Fisheries,large‐scale trade,and conservation of seahorses in Malaysia and Thailand

• 1. All seahorse species (genus Hippocampus) are listed under CITES Appendix II, requiring that exports of these fishes must be regulated for sustainability. Preliminary trade surveys and anecdotal reports suggested Malaysia and Thailand represented an important source for seahorses used globally in traditional medicine, curios, and aquarium display, but few historic trade or fisheries data are available. Baseline information about pre‐CITES catch and trade is essential for managing seahorse fisheries and trade under CITES, and for understanding present‐day effects of CITES regulation on the seahorse trade.
• 2. In 1998–1999, seahorse fisheries and trade in both countries were assessed by interviewing participants at many levels of the trade and corroborating those surveys with official trade documents.
• 3. Seahorses were found to be landed primarily as trawl bycatch. Malaysia's catch of 2900 kg year^?1 was less than the estimated domestic consumption (5500–6000 kg year^?1), whereas Thailand's catch of 6600 kg year^?1 apparently far exceeded domestic consumption (～520 kg year^?1).
• 4. Both countries imported seahorses from and exported to other Asian nations. Import statistics from Hong Kong SAR and Taiwan recorded maximum annual trade from Malaysia at 1280 kg year^?1. Trade surveys indicated that Thailand exported at least 5000 kg annually (similar to the estimation of catch), but national Customs records reported 10 500 kg year^?1 in exports, supported by official import records from Hong Kong SAR and Taiwan which indicated that Thailand was the source of up to 11 400 kg year^?1.
• 5. Fishers and traders in both countries reported decreasing availability of seahorses, raising conservation concerns. These apparent declines, in combination with substantial domestic consumption, point towards the challenges that Malaysia and Thailand face in establishing sustainable levels of exports under CITES. Copyright © 2010 John Wiley & Sons, Ltd.

     

Opportunities and challenges for analysis of wildlife trade using CITES data – seahorses as a case study

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Assessing East African trade in seahorse species as a basis for conservation under international controls

• 1. Seahorses (Hippocampus spp.), many of which are listed as Vulnerable or Endangered on the IUCN Red List, are traded worldwide as souvenirs, aquarium fish and, primarily, for use in traditional medicines. Given concern over the sustainability of this trade, the genus was added to Appendix II of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) in May 2004.
• 2. This paper reports findings of the first ever survey of seahorse trade in Africa, conducted in Kenya and Tanzania in May and June 2000.
• 3. Seahorse trade in Kenya was found to be negligible, with approximately 10 live seahorses exported as aquarium fish annually. Until 1998, however, Kenya may have imported somewhere from 1 to 2.3 t of dried seahorses annually from Tanzania for re‐export to Asian medicine markets. Seahorse trade in Tanzania remained substantial, with at least 630–930 kg of dried seahorse exported directly to Asia each year.
• 4. Accounts of declines in seahorse availability and seahorse size, although few in number, could be early warning signs that wild populations are suffering, at least locally. Close monitoring of future developments in the trade will be essential to allow for timely conservation action as and when necessary, and would contribute to our understanding of the ecological and economical implications of small‐scale, non‐food fisheries.

Copyright © 2004 John Wiley & Sons, Ltd.     

Catch and trade bans for seahorses can be negated by non-selective fisheries

1. All seahorse species (genus Hippocampus) are listed under Schedule I of India's Wild Life Protection Act, making all capture and trade of seahorses illegal. In the more than 15 years since the ban, little work has been done to assess its effects on seahorse conservation.
2. Between 2015 and 2017, fisheries and trade surveys were conducted along the south-east coast of India, in the state of Tamil Nadu, historically known to be a hub for seahorse catches and trade.
3. Seahorses were primarily landed as bycatch, although in greater quantities by traditional drag nets than as trawl bycatch. Total annual catches were estimated between 4.98 million and 13.64 million seahorses, 87% of which were caught by active non-selective gear.
4. Generalized additive models revealed that seahorse catch per unit effort had non-linear relations with depth and latitude, and were higher in biogenic habitats, with active, bottom-used, and non-selective gears (e.g. trawls).
5. The illegal nature of the trade in seahorses hampered an understanding of trade routes and trade volumes. Catch estimates indicated that 11.21–30.31 tonnes of seahorses probably entered trade, yet interviews with traders only documented trade of about 1.6 tonnes.
6. Fishers reported a decreasing availability of seahorses. Since most seahorses come from bycatch in persistent fisheries that are not directly affected by the ban on seahorse capture, this decline is likely to represent a population decline.
7. A fishery and trade ban for incidentally caught species, particularly in a poorly regulated fishery, appears to add little conservation value. There needs to be a shift in the management approach, moving from a ban towards spatial and temporal restrictions, and toward enforcing existing fishery regulations.

     

Revisiting two sympatric European seahorse species: apparent decline in the absence of exploitation

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Striking a balance between retaining populations of protected seahorses and maintaining swimming nets

• 1. The fish family Syngnathidae (seahorses, pipefish, pipehorses and seadragons) is fully protected in New South Wales, Australia, but in some countries certain species are threatened by unsustainable collecting, capture as incidental bycatch, and habitat degradation.
• 2. Within Sydney Harbour, two species of seahorses (Hippocampus abdominalis and Hippocampus whitei) have been found to colonize artificial structures such as jetty pylons and protective netted swimming enclosures. These protective nets are subject to fouling from epibiotic growth (algae, ascidians, bryozoans, etc.) and rubbish, which causes the nets to collapse from the additional weight. Local authorities employ diving contractors on an ad hoc basis to remove the epibiota from nets.
• 3. Surveys showed a significant decline in the numbers of both seahorse species at one site following the replacement of a net, and recovery of the H. whitei population took more than 15 months.
• 4. A manipulative experiment tested the importance of epibiotic growth for seahorses. H. whitei, tagged with individual marks, were allocated to sections of a net that had undergone different cleaning procedures. Seahorse size, position on the net and total population abundance were recorded every 2 weeks over a 3 month period. It was demonstrated that seahorses have a significant positive association with epibiotic growth and proximity to the sea floor. Seahorse populations also showed seasonal variation in abundance with increased numbers on the net during the breeding season (spring–summer).
• 5. This project has led to the development of best practice net cleaning procedures for local authorities in Sydney Harbour to manage growth on the nets while minimizing impacts on seahorse populations. Copyright © 2009 John Wiley & Sons, Ltd.

     

A conservation trade‐off? Interspecific differences in seahorse responses to experimental changes in fishing effort

• 1. A 2‐year experimental seining programme and underwater visual censuses were undertaken to quantify the direct effects of active demersal fishing on the population structure and relative abundance of two sympatric seahorse species of conservation concern: the European long‐snouted seahorse, Hippocampus guttulatus Cuvier 1829 and the short‐snouted seahorse, Hippocampus hippocampus L. The influence of habitat preference on population‐level responses to changes in habitat structure following a reduction in fishing effort was also investigated.
• 2. It was predicted that the benthic habitat would be more structurally complex after fishing ceased and that seahorse densities would increase in response to reduced fishing mortality. Furthermore, it was predicted that the magnitude of the increase in density would be greater for H. guttulatus than for H. hippocampus, because the former species prefers complex vegetated habitats while the latter species uses sparsely vegetated habitats.
• 3. As predicted, the amount of habitat cover increased significantly when seining ceased, primarily through increases in the abundance of drifting macroalgae and unattached invertebrates. Despite similarities in life histories, the two seahorse species responded differently in terms of magnitude and direction to reduced fishing effort: the abundance of H. guttulatus increased significantly while H. hippocampus decreased in abundance.
• 4. Results suggest that active demersal fishing may influence the magnitude and direction of the responses of benthic marine fishes to exploitation through its impacts on habitat structure. An increase in habitat cover appeared to favour higher densities of H. guttulatus when seining effort was reduced. By contrast, repeated seining, which maintained less complex habitats, appeared to favour greater abundances of H. hippocampus.
• 5. Given differences in habitat preference among benthic marine fishes subject to incidental capture in fisheries, simultaneous attempts to manage populations of sympatric species may require complementary strategies that support the persistence of diverse habitat types.

Copyright © 2006 John Wiley & Sons, Ltd.     

Ontogeny of digestive enzymatic capacities in juvenile seahorses Hippocampus guttulatus fed on different live diets

Differences in survival and growth rates in seahorse Hippocampus guttulatus juveniles feeding on Artemia sp. or copepods have been related to specific digestive capacities of seahorse newborn, which are capable of actively forage on available prey from the first day of live. Other seahorse species, such as H. abdominalis and H. hippocampus, show high success feeding on Artemia nauplii suggesting species-specific differences in the digestibility of prey among seahorses. In this study, the profiles of digestive enzyme activity during the initial 15 days after release (DAR) were very low for trypsin, chitinase and α-amylase. In contrast, higher activities towards any of the assayed substrates for lipase (butyrate, octanoate and oleate) were evident from 0 DAR onwards. From 15 DAR onwards, the effect of diet composition became evident in juveniles previously fed on a mixed diet (Artemia + copepods), which showed a clear increase in all the assayed enzymes when compared with juveniles fed on Artemia as a sole prey. As a practical applicability of this study, a feeding schedule ensuring an adequate digestibility of the prey is proposed based on ontogenetic enzymatic activities of seahorse juveniles fed on different prey.     

Frozen mysids as an alternative to live Artemia in culturing seahorses Hippocampus abdominalis

This investigation examined the effects on growth and survival of seahorses Hippocampus abdominalis Leeson 1827 fed a 25% body weight (wet weight) daily ration of live Artemia sp. enriched with Algamac‐3050, frozen mysids Amblyops kempi or a combination of live enriched Artemia and frozen mysids. After 3 months there was no difference in seahorse length, wet weight, condition factor (CF), or food conversion ratios (FCR) between the treatments. Mean daily specific growth rate (SGR) was higher for the Artemia‐only treatment than for the mysid‐only treatment (P<0.05). FCRs ranged from 6.14 g to 8.72 g dry weight of food required to give a 1‐g dry weight increase in seahorses. There was no difference in survival between treatments. Fatty acid analysis revealed that mysids had a higher percentage composition of EPA, 20 : 5n‐3, and DHA, 22 : 6n‐3, but a lower composition of AA, 20 : 4n‐6, than enriched Artemia. Percentage n‐3 highly unsaturated fatty acids (HUFAs) in mysid levels were approximately twice that of Artemia. Proximate analysis revealed mysids to be higher than the enriched Artemia in protein and fats, and lower in water content. This experiment demonstrates that, although no growth advantage was derived from the use of frozen mysids, they can be used successfully as an alternative food to live enriched Artemia for H. abdominalis. The use of frozen mysids is highly recommended in commercial seahorse culture if the seahorses are to be sold into the live aquarium trade, as this may increase their chances of survival after sale.     

Rearing the spotted seahorse Hippocampus kuda by feeding live and frozen copepods collected from shrimp ponds

This study evaluated the use of live and frozen copepods collected from shrimp ponds for rearing juveniles of the spotted seahorse Hippocampus kuda. Protein and HUFA contents in frozen copepods were all higher than in Artemia nauplii, the conventional live food for seahorse juveniles. The results of this study showed that copepods can be used as feed for rearing seahorse fry and juvenile. The spotted seahorse showed obvious preference for live copepods and rarely fed on dead copepods on the tank bottom. Furthermore, the combination of frozen copepods and live Artemia nauplii resulted in highest growth and highest survival of the experimental seahorses. Further research on possible effects of DHA:EPA ratio on survival and growth of young H. kuda is recommended.     

Understanding fishing and conservation of the Pacific seahorse (Hippocampus ingens) in Sinaloa,Mexico, through local ecological knowledge

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Swimming nets have positive effects on populations of the endangered White's seahorse Hippocampus whitei

1. Habitat degradation and destruction arising from rapidly increasing urbanization represents one of the most significant threats to biodiversity. Human populations are continuing to increase around coastal regions, and as marine habitats are displaced by artificial structures it is important to understand how marine species may be impacted by these changes in habitat availability. The endangered seahorse Hippocampus whitei has been observed inhabiting protective swimming nets in Sydney Harbour, Sydney, Australia, even in the presence of natural habitats.
2. This study tested whether the presence of a swimming net results in increased seahorse numbers at sites around Sydney Harbour, or whether seahorses are attracted away from natural habitats. Density surveys and mark–recapture population estimates were done at sites with pre-existing swimming nets and compared to control sites where only natural habitat was present. A manipulative experiment was conducted in which panels of swimming net material were installed at two sites in Sydney Harbour, with comparisons to control sites over a period of 14 months (April 2018 to June 2019) to test whether the installation of swimming nets would affect seahorses on surrounding natural habitat or increase site abundance.
3. The pre-existing and installed swimming nets were found to support greater densities of H. whitei as well as some increases in site-scale abundance, with no effects on seahorse density on natural habitats. It is likely that increased seahorse production is occurring on the nets, with no evidence that seahorses are being attracted away from natural habitat; however, effects may vary across survey occasions and sites. Furthermore, swimming nets may serve as a useful replacement habitat in locations where natural habitat has become sparse or absent.

     

Prey–predator dynamics in seahorses (Hippocampus guttulatus): deciphering fatty acid clues

Understanding the flow of fatty acids between trophic levels can provide important clues on prey–predator dynamics and nutritional requirements of the species. This study investigates the fatty acid flow between enrichment emulsions, Artemia nauplii and Hippocampus guttulatus juveniles, and evaluates the nutritional value of enriched and unenriched Artemia for newborn seahorses. The fatty acid profile of Artemia and seahorses generally reflected the dietary composition, but fatty acids were not linearly transferred between trophic levels. The incorporation of dietary fatty acids showed to be a more complex process involving dietary composition, predator metabolism and nutritional requirements. Artemia composition resulted from a dynamic balance between what was assimilated and metabolized by the nauplii during enrichment. Prey fatty acids were incorporated in seahorses, but HUFA, particularly DHA, were selectively retained to fulfil their high requirements. H. guttulatus newborns were not successfully reared on Artemia nauplii, not even on enriched Artemia, with low survival rates (15.0–26.7%) being observed in all feeding treatments. The high MUFA content and low DHA level of Artemia did not fulfil the high SFA and PUFA requirements of newborn juveniles, particularly their great DHA demands. Higher survivorship was obtained with enriched Artemia, but no differences were detected in juvenile growth.     

Manipulating artificial habitats to benefit seahorses in Sydney Harbour,Australia

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Breeding and juvenile culture of the lined seahorse, Hippocampus erectus Perry, 1810

All seahorse species worldwide have been placed under CITES Appendix II since 2004, because they have been over-exploited for traditional Chinese medicine and aquarium trades. Aquaculture has been recognized as a long-term solution for sustaining the seahorse trade while minimizing wild collection. In this study, we evaluated the breeding and juvenile culture of an important aquarium seahorse species, the lined seahorse Hippocampus erectus, Perry 1810. Pairing, mating and copulation behavior were observed. Gestation time and brood size were 17.33 ± 2.94 days and 272.33 ± 66.45 individuals/brood, respectively. Growth rates differed among juveniles from different broods. Effects of temperature on the growth rates and survivorship of the juveniles during the first two weeks were compared. The highest growth rate and survivorship of the juveniles occurred at 28–29 °C among the temperatures tested (24–33 °C). Growth rate and survivorship of the juveniles during the first 9 weeks at 28 °C were investigated. The final standard length and survivorship of the juveniles were 6.32 ± 0.52 cm and 71.11 ± 10.18%, respectively, and the relationship between the wet weight and the standard length of the juvenile seahorses can be expressed as: W = 0.0034 L^2.5535 (r² = 0.9903, n = 12, P < 0.01). These findings suggest that H. erectus is a good candidate for commercial aquaculture.     

Ex situ growing out of early stages of wild seahorses: Envisioning conservation options for threatened populations

1. Rafting has been proposed as a dispersive mechanism for some species of seahorses. Juvenile Hippocampus patagonicus rafting on the sea surface have been reported. This life stage has high mortality in nature due to ecological and environmental factors usually affecting juvenile planktonic teleosts (e.g. predation).
2. In this study, 50 juvenile seahorses were captured while rafting at the beginning of the reproductive season (December). They were grown out under a standard protocol in a recirculating aquaculture system for 120 days until they reached maturity.
3. During this period, only three seahorses died (6%). Mature seahorses were 65 ± 7 mm average height and showed variable coloration and pigmentation pattern (n = 47; 94%).
4. The availability of juvenile seahorses during the reproductive season and their high survival performance ex situ highlight the feasibility of developing protocols in which juvenile seahorses serve as a novel source of broodstock.

     

Biochemical composition of wild and cultured seahorses (Hippocampus kuda Bleeker)

The seahorse has been used for thousands of years as an important traditional Chinese medicine (TCM) in China. Many species of wild seahorse have become endangered, but demand for them continues to grow rapidly. Therefore, it is urgent to cultivate seahorses to relieve the strain on natural populations and meet the market demand for this TCM. In this study, medicinal components of wild and cultured yellow seahorses (Hippocampus kuda Bleeker) were analysed and compared. Different parts of the body (cortex and bone), male and female specimens, and seahorses of different ages were analysed. Crude protein, crude fat, trace elements, calcium, amino acid, fatty acid, steroid and cholesterol content were measured. The results showed that moisture content accounted for 70% of wet weight and ash content increased with growth. Crude protein and fat contents were higher in cultured seahorses than in wild specimens, and the content of Zn in cultured seahorses (93.26 ± 10.44%) was significantly higher than that of same‐aged wild seahorses (74.20 ± 3.83%). Amino acid and fatty acid contents of cultured seahorses also were higher than those of wild seahorses. These findings show that cultured seahorses can also be used in TCMs and that 1‐year‐old cultured seahorses have the best properties.     

Feeding selectivity of the seahorse,Hippocampus kuda (Bleeker), juveniles under laboratory conditions

This study examined the feeding selectivity of Hippocampus kuda juveniles under captive conditions and evaluates different food organisms that could be used to improve hatchery‐rearing of this species. Newly born H. kuda were reared for 10 days in 60‐L capacity tanks and fed rotifers (Brachionus rotundiformis), zooplankton (mostly Pseudodiaptomus annandalei and Acartia tsuensis) alone or both food sources. The size and amount of food ingested increased as seahorses grew. Selective feeding of seahorses appeared to change as they develop, preferring copepod adults over nauplii and rotifers. A. tsuensis was highly selected by juveniles over P. annandalei. Specific growth rate in terms of body weight (SGR‐BW, 15% day^–1) was the highest and mortality rate (9% at day 10) the lowest in seahorses fed a mixed food sources. Slowest growth rate (0.3% day^–1) and highest mortality rate (60% at day 7) were observed in seahorses fed rotifers alone. These results indicate that copepods are suitable food for seahorse juveniles, but a mixture of food organisms in the rearing tank environment enhances survivorship and growth of H. kuda, thus potentially providing a source of cultured rather than wild specimens for characterizing the life history of this threatened species.     

Identification and characterization of the pathogen associated with skin ulcer syndrome in lined seahorse,Hippocampus erectus

The lined seahorse, Hippocampus erectus, is an Atlantic species, which mainly inhabits shallow sea beds or coral reefs. Seahorse has become very popular in China due to its wide use in traditional Chinese medicine (TCM). However, the aquaculture of the lined seahorse has been threatened by a variety of diseases, especially bacterial infections. Skin ulcer syndrome becomes more and more common in the culture of seahorses, leading to skin ulcer, liver erosion and minority tail rotting. These diseased seahorses die in only 72 hr, causing huge economic losses in aquaculture. Pathogen HMT‐1 was isolated from the lined seahorses with skin ulcer syndrome, which was identified as Vibrio harveyi. The median lethal dose (LD₅₀) of HMT‐1 was 2.88 × 10⁸ cfu/ml. The pathogenic mechanism of HMT‐1 was preliminarily studied, and the pathological changes of the diseased lined seahorses were also investigated. Moreover, the activities of ACP, complement 3, SOD and LZM at different time post injection were measured by commercial kits. Our findings can provide reliable reference for diagnosis and treatment in the future.     

Effects of anthropogenic noise as a source of acoustic stress in wild populations of Hippocampus guttulatus in the Ria Formosa,south Portugal

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