Stiphodon alcedo MAEDA, MUKAI & TACHIHARA, 2011

Etymology

Stiphodon: from the Greek στίφος (stifos), meaning ‘swarm, horde’, and ὀδών (odon), meaning ‘toothed’, in reference to the numerous, closely-packed teeth in the upper lip of member species.

alcedo: from the Latin alcedo, meaning ‘kingfisher’, as the metallic turquoise on the head and body and the orange around the belly of the nuptial coloured male is similar to the plumage of the kingfisher, Alcedo atthis.

Classification

Order: Perciformes Family: Gobiidae

Distribution

Known only from the Ryukyu Islands, Japan, and thus far recorded from just 4 streams on Okinawa island and two on Iriomote island. The type series derived from both islands with Okinawa given as type locality.

It may be more widely-distributed than this however, and was possibly transported to the Ryukyu Islands via the Kuroshio Current, an ocean current similar to the Gulf Stream transporting warm, tropical water northward from an area east of Taiwan past Japan towards the polar region.

This theory is discussed in the description with the conclusion that the species may be extensively-represented further south, e.g., in rivers draining eastern Luzon, Phillipines, which lies close to the origin of the Kuroshio current and is poorly-known in an ichthyological sense.

This may also explain its relatively low abundance in the Ryukyu Islands compared to other congeners found there, especially S. percnopterygionus.

A similar phemoenon has been observed in S. surrufus, which was described from Leyte in the Phillipines but has been recorded on Yaku Island (aka Yakushima), even further north than the Ryukyu chain.

Habitat

Members of this genus are near-exclusive inhabitants of short coastal streams on tropical, often volcanic, islands, with typical habitats lying above waterfalls or cataracts.

This makes them inaccessible to the majority of fishes although other gobies from the genus Sicyopus often occur syntopically, sometimes alongside two or more Stiphodon species. Amphidromous Macrobrachium spp. shrimp and neritid snails are the commonest invertebrates to be found.

The gradient of the streams varies depending on locality, and Stiphodon spp. inhabiting the fastest-flowing and/or living above waterfalls generally lack extended dorsal-fin rays/spines plus the first dorsal-fin is rounded in shape and approximately the same height as the second dorsal-fin.

In contrast those possessing a ‘taller’ first dorsal-fin with one or more extended rays (characters usually if not always more apparent in males) tend to live in slower-moving streams and not climb waterfalls as part of their life cycle (Watson, 2008).

S. alcedo falls into the latter group  and typically occurs in low-gradient biotopes characterised by relatively wide, slow-to-medium flowing riffles or runs broken up by pools and small cascades in some cases.

Substrates are normally of bedrock with scattered jumbles of rocks and boulders, and while riparian vegetation and submerged leaf litter are common aquatic plants aren’t usually present.

Evidence exists to suggest that different Stiphodon spp. actively choose a particular substrate type over another, with some appearing to focus on rocks/boulders within a particular size range for example.

The range of substrate sizes chosen by females also appears to be significantly narrower than that for males in some cases, so resource partitioning may be occurring between and/or within species depending on locality.

The most favourable habitats all contain very clear, well-oxygenated water which, allied with the tropical sun, facilitates the development of a rich biofilm carpeting submerged surfaces.

Sicydiines are such successful colonisers of these niche environments due to aspects of their morphology which allow them to both utilise this as a food source and employ a remarkable breeding strategy.

In nature S. alcedo can be found living syntopically with the congeners S. percnopterygionus and S. atropurpureus, and occasionally with S. imperiorientis.

Maximum Standard Length

45 – 50 mm.

Aquarium SizeTop ↑

An aquarium with base dimensions of ∗ cm should be large enough for a pair or small group but use something bigger if you want to keep multiple species together since males are territorial to an extent.

Maintenance

These gobies aren’t too difficult to keep provided some basic requirements are met.

Most importantly the water must be clean and well-oxygenated at all times so we suggest the use of either an over-sized filter, additional powerheads, flow pumps, or airstones.

While torrential conditions are unnecessary a turnover of 10-15 times tank volume per hour is recommended, though with good oxygenation a lower rate of 5-10 times per hour is feasible.

Base substrate can either be of gravel, sand, or a mixture of both to which should be added a layer of water-worn rocks and pebbles of varying sizes.

Aged driftwood can also be used but avoid new pieces since these usually leach tannins which discolour the water and reduce the effectiveness of artificial lighting.

The latter must be strong to promote the growth of algae and associated micro-organisms because Stiphodon spp. are highly specialised biofilm grazers.

Some aquarists even maintain an open filter sponge in the tank to provide an additional food source.

If keeping multiple males of one or more species structure the rockwork to form plenty of potential hiding places and broken lines-of-sight to reduce the likelihood of excessive aggression.

Also bear in mind that males in particular tend to dig into the substrate when sleeping or spawning meaning larger rocks are best positioned directly on the tank base to prevent any risk of collapse.

They don’t sleep in the same burrow each night and females have been observed to occupy uninhabited ones.

Although not a feature of this species’ natural habitat aquatic plants can be used with hardier genera such as Microsorum, Crinum, and Anubias likely to fare best.

The latter are particularly useful as their leaves tend to attract algal growth and provide hiding places.

Since they need stable water conditions and feed on biofilm these fishes should never be added to immature set-ups and a tightly-fitting cover is necessary since they’re able to climb glass.

While weekly water changes of 30-50% tank volume are essential the rest of the tank needn’t be kept too clean and algae should be allowed to grow on all surfaces except the viewing pane.

Water Conditions

Temperature: 22 – 28 °C; increased surface agitation is needed to maintain dissolved oxygen levels towards the upper end of this range.

In nature this species undergoes a brief cool period between December and April during which water temperature drops to 59 – 66.2°F/15 – 19°C.

pH: 6.5 – 7.5

Hardness: 36 – 215 ppm

Diet

Stiphodon spp. are specialised algal grazers feeding on benthic algae plus associated micro-organisms and possess subterminal, extrusible mouthparts with dentition designed for the purpose including regenerative teeth.

The pelvic disc is also important not only to maintain position in rapidly-flowing water but also to provide leverage.

In the aquarium some sinking dried products and small, meaty foods such as live or frozen bloodworm may be accepted but should only be offered irregularly since the elongate gut is specifically designed to process vegetable matter.

For long-term success it’s thus essential to provide a mature aquarium with a plentiful supply of algae-covered rocks and other surfaces.

If unable to grow sufficient algae in the main tank or you have a community containing numerous herbivorous fishes which consume what’s available quickly, it may be necessary to maintain a separate container in which to grow algae on rocks and switch them with those in the main tank on a cyclical basis.

Such a ‘nursery’ doesn’t have to be very large, requires only strong lighting and in sunny climates can be kept outdoors.

Algal type is also important with diatoms, cyanobacteria (commonly referred to as blue-green ‘algae’) and green varieties preferred to tougher ones like rhodophytic ‘black brush’ algae.

Unfortunately as a result of their specialised diet and oxygen requirements Stiphodon spp. are regularly seen on sale in an emaciated state which can be tricky to correct.

A good dealer will have done something about this prior to sale but if you decide to take a chance with severely weakened specimens they’ll initially require a readily-available source of suitable foods in the absence of competitors if they’re to recover.

Behaviour and CompatibilityTop ↑

Stiphodon spp. can be kept in a community provided tankmates are chosen with care.

Peaceful, similarly-sized species which naturally inhabit well-oxygenated streams such as Tanichthys, Microdevario, or smaller Danio species are the best choices for the upper levels, but we’ve also seen it being maintained with various characins, small poeciliid livebearers, and freshwater shrimp of the genera Caridina and Neocaridina.

Other bottom-dwellers can include small loaches from genera such as Gastromyzon, Pseudogastromyzon, Barbucca, or Acanthopsoides, and in high-turnover set-ups obligate torrent-dwellers like Annamia, Homaloptera, etc.

Avoid those that feed aggressively such as many Schistura spp.

Bigger fishes are best omitted entirely although in large set-ups it may be possible to add a few non-predatory, surface-dwelling species, while the majority of cichlids and other territorial fishes inhabiting the lower reaches should be avoided entirely.

Males tend to be loosely territorial, especially when breeding, but several can be kept together provided sufficient space and suitable foods are available, and other stream-dwelling gobies such as Sicyopus, Sicyopterus, Rhinogobius, or Schismatogobius spp. also make good companions.

Though males aren’t necessarily gregarious females tend to exist in loose groups meaning a single male with two or more females is the recommended minimum purchase.

Females of different species will group together but males appear able to differentiate between them.

Sexual Dimorphism

As with all members of the genus sexual dimorphism is pronounced.

Non-nuptial males have a pale brownish base body colour with the head and dorsal surface of the body reddish brown.

There is a dark lateral stripe extending from the snout to the pectoral-fin base with an additional stripe extending posteriorly from the pectoral-fin to the caudal peduncle, terminating in a dark blotch, and there is a pale blue to gold spot on the upper part of the pectoral-fin base.

The  second dorsal, anal, and caudal fins have a white margin, and the second dorsal fin a series of white spots interspaced with darker spots along the spine and rays.

The caudal-fin has 5-7 whitish transverse bars, and the pelvic-fin a distal white patch.

In nuptial males body colour is variable but the lateral part of the head and lips are always metallic turquoise, dorsum of the head always black, and pectoral-fin base always black with a metallic turquoise spot on the upper part.

Base body colour is normally black with metallic turquoise vertical bars, though the latter are sometimes indistinguishable when the body is very dark.

The dorsal surface also has metallic turquoise or gold spots, while the belly is whitish ventrally and sometimes orange laterally.

The pectoral-fin usually lacks a white marking, but a number of faint bluish-white spots interspaced by black spots are sometimes visible along the rays.

The pelvic-fin is white distally. Smaller males (< 30 mm SL) often have orange markings on the trunk, first and second dorsal, anal, and caudal fins.

While resting on a perch during courtship, the colour pattern changes rapidly and often appears similar to that of non-nuptial males, with paler background and a dark lateral stripe.

Females have a pale cream body with a dark lateral stripe extending from the snout, below the eye to the pectoral-fin base, then continuing posteriorly from the pectoral-fin to the caudal peduncle.

The stripe is composed of 0-3 indistinct blotches anteriorly and 8 regularly-spaced blotches posteriorly, though these are also indistinct in some specimens.

An additional, thinner dark stripe extends dorsolaterally from behind the eye to the base of the caudal-fin.

This is paler than the body stripe and sometimes obscure. There are gold markings on the snout, opercle, and upper pectoral-fin rays, and the fins lack white markings.

Reproduction

Observations of courtship behaviour and the occasional spawning exist but to date no-one has managed to raise fry of any Stiphodon spp. in captivity.

This is undoubtedly attributable to their complex amphidromous breeding strategy in which adults live and spawn in freshwater streams but the initially pelagic post-hatch larvae are washed downstream to the sea where the post-larval fry spend the first part of their life developing in marine conditions.

Once they reach a certain stage of development they begin to migrate upstream, a journey which sometimes includes spectacular climbs up and over waterfalls or other obstructions.

Females are extraordinarily fecund for their size and can deposit as many as 10,000 eggs in a single spawning event.

These are tiny (~ 0.5 mm in diameter), pyriform, and attached to solid surfaces by filaments, normally being placed on the underside of rocks.

It’s thought that reduced egg size and high fecundity are advantageous since the large number of fry offsets risks such as predation or the possibility of excessive dispersal at sea and their small size allows them to feed on microscopic plankton.

Spawning is initiated by the intensely-coloured male as he attempts to coax females to his chosen spawning site while fending off rivals.

It usually occurs under rocks and captive males have also been observed to dive head first into the substrate followed by a female at the climax of courtship.

Once fertilised the mass of eggs, which can number in the thousands, is guarded by the male during the incubation period of less than 24 hours in studied cases.

The fry hatch as undeveloped larvae with a large yolk sac attached and lacking a mouth, anus, or functioning eyes.

The yolk sac is absorbed in 3-4 days and during that period they must reach the ocean, probably the reason why incubation is short as early hatching gives them a better chance of success.

The fact that these gobies are only found in relatively short, steep streams is also thought related to this downstream dispersal.

The larvae initially exist among the plankton in a pelagic form before coming to settle on the substrate within the shallow surf zone.

In one study the pelagic larvae of S. percnopterygionus were found to be transparent and possess an emarginate caudal-fin whereas ‘settled’ larvae (those no longer swimming in the water column) were pigmented.

Interestingly the range of standard length for the pelagic larvae (13.5 – 14.2 mm) was greater than that of settled larvae (12.7 – 13.6 mm).

The pelagic larval duration (PLD) i.e. the length of the larval phase was found to vary between 78 – 146 days and be longer at colder temperatures.

During the annual cool spell between December and April the activity of the gonads reduces considerably in both sexes and the fish probably stop breeding while peak breeding season is June – November.

Once settled on the substrate the larvae begin to lose their temporary specialisations such as the emarginate caudal-fin and begin their journey upstream to join the adults.

They may need to travel several kilometres inland, often over cascades or through stretches of rapidly-flowing water.

The pelvic fins are fused into a disc designed for suction which allow the juveniles to adhere to hard surfaces and climb steep gradients, in some cases even ascending vertical waterfalls with overhanging rocks.

This journey can take several months but the fish are sexually mature within a year and since their natural lifespan is only thought to be around two years are likely to begin spawning soon after, if not immediately, on arrival to the breeding grounds.

Amphidromy in sicydiine gobies isn’t unique to members of Stiphodon and is practised by all other genera.

McDowall (2007) gave a list of potential benefits to fishes employing such a breeding strategy, hypothesising that it may facilitate colonisation of new islands emerging in volcanic areas and/or allow recolonisation of streams following events such as volcanic eruptions/rapid changes in water flow during the wet season.

He also considered that leaving the marine environment can be seen as a trade-off in that since amphidromous gobies are often the only fishes found in their habitats predators are virtually non-existent, but the available food sources are far less diverse than in the ocean.

The ability to graze biofilm appears to be essential for success.

In nature S. alcedo is assumed to breed between the months of October and December on Okinawa island as this was the only period within which nuptial colour pattern was observed in males.

This is a much shorter reproductive season than that seen in the sympatric congener S. percnopterygionus which is reproductively active from May to December.

NotesTop ↑

This species is not in the aquarium trade at time of writing.

It can be told apart from congeners by the following combination of characters: first dorsal-fin with 6 spines and 1 soft ray; second dorsal-fin with 9 soft rays; male with pointed, but not filamentous, first dorsal-fin with spines 4 and 5 elongate; posterior tip of first dorsal-fin normally extending to base of soft rays 2-5 in second dorsal-fin; pectoral-fin rays 15-17 (mode 16); premaxillary teeth 32-40; dentary with 32-45 horizontal teeth;  female with 2 dark lateral stripes with a relatively large space between, lower stripe comprising 8-11 regular blotches, upper stripe thin and pale; all fins of female usually with faint markings; non-nuptial males with a dark lateral stripe below lateral midline, absent in nuptial males; nuptial males with blackish or sometimes orange body, metallic turquoise laterally on head; metallic turquoise spot on upper pectoral-fin base in life; pectoral-fin rays in male often having 1-6 somewhat obscure black spots.

The Gobiidae is the most speciose vertebrate family and notoriously problematic in terms of identifying fishes down to species level.

Stiphodon is often included in the putative subfamily Sicydiinae which currently contains at least six other genera; Cotylopus, Lentipes, Parasicyidium, Sicydium, Sicyopus, and Sicyopterus.

Sicyopus and Lentipes species are omnivorous or carnivorous whereas the others are mostly herbivorous.

All share a similar life-history with many endemic to a particular island or group of islands, though a few are widespread.

They also share some morphological characters including pelvic fins modified into a sucking disc with a strong spine and thickened, highly-branched rays, at the posterior edge of which the pelvic-fin spines and first ray are joined by a membrane forming ‘fleshy pads’ at the tips of the spines.

The tongue is fused to the base of the mouth, a feature shared by some other gobiids.

Following the work of Koumans (1953) Stiphodon was considered a monotypic genus containing only S. elegans for almost half of the twentieth century, despite S. semoni being the original type species, but since the late 1980s a number of species have been described or revalidated.

Over 30 have been described to date with at least a similar number awaiting description (Watson, per. comm.), and while traditionally considered confined to the tropical Indo-Pacific region they’re also found in the eastern Indian Ocean with Sri Lanka representing the known limit of their range.

They can be separated into two generalised groups based on male morphology; those with a first dorsal-fin approximately the same height as the second, e.g., S. atropurpureus, S. semoni, etc., and those in which the first dorsal-fin contains extended, sometimes filamentous spines or rays, e.g., S. percnopterygionus, S. atratus, S. elegans.

Some species also exhibit a patch of white, fatty tissue behind the pectoral-fin in males. The function of this is unknown but it appears to be related to male dominance in some way, with older adults possessing larger patches of tissue (Watson, 2008).

The fused pelvic fins form a structure normally referred to as the pelvic disc, a common feature among gobiids which is used to adhere to rocks and other submerged surfaces.

In Sicyopus and Stiphodon this is short-based and attached to the belly only between the fifth pair of fin rays whereas in other sicydiines it’s attached between all five rays (Watson, 2005).

The role of the disc in ascending waterfalls and cascades has given rise to the common names of ‘rock-climbing’ or ‘cling’ gobies for members of the Sicydiinae in general.

They’re also sometimes referred to as ‘toothed-lip’ gobies in reference to the outwardly-orientated, replaceable teeth of the upper jaw.

Many of those being imported for the aquarium trade have proven difficult to identify for a number of reasons including:

– taxonomic confusion.
– lack of aquarium literature.
– incorrect labelling by exporters and subsequently shops.
– historical over-use of some names.
– likely trade of undescribed species without locality data.
– mixing of species at export facilities.

References

1. Maeda, K., T. Mukai, and K. Tachihara, 2012 - Cybium 35(4): 285-298
   A new species of amphidromous goby, Stiphodon alcedo, from the Ryukyu Archipelago (Gobiidae: Sicydiinae).
2. Keith, P., G. Marquet, and M. Pouilly, 2009 - Publications Scientific du Muséum d'Histoire Naturelle, Paris 31 (3): 471-483
   Stiphodon mele n. sp., a new species of freshwater goby from Vanuatu and New Caledonia (Teleostei, Sicydiinae), and comments about amphidromy and regional dispersion.
3. McDowall, R. M., 2007 - Fish and Fisheries 8(1): 1-13
   On amphidromy, a distinct form of diadromy in aquatic organisms.
4. McDowall, R. M., 2009 - Reviews in Fish Biology and Fisheries 19(1): 1-8
   Early hatch: a strategy for safe downstream larval transport in amphidromous gobies.
5. Parenti, L. R., and K. R. Thomas, 1998 - Journal of Morphology 237(3): 257-274
   Pharyngeal Jaw Morphology and Homology in Sicydiine Gobies (Teleostei: Gobiidae) and Allies.
6. Watson, R. E., 1995 - Ichthyological Exploration of Freshwaters 6(1): 33-48
   Gobies of the genus Stiphodon from French Polynesia, with descriptions of two new species (Teleostei: Gobiidae: Sicydiinae).
7. Watson, R. E., 2008 - Zootaxa 1715: 43-56
   A new species of Stiphodon from southern Sumatra (Pisces: Gobioidei: Sicydiinae).
8. Watson, R. E. and I-S. Chen, 1998 - Aqua, Journal of Ichthyology and Aquatic Biology 3(2): 55-68
   Freshwater gobies of the genus Stiphodon from Japan and Taiwan (Teleostei: Gobiidae: Sicydiini).
9. Watson, R. E. and M. Kottelat, 1995 - Ichthyological Exploration of Freshwaters 6(1): 1-16
   Gobies of the genus Stiphodon from Leyte, Philippines, with descriptions of two new species (Teleostei: Gobiidae: Sicydiinae).
10. Yamasaki, N. and K. Tachihara, 2006 - Icthyological Research 53(1): 13-18
    Reproductive biology and morphology of eggs and larvae of Stiphodon percnopterygionus (Gobiidae: Sicydiinae) collected from Okinawa Island.
11. Yamasaki, N., K. Maeda and K. Tachihara, 2007 - Raffles Bulletin of Zoology Supplement 14: 209-214
    Pelagic larval duration and morphology at recruitment of Stiphodon percnopterygionus (Gobiidae: Sicydiinae).