strait of Hormuz.

Octocorals encountered in this study comprised members of families widespread in the Indo-Pacific region (Fabricius & Alderslade, Reference Fabricius and Alderslade2001; Samimi-Namin & van Ofwegen, Reference Samimi-Namin and van Ofwegen2012). In this study, gorgonians (17 species) clearly had a higher density and diversity than soft corals (five species). In previous studies, this is completely clear; Samimi-Namin & van Ofwegen (Reference Samimi-Namin and van Ofwegen2012) reported eight soft corals and 20 gorgonians. This could be due to the climatic conditions of the Persian Gulf (Riegl & Purkis, Reference Riegl and Purkis2012). Coles (Reference Coles2003) noted that the low abundance and diversity of corals in the Persian Gulf are likely due to harsh conditions such as wide range of temperature changes, high salinity, sedimentation and oil pollution. Therefore, it seems that gorgonians in the Persian Gulf have a higher ability to adapt to harsh climatic conditions than soft corals. Fabricius et al. (Reference Fabricius, Alderslade, Williams, Colin and Golbuu2007) state that the abundance and diversity of soft corals in the shallow waters of the Indo-Pacific region are strongly influenced by factors such as high water temperatures, storms with high wave energy, water pollution and sedimentation.

K Independent sample analyses suggested that two stations (4 and 5) at Larak Island had a significantly higher octocoral abundance and diversity compared with other stations at this island. Interestingly, in terms of community structure, Hengam and Qeshm Islands' octocoral communities were not significantly dissimilar (Figures 4 and 5). Also, based on nMDS analysis, Larak octocoral communities were significantly dissimilar from the two other islands (Figure 6). This is due to the presence of more soft corals (Sinularia, Sarcophyton, Dendronephthya and Briareum) at Larak Island. Also, the existence of two different octocoral communities at Larak Island is due to the fact that gorgonian species at stations 4 and 5 have a higher diversity and density than the other three stations, which include more soft corals. Given that all three islands are adjacent to each other near the Strait of Hormuz, probably localized environmental factors at these study islands may have influenced the octocoral diversity, abundance and community structures. Anthropogenic stresses could perhaps be one contributing factor for the observed differences, particularly in community structures. Field observations of the first author suggest excessive tourism in the coral beaches of Qeshm and Hengam Islands and also uncontrolled harvesting of octocorals for economic and commercial activities is one of the reasons for the decrease in the diversity and abundance of octocorals in these two islands. Rezai et al. (Reference Rezai, Samimi, Kabiri, Kamrani, Jalili and Mokhtari2010) state that due to the rapid expansion of tourism on Qeshm Island, many boats transport tourists to the coral reefs around Hengam Island for recreational activities such as diving. Serious damage to corals has been observed, mostly due to their theft by tourists as well as local people.

Another factor contributing to the observed differences could be the sharp rise in water temperature in recent years and the occurrence of bleaching. Bleaching would primarily affect zooxanthellate species and a few genera (ex: Sarcophyton, Sinularia and Briareum) of these have been reported from the Persian Gulf; this could be a reason for the fact that gorgonians seem to be dominant in the Persian Gulf whereas in places like the northern Red Sea soft corals are very abundant and gorgonians quite rare in shallow water (see Benayahu, Reference Benayahu1985, Reference Benayahu1990, Reference Benayahu2002). Numerous researchers, (Fabricius & De'ath, Reference Fabricius and De'ath2001; Ricklefs, Reference Ricklefs2004; Fabricius et al., Reference Fabricius, Alderslade, Williams, Colin and Golbuu2007), have described the negative effects of bleaching on the frequency and diversity of octocorals in an area. The Persian Gulf has experienced bleaching at least three times in 1996, 1998 and 2002 (Rezai et al., Reference Rezai, Wilson, Claereboudt and Riegl2004). However, unpublished field reports indicate widespread bleaching in recent years. Mohammadizadeh et al. (Reference Mohammadizadeh, Tavakoli-Kolour and Rezai2013) in a study of the coral reefs of Larak Island reported that the island's coral reefs are improving and are likely to be recovered in the coming years. Kavousi et al. (Reference Kavousi, Seyfabadi, Rezai and Fenner2011) in a study of the coral reef communities on Qeshm Island, reported that the island's coral status has not improved as a result of bleaching in recent years. Kavousi et al. (Reference Kavousi, Tavakoli-Kolour, Mohammadizadeh, Bahrami and Barkhordari2014) reported an improvement in the coral ecosystem due to bleaching in the northern Persian Gulf. So, there is disagreement among authors about the health of coral reefs in the area. Sedimentation is another effective factor in reducing octocoral abundance and diversity. Fabricius et al. (Reference Fabricius, Alderslade, Williams, Colin and Golbuu2007) state that sedimentation is one of the causes of reduced octocoral diversity and abundance, which causes suffocation of colonies or inhibition of larval habitat. Kavousi et al. (Reference Kavousi, Seyfabadi, Rezai and Fenner2011) reported sedimentation in coral sites of Qeshm Island as a result of various factors such as human activities.

Conclusions

The present study investigated for the first time the diversity, abundance and species composition of octocorals in the three islands of Larak, Hengam and Qeshm in the Persian Gulf. The data obtained from this study can serve as a baseline for future studies of octocorals in this region. Also, due to various factors in the Persian Gulf, such as special climatic and ecological conditions and human activities, especially in Qeshm (the largest island in the Persian Gulf) and Hengam Islands, the information obtained from this study can help management, conservation and maintenance programmes of octocorals in this region.

Acknowledgements

We would like to acknowledge the Iranian Biological Resource Center. We greatly appreciate and thank the Environment Protection Agencies (EPA) that provided us residency during sampling. We thank Dr Neda Fahimi for their valuable assistance in this work. We are also very grateful to the anonymous reviewers, whose comments have allowed us to improve this paper.

Financial support

This work was supported by Khorramshahr University of Marine Science and Technology (grant number 9434402).

References

Augustin, L, Barbante, C, Barnes, PRF, Barnola, JM, Bigler, M, Castellano, E, Cattani, O, Chappellaz, J, DahlJensen, D and Delmonte, B (2004) Eight glacial cycles from an Antarctic ice core. Nature 429, 623628.Google ScholarPubMed
Bauman, AG, Feary, DA, Heron, SF, Pratchett, MS and Burt, JA (2013) Multiple environmental factors influence the spatial distribution and structure of reef communities in the northeastern Arabian Peninsula. Marine Pollution Bulletin 72, 302312.CrossRefGoogle ScholarPubMed
Bayer, FM (1961) The shallow-water Octocorallia of the West Indian region. Studies on the Fauna of Curaçao and other Caribbean Islands 12, 1373.Google Scholar
Bayer, FM (1981) Key to the genera of Octocorallia exclusive of Pennatulacea (Coelenterata: Anthozoa), with diagnosis of new taxa. Proceedings of the Biological Society of Washington 94, 902947.Google Scholar
Bayer, FM and Grasshoff, M (1994) The genus group taxa of the family Ellisellidae, with clarification of the genera established by JE Gray (Cnidaria; Octocorallia). Senckenbergiana Biologica 74, 2145.Google Scholar
Benayahu, Y (1985) Faunistic composition and patterns in the distribution of soft corals (Octocorallia: Alcyonacea) along the coral reefs of Sinai Peninsula. Proceedings of the 5th International Coral Reef Congress 6, 255260.Google Scholar
Benayahu, Y (1990) Xeniidae (Cnidaria: Octocorallia)from the Red Sea with description of a new species. Zoologische Mededelingen 64, 113120.Google Scholar
Benayahu, Y (2002) Soft corals (Octocorallia: Alcyonacea) of the southern Ryukyu Archipelago: the families Tubiporidae, Clavulariidae. Alcyoniidae and Briareidae Galaxea. Journal of the Japanese Reef Society 4, 1132.Google Scholar
Bilewitch, JP, Ekins, M, Hooper, J and Degnan, SM (2014) Molecular and morphological systematics of the Ellisellidae (Coelenterata: Octocorallia): parallel evolution in a globally distributed family of octocorals. Molecular Phylogenetics and Evolution 73, 106118.CrossRefGoogle Scholar
Cairns, SD (2007) Studies on western Atlantic Octocorallia (Gorgonacea: Ellisellidae). Part 7: The genera Riisea Duchassaing & Michelotti, 1860 and Nicella Gray, 1870. Proceedings of the Biological Society of Washington 120, 138.CrossRefGoogle Scholar
Clarke, KR (1993) Non-parametric multivariate analyses of changes in community structure. Australian Journal of Ecology 18, 117143.CrossRefGoogle Scholar
Clarke, K and Green, R (1988) Statistical design and analysis for a'biological effects’ study. Marine Ecology Progress Series 46, 213226.CrossRefGoogle Scholar
Coles, SL (2003) Coral species diversity and environmental factors in the Arabian Gulf and the Gulf of Oman: a comparison to the Indo-Pacific region. Atoll Research Bulletin 507, 119.CrossRefGoogle Scholar
Coles, SL and Fadlallah, YH (1991) Reef coral survival and mortality at low temperatures in the Arabian Gulf: new species-specific lower temperature limits. Coral Reefs 9, 231237.CrossRefGoogle Scholar
Darvishi, M, Moradinasab, M, Hosseini, SJ, Mohammadnia, R, Aminikhoei, Z, Nasri, S and Nabipour, I (2018) Molecular identification of shallow water zoanthids in the coast of Bushehr – Persian Gulf. Iranian South Medical Journal 21, 147161.Google Scholar
English, S, Wilkinson, C and Baker, V (1994) Survey Manual for Tropical Marine Resource. ASEAN-Australia Marine Science Project: Living Coastal Resource. Townsville: Australian Institute of Marine Science. 368 pp.Google Scholar
Fabricius, K and Alderslade, P (2001) Soft Corals and Sea Fans: A Comprehensive Guide to the Tropical Shallow Water Genera of the Central-West Pacific, the Indian Ocean and the Red Sea. Townsville: Australian Institute of Marine Science.Google Scholar
Fabricius, K and De'ath, G (2001) Environmental factors associated with the spatial distribution of crustose coralline algae on the Great Barrier Reef. Coral Reefs 19, 303309.CrossRefGoogle Scholar
Fabricius, K, Alderslade, P, Williams, G, Colin, P and Golbuu, Y (2007) Octocorallia in Palau, Micronesia: effects of biogeography and coastal influences on local and regional biodiversity. In Kayanne H, Omori M, Fabricius K, Verheij E, Colin P, Golbuu Y and Yurihira H (eds), Coral Reefs of Palau. Palau: Palau International Coral Reef Centre, pp. 79–92.Google Scholar
Gohar, HAF (1948) A description and some biological studies of a new alcyonarian species Clavularia hamra. Publications of the Marine Biological Station, Ghardaqa (Red Sea) 6, 333.Google Scholar
Grasshoff, M (2000) The gorgonians of the Sinai Coast and the Strait of Gubal, Red Sea (Coelanterata, Ostocorallia). Courier Forschungsinstitut Senckenberg 224, 1125.Google Scholar
Hansson, M, Hoffmann, G, Hutterli, MA, Huybrechts, P, Isaksson, E, Johnsen, S, Jouzel, J, Kaczmarska, M, Karlin, T and Kaufmann, P (2006) One-to-one coupling of glacial climate variability in Greenland and Antarctica. Nature 444, 195198.Google Scholar
Hiles, IL (1899) The Gorgonacea Collected by Dr Willey. Zoological Results Based on Material from New Britain, New Guinea, Loyalty Islands and Elsewhere Collected During the Years 1895, 1896 and 1897, by Arthur Willey, part 2. Cambridge, pp. 195206.Google Scholar
Hoegh-Guldberg, O (2011) Coral reef ecosystems and anthropogenic climate change. Regional Environmental Change 11, 215227.CrossRefGoogle Scholar
Hutcheson, K (1970) A test for comparing Shannon–Wiener diversity indices. Journal of Theoretical Biology 29, 151154.CrossRefGoogle Scholar
IPCC (2007) Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. Cambridge: Cambridge University Press.Google Scholar
Kavousi, J, Seyfabadi, J, Rezai, H and Fenner, D (2011) Coral reefs and communities of Qeshm Island, the Persian Gulf. Zoological Studies 50, 276283.Google Scholar
Kavousi, J, Tavakoli-Kolour, P, Mohammadizadeh, M, Bahrami, A and Barkhordari, A (2014) Mass coral bleaching in the northern Persian Gulf, 2012. Scientia Marina 78, 397404.CrossRefGoogle Scholar
Koupaei, AN, Mostafavi, PG, Mehrabadi, JF and Fatemi, SMR (2014) Molecular diversity of coral reef-associated zoanthids off Qeshm Island, northern Persian Gulf. International Aquatic Research 6, 64.CrossRefGoogle Scholar
Koupaei, AN, Mostafavi, PG, Mehrabadi, JF, Fatemi, SMR and Dehghani, H (2016) Diversity of shallow water zoantharians in Hengam and Larak Islands, in the Persian Gulf. Journal of the Marine Biological Association of the United Kingdom 96, 11451155.CrossRefGoogle Scholar
Kumar, Y, Raghunathan, JS, Raghuraman, R, Sreeraj, CR and Venkataraman, K (2014) Gorgonians (Octocorallia) of Andaman and Nicobar Islands. Kolkata: Zoological Survey of India.Google Scholar
Lasker, HR and Coffroth, MA (1983) Octocoral distributions at Carrie Bow Cay, Belize. Marine Ecology Progress Series 13, 2128.CrossRefGoogle Scholar
Lopez-Gonzalez, PJ (2006) A new gorgonian genus from deep-sea Antarctic waters (Octocorallia, Alcyonacea, Plexauridae). Helgoland Marine Research 60, 16.CrossRefGoogle Scholar
McFadden, CS, van Ofwegen, LP, Beckman, EJ, Benayahu, Y and Alderslade, P (2009) Molecular systematics of the speciose Indo-Pacific soft coral genus, Sinularia (Anthozoa: Octocorallia). Invertebrate Biology 128, 303323.CrossRefGoogle Scholar
Mohammadizadeh, M, Tavakoli-Kolour, P and Rezai, H (2013) Coral reefs and community around Larak Island (Persian Gulf). Caspian Journal of Applied Science Research 4, 8592.Google Scholar
Pallas, PS (1766) Elenchus zoophytorum sistens generum adumbrationes generaliores et specierum cognitarum succinctas descriptiones cum selectis auctorum synonymis. Hagae Comitum, 28, 1451.Google Scholar
Pérez, CD, de Moura Neves, B, Cordeiro, RT, Williams, GC and Cairns, SD (2016) Diversity and distribution of Octocorallia. In Goffredo S and Dubinsky Z (eds), The Cnidaria: Past, Present and Future. Cham: Springer, pp. 109123.CrossRefGoogle Scholar
Pous, S, Carton, X and Lazure, P (2004) Hydrology and circulation in the Strait of Hormuz and the Gulf of Oman – results from the GOGP99 experiment: 1. Strait of Hormuz. Journal of Geophysical Research: Oceans 109. https://doi.org/10.1029/2003JC002146.Google Scholar
Rezai, H (1996) Observation of some corals in shallow waters of several remote Iranian islands in the Persian Gulf. Abzeeyan Monthly Magazine 7, 410.Google Scholar
Rezai, H and Savari, A (2004) Observation on reef fishes in the coastal waters off some Iranian Islands in the Persian Gulf. Zoology in the Middle East 31, 6776.CrossRefGoogle Scholar
Rezai, H, Wilson, S, Claereboudt, M and Riegl, B (2004) Coral reef status in the ROPME sea area: Arabian/Persian Gulf, Gulf of Oman and Arabian Sea. Status of Coral Reefs of the World 1, 155170.Google Scholar
Rezai, H, Samimi, K, Kabiri, K, Kamrani, E, Jalili, M and Mokhtari, M (2010) Distribution and abundance of the corals around Hengam and Farurgan islands, the Persian Gulf. Journal of the Persian Gulf 1, 716.Google Scholar
Ricklefs, RE (2004) A comprehensive framework for global patterns in biodiversity. Ecology Letters 7, 115.CrossRefGoogle Scholar
Riegl, BM and Purkis, SJ (2012) Coral reefs of the Gulf: adaptation to climatic extremes in the world's hottest sea. In Riegl BM and Purkis SJ (eds), Coral Reefs of the Gulf. Cham: Springer, pp. 14.CrossRefGoogle Scholar
Salimi, PA, Mostafavi, PG, Chen, CA, Fatemi, SMR and Pichon, M (2018) The Scleractinia (Cnidaria: Anthozoa) of Abu-Musa and Sirri Islands, Persian Gulf. Zoological Studies 57.Google ScholarPubMed
Samiei, JV, Dab, K, Ghezellou, P and Shirvani, A (2013) Some scleractinian corals (Scleractinia: Anthozoa) of Larak Island, Persian Gulf. Zootaxa 3636, 101143.CrossRefGoogle ScholarPubMed
Samimi-Namin, K and van Ofwegen, L (2009) Some shallow water octocorals (Coelenterata: Anthozoa) of the Persian Gulf. Zootaxa 2058, 152.CrossRefGoogle Scholar
Samimi-Namin, K and van Ofwegen, L (2012) The octocoral fauna of the Gulf. In Riegl BM and Purkis SJ (eds), Coral Reefs of the Gulf. Cham: Springer, pp. 225252.CrossRefGoogle Scholar
Seah, JZS, Yap, NWL, Tan, LT and Goh, BPL (2015) Distribution and abundance of octocoral (Octocorallia, Alcyonacea) communities at three southern islands of Singapore. Ocean Science Journal 50, 299306.CrossRefGoogle Scholar
Shahbazi, S, Sakhaei, N, Zolgharnein, H and McFadden, CS (2019) First record of Viminella sp. (Anthozoa: Alcyonacea: Ellisellidae) in the Persian Gulf. Biodiversity Data Journal 7, e33089.CrossRefGoogle Scholar
Shahbazi, S, Sakhaei, N, Zolgharnein, H and McFadden, CS (2021) A molecular systematic survey of the Iranian Persian Gulf octocorals (Cnidaria: Alcyonacea). Marine Biodiversity 51, 118.CrossRefGoogle Scholar
Sheppard, C and Sheppard, A (1991) Corals and Coral Communities of Arabia. Fauna of Saudi Arabia. Basel: Natural History Museum. 170 pp.Google Scholar
Thomson, JA and Simpson, JJ (1909) An Account of the Alcyonarians Collected by the Royal Indian Marine Survey Ship Investigator in the Indian Ocean; with a Report on the Species of Dendronephthya by W.D. Henderson. II. The Alcyonarians of the Littoral Area. Calcutta: The Indian Museum.Google Scholar
Tixier-Durivault, A (1945) Les alcyonaires du Muséum: I. Famille des Alcyoniidae. II. Genre Sinularia. Bulletin du Muséum National d'Histoire Naturelle Paris 2: 17, 1: 55–63, 2: 145–152, 3: 243–250, 4: 321–325.Google Scholar
Walther, GR, Post, E, Convey, P, Menzel, A, Parmesan, C, Beebee, TJ, Fromentin, JM, Hoegh-Guldberg, O and Bairlein, F (2002) Ecological responses to recent climate change. Nature 416, 389395.CrossRefGoogle ScholarPubMed
Williams, G and Chen, J (2011) Illustrated key to the shallow-water gorgonians and pennatulaceans of the Verde Island Passage, northern Philippines, including synopses of the taxa and a glossary of terms (Cnidaria: Anthozoa: Octocorallia). In Williams, G and Gosliner, T (eds), The Coral Triangle: The 2011 Hearst Philippine Biodiversity Expedition. San Francisco, CA: California Academy of Sciences, pp. 67–128.Google Scholar
Williams, GC and Cairns, SD (2013) Biodiversity myth busters, Octocoral Research Center. Available at http://researcharchive.calacademy.org/research/izg/Biodiversity%20Myth%20Busters%202.html (Accessed 3 May 2020).Google Scholar
Figure 0

Fig. 1. Map showing the location of the islands and the sampling stations (1–14) in the northern Persian Gulf (Iran).

Figure 1

Table 1. Coordinates of octocoral sampling stations in the north of the Persian Gulf

Figure 2

Table 2. Octocorals species composition at three islands in the northern Persian Gulf

Figure 3

Fig. 2. Some species identified in this survey. (A) Sarcophyton minusculum Samimi-Namin and Ofwegen, 2009; (B) Echinogorgia sp. a; (C) Sinularia erecta Tixier-Durivault, 1945; (D) Dendronephthya sp. b; (E) Junceella juncea (Pallas, 1766); (F) Verrucella cf. reticulata (Thomson and Simpson, 1909); (G) close up of Astrogorgia fruticosa Samimi-Namin and Ofwegen, 2009; (H) Echinogorgia sp. b; (I) Menella sp. g.

Figure 4

Fig. 3. Per cent composition of octocoral taxa comprising the 22 identified species in the survey. (A) percentages of genera in subordinal groups; (B) percentages of identified octocoral species within Alcyonacea families (rounded to the nearest percentage).

Figure 5

Fig. 4. Mean (± S.E.) abundance (colony number per belt transect) of octocorals at survey stations (n=3 transects per station). Different letters (a, b) indicate significant differences (P < 0.05). (No octocorals found at stations 7, 13 and 14).

Figure 6

Fig. 5. Mean (± S.E.) Shannon-Wiener diversity index (colony number per belt transect) of octocorals at survey stations (n=3 transects per station). Different letters (a, b and c) indicate significant differences (P < 0.05). (No octocorals found at stations 7, 13 and 14.)

Figure 7

Fig. 6. Two-dimensional MDS configuration of octocoral communities at Larak Island (LI), Hengam Island (HI) and Qeshm Island (QI). A stress value of 0.1 gave a good representation of the data.

Figure 8

Table 3. R statistics derived from pairwise tests using ANOSIM to compare dissimilarities of octocoral communities among the three islands