TCRMP 2013: executive summary, part 2
METHODS 32 Methods BENTHIC ASSESSMENTS The University of the Virgin Islands determined the benthic composition at 33 long-‐term monitoring sites between 2001 and 2012 (Fig. 4). Around St. Croix the following 14 sites were assessed: Buck Island-‐St. Croix, Cane Bay, Cane Bay Deep, Castle, Eagle Ray, Great Pond, Jacks/Isaacs Bay, Kings Corner, Lang Bank East End Marine Park (Lang EEMP), Lang Bank Red Hind Fish Spawning Aggregation (Lang Hind), Mutton Snapper, Salt River, Salt River Deep, and Sprat Hole. Four of these sites are within the St. Croix East End Marine Park boundary (Castle, Great Pond, Jacks Bay, Lang EEMP), three sites are within National Park Service boundaries (Buck Island-‐St. Croix, Salt River West , and Salt River Deep), two sites are within federal fisheries marine protected areas (Lang Hind, Mutton Snapper), and four sites can be considered mesophotic coral reefs (Cane Bay Deep, Lang Bank EEMP, Lang Hind Salt River Deep; sensu Ginsburg 2007) (Ginsburg 2007)(Ginsburg 2007)(Ginsburg 2007)(Ginsburg 2007). …
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METHODS 32 Methods BENTHIC ASSESSMENTS The University of the Virgin Islands determined the benthic composition at 33 long-‐term monitoring sites between 2001 and 2012 (Fig. 4). Around St. Croix the following 14 sites were assessed: Buck Island-‐St. Croix, Cane Bay, Cane Bay Deep, Castle, Eagle Ray, Great Pond, Jacks/Isaacs Bay, Kings Corner, Lang Bank East End Marine Park (Lang EEMP), Lang Bank Red Hind Fish Spawning Aggregation (Lang Hind), Mutton Snapper, Salt River, Salt River Deep, and Sprat Hole. Four of these sites are within the St. Croix East End Marine Park boundary (Castle, Great Pond, Jacks Bay, Lang EEMP), three sites are within National Park Service boundaries (Buck Island-‐St. Croix, Salt River West , and Salt River Deep), two sites are within federal fisheries marine protected areas (Lang Hind, Mutton Snapper), and four sites can be considered mesophotic coral reefs (Cane Bay Deep, Lang Bank EEMP, Lang Hind Salt River Deep; sensu Ginsburg 2007) (Ginsburg 2007)(Ginsburg 2007)(Ginsburg 2007)(Ginsburg 2007). Salt River Deep transects 1-‐4 were moved from METHODS 33 40 m depth at the April 2009 sampling to 30 m in the January 2010 sampling due to low coral cover in the deeper transects. Around St. John-‐St. Thomas the following 19 sites were assessed: Black Point, Botany Bay, Brewers Bay, Buck Island-‐St. Thomas, Coculus Rock, College Shoal East, Coral Bay, Fish Bay, Flat Cay, Ginsburgs Fringe, Grammanik Tiger FSA, Hind Bank FSA, Little St. James, Magens Bay, Savana Island, Seahorse Cottage Shoal (Seahorse), Meri Shoal, South Capella, and South Water Island. One site is the within the St. Thomas East End Reserve (Coculus Rock), four sites are within federal fisheries marine protected areas (College Shoal, Ginsburgs Fringe, Grammanik Tiger, Hind Bank), and five sites can be considered mesophotic coral reefs (College Shoal, Ginsburgs Fringe, Grammanik Tiger, Hind Bank, Meri Shoal). Four sites are also part of the Ciguatera Fish Monitoring Program and have been surveyed monthly for benthic structure and coral health since 2010 (Black Point, Coculus Rock, Flat Cay, Seahorse). Benthic Cover. At each site benthic cover and coral health surveys were conducted along six 10 m long permanent transects marked with steel or brass rods. Video sampling consisted of one diver traversing each transect videotaping the benthic cover using a high definition video cassette recorder (Sony FX-‐7 in Light and Motion housing) or an HD digital video recorder with wide angle lens (Canon XF in Light and Motion housing). The diver swam at a uniform speed, pointing the camera down and keeping the lens approximately 0.4 m above the substrate at all times. A guide wand or dropper weight attached to the camera housing was used to help the diver maintain the camera a constant distance above the reef. After taping, approximately 20 -‐ 50 non-‐overlapping images per transect were captured and saved as JPEG files (Fig. 5). Captured images represented an area of reef approximately 0.31 m2 (0.64 m x 0.48 m). Coral Point Count with Excel Extension software (Kohler and Gil 2006) was used to superimpose ten randomly located dots on each image. The substrate type located under each of the dots METHODS 34 was then identified to the most descriptive level possible and entered into a database. Where multiple benthic cover categories fell under a single point, for example macroalgae over bedrock, the upper benthic category was assessed. For each transect, the percent cover of coral, epilithic algae (formerly called dead coral with turf algae), macroalgae, sponges, gorgonians, and sand/sediment were calculated by dividing the number of random dots falling on that substrate type by the total number of dots for that transect. Epilithic algae (sensu Hatcher and Larkum 1983) are diminutive turfs and filamentous algae without thallus structure that cover all rock surfaces of coral reefs not occupied by larger epibenthic organisms. They can also be considered to be grazed surfaces and are often an indicator of healthy grazing communities and high animal cover. Figure 5. A screen grab of benthic video used for the determination of percent cover of coral reef organisms and non-‐living substrate. METHODS 35 Table 1. TCRMP site reef complex type, location coordinates, and depths. FSA = Fish Spawning Aggregation. EEMP = East End Marine Park. Island Site Reef Complex Lat Long Depth (m) St. Croix Buck Island-St. Croix Offshore-Shallow 17.78500 -64.60917 15 Cane Bay Nearshore 17.77388 -64.81350 10 Cane Bay Deep Offshore-MCE 17.77661 -64.81522 38 Castle Offshore-Shallow 17.76278 -64.59743 7 Eagle Ray Offshore-Shallow 17.76150 -64.69880 10 Great Pond Nearshore 17.71097 -64.65221 6 Jacks Bay Nearshore 17.74337 -64.57160 14 Kings Corner Nearshore 17.69116 -64.90008 17 Lang Bank EEMP Offshore-MCE 17.72145 -64.54706 27 Lang Bank Red Hind FSA Offshore-MCE 17.82372 -64.44943 33 Mutton Snapper FSA Offshore-Shallow 17.63660 -64.86240 24 Salt River Deep Offshore-MCE 17.78523 -64.75917 30 Salt River West Offshore-Shallow 17.78530 -64.75940 11 Sprat Hole Nearshore 17.73400 -64.89540 8 St. John Coral Bay Nearshore-Shallow 18.33797 -64.70402 9 Fish Bay Nearshore 18.31417 -64.76408 6 Meri Shoal Offshore-MCE 18.24433 -64.75832 30 St. Thomas Black Point Nearshore 18.34450 -64.98595 9 Botany Bay Nearshore 18.35845 -65.03330 8 Brewers Bay Nearshore 18.34403 -64.98435 6 Buck Island-St. Thomas Offshore-Shallow 18.27883 -64.89833 14 Coculus Rock Nearshore 18.31257 -64.86058 7 College Shoal East Offshore-MCE 18.18568 -65.07677 30 Flat Cay Offshore-Shallow 18.31822 -64.99104 12 Ginsburgs Fringe Offshore-MCE 18.18770 -64.95998 63 Grammanik Tiger FSA Offshore-MCE 18.19113 -64.95032 38 Hind Bank East FSA Offshore-MCE 18.20217 -65.00158 39 Magens Bay Nearshore 18.37425 -64.93438 7 Savana Offshore-Shallow 18.34064 -65.08205 9 Seahorse Cottage Shoal Offshore-Shallow 18.29467 -64.86750 20 South Capella Offshore-Shallow 18.26267 -64.87237 20 South Water Offshore-Shallow 18.28068 -64.94592 20 St James Offshore-Shallow 18.29459 -64.83238 15 METHODS 36 Table 2.TCRMP site date sampled (benthic/health) and type of sampling. Island Site Date Sampled Benthic Health Fish/Urchin St. Croix Buck Island STX 8/13/13 x x x Cane Bay 8/12/13 x x x Cane Bay Deep 8/12/13 x x x Castle 8/15/13 x x x Eagle Ray 8/15/13 x x x Great Pond 8/14/13 x x x Jacks Bay 8/14/13 x x x Kings Corner 8/16/13 x x x Lang Bank EEMP 8/13/13 x x x Lang Bank Red Hind FSA 8/13/13 x x x Mutton Snapper FSA 8/16/13 x x x Salt River Deep 8/11/13 x x x Salt River West 8/11/13 x x x Sprat Hole 8/16/13 x x x St. John Coral Bay 01/20/14 x x x Fish Bay 01/20/14 x x x Meri Shoal 10/13/13 x x x St. Thomas Black Point 10/23/13 x x x Botany Bay 10/29/13 x x x Brewers Bay 10/10/13 x x x Buck Island STT 10/29/13 x x x Coculus Rock 10/22/13 x x x College Shoal East 10/13/13 x x x Flat Cay 10/23/13 x x x Ginsburgs Fringe 12/06/13 x Grammanik Tiger FSA 10/08/13 x x x Hind Bank East FSA 10/11/13 x x x Magens Bay 03/18/14 x x x Savana 10/29/13 x x x Seahorse Cottage Shoal 10/22/13 x x x South Capella 11/05/13 x x x South Water 11/22/13 x x x St James 10/15/13 x x x METHODS 37 Coral Health. Coral health assessments follow methodologies outlined in (Calnan et al. 2008) and (Smith et al. 2008) and are briefly described here. All coral colonies located directly under the transect lines were assessed in situ for signs of mortality and disease following a modified Atlantic and Gulf Rapid Reef Assessment protocol (Kramer et al. 2005). In contrast to previous years where only colonies greater than 10 cm in maximum linear dimension were assessed, starting in 2008 all colonies were assessed, regardless of size. Partial mortality of coral colonies was broken into two categories. Recent partial mortality was characterized visually as skeleton not eroded (fine corallite structure still intact) and bare or with a thin veneer of sheeting or filamentous algae. Recent partial mortality is typically visible for up to three months following tissue loss. Old partial mortality was characterized as skeleton eroded and covered with turf or macroalgae. Old partial mortality is a transition from recent mortality and typically lasts up to 1–6 years (Smith et al. 2008, also see http://www.agrra.org/method/methodcor.html). Diseases were conservatively categorized into recognized Caribbean scleractinian diseases and syndromes that included bleaching, black band disease, dark spots disease, white plague, and yellow band (blotch) disease (following Bruckner 2007). Acroporid corals were extremely rare at the study sites; thus, their associated diseases (white band and white pox) are not presented. Bleaching was assessed as abnormal paling of the colony, and, when present, the severity of the bleaching (paling or total whitening) and the area of the colony affected were assessed. A major bleaching event occurred between September and December 2005, affecting all monitored sites, and a mild bleaching event occurred September and October 2010 (Smith et al. 2013). On St. Croix, a subset of sites were assessed during the 2010 coral bleaching event, and included Cane Bay, Cane Bay Deep, and Jacks Bay. For each transect, the prevalence of coral impairment categories was calculated as the number of colonies with partial mortality, disease, or bleaching divided by the number of METHODS 38 colonies assessed. Also, for affected colonies in each transect the average three-‐ dimensional surface area (%) of the colony affected was also estimated for each impairment category. FISH CENSUS Fish surveys have been conducted at 14 sites around St. Croix and 18 sites around St. Thomas (Table 2). Ten replicate belt transects and three replicate roving dive surveys (RDS) were conducted at each site. Belt transects were 30m x 4m and were conducted in 15 min per replicate. All transects were begun at a random location on the site, and were swum in a random direction. RDS replicates were either 30 min (sites < 25 m depth) or 15 min (sites >25 m depth) (see Table 3). In addition to relative abundance data, specific total length estimates were made for each large grouper, large snapper or hogfish (Lachnolaimus maximus) encountered. In all surveys, all fish encountered were recorded except blennies and gobies. Data were transcribed to Microsoft Excel and Access spreadsheets, and were analyzed for descriptive statistics of reef fish assemblage structure. Divers also counted the number of Diadema antillarum sea urchins within 1 m on either side of transects. From 2001 – 2008 this occurred along the 6 – 10 m long benthic transects. Starting in 2009, urchins were assessed along 25x2m belt transects corresponding to the return of the 10 fish transects. The mean number of sea urchins per 100 m2 was calculated for each site. TCRMP MONITORING SUMMARY 39 Territorial Coral Reef Monitoring Summary BENTHIC COVER & CORAL HEALTH 40 BENTHIC COMMUNITIES AND CORAL REEF HEALTH Benthic cover was monitored at 33 monitoring sites and coral health was monitored at 32 sites in 2013. Coral health was not monitored at the deep (63m) Ginsburgs Fringe. Benthic cover raw data is presented in electronic Appendix I. Coral health raw data is presented in electronic Appendix II. Coral Cover The cover of hard corals decreased at most sites after the 2005 coral bleaching event, but showed little or no change as the results of the 2010 coral bleaching event (Fig. 6). Shallow (<25 m depth), nearshore and offshore sites with greater than about 20% coral cover showed declines in cover, but there was extreme variability in the degree of cover change. For example the Mutton Snapper site on St. Croix lost 87% of its coral cover between 2004 and 2006. Sites that had low coral cover prior to 2005 lost far less relative cover as the result of bleaching. While part of this may be due to detectability at values nearer to 0, these sites tend to be dominated by small massive species that are more resistant to disease related mortality (Smith et al. 2013). Mesophotic coral monitoring sites that were sampled before and after the 2005 coral bleaching event showed slight relative losses of coral cover. Losses ranged from 5.4% (Grammanik Tiger) to 36.0% (Meri Shoal). Since 2010, coral cover has declined slightly at some mesophotic sites, which may reflect the impact of white diseases and a mild bleaching event that occurred in 2012. Recovery since bleaching was marginal at most sites. The majority of sites had apparently level coral cover with recovery potentially inhibited by disease and increased interactions with other organisms. However, slow upward trajectories are notable at some sites. TCRMP MONITORING SUMMARY 41 Figure 6. Coral cover (±SE) across TCRMP monitoring sites over time. Nearshore Cover 0% 20% 40% 60% 80% 100% Black Point Botany Bay Brewers Bay Cane Bay Coculus Rock Coral Bay Fish Bay Great Pond Jacks Bay Kings Corner Magens Bay Salt River West Sprat Hole Offshore Cover 0% 20% 40% 60% 80% 100% Buck Island STT Buck Island STX Castle Eagle Ray Flat Cay Mutton Snapper Savana Island Seahorse South Capella South Water St. James Mesophotic 2001 2002 2003 2004 2005 2005 BL 2006 2007 2008 2009 2010 2011 2012 2013 Cover 0% 20% 40% 60% 80% 100% Cane Bay Deep College Shoal Ginsburgs Fringe Grammanik Tiger Hind Bank FSA Lang Bank EEMP Lang Bank FSA Meri Shoal Salt River Deep BENTHIC COVER & CORAL HEALTH 42 Epilithic Algal Community Cover Algae show the highest inter-‐annual variability of any group of benthic organisms (Fig. 7). This is largely due to seasonality. The cover of epilithic algae is no exception, since it tends to negatively covary with more ephemeral macroalgae. Epilithic algae is important as it can indicate substrates grazed by herbivores and therefore open to the settlement of sessile epibenthic animals, including coral. Nearshore and mesophotic sites showed little inter-‐annual trend in epilithic algal cover. Many offshore sites, such as Eagle Ray and Buck Island-‐St. Croix, appear to have a declining abundance of epilithic algae, indicating an increase in other benthic components, such as macroalgae and filamentous cyanobacteria, and possibly indicating declining grazing. TCRMP MONITORING SUMMARY 43 Figure 7. Epilithic Algal Community cover (±SE) across TCRMP monitoring sites over time. Nearshore Cover 0% 20% 40% 60% 80% 100% Black Point Botany Bay Brewers Bay Cane Bay Coculus Rock Coral Bay Fish Bay Great Pond Jacks Bay Kings Corner Magens Bay Salt River West Sprat Hole Offshore Cover 0% 20% 40% 60% 80% 100% Buck Island STT Buck Island STX Castle Eagle Ray Flat Cay Mutton Snapper Savana Island Seahorse South Capella South Water St. James Mesophotic 2001 2002 2003 2004 2005 2005 BL 2006 2007 2008 2009 2010 2011 2012 2013 Cover 0% 20% 40% 60% 80% 100% Cane Bay Deep College Shoal Ginsburgs Fringe Grammanik Tiger Hind Bank FSA Lang Bank EEMP Lang Bank FSA Meri Shoal Salt River Deep BENTHIC COVER & CORAL HEALTH 44 Macroalgal Cover Macroalgae have been increasing at many reefs, particularly after the 2005 bleaching event (Fig. 8). At sites where there was no loss of coral cover, increased macroalgae may be due to declining grazing, such as at Eagle Ray. At other sites where coral cover dropped after 2005, space opened for algal colonization by coral die-‐off may not have been grazed in reefs where resident herbivores communities are already at the threshold of maximum grazing rates (Williams et al. 2001). These reefs include, the Buck Islands (St. Thomas and St. Croix), Cane Bay, Meri Shoal, South Capella, and Sprat Hole. The same explanation may also apply for filamentous cyanobacteria (see following section). TCRMP MONITORING SUMMARY 45 Figure 8. Macroalgae cover (±SE) across TCRMP monitoring sites over time. Nearshore Cover 0% 20% 40% 60% 80% 100% Black Point Botany Bay Brewers Bay Cane Bay Coculus Rock Coral Bay Fish Bay Great Pond Jacks Bay Kings Corner Magens Bay Salt River West Sprat Hole Offshore Cover 0% 20% 40% 60% 80% 100% Buck Island STT Buck Island STX Castle Eagle Ray Flat Cay Mutton Snapper Savana Island Seahorse South Capella South Water St. James Mesophotic 2001 2002 2003 2004 2005 2005 BL 2006 2007 2008 2009 2010 2011 2012 2013 Cover 0% 20% 40% 60% 80% 100% Cane Bay Deep College Shoal Ginsburgs Fringe Grammanik Tiger Hind Bank FSA Lang Bank EEMP Lang Bank FSA Meri Shoal Salt River Deep BENTHIC COVER & CORAL HEALTH 46 Filamentous Cyanobacteria Filamentous cyanobacteria cover has been increasing at many sites in the TCRMP since the 2005 coral bleaching event (Fig. 9). This is particularly true at many sites on St. Croix that have attained very high cover values in recent years. For example, Salt River West, Jacks Bay, Cane Bay, Sprat Hole, Mutton Snapper, Buck Island-‐St. Croix, Eagle Ray, Lang Bank EEMP, and Lang Bank Hind have all seen cover of filamentous cyanobacteria from 10 – 60%, with 2009 as a particularly high abundance year for offshore sites. The increased incidence of filamentous cyanobacteria can be an indication of disturbance, increased nutrient inputs, and insufficient grazing (Fong and Paul 2011). In addition, filamentous cyanobacteria can promote increases in palatable macroalgae in coral reefs by coating and protecting algae with secondary metabolites that deter grazing (Fong et al. 2006; Smith et al. 2010a). Filamentous cyanobacteria can inhibit the recruitment of coral larvae (Kuffner et al. 2006) and have been observed interacting at the borders of adult coral (Authors, unpub. data). Monitoring the trends of filamentous cyanobacteria in USVI reef systems will be increasingly important in future years in an effort to understand the factors influencing bloom formation and which reefs are most vulnerable. TCRMP MONITORING SUMMARY 47 Figure 9. Filamentous cyanobacteria cover (±SE) across TCRMP monitoring sites over time. Nearshore Cover 0% 20% 40% 60% 80% 100% Black Point Botany Bay Brewers Bay Cane Bay Coculus Rock Coral Bay Fish Bay Great Pond Jacks Bay Kings Corner Magens Bay Salt River West Sprat Hole Offshore Cover 0% 20% 40% 60% 80% 100% Buck Island STT Buck Island STX Castle Eagle Ray Flat Cay Mutton Snapper Savana Island Seahorse South Capella South Water St. James Mesophotic 2001 2002 2003 2004 2005 2005 BL 2006 2007 2008 2009 2010 2011 2012 2013 Cover 0% 20% 40% 60% 80% 100% Cane Bay Deep College Shoal Ginsburgs Fringe Grammanik Tiger Hind Bank FSA Lang Bank EEMP Lang Bank FSA Meri Shoal Salt River Deep BENTHIC COVER & CORAL HEALTH 48 Gorgonian and An+patharian Cover The cover of gorgonians and antipatharians has been fairly constant at most monitoring sites throughout the years of monitoring (Fig. 10). In most cases they are a relatively minor component of cover because of their upright growth form and small branches. However, there are sites that appear to be more favorable to the growth of gorgonians, including Magens Bay, Fish Bay, Coral Bay, Buck Island (St. Croix), Savana Island, South Water, Lang Bank Hind, and Salt River Deep. Note that Black Corals (antipatharians) typically tend to be more prominent in deep monitoring sites, whilst gorgonians tend to be more dominant in shallower and wave-‐washed sites. TCRMP MONITORING SUMMARY 49 Figure 10. Gorgonian and Antipatharian cover (±SE) across TCRMP monitoring sites over time. Nearshore Cover 0% 5% 10% 15% 20% 25% Black Point Botany Bay Brewers Bay Cane Bay Coculus Rock Coral Bay Fish Bay Great Pond Jacks Bay Kings Corner Magens Bay Salt River West Sprat Hole Offshore Cover 0% 5% 10% 15% 20% 25% Buck Island STT Buck Island STX Castle Eagle Ray Flat Cay Mutton Snapper Savana Island Seahorse South Capella South Water St. James Mesophotic 2001 2002 2003 2004 2005 2005 BL 2006 2007 2008 2009 2010 2011 2012 2013 Cover 0% 5% 10% 15% 20% 25% Cane Bay Deep College Shoal Ginsburgs Fringe Grammanik Tiger Hind Bank FSA Lang Bank EEMP Lang Bank FSA Meri Shoal Salt River Deep BENTHIC COVER & CORAL HEALTH 50 Sponge Cover Sponge cover has been constant or variable at many offshore and mesophotic sites, but there is an indication of slightly increasing sponge cover at some nearshore sites (Fig. 11). Nearshore increases were most pronounced at Black Point, Coral Bay, and Magens Bay. This increase in epibenthic and boring sponges may indicate increasing supplies of food, such as bacteria and small eukaryotes, in nearshore environments. This may be a consequence of increasing nearshore nutrient pollution. Further study needs to be done to establish this linkage. TCRMP MONITORING SUMMARY 51 Figure 11. Sponge cover (±SE) across TCRMP monitoring sites over time. Nearshore Cover 0% 5% 10% 15% 20% 25% Black Point Botany Bay Brewers Bay Cane Bay Coculus Rock Coral Bay Fish Bay Great Pond Jacks Bay Kings Corner Magens Bay Salt River West Sprat Hole Offshore Cover 0% 5% 10% 15% 20% 25% Buck Island STT Buck Island STX Castle Eagle Ray Flat Cay Mutton Snapper Savana Island Seahorse South Capella South Water St. James Mesophotic 2001 2002 2003 2004 2005 2005 BL 2006 2007 2008 2009 2010 2011 2012 2013 Cover 0% 5% 10% 15% 20% 25% Cane Bay Deep College Shoal Ginsburgs Fringe Grammanik Tiger Hind Bank FSA Lang Bank EEMP Lang Bank FSA Meri Shoal Salt River Deep FISH COMMUNITIES 52 FISH COMMUNITIES In 2013 a total of 33,058 fish representing 125 species and 37 families were recorded during belt transects across all sites off St. Croix and 39,711 fish representing 132 species and 39 families across all sites off St Thomas/St John. Using roving diver surveys (RDS) 121 species representing 33 families were observed in 2013 off St Croix and 119 species representing 32 families off St. Thomas/St. John (see Appendices III-‐VII). Species richness did not differ significantly between survey method or between nearshore, offshore and mesophotic sites (Table 3) but was lowest in Coral Bay, St. John (16.3±0.4 species/transect) and highest in Cane Bay Shallow, St. Croix (27.7±1.7 species/transect). Overall fish size distribution on both St. Croix and St. Thomas/St. John followed trends seen in earlier years. Fish smaller than 10cm total length (TL) predominated at all sites. Sixty percent of the individuals counted off St. Croix were less than 5cm TL and 84% were less than 10cm TL. Off St. Thomas/St. John, 38% were smaller than 5cm and 78% were under 10cm TL. Large fish (> 40cm TL) constituted less than 0.5% of the numeric total off St. Thomas/St. John (193 fish), and only 0.1% off St. Croix (56 fish). Numerically the most dominant fish across St. Thomas/St. John reefs were creole wrasse (Clepticus parrae), striped parrotfish (Scarus iserti), blue chromis (Chromis cyanae), bluehead wrasse (Thalassoma bifaciatum), bicolor damselfish (Stegastes partitus) and brown chromis (Chromis multilineata). These six species made up over 57% of the numeric total of fish observed on all St. Thomas/St. John sites. On St Croix reefs, creole wrasse, bluehead wrasse, blue chromis, bicolor damselfish and brown chromis contributed over 63% to the numeric total of all sites together. These species were ubiquitous across all sites and have been observed at the highest abundance throughout the years on the Virgin Islands’ reefs. With the exception of the striped parrotfish and bicolor damselfish they are planktivorous or omnivorous feeders, and fairly opportunistic. The creole wrasse, unlike the other common species was more abundant on offshore, mesophotic sites and on nearshore sites adjacent to walls. TCRMP SITE SUMMARIES 53 FISH COMMUNITIES 54 Table 3. Species richness across sites in belt transects and roving diver surveys (RDS). Sites are divided into nearshore, offshore and mesophotic sites as described in the text above. Belt Transects (25x4) RDS Total Number of Species Mean species per transect (±SE) Total Number of Species Nearshore Cane Bay 66 27.7±1.7 63 Great Pond 48 16.8±1.2 42 Jacks Bay 52 22.4±1.1 54 Kings Corner 62 27.5±2.4 67 Salt River West 51 20.0±1.3 55 Sprat Hole 56 25.7±1.0 64 Coculus Rock 45 20.9±1.2 48 Black Point 48 21.4±3.5 44 Brewers Bay 58 23.4±1.4 57 Botany Bay 53 22.6±1.3 59 Buck Island, St. Thomas 66 29.8±3.5 62 Coral Bay 39 16.3±0.4 54 Fish Bay 41 17.2±0.7 25 Magens Bay 48 22.2±1.7 49 Offshore Eagle Ray 63 24.7±1.1 62 Buck Island, St. Croix 53 22.2±1.5 60 Castle 52 23.8±1.1 64 Mutton Snapper 50 22.3±1.5 51 Seahorse Cottage 62 26.3±1.4 70 South Capella 61 21.8±1.2 69 South Water Island 54 21.1±1.3 57 Flat Cay 60 27.4±2.2 61 Meri Shoal 51 24.6±1.1 46 Savana Cay 61 24.4±2.3 69 Little St. James 58 21.2±1.7 59 Mesophotic Cane Bay Deep 47 17.3±1.2 47 Lang EEMP 63 25.0±1.2 62 Lang Bank 45 22.6±1.7 53 Salt River Deep 52 17.6±1.4 51 College Shoal East 64 23.4±1.0 55 Grammanik Bank 63 23.2±1.4 47 Hind Bank East 66 26.9±1.1 51 TCRMP SITE SUMMARIES 55 Fish Abundance Total fish abundances across nearshore, offshore and mesophotic sites and years are shown in Fig.12. Fish abundance in 2013 was similar across all sites to data collected in previous years. Abundance was highly variable across sites and years and shows no obvious pattern across time or space. Very high abundances of fish during most years represented schools of pelagic species such as creole wrasse or blue chromis. No change has been detected in fish communities since the coral bleaching of 2005 and subsequent high coral mortality event. The near shore sites added off St. Thomas/St. John, especially Fish Bay and Coral Bay, St. John, have slightly lower abundances of fish than most of the other sites. FISH COMMUNITIES 56 Figure 12. Fish abundance (±SE) across TCRMP monitoring sites over time. Dotted line separates St. Croix sites (left) from St. Thomas/St. John (right). TCRMP SITE SUMMARIES 57 Fish Biomass Fish biomass across sites is shown in Fig. 13. Across the years, mesophotic sites off St. Thomas (Grammanik Bank, Hind Bank and College Shoal East) have higher, in some years dramatically higher, average biomass of fish throughout the sampling period when compared to the more shallow sites across the territory and the St. Croix mesophotic sites. In 2013, fish biomass was slightly higher on mesophotic sites off St. Thomas/St. John. These sites are in marine reserves, which may be reflected in the average biomass per meter square. The sites are also well offshore and away from land-‐based pollution. Abundance is similar or lower on these deep St. Thomas reefs, indicating a larger average fish size. Juveniles of several species that occur in shallow water are nearly absent on the mesophotic reefs, and pomacentrids and wrasses (except creole wrasse) are much less common. The Grammanik Tiger and Hind Bank sites are near or on multispecies spawning aggregation sites for groupers and snapper. Sampling periods sometimes overlap slightly with the aggregation periods for cubera snapper (Lutjanus cyanopterus) or schoolmaster snapper (Lutjanus apodus); however, in 2013 they did not. Two of the mesophotic sites off St. Croix (Salt River Deep and Cane Bay Deep) are very close to shore and although both are protected areas since 2012, they were previously fished regularly. As with abundance, biomass is highly variable between years. No temporal pattern is evident, and differences in time appear to be seasonal or natural variation. The nearshore sites added in 2012 and re-‐ sampled in 2013 were relatively low in fish biomass, especially Coral Bay and Magens Bay. FISH COMMUNITIES 58 Figure 13. Mean fish biomass (±SE) across TCRMP monitoring sites over time. Dotted line separates St. Croix sites (left) from St. Thomas/St. John (right). SEA URCHINS 59 BLACK SPINY SEA URCHIN DIADEMA ANTILLARUM The abundance of the black spiny sea urchin Diadema antillarum shows tremendous site-‐ to-‐site variability (Fig. 14). In general the shallowest sites, e.g., Great Pond, support the greatest abundance of D. antillarum. These sites also tend to have very low macroalgal cover. Trends are not presented as year-‐to-‐year variability is generally low. Note that urchins have not yet been assessed at Ginsburgs Fringe. At Coral Bay there is a high abundance of Echinometra spp., which seems to be the dominant grazer that effectively removes macroalgal cover. Future monitoring might considered targeted monitoring of these species at certain sites. FISH COMMUNITIES 60 Figure 14. Abundance of the black spiny sea urchin (Diadema antillarum) at TCRMP monitoring sites. Note the log scale. log (Diadema antillarum/100m2) 0.001 0.01 0.1 1 10 100 Cane Bay Deep College Shoal Ginsburg Fringe Grammanik Kings Corner Lang Bank EEMP Lang Bank FSA Meri Shoal Mutton Snapper Salt River Deep Savana Seahorse South Capella South Water Sprat Hole Hind Bank St James Flat Cay Jacks Bay Buck Island STX Buck Island STT Salt River West Fish Bay Eagle Ray Cane Bay Black Point Magens Bay Coral Bay Brewers Bay Botany Bay Castle Coculus Rock Great Pond