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.

Based on the samples collected in Chinese scientific surveys off the Costa Rica Dome from July to August in 2009, statolith microstructure of the jumbo flying squid, Dosidicus gigas, was analysed for studying their age, growth and population structure. Three typical growth zones (postnuclear, dark and peripheral zones), abnormal increments (checks) and aberrant microstructure (additional centre and additional rings) were found in the statoliths examined. Squid sizes ranged from 205 to 429 mm dorsal mantle length (ML) with ages no more than 10 months for females and 8 months for males. Back-calculated hatching dates were from November 2008 to April 2009. Growth in ML was best described by a linear function for both the sexes, while growth in body weight was best quantified by an exponential function for females and a power curve for males. The maximum absolute daily growth rates and instantaneous growth rate in ML were reached during 181–210 and 151–180 days for females and males, respectively. The Costa Rica Dome and its adjacent waters were considered as a potential spawning ground because of presence of not only high proportion of mature squid but also rhynchoteuthion paralarvae, and high primary productivity from the strong upwelling. This study suggests that D. gigas have complicated intra-specific population structure and large spatial variability in the key life history parameters.

The jumbo squid Dosidicus gigas is the only ommastrephid commercially caught in Mexico. Despite the economic and ecological importance of this species, little is known about its early life stages. The relationship between the presence of paralarvae and mesoscale oceanic features was investigated for the first time in the central Gulf of California, Mexico in February, April, June and September of 2008. A total of 86 paralarvae were found only in June and September (summer season), in the well-stratified column water where the thermocline was evident and warm sea surface waters (27.7° to 29.4°C) dominated. The greatest abundance of D. gigas paralarvae was observed within 2.23 to 3.48 km of the main front. The mantle length of the smallest paralarvae corresponded with the mantle length at hatching. The San Pedro Mártir Island–Santa Rosalia transect and Santa Rosalia–Guaymas transect were determined as the main hatching localities in June and September respectively. The number of paralarvae found in this study contrast with the potential fecundity of mature females which are found throughout the year.

The jumbo flying squid, Dosidicus gigas, support an important squid fishery off the Exclusive Economic Zone of Chilean waters. However, we only have limited information about their biology. In this study, age, growth and population structure of D. gigas were studied using statoliths from 533 specimens (386 females and 147 males) randomly sampled in the Chinese squid jigging surveys from 2007 to 2008 off the Exclusive Economic Zone of Chile. Mantle lengths (MLs) of the sample ranged from 206 to 702 mm, and their ages were estimated from 150 to 307 days for females and from 127 to 302 days for males. At least two spawning groups were identified, the main spawning peak tended to occur between August and November (austral spring group), and the secondary peak appeared during March to June (austral autumn group). The ML–age relationship was best modelled by a linear function for the austral spring group and a power function for the austral autumn group, and the body weight (BW)–age relationship was best described by an exponential function for both the groups. Instantaneous relative growth rates and absolute growth rates for ML and BW did not differ significantly between the two groups. The growth rate of D. gigas tended to be high at young stages, and then decreased after the sub-adult stage (>180 days old). This study suggests large spatial and temporal variability in key life history parameters of D. gigas, calling for the collection of more data with fine spatial and temporal scales to further improve our understanding of the fishery biology of D. gigas.

The jumbo or Humboldt squid, Dosidicus gigas, is an important fisheries resource and a significant participant in regional ecologies as both predator and prey. It is the largest species in the oceanic squid family Ommastrephidae and has the largest known potential fecundity of any cephalopod, yet little is understood about its reproductive biology. We report the first discovery of a naturally deposited egg mass of Dosidicus gigas, as well as the first spawning of eggs in captivity. The egg mass was found in warm water (25–27°C) at a depth of 16 m and was far larger than the egg masses of any squid species previously reported. Eggs were embedded in a watery, gelatinous matrix and were individually surrounded by a unique envelope external to the chorion. This envelope was present in both wild and captive-spawned egg masses, but it was not present in artificially fertilized eggs. The wild egg mass appeared to be resistant to microbial infection, unlike the incomplete and damaged egg masses spawned in captivity, suggesting that the intact egg mass protects the eggs within. Chorion expansion was also more extensive in the wild egg mass. Hatchling behaviours included proboscis extension, chromatophore activity, and a range of swimming speeds that may allow them to exercise some control over their distribution in the wild.