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1,478 results for “coral reefs”
Fig. 2 in Preliminary observations of macrobenthic invertebrates and megafauna communities in the upper mesophotic coral ecosystems in Apo Reef Natural Park, Philippines
Fig. 2. Reef fish and marine reptile megafaunal species in Apo Reef Natural Park. A, Eretmochelys imbricata; B, Bolbometopon muricatum; C, Balistoides viridescens; D, Cheilinus undulatus; E, Caranx melampygus; F, Cephalopholis argus; G, Macolor niger; H, Sphyraena qenie; I, Triaenodon obesus.
Fig. 1 in Preliminary observations of macrobenthic invertebrates and megafauna communities in the upper mesophotic coral ecosystems in Apo Reef Natural Park, Philippines
Fig. 1. Map showing the location of Apo Reef Natural Park in the Philippines, as well as, the study sites that were surveyed in March 2016.
Fig. 4 in Preliminary observations of macrobenthic invertebrates and megafauna communities in the upper mesophotic coral ecosystems in Apo Reef Natural Park, Philippines
Fig. 4. Results of the non-metric multidimensional scaling (nMDS) across depths (A) and reef types (B). Analysis of similarity (ANOSIM) results along with the corresponding p values are included in the plots (A and B). Vectors showing the influence (direction and magnitude) of the different benthic cover on the species composition (C).
Fig. 1 in Population dynamics of corallivores (Drupella and Acanthaster) on coral reefs of Koh Tao, a diving destination in the Gulf of Thailand
Fig. 1. Map of survey sites used in this study (after Hoeksema et al., 2012). Six of them were monitored for hard coral cover: Hin Wong Bay, Sairee, Sai Nuan, Chalok Ban Kao, Ao Leuk, and Tanote Bay. These sites and two additional ones (Mango Bay and Twin Rocks=Twins) were also used for predator studies.
Fig. 3 in Population dynamics of corallivores (Drupella and Acanthaster) on coral reefs of Koh Tao, a diving destination in the Gulf of Thailand
Fig. 3. Population dynamics of coral predators around Koh Tao in 2006–2014. a, Relative Drupella abundance showing significant variation over time (p=0.013). b, Mean Acanthaster abundance not varying significantly over time (p=0.189). c, Mean Drupella abundance is significantly higher in shallow quadrats as compared to deeper ones (p <0.001). d, Mean Acanthaster abundance shows no difference by depth (p=0.142). e, Mean Drupella abundance by site varied significantly (p <0.001). f, Mean Acanthaster abundance by site varied significantly p <0.001). g, Seasonal variability in Acanthaster abundance at EMP sites was not significant (p=0.641).
Fig. 5 in Population dynamics of corallivores (Drupella and Acanthaster) on coral reefs of Koh Tao, a diving destination in the Gulf of Thailand
Fig. 5. Coral predator abundance compared to previously published results on Koh Tao's reefs; differences are not significant. Drupella (a) and Acanthaster (b) abundance in low- and high-use sites as designated by Lamb et al. (2014). Similar for the designations as MPA or non-MPA sites used by Hein et al. (2014) concerning Drupella (c) and Acanthaster (d).
Fig. 4 in Population dynamics of corallivores (Drupella and Acanthaster) on coral reefs of Koh Tao, a diving destination in the Gulf of Thailand
Fig. 4. Positive linear correlation between Drupella abundance and live hard coral cover (R2=0.572, p <0.001).
Fig. 2 in Population dynamics of corallivores (Drupella and Acanthaster) on coral reefs of Koh Tao, a diving destination in the Gulf of Thailand
Fig. 2. Variation in mean hard coral cover at Koh Tao over the period 2006–2014 for the six selected sites indicated in Table 1.
Fig. 2 in Ninh Hai waters (south Vietnam): a hotspot of reef corals in the western South China Sea
Fig. 2. Dendrogram of similarity in coral community types, derived from the species–abundances (4th root transformed) of corals in 24 sites using Eucidean distance and complete linkage.
Fig. 1 in Ninh Hai waters (south Vietnam): a hotspot of reef corals in the western South China Sea
Fig. 1. Sites for inventory of reef building scleratinian corals (• in 2003 & 2004 and * in 2011 & 2012), and reef distribution in the Ninh Hai coastal waters
Fig. 4 in Records Of The Hermit Crab Genus Pagurixus Melin, 1939 (Decapoda: Anomura: Paguridae) From Shallow Coral Reefs In The Panglao Islands, The Philippines, With Description Of A New Species
Fig. 4. Pagurixus spiniferore, new species, male (sl 1.4 mm), holotype, NMCR 39060, PANGLAO 2004, stn 23. A, right second pereopod, lateral view; B, same, dactylus, mesial view; C, same, carpus, mesial view; D, left third pereopod, lateral view; E, same, dactylus, mesial view; F, same, carpus, mesial view. Scale bars = 0.5 mm.
Fig. 3 in Records Of The Hermit Crab Genus Pagurixus Melin, 1939 (Decapoda: Anomura: Paguridae) From Shallow Coral Reefs In The Panglao Islands, The Philippines, With Description Of A New Species
Fig. 3. Pagurixus spiniferore, new species, male (sl 1.4 mm), holotype, NMCR 39060, PANGLAO 2004, stn 23. A, right chela, dorsal view; B, right cheliped, mesial view; C, same, lateral view; D, same, carpus, dorsal view; E, left chela, dorsal view; F, left cheliped, mesial view; G, same, lateral view; H, same, carpus, dorsal view. Scale bar = 0.5 mm.
Fig. 1. Pagurixus rubrovittatus Komai, 2010 in Records Of The Hermit Crab Genus Pagurixus Melin, 1939 (Decapoda: Anomura: Paguridae) From Shallow Coral Reefs In The Panglao Islands, The Philippines, With Description Of A New Species
Fig. 1. Pagurixus rubrovittatus Komai, 2010, male (sl 2.5 mm), ZRC 2012.0939, PANGLAO 2004, stn 32-12. Entire animal in dorsal view, showing colouration in life.
Fig. 2 in Records Of The Hermit Crab Genus Pagurixus Melin, 1939 (Decapoda: Anomura: Paguridae) From Shallow Coral Reefs In The Panglao Islands, The Philippines, With Description Of A New Species
Fig. 2. Pagurixus spiniferore, new species, male (sl 1.4 mm), holotype, NMCR 39060, PANGLAO 2004, stn 23. A, shield and cephalic appendages, dorsal view; B, ultimate segment and flagella of left antennule, lateral view; C, left fourth pereopod, lateral view; D, sixth thoracic sternite, ventral view; E, eighth thoracic sternite and coxae of fifth pereopods, ventral view; F, telson, dorsal view. Scale bars = 0.5 mm.
Fig. 4 in Among-Genotype Variation For Sediment Rejection In The Reef-Building Coral Diploastrea Heliopora (Lamarck, 1816)
Fig. 4. Percentage area cleared of sediment over the five-hour duration of the experiment calculated from 12 fragments (four replicates × three treatment) per genotype. Significantly more sediment was cleared under the 'low' sediment load compared to the 'medium' and 'high' loads (Table 2).
Fig. 5 in Among-Genotype Variation For Sediment Rejection In The Reef-Building Coral Diploastrea Heliopora (Lamarck, 1816)
Fig. 5. Percentage of sediment mass cleared after five hours (the duration of the experiment) calculated from 12 fragments (four replicates × three treatment) per genotype.
Fig. 2 in Among-Genotype Variation For Sediment Rejection In The Reef-Building Coral Diploastrea Heliopora (Lamarck, 1816)
Fig. 2. Profiles of natural sediments retrieved from sediment traps positioned at Pulau Hantu (solid line) and the artificial silicon carbide mixture (dotted line).
FIG. 41. — Bretskya scapula n. gen., n in Diversity of chemosymbiotic bivalves on coral reefs: Lucinidae (Mollusca, Bivalvia) of New Caledonia and Lifou
FIG. 41. — Bretskya scapula n. gen., n. sp., Pandanan Island, Philippines:A, dorsal view of paratype (BMNH 20050580); B, protoconch; C, detail of sculpture. Scale bars: A, 1 mm; B, 50 µm; C, 100 µm.
FIG. 40. — Bretskya scapula n. gen., n in Diversity of chemosymbiotic bivalves on coral reefs: Lucinidae (Mollusca, Bivalvia) of New Caledonia and Lifou
FIG. 40. — Bretskya scapula n. gen., n. sp.: A-J, Pandanan Island, Philippines; A-C, holotype (BMNH 20050579), exterior of right valve and interior of right and left valves; D-J, paratype (BMNH 20050580); D-F, exterior of right valve and interior of right and left valves; G, exterior of right valve; H, exterior of right valve; I, J, detail of hinges of left and right valves; K, L, Philippines, MUSORSTOM 3, stn DR 140, 93-99 m (MNHN); M, N, Touho, stn 1249, New Caledonia, exterior and interior right valve. Scale bars: A-H, K-N, 2.0 mm; I, J, 1.0 mm.
FIG. 39 in Diversity of chemosymbiotic bivalves on coral reefs: Lucinidae (Mollusca, Bivalvia) of New Caledonia and Lifou
FIG. 39. — Outline drawings of interiors of right valves of Parvidontia n. gen. and Bretskya n. gen. species: A, P. laevis n. gen., n. sp.; B, B. scapula n. gen., n. sp. Not to scale.
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International Brain Laboratory public data
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OpenNeuro
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