Trait completeness | 100% |
Total data | 250 |
References | 44 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.62-2.09, mean 1.76 [Fertilized eggs before water-hardening] | 1.85 mm | Mansueti, 1964 |
1 | Oocyte diameter | 1.6-2.1 | 1.85 mm | Heidinger and Kayes, 1986 |
1 | Oocyte diameter | About 1.7 | 1.7 mm | Malservisi and Magnin, 1968 |
1 | Oocyte diameter | 1.0-1.9 [Not specified, but seems unswollen] | 1.45 mm | Mittelbach and Persson, 1998 |
2 | Egg size after water-hardening | Mean diameter of 2.26 mm, 1.87 to 2.81 but some describes it to reach 4.5 mm [Water hardening within the first few minutes] | 2.26 mm | Mansueti, 1964 |
2 | Egg size after water-hardening | 1.7-4.5 | 3.1 mm | Heidinger and Kayes, 1986 |
2 | Egg size after water-hardening | 3.5 [Swollen] | 3.5 mm | Scott and Crossman, 1973 |
2 | Egg size after water-hardening | 2.7 [Mean diameter of mature, fully yolked, ovarian oocyte] ??? | 2.7 mm | Olden et al, 2006 |
3 | Egg Buoyancy | Semi-demersal [Strands are slightly heavier than water and float in the current until they become untangled in debris] | Demersal | Mansueti, 1964 |
3 | Egg Buoyancy | Egg masses are semi-buoyant [They undulate with water movement and adhere to submerged vegetation or, at times, to the bottom] | Demersal | Scott and Crossman, 1973 |
3 | Egg Buoyancy | The egg cases are semi-buoyant and attach to submerged vegetation or occasionally to the bottom | Demersal | Anonymous, 2006 Chapter 3 |
4 | Egg adhesiveness | Lose its adhesive properties within 3 minutes in water | Adhesive | Mansueti, 1964 |
5 | Incubation time | 51 [5.4], 27 [8.0°C], 13 [16°C], 6 [19.7°C] | 51.0 days | Heidinger and Kayes, 1986 |
5 | Incubation time | 27 days [8.5-12°C] | 10.25 days | Mansueti, 1964 |
5 | Incubation time | 8-10 | 9.0 days | Scott and Crossman, 1973 |
5 | Incubation time | 20-27 days at peak temperatures | 23.5 days | Rue, 2001 |
5 | Incubation time | 8-10 | 9.0 days | Kerr and Grant, 1999 |
5 | Incubation time | 8-10 | 9.0 days | Anonymous, 2006 Chapter 3 |
5 | Incubation time | 10-20 days | 15.0 days | Whiteside et al, 1983 |
5 | Incubation time | 9.0 [Mean time to egg hatch within the range of average post-spawning the range post-spawning water temperatures] | 9.0 days | Olden et al, 2006 |
5 | Incubation time | Hatching occurred within 12-14 days of fertilization | 13.0 days | Fulford et al, 2006 |
5 | Incubation time | Eggs hatched to days after fertilization | No data | Jentoft et al, 2002 |
6 | Temperature for incubation | 10-20 [Considered to be the optimal temperature] | 15.0 °C | Heidinger and Kayes, 1986 |
6 | Temperature for incubation | 7.8-16.1 is the optimum [Can tolerate 7.7-22.8] | 11.95 °C | Goubier, 1990 |
6 | Temperature for incubation | 15°C [Recommended temperature of 15°C] | 15.0 °C | Kestemont and Mélard, 2000 |
6 | Temperature for incubation | 12 is the optimal temperature | 12.0 °C | Kerr and Grant, 1999 |
6 | Temperature for incubation | The incubation temperature was 11°C, until 4 day at which time the temeprature was slowly increased to 15°C | 11.0 °C | Jentoft et al, 2002 |
6 | Temperature for incubation | Beakers were arranged in a water bath at 10 ± 1°C and individually aerated | 10.0 °C | Peters et al, 2007 |
7 | Degree-days for incubation | 229-300 [About 27 days at 8.5-12°C] | 264.5 °C * day | Mansueti, 1964 |
7 | Degree-days for incubation | From 250, 216, 208 to 118 DD : 51 [5.4], 27 [8.0°C], 13 [16°C], 6 [19.7°C] | 250.0 °C * day | Heidinger and Kayes, 1986 |
7 | Degree-days for incubation | 80-110 [At a temperature of 15°C] | 95.0 °C * day | Kestemont and Mélard, 2000 |
4 | Egg adhesiveness | Adhesive | Adhesive | Williamson et al, 1997 |
2 | Egg size after water-hardening | 3.50 | 3.5 mm | Mansueti, 1964 |
6 | Temperature for incubation | 8.5-12 | 10.25 °C | Mansueti, 1964 |
6 | Temperature for incubation | 18.2 | 18.2 °C | Hinshaw, 1985 |
4 | Egg adhesiveness | Non-adhesive | Non-Adhesive | Clady and Hutchinson, 1975 |
6 | Temperature for incubation | 8-12 | 10.0 °C | Clady, 1976 |
3 | Egg Buoyancy | Demersal | Demersal | Newsome and Aalto, 1987 |
5 | Incubation time | 20 | 20.0 days | Newsome and Aalto, 1987 |
3 | Egg Buoyancy | Demersal | Demersal | Dettmers et al, 2005 |
5 | Incubation time | 10-20 | 15.0 days | Post and McQueen, 1988 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 5.5-6.0 | 5.75 mm | Mansueti, 1964 |
8 | Initial larval size | 4.7-6.6 | 5.65 mm | Heidinger and Kayes, 1986 |
8 | Initial larval size | 4.0-7.0 | 5.5 mm | Brown et al, 1996 |
8 | Initial larval size | 5 | 5.0 mm | Scott and Crossman, 1973 |
8 | Initial larval size | 4.8-6.0 | 5.4 mm | Mittelbach and Persson, 1998 |
8 | Initial larval size | 5 | 5.0 mm | Kerr and Grant, 1999 |
8 | Initial larval size | 4.1-5.5 | 4.8 mm | Anonymous, 2006 Chapter 3 |
8 | Initial larval size | 5.6-6.2 | 5.9 mm | Whiteside et al, 1983 |
8 | Initial larval size | 6.4 | 6.4 mm | Olden et al, 2006 |
8 | Initial larval size | Each model simulation model began with 1000 larvae, and initial size was randomly assigned to each larva from a normal distribution (mean = 5.7 mm, SD = 0.3 mm). | 5.7 mm | Fulford et al, 2006 |
8 | Initial larval size | Deduced from graph => 5.2 mm | 5.2 mm | Peters et al, 2007 |
8 | Initial larval size | The TL of larval yellow perch ranged from 4 to 11 mm on the initial dates of capture | 11.0 mm | Isermann and Willis, 2008 |
9 | Larvae behaviour | Immediatly active swimmer | Demersal | Mansueti, 1964 |
9 | Larvae behaviour | Inactive for about 5 days | Demersal | Scott and Crossman, 1973 |
9 | Larvae behaviour | The swim-up stage occurs within two to five days after hatching [The fry are slow swimmers and gather in dense schools which makes them vary vulnerable) | Pelagic | Kerr and Grant, 1999 |
9 | Larvae behaviour | Pelagic [are inactive for about 5 days until the yolk is absorbed] | Demersal | Anonymous, 2006 Chapter 3 |
9 | Larvae behaviour | Soon after hatching the larvae moved into the limnetic zone where they began feeding [This movement is probably a mechanism to escape intense predation in the littoral zone] | Demersal | Whiteside et al, 1983 |
10 | Reaction to light | Yellow perch are strongly attracted to light before they reach 50 mm | Photopositive | Kestemont and Mélard, 2000 |
11 | Temperature during larval development | Optimum is 20-23°C but can tolerate a range of 2.8-27.8°C for hatch to swim-up and optimum of 20-23.9 and tolerance range of 10-30 for feeding larvae | 21.5 °C | Heidinger and Kayes, 1986 |
11 | Temperature during larval development | 20-23.9 is the optimum [Can tolerate 2.8-27.8] | 21.95 °C | Goubier, 1990 |
11 | Temperature during larval development | In general, water temperatures varied between 10 and 22°C and it is suspected that this range prevails in the shallow waters of the natural spawning grounds. In other studies, specimens were raised under hatchery conditions around 20°C | 10.0 °C | Mansueti, 1964 |
11 | Temperature during larval development | Larvae were maintained in the lab in a 2.4 m diameter tank at 15-18°C under flow-through conditions | 16.5 °C | Fulford et al, 2006 |
11 | Temperature during larval development | Peak larval yellow perch densities generally occurred during late May or early June when surface temperatures were 12-19°C | 15.5 °C | Isermann and Willis, 2008 |
12 | Sibling intracohort cannibalism | Larvae are cannibalistic on their siblings [Cannibalism by adults also takes place weh nlarvae are > 18 mm] | Present | Craig, 2000 |
12 | Sibling intracohort cannibalism | The incidence of perch cannibalism was typically most intense in August when young perch averaged 40-70 mm length | Present | Tarby, 1974 |
12 | Sibling intracohort cannibalism | Yellow perch are known to be cannibaslitic | Absent | Kerr and Grant, 1999 |
13 | Full yolk-sac resorption | 3-5 days | 4.0 °C * day | Rue, 2001 |
14 | Onset of exogeneous feeding | Larvae were initially fed a tank culture of rotifers and small zooplankton four to six times per day. Starting five days posthatch (dph), larvae were fed Artemia nauplii four times per day (at 15-18°C). | 16.5 °C * day | Fulford et al, 2006 |
13 | Full yolk-sac resorption | 7-18 days at 20 C | 12.5 °C * day | Mansueti, 1964 |
12 | Sibling intracohort cannibalism | absent | Absent | Mansueti, 1964 |
12 | Sibling intracohort cannibalism | absent | Absent | Hinshaw, 1985 |
11 | Temperature during larval development | 16-19 | 17.5 °C | Clady, 1976 |
12 | Sibling intracohort cannibalism | absent | Absent | Brown et al, 1996 |
9 | Larvae behaviour | Pelagic | Pelagic | Dettmers et al, 2005 |
10 | Reaction to light | photopositive | Photopositive | Houde, 1969 |
12 | Sibling intracohort cannibalism | absent | Absent | Schael et al, 1991 |
12 | Sibling intracohort cannibalism | absent | Absent | Whiteside et al, 1985 |
9 | Larvae behaviour | Pelagic | Pelagic | Post, 1990 |
13 | Full yolk-sac resorption | 7-14 days | 10.5 °C * day | Post and McQueen, 1988 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 2 [Rare, most at 3-4] | 3.5 year | Heidinger and Kayes, 1986 |
15 | Age at sexual maturity | 3-4 [Sex specified] | 3.5 year | Dabrowski et al, 1996 |
15 | Age at sexual maturity | 4 [Sex specified] | 4.0 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | Female reach sexual maturity during their third or fourth summer | 3.0 year | Kerr and Grant, 1999 |
15 | Age at sexual maturity | 2-3 [Female] | 2.5 year | Anonymous, 2006 Chapter 3 |
15 | Age at sexual maturity | 2.0 [Both sex] | 2.0 year | Olden et al, 2006 |
15 | Age at sexual maturity | Except fot two age II females taken in the summern all fish older than age I were mature | 2.0 year | Brazo et al, 1975 |
15 | Age at sexual maturity | The largest immature females from the stunded population attained just over 10% of the weight of the smallest normal females which had reached maturity. At an average age of 2.84 years, stunted females matured exactly 2 years earlier tnah their normal conspecific (4.84 years). Generally, females mature 1 or more years later than male P. fluviatilis or P. flavescens. This can be as early as during the second year of life for P. flavescens. More commonly, though, females are 3 or 4 years old at first maturity, and in some populations it may take on average 5 years to become mature | 10.0 year | Jansen ,1996 |
16 | Length at sexual maturity | 14-19.1, with a mean of 15.8 [Sex specified] | 16.55 cm | Heidinger and Kayes, 1986 |
16 | Length at sexual maturity | 15.0 [Both sex] | 15.0 cm | Olden et al, 2006 |
16 | Length at sexual maturity | Size of female at age 2 range from 9.9-16.2 | 13.05 cm | Brazo et al, 1975 |
16 | Length at sexual maturity | The smallest stunded female was 8.4 cm long | 8.4 cm | Jansen ,1996 |
17 | Weight at sexual maturity | 30-40 g | 35.0 kg | Dabrowski et al, 1996 |
17 | Weight at sexual maturity | The smallest stunded female weighted 5.52 g | 5.52 kg | Jansen ,1996 |
18 | Female sexual dimorphism | Females less highly coloured | Present | Scott and Crossman, 1973 |
18 | Female sexual dimorphism | Females generally grow faster than males and reach a greater final length | Absent | Anonymous, 2006 Chapter 3 |
19 | Relative fecundity | 79-223 | 151.0 thousand eggs/kg | Heidinger and Kayes, 1986 |
19 | Relative fecundity | 190 | 190.0 thousand eggs/kg | Mittelbach and Persson, 1998 |
19 | Relative fecundity | Although the weight range of stunted and normal perch did not overlap and values had to be extrapolated for stunded fish, the above relationships between fecundity was used to calculate the fecundity of a 100g 'strandard' perch. For the stunted population this hypothetical fish produced approximatively 5000 more eggs (16556 +/-710) than a corresponding female from the normal population (11327 +/-2245). Data from other studies: 130-232 [For females 190-354 mm in Lake Michigan, US], 130-255 [For females 98-168 in Narrow Lake, CDN], 112-199 [For females 135-257, in Lake Ontario, CDN], 82-184 [For females 174-411 mm, in Patuxent River, US], 85-141 [For females 200-305 mm, in Baptiste Lake, CDN], 132-157 [For female 156-353 mm, in Lake Erie, CDN], | 16556.0 thousand eggs/kg | Jansen ,1996 |
20 | Absolute fecundity | 3-109 | 56.0 thousand eggs | Heidinger and Kayes, 1986 |
20 | Absolute fecundity | 8.618-78.741 | 43.68 thousand eggs | Anonymous, 2006 Chapter 3 |
20 | Absolute fecundity | 2-90 | 46.0 thousand eggs | Scott and Crossman, 1973 |
20 | Absolute fecundity | Fecundity ranged from 10.654 eggs for an age II female (190 mm total length, 82g) to 157,594 eggs for an age VI fish (354 mm, 678 g) | 10.65 thousand eggs | Brazo et al, 1975 |
20 | Absolute fecundity | Mean fecundity of 28 stunted females 9.8-16.8 cm, was 3992 eggs (range 1910-11812). The corresponding value for 29 normal perch (20.0-30.5 cm) was 22658 eggs (range: 10639-55592). Data from other studies: 10654-157594 [For females 190-354 mm in Lake Michigan, US], 1910-11812 [For females 98-168 in Narrow Lake, CDN], 3035-61465 [For females 135-257, in Lake Ontario, CDN], 5266-75715 [For females 174-411 mm, in Patuxent River, US], 10639-55952 [For females 200-305 mm, in Baptiste Lake, CDN], 12641-135848 [For female 156-353 mm, in Lake Erie, CDN], | 13.3 thousand eggs | Jansen ,1996 |
21 | Oocyte development | Synchronous oocyte growth | Synchronous | Heidinger and Kayes, 1986 |
21 | Oocyte development | Synchronous oocyte growth | Synchronous | Dabrowski et al, 1996 |
21 | Oocyte development | Group-synchronous development | Group-synchronous | Craig, 2000 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Kestemont and Mélard, 2000 |
22 | Onset of oogenesis | Active growth of ova starts in early september and formation of yolk in November | ['November'] | Dabrowski et al, 1996 |
22 | Onset of oogenesis | Oocyte growth during fall through winter | ['January', 'February', 'March', 'October', 'November', 'December'] | Heidinger and Kayes, 1986 |
22 | Onset of oogenesis | Mid-August until end of September | ['August', 'September'] | Malservisi and Magnin, 1968 |
22 | Onset of oogenesis | Late August until immediately before spawning, increase gradually | ['August'] | Hayes and Taylor, 1994 |
22 | Onset of oogenesis | Rapid increase of oocyte diameter from late July to November-December | ['July', 'August', 'September', 'October', 'November', 'December'] | Kestemont and Mélard, 2000 |
22 | Onset of oogenesis | In September, ovarian weights began to increase again and reached 4-5% of body weight for all age classes by mid-November, when the study was terminated | ['September', 'November'] | Brazo et al, 1975 |
22 | Onset of oogenesis | Began increasing in August and then increased siginificantly from October through March | ['March', 'August', 'October'] | Tansichuk and Mackay, 1989 |
22 | Onset of oogenesis | September | ['September'] | June, 1977 |
22 | Onset of oogenesis | Rapid gonadal development in September and October | ['September', 'October'] | Jansen ,1996 |
23 | Intensifying oogenesis activity | The increase of temperature in March induces the completion of vitellogenesis, resulting in a sharp increase of GSI before spawning | ['March'] | Kestemont and Mélard, 2000 |
23 | Intensifying oogenesis activity | March, but lacks evidence … | ['March'] | Tansichuk and Mackay, 1989 |
23 | Intensifying oogenesis activity | Increase regularly until December (10%) then from December to April | ['January', 'February', 'March', 'April', 'December'] | June, 1977 |
24 | Maximum GSI value | 21.6-22.6 | 22.1 percent | Hayes and Taylor, 1994 |
24 | Maximum GSI value | 22 in wild populations and up to 30.9% in cultured perch | 22.0 percent | Dabrowski et al, 1996 |
24 | Maximum GSI value | From 20 to 31% [Just prior to spawning] | 20.0 percent | Heidinger and Kayes, 1986 |
24 | Maximum GSI value | Mean 18.74% [March] | 18.74 percent | Malservisi and Magnin, 1968 |
24 | Maximum GSI value | The fecundity index gradually increased smoothly for all age classes from April to May reaching a value of 20-25% immediatly before spawning | 22.5 percent | Brazo et al, 1975 |
24 | Maximum GSI value | Mean 14, range 12-14 [March, but note that authors suspect that the Gsi's of yellow perch collected near to spawning (April-May) would have been higher] | 13.0 percent | Tansichuk and Mackay, 1989 |
24 | Maximum GSI value | 18% [April] | 18.0 percent | June, 1977 |
24 | Maximum GSI value | For stunted individuals: GSI vary between 22.5 to 30% and for normal females from 12.5-22.5% | 17.5 percent | Jansen ,1996 |
25 | Oogenesis duration | Period of ova growth and vitellogenesis = 200 days, followed by a short stage of final maturation of oocytes and ovulation (few days) | 200.0 months | Dabrowski et al, 1996 |
25 | Oogenesis duration | The mimimum chill period is 160 days at approximatively 10°C or less | 160.0 months | Heidinger and Kayes, 1986 |
25 | Oogenesis duration | From Mid-August until Mid-April | 9.0 months | Malservisi and Magnin, 1968 |
26 | Resting period | Mid-June until Mid-August | 4.0 months | Malservisi and Magnin, 1968 |
26 | Resting period | May until August | 5.0 months | Dabrowski et al, 1996 |
26 | Resting period | Late April to August | 6.0 months | Hayes and Taylor, 1994 |
26 | Resting period | <1% from July to August | 1.0 months | Tansichuk and Mackay, 1989 |
26 | Resting period | 1% (After the spawning, GSI remain low from May trought August) | 1.0 months | Hayes and Taylor, 1994 |
26 | Resting period | < 1% | 1.0 months | Dabrowski et al, 1996 |
26 | Resting period | Below 1%, in June and July | 1.0 months | Tansichuk and Mackay, 1989 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 1 [Rare but most at 3-4] | 3.5 years | Heidinger and Kayes, 1986 |
27 | Age at sexual maturity | 2 [Sex specified, rarely at 1] | 2.0 years | Dabrowski et al, 1996 |
27 | Age at sexual maturity | 3 [Sex specified] | 3.0 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | Males reach sexual maturity during their second summer | 2.0 years | Kerr and Grant, 1999 |
27 | Age at sexual maturity | 1 [Males] | 1.0 years | Anonymous, 2006 Chapter 3 |
27 | Age at sexual maturity | 2.0 [Both sex] | 2.0 years | Olden et al, 2006 |
27 | Age at sexual maturity | Except fot two age II females taken in the summern all fish older than age I were mature | 2.0 years | Brazo et al, 1975 |
27 | Age at sexual maturity | Out of the 483 stunded males analyzed for maturity status, almost all fish had reached maturity by the time they were two years old, and one male reached maturity after the firstgrowing season. The average age at maturity (1.61 years) of stunded males was nerly 1 year less than that of normal males (2.52 years). Males of P. flavescens and P. fluviatilis typically spawn at age 2, although in some populationsof P. fluviatilis almostall fish mature furing their first year of life, and in one reported case most male P. flavescens mature at age 1 | 483.0 years | Jansen ,1996 |
28 | Length at sexual maturity | 9.2-16.5, with a mean of 10.8 [sex specified] | 12.85 cm | Heidinger and Kayes, 1986 |
28 | Length at sexual maturity | 15.0 [Both sex] | 15.0 cm | Olden et al, 2006 |
28 | Length at sexual maturity | Size of male at age 2 range from 9.9 to 15.9 | 2.0 cm | Brazo et al, 1975 |
28 | Length at sexual maturity | The smallest fish of the stunted males was 5.9 cm. The smallest mature male from the normal population measured 10.0 cm | 5.9 cm | Jansen ,1996 |
29 | Weight at sexual maturity | 5-6 g | 5.5 kg | Dabrowski et al, 1996 |
29 | Weight at sexual maturity | The smallest fish of the stunted males weighted 1.71 g. The smallest mature male from the normal population weighted more than 10 g | 1.71 kg | Jansen ,1996 |
30 | Male sexual dimorphism | Colours of spawning males more intense, bronze-green, bars darker, lower fins suffused with orange to bhroght red | Present | Scott and Crossman, 1973 |
31 | Onset of spermatogenesis | Fast growth of the testes during autumn, begin in September and remain high until spring | ['April', 'May', 'June', 'September', 'October', 'November', 'December'] | Dabrowski et al, 1996 |
31 | Onset of spermatogenesis | GSI increased significantly in August [Testes composition did not change between Septemner and March] | ['March', 'August'] | Tansichuk and Mackay, 1989 |
32 | Main spermatogenesis activity | August: one month | ['August'] | Tansichuk and Mackay, 1989 |
33 | Maximum GSI value | 10 [In mid-october] | 10.0 percent | Heidinger and Kayes, 1986 |
33 | Maximum GSI value | 8-15% | 11.5 percent | Heidinger and Kayes, 1986 |
33 | Maximum GSI value | No value [November] | No data | Dabrowski et al, 1996 |
33 | Maximum GSI value | 5% in September | 5.0 percent | Tansichuk and Mackay, 1989 |
34 | Spermatogenesis duration | Spermatigenesis is completed by December | 2.0 months | Dabrowski et al, 1996 |
34 | Spermatogenesis duration | Rapid, within 6 weeks than testes steadily lose weight to reach 4-6% at spawning | 5.0 months | Heidinger and Kayes, 1986 |
35 | Resting period | Between 1 and 2 [After spawning, declined troughout the summer until August] | 1.0 months | Heidinger and Kayes, 1986 |
35 | Resting period | Below 1%, in June and July | 1.0 months | Tansichuk and Mackay, 1989 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Spawning migrations are usually short-ranged [On lalke system this involves movment from deep water, where the fish over-wintered, to shallow water spawning areas] | No data | Craig, 2000 |
36 | Spawning migration distance | Adults migrate shoreward into the shallows of lakes, and often into tributary rivers to spawn | No data | Scott and Crossman, 1973 |
36 | Spawning migration distance | Perch do not move extensively [Winter migrations take perch into deep water where maximum water temperatures are approximatively 4°C. in the spring fish begin to migrate to the shallow water spawning areas] | 4.0 km | Kerr and Grant, 1999 |
36 | Spawning migration distance | Move to shallower water to spawn | No data | Anonymous, 2006 Chapter 3 |
37 | Spawning migration period | In early Paril, most perch were in deep water (24 m). As water temperatures increased from 2 to 4°C, the fish moved shoreward. By 21 May, water temperature had reached 6-7°C and migration of male perch into shallow water (6-12 km) occurred | ['May'] | Brazo et al, 1975 |
37 | Spawning migration period | In the spring, males move to the shoreline first, followed by females, ans stayed on the spawning grounds longer than female | ['April', 'May', 'June'] | Heidinger and Kayes, 1986 |
37 | Spawning migration period | In the Chesapeake Bay, adult migrate from downstream tidal reaches into the upper reaches during late winter | ['January', 'February', 'March'] | Rue, 2001 |
38 | Homing | Return to their local location to spawn | Present | Craig, 2000 |
39 | Spawning season | Depending on latitudes, the spawning period extends from March to late June | ['March', 'June'] | Craig, 2000 |
39 | Spawning season | March-April | ['March', 'April'] | Mansueti, 1964 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Heidinger and Kayes, 1986 |
39 | Spawning season | April and early May | ['April', 'May'] | Kayes and Calbert, 1979 |
39 | Spawning season | Mid-April to Beginning of May | ['April', 'May'] | Malservisi and Magnin, 1968 |
39 | Spawning season | In the spring, usually from April 15 to early May, but spawning may extend into July in some areas | ['April', 'May', 'June', 'July'] | Scott and Crossman, 1973 |
39 | Spawning season | Spawning period extends from March to late June | ['March', 'June'] | Kestemont and Mélard, 2000 |
39 | Spawning season | Spaws in spring during a period when water temperatures begin to rise (mid-April to early May) | ['April', 'May', 'June'] | Kerr and Grant, 1999 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Anonymous, 2006 Chapter 3 |
39 | Spawning season | Early spring | ['April', 'May', 'June'] | Whiteside et al, 1983 |
39 | Spawning season | The spawning period occurred from the middle of May through the end of June | ['May', 'June'] | Brazo et al, 1975 |
39 | Spawning season | Mean peak spawning 1 May [Range: 14 April-20 May] in Lake Oahe, South and North Dakota | ['April', 'May'] | June, 1977 |
39 | Spawning season | Spawn in April-June and complete most of a year's growthby August | ['April', 'May', 'June', 'August'] | Purchase et al, 2005 |
39 | Spawning season | Yellow perch typically spawn in South Dakota lakes and wetlands from mid-April to mid-May […] On Lake Madison during 2000 and 2001, egg deposition on submerged conifer bundles occurred over 3-15 days periods from 21 April to 5 May at water temperatures between 7 and 17°C, and no new egg deposition was observed after the first week of May | ['April', 'May'] | Isermann and Willis, 2008 |
40 | Spawning period duration | 2-8 [Male arrive on spawnning grounds earlier than female] | 5.0 weeks | Craig, 2000 |
40 | Spawning period duration | Approximatively 2 weeks | 2.0 weeks | Heidinger and Kayes, 1986 |
40 | Spawning period duration | 2-3 | 2.5 weeks | Kayes and Calbert, 1979 |
40 | Spawning period duration | Male remain longer on the spawning grounds than do the females | No data | Scott and Crossman, 1973 |
40 | Spawning period duration | The spawning period lasts between two and four weeks [Adult males arrive on the spawning grounds days or weeks before the females] | No data | Kerr and Grant, 1999 |
40 | Spawning period duration | The spawning period occurred from the middle of May through the end of June | No data | Brazo et al, 1975 |
41 | Spawning temperature | 7-20°C [But optimal temperature at 10-13°C] | 13.5 °C | Craig, 2000 |
41 | Spawning temperature | 2.8-19.9°C [But optimum at 7.8-11.1°C] | 11.35 °C | Heidinger and Kayes, 1986 |
41 | Spawning temperature | 8.0-12.0°C | 10.0 °C | Kayes and Calbert, 1979 |
41 | Spawning temperature | 8.9-12.2 | 10.55 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | 7.8-11.1 | 9.45 °C | Goubier, 1990 |
41 | Spawning temperature | Ranging from 7 to 20°C [Usually 10-13°C] | 11.5 °C | Kestemont and Mélard, 2000 |
41 | Spawning temperature | 6-14 | 10.0 °C | Mittelbach and Persson, 1998 |
41 | Spawning temperature | Range from 5.0-12.8, with peak spawning between 8.5-11.0 | 8.9 °C | Rue, 2001 |
41 | Spawning temperature | Varies between authors: 5-14; 9-12; 7-11; 6.1-8.9 | 9.5 °C | Kerr and Grant, 1999 |
41 | Spawning temperature | 6.7-12.2°C | 9.45 °C | Anonymous, 2006 Chapter 3 |
41 | Spawning temperature | 7 [Temperature at which spawning is typically initiated] | 7.0 °C | Olden et al, 2006 |
41 | Spawning temperature | Mean of 9.2°C | 9.2 °C | June, 1977 |
41 | Spawning temperature | At water temperatures less than 17°C | 17.0 °C | Isermann and Willis, 2008 |
42 | Spawning water type | In the shallows of lakes, and often into tributary, where they live in brackish water, they migrate into fresh water | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Upper reaches of many major tributaries | No category | Mansueti, 1964 |
42 | Spawning water type | Tales place in tidal and non-tidal water | No category | Rue, 2001 |
42 | Spawning water type | Lakes and tributary streams [Sites protected from high winds and fast currents are chosen] | Stagnant water | Kerr and Grant, 1999 |
43 | Spawning depth | Shallow | No data | Scott and Crossman, 1973 |
43 | Spawning depth | Shallow : 60-90 cm deep | 75.0 m | Mansueti, 1964 |
43 | Spawning depth | 0.5-8 | 4.25 m | Craig, 2000 |
43 | Spawning depth | In lakes, spawning occrus at water depth from 0.5-3 m altough depths of up to 8 m have been reported in large lakes and reservoirs | 1.75 m | Kerr and Grant, 1999 |
44 | Spawning substrate | Usually near rooted vegetation, submerged brush, or fallen trees, but at times over sand or gravel | Lithophils | Scott and Crossman, 1973 |
44 | Spawning substrate | Over a wide variety of substrates including boulders and gravel, aquatic macrophytes, roots of trees, dead branches and other materials | Lithophils | Craig, 2000 |
44 | Spawning substrate | Non obligatory plant spawner | Phytophils | Fishbase, 2006 |
44 | Spawning substrate | Eggs adhere to sumerged plants, but other substrata are utilised if suitable plants are absent | Phytophils | Mann, 1996 |
44 | Spawning substrate | A variety of bottom is sused, including aquatic vegetation | Phytophils | Rue, 2001 |
44 | Spawning substrate | Phyto-lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Yellow perch seem to have little preference for bottom type, allowing them a wide variety of habitat choices | No category | Kerr and Grant, 1999 |
44 | Spawning substrate | Usually near rooted vegetation, fallen trees, or brush | Phytophils | Anonymous, 2006 Chapter 3 |
45 | Spawning site preparation | No nest is built | Open water/substratum scatter | Heidinger and Kayes, 1986 |
45 | Spawning site preparation | No nest is built | Open water/substratum scatter | Scott and Crossman, 1973 |
45 | Spawning site preparation | Open water/substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Zygotes are placed in a special habitat (e.g. scattered on vegetation, or buried in gravel) | Susbtrate chooser | Vila-Gispert and Moreno-Amich, 2002 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
46 | Nycthemeral period of oviposition | During the night and early morning | Day | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | The time at which yellow perch spawning occurs has been reported as being both at night and during the day | Day | Kerr and Grant, 1999 |
46 | Nycthemeral period of oviposition | Spawning takes place in the night or early in the morning | Day | Anonymous, 2006 Chapter 3 |
47 | Mating system | One female and two up to five males (even 25 males), it takes several minutes at 14-15°C and up to several days at temperatures below 5°C to extrude the entire egg mass | No category | Heidinger and Kayes, 1986 |
47 | Mating system | One female and two up to five males, during about 30 mn [described in more details] | No category | Craig, 2000 |
47 | Mating system | A single larger female and many males which swim about in a long compact queue, the first males with their snouts pressed against the females | No category | Scott and Crossman, 1973 |
47 | Mating system | Several males fertilize the eggs as they are extruded by the female in a gelatinous, convoluted string | No category | Kerr and Grant, 1999 |
47 | Mating system | Group, communal spawing: a ripe female is followed by several males, the males release sperm as she extrudes a convolued egg strand | Promiscuity | Ah-King et al, 2004 |
48 | Spawning release | Total spawner | Total | Dabrowski et al, 1996 |
48 | Spawning release | Once a year | Total | Craig, 2000 |
48 | Spawning release | All together | Total | Craig, 2000 |
48 | Spawning release | Eggs of the yellow perch are extruded in adhesive strands, eggs are extruted in long adhesive and 'accordion folded' strands about 5 cm thick | No category | Mansueti, 1964 |
48 | Spawning release | All together; | Total | Dabrowski et al, 1996 |
48 | Spawning release | Extruded in a unique transparent, gelatinous, accordion-folded string or tube | No category | Scott and Crossman, 1973 |
48 | Spawning release | Eggs are laid in masses or ribbons on structure suc as aquatic vegetation | No category | Rue, 2001 |
48 | Spawning release | Intermittent spawning | Fractional | Luksiene et al, 2000 |
49 | Parity | Iteroparous | Iteroparous | Dabrowski et al, 1996 |
49 | Parity | Have been reported to live up to 11 years | No category | Anonymous, 2006 Chapter 3 |
50 | Parental care | No protection is given the egg mass or young by either parent | No care | Heidinger and Kayes, 1986 |
50 | Parental care | There is little if any protection of the eggs | No care | Craig, 2000 |
50 | Parental care | No protection is given the egg masses or young by the parents | No care | Scott and Crossman, 1973 |
50 | Parental care | Non guarders | No care | Fishbase, 2006 |
50 | Parental care | No parental care is provided to the eggs or fry | No care | Kerr and Grant, 1999 |
50 | Parental care | No parental care | No care | Ah-King et al, 2004 |