Advances in methods for determining fecundity: application of the new methods to some marine fishes

Estimation of individual egg production (realized fecundity) is a key step either to understand the stock and recruit relationship or to carry out fisheries-independent assessment of spawning stock biomass using egg production methods. Many fish are highly fecund and their ovaries may weigh over a kilogram; therefore the work time can be consuming and require large quantities of toxic fixative. Recently it has been shown for Atlantic cod (Gadus morhua) that image analysis can automate fecundity determination using a power equation that links follicles per gram ovary to the mean vitellogenic follicular diameter (the autodiametric method). In this article we demonstrate the precision of the autodiametric method applied to a range of species with different spawning strategies during maturation and spawning. A new method using a solid displacement pipette to remove quantitative fecundity samples (25, 50, 100, and 200 milligram [mg]) is evaluated, as are the underlying assumptions to effectively fix and subsample the ovary. Finally, we demonstrate the interpretation of dispersed formaldehyde-fixed ovarian samples (whole mounts) to assess the presence of atretic and postovulatory follicles to replace labor intensive histology. These results can be used to estimate down regulation (production of atretic follicles) of fecundity during maturation

Advances in methods for determining fecundity: application of the new methods to some marine fishes

17 pages, 9 figures, 6 tables.Estimation of individual egg production (realized fecundity) is a key step either to understand the stock and recruit relationship or to carry out fisheries-independent assessment of spawning stock biomass using egg production methods. Many f ish are highly fecund and their ovaries may weigh over a kilogram; therefore the work time can be consuming and require large quantities of toxic fixative. Recently it has been shown for Atlantic cod (Gadus morhua) that image analysis can automate fecundity determination using a power equation that links follicles per gram ovary to the mean vitellogenic follicular diameter (the autodiametric method). In this article we demonstrate the precision of the autodiametric method applied to a range of species with different spawning strategies during maturation and spawning. A new method using a solid displacement pipette to remove quantitative fecundity samples (25, 50, 100, and 200 milligram [mg]) is evaluated, as are the underlying assumptions to effectively fix and subsample the ovary. Finally, we demonstrate the interpretation of dispersed formaldehyde-fixed ovarian samples (whole mounts) to assess the presence of atretic and postovulatory follicles to replace labor intensive histology. These results can be used to estimate down regulation (production of atretic follicles) of fecundity during maturation.T his study was jointly funded under Eu ropean Union Frame Work V Q5RS -2002 - 01825 and the Institutes in England (Department of the Environment, Food, and Rural Affairs), Norway (Institute of Marine Research), and Spain (Consejo Superior de Investigaciones Científ icas, and A ZTI Tecnalia (publication number 424))Peer reviewe

Report of the working group on modern approaches to assess maturity and fecundity of warm- and coldwater fish and squids

A workshop was held in Bergen in September 2001 to improve the overall quality of reproduction data used in assessments of marine stocks and egg production surveys by reviewing 1) present practices and 2) establishing a new standard for routine measurements. The selected participants came from different parts of the world and had a broad and varied background in applied reproductive biology. A Plenary Document with specific recommendations is included along with the 15 papers covering both methodological and species-specific aspects. NORSK SAMMENDRAG: Et internasjonalt møte med fokus på hvordan en skal forbedre de reproduksjonsbiologiske dataene som brukes innenfor bestandsvurdering av marine ressursene samt innenfor eggsurvey ble arrangert i Bergen i september 2001. Målet var å vurdere 1) dagens praksis, og 2) lage nye protokoller for pågående undersøkelser. De inviterte deltagerne kom fra ulike deler av verden og hadde en svært variert arbeidsbakgrunn innenfor anvendt reproduksjonsbiologi. Rapporten inneholder et felles dokument med spesifikke anbefalinger, samt 15 artikler som dekker både metodiske forhold og informasjon for den enkelte art

The fate of vitellogenic follicles in experimentally monitored Atlantic cod Gadus morhua (L.): Application to stock assessment

In this paper we report on the fate of vitellogenic follicles (VF) as either alpha atretic follicles (αF) or post-ovulatory follicles (POFs) using histology and captive Atlantic cod (Gadus morhua) in three experiments. In Experiment 1 the production and persistence of αF was determined by taking repeated biopsy samples from tagged females held in temperature regimes (mean ± SD) controlled at 4.5 (0.3) and 8.1 (0.3) °C. The αF lasted (mean ± 2 SE, n) 5.3 days (2.5, 8) and 9.7 days (4.9, 8) in the warmer and cooler water respectively and the combined average was 7.5 days (2.9, 16). In Experiment 2 we took biopsy samples at intervals and monitored egg production from individual females accompanied by a male and used the stage of egg development to age POFs found in the biopsy samples. The females, some immature, were killed at intervals, up to 45 days post-spawning, and then the biopsy and ovary samples were stained by periodic acid Schiffs’ reagent to prepare descriptions of POFs aged from 11 h to 45 days old. Spent female ovaries contained POFs, and a thicker ovarian wall (tunica) exceeding 0.34 mm whilst immature fish lacked POFs and their ovary tunica was thinner (less than 0.15 mm). In Experiment 3 the persistence of POFs was monitored in a simulated North Sea (10–16.1 °C) and Barents Sea (7.5–11.2 °C) regime using ovary sections stained by periodic acid Schiffs’ reagent. In both regimes the POFs regressed at a temperature sensitive rate during the experiment lasting 104 days. Some αF from large VF persisted longer than expected (more than 4 months after spawning) and were called cysts based on their appearance and greater expected lifetime. These histological characteristics were successfully applied to assess maturity of wild cod caught on surveys in the North and Barents Seas after an assumed 150 and 310 days, respectively, after the spawning season. Taken together this article presents reliable figures on the lifetime of atretic and post-ovulatory follicles as well as variation in ovarian thickness with spawning experience, which will be most useful input in the further work to assess reproductive potential

The application of tank experiments to the study of reproductive potential in teleosts using Gadus morhua as a test model

Age-based population assessments (VPA) have often failed to show a clear relationship between spawning stock biomass and either recruitment or biomass estimated from annual egg production. Recent work has shown that the inclusion of reproductive potential (a measurement of both the quality and quantity of eggs produced in relation to female size and age) helps to explain some of the variation in the stock and recruitment curve. Tank experiments will make it possible to develop tools to measure reproductive potential either directly from fecundity or indirectly from maternal reserves. This paper describes such experiments involving first year maturing cod (Gadus morhua), in which egg production has been studied in relation to maternal reserves. Ovary biopsy samples were taken from the start until the end of spawning when the fish were killed in order to study the persistence of postovulatory and atretic follicles (the latter are oocytes that are resorbed during the vitellogenic phase) using histological methods. These results were examined to suggest ways to improve the detection of post spawning females (which is essential when making field assessments of maturity). Using this data it was also possible to quantify atresia in relation to the egg production cycle

Determinacy of fecundity and oocyte atresia in sole (

Changes in the morphology of the ovary are described during maturation and it is established that it is a homogeneous structure for sampling purposes at maturity stages four and five. Several aspects of vitellogenic oocyte growth and recruitement were examined as criteria to ascertain whether the annual fecundity can be determined in Solea solea just prior to spawning. The first criterion was whether a hiatus develops in the size frequency distribution between the previtellogenic and vitellogenic oocytes just prior to spawning. We were unable to demonstrate this feature in sole from division VIId (N = 5) or IVc (N = 5) but it was present in two out of five fish from division VIIe and all fish examined from division VIIa (N = 5) and IVb west (N = 5). The hiates occurred between 175 and 250 µm (cohort size 25 m) in the size frequency distribution and measured between 25 and 75 µm. Oocyte size frequency distribution from mid spawning and late spawning-spent sole from division IVc showed a hiatus in 9 out of 10 fish which became wider as the residual annual potential fecundity declined. Next the rate of recruitment and growth of vitellogenic oocytes was studied in sole sampled at monthly intervals (July 1993 to February 1994) from division VIId in relation to the start and duration of the annual spawning season. The growth rate of the leading oocyte cohort was 2.73 × 10−5 mm3 per day on 20 September and increased to 3.91 × 10−3 at a mean diameter of 839 µm by 10 February just prior to spawning. However, the observed maximum growth rate, even when adjusted for the positive influence of temperature, allowed little scope for previtellogenic oocytes to complete maturation during a spawning period of 60 days. The recruitment of viltellogenic oocytes was 3013 oocytes per day on 3 August and declined rapidly as spawning approached. In the three months prior to spawning no significant increase was found in the annual potential fecundity. An analysis of a sample of spawning fish from IVc demonstrated that 88% had less than 50% of their predicted potential fecundity remaining in the ovary. The mean batch fecundity was 8 400 (SE ± 13 363) and in conjunction with existing data on spawning frequency and duration gave a realised fecundity close to the potential fecundity. It is concluded that for all practical purposes the sole can be regarded as having a determinate fecundity in all the areas studied. The regulation of potential fecundity by follicular atresia was assessed in pre-spawning and spawning sole. In ICES areas IV and VII the prevalence of atretic oocytes in pre-spawning fish varied between 0.04 and 0.69 and the relative intensity varied between 0.017 and 0.076. During spawning in division IVc the prevalence of atresia varied between 0.45 and 0.57 and the relative intensity between 0.022 and 0.058. If we assume a turnover rate of 9 days the loss from the potential annual fecundity, during spawning, in division IVc would be 12.4%

Method development and evaluation of stock reproductive potential of marine fish

28 páginas, 2 figurasWe are grateful to the EU Commission for supporting the RASER project, several agencies for providing collateral funds, as well the four institutes, IMR, AZTI, CSIC and Cefas for being actively involvedPeer reviewe

Fecundity and growth of Atlantic cod (Gadus morhua L.) along a latitudinal gradient

Some fish species have wide distribution areas that span very different habitats. In this investigation we have studied Atlantic cod (Gadus morhua), which is an example of such a species, to demonstrate how this may have caused adaptations to key features such as fecundity, growth and age and size at first spawning. We have studied cod from the Barents Sea, Icelandic waters, North Sea and Irish Sea. The ovary sampling was undertaken over several years, however, not always sequentially, in order to assess whether the relationships between fecundity and other key features were constant or variable. Also, we compared historical maturity ogives and growth from the different regions. There was a clear pattern with fish maturing at a greater age and size in the north compared to the south. For three of the four cod stocks we demonstrated a significant reduction in relative potential fecundity as maturity progressed towards spawning, i.e., as the mean diameter of vitellogenic follicles increased. To be able to compare potential fecundity in a standardised way both in time and space, we constructed models that included mean diameter as one of the independent variables. Our potential fecundity comparisons clearly indicated a north-south gradient with increasing size-specific fecundity towards the south. The higher fecundity of the fish in the south could only partly be explained by the higher condition and temperature that was observed in these waters