Adeonellopsis japonica ( Ortmann, 1890 )

Hirose, Masato, 2016, Diversity and distribution of adeonid bryozoans (Cheilostomata: Adeonidae) in Japanese waters, European Journal of Taxonomy 203 (203), pp. 1-41 : 12-17

Adeonellopsis japonica ( Ortmann, 1890)

Figs 7–9 , 10A

Adeonella japonica Ortmann, 1890: 54 , pl. 4, fig. 11.

Adeonella japonica – Okada 1920: 628, text fig. 6, pl. 8, fig. 9. — Okada & Mawatari 1935: 140, pl. XI, fig. 2. — Okada & Mawatari 1938: 460.

Adeona japonica – Canu & Bassler 1927: 34. — Mawatari 1952: 285 [figured specimen is not A. japonica ].

Adeonellopsis parvipuncta – Harmer, 1957: 798, pl. LIII, fig. 16.

Adeonellopsis japonica – Cheetham et al. 1980: 335–369. — Hirose et al. 2012: 121–136, fig. 9.2.

non Adeonellopsis parvipuncta MacGillivray, 1886: 135 , pl. II, fig. 4a.

Material examined

Lectotype [designated herein]

JAPAN: branched colony, Sagami Bay , 1882, 111̅ 277 m depth, collected by L. Döderlein, MZS 3-3 ( SEM specimen NSMT-Te741).

Paralectotypes [designated herein]

JAPAN: branched colonies, Jogashima, 1882, 185̅ 370 m depth, collected by L. Döderlein, MZS 3-4 ( SEM specimen NSMT-Te742); branched colony, Sagami Bay, 1882, collected by L. Döderlein, MZS 3-1; branched colonies, Sagami Bay, MZS 3-2 ( SEM specimen NSMT-Te739), “ 15 August 1889 / 29 July 1890, 111 m depth, southeast of Jogashima, Sagami Bay” is written on a small label, but the collector and the date are unclear).

Other material examined

JAPAN: eastern side of Sagami Bay (NSMT-BryR36, Bry R 71, Bry R 193, BryR206, BryR225, BryR254, BryR255, BryR259, BryR260, BryR261, BryR277, all in Emperor Showa collection); eastern side of Sagami Bay, collected by NSMT (NSMT-TeS15 to TeS18); NE off Ohakozaki, Otsuchi, collected by M. Hirose (NSMT-Te758, Te759, Te760); west-southwest of Jogashima, Sagami Bay, collected by H. Koutsuka and M. Hirose (NSMT-Te795, Te798); south of Kanae-zaki, Tosashimizu, Kochi (NSMT- Te1051); Seto, Kii Peninsula, Aug. 1936, probably specimen studied by Okada & Mawatari (1938) (SMBL-Brz.17, some fragments NSMT-Te1052); Pacific Ocean, off Honshu Island, 7 May 1900, Albatross Station D.3704, 107̅ 275 m depth ( USNM PAL 271600 A ̅D).

HAWAI’I: off Oahu Island, Albatross Station D.3916, 549̅ 605 m depth, collected 6 May 1902 ( USNM PAL 271601); south coast of Oahu Island, Albatross Station D.3916 ( USNM RB 8450).

Measurements

Autozooids. ZL: 404̅750 (553±71); ZW: 184̅419 (308±52); n = 115. SOrL: 69̅109 (87±11); SOrW: 56̅127 (102±14); n = 67. SAvL: 134̅232 (176±20); SAvW: 62̅133 (90±14); n = 81. FAvL: 75–138 (110±15); FAvW: 40–72 (59±8); n = 47. SpL: 16̅92 (43±16); SpW: 20̅75 (44±14); n = 70.

Gonozooids. ZL: 453̅722 (612±60); ZW: 329̅524 (415±53); n = 35. SOrL: 57 ̅125 (86±13); SOrW: 100̅166 (134±14); n = 34. SAvL: 109̅176 (135±17); SAvW: 52̅104 (73±12); n = 25. SpL: 102̅205 (146±24); SpW: 98̅174 (134±21); n = 33.

Vicarious avicularia at branch margins. L: 358̅399 (385±23); W: 141̅172 (158±16); n = 3.

Description

Colony yellowish brown, erect, dichotomously branching, irregularly spreading; up to 10 cm high ( Fig. 7A ). Branches flattened ( Figs 7B , 9A ), multiserial, with zooids opening both sides, rounded at end; 1.6–4.6 mm wide (average 2.8 mm; n = 27). Autozooids oval or hexagonal, outlined by a distinct deep marginal groove ( Figs 7C , 8C , 9B ), with 6–9 small pores along each lateral margin and two or three small frontal pores just proximal to orifice. Frontal shield umbonuloid ( Fig. 10A ). Young autozooids at growing margin of branch have concave frontal shields surrounded by broad, swollen rim with rows of granulation arranged perpendicular to margin ( Fig. 7 E–F); rim width 41–76 μm (average 57 μm) (n = 31). Mature frontal shield convex, entirely covered with minute granules. Spiramen abuts proximal end of suboral avicularium; subdivided into two or three openings separated by narrow septa, or lobate due to incomplete septa ( Fig. 7C ); with increased calcification, sometimes appearing as single opening ( Fig. 7D ); reduced in size during ontogeny, associated with depression of avicularian rostrum, sometimes occluded ( Figs 7D , 8D ). Secondary orifice nearly circular ( Fig. 7C ) or broader than long ( Figs 7D , 8C ); peristomial rim lacking; primary orifice submerged deep in peristome. Large, suboral avicularium in center of frontal shield, extending from spiramen to proximolateral corner of orifice, or nearly so, usually pointing distolaterally ( Figs 7C, F , 9B ); rostrum slightly raised distally, not hooked; mandible elongate-triangular; no crossbar. Additional smaller frontal avicularium often present near proximal end of zooid; identical in form to suboral avicularium; pointing in any direction ( Fig. 7C ). Gonozooids occur at branch bifurcations ( Fig. 8B, E ); larger than autozooids, with broader, slightly curving orifice; bearing suboral avicularium; smaller frontal avicularia either lacking ( Fig. 8B, E ) or up to three per zooid ( Fig. 7 G–H). Spiramen large, roughly circular in outline, divided into 6–10 pores ( Figs 7 G–H, 8B). Spiramen lacking marginal denticles in both autozooids and gonozooids ( Figs 7C, F , 8E ), although incomplete septa may appear as denticles. Vicarious avicularia at branch margins ( Figs 7D , 8A , 9 C–D) smaller than autozooids; triangular, with mandible directed distally. Basal part of branch consists of kenozooids with secondary orifice occluded by secondary calcification ( Fig. 8D ); about same size as autozooids, 486–631 μm long (average 541 μm) by 199–351 μm wide (average 314 μm) (n = 11). Kenozooids also bearing several small avicularia budded from areolae, near proximal margin of zooid, associated with other marginal pores ( Fig. 8D ), 101–152 μm long (average 121 μm) by 47–75 μm wide (average 59 μm) (n = 15).

Remarks

Ortmann (1890) first described Adeonellopsis japonica as Adeonella japonica , based on Döderlein’s specimens from Sagami Bay. Hayward (1988) discussed this species in his revision of Adeonella , though he did not examine Ortmann’s material; he argued that Adeonella japonica almost certainly belongs in Adeonella because of the elongate avicularia along the edge of the branches, as described by Ortmann. However, the frontal shield of A. japonica is umbonuloid, rather than the lepralioid frontal shield characteristic of Adeonella ; therefore, A. japonica clearly belongs in Adeonellopsis . Harmer (1957) reported a Japanese adeonid species resembling Adeonellopsis parvipuncta MacGillivray (1886) , which has two kinds of spiramina: a small, undivided, slightly denticulate single pore, or a much larger pore region comprising many pores. These features of the spiramen completely correspond to the spiramina of autozooids and gonozooids in A. japonica . Harmer (1957) noted that a few zooids in the middle of the branches have a larger spiramen, which is the condition of gonozooids in A. japonica . Furthermore, his sketch of the larger zooid also indicates a broader, slightly curved orifice. I thus consider Harmer’s A. parvipuncta to be a synonym of A. japonica .

Distribution

Japan: Sagami Bay, Sagami Sea, Suruga Bay, Kii Peninsula, Kouchi, and Otsuchi; 48.7–493 m depth. The current species has also been collected from Hawaii (off Oahu Island), 549–605 m depth, by the R/V Albatross (USNM 271601, IZ cat 8450; RB 8450) ( Fig. 9 ).

Okada & Mawatari (1938) reported this species from Kata, Seto, and off Wakayama, around the Kii Peninsula; the specimens in the SMBL include both A. japonica and Adeonella cf. lichenoides . Mawatari (1952) also reported A. japonica from Wakayama Prefecture, without a description, but with an illustration (pl. XII, fig. 1), which apparently shows proximally swollen zooids and the absence of suboral avicularia, and is more similar to A. cf. lichenoides . Adeonellopsis japonica is one of the common erect species in the Sagami Sea ( Hirose et al. 2012).

Figures

Fig. 7. Adeonellopsis japonica (Ortmann, 1890). A. Lectotype from among Ortmann’s specimens in the Döderlein Collection (MZS 3-3). B. Colonies collected at Otsuchi (NSMT-Te760). C. Autozooids with large suboral avicularium and biporous spiramen (NSMT-Te741, from lectotype, MZS 3-3). D. Lateral vicarious avicularia at branch bifurcation (NSMT-Te741, from lectotype, MZS 3-3). E. Young autozooids at distal end of branch (NSMT-Te741, from lectotype, MZS 3-3). F. Young autozooids, with biporous spiramen surrounded by thick, swollen rim bearing rows of granulation (NSMT-Te741, from lectotype, MZS 3-3). G. Autozooids and gonozooids at branch bifurcation (NSMT-Te742, from paralectotype MZS 3-4). H. Gonozooids showing large multiporous spiramen (NSMT-Te742, from paralectotype MZS 3-4). A–B = optical photographs; C–H = SEM images. Scale bars: A = 2 cm; B = 1 cm; C–D, F, H = 200 μm; E = 300 μm; G = 500 μm.

Fig. 8. Adeonellopsis japonica (Ortmann, 1890). A. Distal end of branch just starting to bifurcate, showing young autozooids and gonozooids (NSMT-BryR277). B. Enlargement of young gonozooids, showing peripheral rim with rows of granulation perpendicular to margin, and large multiporous spiramen (NSMT-BryR277). C. Autozooids in middle of branch, showing immersed spiramen (NSMT- Bry R 193). D. Basal part of branch, showing autozooids, and some kenozooids with closed orifice (NSMT-BryR36). E. Young gonozooids, showing distinct marginal pores and multiporous spiramen (NSMT-Te758). F. Distal end of branch, showing autozooid formation (NSMT-Te758). SEM images. Scale bars: A, C = 1 mm, B, D–E = 300 μm; F = 500 μm.

Fig. 9. Adeonellopsis japonica (Ortmann, 1890). A. Colony collected at Albatross Station D, off Oahu Island, Hawaii (USNM 271601). B. Autozooids of Hawaii specimen, showing suboral avicularia and biporous spiramen (USNM 271601, Hawaii). C. Autozooids and lateral vicarious avicularia at a branch bifurcation (USNM 271601 paper box, Hawaii). D. Enlargement of lateral vicarious avicularia at branch bifurcation (USNM 271601 paper box, Hawaii). A = optical photograph; B–D = photomicrographs. Scale bars: A = 5 mm; B, D = 300 μm; C = 500 μm.

Fig. 10. Interior frontal shield. A. Adeonellopsis japonica (Ortmann, 1890) (NSMT-Te1052). B. A. parvirostrum sp. nov. (NSMT-Te807). Arrowheads indicate ring scar. SEM images. Scale bars: A = 50 μm; B = 25 μm.