The digestive system of 36 paralarvae and 150 juvenile Dosidicus gigas were analysed to determine the diet. The early life stages were collected in the central and south region of the Gulf of California during different years and ranged in dorsal mantle length (ML) from 2.8 to 120.5 mm. The food content was separated first into identifiable material (IM) and non-identifiable material (NIM). All paralarvae contained only NIM stored mainly in the caecum rather than stomach. Juvenile squid feed on nine different prey types: euphausiids, copepods, amphipods, unidentified crustaceans, fishes, cephalopods, pteropods, bivalves and polychaetes. The IM were found mainly in the stomachs of juveniles with increasing number and diversity of prey in a function of increasing squid body size. In fact, juveniles from 60 to 120 mm ML had high stomach fullness percentages in half full and completely full stomachs suggesting improvement of swimming and hunting behaviour as they grow.

The squid Loligo vulgaris has an extended spawning season within the upwelling system off north-west Portugal, and its paralarvae may thus develop under a wide range of environmental conditions. Both temperature and salinity are expected to affect the metabolism of young squid and we tested their effects on growth during the embryonic and post-hatching phase, based on measurements of growth increments in statoliths of juveniles and adults, using generalized additive models. There was no evidence that statolith increments representing early growth become unreadable in adult statoliths. Variability in the statolith size at hatching was weakly but significantly related to the variables in the model. On the other hand, the effects on statolith growth of both sea surface temperature and of sea bottom temperature were significant during early post-hatching life. Thicker increments are deposited in the statoliths of squid living under higher temperatures, which results in summer hatchers having larger statoliths at the age of 90 days. Inspection of the statolith accretion pattern, using a piecewise linear regression method, revealed an ontogenetic shift in increment width, which may be an indication of the age of transition from paralarva to juvenile. On this basis, it is suggested that the planktonic stage lasts 60 or 90 days, depending on whether the paralarvae lived at higher (>15°C) or lower (<15°C) sea surface temperatures. The life strategy under warmer conditions potentially favours survival by reducing the duration of the vulnerable planktonic phase.

Very little is known about the life history of Robsonella fontaniana. In particular, there are no descriptions of the early life stages that enable correct identification of samples taken from the wild. In this work, eggs and hatchlings are described from egg clutches obtained in the field with brooding females and incubated until hatching. Individual eggs exhibited marked differences in stages of embryonic development within egg clutches or even within a single egg string. For one clutch collected at early stages of embryonic development, embryogenesis took 91 days at 11.5 °C and for a second clutch at intermediate developmental stages it took 68 days at 11 °C and 39 days at 14 °C. For the later clutch the hatching period lasts 25 days at 14 °C. The eggs and paralarvae were small, with an egg length of 3.9–5.2 mm, a dorsal mantle length of 2–3 mm and a total paralarvae length of 3.4–6.0 mm. Chromatophore shape and distribution presented a very distinctive pattern. Characteristics of the eggs, egg strings and paralarvae make it possible to distinguish the early stages of R. fontaniana from those of other octopodid species found off the Atlantic coast of Patagonia.

To understand the mechanisms that influence recruitment of the commercially important chokka squid Loligo vulgaris reynaudii, knowledge of its early life history is required. This paper evaluates the influence of food supply on yolk utilization, metabolism and growth of paralarvae. Eggs collected on the spawning grounds were incubated and the paralarvae reared in the laboratory under “fed” and “starved” conditions for 22 d at 16 ± 1 °C. Some paralarvae lasted 42 d in the laboratory. Mantle length (ML), wet and dry weights (WW and DW) and yolk weight (YW) were measured daily from samples of ~30 (10−51) paralarvae from each group. Yolk weight was estimated using image analysis to determined yolk volume. Three methods (growth model, O2 consumption rates and yolk utilization rates) were used to estimate metabolic rates. Input parameters included daily mean wet weight of paralarvae and temperature. Mean ML, WW, DW and YW at hatching were found to be 2.3 mm, 1.86 mg, 0.45 mg and 0.21 mg, respectively. The experiment revealed that daily yolk utilization rates were 86 and 95% d−1 for fed and starved paralarvae respectively, and that the yolk reserve was almost exhausted 3−4 d after hatching. Starved paralarvae survived for 6 days (with 80% mortality), while fed paralarvae attained a growth rate of 7.8% body WW d−1 over the first 22 days after hatching. Results illustrate that temperatures on the chokka squid spawning grounds allow paralarvae to grow at the fastest rates possible without being subjected to a growth “slow down” caused by a high temperature dependent imbalance between sustaining high metabolic and commitment high feeding rates.

Ommastrephid squids undergo remarkable morphological change during the transition from planktonic paralarvae to adults. These changes are characterized by changes in the relative growth of body dimensions and mark phases and stages in post-embryonic development. The following morphometric characters of paralarval and juvenille Illex argentinus ranging in size from 1–55 mm ML were measured: dorsal mantle length (ML), mantle width (MW), head width (HW), eye diameter (ED), right arm lengths (AIL) (AIIL) (AIIIL) (AIVL), proboscis length (PL), proboscis division (PD), fin length (FL), fin width (FW), right tentacle length (TL), club length (CIL), dactylus length (DL) and carpus + manus length (CML). The relative growth of AIL, AIIL, AIIIL, HW and ED, showed discontinuities at c. 14 mm ML, while AIL, AIIL, AIIIL, AIVL, FL, and TL showed other discontinuities at c. 28 mm ML. These discontinuities seem to be related to the activity and ability of the animal to obtain food and survive in different environments. At an early phase (1–14 mm ML), there is a rapid development of the arms, suckers and fins. In the second stage (14–28 mm ML) there is a rapid development of the tentacles and clubs. In the third (>28 mm ML), the juvenile grows more in length in relation to other body parts. No morphological change, besides the proboscis division, takes place at the end of rhynchoteuthion stage. This may indicate the necessity for re-evaluation of the paralarval phase in Ommastrephidae.