36 |
Spawning migration distance |
Often move many males along shore to rech bays and creek mouths; stream residents congregate in pools just before spawning |
No data |
Goodyear et al, 1982 |
36 |
Spawning migration distance |
Move inshore within the same lake |
No data |
Gross and Nowell, 1980 |
37 |
Spawning migration period |
Move inshore beginning at 55°F |
No data |
Goodyear et al, 1982 |
39 |
Spawning season |
May-June |
['May', 'June'] |
Billard, 1997 |
39 |
Spawning season |
May-June |
['May', 'June'] |
Bruslé and Quignard, 2001 |
39 |
Spawning season |
April to Mid-July |
['April', 'May', 'June', 'July'] |
Carrel et al, 2001 |
39 |
Spawning season |
Late spring and ealry summer, probably June in Canada |
['April', 'May', 'June', 'July', 'August', 'September'] |
Scott and Crossman, 1973 |
39 |
Spawning season |
April to July |
['April', 'May', 'June', 'July'] |
Fishbase, 2006 |
39 |
Spawning season |
May-June |
['May', 'June'] |
Gross and Nowell, 1980 |
39 |
Spawning season |
Late spring and early summer |
['April', 'May', 'June', 'July', 'August', 'September'] |
Kerr and Grant, 1999 |
39 |
Spawning season |
April-early August, usually late May-June |
['April', 'May', 'June', 'August'] |
Goodyear et al, 1982 |
39 |
Spawning season |
Nesting was asynchronous both years, occurring from mid-May to mid-July |
['May', 'June', 'July'] |
Noltie and Keenleyside, 1987 |
40 |
Spawning period duration |
4-5 [The nesting period lasted 42 days (20 May-30 June) but most reproductive activity occurred within a 19 day period (21 May-8 June)] |
4.5 weeks |
Gross and Nowell, 1980 |
40 |
Spawning period duration |
In 1981, adult males were first seen on the breeding grounds in early May, designated at the start of the breeding season. Number of males peaked in early June, then declined to zero in late July, the end of the breeding season. The last observation of a female occurred almost 3 weeks earlier, however. The study site breeding season started earlier and finished lated then inlakes studied at similar latitudes |
1981.0 weeks |
Noltie and Keenleyside, 1987 |
41 |
Spawning temperature |
15-27 |
21.0 °C |
Carrel et al, 2001 |
41 |
Spawning temperature |
15.6-21.1 |
18.35 °C |
Scott and Crossman, 1973 |
41 |
Spawning temperature |
Breeding starts when water temperature reach 20-23 |
21.5 °C |
Gross and Nowell, 1980 |
41 |
Spawning temperature |
16-21 |
18.5 °C |
Mittelbach and Persson, 1998 |
41 |
Spawning temperature |
16-21; 15.6; 15.6-21.1 and 20.6-23.3 |
18.5 °C |
Kerr and Grant, 1999 |
41 |
Spawning temperature |
At 57-75°F, i.e., 14-24°C |
66.0 °C |
Goodyear et al, 1982 |
41 |
Spawning temperature |
16 [Temperature at which spawning is typically initiated] |
16.0 °C |
Olden et al, 2006 |
41 |
Spawning temperature |
Nesting began at water temperature lower than in lakes, where they span 20 to 23°C |
20.0 °C |
Noltie and Keenleyside, 1987 |
42 |
Spawning water type |
Lake, near the shorline |
Stagnant water |
Gross and Nowell, 1980 |
42 |
Spawning water type |
Sheltered nearshore areas, including bays, harbors, lagoons, marshes, creek mouths, and lower reaches of tributaries; current-swept lake shoals and ledges; moderateswift water in streams; |
Stagnant water |
Goodyear et al, 1982 |
43 |
Spawning depth |
Shallow waters: mean water depth of nests was 77.4 cm. While nests ranged from 45 to 138 cm depth, the majority of males (64%) nested between 50 and 69 cm |
77.4 m |
Gross and Nowell, 1980 |
43 |
Spawning depth |
50-75 cm in depth |
62.5 m |
Kerr and Grant, 1999 |
43 |
Spawning depth |
To 20 feet, usually less than 6 feet |
20.0 m |
Goodyear et al, 1982 |
43 |
Spawning depth |
Mean water depth over nest is 60.33 ± 0.92 cm |
60.33 m |
Noltie and Keenleyside, 1987 |
44 |
Spawning substrate |
Gravels or plants |
Lithophils |
Billard, 1997 |
44 |
Spawning substrate |
Gravels |
Lithophils |
Carrel et al, 2001 |
44 |
Spawning substrate |
Swamps and gravels shoals |
Lithophils |
Scott and Crossman, 1973 |
44 |
Spawning substrate |
Coarse sand to gravel, nest susbtrate averaging 1.7 cm [No nests were found in muddy, organic substrates] |
Lithophils |
Gross and Nowell, 1980 |
44 |
Spawning substrate |
Sand or gravel bottom, swamps, gravels shoals, coarse sand or gravel bottom |
Lithophils |
Kerr and Grant, 1999 |
44 |
Spawning substrate |
Lithophil |
Lithophils |
Balon, 1975 |
44 |
Spawning substrate |
Gravel, rock, sand, clay, marl or vegetation to expose fibrous plant roolets |
Lithophils |
Goodyear et al, 1982 |
45 |
Spawning site preparation |
Excavations buried on the ground |
No category |
Billard, 1997 |
45 |
Spawning site preparation |
A nest is built |
No category |
Carrel et al, 2001 |
45 |
Spawning site preparation |
The male digs a shallow nest |
Susbtrate chooser |
Scott and Crossman, 1973 |
45 |
Spawning site preparation |
Nesters |
Nest built by both parents |
Fishbase, 2006 |
45 |
Spawning site preparation |
Male constructs a nest [Male extablish territories which each male constructs its nest. Nesting territories are aggressively defended from other fish] |
No category |
Gross and Nowell, 1980 |
45 |
Spawning site preparation |
Male clear shawllow depression up to 0.6 m in diameter |
No category |
Kerr and Grant, 1999 |
45 |
Spawning site preparation |
Nest spawner |
No category |
Balon, 1975 |
45 |
Spawning site preparation |
Eggs are deposited in shallow depression excavated |
Susbtrate chooser |
Goodyear et al, 1982 |
45 |
Spawning site preparation |
Males in our study excavated nests larger than do lakes fish |
No category |
Noltie and Keenleyside, 1987 |
46 |
Nycthemeral period of oviposition |
Spawning occurred more often in early morning (0700-1100: n=10) than either mid-day (1100-1330: n=3) or late evening (2010-2045: n=2) suggesting a temporal preference |
Day |
Gross and Nowell, 1980 |
46 |
Nycthemeral period of oviposition |
Spawning observed in 1981 began inearly afternoon at 1300 D.S.T. (n=43) and typically lasted about 1.5 h. Middle Thames rock bass spawned primarily in early afternoon, consistent with nest starts occuring in early morning and their completion soon after, followed by males beginning to accept the advances of females. This difference with other authors perhaps results from the more leisurely pace at which Lake Opinicon fish constructed their nests, a 2-day interval on average sperating nest start and spaning |
Day |
Noltie and Keenleyside, 1987 |
47 |
Mating system |
More than one female may spawn in the same nest and one female may spawn in more than one nest |
No category |
Scott and Crossman, 1973 |
47 |
Mating system |
By pair, apparent promiscuity [A female may spawn in different nests (3 males maximum). Males may also spawn with more than one female and four males were observed serially spawning with alternating female] |
Promiscuity |
Gross and Nowell, 1980 |
47 |
Mating system |
Individulas may spawn in different nests with different mates |
No category |
Kerr and Grant, 1999 |
48 |
Spawning release |
Multiple spawner |
Multiple |
Carrel et al, 2001 |
48 |
Spawning release |
Multiple spawner |
Multiple |
Gross and Nowell, 1980 |
48 |
Spawning release |
Spawing takes place at short intervals over a period of 1 hour or more but only a few eggs are laid at time |
No category |
Scott and Crossman, 1973 |
48 |
Spawning release |
About 120 dips per spawning and about 3-5 eggs per dip |
No category |
Gross and Nowell, 1980 |
49 |
Parity |
Lake residents than return to lake |
Iteroparous |
Goodyear et al, 1982 |
50 |
Parental care |
The spawning is guarded by male |
Male parental care |
Bruslé and Quignard, 2001 |
50 |
Parental care |
The spawning is guarded by male |
Male parental care |
Billard, 1997 |
50 |
Parental care |
The male guards and fans the eggs and later brrods the young for a short period |
Male parental care |
Scott and Crossman, 1973 |
50 |
Parental care |
The male cares about the young |
Male parental care |
Fishbase, 2006 |
50 |
Parental care |
Male provides care for the eggs and larvae interm of egg fanning and predator defence: on average 14 days |
Male parental care |
Gross and Nowell, 1980 |
50 |
Parental care |
Males guard eggs and fry |
Male parental care |
Kerr and Grant, 1999 |
50 |
Parental care |
Male guards nest and newly hatched fry |
Male parental care |
Goodyear et al, 1982 |
50 |
Parental care |
Brrods are guarded |
Biparental care |
Noltie and Keenleyside, 1987 |