| TAXONOMY | BIOGEOGRAPHY | AGE & GROWTH | REPRODUCTION | MORTALITY | DEMOGRAPHY | HABITAT ASSOCIATION & TROPHIC INTERACTIONS | GENETICS | BEHAVIOR | PATHOLOGY | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CLASS | Life Stage | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chondrichthyes | Seasonal Cycle | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SUBCLASS | Growth Parameters | Fertilization and Pupping Period (^^^^^ = peak fertilization; ***** = peak pupping; ##### = doubtful pupping records) | Juveniles | Adolescents | Adults | Genetic Variance | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Holocephali | Total Length (cm) to Weight (kg) Equation (Location) | Length Conversion Equations (Location) | Max. Reported Length (cm) | Geographic Area (max. length) | Length at Birth (cm) | Geographic Area (length at birth) | Linf in cm | k | t0 | r2 | Growth Model | Ageing Method(s) | Validation | Verification | Geographic Area (Age & Growth Study) | Source (Age & Growth Study) | Longevity | Method of Longevity Estimation | Breeding Behavior Mode of Reproduction | Sexual Dimorphism | Length (cm) & Age at 1st Maturity | 50% Maturity | Geographic Area | Courtship | Fertilization | Egg Deposition | Partuition | Mortality Estimates | Food Habits | Food Habits | Food Habits | Substocks | Haplotype Diversity (Geographic Area) | Nucleotide Diversity (#) | Mean Number of Alleles per Locus (SE) | % Polymorphic Loci | Mean Heterozygosity | Approach | Effective Population Size | Source (Genetic Variance) | Behavioral Interactions | Migration & Movement | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Superorder | Order | Family | Genus | Species | Author | Synonymy | Common Name(s) | Eastern North Pacific | Global | Observed Depth Range (m) | Male | Female | Both | Male | Female | Both | Male | Female | Both | Male | Female | Both | Male | Female | Male | Female | Courtship | Nursery | Jan. | Feb. | March | April | May | June | July | Aug. | Sept. | Oct. | Nov. | Dec. | Source (Location) (Seasonal Cycle) | Reproductive Cycle | Fecundity Range and/or Mean Ovarian Eggs | Uterine Eggs | Embryos | Sex Ratio at Birth (M:F) | Uterine Egg or embryo Number at Female TL (cm) or Age | Size Specific Fecundity Equations (length or weight range) | Gestation Time | Natural (M) | Fishing (F) | Total (Z) | Method of Mortality Estimation | Age Range used to Calculate Mortality | Source (Mortality Estimates) | r | er (lambda) | R0 | G(T) | cx/wx | Method | Geographic Region | Source (Demography Study) | Habitat | Diet | Foraging Strategy | Periodicity | Predators | Habitat | Diet | Foraging Strategy | Periodicity | Predators | Habitat | Diet | Foraging Strategy | Periodicity | Predators | Trophic Level | Expected (SE) | Observed (SE) | Interspecific | Intraspecific | Tagging/Tracking Studies | Movement Patterns | Homing Ability (Home Range) | Parasites | Diseases | ||||||||||||||||||||||||
| Squalimorphii | Rajiformes | Rajidae |
Amblyraja |
badia |
(Garman, 1899) |
Raja badia (Zorzi
and Anderson, 1988) |
broad skate |
Navarin Canyon, Bering Sea to Panama (Ebert,
2003) |
Japanese archipelago: Tohoku slope and Okhotsk slope (Nakaya
and Shirai, 1992) |
846 to 2324 m (Ebert,
2003) |
NF | NF | males: 95 cm TL (Ebert,
2003) females: 99 cm TL (Ebert, 2003) |
NG NG |
23 cm TL (Ebert,
2003) |
NG | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | oviparity |
NF | 86 to 93 cm TL (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | cephalopods, crustaceans, teleosts (Macrouridae) (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii | Rajiformes | Rajidae | Raja |
binoculata |
(Girard, 1855) |
Raja cooperi (Girard,
1858) |
big skate big skate of California (Gates and Frey, 1974) |
eastern Bering sea and southeast Alaska to southern Baja California, Mexico; uncommon south of Point Conception, California (Eschmeyer et al., 1983; Castro-Aguirre et al., 1993; Mecklenburg et al., 2002) | NA | 3 to 800 m (Eschmeyer
et al., 1983) |
both: Log WT= log a + b log TL; Y = -35 + 44.2 x log (x) (Monterey Bay,
California) (Zeiner
and Wolf, 1993) |
both: DW = 15.5 + 0.72 TL (Monterey Bay, California) (Zeiner, 1991) | 240 cm TL (Miller
and Lea, 1972) |
NG | 18 to 23 cm TL (Ebert,
2003) |
NG | 138.8 (S.E. 7.7) |
167.8 (S.E. 13.7) |
151.0 (S.E. 7.6) |
0.43 (S.E. 0.05) |
0.37 (S.E. 0.05) |
0.38 (S.E. 0.04) |
13.3 (S.E. 2.8) |
15.0 (S.E. 3.1) |
15.0 (S.E. 2.2) |
NG | NG | NG | Logistic | vertebral centra: paraffin wax embedding, thin-sectioning |
centrum edge analysis |
NG |
central California |
Zeiner and Wolf,
1993 |
NF |
NF | oviparity |
females larger than males (Zeiner
and Wolf, 1993) |
100 to 110 cm TL; 7 to 8 yrs. (Zeiner,
1991) |
>130 cm TL; 10 to 12 yrs. (Zeiner and Wolf, 1993) |
NF | NF | NF | egg beds observed at 64 m depth off Tillamook Head, OR and between the Siulslaw and Siltcoos Rivers, OR (DeLacy and Chapman, 1935; Hitz, 1964) | Ebert, 2003 (California) |
NF | NF | NF | 1 to 5 per egg case, average 3.25 (Hitz,
1964) 2 to 7, 3 to 4 average per egg case (DeLacy and Chapman, 1935) 1 to 8 per egg case (Ford, 1971) |
1:1 (Hitz, 1964) |
NF | NF | ca. 1 year (DeLacy and
Chapman, 1935; Hitz,
1964) in excess of 12 months (Ford, 1971) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | polychaetes, molluscs, crustaceans, small benthic teleosts (Ebert, 2003) | NF | NF | cephalopods (Octopus dofleini) and pinnipieds (Mirounga angustirostris) prey on egg cases (Anderson, 1996; Love, 1996) | NF | NF | NF | NF | NF | soft substrate (Eschmeyer
et al., 1983) |
crustaceans, benthic teleosts, polychaetes, molluscs
(Hart, 1973; Ebert,
2003) |
NF | NF | elasmobranchs (Notorynchus cepedianus) (Ebert,
1989) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Cestoda (2 families, 6 spp.), Copepoda (4 families, 8 spp.), Digenea (1 family, 1 sp.), Hirudinoidea (1 family, 2 spp.), Monogenea (3 families, 5 spp.), Protozoa (1 family, 1 sp.) (Fraser, 1919; Lloyd, 1938; Kabata, 1974; Love and Moser, 1983) | NF | ||||||||||||
| Squalimorphii | Rajiformes | Rajidae |
Raja |
equatorialis |
Jordan and Bollman, 1890
|
NA |
equatorial ray |
Gulf of California and from Panama south (McEachran and Notarbartolo-di-Sciara, 1995) |
NA | to 100 m (Castro-Aguirre
and Perez, 1996) |
NF | NF | 50 cm TL (McEachran and Notarbartolo-di-Sciara, 1995) |
NG | NF | NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NA | oviparity |
NF | NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
NF | NF | NF | NF | NF | NF | NF | NA | NA | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | benthic from coast to intermediate depths on continental shelf (McEachran and Notarbartolo-di-Sciara, 1995) coastal nearshore (Castro-Aguirre and Perez, 1996) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii | Rajiformes | Rajidae |
Raja |
inornata |
Jordan & Gilbert,
1881 |
Raia inornata inermis (Jordan
& Gilbert, 1881) Raja jordani (Garman, 1885) |
California skate |
Straight of Juan de Fuca to Turtle Bay, Baja California, Mexico, also found in the Gulf of California (Miller and Lea, 1972; McEachran and Notobartolo di Sciara, 1995) | NA | 18 to 671 m (Miller
and Lea, 1972) |
NF | NF | 76 cm TL (Eschmeyer
et al., 1983) |
NG | 15 to 23 TL (Ebert,
2003) |
California |
NF | NF |
NF |
NF |
NF | NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | oviparity |
NF | 47 cm TL (Ebert,
2003) |
52 cm TL (Ebert,
2003) |
NF | NF | NF | NF | Ebert, 2003 (California) |
NF | NF | NF | NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | soft bottoms (Ebert,
2003) |
polychaetes, crustaceans (shrimp) (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Cestoda (2 families, 6 spp.), Copepoda (1 family, 1 sp.) (Love
and Moser, 1983) |
NF | ||||||||||||
| Squalimorphii | Rajiformes | Rajidae |
Raja |
rhina |
Jordan & Gilbert,
1880a |
NA |
longnose skate |
southeastern Bering Sea to Cedros Islands, Baja California, also Gulf
of California (Mecklenburg
et al., 2002) |
NA | nearshore to 1000 m (Ebert,
2003) |
NF | NF | 137 cm TL (Eschmeyer
et al., 1983) |
NG | 12 to 17 cm TL (Ebert,
2003) |
California |
96.7 (S.E. 10) |
106.9 (S.E. 13.1) |
104.7 (S.E. 9.1) |
0.25 (S.E. 0.10) |
0.16 (S.E. 0.05) |
0.17 (S.E. 0.05) |
0.73 (S.E. 1.1) |
-0.3 (S.E. 0.08) |
-0.16 (S.E. 0.62) |
NG | NG | NG | von Bertalanffy growth function |
vertebral centra: thin sectioning |
NG | comparison between readers |
central California |
Zeiner and Wolf,
1993 |
12 to 13 yrs. (132 cm TL) (Zeiner
and Wolf, 1993) |
NG | oviparity |
NF | 61.5 to 74 cm TL (10 to 11 yrs.) (Zeiner
and Wolf, 1993) |
70 cm TL (10 to 12 yrs.) (Zeiner
and Wolf, 1993) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | crustaceans (Ebert,
2003) |
NF | NF | egg cases preyed upon by molluscs (Ebert,
2003) |
NF | crustaceans (Ebert,
2003) |
NF | NF | NF | mud-cobble bottom near boulders, rock ledges, and other areas with vertical
relief (Ebert, 2003) |
benthic crustaceans, teleosts (Ebert,
2003) |
NF | NF | elasmobranchs, cetaceans (Physeter catodon) (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Cestoda (3 families, 7 spp.), Copepoda (2 families, 4 spp.), Digenea (1 family, 1 sp.), Monogenea (1 family, 1 sp.), Nematoda (1 family, 1 sp.), Myxosporea (1 family, 1 sp.) (Love and Moser, 1983; Arthur and Lom, 1985) | NF |
| Squalimorphii | Rajiformes | Rajidae |
Raja |
stellulata |
Jordan & Gilbert,
1880b |
Raja montereyensis (Gilbert,
1915) |
starry skate rock skate (Starks, 1918) prickly skate (Walford, 1935) |
Eureka, California to Coronado Bank, Baja California, Mexico (Miller
and Lea, 1972; Ebert,
2003) |
NA | 18 to 732 m (Miller
and Lea, 1972) |
NF | NF | 76 cm TL (Eschmeyer
et al., 1983) |
NG | 12 to 16 TL (Ebert,
2003) |
California |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | oviparity |
NF | 67 cm TL (Ebert,
2003) |
68 cm TL (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | benthic crustaceans (shrimps), cephalopods, teleosts [Hexagrammidae (Ophiodon elongatus), Scorpaenidae (Sebastes spp.)] (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Monogenea (2 families, 2 spp.) (Love
and Moser, 1983) |
NF |
| Squalimorphii | Rajiformes | Rajidae |
Raja |
velezi |
Chirchirigno,
1973 |
NA |
Velez ray |
Gulf of California to Peru (McEachran
and Notarbartolo di Sciara, 1995) |
NA | 35 to 140 m (McEachran
and Notarbartolo di Sciara, 1995) |
NF | NF | 75.6 cm TL (McEachran and Notarbartolo-di-Sciara, 1995) |
NG | NF |
NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | oviparity |
NG | NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | benthic on the continental shelf (McEachran
and Notarbartolo di Sciara, 1995) |
crustaceans, polychaetes, teleosts (Chirchirigno,
1973) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii | Rajiformes | Urolophidae |
Urobatis | concentricus |
Osburn & Nichols,
1916 |
NF |
bull's-eye stingray reticulated round ray (Beebe and Tee-Van, 1941b) spot-on-spot round ray (McEachran and Notarbartolo-di-Sciara, 1995) |
northern Baja California, Mexico to Nicaragua (McEachran and Notarbartolo-di-Sciara, 1995) |
NA | NF |
NF | NF | 47.5 cm TL (Beebe
and Tee-Van, 1941b) |
NG |
NF |
NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
NF | NF |
have fully developed ovaries by 32.5 to 40 cm (Beebe and Tee-Van, 1941b) | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| California skate | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Squalimorphii | Rajiformes | Urolophidae |
Urobatis | halleri |
(Cooper, 1863) |
Urolophus nebulosus (Garman,
1885) Urolophus umbrifer (Jordan and Starks, 1895) |
round stingray little round stingray (Beebe and Tee-Van, 1941b) Haller's round ray (McEachran and Notarbartolo-di-Sciara, 1995) |
Humboldt Bay, California to Panama Bay, Panama (Miller
and Lea, 1972; McEachran and Notarbartolo-di-Sciara, 1995) |
NA | surface to 91 m (McEachran and Notarbartolo-di-Sciara, 1995) |
NF | both: DW = 1.75*TL (Southern California) (Babel, 1967) |
males: 25 cm DW (Babel,
1967) females: 31 cm DW (Babel, 1967) |
eastern Pacific |
6.3 to 8 cm DW, average 7.5 cm (Babel,
1967) |
southern California |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
immature males and females show cobblestone dentition pattern, mature males have central jaw dentition with a sharp connical cusp (Nordell, 1994) | 14.6 cm DW (2.6 years) (Babel,
1967) |
14.5 cm DW (2.6 years) (Babel,
1967) |
NF | NF | NF | Newport Dunes, southern California (Babel,
1967) |
![]() |
![]() |
Babel, 1967 (Southern
California) |
annual; 2 breeding cycles per year with a portion of the population being 6 months out of sync with the rest of the population and mating and giving birth in the winter (Babel, 1967) | 1 to 8 (Babel, 1967) |
NF | 1 to 6, average 2 to 3 (Ebert,
2003) |
1.6:1 (Babel, 1967) |
litter size increases in larger females; left uterus functional throughout life while right uterus comes into use in larger females (Babel, 1967) | NF | 3 months (Babel,
1967) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | protected inlets and bays with soft substrate (Babel,
1967) shallow waters less than 2 m (Ebert, 2003) |
polychaetes, crustaceans (Decapoda, Amphipoda, Isopoda), nemerteans (Babel, 1967) | burrow into substrate; utilize vision and olfaction in hunting (Babel,
1967) use mouths and discs to dig large pits; feeding rate increases as waters warm in summer and fall, decreases as water temperatures cool (Ebert, 2003) |
feed continuously diurnally (Babel, 1967) |
NF | soft substrate offshore, protected inlets and bays with soft substrate (Babel, 1967) shallow waters less than 2 m (Ebert, 2003) |
polychaetes, bivalves, crustaceans (Decapoda, Mysidae), sipunculids, Leptocardii (Babel, 1967; Valadez-Gonzalez et al., 2001) | burrow into substrate; utilize vision and olfaction in hunting (Babel,
1967) use mouthes and discs to dig large pits; feeding rate increases as waters warm in summer and fall, decreases as water temperatures cool (Ebert, 2003) |
feed continuously diurnally (Babel, 1967) |
NF | soft bottoms of mud or sand, often with eelgrass, usually in less than 15 m; especially abundant in warm, shallow, coastal and bay waters (Babel, 1967) | bivalves [Mytilidae (Mytilus edulis, Mytilus caiforniensis), Cardiidae (Laevicardium substriatum), Veneridae (Saxidomus nuttalli, Chione udatella), Tellinidae (Macoma sp., Macoma nasuta), Solecurtidae (Tagelus sp., Tagelus californiensis), Donacidae (Donax sp., Donax californicus), Solenidae (Solen sp., Solen rosaceus), Mactridae (Spisula sp., Mactra californica, Tresus nuttalii), Pholadidae (Barnea pacifica)], polychaetes [Nephtyidae (Nephtys spp.), Nereididae (Platynereis bicanaliculata), Glyceridae (Glycera americana), Goniadidae (Goniada sp., Goniada brunnea), Eunicidae, Onuphidae (Diopatra sp.), Lumbrineridae (Lumbrineris sp., L. erecta, L. minima), Oenonidae (Arabella sp.), Dorvilleidae (Dorvillea (Schistomeringos) articulata), Orbiniidae (Haploscoloplos elongata), Spionidae (Prionospio sp.), Chaetopteridae (Chaetopterus sp.), Cirratulidae (Tharyx parvus), Capitellidae (Mediomastus ambiseta), Maldanidae, Pectinariidae (Pectinaria sp., Pectinaria californiensis), Terebellidae (Pista alata), Sabellidae (Cione sp.)], nemerteans, nematodes, ophurioids [Ophiuridae (Ophioplocus esmarki)], Holothuroidea, Sipunculoidea, pycnogonids (Phoxichilidiidae), crustaceans [Calliopidae, Gammaridae (Elasmopus rapax), Isaeidae (Photis californica), Corophiidae (Corophium acherusicum), Ampithoidae (Ampithoe sp.), Idoteidae (Idotea resecata), Edotia sp., Edotia sublittoralis), Bodotriidae (Leptocuma sp.), Diastylidae (Diastylopsis tenuis), Mysidacea, Penaeidae (Penaeus sp., Penaeus californiensis), Hippolytidae (Hippolyte sp. Hippolyte californiensis, Spironotcaris sp., Spirontocaris palpator), Crangonidae (Crangon dentipes, Crangon californiensis), Alpheidae (Betaeus longidactylus), Callianassidae (Callianassa sp., Callianassa californiensis), Paguridae (Pagurus sp.), Hippidae (Emerita sp.,), Cancridae (Cancer sp., Cancer productus, Cancer antennarius)], teleosts [Gobiidae (Clevelandia ios), Embiotocidae) (Babel, 1967) | burrow into substrate; utilize vision and olfaction in hunting (Babel,
1967) use mouthes and discs to dig large pits; feeding rate increases as waters warm in summer and fall, decreases as water temperatures cool (Ebert, 2003) |
feed continuously diurnally (Babel, 1967) |
elasmobranchs (large sharks) (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | small fish feed opportunistically in ray pits (Ebert,
2003) |
segregate by age and sex; females tend to live offshore in water deeper than 14 m, while adult males and juveniles occupy
shallower habitats (Babel,
1967) males exhibit copulatory and non-copulatory biting behavior (Nordell, 1994) |
females move inshore to breed from June to September to pup; young remain inshore and as grow move out along open beaches while staying at depths of less than 2 fathoms; at 120 mm DW they gradually move into deeper water (Babel, 1967) | exhibit seasonal movements; young are primarily resident while adults move seasonally with water temperature and feeding opportunities but still do not move great distances; move offshore and deeper in winter; adult females move inshore to mate and give birth during spring and summer; move north of Pt. Conception during periods of warm water such as during El Nino events (Babel, 1967) | NF | Cestoda (4 families, ~18 species), Copepoda (2 families, 3 sp.), Monogenea (1 family, 1 sp.), Protozoa (1 family, 1 sp.) (Love and Moser, 1983) | NF | |||||||||||
| Squalimorphii |
Rajiformes |
Urolophidae |
Urobatis |
maculatus |
Garman, 1913 |
NF |
Cortez round stingray spotted round sting ray (Beebe and Tee-Van, 1941b) spotted round ray (McEachran and Notarbartolo-di-Sciara, 1995) |
Magdalena Bay, Baja California to Gulf of California (McEachran and Notarbartolo-di-Sciara, 1995) |
NA | NF |
NF | NF | 42 cm TL (Beebe
and Tee-Van, 1941b) |
Santa Inez Bay, Mexico |
NF | NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | polychaetes [Eunicidae (Eunice sp.)], crustaceans
(Amphipoda) (Beebe
and Tee-Van, 1941b) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii | Rajiformes | Urolophidae | Urotrygon | aspidera | (Jordan and Gilbert,
1882c) |
Urolophus aspidurus (Jordan
and Gilbert, 1882c) Urotrygon aspidurus (Miyake and McEachran, 1986) |
roughtail round stingray spinetail stingray (Bussing and Lopez, 1994) spiny-tail round ray (McEachran and Notarbartolo-di-Sciara, 1995) Panamic stingray (Allen and Robertson, 1994) |
Mexico to Peru (Allen and Robertson, 1994) |
NA | 5 to 20 m (Allen and Robertson, 1994) |
NF | NF | 42.1 cm TL; 23.3 cm DW (McEachran and Notarbartolo-di-Sciara, 1995) | NG | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | benthically on soft substrates in nearshore waters (McEachran and Notarbartolo-di-Sciara, 1995) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii |
Rajiformes |
Urolophidae |
Urotrygon |
chilensis |
(Günther,
1871) |
Urotrygon goodei (Jordan
and Bollman, 1890) |
thorny round stingray Chilean round ray (McEachran and Notarbartolo-di-Sciara, 1995) |
Gulf of California to Chile (Castro-Aguire, 1965; McEachran and Notarbartolo-di-Sciara, 1995) |
NA | NF |
NF | NF | 41.9 cm TL (McEachran and Notarbartolo-di-Sciara, 1995) |
NG | NF | NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Cestoda (2 families, 7 spp.) (Berman
and Brooks, 1994; Marques
et al., 1997) |
NF |
| Squalimorphii | Rajiformes | Urolophidae | Urotrygon | munda | Gill, 1863b |
Urotrygon mundus (Gill,
1863b) |
shortfin round stingray Munda round ray (McEachran and Notarbartolo-di-Sciara, 1995) |
observed in Mexico, Costa Rica, and Panama (Beebe and Tee Van, 1941b) |
NA | NF | NF | NF | 28.8 cm TL, 16 cm DW (McEachran and Notarbartolo-di-Sciara, 1995) | NG | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | benthically on soft substrates in nearshore waters (McEachran and Notarbartolo-di-Sciara, 1995) | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii |
Rajiformes |
Urolophidae |
Urotrygon |
rogersi |
(Jordan and Starks,
1895) |
NF |
lined round stingray Roger's round ray (McEachran and Notarbartolo-di-Sciara, 1995) |
southern Gulf of California to Gulf de Guayaquil (McEachran and Notarbartolo-di-Sciara, 1995) |
NA | NF |
NF | NF | 46.2 cm TL (McEachran and Notarbartolo-di-Sciara, 1995) |
NG | NF | NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii |
Rajiformes |
Dasyatidae |
Dasyatis |
dipterura |
(Jordan and Gilbert, 1880e) |
Dasyatis dipterurus (Jordan and Gilbert,
1880e) Dasyatis brevis (Garman, 1880) |
diamond stingray |
British Columbia, Canada to Chile, including the Galapagos Islands (Eschmeyer
et al., 1983; Nishida
and Nakaya, 1990) |
Hawaii (Nishida
and Nakaya, 1990) |
shore to at least 28 m (Mathews and Druck, 1975; Eschmeyer et al., 1983) |
NF | NF | 100 cm DW (McEachran and Notarbartolo di Sciara, 1995) |
NG | 17 to 19 cm DW (Mariano
Melendez, 1997) |
NG | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
females larger than males (Mariano Melendez, 1997; W.D. Smith pers. comm.) |
45.5 cm DW (Mariano
Melendez, 1997) 50 cm DW (Mathews and Druck, 1975) |
65.5 cm DW (Mariano
Melendez, 1997) NG |
45.5 cm DW (Mariano Melendez, 1997) |
65.5 cm DW (Mariano
Melendez, 1997) |
NF | NF | ![]() |
![]() |
![]() |
Mariano Melendez, 1997 (Almejas Bay, Baja California Sur, Mexico) |
annual, 9.5 to 10 month diapause (Mariano
Melendez, 1997) |
NF | NF | 2 to 4 (Mariano
Melendez, 1997) |
1:1 (Mariano
Melendez, 1997) |
no relationship (Mariano
Melendez, 1997) larger females produce larger (not more) offspring (W. Smith, pers. obs.) |
NF | 2 to 2.5 months (Mariano
Melendez, 1997) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | sandy areas, often around kelp beds or rocks; more numerous around kelp during winter than on flat bottomed sand (Feder et al., 1974) | NF | NG |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | possible sexual segregation (Mathews
and Druck, 1975) |
NF | range from shore to 6 m during summer (average 2.3 m), concentrated in
13 to 17.7 m averaging 15 m during late fall and winter (Feder
et al., 1974) seasonal shifts in abundance between Magdalena and Almejas Bays, Baja California Sur, Mexico; abundance higher in August (Mathews and Druck, 1975) enter Estero de Punta Banda, Baja California, Mexico during April and leave by September (Beltran-Felix et al., 1986) |
NF | Cestoda (1 family, 4 spp.) (Ghoshroy
and Caira, 2001) |
NF | |||||||||
| Squalimorphii |
Rajiformes |
Dasyatidae |
Dasyatis |
longa |
(Garman, 1880) |
Dasyatis longus (Garman,
1880) Trygon longa (Garman, 1880) |
longtail stingray |
central western coast of Baja and Gulf of California, Mexico to Colombia and Galapagos Islands (Nishida and Nakaya, 1990; Villavicencio-Garyazar et al., 1994, Acero and Franke, 1995) | NA | to at least 80 m (Acero
and Franke, 1995) |
NF | NF | 120 cm DW (McEachran
and Notarbartolo di Sciara, 1995) |
NG | ca. 40 cm DW (Villavicencio-Garyazar et al., 1994) |
Almejas Bay, Baja California Sur, Mexico |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | aplacental viviparity |
females larger than males (Acero
and Franke, 1995) |
ca. 80 cm DW (Villavicencio
et al., 1994) |
ca. 110 cm DW (Villavicencio
et al., 1994) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NG | NF | NF | 1 to 4 (Villavicencio-Garyazar et al., 1994) |
NG | 1 (110 cm DW) (Villavicencio-Garyazar et al., 1994) 2 (131 to 134 cm DW) (Villavicencio-Garyazar et al., 1994) 3 to 4 (154 to 156 cm DW) (Villavicencio-Garyazar et al., 1994) |
NF | 10 to 11 months (Villavicencio-Garyazar et al., 1994) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | crustaceans (Beebe
and Tee-Van, 1941b) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Cestoda (1 family, 2 spp.) (Marques
et al., 1997) |
NF |
| Squalimorphii |
Rajiformes |
Dasyatidae |
Dasyatis |
violacea |
(Bonaparte, 1832) |
Dasyatis atratus (Ishiyama
& Okada, 1955) |
pelagic stingray |
southeast Alaska to equatorial Central America (Mecklenburg
et al., 2002; Mollet,
2002) |
cosmopolitan in tropical and temperate seas ( Mollet,
2002) |
surface to 238 m (Eschmeyer
et al., 1983) |
both: WT = 27 * DW3.01 (wild-caught
specimens) (northeast Pacific) (Mollet
et al., 2002) both: WT = 48.4 * DW3.471 (captive specimens) (Monterey Bay Aquarium, Monterey, California) (Mollet et al., 2002) |
NF | 80 cm DW (Bigelow
and Schroeder, 1965) 96 cm DW (Mollet, 2002) |
western North Atlantic captive; Monterey Bay Aquarium, Monterey, California |
15 to 23.5 cm DW (Mollet
et al., 2002) |
captive births at Steinhart Aquarium, San Francisco, California |
74 (S.E. 2) 70 |
116 (S.E. 5) 101 |
NG NG |
0.35 (S.E. 0.03) 0.58 (S.E. 0.04) |
0.20 (S.E. 0.02) 0.41 (S.E. 0.02) |
NG NG |
17 (S.E. 1) 18 (S.E. 1) |
17 (S.E. 1) 18 (S.E. 1) |
NG NG |
NG NG |
NG NG |
NG NG |
von Bertalanffy growth function Gompertz growth model |
captive growth captive growth |
NG NG |
NG NG |
captive at Monterey Bay Aquarium, Monterey, California captive at Monterey Bay Aquarium, Monterey, California |
Mollet et al.,
2002 Mollet et al., 2002 |
both: 10 yrs. (Mollet
and Cailliet, 2002) |
7 ln/k |
aplacental viviparity |
females larger than males (Wilson
and Beckett, 1970; Mollet
et al., 2002) |
35 to 40 cm DW (ca. 2 yrs.) (Mollet
et al., 2002) |
40 to 50 cm DW (3 yrs.) (Mollet
et al., 2002) |
NF | NF | NF | equatorial waters off Central America (Mollet,
2002) |
Mollet, 2002 (easte | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||