<<

Cainozoic Research, 4(1-2), pp. 19-25, February 2006

First post-Miocene Argonauta from , and its Palaeontological Significance

Susumu Tomida Masahiro Shiba² & Takami Nobuhara³ ¹,

1 Departmentof Management, Chukyo Gakuin University, Nakatsugawa City, Gifu, 509-9195, Japan.

'Natural History Museum, Tokai University, Shizuoka City, Shizuoka, 424-8620, Japan.

J .Science Education (Geology), Faculty of Education, Shizuoka University, Shizuoka City, Shizuoka, 422-8529, Japan.

Received 1 January 2003; revised version accepted 29 July 2003

A ofArgonautahians Lightfoot, 1786,an epipelagic octopod living now in tropical and subtropical oceans, was obtained from the upper Pliocene Dainichi Formation ofthe Kakegawa Group, central Japan. Its occurrence accompaniedby abundant tropical and subtropical benthic molluscs indicates the influence ofthe warm ocean current in the mid-latitudeofNW Pacific during the Late Pliocene

2 This is the first of formation warm episode (c. Ma). record argonautid species from a post-Miocene Japanese and marks the first ap-

in the NW Pacific. In the Middle around the pearance ofa living Argonautaspecies Miocene, many argonautid species flourished Japa- nese Islands, but none are known from the post-Miocene as a result ofthe Late Miocene intensifiedAntarctic glaciation (Robin, 1988)

and the terminal The is the known from the Pliocene the Miocene coolingevent (Beu, 1990). Argonauta only surviving genus to present. The fossil occurrenceofArgonautahians from the Japanese Pliocene suggests that this surviving lineage expandedits distribu- tion mid-latitude Pacific Pliocene into the NW during the warm climatic event.

Key : , Pliocene, words: Argonauta, Japan.

Introduction Geologic setting

In August, 2000, a fossil Argonauta was foundin the upper The Kakegawa Group is a Plio-Pleistocene fore-arc basin

Pliocene Tenno silty sand Member, Dainichi Formation, deposit of the Pacific side of SW Japan. The upper part of

Kakegawa Group, at Koichi, Kakegawa City, Shizuoka the Kakegawa Group is divided into three formations in

Prefecture, central Japan (Figure 1). The specimen is well ascending order: the KamiuchidaFormation(turbidite), the preserved and allows us to identify the fossil as Argonauta Dainichi Formation (shelf sand and silty sand), and the hiansLightfoot, 1786, an epipelagic octopod species living Hijikata Formation (slope silt) (Figure 2, 3) (Shiba et al., now in tropical and subtropical oceans. Shibaetal. (2001) 2000). Shibaet al. (2000) traced volcanic ash layers inter- figured the specimen, but with no systematic description, calated in the three formations and noted that the Kamiu- and did not mention its palaeontological significance. chida, Dainichi, and Hijikata Formations correspond to the

fossil have been all the and Many argonauts reported over lowstand, transgressive, highstand systems tract, re- world in strata ofthe Oligocene to Lower Pliocene, and are spectively, from the viewpoint of sequence stratigraphy.

important indicators of marine climate and palaeo-ocean currents (e.g.. Bellardi, 1872;Hilber, 1915; Martin, 1929; The Dainichi Formation unconformably covers Miocene

Fleming, 1945; Kobayashi, 1954a,b; Kaseno, 1955; To- basement rocks in the northwestern part (landward margin)

mida, 1983; Noda etal., 1986). of the basin, and the volcanic ash layers in the formation

is the first record of fossil from show coastal The ofthe Daini- This paper an argonautid a onlap patterns. geologic age post-Miocene Japanese formation, and it marks the first chi Formation is determined to be latest Pliocene (c. 2.0

Ma) several appearance of a living Argonauta species in the NW Pa- by chronological techniques, e.g., radiometric

cific. We provide a systematic description of Argonauta dating (Shibata et al., 1984) and microbiostratigraphy

hians Lightfoot, 1786 on the basis of the fossil specimen, (planktonic foraminifers: Ibaraki, 1986; calcareous nanno-

and discuss its palaeontological significance in relation to : Kameo, 1998).

Neogene climatic events. - 20 -

1. Index and ofthe northwestern of Shiba b-f: Plio- Figure map geological map part KakegawaCity (after et al., 2001). a: Holocene,

Pleistocene volcanic d: Tenno sand Member KakegawaGroup (b: ash, c: Hijikata Formation, silty ofthe Dainichi Formation, e: Dai-

nichi sand Member ofthe Dainichi f: Kamiuchida Miocene basement rocks. Black circle shows the fossil Formation, Formation), g:

locality from which was recovered.

2. of the and ofthe fossil of hians. Sea level Figure Upper Neogene sequence Kakegawa area, stratigraphic position locality Argonauta

eustatic curve redrawn from Malmgren & Berggren (1987). - 21 -

The in the Dainichi Formation transgression recognized Type-species — Linnaeus, 1758

corresponds to the global sea-level rise at 2.0 - 1.8 Ma

shown by Haq et al. (1987) and Malmgren & Berggren

(1987). Argonauta hians Lightfoot, 1786

Figures 5a-d

A columnar section for the fossil locality is shown in Fig-

3. The DainichiFormationis ofthe Dainichi Selective ure composed synonymy;

sand Member and the Tenno 1786 hians (nearshore facies) silty sand Argonauta Lighttoot, p. 44

1920 hians Member (off shore facies), in ascending order. The fossil Argonauta sensu Bulow-Trummer, p. 269.

(listed Argonauta occurs in a shell-rich sand lens intercalatedin only) 1984 Argonauta hians sensu Bandel & Dullo, 37, figs the Tenno silty sand Member. The sand lens is 40 cm in p. 14, 15. (figured only) maximumthickness, but pinches out rapidly. The sand lens 1993 Argonauta hians sensu Trego, 299, figs 1-J, K. contains clasts and p. muddy rip-up covers the underlying (figured only) silty sand with an erosional contact. Abundantwarm-water 2001 hians Shiba 14. Argonauta sensu et al., p. 86, fig. benthic mollusks occur in the sand lens. Almost all ofthem (figured only) are nearshore, sandy-bottom dwellers, such as Suchium

suchiense suchiense (Yokoyama), perterebra

Material — Yokoyama, Glossaulax hagenoshitensis (Shuto), Babylo- examined An almostcomplete femaleegg case

nia elata(Yokoyama), Scapharca castellata (Yokoyama), (Natural History Museum, Tokai University: Reg. no. is Glycymeris totomiensis Makiyama, Glycymeris albolineata NHMT-KM0023) laterally compressed and lacking the

hom-like rostrum on one side, collected from the (Lischke), Amussiopecten praesignis (Yokoyama), Chla- upper

Pliocene Dainichi Formation at Koichi, mys satoi (Yokoyama), Bathytormus foveolatus (Sowerby), Kakegawa City, Shizuoka Megacardita panda (Yokoyama), Callista chinensis (Hol- Prefecture, Japan (34°46'57” N, 138°0'48” E).

ten) and Paphia takanabensis Shuto. In contrast, the silty

— An rather sand beds just below and above the sand lens yield muddy- Description egg case calcareous, small, thin, bottom dwellers of lower-shelf and with no to slope depths, such as single-chambered septae. Spire coiling very

Yoldia similis Kuroda & Habe and The involutely and rapidly expanding. shallow and Fulgoraria sp. sand closed. section inflated, somewhat lens is interpreted as an infill of a small channel or a local slightly higher

than wide, and Outer side scour on the lower shelf to slope. broadly subtrapezoidal. flattened, wider toward the becoming gradually , and bicari-

nate; widely-spaced double keels formed by two rows of

rather large, obtuse, distally narrow and elongate spinose

nodules nodules; spinose in one row arranged alternately

relative to those in the other; the area between nodule rows

is smooth. Lateral sides ornamentedwith numerous, coarse,

and sinuous radial smooth, prorsiradiate, weakly ribs; ra-

dial 35+ in ribs, numberon the last whorl, bifurcating into

main and intercalatory ones and terminating at spinose

nodules on the keels. Aperture widely subtrapezoidal in section; hom-like a projection on apertural margin near the

umbilicus.

Measurements — Maximum diameter 58.9 mm, max.

width of half23.8 one mm, aperture height c. 44 mm.

Figure 3. Columnar section for the fossil locality. Arrow indi- Comparison — The living and extinct Argonauta species cates the horizon ofthe fossil locality, a: mud to silty sand, b: be classified into three can groups on the basis ofegg case fine-grained sand, c: mud to silty sand intercalating fine- morphology: the first represented by A. hians grained sand layers, d: muddy rip-up clasts, e: shell remains, Lightfoot, f: burrows. 1786 with widely spaced keels and smooth radial ribs, the

second A. represented by argo Linnaeus, 1758 with nar-

rowly spaced keels and smooth radial ribs, and the third

A. nodosa Systematic palaeontology represented by Lightfoot, 1786 with widely

spaced keels and nodulose radial ribs.

Class Cephalopoda Cuvier. 1797 Argonauta hians resembles the following extinct species of

Superorder Dibranchiata Owen, 1836 the first group: Argonauta sismondai Bellardi, 1872 from

Order Octopoda Leach, 1818 the Lower Pliocene of San Stefano, Roero, Torino, Italy;

Family Cantraine, 1841 Argonauta oweri Fleming, 1945 from the Lower Pliocene

Subfamily Argonautinae Berry, 1912 of New Zealand; batavus Martin, 1929 from the

Genus ArgonautaLinnaeus, 1758 Middle Miocene of Palembang, Sumatra. - 22 -

4. of fossil and Figure Geological range living argonautids

Argonauta hians most closely resembles A. sismondai pelago (Nesis, 1977), the Mediterranean and Red Sea

among them, but is distinguished from it by having a (Mienis, 1978), offPapua-New Guinea(Knight, 1989),and

somewhat larger egg case with thinnerand finer radialribs. off South Africa (Norman, 2000).

Moreover, spinose nodules of A. hians are fine, distally

narrow and elongate, whereas those of A. sismondai are

gibbous. Argonauta hians differs fromA. oweri by having Discussion

a smaller shell with coarser radial ribs and coarser spinose

nodules. Argonauta hians is distinguished from Kapal ba- Modern argonauts live and reproduce primarily in tropical

tavus by having an involute spire and less spaced keels. to subtropical seas at epipelagic depths, but they are fre-

drifted into quently neighbouring temperate seas by winds

Distribution— Pliocene: Piemont, Italy (Biilow-Trummer, and currents (Stadum & Saul, 2000). Unlike empty Nauti-

Ponte & lus 1920), near Rimini, Italy (Bandel Dullo, 1984). shells, cases are and without argonautid egg fragile sep-

and Upper Pliocene: Dainichi Formation in Shizuoka Prefec- tae camerae, that is lacking in the buoyancy, and are

ture, central Japan (Shiba et al., 2001; present study). Liv- unlikely to be transported far after death (Stadum & Saul,

ing: Warm Pacific and Atlantic oceanic seas (Abbott & 2000).

Pacific of Archi- Dance, 1998): e.g., W. and Sea E. Indian - 23 -

5. 1786 the Pliocene Dainichi Figure NHMT-KM0023. Argonautahians Lightfoot, from upper Formation, Koichi, KakegawaCity,

Shizuoka Prefecture, Japan; 5a - left lateral side, 5b - ventral side, 5c - right lateral side, 5d - anterior side. All figures xl .5 and with

whitening; Scale bar 10 mm).

Therefore, the fossil occurrence of a well-preserved egg the Late Pliocene, and indicate the strong influence of

case from the Dainichi Formation suggests that Argonauta warm palaeo-Kuroshio current.

hians were living in the epipelagic sea off central Japan in The palaeoclimatic view is consistent with that the Dainichi - 24 -

Formation benthic mol- yields many tropical to subtropical are also due to Dr. Tadashi Kubota, Director ofthe Natural lusks the Tokai for his kind represented by following species. (Luna- History Museum, University, support tica) marmoratus Linnaeus, Thiara scabra (Muller), and critical comment on this study.

Gyrineum cuspidatum (Reeve), Bathytormus foveolatus

(Sowerby) and other species (Tomida & Ozawa, 1996;

Ozawa et al„ 1998). The northern limits of their distribu- References tion are now off or Ryukyu Islands, but were ex- panded to central Japan during the peak of the climatic Abbott, R.T. & Dance, S.P. 1998, Compendium ofseashells. 3rd optimum around 2 Ma (Ozawa et al„ 1995). ed. 411 USA, California, Odyssey Publishing, pp. Besides the palaeoclimatological significance, even more Bandel, K. & Dullo. W.-C. 1984. Zur Schalenstruktur fossiler important is that this fossil occurrence is the first record of und rezenter Argonauta-Gehäuse(Octopoda, Cephalopoda).

from a formation and argonautids post-Miocene Japanese Natur und Mensch, JahresmitteilungenNaturhistorische Ge- marks the earliestappearance ofa living Argonauta species sellschaft Nuernberg, 1984: 33-38, in the NW Pacific. Bellardi, L. 1872. I molluschi dei terreni terziari del Piemonte

della Part 1, In contrast with the Pliocenefossil records, a considerable Liguria, Cephalopoda,Pteropoda, Heteropoda,

( et Memoria Reale numberofargonautid fossil specimens were reported from Tritonidae). Acca- demia Scienza Torino 2, 1-364. the MiddleMiocene (e.g., Hilber, 1915; Martin, 1929; Ko- A.G. 1973. the Aturia from the Beu, Nautiloidsof genus Upper- bayashi, 1954b; Kaseno, 1955; Noda et al., 1986). The most Miocene of Australia and New Zealand. The Science diversity ofargonautid generaalso peaked during the Mid- Reports of the Tohoku University, 2nd Series (Geology), Spe- dle Miocene and seven species of four genera flourished: cial Volume 6 (Professor Kotora Hatai Memorial Volume): Hil- Argonauta tokunagai Yokoyama, 1913, ,A. joanneus 297-308. ber, 1915, Kapal batavus Martin, 1929, Izumonauta lata Beu, A.G. 1990. Molluscan diversity of New Zealand Neogene Kobayashi, 1954b, I. kagana (Kaseno, 1955), I. kasata- stages: extinction and biostratigraphic events. Palaeogeogra- niensis and izumoensis (Kaseno, 1955) Mizuhobaris (Yo- phy. Palaeoclimatology, Palaeoecology77, 279-288. All the koyama, 1913). species disappeared prior to the Bulow-Trummer,E. 1920. Cephalopodadibranchiata. In: Diener,

Miocene, of C. (ed.). Fossilium 11: 1-271. Late and only three species three genera, Ar- Catalogus 1,

C.A. 1945. Some New Zealand gonauta itoigawai Tomida, 1983, Obinautilus awaensis Fleming, Tertiary . Transactions the Zealand 74,411- (Tomida, 1983) and Mizuhobaris lepta Saul & Stadum, of Royal Society of New

from 418. 2005, were reported the upper Miocene (Tomida, Haq, B.V., Hardenbol, J. & Vail. PR. 1987. Chronologyof fluc- 1989, 1996; Yanagisawa, 1990; Saul & Stadum, 2005). tuating sea levels since the Triassic. Science 235,1156-1167, the is the survivor Finally, genus Argonauta only through Hilber, V. 1915. Der alteste bekannte und erste miozane Argo- the Pliocene to the present (Figure 4). This declining trend nauta. Mitteilungen des Naturwissenschatlichen Vereins fur ofargonautid abundance and diversity is similar to that of Steiermark 51, 107-110. the nautiloidAturia. Most ofthe Aturia Neogene species Ibaraki, M. 1986. Neogeneplanktonic foraminiferalbiostratigra- became extinct at the Miocene and mid-upper boundary, phy ofthe Kakegawa area on the Pacific coast ofcentral Ja-

two A. coxi Miller and A. cubaensis only species. (Lea), pan. Reports of Faculty of Science, Shizuoka University survive to the end of the Miocene (Beu, 1973; Ozawa & 20,39-173.

K. 1998. Tomida, 1996), when Aturia went extinct. This declineof Kameo, Upper Neogene and Quaternary stratigraphy in

the Kakegawa district based onthe calcareous nannofossil da- the Neogene cephalopods was probably caused by the re- tum planes -with reference to the stratigraphic position ofthe markableregressions and climatic cooling in relation to the Tamari Formation. The Journal of the Geological Society of intensifiedAntarctic glaciation at 10 Ma(Robin, 1988) and Japan 104: 672-686. [in Japanesewith English abstract] the terminal Miocene event of cooling (e.g., Beu, 1990). Kaseno, Y. 1955. Neogene Argonautinae from Kahoku-gun, For example, in New Zealand 23 percent of the molluscan Ishikawa Prefecture, Japan. The Science Reports ofthe Kana- genera included Aturia was extinct at the end ofMiocene. zawa University 3, 339-344. The fossil occurrence of hians from the Argonauta Japa- Knight, R. 1989. Argonauta in New Guinea. Hawaian Shell nese Pliocene suggests that the surviving lineage of the News 37,5.

its distribution into the mid- genus Argonauta expanded Kobayashi, T. 1954a. A new Palaeogeneparacenoceratoid from latitude NW Pacific the Pliocene climatic during warm southern Kyushu in Japan. Japanese Journal ofGeology and

event. Geography 24, 181-184.

T. 1954b. of the Kobayashi, Izumonauta, a new genus Argo-

nautinae, with a note on their rare but gregariousfossil occur-

rence. Japanese Journal of Geologyand Geography25,21- Acknowledgements 34.

Lightfoot, J. 1786. A catalogue of the Portland Museum lately LouElla Saul of We are very grateful to Dr. R. the Inverte- the the property of Duchess Dowager ofPortland, deceased; brate Paleontology Section ofthe Natural History Museum Which will be sold by auction, by Mr. Skinner & Co.: of Los who useful information Angeles County, provided viii+194 pp. and this Sincere thanks improvements to manuscript. are C. 1758. Linnaeus, Systema naturae, edition 10, 1, 824 pp„ the extended to Mr. Yoshitsugu Okumura of Mizunami Holmiae.

for his of the Thanks Fossil Museum, cleaning specimen. Malmgren, B.A. & Berggren, W.A. 1987. Evolutionary changes - 25 -

in some late foraminiferal and C. 2000. Volcanic ash beds of the Neogene planktonic lineages Ogata, upper Kakegawa

their relationship to paleoceanographic changes. Paleoceano- Group. Science Reports of the Museum Tokai University 2,

graphy 2, 445-456. 53-108. [in Japanese with English abstract]

Martin, K. 1929.Bin neues Argonautiden-Geschlechtvon Suma- Shiba, M., Yokoyama, K., Shinmura. T. & Ito, Y. 2001. Excava-

tra. Leidsche Geologische Mededelingen5,221-226. tion report of Pliocene fossil Cetacea from the Kakegawa

Mienis, 1978. found - H.K. Who or Argonauta on the Group, Kamisaigo, KakegawaCity, central Japan. Geology

Mediterranean of Israel or in the Red Sea. Levantina and environment Science the Mu- coast sedimentary -. Reports of

15, 170-172. seum Tokai University 3, 77-89. [in Japanese with English

K.N. 1977. of Nesis, Biology paper , Argonautaboettgeri abstract]

and Argonauta hians (Cephalopoda, Octopoda), in western Shibata, K., Nishitnura, S. & Chinzei, K. 1984. Radiometric dat-

Pacific and seas of East of Indian Archipelago. Akademiia ing related to Pacific Neogene planktonic datum planes. In:

Nauk USSR, Moskva, Institut Okeanologii, Zoologicheskiy Ikebe, N. & Tsuchi, R. (eds.): Pacific NeogeneDatum Plane,

Zhumal 56,1004-1014.[in Russian, translated by M.J. Gry- University ofTokyo Press, 85-89. [in Japanese with English

gier], abstract]

Noda, H., Ogasawara, K. & Nomura, R. 1986. Systematic and Stadum, C.J. & Saul, L.R. 2000. Argonauts of late Miocene, Los

the Miocene Southern paleobiogeographic studies on Japanese argo- Angeles Basin, California.Annual Report, Western

nautid ",Nautilus” izumoensis. Science Reportof the Institute Society of Malacologists 32, 47-48.

of Geoscience, University ofTsukuba, Section B, Geological Tomida, S. 1983. Two new fossil Argonauta and firstly discov-

Science 7, 15-42. ered Aturia coxi Miller from the Late Tertiary ofBoso Penin-

Norman, M. 2000. World Guide. Cephalopodsa Germany Con- sula, Japan. Bulletin of Mizunami Fossil Museum 10, 107-

chBooks. 116. 320 pp.

Ozawa, T., Inoue, K., Tomida, S., Tanaka. T. & Nobuhara, T. Tomida, S. 1989. Fossil molluscan assemblagefrom the Neogene

1995. An outline of the Neogene warm-water molluscan fau- Senhata Formation around Nokogiriyama, Boso Peninsula,

nas in Japan. Fossils (PalaeontologicalSociety of Japan)58, Japan. Bulletin of Mizunami Fossil Museum 16, 85-108.

20-27. [in Japanese with English abstract] Tomida, S. 1996. Late Neogene tropical and subtropical mollus-

Ozawa, T., Tanaka, T. & Tomida, S. 1998. Pliocene to Early can faunas from the South Fossa-magnaregion, central Japan.

Pleistocene warm water molluscan fauna from theKakegawa Bulletin of Mizunami Fossil Museum 23, 89-140.

Group, Central Japan. Nagoya University Furukawa Mu- Tomida, S. & Ozawa, T. 1996. Occurrence ofTurbo (Lunatica)

1-205. seum, Special Report 7, species (Gastropoda: Turbinidae) in the upper Neogene of

Ozawa, T. & Tomida, S. 1996. Occurrence of Aturia coxi Japan and their implication for Neogene marine climates.

(Cephalopoda:Nautilida) from the uppermostMiocene of Ja- Tertiary Research 17, 65-71.

and its for Late Miocene marine climate in K.D. 1993. in the pan implication Trego, Questionable species cephalopodgenus

the northern Pacific. Journal of Paleontology 70, 795-798. Argonauta. The 36, 298-299.

Robin, G. de O. 1988. The Antarctic ice sheet, its history and Yanagisawa,Y. 1990. Age offossil Argonautidae(Cephalopoda)

level and based response to sea climatic changes over thepast 100 from Hokuriku province (central Honshu, Japan) on

million Pa- diatom Bulletin the years. Palaeogeography, Palaeoclimatology, biostratigraphy. of Geological Survey of

laeoecology 67,31-50. Japan 41, 115-127. [in Japanese with English abstract]

Saul, L.R. & Stadum, CJ. 2005. Fossil argonauts (Mollusca: Yokoyama, M. 1913. On two new fossil cephalopoda from the

Octopodidae) fromLate Miocene siltstones ofthe Los Ange- Tertiary of Izumo. Journal of Geological Society of Japan

les Basin, California. Journal ofPalaeontology79,520-531. 20, 1-3.

Shiba, M., Watanabe, K., Yokoyama, K., Sasaki, A., Udo, F. &