Trait completeness | 88% |
Total data | 257 |
References | 47 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.5-1.7 [Not precised] | 1.6 mm | Mellinger, 2002 |
1 | Oocyte diameter | 1.7-1.9 | 1.8 mm | Internet, 2005 |
1 | Oocyte diameter | 1.5-1.9 | 1.7 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.8 | 1.8 mm | Coad, 2005 |
1 | Oocyte diameter | 1.5 | 1.5 mm | Crivelli, 2001 |
1 | Oocyte diameter | 1.1-1.6 [Newly laid eggs] | 1.35 mm | Fishbase, 2006 |
1 | Oocyte diameter | 1.5-1.7 | 1.6 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | 1.31 ± 0.05 | 1.31 mm | Wallace and Selman, 1979 |
1 | Oocyte diameter | 1.15-1.67 | 1.41 mm | Poizat et al, 2002 |
1 | Oocyte diameter | 1.7 [Large mature oocytes, range 1.31-2.0 for other populations] | 1.66 mm | Copp et al, 2002 |
1 | Oocyte diameter | 1.3 | 1.3 mm | Tyler and Sumpter, 1996 |
1 | Oocyte diameter | Ovulated oocytes reached a diameter of at least 1.4 mm (apart from the overripe ones) | 1.4 mm | Sokolowska and Sokolowska, 2006 |
2 | Egg size after water-hardening | 1.5-1.9 [Swollen eggs] | 1.7 mm | Fishbase, 2006 |
2 | Egg size after water-hardening | 1.52 ± 0.06, n=70 [Eggs stripped from mature females, fertilized and incubated in water: hydrated eggs] | 1.52 mm | Bonislawska et al, 2001 |
2 | Egg size after water-hardening | Mainly 1.5 [Drifting eggs] | 1.5 mm | Copp et al, 2002b |
2 | Egg size after water-hardening | 1.47-1.66 [Eggs swollen] | 1.56 mm | Bonislawska et al, 2000 |
2 | Egg size after water-hardening | Eggs is spherical, about 1.2 to 1.7 mm in diameter | 1.7 mm | Swarup, 1958 |
3 | Egg Buoyancy | Demersal | Demersal | Internet, 2005 |
3 | Egg Buoyancy | Demersal | Demersal | Tyler and Sumpter, 1996 |
3 | Egg Buoyancy | They are opaque and heavier than water. | No category | Swarup, 1958 |
4 | Egg adhesiveness | Highly adhesive to each other but not to substrates | Adhesive | Internet, 2005 |
4 | Egg adhesiveness | Sticky | Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Adhesive to each other | Adhesive | Scott and Crossman, 1973 |
4 | Egg adhesiveness | Adhesive | Adhesive | Bradbury et al, 1999 |
4 | Egg adhesiveness | Stickleback eggs within a nest are stuck together in a large mass | Adhesive | Rebs et al, 1984 |
4 | Egg adhesiveness | The eggs remain together in a mass surrounded by mucus. […] Soon after oviposition the egg capsule hardens and the eggs become firmly attached to one another | Adhesive | Swarup, 1958 |
4 | Egg adhesiveness | Adhesive masses of eggs incubate in nest constructed of sand grains and plant fragments held together by secretions of the male | Adhesive | Goodyear, 1982 |
5 | Incubation time | 7.0 | 7.0 days | Internet, 2005 |
5 | Incubation time | 8 [17-18°C], 15 [8-9°C] | 17.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 6 [17°C] | 6.0 days | Fishbase, 2006 |
5 | Incubation time | 7 [19°C] | 7.0 days | Scott and Crossman, 1973 |
5 | Incubation time | 10-17 | 13.5 days | Poulin and Fitzgerald, 1989 |
5 | Incubation time | 6.5-8.5 [At 20°C], hatcing time is decreased in freshwater | 7.5 days | Belanger et al, 1987 |
5 | Incubation time | Eggs hatch in 4-27 days | 15.5 days | Goodyear, 1982 |
6 | Temperature for incubation | 8-17 | 12.5 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | 18-20 | 19.0 °C | Internet, 2005 |
6 | Temperature for incubation | 17 | 17.0 °C | Fishbase, 2006 |
6 | Temperature for incubation | 19 | 19.0 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | 14.8-20.0 | 17.4 °C | Poulin and Fitzgerald, 1989 |
6 | Temperature for incubation | 20°C | 20.0 °C | Belanger et al, 1987 |
6 | Temperature for incubation | Incubated at 19°C | 19.0 °C | Bohlen, 1999b |
6 | Temperature for incubation | Here the embryos were kept until the yolk was completely used up. During the whole of this time the temperature remained between 18° and 19°C. Under this conditions the embryos take 6-8 days to hatch, and about 4 more days to complete absorption of yolk. | 7.0 °C | Swarup, 1958 |
7 | Degree-days for incubation | About 140 | 140.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 125-140 [7 days at 18-20°C] | 132.5 °C * day | Internet, 2005 |
7 | Degree-days for incubation | About 105 [6 days at 17°C] | 105.0 °C * day | Fishbase, 2006 |
7 | Degree-days for incubation | About 135 | 135.0 °C * day | Scott and Crossman, 1973 |
7 | Degree-days for incubation | 90 | 90.0 °C * day | Bonislawska et al, 2000 |
7 | Degree-days for incubation | 76 [Effective day-degrees] | 76.0 °C * day | Kamler, 2002 |
7 | Degree-days for incubation | 192 hours after fertilization | 192.0 °C * day | Swarup, 1958 |
1 | Oocyte diameter | 1.64-1.66 | 1.65 mm | Belles-Isles and FitzGerald, 1992 |
1 | Oocyte diameter | 1.20-1.60 | 1.4 mm | Lam et al, 1978 |
1 | Oocyte diameter | 1.20-1.70 | 1.45 mm | Swarup, 1958 |
1 | Oocyte diameter | 1.20-1.60 | 1.4 mm | Vrat, 1949 |
2 | Egg size after water-hardening | 1.33-2.16 | 1.75 mm | Glippa et al, 2017 |
2 | Egg size after water-hardening | 1.47-1.51 | 1.49 mm | Crivelli and Britton, 1987 |
2 | Egg size after water-hardening | 1.31 | 1.31 mm | Wallace, 1978 |
2 | Egg size after water-hardening | 1.50-1.90 | 1.7 mm | Vrat, 1949 |
2 | Egg size after water-hardening | 1.50-1.70 | 1.6 mm | Kuntz and Radcliffe, 1917 |
4 | Egg adhesiveness | Adhesive | Adhesive | Kuntz and Radcliffe, 1917 |
4 | Egg adhesiveness | Adhesive | Adhesive | Vrat, 1949 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 4.2-4.5 | 4.35 mm | Internet, 2005 |
8 | Initial larval size | 2-4.5 | 3.25 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 4.2-5 | 4.6 mm | Scott and Crossman, 1973 |
8 | Initial larval size | By the time the embryo hatches it is already 8 days old and measures 3 mm in length. About 24 hours after hathing the larva has a length of nearly 4 mm, has absorbed half of its yolk, and swims about freely. | 3.0 mm | Swarup, 1958 |
8 | Initial larval size | Hatched larvae 6-7 mm SL (6.55 mm in a mean length) can attain a length of about 15 mm within one month of hatching | 6.5 mm | Mori and Magoshi, 1987 |
9 | Larvae behaviour | Newly hatched larvae stay near the bottom | Demersal | Internet, 2005 |
9 | Larvae behaviour | Newly hatched larvae stay within the nest, around the nest in schools and then leave | Demersal | Crivelli, 2001 |
9 | Larvae behaviour | Upon hatching, young leave the the spawning area but remain close to shore in shallow water | Demersal | Bradbury et al, 1999 |
9 | Larvae behaviour | Because of the heavy yolk the larva lies on its side, occasionally swimming swiftly to settle down again at another spot. | Demersal | Swarup, 1958 |
11 | Temperature during larval development | Here the embryos were kept until the yolk was completely used up. During the whole of this time the temperature remained between 18° and 19°C. Under this conditions the embryos take 6-8 days to hatch, and about 4 more days to complete absorption of yolk. | 7.0 °C | Swarup, 1958 |
12 | Sibling intracohort cannibalism | Male could eat some of their guarded eggs | Absent | Bruslé and Quignard, 2001 |
12 | Sibling intracohort cannibalism | Lost of cannibalism | Present | Crivelli, 2001 |
12 | Sibling intracohort cannibalism | Male eat egg and fry | Absent | Fitzgerald, 1983 |
13 | Full yolk-sac resorption | The larva continues to grow by absorption of the yolk which is completely used up 4 days after hatching, giving the larva, now about 6 mm long, a slender appearance. | 4.0 °C * day | Swarup, 1958 |
8 | Initial larval size | 4.71-4.91 | 4.81 mm | Vrat, 1949 |
8 | Initial larval size | 4.2-4.5 | 4.35 mm | Kuntz and Radcliffe, 1917 |
12 | Sibling intracohort cannibalism | present | Present | Hynes, 1950 |
12 | Sibling intracohort cannibalism | present | Present | Semler, 1971 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 1-2 [Both sex] | 1.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 1 [Both sex] | 1.0 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | 1-2 [Not specified] | 1.5 year | Environment agency, ??? |
15 | Age at sexual maturity | 2-3 [Not specified] | 2.5 year | Bradbury et al, 1999 |
16 | Length at sexual maturity | 5.5 [Female] | 5.5 cm | Fishbase, 2006 |
16 | Length at sexual maturity | 3.1-6.4 [Length of adult female during the breeding season] | 4.75 cm | Poizat et al, 2002 |
16 | Length at sexual maturity | 5.2 [SL, smallest individual with ripe eggs] | 5.2 cm | Copp et al, 2002 |
16 | Length at sexual maturity | Length of female producing eggs: mean of 47.9, range 41.0-74.0 mm | 57.5 cm | Wootton, 1973 |
16 | Length at sexual maturity | Lengths of female caught in May anf June: 38.5 ± 1.55 mm and 41.7 mm, respectively in Frongoch and 46.0 ±2.01 mm and 44 ±1.01 mm in Rheidol | 38.5 cm | Wootton et al, 1978 |
16 | Length at sexual maturity | Although the smallest female with mature ova was 43 mm, the majority of females did not have mature ova until 45 mm SL | 43.0 cm | Mori and Magoshi, 1987 |
17 | Weight at sexual maturity | 0.5-3.8 g | 2.15 kg | Poizat et al, 2002 |
17 | Weight at sexual maturity | Weight of females producing eggs after spawning 1.102, range 0.582-3.665 mm | 2.12 kg | Wootton, 1973 |
17 | Weight at sexual maturity | Weights of female caught in May anf June: 0.557 ± 0.0835 g and 0.626 g, respectively in Frongoch and 1.098 ±0.1553 and 0.823 ±0.0525 g in Rheidol | 0.56 kg | Wootton et al, 1978 |
19 | Relative fecundity | About 100, range from 50-130 | 90.0 thousand eggs/kg | Copp et al, 2002 |
19 | Relative fecundity | 5.0 | 5.0 thousand eggs/kg | Tyler and Sumpter, 1996 |
19 | Relative fecundity | A 3 g fish would produce about 270 eggs | 3.0 thousand eggs/kg | Wootton, 1973 |
20 | Absolute fecundity | 1.3-1.8 | 1.55 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | Mean clutch size: 0.366, range 0.116-0.838 | 0.48 thousand eggs | Fitzgerald, 1983 |
20 | Absolute fecundity | 0.090-0.450 | 0.27 thousand eggs | Environment agency, ??? |
20 | Absolute fecundity | The expected fecundity of a stickleback of a standard length of 50 mm was calculated as 163.1 eggs for trachurus females, 154.4 eggs for hybrid females and 132.7 eggs for leiurus females [in the course of a breeding season a large female can produce two to three times its own weight of eggs, that is 2-4 g of eggs] | 3.0 thousand eggs | Wootton, 1973 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
21 | Oocyte development | Simultaneous development of batches of eggs | Synchronous | Borg and Van Veen, 1982 |
21 | Oocyte development | The evidence suggests that a population of oocytes is recuited from pre-vitellogenic oocyes and strats to accumulate yolk shortly before or at the same time as the ovultation of a batch of eggs that have completed their maturation. After the spawning, these vitellogenic oocyes continue to accumulate yolk over the first days of the inter-spawning interval, then undergo maturation over the last hours before ovulation and spawning | No category | Ali and Wooton, 1999 |
21 | Oocyte development | As a result of asynchronous maturatio, the ovaries contained oocytes in various stages of devleopment throughout the year; their proportion varied seasonally | Asynchronous | Sokolowska and Sokolowska, 2006 |
22 | Onset of oogenesis | February | ['February'] | Copp et al, 2002 |
22 | Onset of oogenesis | September-October: A period of slow increase over the autumn and the winter | ['January', 'February', 'March', 'September', 'October', 'November', 'December'] | Wootton et al, 1978 |
22 | Onset of oogenesis | Slight increase in October-November [Relative ovarian weights are low in autum and early spring] | ['April', 'May', 'June', 'October', 'November'] | Borg and Van Veen, 1982 |
22 | Onset of oogenesis | September-October, based on Fig. 5b | ['September', 'October'] | Sokolowska and Sokolowska, 2006 |
23 | Intensifying oogenesis activity | March-April | ['March', 'April'] | Copp et al, 2002 |
23 | Intensifying oogenesis activity | Very rapid increase in the GSI in March and April | ['March', 'April'] | Wootton et al, 1978 |
23 | Intensifying oogenesis activity | May | ['May'] | Borg and Van Veen, 1982 |
23 | Intensifying oogenesis activity | April-May, based on figure 5b | ['April', 'May'] | Sokolowska and Sokolowska, 2006 |
24 | Maximum GSI value | Up to 45 % | 45.0 percent | Bruslé and Quignard, 2001 |
24 | Maximum GSI value | Mean 35, range 32-44 in June [With eviscerated weight !!, about 25-30%] | 38.0 percent | Copp et al, 2002 |
24 | Maximum GSI value | Peak in May: Mean of 19%, up to 21 in 1974 and mean of 12.5, up to 15.5 in 1975 | 19.0 percent | Wootton et al, 1978 |
24 | Maximum GSI value | Mean of 22; up to 25% [In June] | 22.0 percent | Borg and Van Veen, 1982 |
24 | Maximum GSI value | Mean of 19, 18-21, based on fig 5b | 19.5 percent | Sokolowska and Sokolowska, 2006 |
26 | Resting period | September to February | 6.0 months | Copp et al, 2002 |
26 | Resting period | After the breeding season the weights decrease until the lowest level is attained in October | 2.0 months | Borg and Van Veen, 1982 |
26 | Resting period | September | 2.0 months | Sokolowska and Sokolowska, 2006 |
26 | Resting period | The post-spawning phase began in June-July, when part of the population had completed spawning and oogenesis was starting | 3.0 months | Sokolowska and Sokolowska, 2006 |
26 | Resting period | About 5 | 5.0 months | Copp et al, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 1-2 [Both sex] | 1.5 years | Fishbase, 2006 |
27 | Age at sexual maturity | 1 [Both sex] | 1.0 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | 2 [Not specified] | 2.0 years | Environment agency, ??? |
28 | Length at sexual maturity | 4.5 [Male] | 4.5 cm | Fishbase, 2006 |
28 | Length at sexual maturity | Nest-building males were 44.6 ± 3.32 mm, range 39-55 | 44.6 cm | Barber et al, 2000 |
28 | Length at sexual maturity | The breeding coloured male with a nest was 47 mm SL in the smallest body length | 47.0 cm | Mori and Magoshi, 1987 |
29 | Weight at sexual maturity | Nest-building males were 0.94 ± 0.25 g , range 0.60-1.79 g | 0.94 kg | Barber et al, 2000 |
30 | Male sexual dimorphism | Male exhibits breeding color at ca. 12°C and retain their color for a month after spawning season: brilliant, dark green and orange-red spawning coloration | Absent | Internet, 2005 |
30 | Male sexual dimorphism | Breeding males develop a red belly and throat, blue sides, light blue back and have bright blue or turquoise eyes | Present | Coad, 2005 |
30 | Male sexual dimorphism | Breeders displayed a well-developed nuptial colloration and aggressive behavior | Absent | Sokolowska and Sokolowska, 2006 |
31 | Onset of spermatogenesis | February-March | ['February', 'March'] | Copp et al, 2002 |
31 | Onset of spermatogenesis | September | ['September'] | Borg, 1982 |
31 | Onset of spermatogenesis | September, based on Fig 11.b | ['September'] | Sokolowska and Sokolowska, 2006 |
32 | Main spermatogenesis activity | March-April | ['March', 'April'] | Copp et al, 2002 |
32 | Main spermatogenesis activity | In October the testes are to a large extent filled with spermatocytes and spermatids. Sepermatogenesis is completed in November-January | ['January', 'October', 'November'] | Borg, 1982 |
32 | Main spermatogenesis activity | September. In most of the males, spermatogenesis was complete in December, but the spermatozoawere not yet ready to be released | ['September', 'December'] | Sokolowska and Sokolowska, 2006 |
33 | Maximum GSI value | 4.8 [April] | 4.8 percent | Copp et al, 2002 |
33 | Maximum GSI value | The peak of the GSI is reached in October, about a mean of 1.4, up to 1.6, and is followed by a gradual decline until August when the lowest values are reached | 1.4 percent | Borg, 1982 |
33 | Maximum GSI value | Around 1 in September than remained around 0.5 the rest of the year | 1.0 percent | Sokolowska and Sokolowska, 2006 |
35 | Resting period | About 1% [From September to February] | 1.0 months | Copp et al, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Limited home range | No data | Environment agency, ??? |
36 | Spawning migration distance | Move from deeper water to neashore areas, creek mounths, and bays, and often ascend tributaries | No data | Goodyear, 1982 |
37 | Spawning migration period | Migrations of anadromous stickleback into freshwater usually occurs in late psring (June) | ['June'] | Bradbury et al, 1999 |
39 | Spawning season | April-June | ['April', 'June'] | Billard, 1997 |
39 | Spawning season | April to October | ['April', 'May', 'June', 'July', 'August', 'September', 'October'] | Coad, 2005 |
39 | Spawning season | April-May but February-March in southern region | ['February', 'March', 'April', 'May'] | Bruslé and Quignard, 2001 |
39 | Spawning season | May-July [But also February-August] | ['February', 'May', 'June', 'July', 'August'] | Internet, 2005 |
39 | Spawning season | March until July | ['March', 'April', 'May', 'June', 'July'] | Crivelli, 2001 |
39 | Spawning season | Mainly April-June [But in March and September] | ['March', 'April', 'May', 'June', 'September'] | Fishbase, 2006 |
39 | Spawning season | Generally in June-July, but from April to September | ['April', 'May', 'June', 'July', 'August', 'September'] | Scott and Crossman, 1973 |
39 | Spawning season | Thye first nest appear in mid-May and most nest building was finished by mid-June and was extremely rare after June 30 | ['May', 'June'] | Fitzgerald, 1983 |
39 | Spawning season | March-June | ['March', 'June'] | Environment agency, ??? |
39 | Spawning season | April-May | ['April', 'May'] | Terver, 1984 |
39 | Spawning season | Spawning shortly occur after migration, in June [Resident freshwater populations spawn mainly in mid-Summer, during June and July] | ['June', 'July', 'August', 'September'] | Bradbury et al, 1999 |
39 | Spawning season | The breeding season is in late spring-summer | ['April', 'May', 'June', 'July', 'August', 'September'] | Borg and Van Veen, 1982 |
39 | Spawning season | May-June | ['May', 'June'] | Borg, 1982 |
39 | Spawning season | Bred from April to July, but the majority of them were sexually active from May onwards | ['April', 'May', 'June', 'July'] | Sokolowska and Sokolowska, 2006 |
39 | Spawning season | This fish breeds mainly during April and May, but it is possible in tha laboratory to bring into breeding condition during most of the year | ['April', 'May'] | Swarup, 1958 |
39 | Spawning season | April-September | ['April', 'September'] | Goodyear, 1982 |
39 | Spawning season | They have spawned from April to mid June | ['April', 'June'] | Mori and Magoshi, 1987 |
40 | Spawning period duration | 8 : female release 3 to 4 batches of eggs with about 1 week between each of the batch | 8.0 weeks | Bruslé and Quignard, 2001 |
40 | Spawning period duration | The male parental cycle at one site in Canada lasts 9-15 days with female interspawning intervals of 19 days. | 12.0 weeks | Coad, 2005 |
40 | Spawning period duration | Under ideal laboratory control conditions, a pair can spawn six times within an interval of 10-15 days | 12.5 weeks | Internet, 2005 |
40 | Spawning period duration | Several months | No data | Wallace and Selman, 1979 |
40 | Spawning period duration | 4-5 | 4.5 weeks | Fitzgerald, 1983 |
40 | Spawning period duration | 5-6 | 5.5 weeks | Terver, 1984 |
40 | Spawning period duration | This indicates that in 1975, the breeding season in the Rheidol lasted for thrre to four months, but in Frongoch it lasted only about one month | 1975.0 weeks | Wootton et al, 1978 |
40 | Spawning period duration | The prolonged breeding activity of sticklebacks, for as long as five months, enabled the fish to reproduce in the most favourable environmental conditions | No data | Sokolowska and Sokolowska, 2006 |
41 | Spawning temperature | 15.8-18.5 | 17.15 °C | Internet, 2005 |
41 | Spawning temperature | Above 10°C | 10.0 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | >15°C [Little courtship occur when water temperature often exceed 25°C] | 15.0 °C | Fitzgerald, 1983 |
41 | Spawning temperature | In out study, some sticklebacks completed spawning and started a new gametogenetic cycle in June-July. Temperatures as high as 20°C probably limited breeding in the populations examined and a further increase of temperature could have been the reason why the initial phase of gamatogenesis in both sexes was disturbed | 20.0 °C | Sokolowska and Sokolowska, 2006 |
41 | Spawning temperature | At 50-73°F | 61.5 °C | Goodyear, 1982 |
42 | Spawning water type | Shallow weedy areas [Freshwater and brackish water] | Stagnant water | Internet, 2005 |
42 | Spawning water type | Submerged areas | No category | Bruslé and Quignard, 2001 |
42 | Spawning water type | Ponds and rivers | Stagnant water | Poulin and Fitzgerald, 1989 |
42 | Spawning water type | Shallow tidal Pools | No category | Fitzgerald, 1983 |
42 | Spawning water type | Anadromous populations may spawn in brackish or freshwater [Spawning in freshwater has been observed in two distinct habitat types within lakes; open-water areas, or in association with aquatic vegetation | Stagnant water | Bradbury et al, 1999 |
42 | Spawning water type | Pools and rivers in the salt marshes, but most reproduce in pools whose salinity fluctuates between apprimatively 14 and 27 %o, but a considerable number reproduce in the freshwater section | No category | Belanger et al, 1987 |
42 | Spawning water type | Sheltered, current-free / areas along lake shore and in bays, creek mouths, and tributaries, usually close to shore | Stagnant water | Goodyear, 1982 |
43 | Spawning depth | Shallow waters : 5-20 cm | 12.5 m | Bruslé and Quignard, 2001 |
43 | Spawning depth | Shallow | No data | Scott and Crossman, 1973 |
43 | Spawning depth | < 50 cm | 50.0 m | Poulin and Fitzgerald, 1989 |
43 | Spawning depth | Generally nest in water less than 30 cm deep | 30.0 m | Fitzgerald, 1983 |
43 | Spawning depth | Males generally avoid nesting in water shallower than 0.2 m and have been observed nesting at depths of up to 40 m | 0.2 m | Bradbury et al, 1999 |
43 | Spawning depth | About 10 inches, but as shallow as 1-2 inches | 1.5 m | Goodyear, 1982 |
44 | Spawning substrate | Twigs and debris; strands of algae and pieces of aquatic plants; fragments of aquatic plants, algae, and debris | Phytophils | Internet, 2005 |
44 | Spawning substrate | Rich in vegetation | Phytophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Sandy areas | Psammophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Weed | Phytophils | Environment agency, ??? |
44 | Spawning substrate | Ariadnophil | No category | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Ariadnophil | No category | Balon, 1975 |
44 | Spawning substrate | In marine or estuarine habitats, spawning may occur in a variety of habitats including rock crevices, sheltered ellgrass bads, algal mats and sometimes over sand and silt near vegetation | Phytophils | Bradbury et al, 1999 |
45 | Spawning site preparation | Male builts a nest in form of a barrel using parts of plants and renal secretions | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Males builds a barrel-shaped nest with plant fragments and renal secretions | No category | Internet, 2005 |
45 | Spawning site preparation | The male builds a barrel-shaped nest in shallow, sandy areas from plant fragments glued together on the bottom with kidney secretions | No category | Coad, 2005 |
45 | Spawning site preparation | Male builts a nest with rests of plants (Arianophile) | No category | Billard, 1997 |
45 | Spawning site preparation | Male defends a teritory and builts a nest with piece of plants sticking by secretion from kidney | No category | Crivelli, 2001 |
45 | Spawning site preparation | Just before breeding, males become very territorial. The male builds a nest of plant-material glued together with spigging, a protein produced in the kidney. | No category | Fishbase, 2006 |
45 | Spawning site preparation | The nest is constructed of small twigs and plant debris, held together by the mucilaginous kidney secretion emitted by the male | No category | Scott and Crossman, 1973 |
45 | Spawning site preparation | Form nest | No category | Environment agency, ??? |
45 | Spawning site preparation | Nest spawner | No category | Balon, 1975 |
45 | Spawning site preparation | The male constructs a nest of small twigs, algae or plant debris typically over a sandy or mud bottom | No category | Bradbury et al, 1999 |
45 | Spawning site preparation | Male constructs a nest | No category | Belanger et al, 1987 |
45 | Spawning site preparation | Spawn naturally in the nest of a male | No category | Wootton, 1973 |
45 | Spawning site preparation | Following construction of a pit in a sandy substratum, the male lays down a mat of filamentous algae and other vegetation, may cover this partly with substratum carried to the nes by mouth, and finally, forms a tunnel through which the female can pass during spawning. Nest materials are secured by a "glue", produced in the kidney, that contains a glycoprotein, Spiggin, the secretion of which is under the control of androgenic hormone | No category | Barber et al, 2000 |
45 | Spawning site preparation | Breeding males defend their nests in a fixed territory and care for the eggs and offpsring. The kidney of the male secretes a protein glue thatis used in nest building | No category | Sokolowska and Sokolowska, 2006 |
45 | Spawning site preparation | Eggs are deposited in nest built on mud, sand, vegetation, or flat surface of a rock; also scattered onto vegetation | Susbtrate chooser | Goodyear, 1982 |
45 | Spawning site preparation | To examine growth of the fish, 167 progeny hatched from three nests | No category | Mori and Magoshi, 1987 |
46 | Nycthemeral period of oviposition | Courtship of females and fertilization of eggs generally occurred on warm sunny days | Day | Fitzgerald, 1983 |
46 | Nycthemeral period of oviposition | After establishing a territory, building a nest, courting females, and then fertilizing the eggs laid in its nest by one or several females, a male enters the parental phase | Day | Rebs et al, 1984 |
46 | Nycthemeral period of oviposition | Three-spined sticklebacks are typical long-day breeders, and increasing water temperature and the lengthening days in psring stimulate spawning in males and females | Day | Sokolowska and Sokolowska, 2006 |
47 | Mating system | One male and several female, female lay their eggs in several nest | Polygyny | Bruslé and Quignard, 2001 |
47 | Mating system | The male has a complex courtship dance with zig-zag motions and a leading motion to the nest. A responsible female adopts a submissive head up position, which also reveals the egg-swollen belly … | No category | Coad, 2005 |
47 | Mating system | Complex courtship ! | No category | Crivelli, 2001 |
47 | Mating system | By pair, one male and and one female, but both male and female may mate with more than once with different partners | Monogamy | Fishbase, 2006 |
47 | Mating system | Male mate with 2 or 3 different females on average [Polygamous] | No category | Fitzgerald, 1983 |
47 | Mating system | Sneak: pairspawning with sneakers or satellites, About 10% of nests were subjected to egg stealing and sneaking fertilization | No category | Ah-King et al, 2004 |
48 | Spawning release | Multiples | Multiple | Rinchard, 1996 |
48 | Spawning release | Female can spawn several times per year | Multiple | Crivelli, 2001 |
48 | Spawning release | Females may lay eggs in sevreral nests over a period of several days or may be courted by the same male | Multiple | Fishbase, 2006 |
48 | Spawning release | Estimated number of clutches per female is about 14 | No category | Copp et al, 2002 |
48 | Spawning release | 50-300 in several spawnings. mostly less than 100 and more than 50 per batch | Multiple | Internet, 2005 |
48 | Spawning release | 100-400 eggs per batch | Multiple | Bruslé and Quignard, 2001 |
48 | Spawning release | Males and females only complete one spawning in natural conditions though laboratory studies show males capable of 5 reproductive cycles and females of producing a clutch of eggs every 3-4 days. | No category | Coad, 2005 |
48 | Spawning release | Several female can spawn in the same nest | Multiple | Crivelli, 2001 |
48 | Spawning release | The female deposits up to a few hundred eggs | No category | Fishbase, 2006 |
48 | Spawning release | Eggs are laid in clusters | Fractional | Scott and Crossman, 1973 |
48 | Spawning release | Clutches of 112 ± 19 | No category | Wallace and Selman, 1979 |
48 | Spawning release | Clutches of 33-660 eggs | No category | Poizat et al, 2002 |
48 | Spawning release | May ovulate several batches in a season is conditions are favourable | Multiple | Tyler and Sumpter, 1996 |
48 | Spawning release | Eggs are deposited in clusters in the nest | Fractional | Bradbury et al, 1999 |
48 | Spawning release | Several batches during a breeding season | Multiple | Poncin et al, 1987 |
48 | Spawning release | Spawn several in breeding season | Multiple | Wootton, 1973 |
48 | Spawning release | Female have the physiological capacity to spawn several times during a breeding season. A well-fed female spawn 10 or more times in a breeding season | Multiple | Ali and Wooton, 1999 |
48 | Spawning release | The numbers of mature oocytes decreased gradually to the end of breeding as a consequence of multiple spawning | Multiple | Sokolowska and Sokolowska, 2006 |
48 | Spawning release | The female lays about 100 to 150 eggs at a time. | No category | Swarup, 1958 |
48 | Spawning release | Several spawnings may occur each season | Multiple | Goodyear, 1982 |
49 | Parity | Semelparous, broodstock die after the spawning | Semelparous | Bruslé and Quignard, 2001 |
49 | Parity | Can reproduce twice in a year | No category | Billard, 1997 |
49 | Parity | Have a maximum lifespan of about 2 and 1.5 years | No category | Bradbury et al, 1999 |
49 | Parity | All nest builders survived | No category | Barber et al, 2000 |
49 | Parity | Male guards nests and newly hatched larvae fry for maximum of 9 day and then begins return to deeper water | Iteroparous | Goodyear, 1982 |
49 | Parity | After the breeding season, though there was a large mortality, a few of those remaining have experienced two summers and /or two winters. […] Usually, the three-spined stickleback had a life-span of year and a few months | No category | Mori and Magoshi, 1987 |
50 | Parental care | Male guards and ventilates eggs until hatching, and then continue to protect larvae for 2 weeks [Fight between males] | Male parental care | Bruslé and Quignard, 2001 |
50 | Parental care | Male guards and fans the eggs and guards the fry | Male parental care | Coad, 2005 |
50 | Parental care | Male guards eggs and juveniles | Male parental care | Billard, 1997 |
50 | Parental care | Male guards and aerates his nest | Male parental care | Crivelli, 2001 |
50 | Parental care | Male guards and ventilates the eggs and young | Male parental care | Fishbase, 2006 |
50 | Parental care | Male guards the newly hatched fish until they are able to care for themselves | Male parental care | Scott and Crossman, 1973 |
50 | Parental care | Males care for eggs and fry | Male parental care | Fitzgerald, 1983 |
50 | Parental care | Males protect brood | Male parental care | Environment agency, ??? |
50 | Parental care | Male care only | Male parental care | Ah-King et al, 2004 |
50 | Parental care | The male guards and fans the nest and protects the young for up to 2 weeks after hatching or until they are able to fend for themselves | Male parental care | Bradbury et al, 1999 |
50 | Parental care | Male fans its eggs during their development. We found no significant difference when we compared the proportion of time males spent fanning their nests during the day with night levels? However, nocturnal fanning bouts were significantly longer and less numerous than diurnal ones. | No category | Rebs et al, 1984 |
50 | Parental care | After collecting eggs for a period of between 1 and 10 days, the male switches to the parental phase, during which he actively repels potential egg predators, fans oxygenated water through the nest and removes unfertilized eggs and dead or diseased embryos | No category | Barber et al, 2000 |
50 | Parental care | Male guards nests and newly hatched larvae fry for maximum of 9 day and then begins return to deeper water | Male parental care | Goodyear, 1982 |