Trait completeness | 80% |
Total data | 224 |
References | 25 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | >1.6 [Hydrated yolked oocytes] | 1.6 mm | Olney et al, 2001 |
1 | Oocyte diameter | 1.8 [Unfertilized egg] | 1.8 mm | Mills, 2004 |
1 | Oocyte diameter | Two modes for hydrated oocytes: 1.8 and 2.0 [Range from 1.6 to 2.4] | 1.8 mm | Olney and McBride, 2003 |
1 | Oocyte diameter | 0.8-1.27 | 1.04 mm | Anonymous, 2006 Chapter 3 |
2 | Egg size after water-hardening | 2.5-3.5 [Fertilized eggs] | 3.0 mm | Scott and Crossman, 1973 |
2 | Egg size after water-hardening | 2.5-3.5 | 3.0 mm | Mellinger, 2002 |
2 | Egg size after water-hardening | 2.5-3.8 | 3.15 mm | Internet, 2005 |
2 | Egg size after water-hardening | 2.5-3.8 [Min-max] | 3.15 mm | Fishbase, 2006 |
2 | Egg size after water-hardening | 2.5-3.8 [Not specifed] | 3.15 mm | Mills, 2004 |
2 | Egg size after water-hardening | 2.5-3.8 | 3.15 mm | Burdick and Hightower, 2005 |
2 | Egg size after water-hardening | Average egg diameter was 3.4 mm | 3.4 mm | Zydlewski and McCormick, 1997 |
3 | Egg Buoyancy | Demersal, semi-demersal or slightly heavier than fresh water, suspended by water-current [a moderate current (about 1 meter per second or less) will keep eggs floating] | Demersal | Internet, 2005 |
3 | Egg Buoyancy | Only slightly heavier than water, they settle singly and are carried along by the current | No category | Scott and Crossman, 1973 |
3 | Egg Buoyancy | Demersal, semi-demersal or slightly heavier than fresh water, suspended by water-current [a moderate current (about 1 meter per second or less) will keep eggs floating] | Demersal | Everly and Boreman, 1999 |
3 | Egg Buoyancy | Slightly heavier than water and are carried by the currents and gradually sink | Demersal | Mills, 2004 |
3 | Egg Buoyancy | On the bottom (demersal) | Demersal | Fishbase, 2006 |
3 | Egg Buoyancy | Semi-demersal to pelagic | Pelagic | Rue, 2001 |
3 | Egg Buoyancy | In coastal habitats, females lay demersal eggs | Demersal | Anonymous, 2006 Chapter 3 |
3 | Egg Buoyancy | Eggs are released into open water where they are carried along by currents, and being slightly heavier than water, gradually sink to the bottom | Demersal | Bradbury et al, 1999 |
3 | Egg Buoyancy | Shortly after being spawned, the water-hardened eggs start to sink. [described as either demersal or semidemersal depending on whether the researcher assume that eggs stayed on the bottom or were lifted off the bottom by turbulent current. Some eggs remained suspended in the water column for several kilometers] | Demersal | Burdick and Hightower, 2005 |
3 | Egg Buoyancy | Calculations based on eggs ages when collected indicate most eggs traveled only 1 to 4 miles from where spawned. | Pelagic | Marcy, 1972 |
4 | Egg adhesiveness | Initially adhesive or slightly adhesive and then non-adhesive | Non-Adhesive | Internet, 2005 |
4 | Egg adhesiveness | Non-adhesive | Non-Adhesive | Scott and Crossman, 1973 |
4 | Egg adhesiveness | Not sticky | Non-Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Non-adhesive | Non-Adhesive | Everly and Boreman, 1999 |
4 | Egg adhesiveness | Initially adhesive and later become non-adhesive | Non-Adhesive | Mills, 2004 |
4 | Egg adhesiveness | Nonadhesive | Non-Adhesive | Bradbury et al, 1999 |
4 | Egg adhesiveness | Initially adhesive but quickly become non-adhesive | Non-Adhesive | Burdick and Hightower, 2005 |
5 | Incubation time | 8-12 [11-15°C] or 17 [12°C] | 10.0 days | Internet, 2005 |
5 | Incubation time | 8-12 days at 11-15°C | 10.0 days | Scott and Crossman, 1973 |
5 | Incubation time | 7 [15.50°C], 13.50 [12.00°C] | 7.0 days | Fishbase, 2006 |
5 | Incubation time | 2-17 [But 12-15 at 12°C] | 9.5 days | Everly and Boreman, 1999 |
5 | Incubation time | 4-6 [15-18°C], 6-8 [17°C], 8-12 [11-15°C] | 5.0 days | Mills, 2004 |
5 | Incubation time | 2 [24°C], 3 [23.3°C], 7 [15°C], 11 |13.30], 13.5 [12.00] | 2.0 days | Fishbase, 2006 |
5 | Incubation time | 2-17 depeding on temperature | 9.5 days | Rue, 2001 |
5 | Incubation time | 8-12 at 11-15°C | 10.0 days | Bradbury et al, 1999 |
5 | Incubation time | Development of eggs starts between 13°C and 17°C and increases rapidly between 17°C and 20°C | 13.0 days | Burdick and Hightower, 2005 |
5 | Incubation time | Hatching occurred on June 13, i.e. 6-7 days at 16.6-19°C | 6.5 days | Zydlewski and McCormick, 1997 |
5 | Incubation time | Eggs were fertilized and reared in the laboratory at temperatures similar to those in the river (13.8-23.0°C). Hatching occurred 71 to 86 hours after fertilization | 18.4 days | Marcy, 1972 |
5 | Incubation time | Hatched from eggs 6 days after fertilization. […] The temperature of water during the egg incubation and larval development was 17-18°C | 17.5 days | Laiz-Carrion et al, 2003 |
6 | Temperature for incubation | 11-15 | 13.0 °C | Internet, 2005 |
6 | Temperature for incubation | 11-15 | 13.0 °C | Scott and Crossman, 1973 |
6 | Temperature for incubation | 15.5-26.5 [Optimum temperature] | 21.0 °C | Carscadden and Leggett, 1975 |
6 | Temperature for incubation | 17 | 17.0 °C | Fishbase, 2006 |
6 | Temperature for incubation | 12-15.50, up to 27 | 13.75 °C | Fishbase, 2006 |
6 | Temperature for incubation | 12 | 12.0 °C | Everly and Boreman, 1999 |
6 | Temperature for incubation | 17 is considered optimal [The survival rate decreases at 24°C] | 17.0 °C | Mills, 2004 |
6 | Temperature for incubation | 13-26 are required for the development and survival of eggs | 19.5 °C | Rue, 2001 |
6 | Temperature for incubation | 11-15°C | 13.0 °C | Bradbury et al, 1999 |
6 | Temperature for incubation | Filtered Connecticut river water (16.6-19°C during incubation) was supplied to an upwelling jar | 17.8 °C | Zydlewski and McCormick, 1997 |
6 | Temperature for incubation | Eggs required temperatures > 13°C. Incubation temperatures was 17°C | 13.0 °C | Leach and Houde, 1999 |
6 | Temperature for incubation | Glass aquaria contaning fresh water held at room temperature 20.6°C | 20.6 °C | Limburg and Ross, 1995 |
6 | Temperature for incubation | The temperature of water during the egg incubation and larval development was 17-18°C | 17.5 °C | Laiz-Carrion et al, 2003 |
7 | Degree-days for incubation | About 120-150 | 135.0 °C * day | Internet, 2005 |
7 | Degree-days for incubation | 120-140 [8-12 days at 11-15°C] | 130.0 °C * day | Scott and Crossman, 1973 |
7 | Degree-days for incubation | 108.5-162 | 135.25 °C * day | Fishbase, 2006 |
7 | Degree-days for incubation | 130-150 [12-15 days at 12°C] | 140.0 °C * day | Everly and Boreman, 1999 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 6.5-10 | 8.25 mm | Internet, 2005 |
8 | Initial larval size | 9-10 | 9.5 mm | Scott and Crossman, 1973 |
8 | Initial larval size | 8.7 | 8.7 mm | Wiggins et al, 1985 |
8 | Initial larval size | Either 9-10; 6-10 | 9.5 mm | Mills, 2004 |
8 | Initial larval size | Larvae hatch at a size of approximatively 2.5-5.0 mm | 3.75 mm | Anonymous, 2006 Chapter 3 |
9 | Larvae behaviour | Newly larvae are pelagic, and most abundant at the surface | Pelagic | Internet, 2005 |
9 | Larvae behaviour | Both feeding and yolksac larvae are planktonic [Dispersal therefore occurs by passive transport] | Demersal | Everly and Boreman, 1999 |
9 | Larvae behaviour | Larvae are planktonic for about 4 weeks | Demersal | Mills, 2004 |
9 | Larvae behaviour | Larvae are planktonic and do not metamorphose into juveniles for 4-5 weeks | Demersal | Bradbury et al, 1999 |
9 | Larvae behaviour | Larvae drift downstream until they are capable of swimming freely | Demersal | Burdick and Hightower, 2005 |
10 | Reaction to light | The incidence of feeding was higher for larvae reared in continuous light | Photopositive | Wiggins et al, 1985 |
11 | Temperature during larval development | 15.5-26.5 [Optimum temperature] | 21.0 °C | Carscadden and Leggett, 1975 |
11 | Temperature during larval development | 15.6 | 15.6 °C | Wiggins et al, 1985 |
11 | Temperature during larval development | 17-25 for juveniles | 21.0 °C | Mills, 2004 |
11 | Temperature during larval development | Reared at about 20°C | 20.0 °C | Johnson and Dropkin, 1995 |
11 | Temperature during larval development | Rearead at 17°C | 17.0 °C | Everly and Boreman, 1999 |
11 | Temperature during larval development | The temperature was maintained at 20.0 ±1°C | 20.0 °C | Zydlewski and McCormick, 1997 |
11 | Temperature during larval development | Required temperatures are in the range 15.5-26.1°C. Reared at 20°C | 20.8 °C | Leach and Houde, 1999 |
11 | Temperature during larval development | The temperature of water during the egg incubation and larval development was 17-18°C | 17.5 °C | Laiz-Carrion et al, 2003 |
13 | Full yolk-sac resorption | 94 [6 days at 15.6] | 94.0 °C * day | Wiggins et al, 1985 |
13 | Full yolk-sac resorption | 70-85 [Yolksac larvae absorb their yolk in 4-5 days at 17°C] | 77.5 °C * day | Everly and Boreman, 1999 |
13 | Full yolk-sac resorption | [About 4 to 7 days after hatching; 9-12 mm or 12.2 when yolk is absorbed] | 10.5 °C * day | Mills, 2004 |
13 | Full yolk-sac resorption | 4-7 days | 5.5 °C * day | Rue, 2001 |
14 | Onset of exogeneous feeding | 94 [5 days at 15.6] | 94.0 °C * day | Wiggins et al, 1985 |
14 | Onset of exogeneous feeding | The transition from endogenous to exogenous feeding occurred between days 3 and 6, at 20 ± 1.0°C | 20.0 °C * day | Zydlewski and McCormick, 1997 |
14 | Onset of exogeneous feeding | Feeding stage larvae was 6-8 days post-hatch at 19-20°C | 7.0 °C * day | Leach and Houde, 1999 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 4-5 [Not specified] | 4.5 year | Scott and Crossman, 1973 |
15 | Age at sexual maturity | 2-5 [Female] | 3.5 year | Fishbase, 2006 |
15 | Age at sexual maturity | 4-5 [Female] | 4.5 year | Mills, 2004 |
15 | Age at sexual maturity | 4-5 [Female] | 4.5 year | Olney and McBride, 2003 |
15 | Age at sexual maturity | 4-5 [Female] | 4.5 year | Anonymous, 2006 Chapter 3 |
15 | Age at sexual maturity | Most american shad mature and return to spawn at betwenn 3 and 5 years of age [Not specified] | 3.0 year | Burdick and Hightower, 2005 |
15 | Age at sexual maturity | 4.2-4.5 [Female] | 4.35 year | Carscaden and Legget, 1975 |
15 | Age at sexual maturity | The annual spawning run of American shad Alosa sapidissima in the York River, Virginia consists of virgin (ages 3-7 years) and fish that spawned in previous years (repeat spawners, ages 4-10) | 5.0 year | Olney et al, 2006 |
16 | Length at sexual maturity | 45-48 [Not specified] | 46.5 cm | Scott and Crossman, 1973 |
16 | Length at sexual maturity | 38-48 [Female] | 43.0 cm | Fishbase, 2006 |
16 | Length at sexual maturity | Mean of fork length of 42.5-47.3 [For females of 4-8 years] | 44.9 cm | Olney and McBride, 2003 |
16 | Length at sexual maturity | 28.4-30.8 [Female] | 29.6 cm | Anonymous, 2006 Chapter 3 |
16 | Length at sexual maturity | 46.8-49.5 [Mean length of repeat spawners] | 48.15 cm | Carscaden and Legget, 1975 |
17 | Weight at sexual maturity | Mean of 1.241-1.483, range from 0.848 to 1.900 [Female specified] | 1.36 kg | Olney and McBride, 2003 |
17 | Weight at sexual maturity | 1.622-2.095 [Mean weight of repeat spawners] | 1.86 kg | Carscaden and Legget, 1975 |
19 | Relative fecundity | Average batch fecundity (the mean number of oocytes > 1.6 mm per kg of somatic weight) was estimated for six hydrated/running ripe females and ranged from about 20 000 to 70 000 eggs | 1.6 thousand eggs/kg | Olney et al, 2001 |
19 | Relative fecundity | Means varies between 188.3 to 236.3, all variations range from 159.9 to 360. Means of batch sizes vary from 39,658 to 48,113 eggs | 188.3 thousand eggs/kg | Olney and McBride, 2003 |
20 | Absolute fecundity | 155-410 or 2.150 or 30-300 | 282.5 thousand eggs | Internet, 2005 |
20 | Absolute fecundity | Average of 125.166 [Range 58-390] | 224.0 thousand eggs | Scott and Crossman, 1973 |
20 | Absolute fecundity | From various sources, American shad produce 2-300 eggs [Also 116-468 and 98.6-225.6] | 151.0 thousand eggs | Mills, 2004 |
20 | Absolute fecundity | 37-44 | 40.5 thousand eggs | Olney and McBride, 2003 |
20 | Absolute fecundity | 60-300 | 180.0 thousand eggs | Anonymous, 2006 Chapter 3 |
20 | Absolute fecundity | 58,534-659,000 | 596.5 thousand eggs | Burdick and Hightower, 2005 |
20 | Absolute fecundity | 118.929-165.776 [Mean population fecundity] | 142.35 thousand eggs | Carscaden and Legget, 1975 |
21 | Oocyte development | Group-synchronous ovarian development | Group-synchronous | Olney et al, 2001 |
21 | Oocyte development | Oocyte sizes are bimodal, the hydrated oocytes representing a cohort distinct from the smaller oocytes | No category | Olney and McBride, 2003 |
21 | Oocyte development | Groups-synchronous oocyte development | No category | Burdick and Hightower, 2005 |
24 | Maximum GSI value | Mean 20.5, up to 35.4 | 20.5 percent | Olney et al, 2001 |
24 | Maximum GSI value | 14-19 [Calculated from values given by the authors] | 16.5 percent | Olney and McBride, 2003 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 3-5 | 4.0 years | Internet, 2005 |
27 | Age at sexual maturity | 4-5 [Not specified] | 4.5 years | Scott and Crossman, 1973 |
27 | Age at sexual maturity | 2-4, male | 3.0 years | Fishbase, 2006 |
27 | Age at sexual maturity | 3-4 [Males] | 3.5 years | Mills, 2004 |
27 | Age at sexual maturity | 3-4 [Males] | 3.5 years | Anonymous, 2006 Chapter 3 |
27 | Age at sexual maturity | Most american shad mature and return to spawn at betwenn 3 and 5 years of age [Not specified] | 3.0 years | Burdick and Hightower, 2005 |
27 | Age at sexual maturity | 3.8-4.1 [Female] | 3.95 years | Carscaden and Legget, 1975 |
28 | Length at sexual maturity | 45-48 [Not specified] | 46.5 cm | Scott and Crossman, 1973 |
28 | Length at sexual maturity | 30-44, male | 37.0 cm | Fishbase, 2006 |
28 | Length at sexual maturity | 26.5-27.8 | 27.15 cm | Anonymous, 2006 Chapter 3 |
28 | Length at sexual maturity | 42.9-46.9 [Mean length of repeat spawners] | 44.9 cm | Carscaden and Legget, 1975 |
29 | Weight at sexual maturity | 1.210-1.803 [Mean weight of repeat spawners] | 1.51 kg | Carscaden and Legget, 1975 |
30 | Male sexual dimorphism | In all populations and years, males matured at a significantly younger age than females | Absent | Carscaden and Legget, 1975 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | As maturing fish migrate 100 km up the estuary to the freswater spawnig grounds | 100.0 km | Olney et al, 2001 |
36 | Spawning migration distance | Some shad spawn immediately on entering fresh water while others may undertake fairly long journeys, as musch as 630 km upstream, to their favored spawning grounds | 630.0 km | Fishbase, 2006 |
36 | Spawning migration distance | During spawning season, they move to shallower inshore waters to spawn | No data | Anonymous, 2006 Chapter 3 |
36 | Spawning migration distance | York River fish segregate from mixed-stock assemblages and migrate at least 130 river kilometers (rKm) up the estuary to freshwater | 130.0 km | Olney et al, 2006 |
36 | Spawning migration distance | In the Hudson River in New York state, spawning of American shad takes place more than 160 kmfrom the river mouth, and most of the eggs are found above 200 km | 160.0 km | Limburg and Ross, 1995 |
37 | Spawning migration period | Shad begin to enter the estuary as early as fall, the spawning runs occur in March | ['March', 'October', 'November', 'December'] | Internet, 2005 |
37 | Spawning migration period | Peak of spawning run occurs at temperature of about 18.3°C | No data | Scott and Crossman, 1973 |
37 | Spawning migration period | The peak of spawning migrations in all Atlantic coast populations of closely related with a narrow range of water temperatures (13-18°C) | No data | Carscadden and Leggett, 1975 |
37 | Spawning migration period | Adults move into the Hudson River from Atlantic waters in early spring, usually begin in March and April, and temperature must be 12°C or above before the shad begin their run | ['March', 'April', 'May', 'June'] | Everly and Boreman, 1999 |
37 | Spawning migration period | Up stream migrations in southern streams reportdly occur early in the spring and progressively later northward [the upstream migration of Amrican shad in the Sacramento river estuary reportdly takes about 3 months occuring in March, April and May). Migrate upstream in the spring [Take place when water is about 16.0-19.5°C | ['March', 'April', 'May', 'June'] | Mills, 2004 |
37 | Spawning migration period | In eastern Canada, spawing runs of shad enter rivers between late April and late June, with few, if any, entering rivers before water temperatures reach at least 4°C | ['April', 'June'] | Bradbury et al, 1999 |
37 | Spawning migration period | 90% of the run occurred at temperatures between 15/5-19.5°C, and the peak run occurred at about 18°C | No data | Burdick and Hightower, 2005 |
37 | Spawning migration period | Reproductive adults migrate into coastal rivers in the spring when river temperatures are between 14 and 20°C | ['April', 'May', 'June'] | Zydlewski and McCormick, 1997 |
37 | Spawning migration period | The spawing run begins when maturing (prespawning) fish enter the mouth of the river in late January through late February and continues for approximatively4 months through mid-May | ['January', 'February', 'May'] | Olney et al, 2006 |
38 | Homing | The american shad is reported to home to its natal river to spawn | Present | Carscadden and Leggett, 1975 |
38 | Homing | Most sexually mature fish return to natal streams to spawn | Present | Olney et al, 2001 |
38 | Homing | To their natal streams to spawn | Present | Mills, 2004 |
38 | Homing | Return to its natal river to spawn | Present | Bradbury et al, 1999 |
38 | Homing | Return to their natal stram to spawn | Present | Dodson and Legget, 1973 |
38 | Homing | Our life history and meristic data suggest that homing to a tributary within a river system was also occuring [Adlys shad do not feed during the freswater migration and this lack of food would accentuate the effects of temperature and distance of migrating fish) | Present | Carscadden and Legget, 1975 |
39 | Spawning season | April-June | ['April', 'June'] | Internet, 2005 |
39 | Spawning season | May-June, but even as late as July | ['May', 'June', 'July'] | Scott and Crossman, 1973 |
39 | Spawning season | May-June, but also from February until July | ['February', 'March', 'April', 'May', 'June', 'July'] | Fishbase, 2006 |
39 | Spawning season | In most years, spawning begins in late February and ends in early June | ['February', 'June'] | Olney et al, 2001 |
39 | Spawning season | May or early June | ['May', 'June'] | Mills, 2004 |
39 | Spawning season | May-June but as early as February and late as July | ['February', 'May', 'June', 'July'] | Fishbase, 2006 |
39 | Spawning season | May take place anytime between mid-March and early June | ['March', 'May', 'June'] | Rue, 2001 |
39 | Spawning season | Spring | ['April', 'May', 'June'] | Anonymous, 2006 Chapter 3 |
39 | Spawning season | Spawning normally occurs in May and June, but may occur as late as July | ['May', 'June', 'July'] | Bradbury et al, 1999 |
39 | Spawning season | Spawning was detected between February 21 and May 28 in 2003 and between March 16 and May 17 in 2004 | ['February', 'March', 'May'] | Burdick and Hightower, 2005 |
39 | Spawning season | Spawning occurred between 13 May and 27 June, the peak being June in 1967 and May in 1968. | ['May', 'June'] | Marcy, 1972 |
40 | Spawning period duration | The males arrive on the spawning grounds first, soon followed by the females | No data | Scott and Crossman, 1973 |
40 | Spawning period duration | 10-12 [In most years, spawning begins in late February and ends in early June, But spawning duration are unknown] | 11.0 weeks | Olney et al, 2001 |
40 | Spawning period duration | Sevreal weeks of duration | No data | Rue, 2001 |
40 | Spawning period duration | [Spawning was detected between February 21 and May 28 in 2003 and between March 16 and May 17 in 2004] | 21.0 weeks | Burdick and Hightower, 2005 |
41 | Spawning temperature | 8-26 [Max 15-20] | 17.0 °C | Internet, 2005 |
41 | Spawning temperature | Above 12 and will continue until temperaure do not drop below this point | 12.0 °C | Scott and Crossman, 1973 |
41 | Spawning temperature | Diffrente temperatures according to authors: 8-26; 12-17; 14-21; 17-24; 18.5, prefer 16.7-20.0 | 17.0 °C | Mills, 2004 |
41 | Spawning temperature | Generally 12-21 [Range from 8-26°C] | 16.5 °C | Fishbase, 2006 |
41 | Spawning temperature | 12-21 | 16.5 °C | Rue, 2001 |
41 | Spawning temperature | Beginning when water temperatures reach 13 to 15°C, and ending when they exceed 27°C | 13.0 °C | Anonymous, 2006 Chapter 3 |
41 | Spawning temperature | 13-20 | 16.5 °C | Bradbury et al, 1999 |
41 | Spawning temperature | Mean water temperature was 11°C in May 1967 and 15°C in May 1968 | 11.0 °C | Marcy, 1972 |
42 | Spawning water type | Concentrated near the shore, main channel [Freshwater, possibly brackish water] | Stagnant water | Internet, 2005 |
42 | Spawning water type | Rarely if ever in lakes | Stagnant water | Scott and Crossman, 1973 |
42 | Spawning water type | Freshwater of moderate current | Flowing or turbulent water | Everly and Boreman, 1999 |
42 | Spawning water type | In the main channels of rivers, preferred moderate current for spawning, about 0.3-0.93 or 0.15-0.61 m/s | Flowing or turbulent water | Mills, 2004 |
42 | Spawning water type | Primarily in tidal or sometimes in non-tidal freshwater | No category | Rue, 2001 |
42 | Spawning water type | in their native coastal habitats, alewifes spawn in the upper reaches of coastal rivers, in slow-flowing sections of slightly brackish or freshwater. | Flowing or turbulent water | Anonymous, 2006 Chapter 3 |
42 | Spawning water type | Spawn in rivers or brackish estuarine rivers, seldom if ever in lakes [River spawning usually takes place in moderate to strong flowing water, generally where there is sufficient velocity to eliminate silt deposits, and at the same time, far enough upstream for eggs to drift and hatch before reaching saltwater] | Stagnant water | Bradbury et al, 1999 |
42 | Spawning water type | Spawning occurs in open water beyond tidal influence | No category | Zydlewski and McCormick, 1997 |
42 | Spawning water type | Current velocities ranged from 0.5 to 2 ft/sec. | Flowing or turbulent water | Marcy, 1972 |
42 | Spawning water type | American shad choose either tributary and spawn in upsream segments characterized by shallow depths, high dissoled oxygen,and relatively high currents | Flowing or turbulent water | Olney et al, 2006 |
43 | Spawning depth | Near the surface | No data | Internet, 2005 |
43 | Spawning depth | Shallow | No data | Everly and Boreman, 1999 |
43 | Spawning depth | Near the surface: 0.9-12.2; or less than 3 meters | 6.55 m | Mills, 2004 |
43 | Spawning depth | Shallow | No data | Rue, 2001 |
43 | Spawning depth | Shallow, water less than 2 m | 2.0 m | Anonymous, 2006 Chapter 3 |
43 | Spawning depth | Range from 0.2-12 m | 6.1 m | Bradbury et al, 1999 |
43 | Spawning depth | A range of appropriate depths have been described between 0.45 m and 10.0 m. However in Neuse River, Amrican shad spawn almost entirely at depths of less than 2 m | 0.45 m | Burdick and Hightower, 2005 |
43 | Spawning depth | Eggs were found at depths of 0.6 to 7.3 m. An almost equal number of eggs/hr were collected above 3 m as below | 7.3 m | Marcy, 1972 |
44 | Spawning substrate | None, but survival is apparently higher when deposited over sandy and gravel areas | Lithophils | Internet, 2005 |
44 | Spawning substrate | Various substrate | No category | Everly and Boreman, 1999 |
44 | Spawning substrate | Usually spawn over sand and gravel | Lithophils | Mills, 2004 |
44 | Spawning substrate | Sandy or rocky bottoms | Lithophils | Rue, 2001 |
44 | Spawning substrate | Pelagophilous | Pelagophils | Balon, 1975 |
44 | Spawning substrate | It is generally thought that subsrate is unimportant to shad since spawning occurs in the water column and eggs are carried dowstream by the current. Spawning was observed over sand, silt, muck, gravel and boulder substrates, also over sand or gravel. | Lithophils | Bradbury et al, 1999 |
44 | Spawning substrate | Substrates dominated by cobble to be a positive attribute for american shad spawning sites. However, also reported over sandy bottoms free of mud and silt. | Psammophils | Burdick and Hightower, 2005 |
45 | Spawning site preparation | No, eggs are released in the open water | Open water/substratum scatter | Scott and Crossman, 1973 |
45 | Spawning site preparation | Broadcast their eggs in the water | Open water/substratum scatter | Mills, 2004 |
45 | Spawning site preparation | Open substratum spawner | Open water/substratum scatter | Balon, 1975 |
45 | Spawning site preparation | Eggs are released into open water | Open water/substratum scatter | Bradbury et al, 1999 |
45 | Spawning site preparation | Eggs are broadcast | Open water/substratum scatter | Burdick and Hightower, 2005 |
46 | Nycthemeral period of oviposition | Midnight to early morning | Day | Internet, 2005 |
46 | Nycthemeral period of oviposition | Spawning took place in the evening after sundown and continued until midnight or even later | Night | Scott and Crossman, 1973 |
46 | Nycthemeral period of oviposition | Mainly at night | Night | Everly and Boreman, 1999 |
46 | Nycthemeral period of oviposition | Most spawning occurs after dark, taking place between 2100 and 0700 hours, peaking at 2300-2400 | Night | Mills, 2004 |
46 | Nycthemeral period of oviposition | Spawning occurs from sunset to approximatively midnight | Night | Burdick and Hightower, 2005 |
46 | Nycthemeral period of oviposition | Spawning was seen only on dark afternoons and during the evening | Day | Marcy, 1972 |
47 | Mating system | During the spawning act, the female is accompanied by several males | No category | Scott and Crossman, 1973 |
47 | Mating system | The fish pair and swim close together, releasing egg and milt | No category | Fishbase, 2006 |
47 | Mating system | Spawning as several males coming up next to a female | No category | Burdick and Hightower, 2005 |
47 | Mating system | Spawning involves pairs of fish, or presumably several males and a single female. In group spawning, fish swam with their backs exposed. They splashed about forming a closely-packed circle | Promiscuity | Marcy, 1972 |
48 | Spawning release | Broadcast singly | No category | Internet, 2005 |
48 | Spawning release | Batch spawner: an individual female spawns repeatedly during each spawning season [Spawning frequency (every four fays) is preliminary] American shad probably exhibit indeterminate fecundity, contradicting previous studies | Multiple | Olney et al, 2001 |
48 | Spawning release | Batch spawner | Multiple | Fishbase, 2006 |
48 | Spawning release | American shad in the St. Johns river are batch spawners | Multiple | Olney and McBride, 2003 |
48 | Spawning release | Histological evidence that an individual spawn in batches over a period of days or weeks | Multiple | Burdick and Hightower, 2005 |
49 | Parity | After spawning, the spent fish begin to drop back to salt water and vanish until the next spawning season [Some might die] | Semelparous | Scott and Crossman, 1973 |
49 | Parity | Populations may be either semelparous in southern rivers from Florida to North Carolina or predominately iteroparous in more northerly rivers | Iteroparous | Olney et al, 2001 |
49 | Parity | Iteroparous, spawn annualy | Iteroparous | Mills, 2004 |
49 | Parity | Adults descend shortly after spawning | No category | Fishbase, 2006 |
49 | Parity | Iteroparous or semelparous | Iteroparous | Olney and McBride, 2003 |
49 | Parity | Although alewifes generally do not die after spawning, the fluctuating temperatures that the adults are exposed to when they move to inshore waters often results in mortality due to osmotic stress. In some years, temperature changes caused by upwelling may result in a massive die-off of spawning alewifes | Semelparous | Anonymous, 2006 Chapter 3 |
49 | Parity | May spawn up to 7 times and live to be 13 years | No category | Bradbury et al, 1999 |
49 | Parity | Some adults die after spawning with the percentage generally decreasing with increasing latitude | Semelparous | Burdick and Hightower, 2005 |
49 | Parity | The proportions of repeat spawning fish in the sample decreased to 85% for males in 1972 and 78 and 64% for males and females respectively in 1973 | Iteroparous | Carscaden and Legget, 1975 |
49 | Parity | American shad stocks in Virginia may be partially iteroparous (i.e., some proportion of the population dies after spawning), however there is no direct evidence of the phenomenon (e.g., spent carcasses on the shore) in the York River | Iteroparous | Olney et al, 2006 |
50 | Parental care | Non guarders | No care | Fishbase, 2006 |