HOLOCENE OSTRACODS IN THE SOUTHERN BOSO PENINSULA

Paul M. Frydl
Mobil Oil Canada Ltd., Calgary, Canada

Systematic description




Subclass Ostracoda Latreille, 1806
Order Podocopida Sars, 1866
Superfamily Cypridacea Baird, 1845
Family Pontocyprididae G. W. Müller, 1894
Genus Argilloecia Sars, 1866
Argilloecia lunata n. sp.
Pl. 8, figs. 3-7; text.fig.31f.


Explanation of Plate 8
Figs. 1, 2, Trachyleberis straba n. sp.
1. Lateral view, left valve, female (UMUT-CA 15020), detail of the sinuous anterior ridge. × 220.
2. Internal view, right valve, female (UMUT-CA 15021), detail of the muscle scar. × 340.
Figs. 3-7, Argilloecia lunata n. sp.
3. Lateral view, left valve, female (UMUT-CA 15002). × 88. 4. Lateral view, left valve, male (UMUT-CA 15003). × 85. 5. Lateral view, right valve, female (UMUT-CA 15004). × 80.
6. Internal view, left valve, male (UMUT-CA 15001). × 83. 7. Internal view, right valve, female (UMUT-CA 15005). × 83.
Figs. 8-14, 16, 17, Semicytherura sabula n. sp.
8. Internal view, left valve, female (UMUT-CA 15024). × 136. 9. Dorsal view, carapace, male (UMUT-CA 15025). × 136. 10. Dorsal view, carapace, female (UMUT-CA 15023). × 136. 11. Internal view, right valve, female (UMUT-CA 15026). × 133. 12. Internal view, right valve, male (UMUT-CA 15027). × 133. 13. Lateral view, right valve, male (UMUT-CA 15028) × 133. 14. Lateral view, left valve, male (UMUT-CA 15029). × 133. 16. Lateral view, right valve, female (UMUT-CA 15040). × 135. 17. Lateral view, left valve, female (UMUT-CA 15041). × 129.
Figs. 15, 18-20, Nipponocythere haslata n. sp.
15. Internal view, left valve, female (UMUT-CA 15033). × 105. 18. Internal view, right valve, female (UMUT-CA 15034). × 105. 19. Lateral view, right valve, female (UMUT-CA 15032). × 105. 20. Lateral view, left valve, female (UMUT-CA 15035). × 107.

Etymology. —From "lunatus" [Latin, "bent into a crecsent"].

Type. —Holotype, UMUT-CA 15001, left valve, male (Pl. 8, fig. 6), obtained from sample no. 7, from coral bed at Koyatsu, West Coast Valley area, AL sub-biofacies.

Diagnosis. —Species of the genus Argilloecia characterized by relatively broadly rounded posterior margin.

Description. —Elongate in lateral outline, highest at the middle. Dorsal margin convex, ventral margin concave at anterior third. Anterior margin broadly rounded, posterior margin narrowly rounded, extremely at lower third.

Sexual dimorphism moderate: in male, anterior margin obliquely truncated, meets dorsal margin with blunt cardinal angle, posterior margin more narrowly rounded.

Dorsal outline elongate ellipsoid, anterior and posterior margins pointed, widest at the middle. Right valve larger than left, overlaps left valve at second anterior fifth and posterior two-fifths of length.

Surface smooth, normal pores few, scattered.

Inner lamella broad, line of concrescence runs parallel to the margins, coinciding with the inner margin in ventral area. Anterior and posterior vestibule large. Marginal pore canals simple, straight, numerous in anterior end, few in ventral part, moderately numerous in posterior end. Several false radial pore canals occur in posterior end. Muscle scar large, consisting of three anterior, two posterior closely set scars. Hinge adont.

Dimensions. —Holotype, male LV; L, 0.54, H, 0.17; paratypes, female, LV, UMUT-CA 15002 (Pl. 8, fig. 3); L, 0.50, H, 0.18; male, LV, UMUT-CA 15003 (Pl. 8, fig. 4); L, 0.52, H, 0.19; female RV, UMUT-CA 15004 (Pl. 8, fig. 5); L, 0.55, H, 0,20; female RV, UMUT-CA 15005 (Pl. 8, fig. 7); L, 0.54, H, 0.19.

Remarks. —This is the first species of the genus Argilloecia reported from Japan.

Occurrence. —Common in LK biofacies and AL sub-biofacies, rare in AA, KN, K sub-biofacies and sample 162 of the SN biofacies. Absent in Tateyama Bay.


Genus Propontocypris Sylvester-Bradley, 1947
Subgenus Propontocypris Sylvester-Bradley, 1947
Propontocypris (Propontocypris) sp.
Text-fig. 32d.

Illustrated specimen. —A left valve, UMUT-CA 15042.

Remarks. —Assigned to the genus Propontocypris on the basis of typical muscle scar, consisting of three inclined rows of 5 scars, elongated subtriangular outline, and simple marginal pore canals.

Occurrence. —Rare in NL, AA sub-biofacies, and SN biofacies.


Family Candonidae Kaufmann, 1900
Subfamily Paracypridinae Sars, 1923
Genus Paracypris Sars, 1866
Paracypris sp.
Text-fig. 32e.

Illustrated specimen . —A right valve, UMUT-CA 15006.

Remarks. —The elongated, posteriorly tapering carapace, bifurcating marginal pore canals, and a muscle scar consisting of three anterior, two posterior and one upper scars characterize this species as belonging to the genus Paracypris. The species closely resembles Pontocypris? sp. 6, described by Maddocks (1966, p. 44, 45, figs. 32 J-Q) in outline, but differs in muscle scars and marginal pore canals.

Occurrence. —Rare to common in LK biofacies and NK sub-biofacies, rare in A, SN biofacies and K sub-biofacies.


Superfamily Cytheracea Barid, 1850
Family Leptocytheridae Hanai, 1957
Genus Callistocythere Ruggieri, 1953
Callistocythere littoralis group
Callistocythere numaensis n. sp.
Pl. 9, figs. 1-3; text-fig. 31a.


Explanation of Plate 9
Figs. 1-3, Callistorcythere numaensis n. sp.
1. Lateral view, right valve (UMUT-CA 15007) × 100. 2. Lateral view, left valve (UMUT-CA 15008). × 100. 3. Internal view, left valve (UMUT-CA 15009). × 104.
Figs, 4-9, Callistocythere tateyamaensis n. sp.
4. Lateral view, right valve, male (UMUT-CA 15011). × 83. 5. Lateral view, left valve, female (UMUT-CA 15010). × 82. 6. Internal view, left valve, female (UMUT-CA 15012). × 83. 7. Lateral view, right valve, female (UMUT-CA 15013). × 78. 8. Lateral view, left valve, male (UMUT-CA 15043). × 84. 9. Internal view, right valve, female (UMUT-CA 15044). × 80.
Figs. 10, 11, Aurila sp. A
10. Lateral view, right valve (UMUT-CA 15016). × 69. 11. Lateral view, left valve (UMUT-CA 15017). × 63.
Fig. 12, Neomonoceratina sp.
Lateral view, left valve (UMUT-CA 15014). × 107.
Figs. 13, 14. Aurila sp. B.
13. Lateral view, right valve (UMUT-CA 15018). × 57. 14. Lateral view, left valve (UMUT-CA 15019). × 57.
Fig. 15, Hemicythere sp.
Lateral view, right vale (UMUT-CA 15015). × 83.
Figs. 16-18, Trachyleberis straba n. sp.
16. Internal view, left valve, male (UMUT-CA 15022). × 57. 17. Internal view, right-valve, female (UMUT-CA 15021). × 62. 18. Lateral view, left valve, female (UMUT-CA 15020) × 62.

Etymology. —Named after the type locality of the Holocene coral-bearing sediments, village of Numa.

Type. —Holotype, UMUT-CA 15007, right valve (Pl. 9, fig 1), obtained from sample no. 7, from the coral-bearing sediments in Koyatsu, West Coast Valley area. The sample belongs to the AL sub-biofacies.

Diagnosis. —Species of the genus Callistocythere characterized by prominent sub-vertical ridge in the posterocentral area.

Description. —Carapace oblong, reniform, highest at anterior cardinal angle. Dorsal margin gently convex upward, merges with obliquely rounded anterior margin. Anterior margin crenulated at lower half, ventral margin strongly concave at anterior third. Posterior margin meets dorsal margin at a distinct cardinal angle, gently rounded below.

First anterior marginal ridge prominent, sinuous, running from the upper fifth of anterior margin to anterior sixth of ventral margin. Dorsal marginal ridge obscuring the dorsal margin, running from the eye tubercle to posterior fourth, where it bifurcates, one part joining the first posterior marginal ridge, the other running vertically to the posterocentral area. Posterior marginal ridge prominent, running from the posterior fourth of dorsal margin to the ventral sinuosity. First ventral margin starts at the ventral sinuosity and runs obliquely upwards to the posteroventral area, where it turns at a steep angle and continues to the central area. Second ventral marginal ridge running parallel to the ventral margin from anterior fourth to little past half, where it joins the first ventral ridge. Surface ornamented with coarse reticulation. Eye tubercle low, but large. Normal pores moderate in number, simple type, scattered.

Inner lamella moderately wide, radial pore canals simple.

Dimensions. —Holotype, RV; L, 0.43, H, 0.23; paratypes, LV, UMUT-CA 15008 (Pl. 9, fig. 2); L, 0.42, H.0.23; LV, UMUT-CA 15009 (Pl. 9, fig. 3); L, 0.45, H, 0.24.

Remarks. —Development of the hingement and the short, unbranching radial pore canals seem to suggest that these are immature specimens; however, the width of the inner lamella indicates that the forms are adults.

Occurrence. —Common in AL sub-biofacies, rare in KN and K sub-biofacies.


Callistocythere tateyamaensis n. sp.
Pl. 9, figs. 4-9; text-fig. 31b.

Etymology. —Named after Tateyama City.

Type. —Holotype, UMUT-CA 15010, left valve, female (Pl. 9, fig. 5), obtained from sample no. 57, from the village of Shiomi in the West Coast Valley area. The sediment is coarse sand and the sample belongs to the AA sub-biofacies.

Diagnosis. —Species of the genus Callistocythere characterized by large depression developed between the first and second anterior marginal ridges, and reticulation of irregular outline.

Description. —Carapace thick, oblong, subreniform, highest at anterior cardinal angle. Anterior margin broadly obliquely rounded, dorsal margin gently arched. Posterior margin truncated above, meets dorsal margin with a distinct cardinal angle in the left valve, merges with dorsal margin in the right valve. Ventral margin slightly concave at the middle.

Surface sculptured with strong ridges and deep reticulation. First anterior ridge weak, runs from upper third of anterior margin to ventral sinuation. Second anterior ridge prominent, runs from anterior cardinal angle to lower third of anterior margin, where it joins the first anterior ridge. Third anterior ridge prominent, runs from anterior third of dorsal margin to anterior fifth of ventral margin, where it joins the first marginal ridge. Deep depression developed between the second and third marginal ridges and short, but very deep anteriorly oblique depression located behind the upper one third of the third marginal ridge.

Dorsal marginal ridge strong, obscuring the dorsal margin, running from anterior third of the dorsal margin to the posterior fourth, where it merges with the second posterior marginal ridge.

First posterior marginal ridge weak, running from posterodorsal cardinal angle to the ventral sinuation, obscures ventral margin behind the ventral sinuation. Second posterior marginal ridge very prominent, running from the posterior sixth of the dorsal margin, parallel to the posterior margin, and sloping obliquely downwards to the ventral sinuation. It runs parallel to the ventral margin and disappears a little anterior to the ventral sinuation. U-shaped depression present in dorsocentral area.

Anterocentral and posterocentral area ornamented with deep reticulations, commonly separated by thin, low partitions into two or more compartments. Eye tubercle obscure.

Inner lamella moderately wide along anterior and posteroventral margins, line of concrescence nearly coinciding with the inner margin. Anterior vetibule present but very narrow. Radial pore canals moderately numerous, repeatedly polyfurcate. Normal pores small, few, scattered.

Muscle scars located slightly below the center. Four adductor scars in a vertical row, the highest subtriangular, the middle two elongated, horizontal, the lowest circular. Selvage prominent. Snap-knob present in the right valve, corresponding snap-pit in the left. Hingement of the Callistocythere littoralis type.

Dimensions. —Holotype female LV; L, 0.55, H, 0.29; paratypes, male RV, UMUT-CA 15011 (Pl. 9, fig. 4); L, 0.54, H, 0.27; female LV, UMUT-CA 15012 (Pl. 9, fig. 6); L, 0.53, H, 0.26; female RV, UMUT-CA 15013 (Pl. 9, fig. 7); L, 0.58, H, 0.28; male LV, UMUT-CA 15043 (Pl. 9, fig. 8); L, 0.53, H, 0.28; female RV, UMUT-CA 15044 (Pl. 9, fig. 9); L, 0.53, H,0.28.

Occurrence. —Rare to common in AA sub-biofacies, rare in AL and NL sub-biofacies. In Tateyama Bay, common to rare in DS biofacies.


Family Cytheridae Baird, 1850
Subfamily Schizocytherinae Mandelstam, 1960
Tribe Paijenborchellini Deroo, 1966
Genus Neomonocertina Kingma, 1948
Neomonoceratina sp.
Pl. 9, fig. 12.

Illustrated specimen. —A left valve, UMUT-CA 15014.

Remarks. —This species somewhat resembles Neomonocertatina japonica (Ishizaki, 1966) in carapace outline and surface ornamentation, but differs by possessing a dorsally located, downturned caudal process.

Occurrence. —One specimen was found in sample 61 and one in sample 114, both from the Chikura area.


Family Hemicytheridae Puri, 1953
Subfamily Hemicytherinae Puri, 1953
Tribe Hemicytherini Puri, 1953
Genus Hemicythere Sars, 1925
Hemicythere sp.
Pl. 9, fig. 15.

Illustrated specimen. —A right valve, UMUT-CA 15015.

Remarks. —This species somewhat resembles Hemicythere? miii (Ishizaki, 1969) but differs by absence of ridges, and surface ornamentation, consisting of fine reticulation in the marginal areas and punctation in the central area.

Occurrence. —One valve was found in sample 162, belonging to the SN biofacies.


Tribe Aurilini Puri, 1974
Genus Awila Pokorný, 1955
Awila sp. A
Pl. 9, figs. 10, 11.

Illustrated specimens. —A right valve, UMUT-CA 15016; a left valve, UMUT-CA 15017.

Remraks. —This species strongly resembles Aurila cymba (Brady, 1869) in lateral and posterior outline and ornamentation. It. differs by the absence of dorsal, dorsoposterior ridge.

Occurrence. —Abundant in AL sub-biofacies. Common in AA, KN sub-biofacies and SN biofacies, sample 61 and some samples of NL sub-biofacies. In Tateyaroa Bay, common in SFS and Z biofacies, rare in some samples of CBM and IR biofacies.


Awila sp. B
Pl. 9, figs. 13, 14.

Illustrated specimens. —A right valve, UMUT-CA 15018; a left valve, UMUT-CA 15019.

Remarks. —This species resembles Awila sp. A, but in posterior view Awila sp. Bis oval in outline, while Awila sp. A is subtriangular. It further differs in possessing dorsal ridge ending in a tubercle in dorsoposterior area, while the ventral ridge is not as strongly developed as in Awila sp. A. Aurila sp. B might be a sexual dimorph of Aurila sp. A but even though the two forms commonly occur together their abundance is inversely proportional. Further, the differences in dorsal and ventral ridges become more prominent in immature forms.

Occurrence. —Abundant to common in A biofacies. Common in LK, LP, N, SN, and KS biofacies. In Tateyama Bay, common in some samples of the SFS, CBM, DM, IR, and Z biofacies. Rare live specimens found in samples 15 and 27 of the CBM and IR biofacies.


Family Trachyleberididae Sylvester-Bradley, 1948
Subfamily Trachyleberidinae Sylvester-Bradley, 1948
Tribe Trachyleberidini Sylvester-Bradley, 1948
Genus Trachyleberis Brady, 1898
Trachyleberis straba n. sp.
Pl. 8, figs. 1, 2; Pl. 9, figs. 16-18; text-fig. 31e.

Etymology. —From "strabus" [Latin, "squinting"]

Type. —Holotype, UMUT-CA 15020, left valve, female (Pl. 9, fig. 18), obtained from sample no. 107, from Tomoe River area near the village of Kotsuka. Sediment is silty sand, and the sample belongs to the KN biofacies.

Diagnosis. —Species of the genus Trachyleberis distinguished by the presence of a snapknob and absence of eye tubercle.

Description. —Carapace thick, rather small for the genus. In lateral view elongate, subtrapezoidal, tapering toward posterior end. Highest at anterior cardinal angle. Anterior margin broadly rounded. Dorsal margin straight, ventral margin slightly sinuate at the middle. Posterior margin truncated, meets dorsal and ventral margins at a distinct angle. Anterior, ventral, and posterior margins ornamented with spines and tubercles. Carapace ornamented with tubercles, normal pore canals few, mostly located at the top of tubercles.

Anterior marginal ridge prominent, arising from area below anterior cardinal angle and running parallel to anterior margin to the upper half, where it disappears abruptly. A short, slightly sinuous ridges runs vertically from the anterior cardinal angle to a little below the beginning of the anterior marginal ridge.

Marginal infold narrow, line of concrescence coincides with inner margin; no vestibule. Radial pore canals narrow, slightly curved, numerous in anterior and posterior ends. Hingement holamphidont, central bar crenulate. Muscle scars situated in subcentral depression and composed of a V-shaped frontal scar and four horizontally elongated muscle scars in a vertical row.

Sexual dimorphism distinct, males longer and lower than females.

Remarks. —Even though this species strongly resembles Trachyleberis scabrocuneata in shape and ornamentation, the absence of an eye tubercle is remarkable. This is perhaps the only blind species of the genus.

Dimensions. —Holotyps, female LV; L, 0.69, H, 0.40; paratypes, female RV, UMUT-CA 15021 (Pl. 9, fig. 17); L, 0.69, H, 0.39; male LV, UMUT-CA 15022 (Pl. 9, fig. 16); L, 0.77, H,0.41.

Occurrence. —Rare to common in K and KN sub-biofacies.


Family Bythocytheridae Sars, 1926
Genus Bythoceratina Hornibrook, 1952
Bythoceratina sp.

Remarks. —This species resembles Bythoceratina sp. A described by Ishizaki (1968). It differs from Bythoceratina hanaii by near absence of median sulcus, lack of reticulation and less protruding, more broadly rounded posterodorsal margin. Only immature specimens were found.

Occurrence. —Rare in SN and N biofacies.


Family Cytheruridae G, W. Mülller, 1894
Suobfamily Cytherurinae G. W. Müller, 1894
Genus Semicytherura Wagner, 1957
Semicytherwa sabula n. sp.
Pl. 8, figs. 8-14, 16, 17; text-fig. 31d.

Etymology. —From "sabulum" [Latin, "coarse sand"].

Type. —Holotype, UMUT-CA 15023, female carapace (Pl. 8, fig. 10), obtained from sample T10 taken in the Tateyama Bay at depth of about 10 m. Sediment was coarse to medium sand, and the sample belongs to the SCS biofacies.

Diagnosis. —Species of Semicytherura distinguished by its outline and surface ornamentation consisting of wrinkles in the anteroventral area.

Description. —Carapace small, thin, sexual dimorphism pronounced.

Female: Valves slightly asymmetrical, right valve higher than left. Valves reniform in lateral view, greatest height at the middle. Anterior margin broadly rounded, posterior margin more narrowly rounded, extremity at lower third. In right valve posterior margin slightly concave at upper half, meeting the dorsal margin at a distinct cardinal angle. In the left valve posterior margin merges with dorsal margin. Ventral margin gently concave at the middle. In dorsal view, carapace oblong oval, anterior pointed, posterior widely rounded, widest at the middle. Left valve overlaps the right at the anterior and posterior one-sixth; right valve overlaps left at the central two-thirds.

Male: Carapace elongated subrectangular in lateral view. Dorsal margin very gently archped, meets anterior margin with a distinct cardinal angle in left valve and merges with anterior margin in right valve. Anterior margin broadly rounded. Ventral margin gently concave at the middle. Posterior margin broadly rounded in left valve, more narrowly rounded in right valve. Extremity at slightly below middle. Posterior margin slightly concave in upper half in right valve, meeting dorsal margin at a small cardinal angle. In the left valve posterior margin merges with dorsal margin. In dorsal view, oblong, anterior narrowly pointed, posterior bluntly pointed, slightly compressed at middle, widest at posterior fourth.

Surface smooth except at anteroventral and posteroventral area, where it is sculptured with weak, wrinklelike, sinuous ridges parallel to margins. Normal pores few, scattered.

Infold and fused zone moderately wide: one-tenth length anteriorly, four-fifteenth length posteriorly in female, two-fifths in male. Radial pore canals moderate in number, mostly unbranched, often curved. False radial pore canals also present. Adductor muscle scars four in vertical row; frontal scars could not be observed. Hingement lophodont of Cytherwa type.

Dimensions. —Holotype female carapace; L, 0.33, W, 0.10; paratypes, female LV, UMUT-CA 15024 (Pl. 8, fig. 8); L, 0.33, H, 0.16; male carapace, UMUT-CA 15025 (Pl. 8, fig, 9); L, 0.33, W, 0.09; female RV, UMUT-CA 15026 (Pl. 8, fig. 11); L, 0.33, H, 0.15; male RV, UMUT-CA 15027 (Pl. 8, fig. 12); L, 0.32, H, 0.13; male RV, UMUT-CA 15028 (Pl. 8, fig. 13); L, 0.31, H, 0.13; male carapace, UMUT-CA 15029 (Pl. 8, fig. 14); L, 0.33, H, 0.12; female RV, UMUT-CA 15040; L, 0.31, H, 0.15; female LV, UMUT-CA 15041; L, 0,35, H, 0.15.

Occurrence. —Live specimens abundant in SCS biofacies of Tateyama Bay.


Family Loxoconchidae Sars, 1925
Subfamily Loxoconchinae, Sars, 1925
Genus Loxoconcha Sars, 1866
Loxoconcha sp.
Pl. 9, figs. 19, 20.

Illustrated specimens. —A right valve, UMUT-CA 15030; a left valve, UMUT-CA 15031.

Remarks. —A species of Loxoconcha characterized by somewhat converging dorsal and ventral margins and surface ornamented with fine reticulation. Only immature specimens were found.

Occurrence. —Abundant in sample 61 and common in sample 76, both from Chikura area. Common to rare in KS, N, and LP biofacies.In Tateyama Bay one specimen was found in sample 13 of the DS biofacies.


Subfamily Cytheromorphinae Mandelstam, 1960
Genus Nipponocythere Ishizaki, 1971
Nipponocythere hastata n. sp.
Pl. 8, fig. 15, 18-20; text-fig. 31c.

Etymology. —From "hastatus" [Latin, "spear-shaped"].

Type. —Holotype, UMUT-CA 15032, right valve, female, (Pl. 8, fig. 19), obtained from sample no. 7 from the coral-bearing sediment in Koyatsu, West Coast Valley area. The sample belongs to the AL sub-biofacies.

Diagnosis. —Species of the genus Nipponocythere distinguished by strong sinuation of the ventral margin.

Description. —Carapace rather flat, in lateral view elongate subtrapezoidal in outline, highest at anterior cardinal angle. Anterior margin broadly, evenly rounded, dorsal margin straight, ventral margin concave slightly anterior to middle. Posterior end obliquely truncated, narrowly rounded at lower third. Longest at lower third. Sexual dimorphism present, male lower and longer than female.

Surface smooth in anterior, ventral and posterior areas, closely punctate in the central and dorsal areas.

Inner lamella wide anteriorly, narrower ventrally and posteriorly. Line of concrescence parallel to outer, subparallel to inner margin. Vestibule moderate anteriorly, small posteriorly. Radial pore canals few, evenly spaced, straight. False radial pore canals present. Normal pores of simple type with a low lip, moderately numerous, scattered.

Muscle scar consisting of a row of four elongate adductor scars and one inclined reniform anterior scar. Hingement Loxoconchinae gongylodont. In the right valve, anterior tooth is surrounded dorsally by a crescent-shaped extension of the median groove. Median groove narrow, smooth; first posterior tooth small, second large.

Dimensions. —Holotype female RV; L, 0.43, H, 0.20; paratypes, female LV, UMUT-CA 15033 (Pl. 8, fig. 15); L, 0,43, H, 0.20; female RV, UMUT-CA 15034 (Pl. 8, fig. 18); L, 0.41, H,0.20.

Occurrence. —Rare to common in AL aub-biofacies and LK biofacies, rare in AA subbiofacies. Absent in Tateyama Bay.


Family Paradoxostomatidae Brady and Norman, 1889
Subfamily Paradoxostomatinae Brady and Norman, 1889
Genus Paradoxostoma Fisher, 1855
Paradoxostoma sp. 1
Text-fig. 32a.

Illustrated specimen. —A left valve, UMUT-CA 15036.

Remarks. —Species of the genus Paradoxostoma characterized by prominent caudal projection at the lower third of the posterior margin.

Occurrence. —Rare to common in A biofacies. In Tateyama Bay one specimen found in sample 18 (SCS).


Paradoxostoma sp. 2
Text-fig. 32c.

Illustrated specimen. —A right valve, UMUT-CA 15037.

Remarks. —The present species resembles Paradoxostoma lunatum illustrated by Okubo (1976), but differs in more narrowly rounded anterior and posterior margins.

Occurrence. —One specimen was found in sample 60 and one in sample 61.


Paradoxostoma sp. 3
Text-fig. 32b.

Illustrated specimen. —A right valve, UMUT-CA 15038.

Remarks. —This species resembles Paradoxostoma convexum illustrated by Okubo (1977), but differs in more sharply angulated dorsal margin and slightly concave posterodorsal margin.

Occurrence. —Rare in LK, SN and A biofacies.


Genus Cytherois G. W. Müller, 1884
Cytherois? sp.
Text-fig. 32f.

Illustrated specimen. —A right valve, UMUT-CA 15039.

Remarks. —This species somewhat resembles Cytherois zosterae Schornikov, but differs in the much more acutely rounded anterior and posterior margins.

Occurrence. —Rare to common in A biofacies, rare in LK and SN biofacies. In Tateyama Bay common in sample 7 of the CBM biofacies.


Location of samples

West Coast Valley Area: Samples 1, 3, 5, 7, 9, 11, 15, 26, 84-Coral-bearing sediments croping out in the upper part of a valley lying south of Koyatsu village. The outcrop is located about 600 m south of the coastal road. Samples 23, 24-Coral-bearing sediments from the type locality of the coral bed in Numa. Samples were collected from the banks of a water reservoir about 300 m south of the Numa village. Sample 36-Coral-bearing sediments exposed along the banks of a nameless tributary of the Shioiri River joining it slightly upstream of Kamisanakura village. The outcrop is located about 700 m south of the Kamisanakura village. Samples 55, 56, 57-Samples collected from an outcrop along the banks of the little stream flowing through the Shiomi village. Outcrop is located about 300 m south of the coastal road. Samples 87, 88-Outcrop on the bank of a small stream flowing through the Koyatsu valley. The outcrop is located about 40 m downstream of the Ko bridge.

Tateyama Area: Samples 40, 41, 71-Oyster reef located near the village of Nishigo, about 100 m downstream of Nishigo bridge. Samples 43, 44-Sediments above the oyster reef described above. Samples 51, 175-Samples collected from outcrops along the Heguri River upstream of the Nishigo bridge. Samples 67, 52-Sediments exposed along the banks of Taki River, about 1 km upstream from its confluence with Heguri River. Samples 53, 63-Outcrops located near the village of Kokonoe. Sample 53 from a road ditch about 500 m south of Kokonoe station, sample 63 from a construction excavation about 300 m northwest of the station.

Tomoe River Area: Samples 59, 60-Sediments exposed along a small stream flowing through the Tateyama Golf course. The outcrop is located about 500 m upstream from the coastal road. Samples 142, 144, 145, 157-Banks of Tomoe River east of the village of Daijingu. Samples 96, 99, 103,104,151-Banks of Tomoe River tributary flowing into the Tomoe River from the south, about 200 m upstream of the Daijingu village. Samples 162, 128, 110, 107, 111, 112, 123, 125, 126, 127-Outcrops exposed along the Tomoe River and its small tributaries in the vicinity of Kotsuka village. Samples 120, 122-Banks of Tomoe River about 400 m upstream of Kotsuka village. Sample 106-Little stream flowing through the village of Otsukuriba.

Chikura Area: Samples 61, 114-Banks of a north flowing tributary of the Seto River, flowing through an area locally known as Baba. Sample 118-Bank of a small stream flowing into Seto River north of Kanzawa Village. The outcrop is located about 300 m north of the village. Sample 76-Outdrop located above the Seto River, about 100 m west of Ikubyo Center.

Maruyama Area: Sample 134-Outcrop along the banks of Maruyama River, about 300 m east of the railway bridge. Sample 132-Banks of Nuruishi River, about 300 m downstream of the village of Numa.


Acknowledgment

I would like to thank Drs. K. Chinzei, I. Hayami, T. Ozawa, T. Yamaguchi, Y. Okada, M. Yajima and Messrs. K. Abe, R. Matsui, R. Tabuki from the University of Tokyo and Mr. Y. Matsushima from the Kanagawa Pref. Museum. They have aided me in innumerable ways and, through discussions and suggestions both in the field and laboratory, helped to steer this work in the proper direction, and offered the much needed help in the last stage of preparation of this manuscript. Miss M. Kouchi, from the department of Anthropology of the University of Tokyo, patiently helped me with the computer programs. I am particularly grateful to my supervisors, Dr. T, Hanai and Dr. T. Hamada, whose numerous suggestions greatly improved the results of this work.

While conducting research, I was a recipient of the Kajima Foundation Scholarship and Moriya Shogyo Scholarship. I would like to thank them deeply for their long and generous financial support.

Finally, I would like to thank my wife, Kumiko, for her patience and for drafting many of the figures in this report.




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