Anguilla anguilla |
About 0.6 ± 0.28 for the yellow stage and 1.78 ± for the silver stage |
0.6 |
Acou et al, 2003 |
Anguilla anguilla |
> 1.4% for the silver stage |
1.4 |
Marchelidon et al, 1999 |
Aphanius iberus |
From September to February |
6.0 |
Vargas and De Sostoa, 1997 |
Valencia hispanica |
One period of quiescence: August to December |
6.0 |
Caiola et al, 2001 |
Barbatula barbatula |
1 [Short] |
1.0 |
Skryabin, 1993 |
Barbatula barbatula |
1 [Short] |
1.0 |
Saat et al, 2003 |
Barbatula barbatula |
2.8± 0.43 [After spawning in May] |
2.8 |
Skryabin, 1993 |
Barbatula barbatula |
2-8 [In July and beginning of August] |
5.0 |
Saat et al, 2003 |
Barbatula barbatula |
From July to August, the GSI ranges between 3 and 20%, the higher values being largely late-spawners or non-spawners |
3.0 |
Smyly, 1955 |
Cobitis taenia |
Reduction in weight between June and september |
2.0 |
Robotham, 1981 |
Cobitis taenia |
Decrease between August and November |
5.0 |
Marconato and Rasotto, 1989 |
Cobitis taenia |
A phase or relative quiescence in gonad development follows preceeding until the next spring [From July to May] |
12.0 |
Vaino and Saat, 2003 |
Cobitis taenia |
3-6 [In late July] |
4.5 |
Vaino and Saat, 2003 |
Cobitis paludica |
A period of quiescence of 3 month [September-November] |
3.0 |
Oliva-Paterna et al, 2002 |
Blicca bjoerkna |
Relatively long period |
0.0 |
Rinchard et al, 1996 |
Blicca bjoerkna |
About 5 [July until the next spring] |
5.0 |
Rinchard and Kestemont, 1996 |
Blicca bjoerkna |
The ovary of the white bream enters a period of tranquillity between November and March |
5.0 |
Lefler et al, 2008 |
Abramis brama |
About one month |
0.0 |
Witkowski et al, 1989 |
Abramis brama |
The minimum values are found in June and July, which corresponds to a resting period of gonads after spawning |
3.0 |
Kompowski, 1982 |
Abramis brama |
GSI decreases after spawning to 0.88-3.1% in females with single batch spawning, and to 4.6-6.2% in females spawning in batches. In the latter females, the ovary reaches 10-16.3% of body weight again within 14-30 days |
1.99 |
Brylinska and Boron, 2004 |
Alburnoides bipunctatus |
1 [Short in August] |
1.0 |
Yildirim et al, 1999 |
Alburnoides bipunctatus |
Spirlin collected after the spawning season (i.e. in July and especially in August) demosntrated different characteristics compared to those sampled during the spawning season. In July, 3 out of 5 fish ovaries still contained yolked oocytes, however, one female was likely to release one more spawning batch, whereas others appeared undergoing atretic process [...] In August, virtually none of the ovaries analyzed contained yolked oocytes, and the mean diameter was even 0.48 mm lower than that of sample from June 25 [...] |
3.0 |
Polacik and Kovac, 2006 |
Alburnoides bipunctatus |
2.5 ± 0.8 [n=5] |
2.5 |
Yildirim et al, 1999 |
Alburnus alburnus |
Relatively long period |
0.0 |
Rinchard et al, 1996 |
Alburnus alburnus |
>2 (August) |
2.0 |
Rinchard and Kestemont, 1996 |
Aspius aspius |
3-3.5 [Between Mid-May until end of August] |
3.25 |
Shikhshabekov, 1979 |
Aspius aspius |
1.61 [Between May to August] |
1.61 |
Kompowski et Neja, 2004 |
Aspius aspius |
1.1 |
1.1 |
Shikhshabekov, 1979 |
Aspius aspius |
In April, the average female GSI fell to 1.77, which indicates that the majority of the studied fish had already spawned. In May the female GSI value was even lower at 1.04. During the fall from September to November, the average GSI value rose sharply to a level close to that seen in the pre-spawning period. |
1.77 |
Kompowski et Neja, 2004 |
Barbus barbus |
There seems to be a two-month quiescent period (July-August) |
3.0 |
Lobon-Cervia and Fernandez-Delgado, 1984 |
Barbus barbus |
Following early spring spawning oocytes in the stage of primary growth are in majority in the ovary. Mitotically dividing oogonia, non-ovulated oocytes and eggs that were not released during spawning are also present in the ovaries. The latter two groups of cells undergo the process of resorption. Continuous atresia is also in process in the ovary that affects primarily the least developed functioning oocytes during the post-spawning period, i.e., those in the stage of primary growth. In all probability their number will further decrease immediatly after the spawning season |
4.0 |
Lefler et al, 2008 |
Barbus barbus |
As vitellogenesis in the barbel does not stop in winter months, the number of oocytes in the stage of vitellogenesis in samples collected in December reaches that of cells in the stage of cortical alveoli |
5.0 |
Lefler et al, 2008 |
Carassius auratus |
August |
2.0 |
Kobayashi et al, 1986 |
Carassius auratus |
1.0 ± [August] |
1.0 |
Kobayashi et al, 1986 |
Chondrostoma nasus |
Following early spring spawning oocytes in the stage of primary growth are in majority in the ovary. Mitotically dividing oogonia, non-ovulated oocytes and eggs that were not released during spawning are also present in the ovaries. The latter two groups of cells undergo the process of resorption. Continuous atresia is also in process in the ovary that affects primarily the least developed functioning oocytes during the post-spawning period, i.e., those in the stage of primary growth. In all probability their number will further decrease immediatly after the spawning season |
4.0 |
Lefler et al, 2008 |
Cyprinus carpio |
Few weeks after spawning |
0.0 |
Bieniarz et al, 1978 |
Cyprinus carpio |
About two months [June-July] |
3.0 |
Yaron and Levavi-Zermonsky, 1986 |
Cyprinus carpio |
About 5% in December-January |
5.0 |
Smith and Walker, 2004 |
Cyprinus carpio |
Almost 0 [July] |
2.0 |
Yaron and Levavi-Zermonsky, 1986 |
Cyprinus carpio |
Post-spawning period: June-August |
3.0 |
Bieniarz et al, 1979 |
Cyprinus carpio |
July and august are a quiescent period of gonadal activity; a stage of regeneration |
2.0 |
Crivelli, 1981 |
Cyprinus carpio |
Re-maturation of the ovaries requires > 3-4 months |
3.5 |
Smith, 2004 |
Gobio gobio |
1-2 [August-September] |
1.5 |
Kestemont, 1987 |
Gobio gobio |
2-3 [From July through September] |
2.5 |
Rinchard et al, 1993 |
Gobio gobio |
< 3.10 ± 1.53 (July-August-September] |
3.1 |
Rinchard et al, 1993 |
Gobio gobio |
About 3% [August, September] |
3.0 |
Kestemont, 1987 |
Gobio gobio |
From July, the ovary started a recovery phase and only contained stage 1 and 2 ooctyes. One ot two months of quiscence following summer spawning |
1.0 |
Kestemont, 1990 |
Leuciscus cephalus |
July, August |
3.0 |
Unlu and Balci, 1993 |
Leuciscus cephalus |
< 0.5 from July until December |
7.0 |
Kalkan et al, 2005 |
Leuciscus cephalus |
June-September quiescent period, About 1% |
1.0 |
Mann, 1976 |
Leuciscus cephalus |
<1% [From May to September] |
1.0 |
Sasi, 2003 |
Leuciscus cephalus |
Gonads of chub females and males after spawning remain in a resting state until September. |
2.0 |
Zelepien, 1997 |
Leuciscus cephalus |
In June, the GSI diminished because of spawning and continued to do so to the end of July |
3.0 |
Erdogan et al, 2002 |
Leuciscus leuciscus |
< 0.2% [From April to mid-July] |
5.0 |
Mann, 1974 |
Phoxinus phoxinus |
August |
2.0 |
Scott, 1979 |
Phoxinus phoxinus |
2% [August] |
2.0 |
Scott, 1979 |
Phoxinus phoxinus |
Very little growth takes place through the summer months |
4.0 |
Frost, 1943 |
Phoxinus phoxinus |
Between 3 June and 15 July there was a sharp drop in total condition princiapply beacause of a fall in GSI. This decline in GSI continued until late August |
3.0 |
Mills and Eloranta, 1985 |
Rutilus rutilus |
3-4 (May-June-July-August) |
3.5 |
Rinchard, 1996 |
Rutilus rutilus |
Short gonadal quiescent period |
0.0 |
Rinchard et al, 1996 |
Rutilus rutilus |
3 [From June to September] |
3.0 |
Mann, 1973 |
Rutilus rutilus |
1.5-2 months, but could be shorted in heated reservoirs |
1.75 |
Witkowski et al, 1989 |
Rutilus rutilus |
<2% (End of May until Mid-Augsut) |
2.0 |
Rinchard and Kestemont, 1996 |
Rutilus rutilus |
About 1 [June, July until Mid-August] |
1.0 |
Mann, 1973 |
Rutilus rutilus |
May to June, July and stops in August [From graph] |
5.0 |
Tarkan et al, 2006 |
Rutilus rutilus |
After the spawning period, a quiescent period of gonad activity occurs during the summer because warm temperature (>20°C) and the long hours of daulight block the development of gonads until the end of August |
20.0 |
Gillet and Quétin, 2006 |
Scardinius erythrophthalmus |
>1 (August) |
1.0 |
Shikhshabekov, 1979 |
Scardinius erythrophthalmus |
From June to September |
5.0 |
Tarkan et al, 2006 |
Tinca tinca |
Between the last reproduction and the following spring (Period when water temperature is under 10°C) |
10.0 |
Breton et al, 1980 |
Tinca tinca |
Between October and March |
3.0 |
Linhart and Billard, 1995 |
Tinca tinca |
Period of restoration (August) and rest (since September till the end of April) lasted in tench from Lake Drweckie for 9 months. In this period all ovaries were in stage VI/II-III or VI/III, and then in stage III of maturity. Oocyte resorption was observed throughout the year. it was most intensive during fish production, especially in 1979 when water temperature showed considerable variations. |
9.0 |
Pimpicka, 1989 |
Tinca tinca |
August-September |
3.0 |
Alas and Solak, 2004 |
Tinca tinca |
2.25 ± 0.1 (November) |
2.25 |
Pinillos et al, 2003 |
Tinca tinca |
Nearly 0 in July |
2.0 |
Yilmaz, 2002 |
Tinca tinca |
About 4 [October to March] |
4.0 |
Linhart and Billard, 1995 |
Tinca tinca |
After spawning ovaries are in second stage. In that state they are the smallest during the yearly sexual cycle, are bloodshot, and remaining (non-spawned) oocytes are being resorbed. That state lasts 1 month. Later (from Ocotber until the beginning of April) ovaries are in the third stage of maturity. During that time growth of oocytes occurs. At the end of April/beginning of May ovaries are in the fourth maturity stage. Oocytes are being filled with yolk. At that time asynchronous development of oocytes occurs, which is typical for tench. During the next, five th maturity stage asynchrony becomes more deep. The size of ovaries reaches maximum. Four groups of different developmental advancement co-occur in the ovaries. The most mature oocytes continue yolk accumulation, the second group is at the final steps of vacuolisation, oocytes of the third group (=the last group that is going to be spawned during the spawning season) begin vacuolisation. The fourth group, which is the leats developped, will be spawned the next year. The VI-th maturity stage is ovulation (liberation of oocytes from the Graff follicles). Before ovulation nucleus moves from the centre to periphery of oocytes. |
1.0 |
Kubu and Kouril, 1985 |
Vimba vimba |
3 (June until August) |
3.0 |
Shikhshabekov, 1979 |
Vimba vimba |
[July until October] |
5.0 |
Hliwa et al, 2002 |
Gambusia affinis |
1.0-1.1 [From January to April] |
1.05 |
Koya et al, 1998 |
Esox lucius |
3 Months (June to end of August) |
3.0 |
Lenhardt, 1992 |
Esox lucius |
3 months [June to end of August] |
3.0 |
Billard, 1996 |
Esox lucius |
February/April (spawning period) until July |
4.0 |
Lenhardt and Cakic, 2002 |
Esox lucius |
April until August |
6.0 |
Treasurer, 1990 |
Esox lucius |
Almost 0% (June, July, August) |
4.0 |
Lenhardt, 1992 |
Esox lucius |
< 1% [June, July] |
1.0 |
Billard, 1996 |
Lota lota |
0.5 -1.3 [July 29] |
2.0 |
Brylinska et al, 2002 |
Lota lota |
April to August |
6.0 |
Pulliainen and Korhonen, 1990 |
Gasterosteus aculeatus |
September to February |
6.0 |
Copp et al, 2002 |
Gasterosteus aculeatus |
After the breeding season the weights decrease until the lowest level is attained in October |
2.0 |
Borg and Van Veen, 1982 |
Gasterosteus aculeatus |
September |
2.0 |
Sokolowska and Sokolowska, 2006 |
Gasterosteus aculeatus |
The post-spawning phase began in June-July, when part of the population had completed spawning and oogenesis was starting |
3.0 |
Sokolowska and Sokolowska, 2006 |
Gasterosteus aculeatus |
About 5 |
5.0 |
Copp et al, 2002 |
Pungitius pungitius |
September to February |
6.0 |
Copp et al, 2002 |
Pungitius pungitius |
Based on GSI graph, in August and perhaps until november |
2.0 |
Sokolowska and Skora, 2002 |
Pungitius pungitius |
About 5 |
5.0 |
Copp et al, 2002 |
Lepomis gibbosus |
From August to March |
8.0 |
Copp et al, 2002 |
Lepomis gibbosus |
From Setember to May |
2.0 |
Burns, 1976 |
Lepomis gibbosus |
About 1 |
1.0 |
Copp et al, 2002 |
Micropterus salmoides |
2 (September and October); < 1 (between September and October, declined between August, and mid-September) |
2.0 |
Rosenblum et al, 1994 |
Micropterus salmoides |
GSI were minimal ind mid-summer |
4.0 |
Bennett and Gibbons, 1975 |
Dicentrarchus labrax |
April to May (High percentage of atretic female) |
3.0 |
Prat et al. (1990) General And Comparative Endocrinology 78, 361-373 |
Dicentrarchus labrax |
< 0.5 [Between June to October, at Arcachon] |
6.0 |
Zohar et al, 1984 |
Dicentrarchus labrax |
June-October [In Arcachon, France], May-October [In Sète, France], April-July [Tunisia] |
8.0 |
Barnabé, 1980 |
Dicentrarchus labrax |
From June to early August, oocyte development is minimal |
3.0 |
Mayer et al, 1990 |
Morone americana |
June to end of October [From May to September, atretic oocytes were found within their ovaries] |
7.0 |
Jackson and Sullivan, 1995 |
Morone americana |
Mature-spent. Ovaries flacid, few translucent eggs left. Ovarian membrane very vascuar, sac-like, or bloodshot (May-June). Mature-Resting. Ovaries becoming firm, and characterized by a relatively thich doameter. No eggs discernible to the naked eye, color pinkish, texture gelatinous (June-july). |
3.0 |
Mansuetti, 1961 |
Morone americana |
0.61 ± 0.04 (Basal summer level between June to October) |
6.0 |
Jackson and Sullivan, 1995 |
Morone chrysops |
Mid-July to mid-October |
5.0 |
Ruelle, 1977 |
Morone chrysops |
During the post-spawning period (May-September) |
3.0 |
Berlinsky et al, 1995 |
Morone chrysops |
Below 1% |
1.0 |
Ruelle, 1977 |
Morone saxatilis |
In summer, females had nothing more than primaryt growth oocytes |
4.0 |
Woods III and Sullivan, 1993 |
Morone saxatilis |
During the post spawning season (July, Aufgust, and September), when oocyte and ovarian diameters were smallest, sex detemrination was less accurate |
3.0 |
Blythe et al, 1994 |
Gymnocephalus cernua |
2-3 [June, July and August] |
2.5 |
Leino and McCormick, 1997 |
Gymnocephalus cernua |
<1 |
1.0 |
Leino and McCormick, 1997 |
Perca flavescens |
Mid-June until Mid-August |
4.0 |
Malservisi and Magnin, 1968 |
Perca flavescens |
May until August |
5.0 |
Dabrowski et al, 1996 |
Perca flavescens |
Late April to August |
6.0 |
Hayes and Taylor, 1994 |
Perca flavescens |
<1% from July to August |
1.0 |
Tansichuk and Mackay, 1989 |
Perca flavescens |
1% (After the spawning, GSI remain low from May trought August) |
1.0 |
Hayes and Taylor, 1994 |
Perca flavescens |
< 1% |
1.0 |
Dabrowski et al, 1996 |
Perca flavescens |
Below 1%, in June and July |
1.0 |
Tansichuk and Mackay, 1989 |
Perca fluviatilis |
3-4 |
3.5 |
Sulistyo et al,1998 |
Perca fluviatilis |
4-4.5 [From April until August] |
4.25 |
Treasurer and Holliday, 1981 |
Perca fluviatilis |
Mid-summer |
4.0 |
Le Cren, 1951 |
Perca fluviatilis |
After spawning, GSI rapidly decreased to the low values observed during the summer |
4.0 |
Noaksson et al, 2004 |
Perca fluviatilis |
<1% [End of spring and summer corresponds to the post-spawning period] |
1.0 |
Sulistyo et al,1998 |
Sander lucioperca |
From May-June the post-spawning season and from June to September the resting period |
6.0 |
Poulet, 2004 |
Sander vitreus |
By late spring, ovaries were already filled with a large number of non-vitellogenic oocytes; indicating that female have a relatively short post-spawning quiescient period |
4.0 |
Malison and Held, 1996b |
Sander vitreus |
From May to October |
7.0 |
Malison et al, 1994 |
Sander vitreus |
Walleye have a relatively short post-spawning quiescent period |
0.0 |
Kestemont and Mélard, 2000 |
Sander vitreus |
0.7 [July to August] |
3.0 |
Craig, 2000 |
Sander vitreus |
<1% July to August |
1.0 |
Colby et al, 1979 |
Coregonus lavaretus |
After spawning, the gonadosomatic ratio of females fell suddenly and remained low, about 1% of body weight, for 6 months until July[From March to May ovaries contained only primary (pre-vitellogenic) oocytes. Secondary oocytes, wihc chorion and yolkk precursors, appeared in May] |
1.0 |
Fuller et al, 1976 |
Coregonus lavaretus |
After spawning, the gonads were basically resting until April and May |
3.0 |
Heese, 1990 |
Coregonus albula |
2.5-3 but up to 4-4.5 months in low temperature [January until May] |
2.75 |
Demska-Zakes and Dlugosz, 1995 |
Coregonus albula |
2.5-3 months |
2.75 |
Dlugosz and Worniallo, 1985 |
Coregonus albula |
About 2 months |
2.0 |
Witkowski et al, 1989 |
Coregonus albula |
During the winter months, vendace remain in the regenerating and resting phaseses (maturation stages VI and II) for nominate form. For deepwater form, from May until July/August |
8.0 |
Anwand, 1998 |
Oncorhynchus kisutch |
In June to November for broodstock population cultured in a fish farm in Southern Chile |
7.0 |
Estay et all., 1998 |
Oncorhynchus mykiss |
1 [December] |
1.0 |
Bon et al, 1999 |
Oncorhynchus mykiss |
0.5 ± 0.07 [GSI remains at a minimum from December to May= very slow ovarian development phase] |
7.0 |
Bon et al, 1999 |
Salmo trutta fario |
From January until April |
5.0 |
Billard, 1987 |
Salmo trutta fario |
Almost 0 [From January until April] |
5.0 |
Billard, 1987 |
Salvelinus alpinus |
Recruitement of stage II and stage III oocyes was seen 1-2 months after ovulation had occurred, and by February the next year all the post-ovulatory follicles had disappeared |
1.5 |
Frantzen et al, 1997 |
Salvelinus alpinus |
< 0.5% (November to beginning of June) |
3.0 |
Frantzen et al, 1997 |
Salvelinus alpinus |
0.3 (Resting period lasted until July) |
2.0 |
Jamet, 1995 |
Salvelinus fontinalis |
Oocyte development and yolk formation is relatively low from November until May |
7.0 |
Tam et al, 1986 |
Salvelinus fontinalis |
November to June, < 1% |
1.0 |
Wydoski and Cooper, 1966 |
Thymallus thymallus |
About two months: May and June |
3.0 |
Witkowski et al, 1989 |
Thymallus thymallus |
0.8 [May and June] |
3.0 |
Witkowski et al, 1989 |
Ameiurus nebulosus |
6-7 [No significant differences between November to April] |
6.5 |
Burke et al, 1984 |
Ameiurus nebulosus |
About 1 (August-September, then slightly increased) |
1.0 |
Rosenblum et al, 1987 |
Ameiurus nebulosus |
< 1% [No significant differences between November to April] |
1.0 |
Burke et al, 1984 |
Ictalurus punctatus |
About 2 [GSI was low during the summer months: July and August] |
2.0 |
Mackenzie et al, 1989 |
Ictalurus punctatus |
About 4 [From July until November] |
4.0 |
Banks et al, 1999 |
Ictalurus punctatus |
An apparent low point in the annual ovarian cycle was reached immediatly after spawning |
0.0 |
Brauhn and McCraren, 1975 |
Silurus glanis |
July, August: 0.42-0.81% |
3.0 |
Zholdasova and Guseva, 1987 |
Silurus glanis |
September-October: >0.05% |
3.0 |
Alp et al, 2004 |
Anguilla anguilla |
About 0.1 for the silver stage |
0.1 |
Marchelidon et al, 1999 |
Aphanius iberus |
A period of repose from September to February |
6.0 |
Vargas and De Sostoa, 1997 |
Valencia hispanica |
From August to December |
6.0 |
Caiola et al, 2001 |
Barbatula barbatula |
0.3-0.7 [Minimal value in mid-July, and by August GSI increased to about 1% and remained at this level until the next spring] |
6.0 |
Saat et al, 2003 |
Cobitis taenia |
Late June and early July [similar to female cycle] |
3.0 |
Vaino and Saat, 2003 |
Cobitis taenia |
September |
2.0 |
Marconato and Rasotto, 1989 |
Cobitis paludica |
Short quiescence period [August-September] |
3.0 |
Oliva-Paterna et al, 2002 |
Alburnoides bipunctatus |
1.7 [n=3, August] |
1.7 |
Yildirim et al, 1999 |
Aspius aspius |
0.14 [August] |
2.0 |
Kompowski et Neja, 2004 |
Barbus barbus |
No differences in term of GSI between September till January |
3.0 |
Lobon-Cervia and Fernandez-Delgado, 1984 |
Carassius auratus |
0.3 ± 0.1 [August, but a large increased was oberseved in the Autum: about 4%)] |
2.0 |
Kobayashi et al, 1986 |
Cyprinus carpio |
Lower in december-January, about 2% |
2.0 |
Smith and Walker, 2004 |
Gobio gobio |
0.9 [September to October] |
3.0 |
Kestemond, 1989 |
Leuciscus cephalus |
July to November, only germinal cells were evident |
6.0 |
Guerriero et al, 2005 |
Leuciscus cephalus |
April to November <0.5 |
9.0 |
Sasi, 2003 |
Leuciscus cephalus |
June-September quiescent period, About 1% |
1.0 |
Mann, 1976 |
Leuciscus cephalus |
Gonads of females after spawning remain in spawning remain state until September |
2.0 |
Zelepien, 1997 |
Leuciscus leuciscus |
< 0.2% [From mid-April to mid-August] |
6.0 |
Mann, 1974 |
Phoxinus phoxinus |
Almost 0 [From September to February] |
6.0 |
Mills, 1987 |
Rutilus rutilus |
About 1 [During June-August] |
1.0 |
Escaffre and Billard, 1976 |
Rutilus rutilus |
About 1 [June, July until August] |
1.0 |
Mann, 1973 |
Rutilus rutilus |
June, July and August |
4.0 |
Tarkan et al, 2006 |
Tinca tinca |
0.21 (November) |
2.0 |
Pinillos et al, 2003 |
Gambusia affinis |
Resting period is October to April [The GSI values (0.9-2.1%) from January to May] |
1.5 |
Koya and Iwase, 2004 |
Esox lucius |
< 0.1 [June, July, mid-August] |
4.0 |
Lenhardt, 1992 |
Esox lucius |
<0.2 [June-July] |
3.0 |
Billard, 1996 |
Esox lucius |
The resting period last from June until the end of August |
3.0 |
Lenhardt and Cakic, 2002 |
Esox lucius |
Stage I, rest from June to August, and stage IV, stage of post-spawning March to May |
7.0 |
Hoffmann et al, 1980 |
Esox lucius |
The index declined to 0.04-0.08 after spawning in early April and rose from late August |
3.0 |
Treasurer, 1990 |
Lota lota |
0.5-2.7 [July 29th] |
1.6 |
Brylinska et al, 2002 |
Lota lota |
No difference in term of GSI between April and July, and even up to October |
6.0 |
Pulliainen and Korhonen, 1990 |
Gasterosteus aculeatus |
About 1% [From September to February] |
1.0 |
Copp et al, 2002 |
Pungitius pungitius |
About 1% [From September to February] |
1.0 |
Copp et al, 2002 |
Lepomis gibbosus |
October to May |
8.0 |
Burns, 1976 |
Micropterus salmoides |
< 0,1 (September, sharp decrease in August) |
3.0 |
Rosenblum et al, 1994 |
Dicentrarchus labrax |
< 0.5 [March to September] |
8.0 |
Zohar et al, 1984 |
Dicentrarchus labrax |
May-November [In Arcachon, France], May-October [In Sète, France], February-September [Tunisia] |
11.0 |
Barnabé, 1980 |
Dicentrarchus labrax |
From April to October |
8.0 |
Gonzalez and Piferrer, 2003 |
Morone americana |
About 0,2 (Basal summer value: June, July, September) |
5.0 |
Jackson and Sullivan, 1995 |
Morone americana |
Spent. Testes brownish white, flaccid and convoluted, with no flow or white milt upon compresison. April-early June |
3.0 |
Mansuetti, 1961 |
Morone chrysops |
0.1 % |From early August to |
2.0 |
Ruelle, 1977 |
Morone saxatilis |
Male sex determination was lowest in September when testicular diameter was minimal |
2.0 |
Blythe et al, 1994 |
Morone saxatilis |
In June, after the second reproductive season, testes from mature fish strated to regress and spermatozoa were resorbed. In September (the beginning of the third reproductive cycle) only spermatogonia were present in the testes. |
3.0 |
Holland et al, 2000 |
Gymnocephalus cernua |
Periods in which gametogensis is absent occuring between spring and autumn [The coefficients of maturity after discharge of the spermatozoids (in the absence of spermatogensis) is on average 0.8% (range 0.5-1.2%), and after completion of the rearrangement of the somatic elements of the testes less than 0.25% |
7.0 |
Butskaya, 1981 |
Perca flavescens |
Between 1 and 2 [After spawning, declined troughout the summer until August] |
1.0 |
Heidinger and Kayes, 1986 |
Perca flavescens |
Below 1%, in June and July |
1.0 |
Tansichuk and Mackay, 1989 |
Perca fluviatilis |
0.2 ± 0.1 [Late June, July, August) |
4.0 |
Sulistyo et al, 2000 |
Perca fluviatilis |
0.2 [June, July] |
3.0 |
Treasurer and Holliday, 1981 |
Perca fluviatilis |
< 1% [June, July, and most of August] |
1.0 |
Le Cren, 1951 |
Sander vitreus |
0.2 [June-July] |
3.0 |
Colby et al, 1979 |
Sander vitreus |
<1% [From May through September] |
1.0 |
Malison et al, 1994 |
Coregonus lavaretus |
It fell gradually from January to a minimum of 0.4% in June and July |
4.0 |
Fuller et al, 1976 |
Coregonus lavaretus |
Below 1%, between February and May |
1.0 |
Heese, 1990 |
Coregonus albula |
0.13-0.7 % [From December until March] |
5.0 |
Dlugosz and Worniallo, 1985 |
Coregonus albula |
During the winter months, vendace remain in the regenerating and resting phaseses (maturation stages VI and II) for nominate form. For deepwater form, from May until July/August |
8.0 |
Anwand, 1998 |
Oncorhynchus gorbuscha |
5.39 ± 0.5 [Spawning grounds] |
5.39 |
Dye et al, 1986 |
Salmo trutta fario |
< 0 (April and May) |
3.0 |
Billard, 1987 |
Salvelinus alpinus |
Almost 0 (Between December to July, value in July = 0.6%) |
9.0 |
Jamet, 1995 |
Salvelinus fontinalis |
From November to June |
8.0 |
Wydoski and Cooper, 1966 |
Thymallus thymallus |
0.3% [Three months after spawning May -July] |
3.0 |
Witkowski et al, 1989 |
Ameiurus nebulosus |
0.15 (October, November) |
3.0 |
Rosenblum et al, 1987 |
Ameiurus nebulosus |
From 0.100 (September) to 0.158 (mid-April), with no significant differences between the mean values |
3.0 |
Burke et al, 1984 |
Ameiurus nebulosus |
Resting period is between mid-August to mid-April, i.e. 6 months |
6.0 |
Burke and Leatherland, 1984 |
Silurus glanis |
0.12-0.25% at the end of July [June-July] |
3.0 |
Zholdasova and Guseva, 1987 |
Silurus glanis |
Low between August and November |
5.0 |
Alp et al, 2004 |