Trait completeness | 68% |
Total data | 70 |
References | 17 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.8-2.1 but also 2.4-2.8 [Not specified] | 1.95 mm | Internet, 2005 |
1 | Oocyte diameter | 1.6-2.1 | 1.85 mm | Fishbase, 2006 |
1 | Oocyte diameter | 1.5 [Average diameter of the largest oocyte in fully developed ovaries] | 1.5 mm | Vila-Gispert and Moreno-Amich, 2002 |
1 | Oocyte diameter | Mature oocytes were seen in follicles greater than 1.6 mm in diameter, and the number increased as the diameter became larger | 1.6 mm | Koya et al, 2000 |
2 | Egg size after water-hardening | Fertilised eggs began to appear in 1.8-1.9 mm follicles (2.4%) adn Increased to 16.0% in 1.90-2.0 mm follicles [The fertilized eggs were sligtly larger in diameter than mature oocytes] | 1.85 mm | Koya et al, 2000 |
3 | Egg Buoyancy | Demersal [but embedded in the ovary] | Demersal | Internet, 2005 |
4 | Egg adhesiveness | Chorion filaments are adhesive | Adhesive | Internet, 2005 |
5 | Incubation time | The gestation period is 21-28 days | 24.5 days | Internet, 2005 |
5 | Incubation time | A normal gestation period for moquitofish is 3-4 weeks | 3.5 days | Meefe, 1987 |
5 | Incubation time | The ovarian events between two successive parturitions were summarized as follows: active vitellogenesis (days 0-3), maturation and fertilization (days 3-5), progress of embryonic developmentand beginning of vitellogenesis for the following gestation (day 10), and pre-parturition and progress of vitellogenesis (day 20). | 1.5 days | Koya et al, 2000 |
6 | Temperature for incubation | 25°C | 25.0 °C | Koya et al, 2000 |
7 | Degree-days for incubation | 100-120 [Seems to 5-6 days at 25°C] | 110.0 °C * day | Koya et al, 2000 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 7-10 | 8.5 mm | Internet, 2005 |
8 | Initial larval size | 5-10 | 7.5 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 8.5 | 8.5 mm | Olden et al, 2006 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 0.4 | 0.4 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 0.4 [4 months, age at maturation] | 0.4 year | Vila-Gispert and Moreno-Amich, 2002 |
15 | Age at sexual maturity | 0.1 [Both sex] | 0.1 year | Olden et al, 2006 |
16 | Length at sexual maturity | 2.6 [Female specified] | 2.6 cm | Bruslé and Quignard, 2001 |
16 | Length at sexual maturity | 2.4 [Both sex] | 2.4 cm | Olden et al, 2006 |
16 | Length at sexual maturity | Nine females comprised three large individuals (4.5-5 cm) in length born the predecing year, three middle-sized individuals (2.5-3 in length) born early in the year | 4.75 cm | Medlen, 1951 |
16 | Length at sexual maturity | Adult females > 2.3 cm | 2.3 cm | Hughes, 1985 |
18 | Female sexual dimorphism | A small pigmented spot dorsal to the anus occurs in female poecilliid fishes before they are matured. As they become mature and gravid, the spot becomes larger reaching its maximum size shortly before the birth of the brrod. This prigmented spot is referred to as the "gravid spot". After the brrod is born, the gravid spot recedes, but there is never a complete loss of the pigmented mass. | Absent | Medlen, 1951 |
20 | Absolute fecundity | 0.250 [Average number of vitellogenic oocyes of mature females in a single spawning season] | 0.25 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
21 | Oocyte development | Viviparous | No category | Billard, 1997 |
21 | Oocyte development | Viviparous | No category | Koya and Iwase, 2004 |
22 | Onset of oogenesis | April | ['April'] | Koya et al, 1998 |
23 | Intensifying oogenesis activity | May-June | ['May', 'June'] | Koya et al, 1998 |
24 | Maximum GSI value | 23-24.1 [From late June to early October] | 23.55 percent | Koya et al, 1998 |
24 | Maximum GSI value | 20-22% , every 22 days during the reproductive season | 21.0 percent | Koya et al, 2000 |
26 | Resting period | 1.0-1.1 [From January to April] | 1.05 months | Koya et al, 1998 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 0.4 [Both sex] | 0.4 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 0.1 [Both sex] | 0.1 years | Olden et al, 2006 |
27 | Age at sexual maturity | Age at sexual maturity averaged 43.3 and 62.1 days for individually and group-reared males, respectively | 43.3 years | Campton and Gall, 1988 |
28 | Length at sexual maturity | 1.3-2 [Male specified] | 1.65 cm | Bruslé and Quignard, 2001 |
28 | Length at sexual maturity | 2.4 [Both sex] | 2.4 cm | Olden et al, 2006 |
30 | Male sexual dimorphism | Internal fertilization is possible because the anal fin is modified into a copulatory organ | Absent | Fishbase, 2006 |
30 | Male sexual dimorphism | Nine females and two mature males, as determined by the number of segments in the third ray of the gonopodium | Absent | Medlen, 1951 |
30 | Male sexual dimorphism | The anal fin of the adult male is modified into a long and slender intromittent organ, the gonopodium, which the male can extend at various angles and directions from the body | Absent | Martin, 1975 |
31 | Onset of spermatogenesis | Early May | ['May'] | Koya and Iwase, 2004 |
32 | Main spermatogenesis activity | Mid-May to early June [Increase from 0.9-3.2%] | ['May', 'June'] | Koya and Iwase, 2004 |
33 | Maximum GSI value | 3.8 [June to July] | 3.8 percent | Koya and Iwase, 2004 |
35 | Resting period | Resting period is October to April [The GSI values (0.9-2.1%) from January to May] | 1.5 months | Koya and Iwase, 2004 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
39 | Spawning season | April-September | ['April', 'September'] | Internet, 2005 |
39 | Spawning season | Beginning of June until end of September | ['June', 'September'] | Crivelli and Quatre, 2001 |
39 | Spawning season | In both years, no females with embryos were found before April. High percentages of adult females had embryos in June and july and (in 1983) in early august. By late september 1982 no females with embryos were found; and in 1983 only a very few gravid females were found in late September | ['April', 'June', 'September'] | Hughes, 1985 |
40 | Spawning period duration | 24-26 [6.00 months, length of breeding season] | 25.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
40 | Spawning period duration | Total sexual acts peaked on 8 June; howeevr increased numbers of males caused the mean sexual acts per male to be less than on 14 April, the date of maxima sexual activity. In mid and late summer, density, individual sexual acts, and mean male sexual acts all decreased: 28 July was the only date on which females outnumbered males [Other sutdies: the reproductive period in females mosquitofish varied from 8 to 15 weeks in Illinois during July through October, while others reported that "waves" of yound apperared from June to October in their Long Island study area.] | 8.0 weeks | Martin, 1975 |
41 | Spawning temperature | 15.5 up to 30 | 15.5 °C | Internet, 2005 |
41 | Spawning temperature | 17-21 | 19.0 °C | Koya et al, 1998 |
41 | Spawning temperature | 25-30 for the release of neonates | 27.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | 16 [Temperature at which spawning is typically initiated] | 16.0 °C | Olden et al, 2006 |
41 | Spawning temperature | Mosquitofish need more than 18°C temperature and 12.5 h daylength for their reproduction, and that brood interval is kept almost constant if the water temperature and photoperiod are constant. | 18.0 °C | Koya et al, 2000 |
41 | Spawning temperature | Critical temperature sould be near 15.56°C | 15.56 °C | Medlen, 1951 |
41 | Spawning temperature | 25-30°C was an optimal range for reproduction in California mosquitofish | 27.5 °C | Cech et al, 1992 |
42 | Spawning water type | Variable: sluggish water, land-locked ponds, reservoirs, creeks, streams, and sloughs [Mostly in freshwater but oligohaline water] | Stagnant water | Internet, 2005 |
44 | Spawning substrate | Bearer [Viviparous] | No category | Balon, 1975 |
45 | Spawning site preparation | No special placement of zygotes | No category | Vila-Gispert and Moreno-Amich, 2002 |
47 | Mating system | Male fish use a gonodopodium [modified from anal fin rays] to contact's female urogenital tract and transfer sperm. | No category | Internet, 2005 |
47 | Mating system | Male very aggresive, wants to deposit their sperm in the biggest number of females into a special pocket [Sperm can remain viable for three months] | No category | Crivelli and Quatre, 2001 |
48 | Spawning release | Females can have up to six groups of frys during a season | No category | Crivelli and Quatre, 2001 |
48 | Spawning release | Viviparous | No category | Koya et al, 1998 |
48 | Spawning release | Release 10-100 neonates by batch, each 3-4 weeks, i.e. 3 or 5 times per year | Multiple | Bruslé and Quignard, 2001 |
48 | Spawning release | The female carries about 30 alevins and gestation last for a period of 24 days to a month | No category | Fishbase, 2006 |
48 | Spawning release | More than four spawning per year | No category | Vila-Gispert and Moreno-Amich, 2002 |
49 | Parity | Weak longevity: 6 to 18 months. This species is usually annual with fex individuals able to life and reproduce at 2 years of age | No category | Bruslé and Quignard, 2001 |
49 | Parity | No obvious seasonal peak | No category | Fishbase, 2006 |
50 | Parental care | Female is viviparous, internal fecondation: ovovipariy lecitotrophe | No category | Bruslé and Quignard, 2001 |
50 | Parental care | Bearers, internal live bearers: the species is viviparous | No category | Fishbase, 2006 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |