| TAXONOMY | BIOGEOGRAPHY | AGE & GROWTH | REPRODUCTION | MORTALITY | DEMOGRAPHY | HABITAT ASSOCIATION & TROPHIC INTERACTIONS | GENETICS | BEHAVIOR | PATHOLOGY | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CLASS | Life Stage | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chondrichthyes | Seasonal Cycle | Fecundity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SUBCLASS | Growth Parameters | Fertilization and Pupping Period (^^^^^ = peak fertilization; ***** = peak pupping; ##### = doubtful pupping records) | Juveniles | Adolescents | Adults | Genetic Variance | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Elasmobranchii | 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 | Rhinobatidae |
Rhinobatos | glaucostigma | Jordan and Gilbert,
1883a |
Rhinobatus glaucostigmus (Jordan
and Gilbert, 1883a) |
speckled guitarfish slaty-spotted guitarfish (Beebe and Tee-Van, 1941b) |
lower Baja California through Mexico; Peru (Jordan and Gilbert, 1883a; Beebe and Tee-Van, 1941b; McEachran and Notarbartolo-di-Sciara, 1995) | NA | NF | NF | NF | 78 cm TL (Jordan
and Gilbert, 1883a) |
Mazatlan, Mexico |
NF | NF | NF | NF | NF |
NF |
NF |
NF |
NF |
NF | NF | NF | 0.94 |
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 | sandy bottoms, shallow water (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 |
| Squalimorphii | Rajiformes | Rhinobatidae | Rhinobatos | productus |
(Ayers, 1854b) |
Rhinobatis producta (Ayers,
1854b) |
shovelnose guitarfish guitar fish (Starks, 1918) pointed-nosed guitar fish, shovel-nosed shark (Walford, 1935) northern guitarfish (Beebe and Tee-Van, 1941b) shovelnose shark (Roedel, 1953) |
San Francisco, California to Gulf of California, rare north of Monterey
Bay (Miller and Lea,
1972; Eschmeyer
et al., 1983) |
NA | Intertidal to 91.5 m, typically shallower than 12 m (Feder et al., 1974; Love, 1996) |
females: ln WT = -13.4471 + 3.220752 ln TL (Almejas Bay,
Baja California Sur, México) (Villavicencio-Garayzar,
1993b) males: WT = 0.000002 * TL3.14 (Almejas Bay, Baja California Sur, Mexico) (Dowton-Hoffman, 1996) females: WT = 0.000003 * TL3.04 (Almejas Bay, Baja California Sur, Mexico) (Dowton-Hoffman, 1996) |
NF | females: 156 cm TL (Baxter,
1966) males: 114 cm TL (Dowton-Hoffman, 1996) |
San Quintin Bay, Baja California, Mexico Almejas Bay, Baja California Sur, Mexico |
20 to 24 cm TL (Villavicencio-Garayzar
1993b) 15 cm TL (Eschmeyer et al., 1983) |
Almejas Bay, Baja California Sur, Mexico NG |
142 | 594 | 228 |
0.095 |
0.016 |
0.047 |
-3.942 |
-3.800 |
-4.030 |
0.70 |
NF | 0.81 |
NF | vertebral centra: whole centra with transmitted light (dark field) |
Terramycin mark, captive rearing, edge analysis |
triplicate reads, only used those that agreed |
between Seal and Redondo Beaches, California |
Timmons and Bray, 1997 |
both: 11 yrs. (Timmons
and Bray, 1997) |
centra counts (opaque bands) |
aplacental viviparity |
females 40% larger (Villavicencio-Garayzar,
1993b) females 20% larger (Dowton-Hoffman, 1996) |
91 to 100 cm TL; 7.0 to 8.4 yrs. (Timmons and Bray, 1997) <63 cm TL (Villavicencio-Garayzar, 1993b) 80 cm TL (Dowton-Hoffman, 1996) 92 cm TL (Dubois, 1981) 110 cm TL (Talent, 1985) |
99 cm TL; 7 yrs. (Timmons
and Bray, 1997) 66 cm TL (Villavicencio-Garayzar, 1993b) 87 cm TL (Dowton-Hoffman, 1996) NG NG |
NG | 99 cm TL (Timmons and Bray, 1997) |
Almejas Bay, Baja California Sur, Mexico (Villavicencio Garayzar, 1993b) |
Elkhorn Slough, Monterey Bay, California (Herald
et al., 1960) southern California (Love, 1996) Belmont Shores area in Long Beach, California (Timmons and Bray, 1997) Punta Banda estuary, Baja California, Mexico (Beltrán-Félix et al., 1986) Almejas Bay, Baja California Sur, Mexico (Villavicencio-Garayzar, 1993b) Almejas Bay, Baja California Sur, Mexico (Dowton-Hoffman, 1996) |
Herald et al., 1960
(Elkhorn Slough, California) Love, 1996 (southern California) Villavicencio-Garayzar, 1993b (Almejas Bay, Baja California Sur, Mexico) Dowton-Hoffman, 1996 (Almejas Bay, Baja California Sur, Mexico ) |
annual (Herald et
al., 1960; Villavicencio-Garayzar,
1993b) |
NF | NF | up to 28 (Baxter,
1966) 6 to 16, typically 9 to 11 (Villavicencio-Garayzar, 1993b) 4 to18, typically 8 to 10 (Dowton-Hoffman, 1996) |
1:1.06 (Villavicencio-Garayzar,
1993b) 1:1.04 (Dowton-Hoffman, 1996) |
6 to 9 embryos (104 to 110 cm TL) (Villavicencio-Garayzar,
1993b) 11 to 14 embryos (111 to cm 115 TL) (Villavicencio-Garayzar, 1993b) 8 to 9 embryos (116 to 125 cm TL) (Villavicencio-Garayzar, 1993b) 14 to 16 embryos (126 to 130 cm TL) (Villavicencio-Garayzar, 1993b) 16 embryos (131 to 135 cm TL) (Villavicencio-Garayzar, 1993b) 12 embryos (136 to 140 cm TL) (Villavicencio-Garayzar, 1993b) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | very shallow water, usually protected or semi-protected waters (Love,
1996) |
NF | NF | NF | NF | NF | crustaceans [Grapsidae (Hemigrapsus oregonensis)], teleosts, possibly some bivalves (Talent, 1982) | NF | NF | NF | shallow water along beaches and in bays (Roedel
and Ripley, 1950) mud flats, especially those with eelgrass beds, extensively utilized (Dubsky, 1974) sand and mud-sand bottoms in shallow coastal waters, bays, sloughs, and estuaries (Eschmeyer et al., 1983) |
crustaceans [Decapoda (Grapsidae (Hemigrapsus oregonensis),
shrimp)], Amphipoda], bivalves, polychaetes, teleosts [Embiotocidae
(Cymatogaster aggregata), Gobiidae (Gillichthys mirabilis), Cottidae (Leptocottus armatus), Pleuronectiformes)] (Roedel and Ripley, 1950; Talent,
1982; Eschmeyer
et al., 1983; Love,
1996; Ebert, 2003)
|
noted feeding on sand crabs in water less than 3" deep (Baxter,
1966; Baxter,
1980) forage epibenthically off mudflats (Talent, 1982) |
NF | elasmobranchs (Triakis semifasciata) (Talent,
1976) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | observed swimming with (underneath) Triakis semifasciata off Santa Catalina Island, California (Love, 1996) |
solitary or in large aggregations (Michael, 1993) aggregate in shallow waters (Love, 1996) |
NF | nomadic; burrow in sand when resting (Eschmeyer
et al., 1983) enters Punta Banda estuary between May and August (Beltrán-Félix et al., 1986) in Almejas Bay mature females entered the Bay in late April or early May and leave by mid August; mature males enter the Bay in July and leave in mid August; after pupping in July and August, females mate with males before both leave the Bay (Villavicencio-Garayzar, 1993b) |
NF | Nematoda (1 family, 1 sp.), Cestoda (5 families, 10 spp.), Copepoda (4 family, 4 spp.), Digenea (1 family, 1 sp.), Monogenea (2 families, 3 spp.)
(Heinz and Dailey,
1974; Love and Moser,
1983; Adamson
et al., 1987; Deets,
1987; Doijiri
and Deets, 1988; Deets
and Dojiri, 1989; Gomez
del Prado R. and Euzet, 1999)
|
NF | ||||||||||||
| Squalimorphii | Rajiformes | Rhinobatidae |
Platyrhinoidis | triseriata |
(Jordan and Gilbert,
1880c) |
Platyrhina triseriata (Jordan
and Gilbert, 1880c) |
thornback round skate, thornback, guitarfish, California thornback, shovelnose (Gates and Frey, 1974) banjo shark (Love, 1996) |
Tomales Bay, northern California to Thurloe Head, Baja California (Miller
and Lea, 1972; Plant,
1989) |
NA | intertidal to 137 m (Ebert,
2003) |
NF | NF | 91 cm TL (Roedel
and Ripley, 1950) |
NG |
ca. 11 cm (Ebert,
2003) |
NG |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NF |
aplacental viviparity |
NF | NF | 48 cm TL (Ebert,
2003) |
NF | NF | NF | NF | Ebert, 2003 (southern
California) |
annual (Ebert, 2003) |
NF | NF | 1 to15 (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 | fine sand to mud bottoms, sand-bottom kelp holdfast and rocky-bottom kelp-bed
habitat (Feder et al.,
1974; Limbaugh,
1955) kelp bed and adjacent kelpless cobble area (Larson and DeMartini, 1984) mud and sandy bottoms of bays, sloughs, and coastal beaches, also around kelp forests (Ebert, 2003) |
crustaceans, molluscs, polychaetes, cephalopods (Teuthoidea), teleosts [Engraulidae (Engraulis mordax), Gobiidae, Clupeidae (Sardinops sagax), Cottidae, Embiotocidae)] (Limbaugh, 1955, Feder et al., 1974, Van Blaricom, 1982, Ebert, 2003) | NF | NF | elasmobranchs, pinnipeds (Mirounga angustirostris) (Love, 1996; Ebert, 2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF; | NF | NF | NF | NF | NF | NF | NF | Cestoda (3 families, 3 spp.), Digenea (1 family, 1 sp.), Nematoda (1 family,
1 sp.) (Love and Moser,
1983; Ivanov and
Campbell, 1998) |
NF | ||||||||||||
| Squalimorphii | Rajiformes | Rhinobatidae |
Zapteryx |
exasperata |
(Jordan and Gilbert,
1880e) |
Platyrhina exasperata (Jordan
and Gilbert, 1880e) |
banded guitarfish prickly skate (Starks, 1918) mottled guitarfish (Roedel, 1953) striped guitarfish (Ebert, 2003) |
southern California to Puerto Pizzarro, Peru (Eschmeyer et al., 1983; Rubio and Ruiz, 1993; McEachran and Notarbartolo di Sciara, 1995) | NA | intertidal to 23 m; concentrated at 2.5 to 10 m (Feder
et al., 1974) |
NF | NF | 94 cm TL (Villavicencio,
1995b) |
Almejas Bay, Baja California Sur Mexico |
15 to 18 cm TL (Villavicencio,
1995b) |
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 (Villavicencio,
1995b) |
NF | 77 cm TL (Villavicencio,
1995b) |
NF | NF | NF | Alemejas Bay, Baja California Sur, Mexico (Villavicencio,
1995b) |
Villavicencio, 1995b (Almejas Bay, Baja California Sur, Mexico) |
annual (Villavicencio,
1995b) |
NF | NF | 4 to 11 (Villavicencio,
1995b) |
1:1 (Villavicencio,
1995b) |
NF | NF | 3 to 4 months (Villavicencio, 1995b) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | nearshore rocky areas, crevices and caves (Feder et al., 1974) |
NF | NF | NF | NF | nearshore rocky areas, crevices and caves (Feder et al., 1974) |
NF | NF | NF | NF | nearshore rocky areas, crevices and caves (Feder
et al., 1974) |
crustaceans [Decapoda (shrimp, crabs)], benthic
invertebrates (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Monogenea (1 family, at least 1 sp.) (Gomez
del Prado Ruiz and Euzet, 1999) |
NF | ||||||||||||
| Squalimorphii | Rajiformes | Narcinidae |
Diplobatis |
ommata |
(Jordan and Gilbert, in Jordan and Bollman 1890) |
Discopyge ommata Jordan and Gilbert, in Jordan and Bollman 1890 | ocellated electric ray |
Gulf of California to Panama (Beebe
and Tee-Van, 1941b; Jordan
and Bollman, 1890) |
NA | to about 60 m (Jordan
and Bollman, 1890, Beebe
and Tee-Van, 1941b) |
NF | NF | 18.5 cm TL (Beebe
and Tee-Van, 1941b) |
Inez, 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 | 37 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 | NF | NF | NF | NF | NF | NF | 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 [Amphipoda, Decapoda (small shrimp)], polychaetes
(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 | Narcinidae |
Narcine |
entemedor |
Jordan and Starks,
1895 |
NA |
Cortez electric ray ocellated electric ray (Beebe and Tee-Van, 1941b) lesser electric ray (Allen and Robertson, 1994) giant electric ray (McEachran and Notarbartolo di Sciara, 1995) |
Ojo de Liebre lagoon, Baja California Sur, through northern Gulf of California
and south to northern Peru (de
Carvalho, 1999) |
NA | intertidal to 100 m (Chirichigno,
1978) |
males: WT = 0.000067 * TL2.54
(Almejas Bay, Baja California Sur, Mexico) (Villavicencio-Garayzar,
2000) females: WT = 0.000012 * TL2.98 (Almejas Bay, Baja California Sur, Mexico) (Villavicencio-Garayzar, 2000) |
NF | females: 93 cm TL (Villavicencio-Garayzar,
1993c) males: 67 cm TL (Villavicencio-Garayzar, 2000) |
Almejas Bay, Baja California, Mexico Almejas Bay, Baja California, Mexico |
16.3 cm TL (Castro-Aguirre
et al., 1970) 14 to 16 cm TL (Villavicencio-Garayzar, 2000) 11 to 12 cm TL (Allen and Robertson, 1994) |
Gulf of California Almejas Bay, Baja California Sur, Mexico NG |
76.2 (S.E. 11.2) |
82.6 (S.E. 1.1) |
NG |
0.104 (S.E. 0.05) |
0.302 (S.E. 0.04) |
NG |
-5.320 |
-1.140 |
NG | 0.80 | 0.61 |
NG | von Bertalanffy growth function |
vertebral centra: thin sectioned |
marginal increment analysis |
females: APE=10.38%, D=6.1% males: APE=8.35%, D=4.71% |
Almejas Bay, Baja California Sur, Mexico
|
Villavicencio-Garayzar,
2000 |
females:
15 yrs. (Villavicencio-Garayzar,
2000) males: 11 yrs. (Villavicencio-Garayzar, 2000) |
centra thin-sectioned counts centra thin-sectioned counts |
aplacental viviparity |
females larger than males (Villavicencio-Garayzar,
1993c) |
45 cm TL (Villavicencio-Garayzar,
2000) 34.2 to 37.2 cm TL (de Carvalho, 1999) |
63 cm TL (Villavicencio-Garayzar,
2000) NG |
NF | NF | Almejas Bay, Baja California Sur, Mexico (Villavicencio-Garayzar,
2000) |
Almejas Bay, Baja California Sur, Mexico (Villavicencio-Garayzar,
2000) |
Villavicencio-Garayzar,
2000 (Almejas Bay, Baja California Sur, Mexico) |
annual (Villavicencio-Garayzar,
1993c) |
NF | NF | 4 to 15 (Allen and Robertson, 1994) 4 to 20 (Villavicencio-Garayzar, 2000) |
1.2:1 (Villavicencio-Garayzar,
1993c) 1:1.1 (Villavicencio-Garayzar, 2000) |
4 to 12 embryos (71 to 81 DW) (Villavicencio-Garayzar,
1993c) |
Lembryo = 41.82 cm + 1.0025 * L mother, June (Villavicencio-Garayzar,
2000) Lembryo = 75.29 cm + 0.324 * L mother, July (Villavicencio-Garayzar, 2000) Lembryo = 81.364 cm + 0.72 * L mother, August (Villavicencio Garayzar, 2000) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | carbonate sand shelf (20 to 80 m) (Valadez-González
et al., 2000) |
polychaetes, crustaceans (Stomatopoda), teleosts (Anguilliformes) (Valadez-González et al., 2000) | NF | NF | NF | carbonate sand shelf (Valadez-González
et al., 2000) |
polychaetes, teleosts (Anguilliformes), molluscs (Valadez-González et al., 2000) | forage epibenthically on mudflats (Talent, 1982) |
NF | NF | sand and boulder bottom (Breder,
1928) may enter estuarine/brackish water areas (Castro-Aguirre, 1978) benthic in shallow, protected waters with soft bottoms (McEachran and Notarbartolo-di-Sciara, 1995) |
polychaetes, teleosts, tunicates (Beebe
and Tee-Van, 1941b; Castro-Aguirre,
1965) |
NF | nocturnal, move into shallow bays to feed at night (Michael, 1993) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | sexually segregate (Villavicencio-Garayzar,
2000) |
NF | in Almejas Bay, Mexico: most abundant from May to August; enters Bay in May, most abundant in June, leaves in August; females pup in July and August in Bay (Villavicencio-Garayzar, 1993c) | NF | Cestoda (1 family, 2 spp.), Copepoda (1 family, 1 sp.) (Marques
et al., 1997; Braswell
et al., 2002) |
NF | ||||||||||||
| Squalimorphii | Rajiformes | Torpedinidae |
Torpedo |
californica |
Aryes, 1855b |
Tetronarce californica (Ebert,
2003) |
Pacific electric ray |
northern British Columbia to central Baja California (Mecklenburg
et al., 2002) |
NA | 3 to 425 m (Mecklenburg
et al., 2002) |
males: WT = 0.00004 TL2.8753 (Monterey
Bay and Los Angeles Basin, California) (Neer
and Cailliet, 2001) females: y = 0.00002 TL3.0213 (Monterey Bay and Los Angeles Basin, California) (Neer and Cailliet, 2001) |
NF | males: 92 cm TL (Ebert,
2003) females: 137 cm TL (Ebert, 2003) |
NG |
21.4 to 23.1 cm TL (Neer
and Cailliet, 2001) 18 to 23 cm TL (Ebert, 2003) |
Monterey Bay, California |
92.1 (95% C.I. 10.74) |
137.3 (95% C.I. 28.82) |
NG |
0.13 |
0.07 |
NG |
-1.483 |
-1.934 |
NG | NG | NG | NG | von Bertalanffy growth function |
vertebral centra: graphite microtopography |
unsuccessful OTC injection, calcein internal markings, edge analysis |
between reader comparison |
Monterey Bay and Los Angeles Basin, California |
Neer and Cailliet,
2001 |
16 yrs., but possibly up to 24 yrs. (Neer and Cailliet, 2001) |
predicted from von Bertalanffy growth function |
aplacental viviparity |
females grow larger (Neer
and Cailliet, 2001) |
64.5 cm TL; ca. 7yrs (Neer
and Cailliet, 2001) |
73.1 cm TL; ca. 9 yrs (Neer and Cailliet, 2001) |
NF | NF | Neer and Cailliet,
2001 (Monterey Bay, California) |
males: annual (Neer
and Cailliet, 2001) females: biannual (Neer and Cailliet, 2001) |
0 to 55 per ovary (Neer
and Cailliet, 2001) |
NF | 17 (Neer and Cailliet,
2001) |
10:7 (Neer and Cailliet, 2001) |
number of ova increases with increase body size (Neer and Cailliet, 2001) |
NF | NF | NF | NF | 0.277 0.186 |
Hoenig's equation Hoenig's equation |
16 yrs. 24 yrs. |
Neer and Cailliet, 2001 Neer and Cailliet, 2001 |
0.09 |
1.09 |
2.59 |
11.15 |
NG |
age-based life history table |
Monterey Bay, California |
Neer and Cailliet,
2001 |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | around rocky reefs in Southern Calfornia (Lowe
et al., 1994) sandy bottoms, rocky reefs, and near kelp beds (Ebert, 2003) |
teleosts [Engraulidae, Merluccidae, Clupeidae, Scombridae,
Pleuronectiformes, Serranidae (Paralabrax clathratus]) (Ebert,
2003) |
uses electric organ to immobilize prey (Moller,
1995; Lowe et al.,
1994) forage in the water column nocturnally or in turbid condition, using electrical cues; hide on bottom and ambush prey during the day (Ebert, 2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | Cestoda (1 family, 1 sp.), Monogenea (1 family, 1 sp.), Protozoa (1 family,
2 spp.) (Love and Moser,
1983) |
NF | ||||||||||||||
| Squalimorphii | Rajiformes | Arhynchobatidae | Bathyraja |
abyssicola |
(Gilbert, 1896) |
NA | deepsea skate |
Cortes Bank, southern California to eastern Bering Sea (Ishihara
and Ishiyama, 1985) |
western Bering Sea to northern Japan (Ishihara
and Ishiyama, 1985) |
362 to 2904 m (Zorzi
and Anderson, 1988) |
NF | NF | 157 cm TL (Sheiko
and Tranbenkova, 1998) |
northwest of Bering Island in the Commander Islands
|
NG |
NF |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NG | oviparity |
NF | 110.0 cm TL (Zorzi
and Anderson, 1988) |
NF |
NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | annelid worms, cephalopods, crustaceans [Majidae (Chionoecetes
bairdi), Decapoda (shrimps)], teleosts (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 | Arhynchobatidae | Bathyraja |
aleutica |
(Gilbert, 1896) |
NA | Aleutian skate |
Cape Mendocino, northern California to the Bering Sea (Ebert,
2003) |
northern Japan (Ebert,
2003) |
100 to 800m (Mecklenburg
et al., 2002) |
NF | NF | 150 cm TL (Teshima
and Tomonaga, 1986) |
southern Bering Sea, western Gulf of Alaska |
12 to 15 cm DW (Teshima and Tomonaga, 1986) |
Bering Sea |
NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NF |
oviparity |
NF | 113 cm TL (Ebert,
2003) |
125 cm TL (Ebert,
2003) |
NF | NF | NF |
southeastern Bering Sea continental slope from 250 to 500 m depth (Teshima and Tomonaga, 1986) | Teshima and Tomonaga,
1986 (Bering Sea, Gulf of Alaska) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | teleosts [Gadidae (Theragra chalcogramma), Salmonidae (Oncorhynchus nerka)], annelid worms, crustaceans [Decapoda (crabs, shrimps)], cephalopods (Teuthoidea) (Orlov, 1998; 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 | Arhynchobatidae | Bathyraja |
interrupta |
(Gill and Townsend,
1897) |
NA | Bering skate sandpaper skate (Mecklenburg et al., 2002) |
Bering Sea to Cortes Bank, southern California (Mecklenburg
et al., 2002) *southern range uncertain due to confusion between this species and B. kincaidii |
NA | 55 to 1372 m (Mecklenburg
et al., 2002) |
NF | NF | males: 70.0 cm TL (Ishihara
and Ishiyama, 1985) females: 80.0 cm TL (Ishihara and Ishiyama, 1985) |
Bering Sea Bering Sea |
NF |
NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NF |
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 | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | crustaceans (Amphipoda) (Orlov,
1998) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii | Rajiformes | Arhynchobatidae | Bathyraja |
kincaidii |
(Garman, 1908) |
Bathyraja interrupta (Ishihara
and Ishiyama, 1985) |
sandpaper skate black skate (Hart, 1973; Gates and Frey, 1974) Bering skate (Ishihara and Ishiyama, 1985) |
Gulf of Alaska to northern Baja California (Ebert,
2003) |
NA | 55 to 1372 m (Miller
and Lea, 1972) |
NF | NF | males: 53 cm TL (Ebert,
2003) females: 56 cm TL (Ebert, 2003) |
NG | 12 to 16 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 |
disk shape differs between adults (C.Perez, pers. comm.) males have alar thorns (C. Perez, pers. comm.) |
48 cm TL (Ebert,
2003) |
46 to 50 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 | polychaetes, crustaceans [Amphipoda, Decapoda (crabs,
shrimps)] (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 | Arhynchobatidae | Bathyraja |
lindbergi |
Ishiyama and Ishihara,
1977 |
Bathyraja matsubarai (Dolganov,
1999) |
commander skate |
eastern Bering Sea, Aleutian Islands, possibly the western Gulf of Alaska
(Mecklenburg
et al., 2002) |
western Bering Sea and Commander Islands to Sea of Okhotsk (Mecklenburg
et al., 2002) |
180 to 2000 m (Dolganov,
1999; Mecklenburg
et al., 2002) |
NF | NF | 93 cm TL (Mecklenburg
et al., 2002) |
NG | NF |
NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NF |
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 | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | 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 | Arhynchobatidae | Bathyraja |
maculata |
Ishiyama and Ishihara,
1977 |
NA |
whiteblotched skate |
Bering Sea and Aleutian Islands (Mecklenburg
et al., 2002) |
Cape Navarin to Commander Islands, Kamchatka and Kuril Islands, Sea of Okhotsk and northern Sea of Japan (Mecklenburg et al., 2002) | 73 to 1110 m (Mecklenburg
et al., 2002) |
NF | NF | 108 cm TL (Ishiyama
and Ishihara, 1977) 120 cm TL (Mecklenburg et al., 2002) |
Japan NG |
NF |
NF | NF | NF |
NF |
NF |
NF |
NF |
NF |
NF |
NF | NF | NF | NF | NF | NF |
NF | NF |
NF |
NF |
NF |
NF |
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 | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | crustaceans [Amphipoda, Decapoda (shrimps)], mollusks,
teleosts [Scombridae, Cottidae, Gadidae (Theragra chalcogramma)]
(Orlov, 1998) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF |
| Squalimorphii | Rajiformes | Arhynchobatidae | Bathyraja | mariposa |
Stevenson et al., 2004 |
NA | butterfly skate |
Aleutian Islands from Seguam Pass, Tanaga Pass, Petrel Bank, and the Islands
of the Four Mountains (Stevenson et al., 2004) |
NA | 90 to 448 m (Stevenson et al., 2004) |
NF | NF | 76 cm TL (Stevenson et al., 2004) |
Tanaga Pass, Aleutian Islands |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | 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 | Arhynchobatidae | Bathyraja |
microtrachys |
(Osburn and Nichols,
1916) |
Bathyraja trachura (Miller and Lea, 1972; Ishihara and Ishiyama,
1985) |
fine-spined skate |
Washington State to southwest of San Diego, California (Ebert,
2003) |
NA | 1995 to 2900 m (Ebert,
2003) |
NF | NF | females: 70 cm TL (Ebert,
2003) |
Guadalupe Island, Baja California Mexico |
17 cm DW (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 |
NF | 60 to 70 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 | crustaceans [Decapoda (deepwater shrimp)] (Ebert,
2003) |
NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF | NF< | |||||