Syngnathiformes

Wang, X., Zhang, Y., Zhang, H., Qin, G. and Q. Lin. 2019. Complete mitochondrial genomes of eight seahorse and pipefishes (Syngnathiformes: Syngnathidae): insight into the adaptive radiation of syngnathid fishes. BMC Evoluntionary Biology 19(119):1-11.

Longo, S.J., Faircloth, B.C., Meyer, A., Westneat, M.W., Alfaro, M.E. and P.C. Wainwright. 2017. Phylogenetic analysis of a rapid radiation of misfit fishes (Syngnathiformes) using ultraconserved elements. Molecular Phylogenetics and Evolution 111:33-48.

Vincent, A.C.J., Sadovy, Y.J., Fowler, S.L. and S. Lieberman. 2013. The role of CITES in the conservation of marine fishes subject to international trade. Fish and Fisheries 15:563–592.

**Maypa, A. P., et al. 2012. Movement patterns and life history strategies of key coral reef and coastal pelagic fisheries species for consideration in MPA network design in the Coral Triangle. Report submitted to the Coral Triangle Support Partnership:

McClenachan, L., Cooper, A.B., Carpenter, K.E. and N.K. Dulvy. 2012. Extinction risk and bottlenecks in the conservation of charismatic marine species. Conservation Letters 5:73-80.

Pais, M.P., Henriques, S., Costa, M.J. and H.N. Cabral. 2012. A critical approach to the use of published data for baseline characterisation of marine fish assemblages: An exercise on Portuguese coastal waters. Ocean & Coastal Management 69:173-184.

Rajaram, R. and S. Murugan. 2012. Ichthyofaunal Diversity in Great Nicobar Biosphere Reserve. Ecology of Faunal Communities on the Andaman and Nicobar Islands:103-116.

Leysen, H., Dumont, E.R., Brabant, L., Hoorebeke, L.V. and D. Adriaens. 2011. Modelling stress in the feeding apparatus of seahorses and pipefishes (Teleostei: Syngnathidae). Biological Journal of the Linnean Society 104:680-691.

Leysen, H., Roos, G. and D. Adriaens. 2011. Morphological variation in head shape of pipefishes and seahorses in relation to snout length and developmental growth. Journal of Morphology 272:1259-1270.

Mobley, K.B., Small, C.M. and A.G. Jones. 2011. The genetics and genomics of Syngnathidae: pipefishes, seahorses and seadragons.Journal of Fish Biology 78:1624-1646.

Lees, J., Marss, T., Wilson, M.V.H., Saat, T. and H. Spilev. 2011. The sculpture and morphology of postcranial dermal armor plates and associated bones in gasterosteiforms and syngnathiforms inhabiting Estonian coastal waters. Acta Zoologica 93(4):422-435.

Aulostomidae

Centriscidae

Longo, S.J., Goodearly, T. and P.C. Wainwright. 2018. Extremely fast feeding strikes are powered by elastic recoil in a seahorse relative, the snipefish, Macroramphosus scolopax. Proc. R. Soc. B 285:

Noguchi, T., Sakuma, K., Kitahashi, T., Itoh, H., Kano, Y., Shinohara, G., Hashimoto, J. and S. Kojima. 2014. No genetic deviation between two morphotype s of the snipefishes (Macroramphosidae: Macroramphosus) in Japanese waters. Ichthyological Research 62(3):368-373.

Alos, J., Cabanellas-Reboredo, M. and S. Lowerre-Barbieri. 2012. Diel behaviour and habitat utilisation by the pearly razorfish during the spawning season.Marine Ecology-Progress Series 460:207-220.

Bannikov, A.F. and G. Carnevale. 2012. A long-bodied centriscoid fish from the basal Eocene of Kabardino-Balkaria, northern Caucasus, Russia. Die Naturwissenschaften 99(5):379-389.

Paulus, T. 1995. Schnepfenmesserfische. Die seltene und schutzenswerte Fischfamilie Centriscidae. Das Aquarium(312):33-36.

Fistulariidae

Pinnegar, J.K., Tomczak, M.T. and J.S. Link. 2014. How to determine the likely indirect food-web consequences of a newly introduced non-native species: A worked example. Ecological Modelling 272:379-387.

Turker-Cakir, D., Çoktuğ, B. and K. Zengin. 2014. First record of the bluespotted cornetfish, Fistularia commersonii Ruppell, 1835 (Osteichthyes: Fistulariidae) in Edremit Bay (north-eastern Aegean Sea). Journal of Applied Ichthyology 30(1):164-167.

Bariche, M., Kajajian, A. and E. Azzurro. 2013. Reproduction of the invasive bluespotted cornetfish Fistularia commersonii (Teleostei, Fistulariidae) in the Mediterranean Sea. Marine Biology Research 9(2):169-180.

Bariche, M. and A. Kajajian. 2012. Population structure of the bluespotted cornetfish Fistularia commersonii (Osteichthyes: Fistulariidae) in the eastern Mediterranean Sea. Journal of Biological Research 17:74-80.

Bodilis, P., et al. 2011. Further evidence of the establishment of Fistularia commersonii (Osteichthyes: Fistulariidae) in the north-western Mediterranean Sea. Marine Biodiversity Records 4:1-4.

Deidun, A. 2011. On the increasing occurrence of the Bluespotted Cornetfish Fistularia commersonii (Rüppel, 1838) in the Central Mediterranean (Osteichthyes , Fistulariidae). Biodiversity Journal 2:19-26.

Yasemi, M. 2011. On the record of the red cornet fish Fistularia petimba (Syngnathiformes, Fistularidea) in Jask port, the Oman sea. Iranian Journal of Fisheries Sciences 11(1):226-234.

Sanna, D., Merella, P., Lai, T., Farjallah, S., Francalacci, P., Curini-Galletti, M., Pais, A. and M. Casu. 2010. Combined analysis of four mitochondrial regions allowed the detection of several matrilineal lineages of the lessepsian fish Fistularia commersonii in the Mediterranean Sea. Journal of the Marine Biological Association of the United Kingdom 91:1289-1293.

Pegasidae

Pajaro, M. G., et al. 2004. Biology, fishery and trade of sea moths (Pisces: Pegasidae) in the central Philippines. Oryx 38: 432-438.

Gosney, L. 1996. A molecular phylogeny of the Pegasidae (Sea Moths) and the implications for their conservation, Institute of Zoology.

Herold, D. and E. Clark. 1993. Monogamy, spawning and skin-shedding of the Sea Moth, Eurypegasus-draconis (Pisces, Pegasidae). Environmental Biology of Fishes 37(3):219-236.

Myers, R. F. 1991. Syngnathidae & Pegasidae. Micronesian Reef Fishes. Barrigadam, Guam, Coral Graphics:82-90.

Palsson, W. A. and T. W. Pietsch. 1989. Revision of the Acanthopterygian Fish Family Pegasidae (Order Gasterosteiformes). Indo-Pacific (18):1-38.

Li, M., Chen, M., Huang, H., Tao, W., Cui, J. and H. Xiang. 2011. Neuroprotective effects of active ingredients isolated from Pegasus laternarius on cultured cerebral neurons. Cellular and Molecular Neurobiology 31:73-82.

Solenostomidae

Orr, J.W. and R.A. Fritzsche. 1993. Revision of the Ghost Pipefishes, Family Solenostomidae (Teleostei, Syngnathoidei). Copeia 1993(1):168-182.

Fishelso L. 1966. Solenostomus cyanopterus Blecker (Teleostei Solenostomidae) in Elat (Gulf of Akaba). Israel Journal of Zoology 15(3-4):95-103.

Syngnathidae

Álvarez-Hernán, G., Andrade, J.P., Escarabajal-Blázquez, L., Blasco, M., Solana-Fajardo, J., Martín-Partido, G. and J. Francisco-Morcillo. 2019. Retinal differentiation in syngnathids: comparison in the developmental rate and acquisition of retinal structures in altricial and precocial fish species. Zoomorphology 138:371-385.

Manning, C.G., Foster, S.J. and A.C.J. Vincent. 2019. A review of the diets and feeding behaviours of a family of biologically diverse marine fishes (Family Syngnathidae). Reviews in Fish Biology and Fisheries 29(2):197-221.

Zhu, L., Chen, M., Cheng, R., Ge, W., Zhang, G. and Y. Ge. 2018. Complete mitochondrial genome characterization of the alligator pipefish Syngnathoides biaculeatus and phylogenetic analysis of the family Syngnathidae. Conservation Genetic Resources https://doi.org/10.1007/s12686-018-1032-1

Hamilton, H., Saarman, N., Short, G., Sellas, A.B., Moore, B., Hoang, T., Grace, C., Gomon, M., Crow, K. and W. Simison. 2017. Molecular phylogeny and patterns of diversification in syngnathid fishes. Molecular Phylogenetics and Evolution 107:388–403.

Scapin, L., Cavraro, F., Malavasi, S., Riccato, F., Zucchette, M. and P. Franzoi. 2017. Linking pipefishes and seahorses to seagrass meadows in the Venice lagoon: Implication for conservation. Aquatic Conservation Marine and Freshwater Ecosystems 28(2):282-295.

Neutens, C., Adriaens, D., Christiaens, J., De Kegel, B., Dierick, M., Boistel, R. and L. Van Hoorebeke. 2014. Grasping convergent evolution in syngnathids: a unique tale of tails. Journal of Anatomy 224(6):710-723.

Vieira, R.P., Monteiro, P., Ribeiro, J., Bentes, L., Oliveira, F., Erzini, K. and J. Gonçalves. 2014. Length-weight relationships of six syngnathid species from Ria Formosa, SW Iberian coast. Cahiers de Biologie Marine 55(1):9-12.

Williams, S.A., Janetski, N., Abbott, J., Blankenhorn, S., Cheng, B., Crafton, R.E., Hameed, S.O., Rapi, S. and D. Trockel. 2014. Ornamental marine species culture in the coral triangle: Seahorse demonstration project in the Spermonde Islands, Sulawesi, Indonesia. Environmental Management 54(6):1342-1355.

Adriaens, D., Neuten, C., Christiaens, J., Van Loo, D., De Kegel, B., Boistel, R. and L. Van Hoorebeke. 2012. Evolutionary morphology of the caudal musculoskeletal system in syngnathid fish: from swimming to prehension ... in different ways. Integrative and Comparative Biology 52:E2-E2.

Grandcourt, E. 2012. Reef Fish and Fisheries in the Gulf. Coral Reefs of the World 3:127-161.

Hallett, C.S. and N.G. Hall. 2012. Equivalence factors for standardizing catch data across multiple beach seine nets to account for differences in relative bias. Estuarine, Coastal and Shelf Science: 1-9.

Horinouchi, M., Tongnunui, P., Furumitsu, K., Nakamura, Y., Kanou, K., Yamaguchi, A., Okamoto, K. and M. Sano. 2012. Food habits of small fishes in seagrass habitats in Trang, southern Thailand. Fisheries Science 78(3):577-587.

LePage, V. 2012. A Study of Syngnathid Diseases and Investigation of Ulcerative Dermatitis. Master's thesis submitted to the University of Guelph: 128pp.

LePage, V., Dutton, C.J., Kummrow, M., McLelland, D.J., Young, K. and J.S. Lumsden. 2012. Neoplasia of Captive Yellow Sea Horses (Hippocampus kuda) and Weedy Sea Dragons (Phyllopteryx taeniolatus). Journal of Zoo and Wildlife Medicine 43:50-58.

Neal, J.W., Adelsberger, C.M. and S.E. Lochmann. 2012. A Comparison of Larval Fish Sampling Methods for Tropical Streams. Marine and Coastal Fisheries 4(1):23-29.

Oliveira, F., et al. 2012. Habitat preferences of the Syngnathidae in the Ria Formosa coastal lagoon (South Portugal). Poster submitted to the University of Aveiro.

Ahnesjö, I. and J. F. Craig. 2011. The biology of Syngnathidae: pipefishes, seadragons and seahorses. Journal of Fish Biology 78:1597-1602.

Avise JC and Liu JX. 2011. Multiple mating and its relationship to brood size in pregnant fishes versus pregnant mammals and other viviparous vertebrates. Proceedings of the National Academy of Sciences of the United States of America 108:7091-7095.

Azevedo I, Ramos S, Mucha AP, and Bordalo AA. 2011. Applicability of ecological assessment tools for management decision-making: A case study from the Lima estuary (NW Portugal). Ocean and Coastal Management 72:54-63.

Ben Amor MM, Salem BM, Reynaud C, and Capape C. 2011. Length–weight relationships in syngnathid species from Tunisian waters (central Mediterranean). Marine Biodiversity Records 4:1-4.

Leysen, H., et al. 2011. Modeling stress in the feeding apparatus of seahorses and pipefishes (Teleostei: Syngnathidae). Biological Journal of the Linnean Society 104:680-691.

Leysen, H., Roos, G. and D. Adriaens. 2011. Morphological variation in head shape of pipefishes and seahorses in relation to snout length and developmental growth. Journal of Morphology 272(10):1259-1270.

Mobley, K. B., et al. 2011. The genetics and genomics of Syngnathidae: pipefishes, seahorses and seadragons. Journal of Fish Biology 78:1624-1646.

Rosenqvist, G. and A. Berglund. 2011. Sexual signals and mating patterns in Syngnathidae. Journal of Fish Biology 78:1647-1661.

Přikryl, T., et al. 2011. New information about the anatomy of a peculiar fish of the genus Hipposyngnathus Daniltshenko, 1960. Comptes Rendus Palevol 10:559-566.

Scobell, S.K. and D.S. Mackenzie. 2011. Reproductive endocrinology of Syngnathidae. Journal of Fish Biology 78:1662-1680.

Smith, T.M., Hindell, J.S., Jenkins, G.P., Connolly, R.M. and M.J. Keough. 2011. Edge effects in patchy seagrass landscapes: The role of predation in determining fish distribution. Journal of Experimental Marine Biology and Ecology 399:8-16.

Vincent, A.C.J. 2011. Saving the shallows: focusing marine conservation where people might care. Aquatic Conservation: Marine and Freshwater Ecosystems 21(6):495-499.

Vincent, A.C.J., Foster, S.J. and H.J. Koldewey. 2011. Conservation and management of seahorses and other Syngnathidae. Journal of Fish Biology 78:1681-1724.

Vincent, A.C.J., Giles, B.G., Czembor, C. and S.J. Foster. 2011. Trade in seahorses and other syngnathids in countries outside Asia (1998-2001). Fisheries Centre Research Reports 19:181pp.

Wilson, a. B. and J. W. Orr. 2011. The evolutionary origins of Syngnathidae: pipefishes and seahorses. Journal of Fish Biology 78:1603-1623.

Kleiber, D., Blight, L.K., Caldwell, I.R. and A.C.J. Vincent. 2010. The importance of seahorses and pipefishes in the diet of marine animals. Reviews in Fish Biology and Fisheries 21:205-223.

Leysen, H., Jouk, P., Brunain, M., Christiaens, J. and D. Adriaens. 2010. Cranial architecture of tube-snouted Gasterosteiformes (Syngnathus rostellatus and Hippocampus capensis). Journal of Morphology 271(3):255-270.

Leysen, H., Roos, G., Van Wassenbergh, S. and D. Adriaens. 2010. Syngnathid feeding apparatus morphology : long vs short snouts. Integrative and Comparative Biology 50(Suppl 1):E101-E101

Masonjones, H.D., Rose, E., McRae, L.B. and D.L. Dixson. 2010. An examination of the population dynamics of syngnathid fishes within Tampa Bay, Florida, USA. Current Zoology 56(1):118-133.

Paczolt, K.A. and A.G. Jones. 2010. Post-copulatory sexual selection and sexual conflict in the evolution of male pregnancy. Nature 464:401-404.

Paladini, G., et al. 2010. The description of Gyrodactylus corleonis sp n. and G. neretum sp n. (Platyhelminthes: Monogenea) with comments on other gyrodactylids parasitising pipefish (Pisces: Syngnathidae). Folia Parasitologica 57(1):17-30.

Wilson, N. G. and G. W. Rouse. 2010. Convergent camouflage and the non-monophyly of 'seadragons' (Syngnathidae: Teleostei): suggestions for a revised taxonomy of syngnathids. Zoologica Scripta 39(6):551-558.

Shokri, M. R., et al. 2009. The effectiveness of seahorses and pipefish (Pisces: Syngnathidae) as a flagship group to evaluate the conservation value of estuarine seagrass beds. Aquatic Conservation-Marine and Freshwater Ecosystems 19(5):588-595.

Sanna, D., et al. 2008. mtDNA control region and D-HPLC analysis: a method to evaluate the mating system in Syngnathidae (Teleostei). Marine Biology 153(3):269-275.

Martin-Smith, K. and A. C. J. Vincent. 2006. Exploitation and trade of Australian seahorses, pipehorses, sea dragons and pipefishes (Family Syngnathidae). Oryx 40:141-151.

Rosa, I. L., et al. 2006. Collaborative monitoring of the ornamental trade of seahorses and pipefishes (Teleostei: Syngnathidae) in Brazil: Bahia State as a case study. Neotropical Icthyology 4(2):247-252.

Xu, D., et al. 2005. Advance in the research of Syngnathidae in China. Chinese Journal of Marine drugs/Zhongguo Haiyang Yaowu 24(2):51-56.

Choo C. K. and C. Liew Hock 2004. A record of seahorse species (family Syngnathidae) in East Malaysia, with notes on their conservation. Malayan Nature Journal 56(4):409-420.

Fricke, R. 2004. Review of the pipefishes and seahorses (Teleostei: Syngnathidae) of New Calendonia, with descriptions of five new species. Stuttgarter Beiträge zur Naturkunde Serie A (Biologie) 668:1-61.

Vizzini, S. and A. Mazzola. 2004. The trophic structure of the pipefish community (Pisces: Syngnathidae) from a Western Mediterranean seagrass meadow based on stable isotope analysis. Estuaries 27(2):325-333.

Choo, C. K. and H. C. Liew. 2003. Spatial distribution, substrate assemblages and size composition of sea horses (Family Syngnathidae) in the coastal waters of Penninsular Malaysia. Journal of Marine Biology Association U.K. 83:271-276.

CITES. 2003. Seahorses and other members of the family Syngnathidae (Decision 12.54). Universal minimum size limit for seahorses. Nineteenth Meeting of the Animals Committee:7pp.

Riccato, F., et al. 2003. Population structure and reproduction of three pipefish species (Pisces, Syngnathidae) in a sea grass meadow of the Venice Lagoon. Biologia Marina Mediterranea 10(2, pt. 1):138-145.

Wilson, A. B., et al. 2003. The dynamics of male brooding, mating patterns, and sex roles in pipefishes and seahorses (family Syngnathidae). Evolution 57:1374-1386.

Acentronura

Žalohar, J. and T. Hitij. 2012. The first known fossil record of pygmy pipehorses (Teleostei: Syngnathidae: Hippocampinae) from the Coprolitic Horizon; Tunjice Hills, Slovenia. Annales de Paléontologie 98(2):131-151.

Vasquez-Yeomans, L., Quintal-Lizama, C. and M. Pereira-Flota. 2004. First record of Acentronura dendritica (Barbour, 1905) (Gasterosteiformes: Syngnathidae) from Mexico. Bulletin of Marine Science 75(1):127-129.

Acero P., A. 1988. First record of the pipefish Acentronura (Amphelikturus) dendritica (Synganthidae) from the Caribbean. Northest Gulf Science 10(1):61-62.

Anarchopterus

Sazima, C., Carvalho-Filho, A. and I. Sazima. 2009. The pipefish Anarchopterus tectus in western South Atlantic: clarification of its southernmost distribution. Marine Biodiversity Records 2:1-2.

Apterygocampus

Bhanotia

Bryx

Bulbonaricus

Campichthys

Choeroichthys

Corythoichthys

Cosmocampus

Doryichthys

Doryrhamphus

Van Wassenbergh, S., Roos, G., Aerts, P., Herrel, A. and D. Adriaens. 2011. Why the long face? A comparative study of feeding kinematics of two pipefishes with different snout lengths. Journal of Fish Biology 78:1786-1798.

Dunckerocampus

Enneacampus

Entelurus

Festucalex

Filicampus

Halicampus

Ziyadi, M.S.F., Jawad, L.A., and M.A. Al-Mukhtar. 2018. Halicampus zavorensis Dawson, 1984 (Syngnathidae): new record for Iraqi marine waters and for the Arabian Gulf area. Cah. Biol. Mar 59:121-126.

Haliichthys

Heraldia

Hippichthys

Hippocampus

DeBrauwer, M., Gordon, L.M., Shalders, T.C., Saunders, B.J., Archer, M., Harvey, E.S., Collin, S.P., Partridge, J.C. and J.L. McIlwain. 2019. Behavioural and pathomorphological impacts of flash photography on benthic fishes. Scientific Reports 9(748)1-14.

Foster, S.J., Kuo, T.C., Wan, A.K.Y. and A.C.J. Vincent. 2019. Global seahorse trade defies export bans under CITES action and national legislation. Marine Policy 103:33-41.

Francesca, A., Corriero, G., Mirto, S., Oierri, C. Lazic, T. and M. Gristina. 2019. Trophic flexibility and prey selection of the wild long-snouted seahorse Hippocampus guttulatus Cuvier, 1829 in three coastal habitats. Estuarine Coastal and Shelf Science 224:1-10.

Masonjones, H.D. and E. Rose. 2019. When more is not merrier: Using wild population dynamics to understand the effect of density on ex situ seahorse mating behaviours. PLoS ONE 14(7): e0218069.

Masonjones, H., Rose, E., Elson, J., Roberts, B. and J. Curtis-Quick. 2019. High density, early maturing, and morphometrically unique Hippocampus erectus population makes a Bahamian pond a priority site for conservation. Endangered Species Research 39:35-49.

Short, G., Harasti, D. and H. Hamilton. 2019. Hippocampus whitei Bleeker, 1855, a senior synonym of the southern Queensland seahorse H. procerus Kuiter, 2001: molecular and morphological evidecne (Teleostei, Syngnathidae). Zookeys 824:109-133.

Simpson, M., Morris, R.L. Harasti, D. and R.A. Coleman. 2019. The endangered White’s seahorse Hippocampus whitei chooses artificial over natural habitats. Journal of Fish Biology 95:551-561.

Stocks, A.P., Foster, S.J., Bat, N.K., Ha, N.M. and A.C.J. Vincent. 2019. Local fishers’ knowledge of target and incidental seahorse catch in southern Vietnam. Human Ecology 47(3):397-408.

Vaccani, A.C., Freret-Meurer, N.V., Bertoncini, A.A. and L.N. Santos. 2019. Shining in the dark: first record of bioflurescence in the seahorse Hippocampus reidi. PLoS ONE 14(8):e022056.

Zhang, X. and A.C.J. Vincent. 2019. Conservation prioritization for seahorse (Hippocampus spp.) at braod spatial scales considering socioeconomic costs. Biological Conservation 235:79-88.

Zhang, X. and A.C.J. Vincent. 2019. Using cumulative-human-impact models to reveal global threat patterns for seahorses. Conservation Biology doi:10.1111/cobi.1332

Becerril‐Garcia, E. E., Petatan‐Ramirez, D., Ortiz‐Aguirre, I. and A. Ayala‐Bocos. 2018. First record of the Pacific seahorse Hippocampus ingens in Guadalupe Island, Mexico. Journal of Fish Biology 92(4):1207-1210.

Claassens, L. 2018. Aspects of the population ecology, habitat use and behavior of the endangered Knysna Seahorse (Hippocampus capensis Boulenger, 1900) in a residential marina estate, Knysna, South Africa: implications for conservation. PhD thesis, Rhodes University.

Claassens, L. Booth, A.J. and A.N. Hodgson. 2018. An endangered seahorse selectively chooses an artificial structure. Environmental Biology of Fishes 101(8):723-733.

Claassens, L. and A.N. Hodgson. 2018. Monthly population density and structure patterns of an endangered seahorse Hippocampus capensis: a comparison between natural and artificial habitats. Journal of Fish Biology 92:2000-2015.

Correia, M., Campoy, A., Madeira, C. and J.P. Andrade. 2018. Is filament clipping an effective tool for tissue sampling in Hippocampus guttulatus? Environmental Biology of Fishes 101(10):1517-1523.

Correia, M., Koldewey, H.J., Andrade, J.P., Esteves, E., and J. Palma. 2018. Identifying key environmental variables of two seahorse species (H. guttulatus and H. hippocampus) in the Ria Formosa Lagoon, South Portugal. Environmental Biology of Fishes 101(9): 1357-1367.

DeBrauwer, M., Saunders, B.J., Ambo-Rappe, R., Jompa, Jamaluddin, McIlwain, J.L. and E. S. Harvey. 2018. Time to stop mucking around? Impacts of underwater photography on cryptobenthic fauna found in soft sediment habitats. Journal of Environmental Management 218:14-22.

Endo, T., Sekino, M., Fujiwara and A. Sogabe. 2018. Development and characterization of 19 novel microsatellite markers in the Pacific seaweed pipefish Syngnathus schlegali using next-generation sequencing. Molecular Biology Reports 45(6):2831-2834.

Freret-Meurer, N.V. and M.A.S. Alves. 2018. Personality in the longsnout seahorse, Hippocampus reidi Ginsburg, 1993: Are males shyer than females? Behavioural Process 157:106-110.

Giglio, V.J., Ternes, M.L.F, Kassuga, A.D. and C.E.L. Ferreira. 2018. Scuba diving and sedentary fish watching: effects of photographer approach on seahorse behaviour. Journal of Ecotourism 18(2): 142-151.

Han, S., Rho, S., Noh, G.E. and J. Kim. 2018. Interspecific hybridization in seahorses: artificially produced hybrid offspring of Hippocampus kuda and Hippocampus reidi. Fisheries and Aquatic Sciences 21:11.

Kim, M.J. Kim, H.C., Lee, W.C., Park, J.M., Kwak, S.N., Oh. Y., Kang, M.G. and S.H. Lee. 2018. Ecological Characteristics of the new recorded seahorse (Hippocampus haema) in Geoje-Hansan Bay, Korea. Journal of Coastal Research 85:351-355.

Kuo, T-C., Laksanawimol, P., Aylesworth, L., Foster, S.J. and A.C.J. Vincent. 2018. Changes in the trade of bycatch species corresponding to CITES regulations: the case of dried seahorse trade in Thailand. Biodiversity and Conservation 27(13):3447-3468.

Kuo, T-C. and A.C.J. Vincent. 2018. Assessing the changes in international trade of marine fishes under CITES regulations – A case study of seahorses. Marine Policy 88:48–57.

Manning, C.G. Foster, S.J., Harasti, D. and A.C.J. Vincent. 2018. A holistic investigation of the ecological correlates of abundance and body size for the endangered White's seahorse Hippocampus whitei. Journal of Fish Biology 93(4):649-663.

Montes, M.A., Cardoso, M.L.V., Neves, C.H.C.B., Garcia, A.C.L., Da Silva, J.C. and R.B. Silveira. 2018. Genetic diversity and population structure of the seahorse Hippocampus reidi (Syngnathidae) in north-eastern Brazil: A conservation approach. Aquatic Conservation Marine and Freshwater Ecosystems 28(5):1114-1122.

Novelli, B., Otero Ferrer, F., Socorro, J.A. and L. Molina Dominguez. 2018. Early development of the longsnout seahorse Hippocampus reidi (Syngnathidae) within the male brood pouch. Journal of Fish Biology 92(6):1975-1984.

Palma, J., Magalhães, M., Correia, M. and J.P. Andrade. 2018. Effects of anthropogenic noise as a source of acoustic stress in wild populations of Hippocampus guttulatus in the Ria Formosa, south Portugal. Marine and Freshawater Ecosystems 29:751-759.

Pereira, L.C., Silveira, R.B. and V. Abilhoa. 2018. Feeding habits of the seahorse Hippocampus patagonicus (Actinopterygii: Syngnthiformes: Syngnathidae) on the southern coast of Brazil. Acta Ichthyologica et Piscatoria 48(3):267-271.

Qin, G., Johnson, C., Zhang, Y., Zhang, H., Yin, J., Miller, G.., Turingan, R. G., Guisbert, E. and Q. Lin. 2018. Temperature-induced physiological stress and reproductive characteristics of the migratory seahorse Hippocampus erectus during a thermal stress simulation. Biology Open doi: 10.1242/bio.032888

Short, G., Smith, R. Motomura, H., Harasti and H. Hamilton. 2018. Hippocampus japapigu, a new species of pygmy seahorse from Japan, with a redescription of H. pontohi (Teleostei, Syngnathidae). ZooKeys 779:27-49.

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Tanu, Deobagkar, D.D., Khandeparker, R., Sreepada, R.A., Sanaye, S.V. and H.B. Pawar. 2012. A study on bacteria associated with the intestinal tract of farmed yellow seahorse, Hippocampus kuda (Bleeker, 1852): characterization and extracellular enzymes. Aquaculture Research 43:386-394.

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Yasué, M., Nellas, A. and A.C.J. Vincent. 2012. Seahorses helped drive creation of marine protected areas, so what did these protected areas do for the seahorses? Environmental Conservation 39:183-193.

Yin, F., Tang, B., Zhang, D. and X. Zou. 2012. Lipid metabolic response, peroxidation, and antioxidant defence status of juvenile Lined Seahorse, Hippocampus erectus, fed with highly unsaturated fatty acids enriched Artemia nauplii. Journal of the World Aquaculture Society 43(5):716-726.

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Anderson P and Mann D. 2011. Evoked potential audiogram of the lined seahorse, Hippocampus erectus (Perry), in terms of sound pressure and particle acceleration. Environmental Biology of Fishes 91:251-259.

Bahr A and Wilson AB. 2011. The impact of sex-role reversal on the diversity of the major histocompatibility complex: insights from the seahorse (Hippocampus abdominalis). BMC Evolutionary Biology 11:121.

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Faleiro, F. and L. Narciso. 2011. Prey-predator dynamics in seahorses (Hippocampus guttulatus): deciphering fatty acid clues. Aquaculture Research 44(4):618-633.

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Grech, A. and R. Coles. 2011. Interactions between a trawl fishery and spatial closures for biodiversity conservation in the Great Barrier Reef World Heritage Area, Australia. PLoS ONE 6(6):e21094.

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Hellyer, C.B., Harasti, D. and A.G.B. Poore. 2011. Manipulating artificial habitats to benefit seahorses in Sydney Harbour, Australia. Aquatic Conservation:Marine and Freshwater Ecosystems 21:582-589.

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Shin, S. and J. Han. 2011. Identification of scuticociliate Philasterides dicentrarchi from indo-pacific seahorses Hippocampus kuda. African Journal of Microbiology Research 5(7):738-741.

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Szabó, Z., Kimokeo, B.K., Toonen, R.J. and J.E. Randall. 2011. On the status of the Hawaiian seahorses Hippocampus hilonis , H. histrix and H. fisheri (Syngnathidae).Marine Biology Research 7:701-709.

Thangaraj, M. and A. Lipton. 2011. Assessment of genetic variation in closely related seahorse species(Genus: Hippocampus) using mtDNA marker. Indian Journal of Biotechnology 10:140-142.

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Vincent, A.C.J. 2011. Saving the shallows: focusing marine conservation where people might care. Aquatic Conservation: Marine and Freshwater Ecosystems 21(6):495-499.

Vincent, A.C.J., Foster, S.J. and H.J. Koldewey. 2011. Conservation and management of seahorses and other Syngnathidae. Journal of Fish Biology 78:1681-1724.

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Woodall, L.C., Koldewey, H.J. and P.W. Shaw. 2011. Historical and contemporary population genetic connectivity of the European short-snouted seahorse Hippocampus hippocampus and implications for management. Journal of Fish Biology 78:1738-1756.

Zhang, D., Yin, F. and J. Lin. 2011. Criteria for assessing juvenile quality of the lined seahorse, Hippocampus erectus. Aquaculture 322-323:255-258.

Anticamara, J.A., Zeller, D. and A.C.J. Vincent. 2010. Spatial and temporal variation of abundance, biomass and diversity within marine reserves in the Philippines. Diversity and Distributions 16(4):529-536.

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Faleiro, F. and L. Narciso. 2010. Lipid dynamics during early development of Hippocampus guttulatus seahorses: Searching for clues on fatty acid requirements. Aquaculture 307(1-2):56-64.

Foster, R. and M.F. Gomon. 2010. A new seahorse (Teleostei: Syngnathidae: Hippocampus) from south-western Australia. Zootaxa(2613):61-68.

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Foster, S.J. and A.C.J. Vincent. 2010. Using life-history information to assess potential effects of shrimp trawling on small fishes. Journal of Fish Biology 76:2434-2454.

Garcia, L.M.B., Hilomen-Garcia, G.V. and R.L.M. Calibara. 2010. Culturing seahorse (Hippocampus barbouri) in illuminated cages with supplementary acetes feeding. Israeli Journal of Aquaculture-Bamidgeh 62(2):122-129.

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Harasti, D. and T. Glasby. 2010. Striking a balance between retaining populations of protected seahorses and maintaining swimming nets. Marine and Freshwater 166:159-166.

Harasti, D., Glasby, T. and K.M. Martin-Smith. 2010. Striking a balance between retaining populations of protected seahorses and maintaining swimming nets. Aquatic Conservation-Marine and Freshwater Ecosystems 20(2):159-166.

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Koldewey, H.J. and K.M. Martin-Smith. 2010. A global review of seahorse aquaculture.Aquaculture 302(3-4):131-152.

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Kumaravel, K., Ravichandran, S., Balasubramanian, T., Subramanian, K.S. and B.A. Bhat. 2010. Antimicrobial effect of five seahorse species from Indian Coast. British Journal of Pharmacology and Toxicology 1(2):62-66.

Lin, Q., Lin, J. and H. Liangmin. 2010. Effects of light intensity, stocking density and temperature on the air-bubble disease, survivorship and growth of early juvenile seahorse. Hippocampus erectus Perry, 1810. Aquaculture Research 42:91-98.

Lopez, A., Vera, M., Otero-Ferrer, F., Pardo, B.G., Martinez, P., Molina, L. and C. Bouza. 2010. Species identification and genetic structure of threatened seahorses in Gran Canaria Island (Spain) using mitochondrial and microsatellite markers. Conservation Genetics 11(6):2431-2436.

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Martins, M.L., Mouriño, J.L., Fezer, G.F., Buglione Neto, C.C., Garcia, P., Silva, B.C., Jatobá, A. and F. Vieira. 2010. Isolation and experimental infection with Vibrio alginolyticus in the sea horse, Hippocampus reidi Ginsburg, 1933 (Osteichthyes: Syngnathidae) in Brazil. Brazilian Journal of Biology 70(1):205-209.

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Nijman, V. 2010. An overview of international wildlife trade from Southeast Asia. Biodiversity and Conservation 19(4):1101-1114.

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Otero-Ferrer, F., Molina, L., Socorro, J., Herrera, R., Fernández-Palacios, H. and M.S. Izquierdo. 2010. Live prey first feeding regimes for short-snouted seahorse Hippocampus hippocampus (Linnaeus, 1758) juveniles.Aquaculture Research 41(9):e8-e19.

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Planas, M., Quintas, P., Chamorro, A. and C. Silva. 2010. Female maturation, egg characteristics and fatty acids profile in the seahorse Hippocampus guttulatus. Animal Reproduction Science 122:66-73.

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Quintas, P., Planas, M. and G.J. Purser. 2010. Biochemical composition and enzymatic activities in juveniles of the seahorse Hippocampus abdominalis and the effect of Artemia enrichment. Aquaculture Europe 2010 Seafarming 3050:1053-1054.

Raj, S.T., Lipton, A.P. and G.S. Chauhan. 2010. Characterization and infectivity evaluation of Vibrio harveyi causing white patch disease among captive reared seahorses, Hippocampus kuda. Indian Journal of Marine Sciences 39:151-156.

Ranasinghe, R. and E.P.K. Epa. 2010. Breeding of the endangered seahorse, Hippocampus kuda and contraints for larval development under captivity. Proceedings of the 30th Annual Sessions of the Institute of Biology, Sri Lanka, Columbo, 24pp.

Roos, G., Wassenbergh, S.V., Herrel, A., Adriaens, D. and P. Aerts. 2010. Snout allometry in seahorses: insights on optimisation of pivot feeding performance during ontogeny. Journal of Experimental Biology 213(13):2184-2193.

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Ryu, B., Qian, Z.J. and S.K. Kim. 2010. SHP-1, a novel peptide isolated from seahorse inhibits collagen release through the suppression of collagenases 1 and 3, nitric oxide products regulated by NF-kappaB/p38 kinase. Peptides 31(1):79-87.

Saarman, N.P., Louie, K.D. and H. Hamilton. 2010. Genetic differentiation across eastern Pacific oceanographic barriers in the threatened seahorse Hippocampus ingens. Conservation Genetics 11(5):1989-2000.

Santos, C.A., Novaes, L.S. and L.C. Gomes. 2010. Genotoxic effects of the diesel water-soluble fraction on the seahorse Hippocampus reidi (Teleostei: Syngnathidae) during acute exposure. Zoologia (Curitiba, Impresso) 27:956-960.

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Sheppard, J.N. 2010. Structure and functioning of fish assemblages in two South African estuaries, with emphasis on the presence and absence of aquatic macrophyte beds. Master Thesis submitted to Rhodes Universty:310pp.

Silveira, R.B. and N.F. Fontoura. 2010. Fecundity and fertility of the longsnout seahorse, Hippocampus reidi ( Teleostei : Syngnathidae ), in tropical Brazil. Brazilian Journal of Biosciences 8:362-367.

Smith, T.M., Hindell, J.S., Jenkins, G.P. and R.M. Connolly. 2010. Seagrass patch size affects fish responses to edges. Journal of Animal Ecology 79(1):275-281.

Thangaraj, M. 2010. Genetic Identity of Three Indian Populations of Three Spotted Seahorse, Hippocampus trimaculatus. Advances in Biological Research 4:37-41.

Tindemans, D., Rekecki, A. and W. Van Den Broeck. 2010. Development of the digestive tract in the seahorse (Hippocampus erectus P.). Vlaams Diergeneeskundig Tijdschrift 79(3):207-212.

Van Cauter, S., Adriaens, D., Kannan, S., Srigiriraju, S., Praet, T., Masschaele, B., De Beule, M. and B. Verhegghe. 2010. Virtual design from nature : kinematic modeling of the seahorse tail. 2010 SIMULIA Customer Conference Proceedings, SIMULIA:770-783.

Whitfield, A.K. 2010. A century of fish research in South African estuaries. African Journal of Aquatic Science 35:211-225.

Whitfield, A.K. and P.D. Cowley. 2010. The status of fish conservation in South African estuaries. Journal of Fish Biology 76:2067-2089.

Wilson, N.G. and G.W. Rouse. 2010. Convergent camouflage and the non-monophyly of 'seadragons' (Syngnathidae: Teleostei): suggestions for a revised taxonomy of syngnathids. Zoologica Scripta 39(6):551-558.

Xu, Y.J., Lin, J. and S. Chen. 2010. Polyculture of the lined seahorse, Hippocampus erectus Perry, 1810 with two species of macroalgae in aquaria. Acta Oceanologica Sinica 29(1):26-32.

Yasué, M., Kaufman, L. and A.C.J. Vincent. 2010. Assessing ecological changes in and around marine reserves using community perceptions and biological surveys. Aquatic Conservation: Marine and Freshwater Ecosystems 20:407-418.

Zhang, D., Zhang, Y., Lin, J. and Q. Lin. 2010. Growth and survival of juvenile lined seahorse, Hippocampus erectus (Perry), at different stocking densities. Aquaculture Research 42:9-13.

Ban, N.C., Hansen, G.J.A., Jones, M. and A.C.J. Vincent. 2009. Systematic marine conservation planning in data-poor regions: Socioeconomic data is essential. Marine Policy 33:794-800.

Barrows, A.P., Martin-Smith, K.M. and M.S. Baine. 2009. Population variables and life-history characteristics of the alligator pipefish Syngnathoides biaculeatus, in Papua New Guinea. Journal of Fish Biology 74(4):806-819.

Berglund, A. and G. Rosenqvist. 2009. An intimidating ornament in a female pipefish. Behavioral Ecology 20(1):54-59.

Blake, R.W. 2009. On seahorse locomotion. Journal of the Marine Biological Association of the United Kingdom 56(04):939.

Burfeind, D.D., Tibbetts, I.R. and J.W. Udy. 2009. Habitat preference of three common fishes for seagrass, Caulerpa taxifolia, and unvegetated substrate in Moreton Bay, Australia. Environmental Biology of Fishes 84(3):317-322.

da Hora, M.D.C. and J.C. Joyeux. 2009. Closing the reproductive cycle: Growth of the seahorse Hippocampus reidi (Teleostei, Syngnathidae) from birth to adulthood under experimental conditions. Aquaculture 292(1-2):37-41.

Flammang, B.E., Ferry-Graham, L.A., Rinewalt, C., Ardizzone, D., Davis, C. and T. Trejo. 2009. Prey capture kinematics and four-bar linkages in the bay pipefish, Syngnathus leptorhynchus. Zoology 112(2):86-96.

Garcia, L.M.B. and G.B. Hilomen-Garcia. 2009. Grow-out of juvenile seahorse Hippocampus kuda (Bleeker; Teleostei: Syngnathidae) in illuminated sea cages. Aquaculture Research 40(2):211-217.

Gomon, M.F. and R.H. Kuiter. 2009. Two new pygmy seahorses (Teleostei: Syngnathidae: Hippocampus) from the Indo-West Pacific. Aqua: International Journal of Ichthyology 15:37-44.

Goswami, M., Thangaraj, K., Chaudhary, B.K., Bhaskar, L.V.S.K., Gopalakrishnan, A., Joshi, M.B., Singh, L. and W.S. Lakra. 2009. Genetic heterogeneity in the Indian stocks of seahorse (Hippocampus kuda and Hippocampus trimaculatus) inferred from mtDNA cytochrome b gene.Hydrobiologia 621:213-221.

Grémillet, D. and T. Boulinier. 2009. Spatial ecology and conservation of seabirds facing global climate change: a review. Marine Ecology-Progress Series 391:121-137.

Gurkan, S., Taskavak, E. and B. Hossucu. 2009. The reproductive biology of the Great Pipefish Syngnathus acus (Family: Syngnathidae) in the Aegean Sea. North-Western Journal of Zoology 5(1):179-190.

Ishihara, T. and K. Tachihara. 2009. The maturity and breeding season of the bellybarred pipefish, Hippichthys spicifer, in Okinawa-jima Island rivers. Ichthyological Research 56(4):388-393.

Johnson, S.W., Thedinga, J.F. and A.D. Neff. 2009. Invasion by saffron cod Eleginus gracilis into nearshore habitats of Prince William Sound, Alaska, USA. Marine Ecology-Progress Series 389:203-212.

Khan, S.B., Qian, Z., Ryu, B. and S. Kim. 2009. Isolation and biochemical characterization of collagens from seaweed pipefish, Syngnathus Schlegeli. Biotechnology and Bioprocess Engineering 14(4):436-442.

Køie, M. and E. Karlsbakk. 2009. Ellipsomyxa syngnathi sp n. (Myxozoa, Myxosporea) in the pipefish Syngnathus typhle and S. rostellatus (Teleostei, Syngnathidae) from Denmark. Parasitology Research 105(6):1611-1616.

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Lin, Q., Lin, J. and L. Huang. 2009. Effects of substrate color, light intensity and temperature on survival and skin color change of juvenile seahorses, Hippocampus erectus Perry, 1810. Aquaculture 298(1-2):157-161.

Lin, Q., Lin, J. and C. Wang. 2009. Biochemical composition of the wild and cultured seahorses, Hippocampus kuda Bleeker and Hippocampus trimaculatus Leach. Aquaculture Research 40(6):710-719.

Lin, Q., Lin, J., Zhang, D. and Y. Wang. 2009. Weaning of juvenile seahorses Hippocampus erectus Perry, 1810 from live to frozen food. Aquaculture 291(3-4):224-229.

Lin, Q., Zhang, D. and D. Lin. 2009. Effects of light intensity, stocking density, feeding frequency and salinity on the growth of sub-adult seahorses Hippocampus erectus Perry, 1810. Aquaculture 292(1-2):111-116.

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Mai, A.C.G. and I.L. Rosa. 2009. Ecological aspects of the seahorse Hippocampus reidi in the Camurupim/Cardoso estuary, Piauí State, Brazil, as subsidies for the implementation of an Environmental Protection Area. Biota Neotropica 9:85-91.

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Masonjones, H.D. and E. Rose. 2009. Reproductive demographics of syngnathid fishes inhabiting a human-altered landscape. Integrative and Comparative Biology 49:E267-E267.

Mattle, B. and A.B. Wilson. 2009. Body size preferences in the pot-bellied seahorse Hippocampus abdominalis: choosy males and indiscriminate females. Behavioral Ecology and Sociobiology 63(10):1403-1410.

Mobley, K.B. and A.G. Jones. 2009. Environmental, demographic, and genetic mating system variation among five geographically distinct dusky pipefish (Syngnathus floridae) populations. Molecular Ecology 18(7):1476-1490.

Murugan, A., Dhanya, S., Sreepada, R.A., Rajagopal, S. and T. Balasubramanian. 2009. Breeding and mass-scale rearing of three spotted seahorse, Hippocampus trimaculatus Leach under captive conditions. Aquaculture 290(1-2):87-96.

Naud, M.J., Curtis, J.M.R., Woodall, L.C. and M.B. Gaspar. 2009. Mate choice, operational sex ratio, and social promiscuity in a wild population of the long-snouted seahorse Hippocampus guttulatus. Behavioral Ecology 20(1):160-164.

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Otsuka, Y., Suzuki, H. and I. Akagawa. 2009. Occurrence, gonad morphology and maturity of Japanese seahorse Hippocampus mohnikei in Matsushima Bay, Japan. Journal of the School of Marine Science and Technology Tokai University 7(1):11-22.

Ozaka, C., Yamamoto, N. and H. Somiya. 2009. The aglomerular kidney of the deep-sea fish, Ateleopus japonicus (Ateleopodiformes: Ateleopodidae): Evidence of wider occurrence of the aglomerular condition in teleostei. Copeia(3):609-617.

Partridge, C. 2009. The effect of environmental contaminants on mating dynamics and population viability in a sex-role reversed pipefish. Doctoral dissertation submitted to Texas A&M University:179pp.

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Qian, Z., Ryu, B., Kim, M. and S. Kim. 2009. Free radical and reactive oxygen species scavenging activities of the extracts from seahorse, Hippocampus kuda Bleeler. Biotechnology and Bioprocess Engineering 13(6):705-715.

Quintas, P., Planas, M. and G.J. Purser. 2009. The effect of artemia enrichment on the early rearing of the pot-bellied seahorse Hippocampus abdominalis. Journal Of The World Aquaculture Society 3:1055-1056.

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Ripley, J.L. and C.M. Foran. 2009. Elevated whole brain arginine vasotocin with Aroclor 1254 exposure in two Syngnathus pipefishes. Fish Physiology Biochemistry 36(4):917-921.

Roos, G., Leysen, H., Van Wassenbergh, S., Herrel, A., Jacobs, P., Dierick, M., Aerts, P. and D. Adriaens. 2009. Linking morphology and motion: a test of a four-bar mechanism in seahorses.Physiological Biochemical Zoology 82(1):7-19.

Roos, G., Van Wassenbergh, S., Herrel, A. and P. Aerts. 2009. Kinematics of suction feeding in the seahorse Hippocampus reidi. Journal of Experimental Biology 212(21):3490.

Scobell, S.K., Fudicker, A.M. and R. Knapp. 2009. Potential reproductive rate of a sex-role reversed pipefish over several bouts of mating. Animal Behaviour 78(3):747-753.

Shine, R., Greenlees, M., Crossland, M. and D. Nelson. 2009. The myth of the toad-eating frog. Frontiers in Ecology and the Environment 7:359-361.

Shokri, M.R., Gladstone, W. and J. Jelbart. 2009. The effectiveness of seahorses and pipefish (Pisces: Syngnathidae) as a flagship group to evaluate the conservation value of estuarine seagrass beds. Aquatic Conservation-Marine and Freshwater Ecosystems 19(5):588-595.

Silva, K., Almada, V.C., Vieira, M.N. and N.M. Monteiro. 2009. Female reproductive tactics in a sex-role reversed pipefish: scanning for male quality and number. Behavioral Ecology 20(4):768-772.

Smith, T., Gibbs, M. and D. Smith. 2009. Fishing for more effective incentives. Science 323:337-337.

Storero, L.P. and R.A. Gonzalez. 2009. Prey selectivity and trophic behavior of the Patagonian Seahorse, Hippocampus patagonicus, in captivity. Journal of the World Aquaculture Society 40(3):394-401.

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Thomas, G.H. 2009. Bergmann's idiosyncratic rule: a role for fecundity selection? Molecular Ecology 18(6):1027-1029.

Turpie, J., Joubert, A., Babiker, H., Chaudhry, J., Child, M., Hempson, T., Humphrey, G., Joseph, G., La Grange, R., Lipsey, M., Mann, G., Okes, N., Puttick, J. and T. Wistebaar. 2009. Integrated Ecological-Economic Modelling as an Estuarine Management Tool: A Case Study of the East Kleinemonde Estuary. Report submitted to the Water Research Commission:65pp.

Van Wassenbergh, S., Roos, G. and P. Aerts. 2009. Pivot feeding performance in pipefish and seahorses analysed by forward dynamic modelling. Comparative Biochemistry and Physiology - Part A: Molecular & Integrative Physiology 153A(2):S125-S126.

Van Wassenbergh, S., Roos, G., Genbrugge, A., Leysen, H., Aerts, P., Adriaens, D. and A. Herrel. 2009. Suction is kid's play: extremely fast suction in newborn seahorses. Biology Letters 5(2): 200-203.

Weis, J.S., Weis, P., MacDonald, J. and L. Pearson. 2009. Rapid changes in fish utilization of mangrove habitat in Western Madagascar. Wetlands Ecology and Management 17(4):345-354.

Wilson, A.B. 2009. Fecundity selection predicts Bergmann's rule in syngnathid fishes. Molecular Ecology 18(6):1263-1272.

Wilson, A.B. 2009. Opening Pandora's box: comparative studies of genetic mating systems reveal reproductive complexity. Molecular Ecology 18(7):1307-1309.

Woodall, L.C., Koldewey, H.J., Santos, S.V. and P.W. Shaw. 2009. First occurrence of the lined seahorse Hippocampus erectus in the eastern Atlantic Ocean. Journal of Fish Biology 75:1505-1512.

Yasué, M. and P. Dearden. 2009. The importance of supratidal habitats for wintering shorebirds and the potential impacts of shrimp aquaculture. Environmental Management 43(6):1108-1121.

Zalohar, J., Hitij, T. and M. Kriznar. 2009. Two new species of seahorses (Syngnathidae, Hippocampus) from the Middle Miocene (Sarmatian) Coprolitic Horizon in Tunjice Hills, Slovenia: The oldest fossil record of seahorses. Annales De Paleontologie 95(2):71-96.

Ahnesjo, I. 2008. Behavioural temperature preference in a brooding male pipefish Syngnathus typhle. Journal of Fish Biology 73(4):1039-1045.

Anonymous. 2008. Pipefish - No substitute for sandeels if you are a hungry seabird. British Birds 101(7):376-377.

Astporsson, O.S. and J. Palsson. 2008. Recent increase in snake pipefish (Entelurus aequoreus) in Icelandic waters. Natturufraedingurinn 77(1-2):59-62.

Baine, M.S.P., Barrow, A.P.W., Ganiga, G. and K.M. Martin-Smith. 2008. Residence and movement of pygmy seahorses, Hippocampus bargibanti, on sea fans (Muricella spp.).Coral Reefs 27(2):421-421.

Ban, N.C. and J. Alder. 2008. How wild is the ocean? Assessing the intensity of anthropogenic marine activities in British Columbia , Canada. Main 85:55-85.

Ban, N.C., Picard, C. and A.C.J. Vincent. 2008. Moving Toward Spatial Solutions in Marine Conservation with Indigenous Communities. Ecology And Society 13:32pp.

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Bijukumar, A., Abraham, K.M. and D. Soumya. 2008. Morphometry and Meristics of Longnose Seahorse, Hippocampus Trimaculatus (Actinopterygii: Syngnathidae), from Kerala, South-West Coast of India. Acta Ichthyologica Et Piscatoria 38(2):149-155.

Browne, R.K., Baker, J.L. and R.M. Connolly. 2008. Chapter 13: Syngnathids: Seadragons, Seahorses, and Pipefishes of Gulf St Vincent. Natural history of Gulf St Vincent. Royal Society of South Australia (Inc):162-176.

Bruner, R. and V. Bartolino. 2008. Morphological Variation in the Seahorse Vertebral System. International Journal of Morphology 26(2):247-262.

Castro, A.L., Diniz, A., Martins, I.Z., Vendel, A.L., Oliveria, T.P.R. and I.M.L. Rosa. 2008. Assessing diet composition of seahorses in the wild using a non destructive method: Hippocampus reidi (Teleostei: Syngnathidae) as a study-case. Neotropical Ichthyology 6(4):637-644.

Clynick, B.G. 2008. Harbour swimming nets: a novel habitat for seahorses. Aquatic Conservation-Marine and Freshwater Ecosystems 18(5):483-492.

Curtis, J.M.R. and A.C.J. Vincent. 2008. Use of Population Viability Analysis to Evaluate CITES Trade-Management Options for Threatened Marine Fishes. Conservation Biology 22(5):1225-1232.

Dzyuba, B.B., Van Look, K.J., Kholodnyy, V.S., Satake, N., Cheung, S. and W.V. Holt. 2008. Variable sperm size and motility activation in the pipefish, Syngnathus abaster; adaptations to paternal care or environmental plasticity? Reproduction Fertilization and Development 20(4):474-482.

Ebeling, J. and M. Yasué. 2008. Generating carbon finance through avoided deforestation and its potential to create climatic, conservation and human development benefits. Philosophical transactions of the Royal Society of London. Series B, Biological Sciences 363:1917-1924.

Faleiro, F., Narciso, L. and L. Vicente. 2008. Seahorse behaviour and aquaculture: How to improve Hippocampus guttulatus husbandry and reproduction? Aquaculture 282(1-4):33-40.

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Forsgren, K.L. and K.A. Young. 2008. Gonadal morphology of the weedy seadragon, Phyllopteryx taeniolatus (Lacepede): characterisation of ovarian and testicular maturation. Australian Journal of Zoology 56(6):441-446.

Freret-Meurer, N.V. and J.V. Andreata. 2008. Field studies of a Brazilian Seahorse population, Hippocampus reidi Ginsburg, 1933. Brazilian Archives of Biology and Technology 51(4):743-751.

Gehring, G. and E. Ruffing. 2008. When arguments prevail over power: The CITES procedure for the listing of endangered species. Global Environmental Politics 8(2):27pp.

Harris, M.P., Newell, M., Daunt, F. and J.R. Speakman. 2008. Snake Pipefish Entelurus aequoreus are poor food for seabirds. Ibis 150(2):413-415.

Ishihara, T. and K. Tachihara. 2008. Reproduction and early development of a freshwater pipefish Microphis leiaspis in Okinawa-jima Island, Japan. Ichthyological Research 55(4):349-355.

James, N.C., Whitfield, A.K. and P.D. Cowley. 2008. Preliminary indications of climate-induced change in a warm-temperate South African estuarine fish community. Journal of Fish Biology 72:1855-1863.

James, N.C., Whitfield, A.K. and P.D. Cowley. 2008. Long-term stability of the fish assemblages in a warm-temperate South African estuary. Estuarine, Coastal and Shelf Science 76:723-738.

Kawahara, R., Miya, M., Mabuchi, K., Lavoué, S., Inoue, J.G., Satoh, T.P., Kawaguchi, A. and M. Nishida. 2008. Interrelationships of the 11 gasterosteiform families (sticklebacks, pipefishes, and their relatives): A new perspective based on whole mitogenome sequences from 75 higher teleosts. Molecular Phylogenetics and Evolution 46(1):224-236.

Kéry, M. and B. Schmidt. 2008. Imperfect detection and its consequences for monitoring for conservation. Community Ecology 9(2):207-216.

Kitsos, M.S., Tzomos, T., Anagnostopoulou, L. and A. Koukouras. 2008. Diet composition of the seahorses, Hippocampus guttulatus Cuvier, 1829 and Hippocampus hippocampus (L., 1758) (Teleostei, Syngnathidae) in the Aegean Sea. Journal of Fish Biology 72(6):1259-1267.

Krupczynski, R. 2008. Diversity of fin-activation patterns in the longsnout seahorse, Hippocampus reidi. Comparative Biochemistry and Physiology a-Molecular & Integrative Physiology 150(3):S108-S109.

Li, Y., Qian, Z. and S. Kim. 2008. Cathepsin B inhibitory activities of three new phthalate derivatives isolated from seahorse, Hippocampus kuda Bleeler. Bioorganic & Medicinal Chemistry Letters 18(23):6130-6134.

Lin, Q., Lin, J. and D. Zhang. 2008. Breeding and juvenile culture of the lined seahorse, Hippocampus erectus Perry,1810. Aquaculture 277(3-4):287-292.

Lin, Q., Lin, J., Lu, J. and B. Li. 2008. Biochemical composition of six seahorse species, Hippocampus sp., from the Chinese coast. Journal of the World Aquaculture Society 39(2):225-234.

Lourie, S.A. and R.H. Kuiter. 2008. Three new pygmy seahorse species from Indonesia (Teleostei: Syngnathidae: Hippocampus). Zootaxa 68:54-68.

Lunn, K., Noriega, V.M.J. and A.C.J. Vincent. 2008. Souvenirs from the sea: an investigation into the curio trade in echinoderms from Mexico. Traffic Bull 22:19-32.

Martinez-Cardenas, L., Porter, M. and G.J. Purser. 2008. Light-dark variations in plasma melatonin concentrations in the pot-bellied seahorse Hippocampus abdominalis Lesson, 1827. Journal of Fish Biology 72(7):1799-1803.

Morgan, S.K. and H.M. Panes. 2008. Threatened fishes of the world: Hippocampus spinosissimus Weber 1913 (Syngnathidae). Environmental Biology of Fishes 82(1):21-22.

Murugan, A., Dhanya, S. and S. Rajagopal. 2008. Seahorses and pipefishes of the Tamil Nadu coast. Current Science 95(2):253-260.

Nadeau, J.L., Curtis, J.M.R. and S.A. Lourie. 2008. Preservation causes shrinkage in seahorses: implications for biological studies and for managing sustainable trade with minimum size limits. Aquatic Conservation: Marine and Freshwater Ecosystems 19(4):428-438.

Naud, M.J., Curtis, J.M.R., Woodall, L.C. and M.B. Gaspar. 2008. Mate choice, operational sex ratio, and social promiscuity in a wild population of the long-snouted seahorse Hippocampus guttulatus. Behavioral Ecology 20:160-164.

Okuzawa, K., Maliao, R.J., Quinitio, E.T., Buen-Ursua, S.M.A., Lebata, M.J.H.L., Gallardo, W.G., Garcia, L.M.B. and J.H. Primavera. 2008. Stock enhancement of threatened species in Southeast Asia. Reviews in Fisheries Science 16(1-3):394-402.

Olivotto, I., Avella, M.A., Sampaolesi, G., Piccinetti, C.C., Ruiz, P.N. and O. Carnevali. 2008. Breeding and rearing the longsnout seahorse Hippocampus reidi: Rearing and feeding studies. Aquaculture 283(1-4):92-96.

Palma, J., Stockdale, J., Correia, M. and J.P. Andrade. 2008. Growth and survival of adult long snout seahorse (Hippocampus guttulatus) using frozen diets. Aquaculture 278(1-4):55-59.

Patron, J.J., Herrera, A.A. and E.P. Oconer. 2008. Prolactin and growth hormone levels in the pouch fluid of gravid male seahorse, Hipocampus barbouri Jordan and Richardson 1908. Asia Life Sciences 17(2):261-269.

Planas, M., Chamorro, A., Quintas, P. and A. Vilar. 2008. Establishment and maintenance of threatened long-snouted seahorse, Hippocampus guttulatus, broodstock in captivity. Aquaculture 283:19-28.

Polte, P. and C. Buschbaum. 2008. Native pipefish Entelurus aequoreus are promoted by the introduced seaweed Sargassum muticum in the northern Wadden Sea, North Sea. Aquatic Biology 3(1):11-18.

Qian, Z.J., Ryu, B., Kim, M. and S. Kim. 2008. Free radical and reactive oxygen species scavenging activities of the extracts from seahorse, Hippocampus kuda Bleeler. Biotechnology and Bioprocess Engineering 13(6):705-715.

Ripley, J.L. and C.M. Foran. 2008. Interspecific differences of parental polychlorinated biphenyl exposure on nutrient availability, egg production and brooding in two Syngnathus species. Journal of Fish Biology 72(6):1369-1385.

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Histiogamphelus

Hypselognathus

Ichthyocampus

Kaupus

Kimblaeus

Kyonemichthys

Leptoichthys

Leptonotus

Luzzatto, D.C. and Estalles, M.L. 2019. Leptonotus vincentae, a new pipefish species (Syngnathidae: Syngnathinae) from south-west Atlantic Ocean near northern Patagonia. Journal of Fish Biology 95(2):624-632.

Caille, G.M. 2012. Leptonotus blainvilleanus. Open Journal of Ecology 02(02):58-59.

Lissocampus

Maroubra

Micrognathus

Randall, J.E., McKeon, C.S., Anker, A. and P. Bacchet. 2010. First records of the pipefishes Minyichthys myersi and Micrognathus andersonii from the Society Islands. Cybium 34(3):315-316.

Microphis

Martinez-Cardenas, L., Valdez-Hernandez, E.F., Gonzalez-Diaz, A.A., Soria-Barreto, M., Castaneda-Chavez, M.R., Lango-Reynoso, F., Ruiz-Velazco, J.M. and E. Pena-Messina. 2014. Effect of salinity on growth and survival in juvenile opossum pipefish, Microphis brachyurus, in culture conditions. Journal of the World Aquaculture Society 45:577-585.

Martinez-Cardenas, L., Sumaya-Martinez, M.T., Valdez-Hernandez, E.F., Gonzalez-Diaz, A.A., Soria-Barreto, M., Castañeda-Chavez, M.R., Ruiz-Velazco, J.M. and E. Peña-Messina. 2013. Effect of temperature on growth and survival in juvenile oppossum pipefish, Microphis brachyurus: First observations on the species in culture conditions. Journal of the World Aquaculture Society 44(5):735-742.

Burkhead, N. 2012. Extinction Rates in North American Freshwater Fishes, 1900–2010. Bioscience 62(9):798-808.

Sumith, J.A., Munkittrick, K.R. and N. Athukorale. 2011. Fish assemblage structure of two contrasting stream catchments of the Mahaweli River basin in Sri Lanka: Hallmarks of human exploitation and implications for conservation. The Open Conservation Biology Journal 5:25-44.

Minyichthys

Randall, J.E., McKeon, C.S., Anker, A. and P. Bacchet. 2010. First records of the pipefishes Minyichthys myersi and Micrognathus andersonii from the Society Islands. Cybium 34(3):315-316.

Mitotichthys

Nannocampus

Nerophis

Monteiro, N. Cunha, M., Ferreira, L. Viera, N., Antunes, A., Lyons, D. and A.G. Jones. 2017. Parabolic variation in sexual selection intensity across range of cold-water pipefish: implication for susceptibility to climate change. Global Change Biology  23(9):3600-3609.

Monteiro, N.M., Silva, R.M., Cunha, M., Antunes, A., Jones, A.G. and M.N. Vieira. 2014. Validating the use of colouration patterns for individual recognition in the worm pipefish using a novel set of microsatellite markers. Molecular Ecology Resources 14(1):150-156.

Dziubinska, A. and M. Sapota. 2013. Hydroid Gonothyraea loveni found on the straightnose pipefish (Nerophis ophidion) in the Gulf of Gdansk - symbiosis, parasitism, or biofouling? Oceanological and Hydrobiological Studies 42(3):332-335.

Myhren, S. 2013. Mate choice in straight-nosed pipefish (Nerophis ophidion) may be affected by increasing turbidity in the Baltic Sea. Thesis submitted to the Norwegian University of Science and Technology:26 pp.

Sarria, M.P., Santos, M.M., Castro, L.F., Vieira, N.M. and N.M. Monteiro. 2013. Estrogenic chemical effects are independent from the degree of sex role reversal in pipefish. Journal of Hazardous Materials 263:746-753.

Sundin, J. 2013. Sex in murky waters: Anthropogenic disturbance of sexual selection in pipefish. Ph.D. thesis submitted to the University of Uppsala:35 pp.

Gurkan, S., Sever, T.M. and E. Taskavak. 2011. Seasonal food composition and prey-length relationship of pipefish Nerophis ophidion (Linnaeus, 1758) inhabiting the Aegean Sea. Acta Adriatica 52:5-14.

Sogabe, A. and I. Ahnesjö. 2011. The ovarian structure and mode of egg production in two polygamous pipefishes: a link to mating pattern. Journal of Fish Biology 78:1833-1846.

Sundin, J., Jacobsson, O., Berglund, A. and G. Rosenqvist. 2011. Straight-nosed pipefish Nerophis ophidion and broad-nosed pipefish Syngnathus typhle avoid eelgrass overgrown with filamentous algae. Journal of Fish Biology 78:1855-1860.

Monteiro, N. M., et al. 2006. Reproductive migrations of the sex role reversed pipefish Nerophis lumbriciformis (Pisces; Syngnathidae). Journal of Fish Biology 69(1):66-74.

Monteiro, N. M., et al. 2005. Brief Communications: Temporal patterns of breeding and recruitment in Nerophis lumbriciformis(Pisces; Syngnathidae) related to seawater temperatures. Journal of Fish Biology 67(5):1475-1480.

Monteiro, N. M., et al. 2005. Homing behaviour and individual identification of the pipefish Nerophis lumbriciformis (Pisces; Syngnathidae): a true intertidal resident? Estuarine, Coastal and Shelf Science 63(1-2):93-99.

Zander, C. D. 2005. On the prey of two pipefish, Syngnathus typhle and Nerophis ophidion (Teleostei, Syngnathidae) from the Baltic Sea, in combination with the transfer of parasites. Zeitschrift fuer Fischkunde 7(2):155-159.

Notiocampus

Penetopteryx

Phoxocampus

Phycodurus

Stiller, J., Wilson, N.G. and G.W. Rouse. 2015. A spectacular new species of seadragon (Syngnathidae). Royal Society Open Science 2:140458.

Larson, S., Ramsey, C., Tinnemore, D. and C. Amemiya. 2014. Novel microsatellite loci variation and population genetics within leafy seadragons, Phycodurus eques. Diversity 6(1):33-42.

Connolly, R.M., Melville, A.J. and J.K. Keesing. 2002. Abundance, movement and individual identification of leafy seadragons, Phycodurus eques (Pisces: Syngnathidae). Marine and Freshwater Research 53(4):777-780.

Phyllopteryx

LePage, V., Young, J., Dutton, C.J., Crawshaw, G., Pare, J.A., Kummrow, M., McLelland, D.J., Huber, P., Young, K., Russell, S., Al-Hussinee, L. and J.S. Lumsden. 2014. Diseases of captive yellow seahorse Hippocampus kuda Bleeker, pot-bellied seahorse Hippocampus abdominalis Lesson and weedy seadragon Phyllopteryx taeniolatus (Lacepede). Journal of Fish Diseases 38(5):439-450.

Forsgren, K. L. and C. G. Lowe. 2006. The life history of weedy seadragons, Phyllopteryx taeniolatus (Teleostei : Syngnathidae). Marine and Freshwater Research 57(3):313-322.

Sanchez-Camara, J., et al. 2006. Density, habitat use and behaviour of the weedy seadragon Phyllopteryx taeniolatus (Teleostei : Syngnathidae) around Sydney, New South Wales, Australia. Marine and Freshwater Research 57(7):737-745.

Sanchez-Camara, J. and D.J. Booth. 2004. Movement, home range and site fidelity of the weedy seadragon Phyllopteryx taeniolatus (Teleostei: Syngnathidae). Environmental Biology of Fishes 70(1):31-41.

Martin-Smith, K.M. 2011. Photo-identification of individual weedy seadragons Phyllopteryx taeniolatus and its application in estimating population dynamics. Journal of Fish Biology 78:1757-1768.

Sanchez-Camara, J., Martin-Smith, K., Booth, D.J., Fritschi, J. and X. Turon. 2011. Demographics and vulnerability of a unique Australian fish, the weedy seadragon Phyllopteryx taeniolatus. Marine Ecology Progress Series 422:253-264.

Pseudophallus

Pugnaso

Siokunichthys

Solegnathus

Stigmatopora

Dawson, M.N. 2012. Parallel phylogeographic structure in ecologically similar sympatric sister taxa. Molecular Ecology 21:987-1004.

Parkinson, K.L., Booth, D.J. and J.E. Lee. 2012. Validation of otolith daily increment formation for two temperate syngnathid fishes: the pipefishes Stigmatopora argus and Stigmatopora nigra.Journal of Fish Biology 80:698-704.

Smith, T.M., Hindell, J.S., Jenkins, G.P., Connolly, R.M. and M.J. Keough. 2011. Fine-scale spatial and temporal variations in diets of the pipefish Stigmatopora nigra within seagrass patches. Journal of Fish Biology 78:1824-1832.

Smith, J.E., Macreadie, P.I. and S.E. Swearer. 2010. An osmotic induction method for externally marking saltwater fishes, Stigmatopora argus and Stigmatopora nigra ,with calcein. Journal of Fish Biology 76:1055-1060.

Stripecampus

Syngnathoides

Zhu, L., Chen, M., Cheng, R., Ge, W., Zhang, G. and Y. Ge. 2018. Complete mitochondrial genome characterization of the alligator pipefish Syngnathoides biaculeatus and phylogenetic analysis of the family Syngnathidae. Conservation Genetic Resources https://doi.org/10.1007/s12686-018-1032-1

Sanaye, S.V., Rivonker, C.U., Sreepada, R.A. and Z.A. Ansari. 2018. Natural diet of the alligator pipefish, Syngnathoides biaculeatus (Bloch, 1785) inhabiting Palk Bay, southest coast of India. Indian Journal of Geo-Marine Sciences 47(7):1391-1397.

Syngnathus

Anderson, A. and A.G. Jones. 2019. Choosy Gulf pipefish males ignore age but prefer active females with deeply keeled bodies. Animal Behaviour 155:37-44.

Garcia, E., Rice, C.A., Eernisse, D.J., Forsgren, F.L., Quimbayo, J.P. and G.W. Rouse. 2019. Systematic relationships of sympatric pipefishes (Syngnathus spp.): a mismatch between morphological and molecular variation. Journal of Fish Biolgy https://doi.org/10.1111/jfb.14073

Cunha, M., Berglund, A. Mendes, S. and N. Monteiro. 2018. The "Woman in Red" effect: pipefish males curb pregnancies at the sight of an attractive female. Proceedings of the Royal Society B 285.

Cunha, M.A.B., Berglund, A. and Monteiro, N.M. 2017. Female ornaments signal own and offspring quality in a sex-role-reversed fish with extreme male parental care. Marine Ecology 38(5):1-8.

Monteiro, N. and N.B. Viera. 2017. Rendez-vous at the Baltic? The ongoing dispersion of the Black-striped pipefish, Syngnathus abaster. Oceanagraphy & Fisheries 3(2)

Müller, C. and K. Erzini. 2017. Interspecific differences in habitat selection of syngnathids in the Ria Formosa lagoon, Portugal. Estuarine, Coastal and Shelf Science 189:235–242.

Whitfield, A.K., Mkare, T.K., Teske, P.R., James, N.C. and P.D. Cowley. 2017. Life-histories explain the conservation status of two estuary-associated pipefishes. Biological Conservation 212:256–264.

Goncalves, I.B., Mobley, K.B., Ahnesjo, I., Sagebakken, G., Jones, A.G. and C. Kvarnemo. 2015. Effects of mating order and male size on embryo survival in a pipefish. Biological Journal of the Linnean Society 114:639–645.

Biagi, F., Piras, F., Farina, V., Zedda, M., Mura, E., Floris, A., Franzoi, P., Fausto, A.M., Taddei, A.R. and M. Carcupino. 2014. Testis structure, spermatogenesis and sperm morphology in pipefishes of the genus Syngnathus. Acta Zoologica 97:90-101.

Correia, M., Palma, J. and J.P. Andrade. 2014. Growth performance of the early life stages of broad-nosed pipefish, Syngnathus typhle (L.) fed different live or frozen diets. Aquaculture Research-Early Online.

Flanagan, S.P., Johnson, J.B., Rose, E. and A.G. Jones. 2014. Sexual selection on female ornaments in the sex-role-reversed Gulf pipefish (Syngnathus scovelli). Journal of Evolutionary Biology 98(4):1047-1058.

Landis, S. 2014. Coping with a changing ocean: Responses to global warming in host-parasite interactions between the broad-nosed pipefish (Syngnathus typhle) and its parasites. Doctoral thesis submitted to the Universität zu Kiel: 114pp.

Mobley, K.B., Chakra, M. and A.G. Jones. 2014. No evidence for size-assortative mating in the wild despite mutual mate choice in sex-role-reversed pipefishes. Ecology and Evolution 4(1):67-78.

Mwale, M., Kaiser, H. and P.C. Heemstra. 2014. Reproductive biology and distribution of Syngnathus temminckii and S. watermeyeri (Pisces: Syngnathidae) in southern Africa. African Journal of Marine Science 36:175-184.

Roth, O., Sundin, J., Berglund, A., Rosenqvist, G. and K.M. Wegner. 2014. Male mate choice relies on major histocompatibility complex class I in a sex-role-reversed pipefish. Journal of Evolutionary Biology 27:929-938.

Whitcombe, C.D. 2014. Dietary and stable isotope analyses reveal the role of kelp pipefish (Syngnathus californiensis), a presumed cryptic prey, in the diet of the elegant tern (Thalasseus elegans) in southern California waters. Master’s thesis submitted to California State University, Fullerton. 66pp.

Aronsen, T., Mobley, K.B., Berglund, A., Sundin, J., Billing, A.M. and G. Rosenqvist. 2013. The operational sex ratio and density influence spatial relationships between breeding pipefish. Behavioral Ecology 24(4):888-897.

Cone, D.K.A., Appy, R., Baggett, L., King, S., Gilmore, S. and C. Abbott. 2013. A new Gyrodactylid (Monogenea) parasitizing bay pipefish (Syngnathus leptorhynchus) from the Pacific coast of North America.Journal of Parasitology 99(2):183-188.

Fehr, A., Walther, E., Schmidt-Posthaus, H., Nufer, L. and A. Wilson. 2013. Candidatus Syngnamydia Venezia, a novel member of the phylum Chlamydiae from the Broad-nosed pipefish, Syngnathus typhle. PLoS ONE 8(8):e70853.

Haase, D., Roth, O., Kalbe, M., Schmiedeskamp, G., Scharsack, J.P., Rosenstiel, P. and T.B. Reusch. 2013. Absence of major histocompatibility complex class II mediated immunity in pipefish, Syngnathus typhle: evidence from deep transcriptome sequencing. Biology Letters 34(8):1-6.

Hubner, K., Gonzalez-Wanguemert, M., Diekmann, O.E. and E.A. Serrão. 2013. Genetic evidence for polygynandry in the black-striped pipefish Syngnathus abaster: A microsatellite-based parentage analysis. Journal of Heredity 104(6):791-797.

Ivankov, V.N., Ivankova, E.V., Borisovets, E.E. and D.I. Vyshkvartsev. 2013. Interpopulation morphological variability of the viviparous pipefish Syngnathus acusimilis Gunther, 1873 (Teleostei: Syngnathidae). Russian Journal of Marine Biology 39(5):340-349.

Keightley, M.C., Wong, B.B. and G.J. Lieschke. 2013. Immune priming: Mothering males modulate immunity. Current Biology 23(2):R76-R78.

Kiryukhina, N.A. 2013. Morphological variability in black-striped pipefish Syngnathus nigrolineatus in relation to its invasion into the Volga Basin reservoirs. Russian Journal of Biological Invasions 4(3):149-155.

Mwale, M., Kaiser, H., Barker, N.P., Wilson, A.B. and P.R. Teske. 2013. Identification of a uniquely southern African clade of coastal pipefishes Syngnathus spp. Journal of Fish Biology 82(6):2045-2062.

Partridge, C., Boettcher, A. and A.G. Jones. 2013. The role of courtship behavior and size in mate preference in the sex-role reversed gulf pipefish, Syngnathus scovelli. Ethology 119(8):692-701.

Rose, E., Paczolt, K.A. and A.G. Jones. 2013. The contributions of premating and postmating selection episodes to total selection in sex-role-reversed Gulf pipefish. American Naturalist 182(3):410-420.

Rose, E., Paczolt, K.A. and A.G. Jones. 2013. The effects of synthetic estrogen exposure on premating and postmating episodes of selection in sex-role-reversed Gulf pipefish. Evolutionary Applications 6(8):1160-1170.

Sanna, D., Biagi, F., Alaya, H.B., Maltagliati, F., Addis, A., Romero, A., De Juan, J., Quignard, J.P., Castelli, A., Franzoi, P., Torricelli, P., Casu, M., Carcupino, M. and P. Francalacci. 2013. Mitochondrial DNA variability of the pipefish Syngnathus abaster. Journal of Fish Biology 82(3):856-876.

Sarria, M.P., Santos, M.M., Castro, L.F., Vieira, N.M. and N.M. Monteiro. 2013. Estrogenic chemical effects are independent from the degree of sex role reversal in pipefish. Journal of Hazardous Materials 263:746-753.

Small, C.M., Harlin-Cognato, A.D. and A.G. Jones. 2013. Functional similarity and molecular divergence of a novel reproductive transcriptome in two male-pregnant Syngnathus pipefish species. Ecology and Evolution 3(12):4092-4108.

Sundin, J. 2013. Sex in murky waters: Anthropogenic disturbance of sexual selection in pipefish. Ph.D. thesis submitted to the University of Uppsala:35 pp.

Sundin, J.Rosenqvist, G. and A. Berglund. 2013. Altered oceanic pH impairs mating propensity in a pipefish. Ethology 119(1):86-93.

Sundin, J., Sagebakken, G. and C. Kvarnemo. 2013. Female mate choice is not affected by mate condition in a fish with male care. Acta Ethologica 16(3):189-194.

Able, K.W., Wuenschel, M.J., Grothues, T.M., Vasslides, J.M. and P.M. Rowe. 2012. Do surf zones in New Jersey provide “nursery” habitat for southern fishes? Environmental Biology of Fish 96(5):661-675.

Alaya, H.B., Trabelsi, M. and M. Longshaw. 2012. Pathogens and parasites of the black-striped pipefish (Syngnathus abaster) from the Tunis North Lake, Tunisia. Journal of Environmental and Occupational Science 1(2):99-104.

Becker, A., Coppinger, C. and A.K. Whitfield. 2012. Influence of tides on assemblages and behaviour of fishes associated with shallow seagrass edges and bare sand. Marine Ecology-Progress Series 456:187-199.

Birrer, S.C., Reusch, T.B. and O. Roth. 2012. Salinity change impairs pipefish immune defence. Fish Shellfish Immunology 33(6):1238-1248.

Gurkan, S. and E. Taskavak. 2012. Sexual dimorphism of the broad-nosed pipefish, Syngnathus typhle, from Aegean Sea (Turkey).North-Western Journal of Zoology 8(1):41-45.

Landis, S.H., Kalbe, M., Reusch, T.B. and O. Roth. 2012. Consistent pattern of local adaptation during an experimental heat wave in a pipefish-trematode host-parasite system. PloS One 7(1):e30658.

Landis, S.H., Sundin, J., Rosenqvist, G. and O. Roth. 2012. Behavioral adjustments of a pipefish to bacterial Vibrio challenge. Behavioral Ecology and Sociobiology 66(10):1399-1405.

Miersch, L. 2012. Life History Patterns of Syngnathus typhle: An experimental approach. Diploma thesis submitted to the Christian-Albrecht-Universität Kiel:64pp.

Mobley, K.B. and A.G. Jones. 2012. Overcoming Statistical Bias to Estimate Genetic Mating Systems in Open Populations: A Comparison of Bateman's Principles between the Sexes in a Sex-Role-Reversed Pipefish. Evolution 67(3):646-660.

Ondračková, M., Slováčková, I., Trichkova, T., Polačik, M. and P. Jurajda. 2012. Shoreline distribution and parasite infection of black-striped pipefish Syngnathus abaster Risso, 1827 in the lower River Danube. Journal of Applied Ichthyology 28(4):590-596.

Roth, O., Keller, I., Landis, S.H., Salzburger, W. and T.B. Reusch. 2012. Hosts are ahead in a marine host-parasite coevolutionary arms race: innate immune system adaptation in pipefish Syngnathus typhle against Vibrio phylotypes. Evolution 66(8):2528-2539.

Scobell, S.K., Mackenzie, D.S., Jaques, J.T. and A.G. Jones. 2012. Androgens and female intrasexual aggression in the sex-role reversed Gulf pipefish. Integrative and Comparative Biology 52:E156-E156.

Sogabe, A., Mohri, K. and J. Shoji. 2012. Reproductive seasonality of the seaweed pipefish Syngnathus schlegeli (Syngnathidae) in the Seto Inland Sea, Japan. Ichthyological Research 59(3):223-229.

Sogabe, A., Takata, H. and Y. Kobayashi. 2012. Ovarian structure and mode of egg production in the seaweed pipefish Syngnathus schlegeli (Syngnathidae). Ichthyological Research 60(1):85-88.

Tutman, P., Burić, M. and B. Skaramuca. 2012. First substantiated record of the Black-Striped Pipefish, Syngnathus Abaster (Actinopterygii: Syngnathiformes: Syngnathidae), in the freshwaters of Bosnia and Herzegovina. Acta Ichthyologica Et Piscatoria 42(3):259-262.

Verdiell-Cubedo, D., Torralva, M., Ruiz-Navarroa, A. and F.J. Oliva-Paterna. 2012. Fish assemblages in different littoral habitat types of a hypersaline coastal lagoon (Mar Menor, Mediterranean Sea). Italian Journal of Zoology 80(1):104-116.

Wang, M., Nie, Y., Peng, Y., He, F., Yang, J., Wu, C. and X. Li. 2012. Purification, characterization and antitumor activities of a new protein from Syngnathus acus, an officinal marine fish. Marine Drugs 10(1):35-50.

Alaya HB, Galzin R, Quignard JP, and Trabelsi M. 2011. Spinal deformities in the black-striped pipefish Syngnathus abaster (Pisces, Syngnathidae) from the Tunis North Lake, Tunisia. Chemosphere 82:318-320.

Ben Alaya H, Sanna D, Casu M, Biagi F, Francalacci P, Carcupino M, Galzin R, Quignard JP, and Trabelsi M. 2011. Analysis of meristic and mitochondrial DNA variation in Syngnathus abaster (Teleostea: Syngnathidae) from two western Mediterranean lagoons. Biologia 66:1140-1147.

Birrer S. 2011. How salinity affects the pipefish-Vibrio interaction. Department of Biology at Swiss Federal Institute of Technology Zurich:66pp.

Braga Goncalves I, Ahnesjö I, and Kvarnemo C. 2011. The relationship between female body size and egg size in pipefishes. Journal of Fish Biology 78:1847-1854.

Hablützel, P.I. and A.B. Wilson. 2011. Notes on the occurrence of Syngnathus rostellatus (Teleostei: Syngnathidae) in the Mediterranean. Marine Biodiversity Records 4:2007-2010.

Kiryukhina, N. and M.V. Kholodova. 2011. Mitochondrial DNA control region analysis in aboriginal and invasive populations of Black Sea pipefish Syngnathus nigrolineatus Eichwald 1831. Doklady Biological Sciences : Proceedings of the Academy of Sciences of the USSR, Biological sciences sections-translated from Russian 437: 88-90.

Kvarnemo, C., Mobley, K.B., Partridge, C., Jones, A.G. and I. Ahnesjö. 2011. Evidence of paternal nutrient provisioning to embryos in broad-nosed pipefish, Syngnathus typhle. Journal of Fish Biology 78:1725-1737.

Lim, A.C.O., Chong, V.C., Wong, C.S. and C.K. Choo. 2011. Diversity, habitats and conservation threats of syngnathid (Syngnathidae) fishes in Malaysia.Tropical Zoology 24(2):193-222.

Lindqvist, C., Sundin, J., Berglund, A. and G. Rosenqvist. 2011. Male broad-nosed pipefish Syngnathus typhle do not locate females by smell.J ournal of Fish Biology 78:1861-1867.

Mobley, K.B., Kvarnemo, C., Ahnesjö, I., Patridge, C., Berglund, A. and A.G. Jones. 2011. The effect of maternal body size on embryo survivorship in the broods of pregnant male pipefish. Behavioral Ecology and Sociobiology 65:1169-1177.

Rosenqvist, G. and A. Berglund. 2011. Sexual signals and mating patterns in Syngnathidae. Journal of Fish Biology 78:1647-1661.

Roth, O., Scharsack, J.P., Keller, I. and T.B. Reusch. 2011. Bateman's principle and immunity in a sex-role reversed pipefish. Journal of Evolutionary Biology 24:1410-1420.

Ryu, B., Himaya, S.W., Qian, Z.J., Lee, S.H. and S.K. Kim. 2011. Prevention of hydrogen peroxide-induced oxidative stress in HDF cells by peptides derived from seaweed pipefish, Syngnathus schlegeli. Peptides 32:639-647.

Sagebakken, G., Ahnesjö, I., Goncalves, I.B. and C. Kvarnemo. 2011. Multiply mated males show higher embryo survival in a paternally caring fish. Behavioral Ecology 22:625-629.

Sárria, M.P., Santos, M.M., Reis-Henriques, M.A., Vieira, N.M. and N.M. Monteiro. 2011. The unpredictable effects of mixtures of androgenic and estrogenic chemicals on fish early life. Environment International 37:418-424.

Sárria, M.P., Santos, M.M., Reis-Henriques, M.A., Vieira, N.M. and N.M. Monteiro. 2011. Drifting towards the surface: a shift in newborn pipefish's vertical distribution when exposed to the synthetic steroid ethinylestradiol. Chemosphere 84:618-624.

Rozas, L.P., Minello, T.J. and D.D. Dantin. 2011. Use of Shallow Lagoon Habitats by Nekton of the Northeastern Gulf of Mexico. Estuaries and Coasts 35(2):572-586.

Sheppard, J.N., James, N.C., Whitfield, A.K. and P.D. Cowley. 2011. What role do beds of submerged macrophytes play in structuring estuarine fish assemblages? Lessons from a warm-temperate South African estuary. Estuarine, Coastal and Shelf Science 95:145-155.

Schein, A., Courtenay, S.C., Crane, C.S., Teather, K.L. and M.R. Van Den Heuvel. 2011. The role of submerged aquatic vegetation in structuring the nearshore fish community within an estuary of the southern Gulf of St. Lawrence. Estuaries and Coasts 35:799-810.

Scobell, S.K. 2011. The role of androgens in male pregnancy and female competitive behavior in a sex role reversed pipefish. Doctoral dissertation submitted to Texas A&M University:157pp.

Sogabe, A. and I. Ahnesjö. 2011. The ovarian structure and mode of egg production in two polygamous pipefishes: a link to mating pattern. Journal of Fish Biology 78:1833-1846.

Sundin, J., Jacobsson, O., Berglund, A. and G. Rosenqvist. 2011. Straight-nosed pipefish Nerophis ophidion and broad-nosed pipefish Syngnathus typhle avoid eelgrass overgrown with filamentous algae. Journal of Fish Biology 78:1855-1860.

Van Bibber, N. 2011. Population Genetics of Gulf Pipefish, Syngnathus Scovelli, Along the Southeast Coast of Florida. Thesis submitted to Eckerd College: 40pp.

Wijesekara, I., Qian, Z., Ryu, B., Ngo, D. and S. Kim. 2011. Purification and identification of antihypertensive peptides from seaweed pipefish (Syngnathus schlegeli) muscle protein hydrolysate. Food Research International 44:703-707.

Winkler, J.D., Stölting, K.N. and A.B. Wilson. 2011. Sex-specific responses to fecundity selection in the broad-nosed pipefish. Evolutionary Ecology 26(3):701-714.

Downey-Wall, A.M. 2010. Molecular Population Structure of the Chain Pipefish, Syngnathus Louisianae, in Florida Waters. Thesis submitted to Eckerd College: 32pp.

Gonçalves, I.B. 2010. Egg size evolution and paternal care in pipefishes. Thesis submitted to the University of Gothenburg:41pp.

Gonçalves, I.B., Mobley, K.B., Ahnesjö, I., Sagebakken, G., Jones, A.G. and C. Kvarnemo. 2010. Reproductive compensation in broad-nosed pipefish females. Proceedings of the Royal Society B:Biological Sciences 277(1687):1581-1587.

Gwynne, D.T., Judge, K.A. and C.D. Kelly. 2010. Evidence for male allocation in pipefish? Nature 466:E11; discussion E12.

Mobley, K.B., Small, C.M., Jue, N.K. and A.G. Jones. 2010. Population structure of the dusky pipefish (Syngnathus floridae) from the Atlantic and Gulf of Mexico, as revealed by mitochondrial DNA and microsatellite analyses. Journal of Biogeography 37(7):1363-1377.

Paladini, G., Fioravanti, M.L., Cable, J. and A. Shinn. 2010. The description of Gyrodactylus corleonis sp n. and G. neretum sp n. (Platyhelminthes: Monogenea) with comments on other gyrodactylids parasitising pipefish (Pisces: Syngnathidae). Folia Parasitologica 57(1):17-30.

Partridge, C., Boettcher, A. and A.G. Jones. 2010. Short-term exposure to a synthetic estrogen disrupts mating dynamics in a pipefish. Hormones and Behavior 58:800-807.

Ripley, J.L. and C.M. Foran. 2010. Elevated whole brain arginine vasotocin with Aroclor 1254 exposure in two Syngnathus pipefishes. Fish Physiology and Biochemistry 36:917-921.

Ripley, J.L. and C.M. Foran. 2010. Quantification of whole brain arginine vasotocin for two Syngnathus pipefishes: elevated concentrations correlated with paternal brooding. Fish Physiology and Biochemistry 36(4):867-874.

Ripley, J.L., Williams, P.S. and C.M. Foran. 2010. Morphological and quantitative changes in paternal brood-pouch vasculature during embryonic development in two Syngnathus pipefishes. Journal of Fish Biology 77(1):67-79.

Sagebakken, G., Ahnesjö, I., Mobley, K.B., Gonçalves, I.B. and C. Kvarnemo. 2010. Brooding fathers, not siblings, take up nutrients from embryos. Proceedings. Biological sciences / The Royal Society 277:971-977.

Silva, K., Vieira, M.N., Almada, V.C. and N.M. Monteiro. 2010. Reversing sex role reversal: compete only when you must. Animal Behaviour 79(4):885-893.

Sundin, J., Berglund, A. and G. Rosenqvist. 2010. Turbidity hampers mate choice in a pipefish. Ethology 116(8):713-721.

Taskavak, E., Gürkana, S., Severa, T.M., Akalına, S. and O. Özaydına. 2010. Gut contents and feeding habits of the Great Pipefish, Syngnathus acus Linnaeus, 1758, in Izmir Bay (Aegean Sea, Turkey). Zoology in the Middle East 50:75-82.

Vaughan, D.B., Christison, K.W., Hansen, H. and A.P. Shinn. 2010. Gyrodactylus eyipayipi sp. n. (Monogenea: Gyrodactylidae) from Syngnathus acus (Syngnathidae) from South Africa. Folia Parasitol (Praha) 57(1):11-15.

Cakić, P., Lenhardt, M., Mićković, D., Sekulić, N., & Budakov, L. J. 2002. "Biometric analysis of Syngnathus abaster populations. Journal of Fish Biology 60(6): 1562-1569.

Trachyrhamphus

Wang, M., He, Y., Nie, Y. and X. Li. 2011. Chemical constituents from the antitumor fraction of Trachyrhamphus serratus. Chemistry of Natural Compounds 47:465-466.

Urocampus

Sogabe, A., Kawanishi, R., Takata, H. and Y. Kobayashi. 2011. Basic reproductive biology of the barbed pipefish Urocampus nanus (Syngnathidae) under laboratory conditions. Ichthyological Research 59:77-82.

Vanacampus


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