Adaptive spatial utilization of host mussels by the Japanese rosy bitterling Rhodeus ocellatus kurumeus

The spatial pattern of resource utilization for oviposition in the Japanese rosy bitterling Rhodeus ocellatus kurumeus was investigated in two field experiments. The distribution of rosy bitterling eggs deposited in the four demibranchs of the gills of the test mussel species, Anodonta woodiana , differed with mussel reproductive state in pair spawnings, but not in group spawnings. In pair spawnings, female rosy bitterling may have had more time to select the site of oviposition in the gill in relation to the sex and reproductive state of the mussel, thereby maximizing embryo survival. Thus, the inner gill of female mussels may have been selected in preference to the outer gills to avoid mortalities of eggs due to the presence of the mussel's own embryos (glochidia) in the outer gill chambers. In male mussels, female rosy bitterling distributed their eggs equally among all parts of the mussel gill, thereby minimizing density-dependent mortality of embryos. During group spawnings, however, female rosy bitterling may have been more constrained in their decision making, ovipositing in the inner gills irrespective of mussel sex.     

Factors affecting seasonal mortality of rosy bitterling (Rhodeus ocellatus kurumeus) embryos on the gills of their host mussel

I investigated the seasonal change in factors affecting embryonic mortality in the rosy bitterling, Rhodeus ocellatus kurumeus, a freshwater fish that spawns on the gills of living unionid mussels. Research was conducted in a small pond during 1999 and 2001 in which bitterling were provided with Anodonta sp. mussels for spawning. Bitterling spawned between April and July, peaking mid–late May. Seasonal survival rate of bitterling embryos in their mussel hosts was unimodal, with a peak between late April and mid May (about 70% of total spawnings). In mid April, survival was about 50%. The lowest survival was from late May to July (0%). Losses of bitterling embryos from mussels were identified by ejections from the mussel host. Ejections were categorized as either ejections of live embryos, or ejections of embryos that died in the mussel and were subsequently expelled from the mussel. Ejection rates of live embryos were higher in the earlier part of the spawning period (early–mid April) and dead embryo ejections in the later period (after June). The ejection rate of live embryos was higher among younger embryos earlier in the season, probably because of the incomplete development of morphological and behavioural traits associated with maintaining the embryo inside the mussel gill chambers, and as a consequence of a more protracted developmental period at low temperatures making them more susceptible to ejection. The ejection rate of dead embryos was higher in older embryos later in the season, and in larger mussels and at high embryo densities. The survival of embryos in mussels was probably related to oxygen availability, with mortalities probably caused by asphyxiation. Increased embryo mortalities may arise through competition among embryos, between embryos and mussel, and ambient dissolved oxygen levels. The optimal period for bitterling to spawn may represent a balance between two opposing factors; with positive and negative effects of a seasonal rise in temperature directly affecting embryonic growth rate and oxygen availability.An erratum to this article can be found at This revised version was published online January 2005 with the correction of the authors name.     

Histological structure of the female gonads and ovipositor of the European bitterling,Rhodeus amarus (Bloch, 1782) (Cyprinidae: Acheilognathinae)

We investigated the histological structure of the female gonads and ovipositor of the European bitterling, Rhodeus amarus. The base of the ovipositor was formed by the conical organ or ‘eminence’. Based on the structure of the conical organ, including a special distribution of collagenous and muscular fibrils, a well‐developed vascular system and numerous scyphoid mucous cells in the internal epithelium, this organ was used for temporary storage of oocytes during the spawning period and for their movement along the ovipositor. An extensive network of blood vessels, muscular fibrils and numerous collagenous fibrils in the connective tissue of the ovipositor may make a functional contribution to the ovipositor by making it firmer during egg laying. Mucous cells were detected in the medial and distal regions of the ovipositor, which may play a role in facilitating insertion of the ovipositor into the exhalant siphon of a mussel during oviposition. European bitterling are batch spawners, and the female spawns eggs in clutches at intervals during the breeding season, which were visible as three distinct cohorts of oocytes in the ovary.     

Timing of juvenile emergence from host mussels in the Japanese rosy bitterling, <Emphasis Type="Italic">Rhodeus ocellatus kurumeus</Emphasis>

The diel rhythm of juvenile emergence from host mussels in the Japanese rosy bitterling, Rhodeus ocellatus kurumeus, was investigated in a small pond in Osaka prefecture, Japan. The emergence of juvenile bitterling from host mussels occurred principally at night, with a peak in the early part of the night. The pattern of juvenile bitterling emergence was discussed in the context of an adaptive response to diurnal predation.     

Minute tubercles in bitterling larvae: Developmental dynamic structures to prevent premature ejection by host mussels

1. Bitterlings are small freshwater fish that use long ovipositors to lay eggs in host mussels, and they have morphological adaptations to increase larval survival. The most well‐known adaptation is the minute tubercles on the skin surface of larvae; they are developed in early‐stage larvae with weak swimming ability and disappear in free‐swimming larvae before they leave the host mussel.
2. In the present study, I comprehensively analyzed the developmental stages of Rhodeus pseudosericeus larvae, their morphological and physiological characteristics, their migration inside mussels, and the development of minute tubercle in order to elucidate the morphological function of the minute tubercles. These tubercles began to develop 1 day after hatching (formation stage), grew for 2–5 days (growth stage), reached the peak height after 6–7 days (peak stage), abruptly reduced in height after 8–10 days (abrupt reduction stage), and gradually reduced in height (reduction stage) until completely disappearing 27 days after hatching (disappearance stage).
3. The larvae remained in the mussels’ interlamellar space of the gill demibranchs until 10 days after hatching and began to migrate to the suprabranchial cavity 11 days after hatching. At this time, the larvae had a heart rate and the caudal fin began to develop. At 24 days after hatching, the minute tubercles had almost disappeared, and some individuals were observed swimming out of the mussels.
4. The results presented herein elucidate that the minute tubercles are the developmental dynamic structures that the bitterling larvae have morphologically adapted to prevent premature ejection from the mussel.