Trait completeness | 94% |
Total data | 204 |
References | 31 |
Author: Fabrice Téletchéa
License: All rights reserved
Trait id | Trait | Primary data | Secondary Data | References |
---|---|---|---|---|
1 | Oocyte diameter | 1.5 | 1.5 mm | Spillmann, 1961 |
1 | Oocyte diameter | 2 | 2.0 mm | Bruslé and Quignard, 2001 |
1 | Oocyte diameter | 1.5 [Not specified] | 1.5 mm | Persat, 2001 |
1 | Oocyte diameter | 1.7 | 1.7 mm | Tyler and Sumpter, 1996 |
1 | Oocyte diameter | 1.50 [Average diameter of the largest oocyte in fully developed ovaries] | 1.5 mm | Vila-Gispert and Moreno-Amich, 2002 |
1 | Oocyte diameter | 1.5 [Not specified] | 1.5 mm | Copp et al, 2002b |
1 | Oocyte diameter | Mean 1.2, range 1.1-1.4 [Egg within ovary] | 1.25 mm | Lobon-cervia et al, 1996 |
1 | Oocyte diameter | Diameter means range from 1.34 to 1.56 [Unfertilized eggs] | 1.34 mm | Mann and Mills, 1985 |
2 | Egg size after water-hardening | Mainly 1.5 [Drifting eggs] | 1.5 mm | Copp et al, 2002b |
2 | Egg size after water-hardening | 2.0-2.5, mostly 2.4-2.5 [Ova] | 2.25 mm | Kennedy, 1969 |
2 | Egg size after water-hardening | About 1.5 [Eggs] | 1.5 mm | Wurtz-Arlet, 1950 |
2 | Egg size after water-hardening | Eggs found on the field range from 1.33 to 1.51 mm | 1.51 mm | Mills, 1981 |
2 | Egg size after water-hardening | 2.0 [Not specified] | 2.0 mm | Kamler and Wolnicki, 2006 |
2 | Egg size after water-hardening | 2.5 [Not specified] | 2.5 mm | Kestemont and Mélard, 1994 |
3 | Egg Buoyancy | Demersal | Demersal | Spillmann, 1961 |
3 | Egg Buoyancy | Demersal | Demersal | Persat, 2001 |
3 | Egg Buoyancy | Demersal | Demersal | Tyler and Sumpter, 1996 |
3 | Egg Buoyancy | Negatively bouyant | No category | Mills, 1981 |
4 | Egg adhesiveness | Stick to gravel | Adhesive | Spillmann, 1961 |
4 | Egg adhesiveness | Adhesive | Adhesive | Bruslé and Quignard, 2001 |
4 | Egg adhesiveness | Adhesive | Adhesive | Persat, 2001 |
4 | Egg adhesiveness | Fixed on plant or stone | Non-Adhesive | Fishbase, 2006 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mills, 1986 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mann, 1996 |
4 | Egg adhesiveness | Eggs, singly or in clumps or two to five, were also found adhering to pebbles on the bottom, especially in the eddis behind larger stones | Adhesive | Kennedy, 1969 |
4 | Egg adhesiveness | Strongly adhesive on stones | Adhesive | Wurtz-Arlet, 1950 |
4 | Egg adhesiveness | Adhesive | Adhesive | Mills, 1981 |
5 | Incubation time | 25 | 25.0 days | Spillmann, 1961 |
5 | Incubation time | 25-30 days at 11-13°C | 27.5 days | Bruslé and Quignard, 2001 |
5 | Incubation time | About 4 weeks, more precisely 20-23 [12°C], 29-30 [10°C] | 21.5 days | Kennedy, 1969 |
5 | Incubation time | 25 [At 13°C] and 28 [At 12°C] | 25.0 days | Wurtz-Arlet, 1950 |
5 | Incubation time | Take 25-30 days to hatch in a typical river temperatures | 27.5 days | Mills, 1981 |
5 | Incubation time | Fertilization to larvae (2-4 days after hatching): 26-32 days (mostly 30) at 10°C | 3.0 days | Mann and Mills, 1985 |
6 | Temperature for incubation | 13 | 13.0 °C | Spillmann, 1961 |
6 | Temperature for incubation | 11-13 | 12.0 °C | Bruslé and Quignard, 2001 |
6 | Temperature for incubation | Mean of 9.7, range 5.6-11.3°C in natural conditions | 8.45 °C | Mills, 1986 |
6 | Temperature for incubation | 11-14, mean of 12 [Laboratory water temperatures] | 12.5 °C | Kennedy, 1969 |
6 | Temperature for incubation | 6.75-15 range in which normal development occurs | 10.88 °C | Herzig and Winkler, 1986 |
6 | Temperature for incubation | 12-13 | 12.5 °C | Wurtz-Arlet, 1950 |
6 | Temperature for incubation | Typical spring water temperature is 10°C | 10.0 °C | Mills, 1981 |
6 | Temperature for incubation | Incubated at a constant 10°C in chalk spring water | 10.0 °C | Mann and Mills, 1985 |
6 | Temperature for incubation | Viable range 4-17.5, threshold temperature at which ontogeny is theoretically arrested: 5.1 | 10.75 °C | Kamler and Wolnicki, 2006 |
7 | Degree-days for incubation | 325 [25 days at 13°C] | 325.0 °C * day | Spillmann, 1961 |
7 | Degree-days for incubation | 320-330 | 325.0 °C * day | Bruslé and Quignard, 2001 |
7 | Degree-days for incubation | 240-300 [24-30 days at 9.7] in natural conditions | 270.0 °C * day | Mills, 1986 |
7 | Degree-days for incubation | About 300-350 | 325.0 °C * day | Wurtz-Arlet, 1950 |
7 | Degree-days for incubation | 143 [Effective day-degrees] | 143.0 °C * day | Kamler, 2002 |
7 | Degree-days for incubation | 250-300 [25-30 days at 10°C] | 275.0 °C * day | Mills, 1981 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
8 | Initial larval size | 7.5 | 7.5 mm | Spillmann, 1961 |
8 | Initial larval size | 7-7.5 | 7.25 mm | Bruslé and Quignard, 2001 |
8 | Initial larval size | 7.5 | 7.5 mm | Persat, 2001 |
8 | Initial larval size | 8.6 | 8.6 mm | Kennedy, 1969 |
8 | Initial larval size | 7.5 | 7.5 mm | Wurtz-Arlet, 1950 |
8 | Initial larval size | Means range from 8.24 to 9.38, for larvae 2 to 4 days old | 8.24 mm | Mann and Mills, 1985 |
9 | Larvae behaviour | 24 hours after hatching, fry swim strongly in all directions | Demersal | Wurtz-Arlet, 1950 |
9 | Larvae behaviour | The water current may play an important role at the time of hatching as newly-hatched fry are feeble swimmers and will be swept dowstream off the site until either chance or perhaps a response to some environmental gradient such as temperature, depth or current itself enables them to aggregate in slack marginal areas | Demersal | Mills, 1981 |
10 | Reaction to light | Larvae are intially photophobic | Photophobic | Mann, 1996 |
10 | Reaction to light | Slight preference for the mostly bright side of the aquarium | Photopositive | Wurtz-Arlet, 1950 |
11 | Temperature during larval development | 11-14, with a mean of 12 | 12.5 °C | Kennedy, 1969 |
11 | Temperature during larval development | About 15 | 15.0 °C | Wurtz-Arlet, 1950 |
11 | Temperature during larval development | Between 20 and 25 April 1977 and 1978 the fry (<48 h old) were stocked into cages [Heavy mortalities in starved fry kept at 10°C ( a typical mean river water temperature in late April and May) | 20.0 °C | Mills, 1982 |
11 | Temperature during larval development | Reared at 16-25 | 20.5 °C | Kamler and Wolnicki, 2006 |
13 | Full yolk-sac resorption | 90-120 [The yolk-sac was absorbed in a week or to ten days, when the larvae were about 10 mm long] | 105.0 °C * day | Kennedy, 1969 |
13 | Full yolk-sac resorption | After 10 days at about 15°C, the yolk sac is fully resorbed | 10.0 °C * day | Wurtz-Arlet, 1950 |
13 | Full yolk-sac resorption | [The exhaustion of endogeneous supplies; heavy mortalities in starved fry kept at 10°C only began after three weeks] | 10.0 °C * day | Mills, 1982 |
14 | Onset of exogeneous feeding | About 100 [Feeding begin before the yolk-sac was fully absorbed] | 100.0 °C * day | Kennedy, 1969 |
14 | Onset of exogeneous feeding | After 7 days at 15°C, fry start to eat | 7.0 °C * day | Wurtz-Arlet, 1950 |
14 | Onset of exogeneous feeding | About 4-6 days at 10°C | 5.0 °C * day | Mills, 1982 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
15 | Age at sexual maturity | 2 but 3-4 [Sex not precised] | 3.5 year | Bruslé and Quignard, 2001 |
15 | Age at sexual maturity | 3 [Female] | 3.0 year | Fishbase, 2006 |
15 | Age at sexual maturity | 2 [48 months, age at maturation] | 2.0 year | Vila-Gispert and Moreno-Amich, 2002 |
15 | Age at sexual maturity | 3-4 [Not specified] | 3.5 year | Environment agency, ??? |
15 | Age at sexual maturity | The smallest female about to spawn was 5 years old [Siberia, 3-5 Not specified for various populations] | 4.0 year | Lobon-cervia et al, 1996 |
15 | Age at sexual maturity | 3-4, yet mostly at 4 [Female] | 3.5 year | Mann, 1974 |
15 | Age at sexual maturity | Both sex reach sexual maturity after four years growth, although some fast-growing individuals may do so after three years | 4.0 year | Mann and Mills, 1985 |
15 | Age at sexual maturity | 2-5 [Sex not specified] | 3.5 year | Kestemont and Mélard, 1994 |
16 | Length at sexual maturity | 16 | 16.0 cm | Bruslé and Quignard, 2001 |
16 | Length at sexual maturity | 14-15 [Unsexed] | 14.5 cm | Fishbase, 2006 |
16 | Length at sexual maturity | The smallest female about to spawn was 14.9 cm [12-15.9 not specified for various populations] | 13.95 cm | Lobon-cervia et al, 1996 |
16 | Length at sexual maturity | 16 ±1 [Female] | 16.0 cm | Mann, 1974 |
17 | Weight at sexual maturity | 29.5-46.4 g for age 3 and 53.0-84.5 for age 4 in two populations respectively [female] | 37.95 kg | Mann, 1974 |
19 | Relative fecundity | 75 | 75.0 thousand eggs/kg | Bruslé and Quignard, 2001 |
19 | Relative fecundity | [F=-3.6284+4.0424*log L, and Log W=-5.1261 + 3.2483 log L, used with 16.2 and 20.3 cm] | 3.63 thousand eggs/kg | Lobon-Cervia et al;, 1996 |
20 | Absolute fecundity | 8-10 | 9.0 thousand eggs | Bruslé and Quignard, 2001 |
20 | Absolute fecundity | 15-30 | 22.5 thousand eggs | Spillmann, 1961 |
20 | Absolute fecundity | 8.714 [Average number of vitellogenic oocyes of mature females in a single spawning season] | 8.71 thousand eggs | Vila-Gispert and Moreno-Amich, 2002 |
20 | Absolute fecundity | 6.5-9.5 eggs for 20 cm females | 8.0 thousand eggs | Environment agency, ??? |
20 | Absolute fecundity | Log egg number = 4038 log length (mm) - 5474 or log egg number=3900 log length (mm)-5128 | 4038.0 thousand eggs | Mann, 1974 |
20 | Absolute fecundity | 5.973-8.714 for a female 200 mm | 7.34 thousand eggs | Mann and Mills, 1985 |
20 | Absolute fecundity | About 100 000 eggs | 100.0 thousand eggs | Kestemont and Mélard, 1994 |
21 | Oocyte development | Group-synchronous | Group-synchronous | Rinchard, 1996 |
22 | Onset of oogenesis | Elaboration of gonad tissue was not significant until August/September, from which time devolpment continued through winter months | ['January', 'February', 'March', 'August', 'September'] | Mann, 1974 |
22 | Onset of oogenesis | Maturation of gonads is synchronous and complete in the previous autumn | ['October', 'November', 'December'] | Fredrich et al, 2003 |
23 | Intensifying oogenesis activity | From Mid-August to November, 2 to 10% | ['August', 'September', 'October', 'November'] | Mann, 1974 |
24 | Maximum GSI value | The average GSI for females about to spawn was 13.8% [Range 8.9-19.4%] | 14.15 percent | Lobon-cervia et al, 1996 |
24 | Maximum GSI value | Mean of 16%, range 15-17% [Mid-March] | 16.0 percent | Mann, 1974 |
25 | Oogenesis duration | From August to mid-March | 8.0 months | Mann, 1974 |
26 | Resting period | < 0.2% [From April to mid-July] | 5.0 months | Mann, 1974 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
27 | Age at sexual maturity | 2 but 3-4 [Sex not precised] | 3.5 years | Bruslé and Quignard, 2001 |
27 | Age at sexual maturity | 2-3 [Male] | 2.5 years | Fishbase, 2006 |
27 | Age at sexual maturity | 3-4 [Not specified] | 3.5 years | Environment agency, ??? |
27 | Age at sexual maturity | 3-5 |Not specified for vairous populations] | 4.0 years | Lobon-cervia et al, 1996 |
27 | Age at sexual maturity | 3-4, rarely 2 [Male] | 3.5 years | Mann, 1974 |
27 | Age at sexual maturity | Both sex reach sexual maturity after four years growth, although some fast-growing individuals may do so after three years | 4.0 years | Mann and Mills, 1985 |
28 | Length at sexual maturity | 16 [Sex not precised] | 16.0 cm | Bruslé and Quignard, 2001 |
28 | Length at sexual maturity | 16.3 [Male] | 16.3 cm | Fishbase, 2006 |
28 | Length at sexual maturity | 12-15.9 [Not specified for various populations] | 13.95 cm | Lobon-cervia et al, 1996 |
28 | Length at sexual maturity | 15.9 ± 0.5 [Male] | 15.9 cm | Mann, 1974 |
29 | Weight at sexual maturity | 29.1-46 g for age 3 and 52.8-82.0 for age 4 in two populations respectively [female] | 37.55 kg | Mann, 1974 |
30 | Male sexual dimorphism | Bears whitish nuptial tubercules on snout, head, cheeks, opercules, sides and belly. Pectoral fin are longer in male than female | Present | Spillmann, 1961 |
30 | Male sexual dimorphism | Male bears whitish nuptial tubercule | Absent | Bruslé and Quignard, 2001 |
30 | Male sexual dimorphism | Breeding tubercles are present on the head, trunk, and pectoral fin | Present | Witkowski and Rogowska, 1991 |
31 | Onset of spermatogenesis | August [Elaboration of gonad tissue was not significant until August/September, from which time development continued through winter months] | ['January', 'February', 'March', 'August', 'September'] | Mann, 1974 |
32 | Main spermatogenesis activity | October-November | ['October', 'November'] | Mann, 1974 |
33 | Maximum GSI value | Average 1.2% | 1.2 percent | Lobon-cervia et al, 1996 |
33 | Maximum GSI value | Mean 1.5, range 1-2% [November through December] | 1.5 percent | Mann, 1974 |
34 | Spermatogenesis duration | [From mid-April to mid-August] | 6.0 months | Mann, 1974 |
35 | Resting period | < 0.2% [From mid-April to mid-August] | 6.0 months | Mann, 1974 |
Trait id | Trait | Primary Data | Secondary Data | References |
---|---|---|---|---|
36 | Spawning migration distance | Short migration | No data | Spillmann, 1961 |
36 | Spawning migration distance | Large home range | No data | Environment agency, ??? |
37 | Spawning migration period | Migration prior and after spawning | No data | Bruslé and Quignard, 2001 |
38 | Homing | Spawning areas are not fixed | Present | Spillmann, 1961 |
38 | Homing | Tendendy to return to the same spawning ground (reproductive homing) | Present | Fredrich et al, 2003 |
39 | Spawning season | March-April | ['March', 'April'] | Billard, 1997 |
39 | Spawning season | February until May | ['February', 'March', 'April', 'May'] | Spillmann, 1961 |
39 | Spawning season | End of March-Beginning of April until May-June | ['March', 'April', 'May', 'June'] | Bruslé and Quignard, 2001 |
39 | Spawning season | March-April | ['March', 'April'] | Persat, 2001 |
39 | Spawning season | March-April | ['March', 'April'] | Fishbase, 2006 |
39 | Spawning season | March-April | ['March', 'April'] | Mills, 1986 |
39 | Spawning season | February-April | ['February', 'April'] | Mann, 1996 |
39 | Spawning season | Might spawn in early March, possibly even in February | ['February', 'March'] | Kennedy, 1969 |
39 | Spawning season | March-April | ['March', 'April'] | Environment agency, ??? |
39 | Spawning season | March-April | ['March', 'April'] | Terver, 1984 |
39 | Spawning season | March / April-May | ['March', 'April', 'May'] | Herzig and Winkler, 1986 |
39 | Spawning season | Varies according to latitude, mainly March-April [Full range February to July] | ['February', 'March', 'April', 'May', 'June', 'July'] | Lobon-cervia et al, 1996 |
39 | Spawning season | Spawning occurred during the second half of March and no ripe fish were found at either site in April | ['March', 'April'] | Mann, 1974 |
39 | Spawning season | Late winter or early spring | ['January', 'February', 'March', 'April', 'May', 'June'] | Fredrich et al, 2003 |
39 | Spawning season | A small number of eggs were found on 21 March 80, but the following week a large shoal of ripe dace collected in a pool above the spawning site and spawned on 28 March 80 | ['March'] | Mills, 1981 |
39 | Spawning season | Between late February and early April | ['February', 'April'] | Mann and Mills, 1985 |
39 | Spawning season | Mid to late March | ['March'] | Clough et al, 1998 |
39 | Spawning season | (February) March-May | ['February', 'March', 'May'] | Kamler and Wolnicki, 2006 |
39 | Spawning season | March-April | ['March', 'April'] | Kestemont and Mélard, 1994 |
39 | Spawning season | In the Trent, dace hatched between the third week of April (2003) and the first week of May (2002), whereas in the Ouse catchment hatching occurred 3 or 4 weeks later | ['April', 'May'] | Nunn et al, 2007 |
40 | Spawning period duration | 4-5 [Southern populations from 10 February to 24 March] | 4.5 weeks | Spillmann, 1961 |
40 | Spawning period duration | 4 [1.00 month, length of breeding season] | 4.0 weeks | Vila-Gispert and Moreno-Amich, 2002 |
40 | Spawning period duration | 8-9 | 8.5 weeks | Terver, 1984 |
40 | Spawning period duration | Spawing of all the age-groups togehter occurred within a 5-day period [In Siberia] | 5.0 weeks | Lobon-cervia et al, 1996 |
40 | Spawning period duration | Spawning occurred during the second half of March and no ripe fish were found at either site in April | No data | Mann, 1974 |
40 | Spawning period duration | Spawn over a two or three week period | No data | Mann and Mills, 1985 |
41 | Spawning temperature | 11-12 | 11.5 °C | Bruslé and Quignard, 2001 |
41 | Spawning temperature | From 10°C | 10.0 °C | Persat, 2001 |
41 | Spawning temperature | 5-12 | 8.5 °C | Mann, 1996 |
41 | Spawning temperature | About 10 | 10.0 °C | Kennedy, 1969 |
41 | Spawning temperature | 9-10 | 9.5 °C | Environment agency, ??? |
41 | Spawning temperature | > 8 | 8.0 °C | Herzig and Winkler, 1986 |
41 | Spawning temperature | About 6 [In Siberia] | 6.0 °C | Lobon-cervia et al, 1996 |
41 | Spawning temperature | 6-13 | 9.5 °C | Kamler and Wolnicki, 2006 |
41 | Spawning temperature | >13°C | 13.0 °C | Kestemont and Mélard, 1994 |
42 | Spawning water type | Riffles : water with current | Flowing or turbulent water | Bruslé and Quignard, 2001 |
42 | Spawning water type | Water with current | Flowing or turbulent water | Spillmann, 1961 |
42 | Spawning water type | Flowing water | Flowing or turbulent water | Fishbase, 2006 |
42 | Spawning water type | Current velocities: 20-50 cm/s | Flowing or turbulent water | Mann, 1996 |
42 | Spawning water type | Prefers swifter currents | Flowing or turbulent water | Kennedy, 1969 |
42 | Spawning water type | Fast-flowing waters | Flowing or turbulent water | Mills, 1981 |
42 | Spawning water type | Fast flowinf rivers and streams | No category | Mann and Mills, 1985 |
43 | Spawning depth | Shallow waters | No data | Bruslé and Quignard, 2001 |
43 | Spawning depth | Shallow waters | No data | Persat, 2001 |
43 | Spawning depth | Shallow waters | No data | Fishbase, 2006 |
43 | Spawning depth | The eggs were, however, widely and adundantly distributed in the riffle in depths of 25 to 40 cm from just above the pool | 25.0 m | Kennedy, 1969 |
44 | Spawning substrate | Lithophile: sand or gravel | Lithophils | Bruslé and Quignard, 2001 |
44 | Spawning substrate | Gravel | Lithophils | Persat, 2001 |
44 | Spawning substrate | Gravel and stones | Lithophils | Fishbase, 2006 |
44 | Spawning substrate | Gravel | Lithophils | Mills, 1986 |
44 | Spawning substrate | Eggs adhere to submerged plants, but other substrata are utilised if suitable plants are absent, 3-25 cm in diameter | Phytophils | Mann, 1996 |
44 | Spawning substrate | Is clearly a lithophil spawner | Lithophils | Kennedy, 1969 |
44 | Spawning substrate | Gravel, typically 10-40 mm diameter | Lithophils | Environment agency, ??? |
44 | Spawning substrate | Phytolithophil | Lithophils | Wolter and Vilcinskas, 1997 |
44 | Spawning substrate | Phyto-lithophils | Lithophils | Balon, 1975 |
44 | Spawning substrate | Gravel spawning sites | Lithophils | Mills, 1981 |
44 | Spawning substrate | Gravel spawner | Lithophils | Mann and Mills, 1985 |
44 | Spawning substrate | Lithophilous | Lithophils | Clough et al, 1998 |
44 | Spawning substrate | Plants or sand | Phytophils | Kestemont and Mélard, 1994 |
44 | Spawning substrate | Spawn in the main river channel over gravel substrata | Lithophils | Smith, 2004 |
45 | Spawning site preparation | No, eggs are deposited on the substrates | Susbtrate chooser | Persat, 2001 |
45 | Spawning site preparation | Open water/susbtratum egg scatterers | Open water/substratum scatter | Fishbase, 2006 |
45 | Spawning site preparation | Open substratum spawners | Open water/substratum scatter | Mann, 1996 |
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 | Night | Night | Spillmann, 1961 |
46 | Nycthemeral period of oviposition | Night | Night | Persat, 2001 |
48 | Spawning release | Unique | No category | Rinchard, 1996 |
48 | Spawning release | Spawning is synchronous: each female deposited 15000-25000 eggs | No category | Persat, 2001 |
48 | Spawning release | Single spawning per year | Total | Vila-Gispert and Moreno-Amich, 2002 |
48 | Spawning release | Single spawning | Total | Environment agency, ??? |
48 | Spawning release | Spawn once a year | Total | Fredrich et al, 2003 |
48 | Spawning release | Release one batch of egg | Multiple | Mann and Mills, 1985 |
48 | Spawning release | Shed a single batch of eggs in a well-defined spawning period | Multiple | Nunn et al, 2007 |
49 | Parity | Iteroparous | Iteroparous | Bruslé and Quignard, 2001 |
49 | Parity | Female dace did not necessarily spawn every year once they had reached maturity | Iteroparous | Mann, 1974 |
49 | Parity | Release one batch of eggs annually for up to seven successive years. There was no evidence that any female had a rest year from spawning once they were mature | No category | Mann and Mills, 1985 |
49 | Parity | Iteroparous | Iteroparous | Clough et al, 1998 |
50 | Parental care | Non guarders | No care | Fishbase, 2006 |
50 | Parental care | Non-guarders | No care | Mann, 1996 |
50 | Parental care | No parental protection of zygotes, embryo and larvae | No care | Vila-Gispert and Moreno-Amich, 2002 |