Statolith growth increments were analysed in the bigfin reef squid, Sepioteuthis lessoniana lineage B, for estimating the age and growth in the Gulf of Mannar Biosphere Reserve (GOM), southeast coast of India. The identification of S. lessoniana lineage B was determined by mitochondrial cytochrome c oxidase I gene sequence. The statolith increment age analysis indicated that the wild-captured squid population of S. lessoniana in the study area undergoes rapid growth. The age of S. lessoniana in males ranged from 61 (95 mm dorsal mantle length (DML)) to 220 d (390 mm DML), while it was 64 (98 mm DML) to 199 d (340 mm DML) in females. The average daily growth rate in males and females was 1.63 and 1.55 mm DML d−1, respectively. The instantaneous growth rate varied from 0.85 (210 d) to 4.1% (110 d) for males and 0.65 (190 d) to 3.7% (110 d) for females. The age at first maturity was 114 and 120 d for males and females, respectively. Back-calculated hatching dates and the attainment of maturity in females suggested that the reproduction of S. lessoniana is year-round, with two distinct spawning peaks during July–August and February months; accordingly, the hatching dates were spread throughout the year, with the presence of two cohorts. Based on the statolith data, it can be concluded that S. lessoniana lineage B in the GOM has a potential lifespan of up to 7 months. This finding contradicts the previous growth estimates based on length-frequency data, which underestimated the true growth potential of this species.

The strontium-to-calcium ratio (Sr/Ca) in aragonitic shells and statoliths often depends on temperature, and has been investigated for its potential availability as a sclerochronological record of the temperatures experienced during the life of the animal. Only a few cephalopod species have been subjected to rearing experiments to validate the temperature dependence of statolith Sr/Ca despite the strong demand for estimating their historical ecology, particularly of migratory squid populations. In this context, we examined the relationship between temperature and statolith Sr/Ca in the spear squid, Heterololigo bleekeri, by maintaining wild-caught immature individuals at one of three constant temperatures: 12, 14 or 16°C. A portion of statolith precipitated during the experiment was optically identified by daily increment analysis, and then subjected to Sr/Ca measurement using an electron probe micro-analyser. Regression analysis (N = 29) demonstrated the dependence of statolith Sr/Ca on temperature and the relationship was estimated as an equation Y = 9.93 (±0.29) − 0.11 (±0.02) X. However, ~90% of the total residual variance was accounted for by the among-individual variation of statolith Sr/Ca within each temperature group. Consequently, the 95% confidence interval ranged over ± 7.85°C when the temperature was estimated by inserting a Sr/Ca value into this equation. The statolith Sr/Ca values are unlikely to provide reliable estimates for absolute temperatures, but it may allow reconstruction of a time-series of relative temperatures experienced by a particular individual.

Age and growth of the little Indian squid Loliolus hardwickei (Gray, 1849) were studied using samples collected in the coastal waters of Arabian Sea. Statolith increment counts demonstrated that L. hardwickei has a fast growth rate (dorsal mantle length: 0.31–0.73 mm day−1 in females and 0.27–0.56 mm day−1 in males) and a short lifespan of less than 6 months. Females are the larger sex and their daily growth rates were higher than in males. The oldest male and female were 110 and 130 days old; the youngest mature female and male were 62 and 52 days old respectively. The oviducal fecundity ranged from 104–480 eggs, mean = 360 eggs (14–23 eggs g−1 body weight).

Statoliths are nonskeletal calcified structures included in most invertebrates’ gravireceptors. They have been identified and characterized in several gastropod and cephalopod molluscs and have proved to be very useful for age estimation, growth studies, and connectivity analysis, among other applications. Beyond the scarce available records on their occurrence in Class Bivalvia, statoliths are yet to be documented in the grooved carpet shell, Ruditapes decussatus, a species of high ecological and commercial value. An easy method for the extraction and processing of R. decussatus statoliths is described herein. The statolith growth was followed from the initial shell length (SL) of 2.5–3.5 mm (seed commercial size T1.5) for a period of 6 months in a nursery facility located in the Ria de Aveiro (an estuarine system in NW Portugal). The relationship between statolith diameter (StD) and SL follows the function StD=14.305 SL0.254 (N=173; r=0.855, p<0.001). All statoliths observed showed similar morphostructure and general chemistry: hard, translucent spheres of crystalline calcium oxalate (whewellite), with a central nucleus delimited by a growth check of 6.7±1.0 µm in diameter, possibly as a result of growth arrest during metamorphosis, a metamorphic ring, as described for their gastropod counterparts. Subsequent studies should validate this and will involve a search for the occurrence of additional checks that may potentially be present in older specimens and if they are, would open a new range of most promising applications for bivalve statoliths.

The bigfin reef squid Sepioteuthis lessoniana is a neritic species widely distributed in coastal waters of the Indo-Pacific region and is of interest to fisheries for its high commercial value. Squid samples were collected from Keelung (KL) and Penghu (PH), around northern Taiwan from October 2012 to September 2013. A total of 949 squid were examined, and 620 squid were aged using statoliths. The age range of the squid in KL (55–183 days) was similar to that in PH (77–186 days). The squid hatched almost year-round, except in January and December in KL. Two seasonal cohorts were identified: a spring cohort (hatched in March to May) and an autumn cohort (July to October). Concentrations of nine trace elements in statoliths were analysed using solution-based inductively coupled plasma mass spectrometry (ICP-MS). Significant differences in Fe/Ca, Cu/Ca and Sr/Ca were found between the two locations, while significant differences in concentration ratios of Sr/Ca and Ba/Ca were noted between the two seasonal cohorts. Results of a principal component analysis and cluster analysis varied in life-history traits between the two geographic stocks and in elemental concentrations between the two seasonal cohorts. Squid in KL and PH might undertake different migration routes, while seasonal variability in oceanographic conditions was apparent in the two locations.

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.

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.

Through rearing known age individuals and maintaining chemically marked adults in captivity, this study explored the rate of increment formation in southern calamary (Sepioteuthis australis) statoliths over seasonal (summer and winter) and ontogenetic (hatchlings and adults) extremes. A ‘one increment–one day’ relationship was verified for captive-reared hatchlings up to 40 days post-hatching which remained stable across the seasonal extremes. This relationship, however, was not evident in the chemically marked adults as inconsistencies of up to 44 days were detected between the number of days elapsed post-stain and the increment count. No seasonal effect was detected in the ratio between increment count and days elapsed, however, the degree of underestimation was consistently greater for winter-caught adults by approximately 2.5 increments relative to summer-caught adults. This less-than-daily increment formation in adults may be due to: (1) the periodicity of increment formation changing throughout the squid's lifespan; (2) deleterious effects associated with rearing squid in captivity; and/or (3) compromised interpretation of the statolith microstructure as a result of the preparation method.

Growth increments in statoliths of Idiosepius paradoxus were observed for aging analysis. The rate of increment formation was examined by staining the statoliths with tetracycline at 5–14 d intervals. In 6 of 16 specimens, increments formed daily, but in the other specimens, increments formed less than one per day. The maximum number of increments observed in males and females were more than 150 and 140, respectively, suggesting a life span of ≥150 and ≥140 d. During the cool season (from November to April), the dorsal mantle length (DML) and the number of increments gradually increased. Specimens collected in June showed bi-modal patterns in DML and the number of increments. Only small specimens were collected from August to October. These results suggest that two generations alternately occurred in the cool season and in the warm season.

Martialia hyadesi were collected from fishing vessels at the Antarctic Polar Frontal Zone (APFZ) and the Patagonian Shelf Edge (PASE) during the 1989 austral autumn and winter. Squid were measured, weighed, assigned a maturity stage and the paired statoliths were removed. Statolith sections revealed concentric growth rings using light and scanning electron microscopy. Counts of these putative daily micro-growth increments were made directly and by an estimating procedure. Energy dispersive (ED) and wavelength dispersive (WD) x-ray analyses of Sr and Ca content were made on subsamples of statolith sections. Estimated increment counts, which were generally higher than direct counts, were adopted for routine application. Back calculated hatching dates showed that a single cohort, with a relatively narrow size range, was sampled in each geographical area. Back calculations suggested that M. hyadesi at the APFZ had hatched in the austral winter and those at the PASE had hatched in the spring. At the PASE, growth rate was estimated to be some 30% higher than at the APFZ and PASE squid were more mature at a given age. The hypothesis that the Sr:Ca ratio along the growth axis of the statolith contains information on thermal history was examined. Sr:Ca ratios in the statolith fell in the range 0.009–0.017 and varied systematically but this variation did not apparently relate to season and ratios were not significantly different between geographical areas. A consistent feature was a relatively low Sr:Ca ratio at the time of hatching. According to the Sr:Ca thermometer hypothesis this is consistent with spawning in relatively warm water but it could equally be due to depositional differences during early statolith growth. The Sr:Ca thermometer hypothesis could neither be confirmed nor rejected by the data but there is evidence that strontium varies systematically with age in the squid statolith.

The statolith microstructure was studied in 142 females (mantle length, ML, ranging from 77–402 mm) and 119 males (72–328 mm ML) of Martialia hyadesi caught on the Patagonian and Falkland shelves and at the Antarctic Polar Frontal Zone between 1989–94. The statolith microstructure dark zone in this species, contains narrower and more numerous growth increments than the dark zones of other ommastrephid squids. Assuming daily production of putative growth increments within statoliths males live up to 12 months, and females live up to 13 months. It is likely that the life cycle lasts c. 1 yr, but immature squids with ages >330–340 d suggest that a part of M. hyadesi populations could have life span >1 yr. Growth in length was best described by the Gompertz function, whereas growth in weight was best described by the logistic function. M. hyadesi is characterized by slow juvenile growth (<100 mm ML), fast growth of immature squids and a sharp decrease in growth rates during maturation. M. hyadesi mature later (at ages >270 d) than other temperate ommastrephids, but maturation is rather rapid (2–3 months). In the south-west Atlantic, M. hyadesi hatch throughout the year.

In the English Channel, the French cuttlefish landings of the smallest commercial category (body weight < 100 g) indicate that recruitment begins in autumn. Samples of recruits were collected in the Port-en-Bessin (Normandy) fish market once every fortnight from October to December 2000 to determine age-at-recruitment and juvenile growth variability. In addition, pre-recruit samples (mantle length: 53–90 mm) were collected in the Bay of Seine from August. Age was determined by statolith analysis: daily growth increments on the statolith lateral dome were observed under a light microscope. Increments were counted automatically, and manually when necessary, using the image analysis software TNPC. Readable statoliths were obtained in 236 cuttlefish, which revealed changes in age-at-recruitment during the study period. The cohort 2000 is recruited at an age ranging between 2 and 5.5 months (the bulk of recruits are 60–120 d old) and an increasing trend in average age is observed in autumn. The duration of the hatching period was derived from back-calculated hatching dates. A main hatching peak was observed between June and August. Juvenile growth variability was analysed at the individual level and between batches of hatchlings. Growth rates suggest that early hatched individuals grow faster than animals hatched later in the summer.

Morphology of statoliths and anatomy of statocysts were studied in five species of Gonatidae, Moroteuthis robusta (Onychoteuthidae) and Galiteuthis phyllura (Cranchiidae) from the northern Bering Sea, and Todarodes pacificus (Ommastrephidae) from the Pacific waters near Japan. A special experiment was carried out in order to observe statolith mobility on the macula statica and possible endolymph flows within the statocyst in freshly caught gonatid squid Berryteuthis magister. It was found that the statolith may deviate at small acute angles around three axes running through its centre of rotation (located near the spur) without any visual damage of its attachment area to the macula. This finding enabled us to re-consider previous theories and to create a new model of the squid statocyst functioning with the statolith as detector of multidimensional movement. Two types of statolith morphology are distinguished: demersal type statoliths characteristic of near-bottom decapods, and pelagic type statoliths characteristic of all pelagic squids and not dependent on their systematic position. Phylogenetic and ecological features of the statocyst and statolith structure are established. Possible evolutionary trends in development of different types of statocysts in decapods are discussed.