Trait completeness | 82% |
Total data | 145 |
References | 19 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.2-1.5 | 1.35 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1-1.5 | 1.25 mm | Fishbase, 2006 |
1 | Oocyte diameter | Mean of 1.366, from 0.52 to 1.872 [Maturing eggs] | 1.37 mm | Sokolowska and Skora, 2001 |
1 | Oocyte diameter | 1.7 [Large mature oocytes] | 1.7 mm | Copp et al, 2002 |
1 | Oocyte diameter | 1.2 [Not specified] | 1.2 mm | Copp et al, 2002b |
1 | Oocyte diameter | Means or most common values and ranges in parentheses => 1.42 (1.18-1.55) in Alaskan Lake; 1.3 in Newfoundland; 1.76 (1.53-1.98) in Lake Superiour USA; (1.4-1.8) in Indiana Lake USA | 1.36 mm | Heins et al, 2003 |
2 | Egg size after water-hardening | Mainly 1.2, varying between 1.2-1.25 [Drifting eggs] | 1.23 mm | Copp et al, 2002b |
3 | Egg Buoyancy | Demersal | Demersal | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Sticky | Adhesive | Fishbase, 2006 |
5 | Incubation time | 8-15 at 10°C | 11.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | 10-20 | 15.0 days | Lafaille and Feunteun, 2001 |
5 | Incubation time | 7 days at 18°C | 7.0 days | Fishbase, 2006 |
5 | Incubation time | 4-6.75 days [96 hours at 20°C, 162 hours at 15°C] | 5.38 days | Shadrin, 1996 |
5 | Incubation time | Embryogenesis lasts about seven days (162 hours) at 15°C | 162.0 days | Shadrin and Ozernyuk, 2002 |
5 | Incubation time | Eggs hatch in 9 days or less; in 4 or 5 days at 64-66°F | 65.0 days | Goodyear, 1982 |
6 | Temperature for incubation | 10 | 10.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | 18 | 18.0 °C | Fishbase, 2006 |
6 | Temperature for incubation | 15-20 can be considered the optimum [5° is beyond the lower limit of tolerant zone, 28-30 the upper limit] | 17.5 °C | Shadrin, 1996 |
6 | Temperature for incubation | 15 | 15.0 °C | Shadrin and Ozernyuk, 2002 |
7 | Degree-days for incubation | 100-150 | 125.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | About 130 [7 days at 18°C] | 130.0 °C * day | Fishbase, 2006 |
7 | Degree-days for incubation | 80-100 [96 hours at 20°C, 162 hours at 15°C] | 90.0 °C * day | Shadrin, 1996 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 2-3 | 2.5 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 4.2-4.57 | 4.38 mm | Shadrin, 1996 |
9 | Larvae behaviour | Newly hatched larvae move to the top of the nest and settle to it | Demersal | Fishbase, 2006 |
9 | Larvae behaviour | Newly hatched larve move to the top of the nest where they remain relativelt inactive | Demersal | Bradbury et al, 1999 |
11 | Temperature during larval development | 15 | 15.0 °C | Shadrin and Ozernyuk, 2002 |
12 | Sibling intracohort cannibalism | Male eat egg and fry | Absent | Fitzgerald, 1983 |
14 | Onset of exogeneous feeding | About five days after hatching at 15°C, begin the transition to mixed feeding | 15.0 °C * day | Shadrin and Ozernyuk, 2002 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 1 [Sex not precised] | 1.0 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 1 [Sex not precised] | 1.0 year | Lafaille and Feunteun, 2001 |
15 | Age at sexual maturity | 1-2 [Unsexed] | 1.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 2 [Adult female] | 2.0 year | Heins et al, 2003 |
15 | Age at sexual maturity | 1 [Not specified] | 1.0 year | Environment agency, ??? |
15 | Age at sexual maturity | Mean or most common values and ranges in parenthses => 2+ in Alaskan Lake; 1+ (2+) in Québec river, 2+ in Québec Lake; 2+ (1-5+) in Lake Superior USA; 1+ (2-3) in English stream | 3.0 year | Heins et al, 2003 |
16 | Length at sexual maturity | 3.7 [Unsexed] | 3.7 cm | Fishbase, 2006 |
16 | Length at sexual maturity | 3.8-5.7 [Female] | 4.75 cm | Sokolowska and Skora, 2001 |
16 | Length at sexual maturity | 5.33-5.8 [Mean size of reproducing female], with smallest of 4.47-4.81 | 5.56 cm | Heins et al, 2003 |
16 | Length at sexual maturity | 3.5 [SL, smallest individual with ripe eggs] | 3.5 cm | Copp et al, 2002 |
16 | Length at sexual maturity | Mean or most common values and ranges in parenthses => 53.1 (39.9-71.8) Ls in Alaskan Lake; 38 (30-54) in Québec river, 47 (c. 35-54) in Québec Lake; (48-61) in Indiana Lake USA; (28-48) in English stream | 55.85 cm | Heins et al, 2003 |
17 | Weight at sexual maturity | 0.244-0.953 g | 0.6 kg | Sokolowska and Skora, 2001 |
17 | Weight at sexual maturity | 1.095-1.298 g and smallest female were 0.66-0.69 | 1.2 kg | Heins et al, 2003 |
17 | Weight at sexual maturity | The mean size of reproducing (clutch bearing) females was 58.1 mm Ls (1.298 g) in 1994 and 53.3 mm Ls (1.092 g) in 1998 | 58.1 kg | Heins et al, 2003 |
19 | Relative fecundity | Mean of 109 [Range from 47 to 393] | 109.0 thousand eggs/kg | Sokolowska and Skora, 2001 |
19 | Relative fecundity | About 100 | 100.0 thousand eggs/kg | Copp et al, 2002 |
20 | Absolute fecundity | Maximum fecundity recorded is 0.199 | 0.2 thousand eggs | Sokolowska and Skora, 2001 |
20 | Absolute fecundity | Mean clutch size: 0.076, range 0.37-0.176 | 0.27 thousand eggs | Fitzgerald, 1983 |
20 | Absolute fecundity | Cluth size in different areas, means or most common values whereas ranges are in parentheses => 126 (63-269) in Alaskan Lake; 31 (10-71) in Québec River; 76 (37-176) in Québec tidal creek; (32-170) in English stream | 166.0 thousand eggs | Heins et al, 2003 |
22 | Onset of oogenesis | Based on GSI graph, slight increase between November to February | ['January', 'February', 'November'] | Copp et al, 2002 |
22 | Onset of oogenesis | Based on GSI graph, slight increase between August and September and another between November and December | ['August', 'September', 'November', 'December'] | Sokolowska and Skora, 2002 |
23 | Intensifying oogenesis activity | Based on GSI graph, in February GSI increased from 5 to 35% in females | ['February'] | Copp et al, 2002 |
23 | Intensifying oogenesis activity | Based on GSI graph, from April until July (during the spawning season) | ['April', 'May', 'June', 'July'] | Sokolowska and Skora, 2002 |
24 | Maximum GSI value | About 35 in end of March [With eviscerated weight, i.e. about 25%] | 35.0 percent | Copp et al, 2002 |
24 | Maximum GSI value | In females, the ovaries wan make up as much as 20% of the total weight during the reproductive period | 20.0 percent | Sokolowska and Skora, 2002 |
26 | Resting period | September to February | 6.0 months | Copp et al, 2002 |
26 | Resting period | Based on GSI graph, in August and perhaps until november | 2.0 months | Sokolowska and Skora, 2002 |
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 [Sex not precised] | 1.0 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 1 [Sex not precised] | 1.0 years | Lafaille and Feunteun, 2001 |
27 | Age at sexual maturity | 1-2 [Unsexed] | 1.5 years | Fishbase, 2006 |
27 | Age at sexual maturity | 1 [Not specified] | 1.0 years | Environment agency, ??? |
27 | Age at sexual maturity | Mean or most common values and ranges in parenthses => 2+ in Alaskan Lake; 1+ (2+) in Québec river, 2+ in Québec Lake; 2+ (1-3+) in Lake Superior USA; 1+ (2-3) in English stream | 2.0 years | Heins et al, 2003 |
28 | Length at sexual maturity | 3.7 [Unsexed] | 3.7 cm | Fishbase, 2006 |
28 | Length at sexual maturity | Average of 4.97-5.02 | 4.99 cm | Heins et al, 2003 |
28 | Length at sexual maturity | Mean or most common values and ranges in parenthses => 53.1 (39.9-71.8) Ls in Alaskan Lake; 38 (30-54) in Québec river, 47 (c. 35-54) in Québec Lake; (48-61) in Indiana Lake USA; (28-48) in English stream | 55.85 cm | Heins et al, 2003 |
29 | Weight at sexual maturity | Average 1.015-1.03 g ! | 1.02 kg | Heins et al, 2003 |
29 | Weight at sexual maturity | The mean size of reproducing (clutch bearing) females was 58.1 mm Ls (1.298 g) in 1994 and 53.3 mm Ls (1.092 g) in 1998 | 58.1 kg | Heins et al, 2003 |
31 | Onset of spermatogenesis | February-March | ['February', 'March'] | Copp et al, 2002 |
31 | Onset of spermatogenesis | Early spermatogenetic stages, e.g. spermatogonia and spermatocytes began to dominate after spawning in August | ['August'] | Sokolowska and Skora, 2002 |
31 | Onset of spermatogenesis | Based on GSI graph: strong increase between July and August and then remained relativelt constant | ['July', 'August'] | Sokolowska and Skora, 2002 |
32 | Main spermatogenesis activity | March-April | ['March', 'April'] | Copp et al, 2002 |
32 | Main spermatogenesis activity | Based on GSI graph: strong increase between July and August and then remained relativelt constant | ['July', 'August'] | Sokolowska and Skora, 2002 |
33 | Maximum GSI value | 7.4-8 [August] | 7.7 percent | Copp et al, 2002 |
33 | Maximum GSI value | Based on GSI graph: 1.0 in February | 1.0 percent | Sokolowska and Skora, 2002 |
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 | No migration | No data | Agence de l'eau, |
36 | Spawning migration distance | Move inshore to shoals and harbors or upstream into creeks | No data | Goodyear, 1982 |
39 | Spawning season | April-June | ['April', 'June'] | Billard, 1997 |
39 | Spawning season | April-May and in July in Nothern region | ['April', 'May', 'July'] | Bruslé and Quignard, 2001 |
39 | Spawning season | April-June | ['April', 'June'] | Lafaille and Feunteun, 2001 |
39 | Spawning season | May-June [Also in April until August] | ['April', 'May', 'June', 'July', 'August'] | Fishbase, 2006 |
39 | Spawning season | Summer | ['July', 'August', 'September'] | Scott and Crossman, 1973 |
39 | Spawning season | May-June | ['May', 'June'] | Heins et al, 2003 |
39 | Spawning season | Last week of May and most nest building was finished by mid-June and was extremely rare after June 30 [Sexually mature individuals were found in the pools in early May] | ['May', 'June'] | Fitzgerald, 1983 |
39 | Spawning season | April-July | ['April', 'July'] | Environment agency, ??? |
39 | Spawning season | April-May | ['April', 'May'] | Terver, 1984 |
39 | Spawning season | In most areas thoughout its range, spawning occurs in the summer in relatively shallow areas containing dense aquatic vegetation | ['July', 'August', 'September'] | Bradbury et al, 1999 |
39 | Spawning season | May-July | ['May', 'July'] | Goodyear, 1982 |
39 | Spawning season | The breeding season in the Bay begins at the end of April and ends in July | ['April', 'July'] | Sokolowska and Skora, 2002 |
39 | Spawning season | May-June [Alaskan Lake], Late June-early July [Alaskan Lake], June-July [Newfoundland, Québec River], Early May-Late June [Québec tidal creek], Mid-June-late July [Lake Superior, U.S.A], April-August [Indiana Lake, U.S.A], April-May [English Stream], June-July (North) and April-May (South) [In Europe], Late January-late June [Japan] | ['January', 'April', 'May', 'June', 'July', 'August'] | Heins et al, 2003 |
40 | Spawning period duration | 4-6 | 5.0 weeks | Fitzgerald, 1983 |
40 | Spawning period duration | 4-5 | 4.5 weeks | Terver, 1984 |
40 | Spawning period duration | The females were able to spawn for almost four months of the year in Puck Bay | No data | Sokolowska and Skora, 2002 |
41 | Spawning temperature | >15°C [Little courtship occur when water temperature often exceed 25°C] | 15.0 °C | Fitzgerald, 1983 |
41 | Spawning temperature | At 49-62°F; peak spawning occurs at 52-54°F | 55.5 °C | Goodyear, 1982 |
42 | Spawning water type | Shallow tidal Pools | No category | Fitzgerald, 1983 |
42 | Spawning water type | Although ninespine stickleback have a relatively high salinity tolerance, they have only been reported to spawn in freshwater | No category | Bradbury et al, 1999 |
42 | Spawning water type | Quiet areas in vegetated bays and creeks, 1-5 feet from shore; may also spawn along exposed shoreline but this is not as successful | Stagnant water | Goodyear, 1982 |
43 | Spawning depth | Generally nest in water less than 30 cm deep | 30.0 m | Fitzgerald, 1983 |
43 | Spawning depth | Shallow areas, yet spawning has been observed at depths of 5-40 m in some areas | 22.5 m | Bradbury et al, 1999 |
43 | Spawning depth | To 144 feet, but usually less than 60 feet; usually nests 1-8 inches above substrates | 4.5 m | Goodyear, 1982 |
44 | Spawning substrate | Aquatic plants | Phytophils | Lafaille and Feunteun, 2001 |
44 | Spawning substrate | Among the weeds | Phytophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Prefers to nest in relatively thick vegetation, but are not confined to these areas (rocks) | Lithophils | Fitzgerald, 1983 |
44 | Spawning substrate | Weed | Phytophils | Environment agency, ??? |
44 | Spawning substrate | Ariadnophil | No category | Balon, 1975 |
44 | Spawning substrate | Areas containing dense aquatic vegetation | Phytophils | Bradbury et al, 1999 |
44 | Spawning substrate | Eggs are deposited in nest built on vegetation, rock, or rubble, or inhighly organic mud or sand | Lithophils | Goodyear, 1982 |
45 | Spawning site preparation | Male built a nest with parts of aquatic plants | No category | Bruslé and Quignard, 2001 |
45 | Spawning site preparation | Male builts a nest among aqutic plants, using piece of plants | No category | Lafaille and Feunteun, 2001 |
45 | Spawning site preparation | The male builts the nest with plant fragments and binds it together with a kidney secretion | No category | Fishbase, 2006 |
45 | Spawning site preparation | Both sex are aggresive in breeding season. The male builts a nest, usually off the bottom, in the plants, using fragments of aquatic vegetation bound together (gluing) by the threadlike, kidney secretion that hardens on contact with water | Nest built by both parents | Scott and Crossman, 1973 |
45 | Spawning site preparation | The sexually mature male establishes a territory on or near the substrate and then builts a nest | Susbtrate chooser | Fitzgerald, 1983 |
45 | Spawning site preparation | Male builds nest | No category | Environment agency, ??? |
45 | Spawning site preparation | Nest spawner | No category | Balon, 1975 |
45 | Spawning site preparation | Male have territories and have nests | No category | Ah-King et al, 2004 |
45 | Spawning site preparation | Males construct a nest made of algae and other plants debris. | No category | Bradbury et al, 1999 |
45 | Spawning site preparation | Eggs incubate in nest constructed of fine plant fragments held together by secretions of the male | No category | Goodyear, 1982 |
45 | Spawning site preparation | In the nest of a single male | No category | Heins et al, 2003 |
46 | Nycthemeral period of oviposition | Courtship of females and fertilization of eggs generally occurred on warm sunny days | Day | Fitzgerald, 1983 |
47 | Mating system | More than one female may deposit eggs in the nest | No category | Fishbase, 2006 |
47 | Mating system | By pair, but a nest contains eggs coming from different females | Monogamy | Bruslé and Quignard, 2001 |
47 | Mating system | As many as 7 females may be encouraged to deposit eggs in one nest | No category | Scott and Crossman, 1973 |
47 | Mating system | Males mate with 4 different females [Polygamous] | Polygyny | Fitzgerald, 1983 |
47 | Mating system | Sneak: pairspawning with sneakers or satellites | No category | Ah-King et al, 2004 |
48 | Spawning release | Multiple spawner | Multiple | Fitzgerald, 1983 |
48 | Spawning release | Female release about 100 eggs | No category | Bruslé and Quignard, 2001 |
48 | Spawning release | Female lays about 50 to 80 eggs | No category | Fishbase, 2006 |
48 | Spawning release | 20-30 batches of eggs | Multiple | Scott and Crossman, 1973 |
48 | Spawning release | Estimated number of clutches per female is about 21.3 | No category | Copp et al, 2002 |
48 | Spawning release | The range of clutch size in the two lakes was similar accross the 2 years. In Airolo Lake clutches ranged in size from 43 to 291 eggs (females 40.3-70.4mm Ls), whereas clutches in Dog Bone Lake contained 36-261 eggs (females 40.5-68.7 mm Ls) | No category | Heins et al, 2005 |
48 | Spawning release | May spawn more than once a season | Multiple | Goodyear, 1982 |
48 | Spawning release | The presence of partly spent females shows that spawning in this species is portioned: a female can spawn several times during one breeding season. After one clutch of eggs has been laid in the nest the next batch of oocytes begins to mature in the ovaries | Multiple | Sokolowska and Skora, 2002 |
48 | Spawning release | In most populations probably produce multiple clutches of eggs during a spawning season | Multiple | Heins et al, 2003 |
49 | Parity | Several spawns per year | Iteroparous | Billard, 1997 |
49 | Parity | Die few weeks after spawning | Semelparous | Lafaille and Feunteun, 2001 |
49 | Parity | Longevity of the river form was 1 year and some months, whereas the lake form lived for more than 2 years | No category | Bradbury et al, 1999 |
50 | Parental care | Male guard its nest and the spawning until and after the htaching of eggs | Male parental care | Bruslé and Quignard, 2001 |
50 | Parental care | The male guards and aerates the eggs | Male parental care | Fishbase, 2006 |
50 | Parental care | The nest is guarded by the male who engages in considerable fanning at the entrance, causing a current ot flow through the nest and aerate the eggs within [The male may build a second nest] | Male parental care | Scott and Crossman, 1973 |
50 | Parental care | Males care for eggs and fry | Male parental care | Fitzgerald, 1983 |
50 | Parental care | Male guarding and fanning | Male parental care | Ah-King et al, 2004 |
50 | Parental care | Male guards the nest and aerate the eggs through fanning with their pectoral fins | Male parental care | Bradbury et al, 1999 |
50 | Parental care | Male guards nest and fry | Male parental care | Goodyear, 1982 |
50 | Parental care | The fry remain close to the males and do not swim far from the nest | No care | Sokolowska and Skora, 2002 |