Shell growth of the razor clam Ensis siliqua (Mollusca: Bivalvia) from southern Portugal has been analysed using both surface growth rings and internal shell microgrowth patterns. The growth rate estimated from an analysis of the growth rings is slower (von Bertalanffy growth, constant K=0·27) than that determined from the annual narrowing of the internal microgrowth patterns present in shell sections (K=0·65), although both methods predict a similar asymptotic length, L∞, of 144·8 and 139·6 mm, respectively.

The Barrinha razor clam population occurs in a heavily dredged area and an analysis of shell sections reveals the presence of a series of shell margin breaks consisting of deep clefts in the outer shell layer in which sand grains are embedded. It is suggested that these disturbances to shell growth are the result of repeated dredge damage. The frequency of the clefts increases with the size and age of the razor clams, and thus the shells provide a record of the intensity and frequency of unsuccessful capture or retrieval attempts. Cleft formation also occurred seasonally with the deposition of a small cleft during June, but these annual clefts were much less pronounced than those caused by dredge damage.

Annual reproductive cycles of two commercially important bivalves, the razor clam Ensis siliqua and the clam Venus striatula were investigated. Specimens of both species were sampled monthly from a site off Vilamoura, south of Portugal, between June 1992 and May 1993. Gonadal development was monitored using standard histological methods. Observed gametogenic progression was categorized by six stages: (0) inactive; (I) early active gametogenesis; (II) late active gametogenesis; (HI) ripe; (IV) partially spawned; and (V) spent. Both males and females showed a synchronism in gonadal development. The gametogenesis in the razor clam began in December and by late April the gonads were characterized morphologically by an abundance of ripe eggs and sperm. Partially spawned individuals were first encountered in May. All were spent by July. The gametogenic activity in V. striatula began in the months of October/November and continued until March. Spawning occurred between April and early August. Both species reached maturity during the first year of life.

The gametogenic cycle of the smooth clam Callista chione off the Arrábida region was studied throughout a 17-month period (from January 2004 to May 2005) using standard histological techniques, mean oocyte diameters and a condition index. This species showed a synchronism between sexes both in terms of gametogenic development and spawning. The results indicated that sex-ratio was not significantly different from parity. In January 2004, the gametogenic cycle had already begun and ended in late October 2004. Three spawning peaks were detected: January–March, April–May and August–October. No resting period was observed and a new gametogenic cycle began in early November, immediately after the spawning period. The analysis of the oocyte diameter enabled predicting the main spawning periods, which appear to be largely governed by seawater temperature. The condition index evolved according to the reproductive cycle of the species, with the highest values being observed prior to the main spawning periods. The size at first maturity estimated for C. chione was 50.81 mm.

The effect of dredging on bottom structure was assessed, to estimate the damage inflicted on the benthic macrofauna left on the dredge path and to evaluate aggregations of scavengers within the track. Sediment suspended during dredging rapidly resettled both on sand and sandy-mud bottoms. Dredge tracks were deeper on sandy-mud sediments and persisted longer than in sandy sediments. The disappearance of tracks in both sediment types depended both on current strength and wave action. Damage and mortality induced by dredging on the macrobenthic animals left on the dredge path was relatively low. Post-fishing SCUBA diver observations showed that damaged animals left on the dredge path rapidly attracted scavengers, mainly Ophiura albida. Immediately after the tow ophiuroids reached densities eight times greater in the track region than in the background. However, they dispersed again rapidly because only few damaged fauna were available on the dredge tracks. Undamaged or slightly damaged shellfish started to rebury immediately after escaping from the dredge.

An experiment was carried out to estimate the rate of indirect fishing mortality on juvenile Spisula solida due to the exposure time on deck. Samples were collected using a dredge from a site off Vilamoura, south coast of Portugal, during July 1994. Length of deck exposure is directly related to mortality of juveniles. It was estimated a fishing mortality rate of 0.00335 per min, due to length of exposure.

Seasonal variations in reproductive cycle of Spisula solida were studied between June 1995 and June 1996 at a site off Vilamoura, southern Portugal. Sex ratio was found to be in favour of males. Both males and females showed a synchronism in gonadal development and spawning. Gametogenic activity started with decreasing temperature at the beginning of autumn. The onset of spawning took place in February when the seawater temperature began to increase. Spawning ended in May. It is possible that the white clam does not spawn at a definite temperature, rather responding to the increase in seawater temperature. Between June and September, the specimens were found to be in the resting stage and the condition index increased, probably due to the accumulation of reserves. Spisula solida reached maturity during the first year of life.