About Hippocampus abdominalis Lesson, 1827
The big-belly seahorse (scientific name Hippocampus abdominalis Lesson, 1827) has a forward-tilted, long-snouted head, a distended but narrow pot belly, and a long coiled tail. Its colour can be yellow, brown, or sometimes white. It swims with a vertical stance using its dorsal fin; when not swimming, it coils its prehensile tail around suitable growth such as seaweed, and waits for planktonic animals to drift close enough to be sucked up by its small mouth located at the tip of the snout, in a motion similar to a vacuum cleaner. Big-belly seahorses are voracious feeders, that eat mainly crustaceans such as shrimp, and other small animals that live among seaweed, such as copepods and amphipods. They do not chew food, and can eat to excess because they have a small gut tract. Each of their eyes moves independently, which makes it easier for them to spot both food and predators. It is easy to distinguish males from females: males have a smooth, soft pouch-like area at the base of the abdomen, on the front side where the stomach meets the tail. Males also have a fin in this area, but it is not obvious. Females have a more pointed stomach, with a very obvious fin at its base. Big-belly seahorses are found in the waters of Southeast Australia and New Zealand, and typically live in shallow environments such as large low-tide rock pools. They can stay motionless within seaweed, which helps them avoid predators. These habitats are preferred because they are the most productive for the seahorse's ambush predation strategy. Juvenile big-belly seahorses are pelagic or attach themselves to drifting seaweed, while adults feed on minute crustaceans including copepods and amphipods. This species is nocturnal and ovoviviparous, with males carrying eggs in a brood pouch located under the tail. These seahorses are often seen in groups at night, and can attach themselves to sponges, colonial hydroids, or man-made structures such as jetty piles in deeper water. They are typically found in water less than 50 m (160 ft) deep, though individuals have been observed at depths as great as 104 m (340 ft). Notably, this is the largest seahorse species in southeastern Australia, and it has more dorsal fin rays and tail rings than any other seahorse species. When given a choice, both juvenile and adult big-belly seahorses prefer vegetated areas, even areas with artificial seagrass, over open water. They consistently choose vegetated areas even when mysid prey is present in adjacent open water. This preference is tied to their predatory behaviour, as they rely on ambush predation. Vegetation density also affects the seahorses' foraging success. Increasing vegetation density from low to medium habitat complexity improves prey capture success for both juvenile and adult big-belly seahorses feeding on mysid swarms. However, juvenile seahorses make fewer prey attacks in higher-density vegetation, while adult seahorses show no change in attack rate. The lower number of attacks in juveniles may happen because high vegetation density disrupts the structure of prey swarms, which normally form defensive formations. Large, cohesive prey swarms are more effective at defending against lunging predators, but dense vegetation breaks up this structure, making the prey more vulnerable to ambush predators like seahorses. Studies of substrate preference have found a strong preference for substrates with the largest diameter (0.9 mm) and the lowest density (24 mm bar length). Big-belly seahorses, which have prehensile tails, often attach to both natural and artificial substrates such as coral and aquaculture nets. While early juveniles are pelagic during their first month of life, they already attach to substrates, which suggests they may prefer substrates with specific characteristics. This matches earlier findings that highlight the need for appropriately sized substrates in seahorse rearing to promote optimal distribution and minimise stress. This species' complex use of space also relates to its mating system, suggesting that genetic monogamy in this species arises from factors beyond mate availability, and also involves intricate ecological and behavioural considerations. Juvenile big-belly seahorses have optimal growth when held at lower densities. At higher densities, physical interference such as tail-grasping during feeding hinders growth and survival, and crowding negatively impacts juvenile development. Gender segregation does not significantly affect the growth of sexually mature seahorses, though same-sex courtship behaviours have been observed. This indicates that social dynamics among juveniles are more influenced by density than by gender. This finding highlights the importance of managing stocking densities in aquaculture to support healthy growth and reduce competition during feeding. Big-belly seahorses do not show typical stress responses (such as changes in plasma cortisol, glucose, or lactate levels) after brief acute stress (60 seconds of air exposure), which indicates a lack of adrenergic activation. Chronic stress (such as confinement or transportation) significantly raises stress marker levels, but these levels return to normal within six hours, demonstrating the species' capacity for recovery. This rapid recovery suggests that big-belly seahorses tolerate handling and extended confinement (up to 35 hours) with minimal adverse effects, reflected in a low 1% mortality rate during recovery. Research analysing seahorse breathing patterns has found that both wild and captive big-belly seahorses show an increase in opercular beat rate (gill movements) after being handled. While wild seahorses have lower opercular beat rates at rest than captive seahorses, both groups show a significant increase after manipulation. This suggests that current captivity protocols should allow more than 24 hours of acclimation to ensure good recovery. In the wild, breeding starts when seahorses are around one year old; in captivity, this age can drop to around eight months. Big-belly seahorses breed year-round, with breeding peaks in warmer months. Courtship begins with a series of colour changes and postural displays. The male slightly dilates the opening of his brood pouch, inflates the pouch to a balloon-like shape with water by swimming forwards or pushing his body forwards in a pumping action, then closes the pouch opening. At the same time, he lightens the colour of his pouch to white or pale yellow, and brightens his overall body colour, typically intensifying yellow tones. The male repeatedly approaches his chosen female with his head tucked down, and rapidly flutters his dorsal and pectoral fins. If the female is not receptive, she ignores the male, who will then look for another potential mate. If no females are receptive, the male stops displaying and deflates his pouch by dilating the opening, bending forwards, and expelling the water inside. If a female is receptive to a courting male, she responds with her own colour changes and head tucking, typically intensifying lighter colours such as yellow and white to highlight the contrast between these lighter colours and her overall darker blotching and banding patterns. Next, the pair performs a series of short bursts of tandem swimming, sometimes with their tails entwined, or with the female tightly rolling her tail up. This sequence is often described as 'dancing'. After coming to rest, the male repeatedly points his snout upwards to attempt to lead the female to swim towards the water surface with him. If the female responds by also pointing her snout upwards, the final stage of courtship begins: both the male and female swim directly upwards toward the water surface, with their heads pointing up and tails pointing straight down. When they reach the water surface, one or both seahorses can often be seen and heard snapping their heads. To transfer her eggs to the male, the female faces the male, positioned slightly above him. She presses the base of her abdomen against the male's pouch, then squirts her eggs through the opening in the front of his dilated pouch. Male big-belly seahorses brood 300 to 700 young at a time, and can have up to four broods in a single summer. Newly brooded young have variable brown colouring, mottled with yellow-brown and marked with darker splotches. The tail often has yellow bands circling it. In deeper water, where the tail anchors to other colourful organisms such as sponges and hydroids, big-belly seahorses often take on the colours of these anchor organisms.
