Christmas tree worms (Serpulidae: Spirobranchus) occur in shallow parts of coral reefs, where they
live as associates of a large number of stony coral species [1,2]. They dwell inside a calcareous tube,
which is usually overgrown by the host coral and partly embedded deep inside the coral skeleton,
except for the tube’s opening and the worm’s operculum [3]. Even if host corals and worm tubes
become overgrown by other invertebrates, the worms continue to grow and are able to keep their tube
openings free [4,5].
Despite their wide distribution, high densities, and the damage these tube-dwelling worms
may cause to corals [6,7], little is known about their natural enemies. They appear well protected
by the tube, which is armed by a long spine on the opening margin. Although they may live up
to 40 years [3], mortality of Spirobranchus worms in dense populations is not uncommon, and most
obvious when their vacated tubes are inhabited by small fish and crustaceans [6,8]. There are a few
reports on attempted feeding of Christmas tree worms by fish and on Spirobranchus remnants found in
fish stomachs ([9], references therein), but no information is available on other predators.
Therefore, it is surprising that a West Atlantic batwing coral crab, Carpilius corallinus Herbst, 1783,
was observed preying on two individuals of Spirobranchus giganteus (Pallas, 1766) during a night dive at
Playa Pabou (1209041.8” N, 06817001.0” W), Kralendijk, Bonaire on 18 October 2020; time 18:45–21:15
(Electronic Supplementary Material). The worms were living in a colony of the scleractinian coral
Porites astreoides Lamarck, 1801, at a depth of 7 m. The crab was using its slender left claw to break away
the thick calcareous tubes of the worms, which resulted in a deposit of limestone debris aside the coral
(Figure 1a). The crab seemed to extract soft parts of the worm from the tube and manipulate them by
using its second pair of pereiopods, which are the first pair of walking legs (Electronic Supplementary
Material). The use of walking legs during feeding is not uncommon in other brachyuran lineages.
Some spider crabs (Majidae) use walking legs to pry and wedge open gastropod and bivalve shells [10]
and box crabs (Calappidae) can be seen to use the first two pairs of walking legs to rotate prey shells
to find an opening for easier access and grip for their specialized right claw (W.d.G. pers. obs.).
During another night dive, two days later, the crab was no longer present but the extent of damage
to the worm tubes and the coral was evident (Figure 1b). The worm in the longest of the two tubes
was gone, while the other worm had survived in a part of the tube that was inside the host coral.
Its operculum appeared lost (Figure 1b).
This observation is interesting because little is known about species predating on Christmas tree
worms (see above), while also hardly anything has been published on the diet of the Batwing coral
crab. Carpilius corallinus is well known for its nocturnal activities [11] and it is the onlyWest Atlantic
member of Carpiliidae, a family of three congeneric species [12]. All three species possess an enlarged
right cheliped (claw-bearing leg), with a blunt molariform tooth found proximally on the cutting edge
of the pollex, which is the fixed ‘finger’ of the claw.
In laboratory conditions in Guam, the Indo-West Pacific species C. convexus (Forskål, 1775) and
C. maculatus (Linnaeus, 1758) have been observed to use their major claw to crush shells of various
species of gastropods [13]. The latter crab species has also been reported as predator of a commercially
important abalone, Haliotis asinina Linnaeus, 1758, in the Philippines [14], and was found in the field
between the remains of freshly-killed gastropods on two separate occasions in Guam [15].
Individuals of the West Atlantic C. corallinus were also found to be feeding on gastropods in
captivity, while they were also fed with sardines [16]. In another case, a female individual in an
aquarium was observed to break apart shells inhabited by hermit crabs in an attempt to remove
them from their homes [11]. Only one published record was found on the diet of C. corallinus in its
natural environment, consisting of Diadema sea urchins [11]. There is also unpublished data concerning
C. corallinus feeding on sea urchins, as well as on a topshell, Calliostoma javanicum (Lamarck, 1822),
all from Bonaire (E.M., pers. obs.).
It seems that information on the diet of Carpilius species is rare, but considering the armor of
previously reported prey species, the crushing of serpulid worm tubes seems to be within their capacity
when they use their right claw. The crab at Bonaire was, however, using its slender left claw to feed
from the worm tube. We do not know if the crab had initially crushed the tube using its specialized
right claw and continued feeding using its left claw, or if the crab initially used its left claw to break
the tube.
The extent of damage on worm tubes is striking (Figure 1). In spite of many dives on Bonaire,
this kind of harm was not reported before. Because Spirobranchus tubes may easily become covered
by coral tissue and algae [3,6,7], it is possible that damaged worm tubes may get unnoticed due
to similar overgrowth. All in all, we do not expect Spirobranchus to be a regular part of the diet
of Carpilius corallinus. The present observation and previously published information suggest that
Carpilius species are not prey specific. More research on the diet and foraging behavior of these
commercially important crab species will teach us more about their role in the food chains of coral reefs.
