/30 BULLETIN SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUME 1 Mations/mi n. 200 160 120 --20 0 2 2 0, conc. (Val Figure 3. The effect of oxygen concentration on the rate of gill ventilation. Points are means for five fish, with 5 measurements of ventilation per minute and averaged for each fish. fairly constant rates of oxygen consumption ( Warren, 1971). The unarmored stickleback shows this homeostatic ability quite well above 2.0 ppm. In oxygen concentrations below 2.0 ppm, oxygen consumption drops rapidly. A strong correlation exists between the level of no excess activity point, when oxygen consumption begins to rapidly decrease, and the oxygen concentration an organism is exposed to in its particular habitat ( Macan, 1963). Goldfish (Carassius aurains) have a considerably tower incipient limiting point than do brook trout (Sardinia fontinalis) (Fry and Hart, 1948; (i raham, 1949; Beamish, 1964). Undoubtedly the critical dissolved oxygen concentration which causes the rate of oxygen consumption to drop can he influenced by acclimation. Sim ilatly, the critical or lethal low oxygen concentration is also effected by acclimation. Shepard ‘i1955) found that the survival time of brook tro in a lethal oxygen concentration of 1.06 pp creased when fish were held for 150 hours i .8 ppm 02. Fry and Hart (1948) and Graha 1949) also showed that temperature also affe the point of no excess activity. The small mere- in respiratory rate (Fig. 2) in oxygen co trations slightly above the level of no exce . activity has also been reported by Beamish (1964). This increase is believed to he caused by the large energy requirement needed for providing sufficient gill ventilation at low oxygen concentrations. Gill ventilation data for 73 the unarmored stickleback (Fig. 3) indicates the great increase in ventilation rate required to allow respiratory independence to exist as oxygen concentration decreases. These data show that even though a field oxygen concentration of 3.0 pp would not be lethal, a sizeable amount of energy would be required for ventilation. Such a s'ination would probably reduce both growth and *roductive abilities as well as general activiiir as energy would be diverted to maintain a s icicnt metabolic rate. Jones (1952) found that G rosteus aculeattu would avoid water with lean than 2.0 ppm 02. When a fish entered water with a dissolved oxygen concentration less than 2.0 ppm it immediately turned around or hacked out of it. Data presented in this paper indicate that although the unarmored stickleback also ears to be capable of tolerating oxygen levels 416 low as 2.0 ppm, below this concentration death would soon occur. Hence there appears to be a good correlation between the behavioral observations of Jones and our oxygen consumption data. The daytime oxygen concentrations in the upper Santa Clara River (mean 02 = 7.18 ppm) appear to he well above this limiting level. However, in isolated stagnant pools and perhaps on warm summer nights, when photosynthetic 02 production would be absent, lower oxygen levels might occur. The relatively high critical oxygen concentration of 2.0 ppm for this species probably indicates a preference for moving, well-oxygenated waters. Field observations show that sticklebacks have a strong preference for flowing water, and are entirely absent in ponds lacking flow. With respect to physiological adaptations, the unarmored stickleback again appears to be intermediate between fishes such as carps, which inhabit stagnant waters and tolerate low 02 levels, and those inhabiting cold mountain streams (sal- . 6 TEMPERATURE AND OXYGEN TOLERAN CE LITERATURE CITED mish, F. W. H. 1964. Respiration of fishes with special emphasis on standard oxygen consumption III. Influence of oxygen. Canadian J. Zool., 42:355-366. rest, J. R. 1956. Some principles in the thermal requirements of fishes. Quart. Rev. Biol., 31: 4 . 75-87. ksen, C. H. 1976. Physiological ecology and management of the rare "southern" grayling, Thymallus aerials tricolor Cope. Verb. Inte • Verein. Limnol. 19. In press. ment on of, F. E. J. 1947. Effects of e - animal activity. Univ. Toronto Biol. Ser. No. 55, Publ. Ontario Fisheries Res. Lab., 68. OF THE UNARMORED STICKLEBACK 131 Fry, F. E. J., and J. S. Hart. 1948. The relation of temperature to oxygen consumption in the g fish. Biol. Bull., 94:66-77. temperature Graham, J. M. 1949. Some eff metabolism and and oxygen pressure o lontinalis. Salvelinus , activity of the speckle 7:270-288. Canadian J. Re ., and G. N. Somero. 1973. of biochemical adaptation. W. B. ders Co., 358 pp. Hochachka St ewis, D. B., M. Walkey, and H. J. B. Hannan. 1972. Some effects of low oxygen tensions on the distribution of the three-opined stickleback Gasterosteus aculeatus L. and the nine-opined stickleback Pungitius pungitius (L.). J. Fish. Biol., 4:103-108. . 1967. Responses of vertebrate poikilo- Lowe, C. H., and W. G. Heath. 1969. Behavioral and physiological responses to temperature in the : therms to temperature. In Thermobiology, (A. H. Rose, ed.) Academic Press. New York. desert pupfish (Cyprinodon tnacularius). Physiol. Zool., 42:53-59. . 1971. The effect of environmental factors the physiology of fish. In Fish physiology. Vol. 6. ( W. S. Hoar and D. 5. Randall, eds.) Academic Press, New York. pp. 1-98. Accepted for publication May I, 1976. FISH REMAINS FROM AN ARCHAEOLOGICAL SITE AT RANCHO CARRILLO ON THE SILVER STRAND, SAN DIEGO COUNTY, CALIFORNIA W. I. FOLLETT' Aesrancr: A collection of 170 fish remains from an archaeological site on the Silver Strand, species, all of which are ../immediately west of San Diego Bay, California, represents nine calijorniensis, Paralabrar sp., edible: Mustelus calijornicus, Sardinops sagas, A therinopsis argentea, and Roncador stearnsii, Genyonentas lineatus, Cyno.scion parripinnis, Sphyraena Pneuntatophorus japonicas. Remains of Cynoscion parvipinnis, a subtropical fish unknown from California in recent years, indicate the occurrence of a former warmwater fauna in this vicinity, probably during more than two centuries. probably caught in Remains of large Sphyraetta argentea and Pneurnatophorus japonicas, the ocean, suggest aboriginal use of the tule balsa. monids). ACKNOWLEDGMENTS We wish to thank the following people and organizations-the members and advisors of the Unarmored Threespine Stickleback Recovery Team and J. MacKinin, owner of the study site land, for their cooperation; James Herman, Thomas Williams and Deborah Flores for assistance in the field; the California State Department of Fish and Game for support through conti act AB-27. pis is a report on a collection of fish remains land masses, Coronado and Coronado Heights 10 km apart), and separating the moderrecovered by Carl L. Hubbs and Laurence G. (about ately surf-beaten ocean beach from the extensive Jones during July 1962 from an archaeological site mud flats and open water of San Diego Bay (U.S. at Rancho Carrillo, a former Spanish ranch on the Silver Strand (Coronado Strand), San Diego Co, Academy of SciCalifornia. The narrow, gently curving Silver ' 13W. Ichthyology, California94118. ,Strand is a sandspit connecting two low-terrace ences, San Francisco, California II- 132 BULLETIN SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUME 75 of 17.2 kg, but few exceed 107 cm or 4.1 kg (Fitch, 1972:104). It was said to be the commonest shark in southern California, great numbers being taken in seines and on setlines in San Diego Bay (Starks and Morris, 1907:163). Material: I vertebral centrum, diameter 5.7 mm. Identified from radiographs. For a photograph of a vertebral centrum of this species, see Follett ( I 966:fig. la). Records front other archaeological sites: Irvine, Ora-1190 (Follett, 1966:190, 191); Ventura, Ven-3 (Fitch, 1969a:62); Diablo Cove, SLO-2 (Fitch, 1972: 104), Coast and Geodetic Survey Chart 5107). The primitive topography of the Silver Strand and its vicinity is shown on a map of San Diego Bay made in 1782 by Juan Pantoja (Pomade, 1961:80). The approximate location of the site is indicated by Kroeber (1925:920, fig. 75, third site from bottom). Fish remains were recovered only at Stations B and C of this site. Station B represents a Diegueno camp with an abundance of pottery—a culture still extant when the Spaniards arrived (Moriarty, 1961:13, 16). This station is on the light-colored, unconsolidated upper sand, among low sand dunes cast of the south extension of Silver Strand State Park. It is at an elevation of 6.4 m above sea level, about 600 m from Stale Park Monument No. 5. A radiocarbon date of 270 ± 150 years B.P. (A.D. 1680) from material from the surface midden (LJ-210, 32°37'27"N, 117°08'09"W) was noted by Hubbs, Bien, and Suess (1962:212: 1965:104). Station C, 0.1 km northwest Irons Station B, very likely represents the late stage of the La JoIlan (prepottery) culture, which preceded the Diegueno; material Irons superficial layers of Station C is much more ancient than that from Station II. Station C is on the upper layer of the swale to the west of a sand ridge and at a much lower elevation, not much above sea level. A radiocarbon date of 3470 ± 175 years B.P. (1520 B.C.) from material from a depth of 5 to 15 ens (1J-593) was noted by Hubbs, Bien, and Suess (1965:104). Since the material from Station C appears to represent a redeposit from the adjacent slopes to the cast (Carl L. Hubbs, pers. comm.), the possibility cannot be excluded that the fish material at Station C was derived by surface wash Irons the Dieguetio material of Station B. The specimens are deposited at the Scripps Institution of Oceanography, under Accdsion No. 1962-VII:21. FISHES REPRESENTED The collection comprises 170 fish remains, most of which are incomplete or fragmentary. The stations and depths from which they were recovered are shown in Table I. At least nine species, referable to nine genera and seven families, are represented. Family Triakidae Mustehts californicus Gill, 1864 The gray smoothhound (Roedel and Ripley, 1950: fig. 37) attains a total length of 163 cm and a weight Family Clupeidae Sardinops sagas (Jenyns, 1842) The l'acific sardine (Hart, 1973:100, unnumbered fig.) has been known to attain a fork length of 41.3 cm, but usually does not exceed 33 cm (Roedel, 1953:33). A fork length of 41.3 cm would correspond to a total length of about 46 cm. At times, sardines have occurred in San Diego Bay in such abundance that bushels were left at low tide in the small puddles about piles (Eigenmann, 1892:136, 137, as Clupea sagas). Under such conditions, sardines could have been caught by a seine or a gill net. If the Dieguefic, used a seine, they might have manipulated it from balsas. By so doing, they could have avoided being stung by the round stingray, Urolopluts halleri Cooper, which has been very common in San Diego Bay (Eigenmann, 1892:134). Material: Articular (1 ), dentary (1 ), frontal (2). supplemental maxillary (1), opercle (3), preopercle ( I ), scale (4), sphenotic (1), and vertebra (10)— representing fish about 13 to 23 cm in total length. For figures of the skeletal elements of this species, see Phillips (1942). Records from other archaeological sites: Conejo Rock Shelter, Ven-69 (Follett, 1965:83); Tomales Bay, Mann Co (Follett, I968a:3); Century Ranch, LAn-229 ( Follett, 1968b: 134); Rincon Point, SBa-1 (Filch, 1969b:72, as Sardinops caeruleus); Swoape, Ven-168 (Fitch, 19696:72, as Sardinops caertrieus); Diablo Cove, SLO-2 (Fitch, 1972:105, as Sardinops caeruleus); San Buenaventura Mission, Ven-87 (Fitch, 1975:442). Family Athcrinidae Atherinopsis californiensis Girard, 1854 The jacksmelt (Jordan and Evermann, 1900:pl. 125 fig. 341) seldom exceeds a total length of 33 cm south of Point Conception (Cannon, 1964:234). The largest measured specimen was 44.4 cm in total length (Miller and Lea, 1972:82). Jacksmelt were abundant in San Diego Bay (Eigenmann, 1892:129, 145); they could have been caught by hook and line or by seine. Material: Articular ( I; from a fish about 23 cm in total length). 133 FISH REMAINS FROM ARCHAEOLOGICAL SITE Moriarty, 1961:104); Conejo Rock Shelter, Ven-69 Records f coin other archaeological sites: Ventura, Vert-3 (Fitch, 1969a:64); Shelter Hill, 4-Mm-14 (Follett, 1965:84); Ventura, Ven-3 (Fitch, 1969a:65); (Fitch, 19696:73); Swoape, (Follett, 1974:146); West Berkeley, CA-Ala-307 Rincon Point, SBa-1 Ven-168 (Fitch, 1969b:73); Diablo Cove, SLO-2 (Follett, 1975:78). (Fitch, 1972:111, 120); San Pedro, LAn-283 (Frey, 1974:92); San Buenaventura Mission, Ven-87 (Fitch, Family Serranidae 1975:449). Paralabrax sp. Cynoscion parvipinnis Ayres, 1862 Three species of bass (Paralabrar eh:donuts, P. maculatofasciants, and P. nebulifer) were abundant The shortfin corvina (Croker, 1932:0g. 89) was in the vicinity of San Diego and were known to enter San Diego Bay (Eigenmann, 1892:130, 150-151). said by Jordan and Gilbert (1881:48) to reach a length of about 61 cm and a weight of 3.6 kg. That All are food fish, readily caught by hook and line. appears to have been an inadvertent overstatement of In the skeletal elements represented in this collection, at that length: a specimen of normal apthese three species are but slightly differentiated from the weight collected by W. I. Follett and Richard S. one another. Identification is therefore to genus only. pearance, Croker off San Felipe, Baja California, measured 59.7 Material: Basipterygium (I), ceratohyal (1), cm in total length and weighed 1.8 kg. Shortfin cleithrum (1), vertebra (I)—representing fish to per- corvinas are readily caught by hook and line. This haps 46 cm in total length. species was common in southern California, where it Records front other archaeological sites: Century now seems to have been absent for many years, though Paralabrax 1963a:302, (Follett, Ranch, LAn-227 it remains abundant in central Baja California (Hubbs, clatitratus); Arroyo Sequit, LAn-52 (Follett, 1963b: 1948:466). It was originally described from the coast 115, Paralabrax clathratus); Irvine, Ora-I I8A and of Baja California at about 27°N (Ayres, 1862:156), Ora-119B (Follett, 1966:191, 193, Paralabrax macu- in the vicinity of Punta San Hip6lito; it was recorded latofasciatus); Corona del Mar, Ora-I90 (Fitch, 1967: from San Diego by Jordan and Gilbert (1880:28, as 188, Paralabrax sp.). Cynoscion magdalettae), Eigenmann (1892:130, 154), Starks and Morris (1907:198). Family Sciaenidae Material: Ceratohyal (1), epibranchial (I), epihyal Roncador stearnsii (Steindachner, 1875) (1), metapterygoid (1), palatine (1; fig. IA), and lower pharyngeal (1)—representing fish from about The spotfin croaker (Roedel, 1953:fig. 93) is to 51 cm in total length. known to attain a weight of 4.76 kg; a 673 mm speci- 43Although in certain skeletal elements this species is men weighed 4.2 kg (Baxter, 1960:39). Spotfin but slightly differentiated from the white seabass, croakers were said to be "only occasionally absent Cynoscion nobilis (Ayres), which was also abundant from" San Diego Bay (Eigenmann, 1892:152). They in the region of San Diego, the identification of the are readily caught by hook and line. present material appears satisfactory. In particular, Material: Dentary (1), maxillary (1), pelvic spine dorsal ridge of the palatine is more prominent (I), upper pharyngeal (I ), sagitta (1), scale (24), the in C. nobilis, the lower pharyngeal is wider in and vertebra (3)—representing fish about 48 to 56 than proportion to its length, the epibranchial is less striate, cm in total length. and the ceratohyal is more deeply concave along its Records from other archaeological sites: Scripps superior margin. Hubbs, and (Shttmway, Estate, San Diego Co Records front other archaeological sites: I have Moriarty, 1961:104); San Pedro, LAn-283 (Frey, found no published records of archaeological material 1974:92); San Buenaventura Mission, Ven-87 (Fitch, of this species. 1975:450). Family Sphyraenidac Genyonemus lineatus (Ayres, 1855) Sphyraena argentea Girard, 1854 The white croaker (Roedel, 1953:fig. 97) attains a The California barracuda (Watford, 1937:colored total length of 413 mm and a weight of 1.1 kg (Fitch, 66 fig, a) is known to attain a length of 118 cm 1975:450). It was abundant in San Diego Bay during pl. a weight of 8.2 kg (not the same fish) (Fitch and December and January (Eigenmann, 1892:130, 153), and Lavenberg, 1971:142). Barracudas were abundant at but it is caught throughout the year (Baxter, 1960:38). San Diego throughout the summer, the young (about In southern California this is one of the fishes most 30 cm in length), but not the adults, entering San readily caught by hook and line from the shore. Diego Bay in large schools (Eigenmann, 1892:147). Material: Maxillary (1), lower pharyngeal (I), sagitta (2), scale (2)—representing fish about 23 to The large individuals represented in the collection were probably caught in the ocean, presumably by hook 25 cm in total length. lute balsa. Records from other archaeological sites: Scripps and line trolled from a Material: Cleithrum (1), hyomandibular (2), Estates, San Diego Co (Shumway, Hubbs, and 1976 134 BULLETIN SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUME 75 1892:148, as Scomber colias). The large individuals represented in the collection were probably caught in the ocean by hook and line from a tule balsa; the small ones, in San Diego Bay by net or possibly by hook and line. Material: Anal spine (1), cleithrum ( I ), dentary ( I ), hyomandibular (1), interhaemal spine (1 ), maxillary (I), positemporal (1), premaxillary (2), pterygokl (1). and vertebra (69; one shown in fig. 1C)—representing fish about 18 to 50 cm in total length. Records from other archaeological sites: Century Ranch, LAn-227 and LAn-229 (Follett, I963a:304, 1968b:135; as Scomber japonicas diego); Arroyo Sequit, LAn-52 (Follett, I963b: 116, as Scomber japonicas diego); Conejo Rock Shelter, Ven-69 (Follett, 1965:84, as Scomber japonicas diego); Ventura, Ven-3 (Fitch, 1969a:65, as Scomber diego). DISCUSSION Indications of Former Warmtvater Faunas.—Re- mains of Cynoscion parvipinnis recovered from Figure I. Fish remains from Rancho Carrillo: A, right palatine, length 39 mm, of Cynoscion parripinnis (total length about 50 cm) from Station B, on slope, decimeter 2; B, right palatine (mesial aspect), length 73 mm, of Sphyraena argentea (total length about 92 cm) from Station B. on slope, decimeter 4; C. caudal vertebra, length 6.3 mm, of Pneumatophorus japonicas (total length about 28 cm) from Station B, on slope, decimeter I. hypural (2), maxillary ( I ), palatine (I; fig. IB), vertebra (7), vomer ( I )—representing fish about 86 to 110 cm in total length. Records front other archaeological sites: Century Ranch, LAn-227 and LAn-229 (Follett, 1963a:303; 1968b:135); Arroyo Sequit, LAn-52 (Follett, 1963b: 115): Conejo Rock Shelter, Ven-69 (Follett, 1965: 84); Ventura, Ven-3 (Fitch, I969a:64); San Buenaventura Mission. Ven-87 (Fitch, 1975:455); Swoape, Ven-168 (Fitch, 1975:466). Family Scornhridae Pneumatophorits japonicus (Houttuyn, 1782) The Pacific mackerel ( Watford. I937:colored pl. 37 fig. b) has been known to attain a total length of 63.5 cm and a weight of 2.9 kg, but usually is under 38 cm in length ( Roedel, 1953:84, as Plicanwtophoras diego). Half-grown individuals were exceedingly abundant in San Diego Bay during the autumn, but very few large ones were caught there (Eigenmann, this site strongly corroborate the conclusions expressed by Carl L. Hubbs, some 14 years before the Rancho Carrillo collection was made, that former northward occurrences of subtropical fishes along the southern California coast did not represent merely single-season waves, but longlasting warmwater faunas (Hubbs, 1948:465). These remains indicate that C. parvipinnis had persisted in the San Diego area for a considerable period of time, probably for more than two centuries. The material of this species was recovered Irons Station B at three distinct levels. The remains of 0--± 1 decimeter were presumably contemporaneous with the material from the surface midden that yielded a radiocarbon date of 270 ± 150 years B.P. (A.D. 1680). Presumably, the remains from decimeter 2 were older, and those from decimeter 3 were older still. Doubtless in addition to the long-lasting warm. water periods, there has been an occasional warmwater year that may have brought C. parvipinnis into southern California for a short interval. Between 1927 and 1929, shortfin corvinas from 1.4 to 1.8 kg in weight were netted on several occasions in salt ponds at the southern part of San Diego Bay (John E. Fitch, pers. comm.). These fish may have been holdovers in this favorable habitat from a possible northward occurrence of this species in I926—a year when other fishes are known to have strayed north of their usual range (Hubbs and Schultz, 1929). Another subtropical species, the bonefish, Alhula ',tripes 135 FISH REMAINS FROM ARCHAEOLOGICAL SITE 1976 TABLE I. Number of fish remains recovered from Rancho Carrillo site. On flat dm Mustelus californicus Sardinops sagar A therinopsis californiensis Paralabrar sp. Roncador stearnsii Genyonennis lineatus Cynoscion parvipinnis Sphyraena argentea Pnettttt atophorits japonicas 1 1 dm 2 1 " Station C. Station B. On slope ' dm 1 dm 2 dm 3 dm 4 II 1 I 5 1 3 8 2 lt dm 6 3 3 2 30 8 1 1 3 15 8 Surface misc. levels dm 1 dm 2 2 4 dm 3 1 1 2 1 4 2 3 1 7 6 20 A radiocarbon date of 270:-. 150 years B.P. (A.D. 1680) was obtained from Pismo clam (Tirtla stubortun) valves from Station B ( Dieguerio) surf ace midden. B.P. (1520 B.C.) was obtained from Pismo clam (TIvela stultornm) valves front r A radiocarbon date of 3470 -± 1755 years Station C (La Jollan1) at a depth of to 15 cm. (Linnaeus), is known to have occurred in some numbers in Los Angeles Co, California, during 1926. Between 25 September and 7 November 1926, while employed at the California State Fisheries Laboratory at Terminal Island, I caught three bonefish from the Terminal Island seawall, saw another, and examined two that another angler had caught. These observations, on five distinct occasions, caused me to believe, erroneously, that the bonefish was normally a member of the southern California fauna ( Follett, 1928 :285 ). Indications of Dieguelio Use of the Tule Balsa. —The presence of remains of barracudas and mackerel, of large size, indicates the use of some type of watercraft for fishing in the ocean. Large individuals of these two species were probably not caught from the shore, since they surely did not occur either on the mud flats or in the surf. According to Eigenmann (1892:147, 148), adult bariacudaenever or very rarely entered San Diego Bay, and very few large mackerel were caught there, although the young and half-grown of both species abounded in the bay. These remains suggest the use off San Diego, during aboriginal times, of a tule balsa such as that ascribed to the historic Dieguelio by Costanso (1910:121), Menzies (1924:340), Kroeber (1925:723), and Heizer and Massey (1953:295). Presumably, the Rancho Carrillo people were able to launch their balsas from the steep beach on the ocean side of their area of occupation. Once under way, they could have taken advantage of the local drift to reach (and to return from) an eddy in the lee of Point Loma, which may have been their most favorable fishing grounds. The dominant southeastward coastwise current, de- fleeted by Point Loma, creates a back-set beach drift along the Silver Strand and forms a counterclockwise eddy several kilometers in extent (Davis, 1933:235). That eddy would seem to have been a feeding area for the large barracudas and large mackerel that were captured by the people of Rancho Carrillo. ACKNOWLEDGMENTS I wish to express my appreciation to Carl L. Hubbs for permitting me to study this collection of fish remains and for making available to me an unpublished report on the site by Carl L. Hubbs and Laurence G. Jones; to Leonard J. V. Compagno (Stanford Univ.) for assistance in identifying the shark vertebra; to Lillian 3. Dempster (California Acad. Sci.) for assistance with the manuscript; to John E. Fitch (California Dept. Fish and Game) for identifying the otoliths, for providing the vernacular "Swoape Site" for Ven-168, and for information regarding shortfin corvinas in San Diego Bay; and to Maurice C. Giles (California Acad. Sci.) for enlarging the photographs. LITERATURE CITED Ayres, W. 0. 1862. [Description of Cynoscion parripinnis.] Proc. California Acad. Nat. Sci., 2:156-158: Baxter, J. L. 1960. Inshore fishes of California. California Dept. Fish and Game. Sacramento, 80 pp. Cannon, R. 1964. How to fish the Pacific coast. Lane Book Co., Menlo Park, California, Second Edition, xi + 337 pp. 136 BULLETIN SOUTHERN CALIFORNIA ACADEMY OF SCIENCES VOLUME 75 Costanso, M. 1910. The narrative of the Portola expedition of 1769-1770. (A. van Hemert-Engert and F. J. Teggart, eds.) Publ. Acad. Pac. Coast Hist., 1(4):91-159. 1963b. Fish remains from Arroyo Sequit shellmound (LAn-52), Los Angeles County, Croker, R. S. 1932. The white sea-bass and related 1965. Fish remains from the Conejo Rock Shelter site (Ven-69), Ventura County, California. Univ. California Los Angeles Archaeol. Surv. Ann. Rept., 7:81-90. species that are sold in California fish markets. California Fish and Game, I8(4):318-327. Davis, W. M. 1933. The lakes of California. California J. Mines and Geol., 29(I-2):175-236. Eigenmann, C. H. 1892. The fishes of San Diego, California. Proc. U.S. Natl. Mus., 15(897):123178. Fitch, J. E. 1967. Fish remains recovered from a Corona del Mar, California, Indian midden (Ora-190). California Fish and Game, 53(3): 185-191. . 1969a. Fish remains. primarily otoliths, from a Ventura. California, Chumash village site (Ven-3 ). Mem. So. California Acad. Sci., 8: 56-7 1 . . 19696. Fossil records of certain schooling fishes of the California Current System. California Mar. Res. Comm.. CalC0F1 Rept., 13:7180. California. California Div. Beaches and Parks Archaeol. Rept., No. 9:113-121. . 1966. Fish remains front archaeological sites at Irvine, Orange County, California. Univ. California Los Angeles Archaeol. Surv. Ann. Rept., 8:185-195. . 1968a. Fish remains from two submerged deposits in Tomales Bay, Mann County, California. Occas. Pap. California Acad. Sci., No. 67:1-8. I968b. Fish remains from Century Ranch site LAn-229, Los Angeles County, California. Univ. California Los Angeles Archaeol. Surv. Ann. Rcpt., 10:132-143. . 1974. Fish remains from the Shelter Hill site, Mann County, California. San Francisco State Univ. Treganza Anthrop. Mils. Pap., No. 15 (MAPOM Pap., No. 2):I45-159. -.1975. Fish remains from the West Berkeley shellmound (CA-Ala-307), Alameda County, California. Contrib. Univ. California Archaeol. -.1972. Fish remains, primarily otoliths, Res. Facility, No. 29:71-98. from a coastal Indian midden (SLO-2) at Diablo Cove, San Luis Obispo County, California. San Luis Obispo County Archaeol. Soc. Occas. Pap., No. 7:101-120. . 1975. 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