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174 results for “seahorse”
Figure 2 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
Figure 2 Comparison of non-type specimens of AHippocampusprocerus CAS 241511, preserved adult female, 142.7 mm SL, Southport, QLDBHippocampusprocerus CAS 241512, preserved juvenile, 112.7 mm SL, Southport, QLD1Hippocampuswhitei PSFC-DH-1, preserved adult male, 122.1 mm SL, Nelson Bay, NSWDHippocampuswhitei CAS PSFC-DH-2, preserved subadult female, 47.7 mm SL, Nelson Bay NSW. Note the differences in coronet profile between juvenile/subadult and adult: projecting anteriad in juvenile/subadult versus lower or projecting posteriorly in adults.
Figure 13 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
Figure 13 Neighbor-joining tree based on mtDNA COI sequences showing the relationships among specimens of H.whitei collected from various sites in NSW and H.procerus from Southport, Gold Coast Harbour, QLD. Numbers in branches indicate bootstrap probabilities obtained from 1000 bootstrap replications. Scale bar = genetic distance of 0.02.
Figure 8 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
Figure 8 Hippocampusprocerus, QM I.39230, adult male, non-type, Elliot Heads, Queensland, Australia (photograph Jeff Johnson).
Figure 12 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
Figure 12 Hippocampusprocerus, QM I.39656, adult female, non-type, Waddy Point Queensland, Australia (photograph Jeff Johnson).
Figure 11 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
Figure 11 Hippocampusprocerus, AMS I.A4205, juvenile female, non-type, Point Curtis, Queensland, Australia (photograph Jeff Johnson).
Figure 10 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
Figure 10 Hippocampusprocerus, CAS-ICH 13406, adult male, non-type, 113.4 mm SL, Mackay, Queensland, Australia (photograph Jon Fong).
Supplementary material 2 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
: Data type: molecular data
Supplementary material 1 from: Short G, Harasti D, Hamilton H (2019) Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidence (Teleostei, Syngnathidae). ZooKeys 824: 109-133. https://doi.org/10.3897/zookeys.824.30921
: Data type: molecular data
Figure 3 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 3 Comparison of AHippocampus denise in situ, Orchid Island, Taiwan at 28 m depth, with its most similar congener BHippocampus bargibanti in situ, Green Island, Taiwan. Note the differences in body colouration (orange in H. denise vs. purple in H. bargibanti), the number and size of tubercles (fewer and less pronounced in H. denise), snout length (bulbous tip in H. bargibanti vs. non-bulbous in H. denise) and overall shape (slender and elongate in H. denise vs. rotund in H. bargibanti) (Photographs A Yung-Kuang Ting B Ryan Ku).
Figure 2 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 2 Hippocampus japapigu in situ A Green Island, Taiwan B Hejie, Kenting, Taiwan at 5 m depth C Hejie, Kenting, Taiwan D 82.5 k near Longdong, northern Taiwan (Photographs A Jolly Huang B Jay Chiu C Chao-Tsung Chen D Jung-Chao Yeh).
Figure 4 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 4 Comparison of A–CHippocampus colemani in situ, Green Island, Taiwan with D–FHippocampus pontohi in situ, Green Island, Taiwan. Note the differences in the shape and angle of the coronet (low and rounded in H. colemani vs. distinct and angular in H. pontohi), as well as differences in body colouration (H. colemani is known only to occur in shades of off-white, whereas H. pontohi is highly variable) (Photographs A Joe Chiu B Ryan Ku C, E, F Ming-Hung Yu D Ryan Ku).
Figure 1 from: Heard J, Chen J-P, Wen CKC (2019) Citizen science yields first records of Hippocampus japapigu and Hippocampus denise (Syngnathidae) from Taiwan: A hotspot for pygmy seahorse diversity. ZooKeys 883: 83-90. https://doi.org/10.3897/zookeys.883.39662
Figure 1 Map showing A the original collection locations of specimens for the five pygmy seahorse species recorded in Taiwan during this study, as well as B their distributions in Taiwan and surrounding islands (Penghu islands, Green Island, and Orchid Island). Symbols are scaled relatively according to the number of observations per species at each location obtained through social media.
Figure 2 in First record of the near threatened native seahorse Hippocampus reidi (Teleostei: Syngnathidae) in an ecosystem dominated by the invasive seagrass Halophila stipulacea in the Caribbean Sea
Figure 2. – Map of the study area with observation site; Madiana beach, Schoelcher, West coast of Martinique Island. June 2017.
Figure 5 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 5 - Muricella sp. 1 (RMNH Coel. 39871)A spindles from coenenchyme and polyp B smaller spindles from coenenchyme and polyp C capstans from adaxial layer D rods from tentacle. Scale bars represent 0.1 mm.
Figure 2 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 2 - In-situ photographs A Hippocampus bargibanti on Muricella sp. 3 (RMNH Coel. 39866, see Fig. 7), Turtles Reef, Raja Ampat (photo F.R. Stokvis) B Hippocampus denise on Annella reticulata (RMNH Coel. 39880, see Fig. 10); W Mansuar, Raja Ampat (photo B.W. Hoeksema) C Hippocampus pontohi (host not collected) Timur I, Bunaken (photo S.E.T. van der Meij) D Hippocampus severnsi (host not collected) Siladen I, SE Siladen (photo B.T. Reijnen).
Figure 11 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 11 - Annella mollis (RMNH Coel. 39875) A spindles from the coenenchyme B tentacle rods C medulla spindles from the axis D double heads from the surface layer. Scale bar represents 0.1 mm, except for D which is 0.05 mm.
Figure 1 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 1 - Map showing the fieldwork localities in Indonesia and Malaysia; BUN (Bunaken), RAJ (Raja Ampat), SEM (Semporna) and TER (Ternate).
Figure 8 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 8 - Euplexaura reticulata (ZMA Coel. 3504 - holotype) A spindles from the coenenchyme B tentacle rods C medulla spindles from the axis D double heads from the surface layer. Scale bar represents 0.1 mm, except for D which is 0.05 mm.
Figure 13 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 13 - A rare occurrence, Hippocampus denise on Muricella sp. 2 (RMNH Coel. 39873) at Raja Ampat (photo F.R. Stokvis).
Figure 12 from: van der Meij S, Reijnen B, van Ofwegen L (2011) Fish, fans and hydroids: host species of pygmy seahorses. ZooKeys 103: 1-26. https://doi.org/10.3897/zookeys.103.953
Figure 12 - Annella cf. mollis (RMNH Coel. 39877) A spindles from the coenenchyme B tentacle rods C medulla spindles from the axis D double heads from the surface layer. Scale bar represents 0.1 mm, except for D which is 0.05 mm.
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