Capitulum mitella is a tropical/sub-tropical intertidal barnacle of high economic value. However, no studies have yet focused on the effects of the extrinsic and intrinsic factors that affect the metamorphosis of this species. The current study stored cyprids at room temperature (24–26°C) and low temperature (7°C) and then compared the effects of age and storage temperature on cyprid metamorphosis. The effects of salinity and temperature on cyprid metamorphosis and survival were examined. Results showed the following. (1) Young 0-day cyprids were not competent to metamorphose, and C. mitella cyprids had a pre-competent phase. (2) The cyprid metamorphosis percentage at different storage temperatures with the same age was higher at room temperature than at 7°C. Low temperature storage of cyprids appeared to be unsuitable for C. mitella. The ideal storage time at room temperature for cyprids was 3–5 days. (3) The cyprids could complete metamorphosis at a salinity range of 20–45 mg l−1, and the optimum salinity range for metamorphosis was 25–35 mg l−1. At 15 mg l−1 salinity, the cyprids could survive but failed to metamorphose. (4) The cyprids could survive and complete metamorphosis at 18–36°C, and the optimum temperature range for metamorphosis was 21–33°C. The metamorphosis of C. mitella cyprids can tolerate a wide spectrum of salinity and temperature, which is related to the distribution location, habitat environment and lifestyle. Results of this study may provide a basis for the settlement biology, recruitment ecology and aquaculture of this species.

In this paper, metamorphosis of laboratory-reared cyprids of the pedunculate cirripede, Capitulum mitella was successfully induced. A timeline and a detailed description of morphological events during metamorphosis were derived from light microscopy and scanning electron microscopy analyses. The metamorphic process of cyprids involves five main events. (1) Triggering of metamorphosis: after 0–6 h of reagent exposure, the epidermis ventral to the compound eyes gradually invaginates. (2) Invagination and separation of epidermis: after 6–36 h, the invagination bypasses the compound eyes, the cypris epidermis separates slightly from the carapace and the nauplius eye gradually migrates ventrally. (3) Formation of juvenile rudiment: after 36–72 h, the metamorphosing specimen shape slightly resembles that of a juvenile. (4) Shedding of thoracopodal exuvium: after 72–96 h, the cyprid finally sheds the thoracopodal exuvium and metamorphoses into a juvenile barnacle. (5) Early development of juvenile barnacle: the juvenile shed the cirrum cuticle for the first, second, third and fourth time at 1.5–2, 1.5–2, 4–5 and 5–6 days, respectively. The newly formed juvenile completely assumes the shape and armature of all shell-plates found in adult barnacle. Rostro-carnal length of the juvenile is 240–260 μm. Tergum, scutum and upper latus are paired, and carina and rostrum are unpaired. Uniform circular depressions are dispersed on the surface of the tergum, scutum and carina. The rostrum and upper latus, which have the shape of small triangle, are not clear. The entire surface of the peduncle is covered with convoluted cuticular ridges. The metamorphosis of C. mitella is similar to that of Lepas.

Adult specimens of Capitulum mitella were collected in August 2011 in the intertidal zone of Dinghai, Fuzhou, Fujian, China (26°16′N 119°48′E). The morphology of the cypris larva reared under our conditions was determined using scanning electron microscopy (SEM). Special emphasis was given to the carapace, lattice organs, antennules, thoracopods and furcal rami. The whole carapace surface is sculptured by slender ridges demarcating rectangular or irregular polygonal areas with very fine pores. The cyprid possesses five pairs of lattice organs, arranged as two anterior and three posterior pairs. The second segment carries a preaxial seta 2 and a postaxial seta 2. The third segment carries a postaxial seta 3 outside the attachment disc, whereas a postaxial disc seta, an axial disc seta and two radial disc setae are located inside the attachment disc. The attachment disc is somewhat bell shaped. A series of slender cuticular flaps forms a distinct ‘velum’ around the base of the disc. The fourth segment carries four subterminal setae and five terminal setae. The cyprid bears six pairs of biramous natatory thoracopods consisting of a protopod (coxa + basis), a two-segmented exopod and a two-segmented endopod. The cyprid possesses a rudimentary abdomen and an almost completely cleaved telson with a pair of one-segmented furcal rami. The morphology and setation of the antennules of C. mitella resemble those of Balanus amphitrite (=Amphibalanus amphitrite) and Megabalanus rosa, but differ in some morphological details.