Anguilla anguilla |
Pelagic |
Pelagic |
Spilmann, 1961 |
Anguilla anguilla |
Pelagic |
Pelagic |
Deelder, 1970 |
Anguilla anguilla |
The prolarvae on hatching settled at the bottom of the incubation containers and remained lying with the back down, periodically making spiral movements and rising into the water column. The large fat droplet, broad fin border and head sinus ensured buoyancy of the prolarvae |
Demersal |
Prokhorchik, 1987 |
Anguilla anguilla |
Pelagic |
Pelagic |
Bruslé and Quignard, 2001 |
Alosa alosa |
Remains in the gravel |
Demersal |
Bruslé and Quignard, 2001 |
Alosa alosa |
After hatching, the young remain in the slow-flowing reaches of the lower parts of rivers, then move into the estuary and eventually into coastal waters and the open sea |
Demersal |
Maitland and Hatton-Ellis, 2000 |
Alosa alosa |
Remain close to the bottom |
Demersal |
Bensettiti and Gaudillat, 2002 |
Alosa alosa |
It has been observed that larvae would grow under the gravel, which could suggest that their photoresponse evolves from a strong positive photoresponse at hatching to negative photoresponse in the course of larval stage. […] larvae were caught near the surface |
Demersal |
Jatteau and Bardonnet, 2008 |
Alosa alosa |
After hatching, yolk sac larvae swam directly from the jars into the small containers equipped with a net at their outflow to prevent any larval escapement |
Demersal |
Bardonnet and Jatteau, 2008 |
Alosa fallax |
The young fish then drop quickly dowstream in the current to the quieter waters of the upper estuary where they start to feed and grow [Both eggs and larvae are transparent] |
Demersal |
Maitland and Hatton-Ellis, 2000 |
Alosa sapidissima |
Newly larvae are pelagic, and most abundant at the surface |
Pelagic |
Internet, 2005 |
Alosa sapidissima |
Both feeding and yolksac larvae are planktonic [Dispersal therefore occurs by passive transport] |
Demersal |
Everly and Boreman, 1999 |
Alosa sapidissima |
Larvae are planktonic for about 4 weeks |
Demersal |
Mills, 2004 |
Alosa sapidissima |
Larvae are planktonic and do not metamorphose into juveniles for 4-5 weeks |
Demersal |
Bradbury et al, 1999 |
Alosa sapidissima |
Larvae drift downstream until they are capable of swimming freely |
Demersal |
Burdick and Hightower, 2005 |
Cobitis taenia |
Live on the bottom, at the age of 3-4 days their activity increases |
Demersal |
Vaino and Saat, 2003 |
Cobitis taenia |
After the onset of negative phototaxis, the free-embryos will accumulate at the darkest point in the surrounding, i.e. the bottom beneath the centre part of the vegetation |
Demersal |
Bohlen, 2000 |
Cobitis taenia |
Benthic |
Demersal |
Bensettiti and Gaudillat, 2002 |
Abramis brama |
Remain fixed to plants until the full resorption of yolk sac |
Demersal |
Bruslé and Quignard, 2001 |
Abramis brama |
Remain fixed to plants until the full resorption of yolk sac [TL of 7.6-8.4] |
Demersal |
Olivier, 2001 |
Abramis brama |
Larvae motionless, attached to vegetation or resting on bottom. Feed only on yolk |
Demersal |
Backiel and Zawiska, 1968 |
Abramis brama |
The hatched embryos mostly rested in a passive way on the bottom and only some of them hung themselves by their sticky glands onto walls or onto submerged silon threads; under natural conditions, the embryos stuck themselves onto submerged plants |
Demersal |
Penaz and Gajdusek, 1979 |
Abramis brama |
Eleutheroembryos hangs attached to plants or lies on the bottom. |
Demersal |
Brylinska and Boron, 2004 |
Aristichthys nobilis |
Motile under natural conditions, however, it is carried out by the water current |
Demersal |
Jennigs, 1988 |
Aristichthys nobilis |
One day after fertilization, larval bighead haTch and enter the ichthyoplankton drift. Seven days after hatching, bighead carp larvae migrate to shore |
Demersal |
Schrank, 1999 |
Barbus barbus |
The hatched embryos lie on one side motionless, showing quite isolated, feeble movements. However, they respond to external stimuli (by light or touch) by very rapid movements along the bottom of the tank. They show no tendency towards hiding in shelters or dark places |
Demersal |
Penaz, 1973 |
Barbus barbus |
After hatching the embryos rested on the bottom of the hatching apparatus, performing only occassional short movements, most frequently when disturbed by handling the apparatus |
Demersal |
Krupta, 1988 |
Carassius auratus |
Benthic, remain near the spawning area, then near the surface after yolk sac is absorbed |
Demersal |
Internet, 2005 |
Carassius auratus |
At hatching, the larva is restricted in the movement by the weight of the yolk sac. The larva shows a positive thigmotropism, adhering to the aquarium walls or any fragments of plants. |
Demersal |
Battle, 1940 |
Carassius auratus |
During 3 days after hatching yolk-feeding larva is fixed to submerged plants |
Demersal |
Szczerbowski and Szczerbowski, 1996 |
Carassius carassius |
In nature, the free embryo are passive and often attach themselves to plants, where they stay hiding for the first 1-2 days of the endogenous feeding period |
Demersal |
Laurila et al, 1987 |
Carassius carassius |
Eggs are deposited on plants to which they remain fixed during endogeneous feeding |
Demersal |
Szczerbowski and Szczerbowski, 1996 |
Carassius carassius |
The newly hatched larvae are passive: they lie on the bottom of the aquarium, for example. In the second day after hatching they try to swimupwards, towards the light (positive phototaxis) and attach to plants |
Demersal |
Laurila and Holopainen, 1990 |
Chondrostoma nasus |
Benthic, remains in the grounds |
Demersal |
Bruslé and Quignard, 2001 |
Chondrostoma nasus |
The starvating larvae show limited mobility already during the terminal phase of resorption of their yolk sac and mostly keep at the bottom of the aquarium, whereras the feeding larvae move throughout the water column and near water surface. During the last two or three days of their life, the fishes were in agony, showing but quite feeble signs of life. |
Demersal |
Penaz, 1971 |
Chondrostoma nasus |
Although the hatched embryos still spend most of their times lying passively on one side of the bottom of the through, they sometimes rise to the surface and then sink pasively to the bottom again |
Demersal |
Penaz, 1974 |
Chondrostoma nasus |
Benthic larvae |
Demersal |
Keckeis, 2001 |
Chondrostoma toxostoma |
Benthic larvae [The free embryos laid more or less on the bottom of the tank, but from time to time darted horizontally. Then, they fell back to the bottom and rest passively for some time.] |
Demersal |
Gozlan et al, 1999 |
Ctenopharyngodon idella |
Pelagic and could derive |
Pelagic |
Bruslé and Quignard, 2001 |
Ctenopharyngodon idella |
The pelagic larvae then have a behavior of alternately sinkink and swimming giving them the potential for extensive downstream migration |
Pelagic |
Cudmore and Mandrake, 2004 |
Ctenopharyngodon idella |
Currents carry the eggs and larvae to the quiet water at the tributary mouth |
Demersal |
Brown and Coon, 1991 |
Ctenopharyngodon idella |
Eggs and prolarvae drift more than 500 km dowstream in the Amur |
Demersal |
Gorbach and Krykhtin, 1988 |
Ctenopharyngodon idella |
The pelagic larvae then have a behavior of alternately sinkink and swimming, which allows them to migrate farther downstream. Also: it lies on the bottom and occasionally swim vertically to the surface and drifts back to the bottom |
Demersal |
Shireman and Smith, 1983 |
Cyprinus carpio |
First fixed on aquatic plants then free |
Demersal |
Bruslé and Quignard, 2001 |
Cyprinus carpio |
At bottom or attached to aquatic vegetation immediatly after hatching, then gradually in shallow water at bottom amon vegetation, occassionally in water column [Newly hatched larvae lay on their sides at the bottom of the aquarium] |
Demersal |
Internet, 2005 |
Cyprinus carpio |
Remain fixed the first 2-3 days |
Demersal |
Lafaille and Crivelli, 2001 |
Cyprinus carpio |
Immedialty after hatching the embryos remain passively on the bottom of the tank, with occasional jerly movements, and someindividuals begin to attach themselves by means of their special adhesive glands |
Demersal |
Penaz et al, 1983 |
Cyprinus carpio |
After hatching, carp larvae a cement attach themselves to surface vegetation via cement glands on their head. They remain attached for 4-5 days while yolk is absorbed from a large yolk-sac and undergo organogenesis and other development |
Demersal |
Smith, 2004 |
Cyprinus carpio |
Prolarvae settle to bottom immediatly after hatching and attach to plants or other objects; fry tend to leave spawning areas about 2 weeks after hatching but remain along shore among vegetation through summer |
Demersal |
Goodyear et al, 1982 |
Gobio gobio |
Tend to keep to the bottom. where they rest upright with the spread out of their pectoral fins |
Demersal |
Kennedy and Fitzmaurice, 1972 |
Gobio gobio |
Benthic larvae |
Demersal |
Mann, 1996 |
Gobio gobio |
The hatched embryos mostly lie still on the bottom |
Demersal |
Penaz and Prokes, 1978 |
Hypophthalmichthys molitrix |
Pelagic eggs and larvae are carried more than 500 km from the spawning grounds |
Pelagic |
Gorbach and Kryhtin, 1988 |
Leucaspius delineatus |
Pelagic, highly active near the surface |
Pelagic |
Bruslé and Quignard, 2001 |
Leucaspius delineatus |
Newly-emerged larvae swim actively |
Demersal |
Mann, 1996 |
Leucaspius delineatus |
The earliest embryos to hatch were onyl able to perform sudden bursts of activity and appeared to be able to swim a few centimetres from the bottom before sinking again. Those embryos that hatched lated, however, were able to perform more sustained swimming that were soon able to swim to the surface |
Demersal |
Pinder and Gozlan, 2004 |
Leucaspius delineatus |
A specific prolongation of embryonic development within the membane seems to be a fairly unusual development phenomenon; as a result the hatching larvae is capable of an independent life in water [Others described as: hatched larvae had no cement glands and were so advanced in develoment that were able to commence active life and form soals under the water surface as soon as they left the egg membranes while also described as that sun bleak larvae, as of other cyprinids, first attached themselves to the substraum, and sawm upward, to the surface, to fill the air bladder, only after having resorbed the yolk sac] |
Demersal |
Bonislawska et al, 1999 |
Leuciscus cephalus |
Newly hatched larvae stayed mainly motionless at the bottom of the tank; however time to time performed short and sudden jerky anguilliform movements [Schooling behavior for the entire period of larvae and juvenile development] |
Demersal |
Calta, 2000 |
Leuciscus cephalus |
The embryos are positioned sideways on the bottom of the contained in the immobile condition, and only at times they give violent jerks ahead |
Demersal |
Penaz, 1968 |
Leuciscus idus |
Larvae have well developped cement glands with which they fix themselves to plants where their development occurs. Active swiimming in horizontal position begins 4 days after hatching. At that time their swim bladder is being filled with air |
Demersal |
Witkowski et al, 1997 |
Leuciscus leuciscus |
24 hours after hatching, fry swim strongly in all directions |
Demersal |
Wurtz-Arlet, 1950 |
Leuciscus leuciscus |
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 |
Phoxinus phoxinus |
After hatching, the prolarvae disperse on the bottom of the aquarium. They lie on the side completely still, not reacting to light, water fluctuations or sounds. [The hatched embryos are under stones, described in other studies] |
Demersal |
Soin et al, 1982 |
Phoxinus phoxinus |
From birth they were most active |
Demersal |
Frost, 1943 |
Pimephales promelas |
Newly hatched fry are translucent |
Demersal |
Kerr and Grant, 1999 |
Pseudorasbora parva |
After hatching the prolarvae swim actively in jerks |
Demersal |
Makeyeva and Mokamed, 1982 |
Rhodeus sericeus |
Remain in the mussel |
Demersal |
Bruslé and Quignard, 2001 |
Rhodeus sericeus |
Positively rheotaxic, remains in the mussel |
Demersal |
Smith et al, 2004 |
Rutilus rutilus |
Fixed to the aquatic plants or stones by their adhesive gland |
Demersal |
Bruslé and Quignard, 2001 |
Rutilus rutilus |
Roach spawned in the middle of May, and on 24 May the yolk sac larvae were observed hanging on plants. Two days later almost all the roach larvae caught had gas in the swim bladder, although the majority still had some yolk left. Most of the orach larvae caught the next day had started feeding. By the last day of May, the mean length of roach larvae was 8.5 mm and the flecxion stage was just beginning with temperature between 12-14°C |
Demersal |
Urho, 1996 |
Scardinius erythrophthalmus |
Stick to aquatic plants with a cement cephalic gland |
Demersal |
Bruslé and Quignard, 2001 |
Scardinius erythrophthalmus |
Remain fixed on plants until full resorption of the yolk sac |
Demersal |
Lafaille et al, 2001 |
Scardinius erythrophthalmus |
The newly larva glues its head to the substrate and remains restive until the yolk sac is completely resorbed |
Demersal |
Korzelecka and Winnicki, 1998 |
Tinca tinca |
Larvae remains fixed on plants by a ceplalic cemant, then becoming free |
Demersal |
Bruslé and Quignard, 2001 |
Tinca tinca |
Larvae remains fixed on plants until full resorption of the yolk sac [4-6 days] |
Demersal |
Feunteun et al, 2001 |
Tinca tinca |
In the first stage - from 12 h to 3 days - larave that attained 4 mm were photophilous, non motile lying at the bottom or hanged on the aquarium wall |
Demersal |
San Juan, 1995 |
Tinca tinca |
By means of their adhesive glands, they "hang" themselves on the walls of the jars as well on submerged objects, remaining 'hung' in a vertical position psssively througout this step |
Demersal |
Penaz et al, 1981 |
Tinca tinca |
Larvae attach themselves with cement glands to submerged plants on which they spend all the yolk-feeding period. However, in larvae hatched prematurely cement glands are under-developed and larvae fail to attach |
Demersal |
Kubu and Kouril, 1985 |
Vimba vimba |
Hathing proceeds initially in hiding between stones. Then, after a few days, the hatched fish either swim actively down the river or are swept down by the current to the reservoir |
Demersal |
Wajdowicz, 1974 |
Esox masquinongy |
Newly hatched young lack the swim-up and vegetation-attachment behavior characteristic of other esocid larvae. Instead they remain quiescent at the bottom, becoming active only after yolk-sac cosumption |
Demersal |
Dombeck et al, 1984 |
Esox masquinongy |
May remain dormant in the vegetation for about 10 days or until the yolk is consumed, at which they become active and begin feeding |
Demersal |
Scott and Crossman, 1973 |
Esox masquinongy |
Prolarvae remain among vegetation for about 10 days |
Demersal |
Goodyear et al, 1982 |
Esox masquinongy |
The fry attach themselves to sunken debris as they absorb their egg sacs |
Demersal |
Pennslylvania fishes, 2006 |
Esox masquinongy |
Five days after the larvae swam up from the bottom |
Demersal |
Anonymous, 1982 |
Esox niger |
The fry have an adhesive gland on the tip of the nose by witch they attch themselves to the substrate of surface scum |
Demersal |
Coffie, 1998 |
Esox niger |
Possess a cephalic cement gland, used for attachment to macrophytes during yolk sac absorption |
Demersal |
Dombeck et al, 1984 |
Esox niger |
They sink to the bottom where they attch themsleves to vegetation by an adhesive gland on the tip og the snout |
Demersal |
Scott and Crossman, 1973 |
Esox niger |
Just-hatched chain pickerel fry attach themselves to plant stems during the absorption of yolk sac |
Demersal |
Pennslylvania fishes, 2006 |
Esox niger |
Hatchlings sink to bottom and attach to vegetation by adhesive spot on snout and remain until able to begin active feeding (app. 1 week) |
Demersal |
Anonymous, 2006 |
Esox niger |
Pickerel fry attach to the vegetationby an adhesive gland located on the snout |
Demersal |
Wynne, 2006 |
Esox lucius |
Prolarvae remain motionless during all the priod of resorption of yolk |
Demersal |
Souchon, 1983 |
Esox lucius |
Remain fixed on aquatic plants until the resorption of the yolk sac |
Demersal |
Bruslé and Quignard, 2001 |
Esox lucius |
Remain fixed for about 10-12 days at 11.5°C |
Demersal |
Dorier, 1938 |
Esox lucius |
Many were attached to any available surface, usually vertical for 4-6 days, then are free |
Demersal |
Frost and Kipling, 1967 |
Esox lucius |
The fry did not swim about freely, but remained hidden, apparently attached to vegetation for the first week after hatching |
Demersal |
Bryan, 1967 |
Esox lucius |
Remain motionless, fixed, during about one week |
Demersal |
Balvay, 1983 |
Esox lucius |
Remain fixed by cemant gland |
Demersal |
Le Louarn and Feunteun, 2001 |
Esox lucius |
Remain fixed vertically for about 130 DD, then swin near the surface |
Demersal |
Chauveheid and Billard, 1983 |
Esox lucius |
They remain inactive, often attached to vegetation by means of adhesive glans on the head, for 6-10 days, and feed on the stored yolk |
Demersal |
Scott and Crossman, 1973 |
Esox lucius |
Attached to vegetation, the sac fry remain inactive for 6-10 days until the yolk is absorbed |
Demersal |
Kerr and Grant, 1999 |
Esox lucius |
Larvae remain atatched to vegetation for 6 to 10 days |
Demersal |
Bradbury et al, 1999 |
Esox lucius |
Just after hatching, the young fry remain on the bottom. Then, about few hours, they stich, using their cemand gland, to various objects in the water: plants, … Remain there, motionless |
Demersal |
Wurtz, 1944 |
Esox lucius |
The fry attached to this substrate using the adhesive organ on the head |
Demersal |
Giles et al, 1986 |
Esox lucius |
Pike perch hatched in the middle of May. After using their yolk whille still hanging on plants, pike larvae with some gas in the swim bladder were caught among the vegetation at the same time as the first roach and perch larvae hatched (24 May) |
Demersal |
Urho, 1996 |
Esox lucius |
Prolarvae remain in attached to vegetation at spawning site for 5-10 days |
Demersal |
Goodyear et al, 1982 |
Esox lucius |
Newly hatched larvae attached to plants remain nonmotile for the first few days of life |
Demersal |
Vehniäinen et al, 2007 |
Esox lucius |
Remain attached to vegetation during the first 4-6 days. Thereafter, the larvae are 11-12 mm long, almost all of the yolk sac has been used, and they start to seek food |
Demersal |
Lappalainen et al, 2008 |
Lota lota |
Pelagic until 6-7 mm then become benthic |
Pelagic |
Bruslé and Quignard, 2001 |
Lota lota |
Small pelagic larvae |
Pelagic |
Van Houdt, 2003 |
Lota lota |
Pelagic, gregarious, steadily remain under the surface of water |
Pelagic |
Persat, 2001 |
Lota lota |
At hatching, the offspring are at first pelagic, threafter they are found in shallow littoral waters |
Pelagic |
Hudd and Kjellman, 2002 |
Lota lota |
Buoyant larvae are carried downstream in water currents |
Demersal |
Mann, 1996 |
Lota lota |
Immediate dispersion after hatching |
Demersal |
Urho, 2002 |
Lota lota |
Upon hatching larvae are pelagic |
Pelagic |
Bradbury et al, 1999 |
Lota lota |
Dispersed earlier at the yolk-stage and ended up in the littoral |
Demersal |
Urho, 1996 |
Lota lota |
Newly hatched larvae repeatedly swim up and sink, later they sink to the bottom where they remain until final resoprtion of yolk sac. When a major part of the yolk sac is resorbed fish start swimming searching for food. They aggregate in the surface layers of shallow waters, where they fed on phytoplankton and rotifers. |
Demersal |
Kujawa et al, 2002 |
Gasterosteus aculeatus |
Newly hatched larvae stay near the bottom |
Demersal |
Internet, 2005 |
Gasterosteus aculeatus |
Newly hatched larvae stay within the nest, around the nest in schools and then leave |
Demersal |
Crivelli, 2001 |
Gasterosteus aculeatus |
Upon hatching, young leave the the spawning area but remain close to shore in shallow water |
Demersal |
Bradbury et al, 1999 |
Gasterosteus aculeatus |
Because of the heavy yolk the larva lies on its side, occasionally swimming swiftly to settle down again at another spot. |
Demersal |
Swarup, 1958 |
Pungitius pungitius |
Newly hatched larvae move to the top of the nest and settle to it |
Demersal |
Fishbase, 2006 |
Pungitius pungitius |
Newly hatched larve move to the top of the nest where they remain relativelt inactive |
Demersal |
Bradbury et al, 1999 |
Ambloplites rupestris |
Nine days before leaving the nest |
Demersal |
Gross and Nowell, 1980 |
Ambloplites rupestris |
Prolarvae remain in nest 2-3 days |
Demersal |
Goodyear et al, 1982 |
Ambloplites rupestris |
Wrigglers, initially translucent and immobilie with large golden yolk sacs, gradually darkened as they grew and absorbed yolk allowing their developing eyes to become conspicuous. Wrriggler movement gradually increased, the young formaing a churning cloud of free-swimming fry above the substrate just before their synchronous liberation from each nest |
Demersal |
Noltie and Keenleyside, 1987 |
Lepomis gibbosus |
Remain at the bottom of the nest for as short period and then inhabit dense vegetation and also venture out into open waters |
Demersal |
Internet, 2005 |
Lepomis gibbosus |
Gregarious |
Demersal |
Bruslé and Quignard, 2001 |
Lepomis gibbosus |
Newly hatched inhabit nearshore open water areas |
Demersal |
Kerr and Grant, 1999 |
Lepomis gibbosus |
From preliminary field observations, I found that larvae were usually scattered throughout the nest despite some clumping |
Demersal |
Shao, 1997 |
Lepomis gibbosus |
Fry leave nest soon after hatching |
Demersal |
Goodyear, 1982 |
Micropterus dolomieui |
Remain in the nest for several days and them swim in dense schools, protected by male for 2-3 weeks |
Demersal |
Internet, 2005 |
Micropterus dolomieui |
Remain in the nest until the resorption of the yolk and then rise off the bottom |
Demersal |
Scott and Crossman, 1973 |
Micropterus dolomieui |
The larvae became free-swimming 6 days after hatching at a length of approximatively 8.7 millimeters |
Demersal |
Meyer, 1970 |
Micropterus dolomieui |
After rising from the nest, the young free-swimming bass remained in a dense mass close to the bottom and directly over the nest. |
Demersal |
Turner and MacCrimmon, 1970 |
Micropterus dolomieui |
Fry gradually disperse from nest when 1-2 weeks old and are then found along edges of vegetation beds |
Demersal |
Goodyear et al, 1982 |
Micropterus salmoides |
Remain in the nest, postlarvae venture to the surface in small schools and eventualy disperse |
Demersal |
Heidinger, 1976 |
Micropterus salmoides |
Remain in the nest during 2-3 month, and than leave the nest but stay together during 2-3 months |
Demersal |
Spillmann, 1961 |
Micropterus salmoides |
Newly hatched larvae remain in the nest, postlarvae venture to the surface in small schools and eventually disperse into shallow weedt waters |
Demersal |
Internet, 2005 |
Micropterus salmoides |
They remain in the bottom of the nest until the yolk is absorbed, usually 6-7 days, then they rise, begin feeding and schooling |
Demersal |
Scott and Crossman, 1973 |
Micropterus salmoides |
Three of four days after hatching, larvae became free-swimming at approximatively 6.1 millimetres |
Demersal |
Meyer, 1970 |
Micropterus salmoides |
Larvae remain in nest for 5-10 days |
Demersal |
Goodyear et al, 1982 |
Dicentrarchus labrax |
Planktonic |
Demersal |
Fishbase, 2006 |
Dicentrarchus labrax |
Larvae are transported into embayments and estuarine nursery habitats |
Demersal |
Secor, ??? |
Dicentrarchus labrax |
Pelagic |
Pelagic |
Barnabé, 1980 |
Dicentrarchus labrax |
Eggs and pre-larvae drift passively towards coastal zones |
Demersal |
Giffard-Mena et al,2006 |
Morone americana |
White perch larvae are one of the major species in ichthyoplankton in upper Chesapeake Bay during spring months [Larvae are trasnported down-stream after hatching] |
Demersal |
Shoji et al, 2005 |
Morone americana |
Newly hatched prolarvae remain in the general spawning area during the first 4 to 13 days [Prolarvae have limited mobility] |
Demersal |
Stanley and Danie, 1983 |
Morone americana |
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 |
Morone americana |
Eggs and larvae were discovered in plankton collections |
Demersal |
Mansuetti, 1961 |
Morone chrysops |
Pelagic |
Pelagic |
Anonymous, 2006 Chapter 3 |
Morone chrysops |
Sac larvae of the white bass exibited a unique swimming behavior. They swam vertically to near the surface, where they became inactive and dropped, head down, to the bottom of chamber. Upon touching, they sawm actively to the surface again |
Demersal |
Siefert et al, 1974 |
Morone chrysops |
Many of its semibuoyant eggs and early-life stage larvae were carried downstream of the actual spawning sites by current |
Demersal |
June, 1977 |
Morone saxatilis |
Planktonic |
Demersal |
Will et al, 2002 |
Morone saxatilis |
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 |
Gymnocephalus cernua |
Embryo remains sedentary on the bottom for 3 to 7 days until reaching a size of 4.5-5.0 |
Demersal |
Ogle, 1998 |
Gymnocephalus cernua |
Remain sedentary for 3-7 days |
Demersal |
Crosier et al, 2005 |
Gymnocephalus cernua |
Most to the time they stay at the bottom |
Demersal |
Kovac, 1998 |
Gymnocephalus cernua |
Immediate dispersion after hatching |
Demersal |
Urho, 2002 |
Gymnocephalus cernua |
The larvae easily stayed in the water column and were fully prepapred for independent living in external environment |
Demersal |
Bonislawska et al, 2004 |
Gymnocephalus cernua |
Larval ruffe hatch and become pelagic within 1 to 2 weeks after egg deposition and could possibly be netrained in ballast water duting the pelagic period |
Pelagic |
Brown et al, 1998 |
Perca flavescens |
Immediatly active swimmer |
Demersal |
Mansueti, 1964 |
Perca flavescens |
Inactive for about 5 days |
Demersal |
Scott and Crossman, 1973 |
Perca flavescens |
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 |
Perca flavescens |
Pelagic [are inactive for about 5 days until the yolk is absorbed] |
Demersal |
Anonymous, 2006 Chapter 3 |
Perca flavescens |
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 |
Perca fluviatilis |
Gregarious |
Demersal |
Bruslé and Quignard, 2001 |
Perca fluviatilis |
Larvae are known to move out into the pelagic area and after some time return to shallow-water areas |
Pelagic |
Urho, 1996 |
Perca fluviatilis |
Pelagic larval stock |
Pelagic |
Treasurer, 1983 |
Perca fluviatilis |
During the next four days, the yolk sac larvae of perch were mainly caught in the pelagic area [Perch start to swim immediatly without filling the swimbladder first] |
Pelagic |
Urho, 1996 |
Sander lucioperca |
Active |
Demersal |
Olivier and Schlumberger, 2001 |
Sander lucioperca |
Larvae leave the nest immediatly after hatching |
Demersal |
Deeler and Willemsen, 1964 |
Sander lucioperca |
Immediate dispersion after hatching |
Demersal |
Urho, 2002 |
Sander lucioperca |
The larvae live during the first two weeks post hatching near the bottom and then change their habitat from the benthic to the pelagic |
Demersal |
Lehtonen et al, 1996 |
Sander lucioperca |
Larvae alternate between pelagic and benthic phases |
Pelagic |
Schlumberger and Proteau, 1993 |
Sander lucioperca |
Show alternate phases of upward swimming to the water surface and passive falling to the tank bottom |
Demersal |
Schlumberger and Proteau, 1996 |
Sander vitreus |
Fry are pelagic |
Pelagic |
Malison and Held, 1996b |
Sander vitreus |
Embryos characteistically suspend themselves at the water surface; vertically, with head up and ventral abdominal surface of the yolk and oil near the surface |
Demersal |
Krise and Meade, 1986 |
Sander vitreus |
The fry are able to swim and feed within one week after hatching |
Demersal |
Kerr and Grant, 1999 |
Sander vitreus |
As the young walleye began to hatch, they usually swam to the surface of the side-arm tube |
Demersal |
Hurley, 1972 |
Sander vitreus |
Walleye larvae typically leave the spawning bed immediatly after hatching |
Demersal |
Johnston, 1997 |
Sander vitreus |
The prolarvae are weak swimmers, so water currents in culture banks should be low, because larvae are quickly exhausted |
Demersal |
Summerfelt, 1996 |
Coregonus albula |
Immediatly after hatching vendace larvae accumulate in patches near the water surface, but true schools are not formed until somme weeks later |
Demersal |
Karjalainen, 1991 |
Coregonus clupeaformis |
Tend to remain in the spawning gravel |
Demersal |
Kerr and Grant, 1999 |
Coregonus clupeaformis |
Rise to surface soon after hatching |
Demersal |
Goodyear et al, 1982 |
Coregonus clupeaformis |
Young typically hatch from mid-May to mid-June and remain within the general vicinity of the spawning area |
Demersal |
Bradbury et al, 1999 |
Coregonus clupeaformis |
After the third week, the larvae swam incessantly in tight formation in a circular motion from feeding station to feeding station. There, they congregated and swarmed around the point of entry of nauplii. Displaced larvae swam rapidly to the opposing feeding station where they strived aggressively to regain and advantageous feeding position. Between feedings the larvae continued swimming in tight schools near the surface. |
Demersal |
Drouin et al, 1986 |
Coregonus clupeaformis |
Throughout the trial, larvae in all tanks formed a school only when startled but then soon disassociated |
Demersal |
Zitzow and Millard, 1988 |
Hucho hucho |
Fry remain on the spawning ground until they reach 40 mm |
Demersal |
Jatteau, 1991 |
Hucho hucho |
Once the vesicle is reabsorbed, young stays near spawning area feeding on bottom fauna |
Demersal |
Fishbase, 2006 |
Hucho hucho |
The larvae keep close to the ground, near the spawning place |
Demersal |
Prawochensky and Kolder, 1968 |
Hucho hucho |
After hatching they mostly remain motionless at the bottom of the trough, lying sideways on the yolk sac |
Demersal |
Penaz and Prihoda, 1981 |
Oncorhynchus gorbuscha |
The fry emerge from the gravel at night, mainly in April and May, and immediatly migrate to sea |
Demersal |
Groot, 1996 |
Oncorhynchus gorbuscha |
The alevins remain in the gravel until the yolk is absorbed in April or early May (rarely late February) when they struggle up out of the nest and become free swimming)] |
Demersal |
Scott and Crossman, 1973 |
Oncorhynchus gorbuscha |
Remain in the gravel until yolk is absorbed, emerge in April-May, mainly mid-April |
Demersal |
Goodyear et al, 1982 |
Oncorhynchus gorbuscha |
Swim-up from fertilization: 805 degree-days [From hatching 805 less 500] |
Pelagic |
Bascinar and Okumus, 2004 |
Oncorhynchus gorbuscha |
Upon hatching the alevins migrated through the spawces in the base of each basket into the gravel where they remained until 80-90% of their yolk had been absorbed |
Demersal |
Macquarrie et al, 1979 |
Oncorhynchus keta |
Remain in the gravel until conditions. During the waiting period they live on the yolk |
Demersal |
Scott and Crossman, 1973 |
Oncorhynchus keta |
After hatching, the prolarvae stay in the ground for 1-1.5 month |
Demersal |
Volobuev and Volobuev, 2000 |
Oncorhynchus keta |
Swim-up from fertilization: 960 degree-days [From hatching 960 less 560] |
Pelagic |
Bascinar and Okumus, 2004 |
Oncorhynchus keta |
Alevins remain in the gravel until their yolk sacs are completety or almost completely absorbed. |
Demersal |
Bakkala, 1970 |
Oncorhynchus kisutch |
After hatching, tha alevins move down into the gravel and then hold for several weeks [emergence primarily occur at night] |
Demersal |
Groot, 1996 |
Oncorhynchus kisutch |
The alevin remain 2-3 weeks in the gravel, at least until yolk is absorbed |
Demersal |
Scott and Crossman, 1973 |
Oncorhynchus kisutch |
The young fish, called alevins, remain under the gravel until they are anywhere from two weeks to four months old |
Demersal |
Kerr and Grant, 1999 |
Oncorhynchus kisutch |
Remain in the gravel until yolk is absorbed |
Demersal |
Goodyear et al, 1982 |
Oncorhynchus kisutch |
Swim-up from fertilization: 970 degree-days [From hatching 970 less 420] |
Pelagic |
Bascinar and Okumus, 2004 |
Oncorhynchus mykiss |
Fry remain in the gravel for about 2 to 3 weeks after hatching before emerging from the gravel at night |
Demersal |
Groot, 1996 |
Oncorhynchus mykiss |
Immediate move downward into the gravel [prior to dispersal the alevins exhibt both horizaontal and vertical movements within the gravel] |
Demersal |
Kerr and Grant, 1999 |
Oncorhynchus mykiss |
Swim-up from fertilization: 500 degree-days [From hatching 500 less 310] |
Pelagic |
Bascinar and Okumus, 2004 |
Oncorhynchus nerka |
Alevins stay in the gravel for varying amounts of time after hatching and then ermge as fry from the gravel at night. Fry migration generally peas before midnight with sometimes a small peak before dawn |
Demersal |
Groot, 1996 |
Oncorhynchus nerka |
Remain in the gravel until some weeks or months after the yolk is absorbed, and emerge in April to June |
Demersal |
Scott and Crossman, 1973 |
Oncorhynchus nerka |
Remain in the gravel |
Demersal |
Hendry et al, 1998 |
Oncorhynchus nerka |
Emerge from redd in early January-May |
Demersal |
Goodyear et al, 1982 |
Oncorhynchus nerka |
Swim-up from fertilization: 1000 degree-days [From hatching 1000 less 670] |
Pelagic |
Bascinar and Okumus, 2004 |
Oncorhynchus tshawytscha |
Newly hatch larvae stay in the gravel 2-3 weeks until the yolk is absorbed, then become free swimming, and remain in the sapwning area or more dowstream |
Demersal |
Internet, 2005 |
Oncorhynchus tshawytscha |
Inittially fry hide in the gravel and undr banks during daylight hours, then appear along open shorelines and finally move into higher velocity waters along the shore or farther in the sream |
Demersal |
Groot, 1996 |
Oncorhynchus tshawytscha |
The alevins spend 2-3 weeks in the nest while the yolk is absorbed |
Demersal |
Scott and Crossman, 1973 |
Oncorhynchus tshawytscha |
Following hatching the young fry, called alevin, remain in thegravel for several weeks |
Demersal |
Kerr and Grant, 1999 |
Oncorhynchus tshawytscha |
Emerge from gravel a few weeks after hatching |
Demersal |
Goodyear et al, 1982 |
Oncorhynchus tshawytscha |
Swim-up from fertilization: 890 degree-days [From hatching 890 less 420] |
Pelagic |
Bascinar and Okumus, 2004 |
Salmo salar |
Benthic, the alevins hatch in March and April and the fry emergence from the gravel in May or June |
Demersal |
Groot, 1996 |
Salmo salar |
Remain in the gravel until the resoprtion of the yolk-sac |
Demersal |
Bruslé and Quignard, 2001 |
Salmo salar |
Remain in the gravel until the resoprtion of the yolk-sac |
Demersal |
Porcher and Baglinière, 2001 |
Salmo salar |
The young remain buried in the gravel, absorbing the yolk sac and finally emerging from the gravel in May or June |
Demersal |
Scott and Crossman, 1973 |
Salmo salar |
The newly hatched fish, remain buried in the gravel until the yolk sac is fully absorbed |
Demersal |
Kerr and Grant, 1999 |
Salmo salar |
Swim-up from fertilization: 800 degree-days, also from 387-765 [From hatching 800 less 430] |
Pelagic |
Bascinar and Okumus, 2004 |
Salmo salar |
Alevins remain in the gravel for a few weeks until their yolk sac is absorbed |
Demersal |
Bradbury et al, 1999 |
Salmo salar |
Remain in the gravel for about 1.5 month |
Demersal |
Bensettiti and Gaudillat, 2002 |
Salmo salar |
Following hatch,alevins remain buried in the river gravel and growth is at the expense of endogenous yolk |
Demersal |
Johnston and McLay, 1997 |
Salmo salar |
Remain in gravel fro 4-6 weeks; emerge in May and June |
Demersal |
Goodyear et al, 1982 |
Salmo trutta fario |
The alevins stay in the gravel until the yolk sac has almost been absorbed |
Demersal |
Groot, 1996 |
Salmo trutta fario |
Remains in the substrate until the yolk sac completion |
Demersal |
Ombredane et al, 2001 |
Salmo trutta fario |
delayed, gradual dispersion after a passive phase |
Demersal |
Urho, 2002 |
Salmo trutta fario |
Pre-emergent fry remain in the gravel until the yolk sac is absorbed |
Demersal |
Kerr and Grant, 1999 |
Salmo trutta fario |
From hatch until two-thirds of the yolk sac was resorbed; this time intervalwas deliberately selected because from hatch until two-thirds of the yolk sac has been resorbed, the trout larvae, or -strickly speaking-, eleutherembryo, excessevely weighted by the yolk sac, stays immobile and close to the bottom and performs only slight movement in the water column |
Demersal |
Formicki et al, 2004 |
Salvelinus alpinus |
Rest near the bottom |
Demersal |
Guillard et al, 1992 |
Salvelinus alpinus |
The newly hatched embryos remain in the gravel of the redd, emerging as young fry (alevins) in about to three months |
Demersal |
Kerr and Grant, 1999 |
Salvelinus alpinus |
Upon hatching remain in the gravel until the yolk is absorbed |
Demersal |
Bradbury et al, 1999 |
Salvelinus fontinalis |
Alevins emerge from the redd after absorbing most of their yolk sac and then rest on the substrate outside the redd reabsorbing of the yolk sac before dispersing in the stream or the lake |
Demersal |
Mirza et al, 2001 |
Salvelinus fontinalis |
When hatched, the larvae or sac fry remain in the gravel within the redd until the yolk is absorbed |
Demersal |
Scott and Crossman, 1973 |
Salvelinus fontinalis |
Remain in the substrate after hatching before emerging |
Demersal |
Snucins et al, 1992 |
Salvelinus fontinalis |
After hatcing, alevins remain in the gravel, deriving nourishment from their yolk sacas until March, when they emerge as new fry |
Demersal |
Fraser, 1985 |
Salvelinus fontinalis |
Alevins remain in the nest until the yolk sac is absorbed |
Demersal |
Bradbury et al, 1999 |
Salvelinus fontinalis |
Newly hatched sac fry remain in the gravel within the redd for between 30 and 80 days until the yolk is absorbed |
Demersal |
Kerr and Grant, 1999 |
Salvelinus fontinalis |
Swim-up from fertilization: 675 degree-days, also from 387-618 [From hatching 675 less 415] |
Pelagic |
Bascinar and Okumus, 2004 |
Salvelinus fontinalis |
Emerge from gravel in January-March |
Demersal |
Goodyear et al, 1982 |
Salvelinus namaycush |
Fry remain on the spawing shoals about a month or so after hatching while the yolk sac is being absorbed |
Demersal |
Kerr and Grant, 1999 |
Salvelinus namaycush |
Upon hatching alevins remain near the bottom in spawning areas for several weeks to three months before moving to deeper water |
Demersal |
Bradbury et al, 1999 |
Salvelinus namaycush |
Remain in crevices in susbrate for about 1 month |
Demersal |
Goodyear et al, 1982 |
Thymallus thymallus |
Stay in the gravel the first week, then become pelagic |
Demersal |
Bruslé and Quignard, 2001 |
Thymallus thymallus |
Prolarvae concentrated in groups at the bottom in the corners on the trough, rarely mouving around |
Demersal |
Zaytsev, 1986 |
Thymallus thymallus |
Stay in the gravel the first week, until the full absorption of yolk sac |
Demersal |
Persat, 2001 |
Thymallus thymallus |
At 12-18°C, larvae spend 5-10 days in the gravel |
Demersal |
Northcote, 1995 |
Thymallus thymallus |
The yolk_sac larvae remain buried until the yolk is exhausted |
Demersal |
Haugen and Vollestad, 2000 |
Thymallus thymallus |
After emergence from the gravel |
Demersal |
Sempeski and Gaudin, 1995b |
Thymallus thymallus |
The larvae spend a further 4-5 days in the gravel susbtrate before emerging and beginning to feed near the water surface |
Demersal |
Scott, 1985 |
Thymallus thymallus |
The hatched embryos are little mobile and mostly lie on one side of the body. From time to time, the embryo swims up to the water column or even to the water surface, then slowly sinks back to the bottom |
Demersal |
Penaz, 1975 |
Thymallus thymallus |
Hatching occurs within the gravel, and yolk sac larvae remain within the gravel until the yolk is resorbed. The larvae then emerge from the gravel, fill their swim bladders with air and, for a period, stay in mid-water shoals. After a few days, the take the position closer to the bottom, and the shoals reduce to small groups or single individuals |
Demersal |
Gregersen et al, 2008 |
Thymallus arcticus |
First 3-4 day period of sub-gravel residence for hatched larvae |
Demersal |
Northcote, 1995 |
Thymallus arcticus |
Remain in the gravel during 3-4 days |
Demersal |
Northcote, 1993 |
Thymallus arcticus |
A post-hatching sub-gravel stage of 3 to 4 days'duration appears to be a normal feature of the life cycle of Arctic grayling in the Fond Lac River |
Demersal |
Kratt and Smith, 1977 |
Cottus gobio |
When scuba diving I have observed that the larvae remain under a stone in the care of their parent at least until their fins have differentiated |
Demersal |
Urho, 2002 |
Cottus gobio |
On hatching, larvae become planktonic in the stream eastuary or in lakes and do not take up a bottom-dwelling or benthic life until about 32-35 days after hatching |
Demersal |
Wanzenböck et al, 2000 |
Cottus gobio |
The young absorb their yolk sac after which, as fry (9 mm in length) they are ready to disperse |
Demersal |
Tomlinson and Perrow, 2003 |
Ameiurus nebulosus |
Remain in the nest for about one week, stay as a tight mass at the bottom [Possess a very large yolk sac] |
Demersal |
Internet, 2005 |
Ameiurus nebulosus |
The yolk sac is too large to enable them to swim and they lie on their sides in the the nest until about the seventh day |
Demersal |
Scott and Crossman, 1973 |
Ameiurus nebulosus |
Young stay in the nest for about 7 days |
Demersal |
Kerr and Grant, 1999 |
Ameiurus nebulosus |
Larvae remain in the nest up to 12 days |
Demersal |
Goodyear et al. et al, 1982 |
Ictalurus punctatus |
Stay at or near the nest for several days then disperse into shallow water |
Demersal |
Internet, 2005 |
Ictalurus punctatus |
All prelarvae are in contact with one another |
Demersal |
Makeeva and Emel'yanova, 1993 |
Ictalurus punctatus |
Newly hatched fish have large yolks and remain on the bottom for 2-5 days and then swim to the surface adn begin to feed |
Demersal |
Scott and Crossman, 1973 |
Ictalurus punctatus |
Newly hatched larvae fish remain on bottom for 2-5 days then swim to surface and begin to feed |
Demersal |
Kerr and Grant, 1999 |
Ictalurus punctatus |
Remain in the nest up to 8 days |
Demersal |
Goodyear et al. et al, 1982 |
Ictalurus punctatus |
Remain near the nest for a few days than disperse to shallow water |
Demersal |
Anonymous, 2006 Chapter 3 |
Silurus glanis |
To start with the yellow and helpless larvae lay at the bottom of the boxes. On the 2nd and 3rd day, as they became greyish, they gathered in the darker corner |
Demersal |
Horvath, 1977 |
Silurus glanis |
Remains fixed to roots of the nest by a ceplalic cement glands |
Demersal |
Bruslé and Quignard, 2001 |
Silurus glanis |
Remain motionless on the bottom, 5-6 days after they swim well |
Demersal |
Linhart et al, 2002 |
Osmerus eperlanus |
After hatching, the larvae drift dowstream, where they are concentrated near the surface |
Demersal |
Buckley, 1989 |
Osmerus eperlanus |
Pelagic |
Pelagic |
Urho, 2002 |
Osmerus eperlanus |
After hatching, the larvae passively drift downstream into the estuary, where they begin to feed on zooplankton |
Demersal |
Quigley et al, 2004 |
Sander canadensis |
benthic |
Demersal |
Scott and Crossman, 1998 |
Sander canadensis |
Pelagic |
Pelagic |
Walburg, 1972 |
Thymallus arcticus |
(benthic); found over silt or sand substrates within 10-20 mm of bottom |
Demersal |
Stewart et al, 2007b |
Ptychocheilus lucius |
benthic |
Demersal |
Schaugaard, 1997 |
Acipenser brevirostrum |
benthic |
Demersal |
Jones et al, 1978 |
Acipenser brevirostrum |
benthic |
Demersal |
Meehan, 1910 |
Acipenser brevirostrum |
benthic |
Demersal |
Dadswell et al, 1984 |
Dorosoma petenense |
benthic |
Demersal |
Shelton and Stephens, 1980 |
Hiodon tergisus |
Pelagic |
Pelagic |
D'Amours et al, 2001 |
Cottus aleuticus |
Pelagic |
Pelagic |
Asper, 1976 |
Etheostoma flabellare |
benthic? |
Demersal |
Paine and Belon, 1986 |
Etheostoma caeruleum |
benthic |
Demersal |
Paine and Belon, 1984 |
Scaphirhynchus platorynchus |
diurnal migration 0-4 days; switch to nocturnal later in development |
Demersal |
Kynard and Horgran, 2002 |
Scaphirhynchus platorynchus |
transition from drifting to benthic life stage initiated at 6 days post hatch and at a mean length of 15.6mm |
Demersal |
Braaten, 2008 |
Scaphirhynchus albus |
pallid sturgeon remained diurnal in their migration patterns |
Demersal |
Kynard and Horgran, 2002 |
Scaphirhynchus albus |
transition from drifting to benthic life stage initiated at 11-17 days post hatch and at a mean length of 18.1-20.3mm |
Demersal |
Braaten, 2008 |
Scaphirhynchus albus |
Pelagic behavior observed in days 0-8 post hatch, and benthic behavior observed in 8+ days post hatch |
Pelagic |
Kynard and Horgran, 2002 |
Polyodon spathula |
Pelagic |
Pelagic |
Jennings and Zigler, 2009 |
Perca flavescens |
Pelagic |
Pelagic |
Dettmers et al, 2005 |
Perca flavescens |
Pelagic |
Pelagic |
Post, 1990 |
Atractosteus spatula |
Pelagic |
Pelagic |
Butler et al, 2018 |
Atractosteus spatula |
Pelagic |
Pelagic |
Mendoza et al, 2002 |
Percina caprodes |
benthlic |
Demersal |
Turner, 2001 |
Percina caprodes |
benthic |
Demersal |
French and Jude, 2001 |
Percina caprodes |
benthoPelagic |
Pelagic |
Faith and Reid, 2004 |
Lota lota |
Pelagic for 3 months after hatching then switch to benthic |
Pelagic |
Donner et al, 2011 |
Lepisosteus osseus |
benthic |
Demersal |
Jones et al, 1978 |
Lepisosteus osseus |
benthic |
Demersal |
Echelle and Riggs, 1972 |
Lepisosteus osseus |
benthic |
Demersal |
Goff, 1984 |
Esox masquinongy |
benthic |
Demersal |
Cooper, 2008 |
Catostomus commersonii |
Pelagic |
Pelagic |
McElman and Balon, 1980 |
Catostomus commersonii |
benthic |
Demersal |
Johnson and Dropkin, 1995 |
Lepomis megalotis |
benthic, smaller larvae may swim upward at night |
Demersal |
Taber, 1969 |
Aplodinotus grunniens |
Pelagic |
Pelagic |
Davis, 1959 |
Acipenser oxyrinchus |
free embryos do not disperse; larvae disperse downstream near the bottom (benthic) for 6-12 days |
Demersal |
Hilton et al, 2016 |
Acipenser oxyrinchus |
embryos stayed at bottom; however, day 13-14 fish swam to the water column |
Demersal |
Kynard and Horgan, 2002 |
Acipenser oxyrinchus |
early migrants were nocturnal while late migrants were diurnal |
Demersal |
Kynard and Horgan, 2002 |
Etheostoma exile |
Phototactic |
Demersal |
Simon and Faber, 1987 |
Hiodon alosoides |
Pelagic |
Pelagic |
Wallus, 1989 |
Etheostoma nigrum |
benthic |
Demersal |
Scott and Crossman, 1998 |
Semotilus atromaculatus |
Pelagic |
Pelagic |
Magnan and FitzGerald, 1984 |
Acipenser medirostris |
once exogenous feeding begins they begin a 12 day nocturnal downstream migration |
Demersal |
Moser et al, 2016 |
Acipenser medirostris |
nocturnal behavior |
Demersal |
Van Eenennaam, 2001 |
Acipenser medirostris |
free embryos and larvae exhibit benthic preference |
Demersal |
Moser et al, 2016 |
Acipenser medirostris |
larvae are benthic |
Demersal |
Kynard, 2005 |
Lepomis macrochirus |
benthic |
Demersal |
Coleman and Fischer, 2010 |
Neogobius melanostomus |
Pelagic |
Pelagic |
Kornis et al, 2012 |
Leuciscus idus |
benthic |
Demersal |
Witaska et al, 2014 |
Leuciscus idus |
Pelagic |
Pelagic |
Witaska et al, 2014 |
Leuciscus idus |
Pelagic |
Pelagic |
Kupren et al, 2015 |
Dorosoma cepedianum |
Pelagic |
Pelagic |
Downey and Toetz, 1983 |
Fundulus heteroclitus |
benthoPelagic |
Pelagic |
Baensch and Riehl, 1995 |
Ameiurus nebulosus |
benthic |
Demersal |
Rafferty et al, 2009 |
Noturus flavus |
benthic |
Demersal |
Pollard, 2004 |
Notropis atherinoides |
Pelagic |
Pelagic |
Scott and Crossman, 1998 |
Notropis atherinoides |
benthoPelagic |
Pelagic |
Schaap, 1989 |
Cycleptus elongatus |
Pelagic |
Pelagic |
Adams et al, 2006 |
Cycleptus elongatus |
Pelagic |
Pelagic |
Semmens, 1985 |
Chasmistes cujus |
benthic |
Demersal |
Snyder, 1983 |
Chasmistes cujus |
Pelagic |
Pelagic |
Scoppettone et al, 1986 |
Ammocrypta pellucida |
benthic |
Demersal |
COSEWIC, 2009 |
Noturus eleutherus |
benthic |
Demersal |
Starnes and Starnes, 1985 |
Culaea inconstans |
benthic |
Demersal |
Tompkins, 1983 |
Prosopium coulterii |
typically benthic |
Demersal |
COSEWIC, 2016 |
Cyprinella analostana |
benthic |
Demersal |
Gale and Buynak, 1978 |
Carassius auratus |
benthic |
Demersal |
Becker, 1983 |
Labidesthes sicculus |
Pelagic |
Pelagic |
Baensch and Riehl, 1997 |
Labidesthes sicculus |
Pelagic |
Pelagic |
Hubbs, 1921 |
Labidesthes sicculus |
Pelagic |
Pelagic |
Cahn, 1927 |
Cottus asper |
Pelagic |
Pelagic |
Ladell et al, 2007 |
Cottus cognatus |
benthic |
Demersal |
Ladell et al, 2007 |
Acipenser fulvescens |
Pelagic |
Pelagic |
D'Armours et al, 2001 |
Crystallaria cincotta |
benthic |
Demersal |
Ruble, 2014 |
Percina copelandi |
Pelagic |
Pelagic |
Douglas, 2013 |
Percina aurantiaca |
pelagic |
Pelagic |
Douglas, 2013 |
Percina tanasi |
Pelagic |
Pelagic |
Douglas, 2013 |
Percina aurolineata |
Pelagic |
Pelagic |
Douglas, 2013 |
Percina sciera |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma etowahae |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma maculatum |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma Moorei |
Pelagic |
Pelagic |
Douglas, 2013 |
Nothonotus sanguifluus |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma vulneratatum |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma wapiti |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma susanae |
benthic |
Demersal |
Douglas, 2013 |
Etheostoma Marmorpinnum |
benthic |
Demersal |
Douglas, 2013 |
Etheostoma percnurum |
benthic |
Demersal |
Douglas, 2013 |
Etheostoma sitikuense |
benthic |
Demersal |
Douglas, 2013 |
Etheostoma stigmaeum |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma parvipinne |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma spilotum |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma boschungi |
benthic |
Demersal |
Douglas, 2013 |
Etheostoma variatum |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma cyanoprosopum |
Pelagic |
Pelagic |
Douglas, 2013 |
Etheostoma caeruleum |
Pelagic |
Pelagic |
Douglas, 2013 |
Cyprinella monacha |
benthic |
Demersal |
Rakes, 1999 |
Coregonus kiyi |
Pelagic |
Pelagic |
Lepak, 2017 |
Coregonus nasus |
Pelagic |
Pelagic |
Scott and Crossman, 1998 |
Hypomesus transpacificus |
Pelagic |
Pelagic |
Lindberg, 2019 |
Hypomesus transpacificus |
Pelagic |
Pelagic |
Kurobe, 2016 |
Spirinchus thaleichthys |
Pelagic |
Pelagic |
Emmett, 1991 |
Spirinchus thaleichthys |
Pelagic |
Pelagic |
Rosenfield, 2007 |
Thaleichthys pacificus |
Pelagic |
Pelagic |
Hay, 2000 |
Thaleichthys pacificus |
Pelagic |
Pelagic |
Emmett, 1991 |
Fundulus diaphanus |
benthoPelagic |
Pelagic |
Page and Burr, 1991 |
Etheostoma raneyi |
Pelagic |
Pelagic |
Ruble et al, 2019 |
Entosphenus tridentatus |
benthic |
Demersal |
Wade and Beamish, 2012 |
Micropterus cataractae |
benthic |
Demersal |
Johnston and Kennon, 2007 |
Erimyzon sucetta |
benthic |
Demersal |
Balon, 1981 |
Ichthyomyzon fossor |
benthic |
Demersal |
Reighard and Cummins, 1916 |
Moxostoma pappillosum |
Pelagic |
Pelagic |
Weyers et al, 2003 |
Moxostoma robustum |
Pelagic |
Pelagic |
Weyers et al, 2003 |
Moxostoma macrolepidotum |
benethic |
Demersal |
Buynak and Mohr, 1979 |
Noturus insignis |
benthic |
Demersal |
Stoekel and Neves, 2000 |
Leuciscus idus |
pelagic |
Pelagic |
Kupren et al, 2015 |
Neogobius melanostomus |
Benthic |
Demersal |
Grabowska et al, 2008 |
Neogobius melanostomus |
Benthic |
Demersal |
Miller, 1984 |
Acipenser ruthenus |
Benthic "sterlet's prolarvaes passes to a bottom mode of life" |
Demersal |
Kalmykov et al, 2010 |
Atractosteus spatula |
pelagic |
Pelagic |
Snow, 2014 |
Ponticola kessleri |
Benthic |
Demersal |
Hirsch et al, 2016 |
Ponticola kessleri |
Benthic |
Demersal |
Hohenadler, 2012 |
Ponticola kessleri |
Benthic |
Demersal |
Kessel et al, 2016 |
Ponticola kessleri |
Benthic |
Demersal |
Borcherding et al, 2013 |
Ponticola kessleri |
Benthic |
Demersal |
Adrian-Kalchhauser et al, 2016 |
Acipenser transmontanus |
pelagic |
Pelagic |
Buddington and Doroshov (, 1986) |
Aplodinotus grunniens |
Pelagic |
Pelagic |
Holland, 1986 |
Proterorhinus semilunaris |
Benthic |
Demersal |
Valová et al., 2015 |
Leuciscus aspius |
Benthic |
Demersal |
https://www.fishbase.se/Reproduction/LarvaeInfoSummary.php?stockcode=5007 and genusname=Leuciscus and speciesname=aspius and LarvalArea=hide%, 20under%, 20stones%, 20in%, 20the%, 20spawning%, 20grounds |
Pseudorasbora parva |
benthic for the first 3 days, pelagic thereafter |
Pelagic |
Pinder, 2005 |
Pomoxis annularis |
Zooplanktivorous juveniles of the white crappie, Pomoxis annularis, are saltatory searchers; they search briefly while stationary and, if they do not locate a prey, swim a short distance before stopping to scan again. In this paper, we report on the development of foraging behavior in white crappie larvae, compare it to the search strategy of juveniles. |
Pelagic |
Browman and O'Brien, 1992 |
Pomoxis annularis |
Estimates of visual acuity in a pelagic freshwater zooplanktivorous fish, the white crappie (Pomoxis annularis, Centrarchidae). |
Pelagic |
Browman et al, 1990 |
Acipenser baeri |
Benthic |
Demersal |
Gisbert and Williot, 1997 |