Trait completeness | 92% |
Total data | 208 |
References | 44 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.0-1.35 [Before extrusion] | 1.18 mm | Scott and Crossman, 1973 |
1 | Oocyte diameter | 0.7 [Final egg size] | 0.7 mm | Tyler and Sumpter, 1996 |
1 | Oocyte diameter | 0.8 [Mean diameter of mature, fully yolked, ovarian oocyte] | 0.8 mm | Olden et al, 2006 |
1 | Oocyte diameter | Fully mature and ovulated oocytes have a diameter of approximatively 1-1.2 mm before water hardening | 1.1 mm | Woods III and Sullivan, 1993 |
1 | Oocyte diameter | 0.911 ± 0.177 in May | 0.91 mm | Blythe et al, 1994 |
1 | Oocyte diameter | Oocyte diameter reached their maximum in April: 0.84 ± 0.014 | 0.84 mm | Vuthiphandchai et al, 2002 |
1 | Oocyte diameter | Mean ooocyte diameter from all females at the second sampling (20 March) was 0.838 +/- 0.018 mm. When oocytes completed FOM and were ovulated (1.131 +/- 0.020 mm in diameter) | 0.84 mm | Mylonas et al, 1997 |
2 | Egg size after water-hardening | 3.6 [Not precised] | 3.6 mm | Mellinger, 2002 |
2 | Egg size after water-hardening | Mean 3.3, or range 3.4-4.2 | 3.8 mm | Internet, 2005 |
2 | Egg size after water-hardening | 2.4-3.9 | 3.15 mm | Fishbase, 2006 |
2 | Egg size after water-hardening | 3.6 [A few hours after they are fertilized and have undergone swelling] | 3.6 mm | Scott and Crossman, 1973 |
2 | Egg size after water-hardening | 3.6 [Eggs] | 3.6 mm | Merriman, 1937 |
2 | Egg size after water-hardening | 3.2 [Mean diameter of mature, fully yolked, ovarian oocyte] ??? | 3.2 mm | Olden et al, 2006 |
3 | Egg Buoyancy | Slightly heavier than freswater, suspended near bottom; planktonic | Pelagic | Internet, 2005 |
3 | Egg Buoyancy | Planktonic | Pelagic | Will et al, 2002 |
3 | Egg Buoyancy | Buoyant (pelagic) | Pelagic | Fishbase, 2006 |
3 | Egg Buoyancy | Semibuoyant and may be swept by the current | Pelagic | Scott and Crossman, 1973 |
3 | Egg Buoyancy | Semibuoyant | Pelagic | Everly and Boreman, 1999 |
3 | Egg Buoyancy | The semi-buoyant eggs are spawned near the surface where they rely on water turbulence to keep from sinking | Pelagic | Burdick and Hightower, 2005 |
3 | Egg Buoyancy | Pelagic | Pelagic | Secor, ??? |
3 | Egg Buoyancy | Spawn pelagic eggs, the slighly heavy eggs are suspended by current greater than 0.3 m/s | Pelagic | North and Houde, 2001 |
3 | Egg Buoyancy | Semibuoyant: that is they sink but are swpet up from the bottom by the slightest disturbance of the water | Demersal | Merriman, 1937 |
3 | Egg Buoyancy | Most eggs were maintained in the water column by the upwelling current generated by micropore aeration around the central standpipe and the 1.1 liter per min circular flow of incoming water below the surface | No category | Martin-Robichaud and Peterson, 1998 |
4 | Egg adhesiveness | Non-adhesive | Non-Adhesive | Internet, 2005 |
4 | Egg adhesiveness | Lack of adhesiveness | Adhesive | Burdick and Hightower, 2005 |
5 | Incubation time | 2 days at 17-18°C | 17.5 days | Internet, 2005 |
5 | Incubation time | 48 hours at 17-20 | 18.5 days | Rue, 2001 |
5 | Incubation time | 3.0 [Mean time to egg hatch within the range of average post-spawning the range post-spawning water temperatures] | 3.0 days | Olden et al, 2006 |
5 | Incubation time | 29-48 hours | 38.5 days | Burdick and Hightower, 2005 |
5 | Incubation time | In about 2 days | 2.0 days | North and Houde, 2001 |
5 | Incubation time | 74 hours at 58°F and 48hours at 67°F | 74.0 days | Merriman, 1937 |
5 | Incubation time | 34-36 hours at 21-22°C | 35.0 days | Woods III et al, 1992 |
5 | Incubation time | Hatching of viable eggs was completed by 54 h after fertilization at 19 +/- 0.5°C | 19.0 days | Monteleone and Houde, 1990 |
5 | Incubation time | Larvae hatched within 3 days post-fertilization at 16.1°C | 3.0 days | Martin-Robichaud and Peterson, 1998 |
5 | Incubation time | Hatched in approximatively 42 hours at 19°C | 42.0 days | Harrell et al, 2002 |
5 | Incubation time | Development is rapid, eggs hatch in about 48 hours | 48.0 days | Macintosh and Duston, 2007 |
6 | Temperature for incubation | 14-15.6 or 17.8-19.4 | 14.8 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | 17-18 | 17.5 °C | Internet, 2005 |
6 | Temperature for incubation | Temperatures <12°C are considered lethal to eggs | 12.0 °C | Rue, 2001 |
6 | Temperature for incubation | 16.7-17.9°C | 17.3 °C | Burdick and Hightower, 2005 |
6 | Temperature for incubation | Incubated at 14-16°C | 15.0 °C | Rogers and Westin, 1981 |
6 | Temperature for incubation | Rapid drops in temperature to below 12°C are lethal to striped bass eggs and larvae | 12.0 °C | Rutherford and Houde, 1994 |
6 | Temperature for incubation | 21-22 | 21.5 °C | Woods III et al, 1992 |
6 | Temperature for incubation | Optimal calculated temperatures were 18.2°C | 18.2 °C | Kamler and Kato, 1983 |
6 | Temperature for incubation | Water temperature was adjusted to 19 +/- 0.5°C | 19.0 °C | Monteleone and Houde, 1990 |
6 | Temperature for incubation | Water temperature for all tests were set at 19°C | 19.0 °C | Harrell et al, 2002 |
7 | Degree-days for incubation | 40-50 [70-74 hours at 14.4-15.6°C, and 48 hours at 17.8-19.4°] | 45.0 °C * day | Scott and Crossman, 1973 |
7 | Degree-days for incubation | 40 [2 days at 17-18°C] | 17.5 °C * day | Internet, 2005 |
7 | Degree-days for incubation | [33-36 hours at 21-22°C] | 34.5 °C * day | Woods III et al, 1992 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 2.9-5.0 | 3.95 mm | Internet, 2005 |
8 | Initial larval size | 5.2-6.0 | 5.6 mm | Scott and Crossman, 1973 |
8 | Initial larval size | 5.0 | 5.0 mm | Harrell, 1997 |
8 | Initial larval size | 3.3 | 3.3 mm | Olden et al, 2006 |
8 | Initial larval size | About 3.1 | 3.1 mm | North and Houde, 2001 |
8 | Initial larval size | 3.9 ±0.6 mm, standard length at hatching | 3.9 mm | Eldridge et al, 1982 |
8 | Initial larval size | At 5 dph, the mean length of larvae from the large females was 5.7 mm | 5.7 mm | Monteleone and Houde, 1990 |
9 | Larvae behaviour | Planktonic | Demersal | Will et al, 2002 |
9 | Larvae behaviour | Both stripped bass and white perch yolksac larvae may have the ability to swim actively toward surface waters during the day | Demersal | North and Houde, 2001 |
10 | Reaction to light | Light sensitive and become stressed in bright sunlight | Photopositive | Harrell, 1997 |
10 | Reaction to light | Exhibit positive phototaxis upon hatching in the laboratory | Photopositive | North and Houde, 2001 |
10 | Reaction to light | Photopositive fish larvae of walleye (Sander vitreus) and striped bass are attracted to the sides of the tanks (mirror effect) in light-rearing conditions, which negatively affects prey consumption | Photopositive | Jentoft et al, 2006 |
11 | Temperature during larval development | 26.5-30.3 [Temperature range corresponding to 90% of mawimum growth] | 28.4 °C | Kellog and Gift, 1983 |
11 | Temperature during larval development | 16-17 is around the optimal for larval development and survival | 16.5 °C | Sullivan et al, 1997 |
11 | Temperature during larval development | Larvae can tolerate temperatures of 12-23°C, but 18-21 is optimum |Lower limit is 12 and upper limit is 28.9°C] | 17.5 °C | Rue, 2001 |
11 | Temperature during larval development | 18°C | 18.0 °C | Secor, ??? |
11 | Temperature during larval development | Reared at 15, 18, 21 and 24°C | 15.0 °C | Rogers and Westin, 1981 |
11 | Temperature during larval development | Rapid drops in temperature to below 12°C ar elethal to striped bass eggs and larvae | 12.0 °C | Rutherford and Houde, 1994 |
11 | Temperature during larval development | Temperatures were maintained at 18°C | 18.0 °C | Eldridge et al, 1982 |
11 | Temperature during larval development | The water temperature increased from 15.7 to 18.7°C during the 2-week experiment | 15.7 °C | Martin-Robichaud and Peterson, 1998 |
11 | Temperature during larval development | Rearing temperature was 17°C to 5 dph, 19°C from 6 to 10 dph and 20°C from 10 dph onwards | 17.0 °C | Macintosh and Duston, 2007 |
12 | Sibling intracohort cannibalism | The growth differential among fry of the same age probably accounts for most cannibalistic activities starts about 2-3 weeks after hatching | Present | Braid, 1981 |
12 | Sibling intracohort cannibalism | Cannibalism can be a serious problem in intensive culture of striped bass [could start when striped bass larvae were only 6 days | Present | Katavic et al, 1989 |
12 | Sibling intracohort cannibalism | Cannibalism described | Present | Bry et al, 1992 |
12 | Sibling intracohort cannibalism | Present | Present | Hecht and Pienaar, 1993 |
13 | Full yolk-sac resorption | The yolk sas larval stage runs 3-6 days | 4.5 °C * day | Everly and Boreman, 1999 |
13 | Full yolk-sac resorption | Absorb their yolk sac until they are >5 d old and > 5 mm in length | 5.0 °C * day | North and Houde, 2001 |
13 | Full yolk-sac resorption | Striped bass survive on endogenous yolk for the first 5 days of life | 5.0 °C * day | Harell and Curry Woods III, 1995 |
13 | Full yolk-sac resorption | In stripped bass, inflated swibladders are first detected at 5-7 days post-hatching (dph) at 18°C, which coincides with the completion of yolk absorption, initiation of first feeding and peak larval specific gravities | 6.0 °C * day | Martin-Robichaud and Peterson, 1998 |
14 | Onset of exogeneous feeding | Larvae in all experiments began active feeding 5 days after hatching at a temperature of 18°C | 5.0 °C * day | Eldridge et al, 1982 |
14 | Onset of exogeneous feeding | Beginning at 5 dph, larvae were provided with a diet that consisted of Artemia nauplii maintained at 100per liter, on days 5,6 and 7, 500-1000 rotifers Brachinonus plicatilis per liter also were provided | 750.0 °C * day | Monteleone and Houde, 1990 |
14 | Onset of exogeneous feeding | Larvae were fed Artemia from 6 days post-hatching. Larvae with food in their gut were first observed at 7 dph in the black tanks and one day later in white tanks | 6.0 °C * day | Martin-Robichaud and Peterson, 1998 |
14 | Onset of exogeneous feeding | At 16-19°C, striped bass larvae make the transition to exogenous feeding by 5 d posthatch | 17.5 °C * day | Harrell et al, 2002 |
14 | Onset of exogeneous feeding | The larvae grow quickly from 6 mm total length (Lt) at first feeding (6 days post-hatch, dph) […] Swimbladder inflation and first feeding occurred between 5 and 7 dph (at 19°C) | 6.0 °C * day | Macintosh and Duston, 2007 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | Most of the studies indicate that females do not mature until at least 4 years, and, in most cases, not until 5 years of age | 4.0 year | Will et al, 2002 |
15 | Age at sexual maturity | 4-7 [Female] | 5.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | >4 | 4.0 year | Berlinsky et al, 1995 |
15 | Age at sexual maturity | 3-5 | 4.0 year | Sullivan et al, 1997 |
15 | Age at sexual maturity | Spawn for the first time at 3 to 6 years of age [Not specified] | 1.0 year | Burdick and Hightower, 2005 |
15 | Age at sexual maturity | 5.5 [Both sex] | 5.5 year | Olden et al, 2006 |
15 | Age at sexual maturity | 5-8 [Female specified] | 6.5 year | Secor, ??? |
15 | Age at sexual maturity | A few of the female striped bass become mature by the end of their 3rd year, while the majority attain maturity at the end of their 4th year | 3.0 year | Merriman, 1937 |
15 | Age at sexual maturity | In 1976: female were mature at age VI (47%), VII (87%), VIII (90%), IX (100) | 1976.0 year | McLaren et al, 1981 |
15 | Age at sexual maturity | About 44% of age-3 females were sexually mature and that all females examined were mature by age 6 [Female stripped bass from the Atlantic coast of the USA mature mainly at age 5-6, yet some mature at 3-4] | 5.5 year | Olsen and Rulifson, 1992 |
15 | Age at sexual maturity | All females whose age at next potential spawning was and older were mature. Our empirical observations indicated that 12% of fish in age-class 4, 34% of fish in age-class 5, and 77% of fish in age-class 6 were mature | 10.0 year | Berlinsky et al, 1995b |
15 | Age at sexual maturity | In the mid-Atlantic region, females mature between 3 to 7 years | 3.0 year | Holland et al, 2000 |
16 | Length at sexual maturity | 45 [Both sex] | 45.0 cm | Olden et al, 2006 |
16 | Length at sexual maturity | In 1976: female were mature at size 57.7 (47%), 69.0 (87%), 73.7 (90%), 90.6 (100%) | 1976.0 cm | McLaren et al, 1981 |
16 | Length at sexual maturity | Size of females sampled in Albemarle Sound in spring 1989-1990: mean 50.4, range 45.7-55 [Age 3]; mean 56.8, range 49.2-62.8 [Age 4], mean 58.9, range 53.4-65.4 Age 5], mean 62.7, range 57.5-69.6 (Age 6 | 1989.5 cm | Olsen and Rulifson, 1992 |
16 | Length at sexual maturity | Size of mature females in spring : 47.8 ±3.18 [Age 4], 51.6 ± 0.87 [Age 5], 58.2 ± 0.84 [Age 6] and 66.9 ± 1.2 [Age 7 | 47.8 cm | Berlinsky et al, 1995b |
17 | Weight at sexual maturity | >2 | 2.0 kg | Berlinsky et al, 1995 |
19 | Relative fecundity | 50-70 | 60.0 thousand eggs/kg | Tyler and Sumpter, 1996 |
19 | Relative fecundity | Fecundity of domesticated fish is similar to that of wild fish, approximatively 200 000 eggs/kg | 200.0 thousand eggs/kg | Harell and Curry Woods III, 1995 |
19 | Relative fecundity | Fecundity of two females of the control group : 137.644 and 167.718 for females Three-year-old, with an average weight of 1.01 kg | 137.64 thousand eggs/kg | Clark et al, 2005 |
19 | Relative fecundity | 46-86 [Fecundity measured are 201 000 [Mass 4300 g], 417 000 [Mass 5300 g], 704 000 [Mass 8500 g], 1390 [Mass 15 500 g]] | 66.0 thousand eggs/kg | Will et al, 2002 |
20 | Absolute fecundity | 11-5300 | 2655.5 thousand eggs | Internet, 2005 |
20 | Absolute fecundity | 14-3220 [Most fish yield about 180-700] | 1617.0 thousand eggs | Scott and Crossman, 1973 |
20 | Absolute fecundity | Mean fecundity for striped bass were 349.095 ± 157.343 [Size class I] and 463.130 ± 192.302 [Size class II] | 349.1 thousand eggs | Will et al, 2002 |
20 | Absolute fecundity | Average 181,000 [Age 3] to 5,000,000 [Age 16] | 181.0 thousand eggs | Burdick and Hightower, 2005 |
20 | Absolute fecundity | 8,000 [Maximum fecundity] | 8.0 thousand eggs | Secor, ??? |
20 | Absolute fecundity | Very prolific, a female of only 12 pounds has been known to yield 1280000 eggs, while a 75 pound fish would produce as many as 10000000. | 12.0 thousand eggs | Merriman, 1937 |
20 | Absolute fecundity | Age-3 females produced approximatively 200,000 eggs, one age 16-female produced approximatively 5,000,000 eggs. Fecundity of female stripped bass increased about 100,000-200000 eggs with year of growth | 100000.0 thousand eggs | Olsen and Rulifson, 1992 |
21 | Oocyte development | Group-synchronous type, single clutch [One clutch of oocytes is recruited through development, maturation, and ovulation for the single annual spawning] | Group-synchronous | Sullivan et al, 1997 |
21 | Oocyte development | Group-synchronous development | Group-synchronous | Will et al, 2002 |
22 | Onset of oogenesis | Vitellogenesis may be initiated as early as late-September, but this could vary | ['September'] | Sullivan et al, 1997 |
22 | Onset of oogenesis | Initiate ovarian maturation near autumnal equinox | ['October', 'November', 'December'] | Sullivan et al, 1997 |
22 | Onset of oogenesis | Vitellogenic from late October. E2 and T levels covaried in females and were low in summer, increased by late October to intermediate levels maintained until January, and increased again to maximum values observed just prior to the spawning season. | ['January', 'July', 'August', 'September', 'October'] | Woods III and Sullivan, 1993 |
22 | Onset of oogenesis | Differentiation of females was more accurate from October to May, when maximum ovarian diameters exceeded 16 mm | ['January', 'February', 'March', 'April', 'May', 'October', 'November'] | Blythe et al, 1994 |
22 | Onset of oogenesis | In October and November of the third year, SG-I oocytes became more numerous. By December, 50% of the fish contained two populations of oocytes in captive maturing females | ['October', 'November', 'December'] | Holland et al, 2000 |
22 | Onset of oogenesis | Significant oocyte (follicle) growth was detected in females from all treatment groups around the time of the autumnal equinox, on or between experimental days 106-139 | ['October', 'November', 'December'] | Clark et al, 2005 |
23 | Intensifying oogenesis activity | There is a surge in oocyte growth and circulating levels of sex steroids around the vernal equinox | No data | Sullivan et al, 1997 |
23 | Intensifying oogenesis activity | In early March 1989, the GSI of age-3 fish was 1.95. The Gsi had increased to only 2.11 by mid-April but jumped to 10.77 in May | ['March', 'April', 'May'] | Olsen and Rulifson, 1992 |
23 | Intensifying oogenesis activity | Final oocyte maturation in late April and May | ['April', 'May'] | Woods III and Sullivan, 1993 |
23 | Intensifying oogenesis activity | Significant egg growth from September to March | ['January', 'February', 'March', 'September', 'October', 'November'] | Blythe et al, 1994 |
23 | Intensifying oogenesis activity | January and February in maturing captive females | ['January', 'February'] | Holland et al, 2000 |
24 | Maximum GSI value | Vary according to the age of female from: 10.77 ±3.28 [Age 3]; 12.10 ± 4.65 [Age 4]; 13.58 ± 4.30 [Age 5]; 18.19 ± 4.09 [Age 6] in May | 10.77 percent | Olsen and Rulifson, 1992 |
24 | Maximum GSI value | Mean of 4% in April, for maturing captive females | 4.0 percent | Holland et al, 2000 |
26 | Resting period | In summer, females had nothing more than primaryt growth oocytes | 4.0 months | Woods III and Sullivan, 1993 |
26 | Resting period | During the post spawning season (July, Aufgust, and September), when oocyte and ovarian diameters were smallest, sex detemrination was less accurate | 3.0 months | Blythe et al, 1994 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 5 [Male] | 5.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | 3 [Male] | 3.0 years | Sullivan et al, 1997 |
27 | Age at sexual maturity | 5.5 [Both sex] | 5.5 years | Olden et al, 2006 |
27 | Age at sexual maturity | Spawn for the first time at 3 to 6 years of age [Not specified] | 1.0 years | Burdick and Hightower, 2005 |
27 | Age at sexual maturity | In 1976: male were mature at age III (48%), age IV (67%), age V (87%), age VI (78%) and age VII (100%) | 1976.0 years | McLaren et al, 1981 |
27 | Age at sexual maturity | In the mid-Atlantic region, males reach sexual maturity during their second and third year | 2.0 years | Holland et al, 2000 |
28 | Length at sexual maturity | About 50 or more | 50.0 cm | Rue, 2001 |
28 | Length at sexual maturity | 45 [Both sex] | 45.0 cm | Olden et al, 2006 |
28 | Length at sexual maturity | In 1976: male were mature at size 38.5 (48%), 43.9 (67%), 52.1 (87%), 56.5 (78%) and 64.0 (100%) | 1976.0 cm | McLaren et al, 1981 |
31 | Onset of spermatogenesis | Males initiated spermiogenesis by late september and spermiation by late February or early March | ['February', 'March'] | Woods III and Sullivan, 1993 |
31 | Onset of spermatogenesis | Ultrasonic sex detemrination was accurate from october to May, even tough all males were spermiating only during April | ['April', 'May'] | Blythe et al, 1994 |
31 | Onset of spermatogenesis | In October-November, spermatogenesis began in all males in reared conditions | ['October', 'November'] | Holland et al, 2000 |
32 | Main spermatogenesis activity | GSI increased rapidly from December to April, mainly December to February in reared conditions | ['January', 'February', 'March', 'April', 'December'] | Holland et al, 2000 |
33 | Maximum GSI value | Mean of 9.5, up to 10.5 [Mid-April] in reared conditions | 9.5 percent | Holland et al, 2000 |
35 | Resting period | Male sex determination was lowest in September when testicular diameter was minimal | 2.0 months | Blythe et al, 1994 |
35 | Resting period | In June, after the second reproductive season, testes from mature fish strated to regress and spermatozoa were resorbed. In September (the beginning of the third reproductive cycle) only spermatogonia were present in the testes. | 3.0 months | Holland et al, 2000 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Prespawning may travel long distances upriver, in fresh water | No data | Scott and Crossman, 1973 |
36 | Spawning migration distance | The 165-km upriver migration took about a week | 165.0 km | Carmichael et al, 1998 |
36 | Spawning migration distance | Spawning occurs in several deltaic channels c. 16-50 km inland from the Atlantic Ocean in the freshwater portion | 33.0 km | Will et al, 2002 |
36 | Spawning migration distance | Can migrate as far inland as 320 km to find suitable spawning habitat | 320.0 km | Burdick and Hightower, 2005 |
36 | Spawning migration distance | Local fishermen catch adult striped bass more than 300 km upstream in the Savannah River from May to September and catch fish in the extreme dowstream tidal reaches of the river during the winter. The major spawning area for striped bass in the Savannah River is in the tidally influenced area 30 to 40 km upstream from the river mouth | 300.0 km | Dudley et al, 1977 |
36 | Spawning migration distance | Following spawning, most striped bass leave the Hudson River and move generally northeast-ward in Long island Sound and the Atlantic Ocean, but the majority are restricted to within 50 km of the river mouth | 50.0 km | McLaren et al, 1981 |
37 | Spawning migration period | There is a fall migration upriver, the potential spawners spend the winter in the river, then swim up to their spaning grounds in the spring | ['January', 'February', 'March', 'April', 'May', 'June', 'October', 'November', 'December'] | Scott and Crossman, 1973 |
37 | Spawning migration period | Migration began in mid- to late April when water temperature in the lower river reached 17-18°C | ['April'] | Carmichael et al, 1998 |
37 | Spawning migration period | Anadromous, coming in from the sea to spawn in brackish or fresh water | No data | Merriman, 1937 |
37 | Spawning migration period | Ascend rivers to spawn in fresh or brackosh water in March to June when water temperature reach 15 to 19°C | ['March', 'April', 'May', 'June'] | Dudley et al, 1977 |
38 | Homing | Return to their natal river in the spring to spawn | Present | Burdick and Hightower, 2005 |
38 | Homing | These fish return to wintering areas prior to entering home streams to spawn | Present | Dudley et al, 1977 |
39 | Spawning season | April-June, can extend to mid-summer | ['April', 'June', 'July', 'August', 'September'] | Internet, 2005 |
39 | Spawning season | Mainly May, but April-June | ['April', 'May', 'June'] | Fishbase, 2006 |
39 | Spawning season | Usually in June | ['June'] | Scott and Crossman, 1973 |
39 | Spawning season | About mid-April to mid-June, peaking in mid-May | ['April', 'May', 'June'] | Carmichael et al, 1998 |
39 | Spawning season | Occurs primarily in April and May | ['April', 'May'] | Sullivan et al, 1997 |
39 | Spawning season | Early May to June | ['May', 'June'] | Everly and Boreman, 1999 |
39 | Spawning season | Genreally from April to June | ['April', 'May', 'June'] | Rue, 2001 |
39 | Spawning season | Peaks in April and May | ['April', 'May'] | North and Houde, 2001 |
39 | Spawning season | Spawn in Chesapeake Bay tributaries from April to Hune | ['April'] | Rutherford and Houde, 1994 |
39 | Spawning season | April through June, the excat time depending on the latirude and temperature | ['April', 'June'] | Merriman, 1937 |
39 | Spawning season | Most fish observed left the spanwing area between 16 April and 1 May | ['April', 'May'] | Dudley et al, 1977 |
39 | Spawning season | April | ['April'] | Vuthiphandchai et al, 2002 |
39 | Spawning season | Normally spawn at Chesapeake latitude (April-May) | ['April', 'May'] | Clark et al, 2005 |
39 | Spawning season | Striped bass spawn in spring in numerous estuaries on the east coast of North America | ['April', 'May', 'June'] | Macintosh and Duston, 2007 |
40 | Spawning period duration | Males remain on the spawning grounds for as long as 30 days while females spend about 7-10 days there | 8.5 weeks | Sullivan et al, 1997 |
40 | Spawning period duration | Males remained on the spawning grounds for averages of 22 and 21 days, females for 8 and 11 days | 22.0 weeks | Carmichael et al, 1998 |
40 | Spawning period duration | From 5 to 9 weeks | 5.0 weeks | Rue, 2001 |
41 | Spawning temperature | Starts at 14-15, bulk of spawn 16-18°C | 14.5 °C | Internet, 2005 |
41 | Spawning temperature | About 18 | 18.0 °C | Carmichael et al, 1998 |
41 | Spawning temperature | Around 16-17 | 16.5 °C | Sullivan et al, 1997 |
41 | Spawning temperature | Between 14.4-21.2, with peak spawning between 17.8-20.0 | 17.8 °C | Rue, 2001 |
41 | Spawning temperature | 14 [Temperature at which spawning is typically initiated] | 14.0 °C | Olden et al, 2006 |
41 | Spawning temperature | Spawning activity start not until water temperatures reached 18°C, with 70 percent of spawning occuring between 20.0 and 23.9°C [Also start at 14.4, and peak at 15.6-19.4°C] | 17.5 °C | Burdick and Hightower, 2005 |
41 | Spawning temperature | In the Chesapeeke Bay, females undergoing FOM can be found at temperatures as low as 13°C, whereas spawning takes place at water temperatures of 16-20°C | 18.0 °C | Mylonas et al, 1997 |
42 | Spawning water type | Move into fresh or brackish water to spawn | No category | Fishbase, 2006 |
42 | Spawning water type | Areas with good flow and/or tidal action which provides increased agitation and aeration to the eggs and help keeps tehm in suspension | No category | Internet, 2005 |
42 | Spawning water type | Deltaic channels | No category | Will et al, 2002 |
42 | Spawning water type | With some current | Flowing or turbulent water | Rue, 2001 |
42 | Spawning water type | Current velocities averaging 0.49-0.55 m/s [Areas with rapids, boulders and strounfg currents, typically associated with the fall line] | Flowing or turbulent water | Burdick and Hightower, 2005 |
42 | Spawning water type | In the headwaters of Chesapaekae Bay and its tributaries | No category | North and Houde, 2001 |
42 | Spawning water type | In these rapids, where the muddy current is exceedingly strong and rendered very erratic by islands, boulders and rocks, the fish spaws. Spawn in low-lying flooded delta country adjacent to Suisun Bay, where the borders between brackish and purely fresh | Flowing or turbulent water | Merriman, 1937 |
42 | Spawning water type | Anadromous, spawning in tidal rivers and migrating to estuarine and marine coastal waters to feed and mature | No category | McLaren et al, 1981 |
43 | Spawning depth | Release gametes at the water surface | No data | Sullivan et al, 1997 |
43 | Spawning depth | Spawn near the surface | No data | Burdick and Hightower, 2005 |
44 | Spawning substrate | No substrate | No category | Internet, 2005 |
44 | Spawning substrate | Over bottoms of sand or mud | Psammophils | Rue, 2001 |
44 | Spawning substrate | Litho-pelagophil | Pelagophils | Balon, 1975 |
44 | Spawning substrate | Egg survival is increased when spawning takes place over large substrates or conditons cause them to stay suspended. In a controlled experiment, it was showed that egg survival was 22.6% higher for eggs deposited over coarse sand than those deposited over a mix of silt and clay. Eggs deposited over a mix of organic matter, sand, silt and clay showed no survival. | Psammophils | Burdick and Hightower, 2005 |
45 | Spawning site preparation | Open water/substratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
46 | Nycthemeral period of oviposition | It remains unclear whether spawning occurs predominantly during the day or the night | Day | Sullivan et al, 1997 |
46 | Nycthemeral period of oviposition | Over their entire range, accounts of stripped bass spawning span all times of the day. However, in North Carolina, striped bass have been reported to broadcast their eggs late in the afternoon and early in the evening | Day | Burdick and Hightower, 2005 |
47 | Mating system | Spawning can involve multiple males and more than one female, but it is characterized by one female and many males releasing gametes at the water surface [Once a group of males has spawned, they will continue to chase the spent female or court the next available one] | Polyandry | Sullivan et al, 1997 |
48 | Spawning release | Once, single clutch. Females releases one long continuous cloud of eggs for less than ten seconds, sometimes another (minor) synchronous gamete release can be observed | Total | Sullivan et al, 1997 |
48 | Spawning release | Females spawn more than once in a season [One clear seasonal peak per year] | Multiple | Fishbase, 2006 |
49 | Parity | Iteroparous | Iteroparous | Sullivan et al.. Reproduction in Harrel Editor 1997 |
49 | Parity | Females don't necessarily spawn every year | Iteroparous | Fishbase, 2006 |
49 | Parity | Although females spawn more than once, they do not necesseraliy spawn every year | Iteroparous | Scott and Crossman, 1973 |
49 | Parity | Iteroparous | Iteroparous | Burdick and Hightower, 2005 |
49 | Parity | After spawning, followed perhaps by a short stay in fresh waters, most adult striped bass return to marine waters | Iteroparous | Dudley et al, 1977 |
49 | Parity | Spawn once a year during a relatively short period in the psring | Iteroparous | Vuthiphandchai et al, 2002 |
50 | Parental care | Nonguarders | No care | Fishbase, 2006 |