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146 W. Song et al.<br />

Petz et al. 1995, Wilbert 1995, Song <strong>and</strong> Packr<strong>of</strong>f 1997,<br />

Berger 1999, Song <strong>and</strong> Hu 1999).<br />

The current work forms part <strong>of</strong> a faunistic study <strong>of</strong><br />

ciliates in <strong>the</strong> coastal waters <strong>of</strong> <strong>the</strong> north China seas,<br />

which has been carried out for a period <strong>of</strong> over 10 years.<br />

In this paper, 4 previously known but poorly described<br />

species <strong>of</strong> hypotrichs, collected from <strong>of</strong>fshore mariculture<br />

waters near Qingdao, China, are redescribed following<br />

examination using modern techniques.<br />

MATERIALS AND METHODS<br />

Sample sites. All samples were collected from mariculture waters<br />

near <strong>the</strong> coast <strong>of</strong> Qingdao (Tsingtao, 36 o 08’N; 120 o 43’E), China.<br />

Bakuella agamalievi <strong>and</strong> Cyr<strong>to</strong>hymena marina were isolated (6 May<br />

1997) from a semi-closed pond used for mollusc culture (salinity<br />

10-15 ‰). Pseudokeronopsis flavicans was isolated on two occasions<br />

(6 <strong>and</strong> 12 May 1997) from <strong>the</strong> same sampling site as above.<br />

Two populations <strong>of</strong> Holosticha heter<strong>of</strong>oissneri were collected on<br />

separate occasions (31 March 1995 <strong>and</strong> 28 Oc<strong>to</strong>ber 1997) from an<br />

open scallop (Chlamys farreri) farming pond (salinity 31-32 ‰).<br />

General methods. After collection <strong>and</strong> isolation, specimens were<br />

maintained in <strong>the</strong> labora<strong>to</strong>ry for several weeks, ei<strong>the</strong>r as pure or raw<br />

cultures in Petri dishes, with rice grains as food source for bacteria.<br />

Observations on living morphology were undertaken using Nomarski<br />

optics. Protargol staining (Wilbert 1975) was performed for revealing<br />

<strong>the</strong> infraciliature <strong>and</strong> nuclear apparatus. Counts <strong>and</strong> measurements<br />

were made at a magnification <strong>of</strong> x1250. Drawings were made with <strong>the</strong><br />

help <strong>of</strong> a camera Lucida. Terminology is mainly according <strong>to</strong> Foissner<br />

(1982) <strong>and</strong> Hemberger (1985).<br />

<strong>New</strong> type specimens. Since no type specimens <strong>of</strong> Bakuella<br />

agamalievi, Cyr<strong>to</strong>hymena marina or Pseudokeronopsis flavicans are<br />

known <strong>to</strong> exist, one neotype slide <strong>of</strong> protargol impregnated cells <strong>of</strong><br />

each species has been deposited in <strong>the</strong> collection <strong>of</strong> <strong>the</strong> Natural<br />

His<strong>to</strong>ry Museum, London, UK with <strong>the</strong> following registration numbers:<br />

Bakuella agamalievi, 2001:1z:z8:01; Cyr<strong>to</strong>hymena<br />

marina, 2001:1z:z8:02; Pseudokeronopsis flavicans, 2001:1z:z8:03.<br />

In addition one paraneotype <strong>of</strong> each has been deposited in <strong>the</strong><br />

Labora<strong>to</strong>ry <strong>of</strong> Pro<strong>to</strong>zoology, Ocean University <strong>of</strong> Qingdao, People’s<br />

Republic China.<br />

RESULTS<br />

Bakuella agamalievi Borror & Wicklow, 1983<br />

(Figs 1-8, 52-53; Table 1)<br />

Syn. Holosticha manca sensu Agamaliev, 1972<br />

Borror <strong>and</strong> Wicklow (1983) reclassified this species<br />

but did not give a clear definition; hence we supply here<br />

<strong>the</strong> species diagnosis based on <strong>the</strong> present studies.<br />

Improved diagnosis. <strong>Marine</strong> Bakuella with elongated<br />

body shape, 100-150 x 30-50 µm in vivo; about<br />

30 adoral membranelles; on average, 33 left <strong>and</strong> 43 right<br />

marginal cirri; 4-7 fron<strong>to</strong>terminal, 4 frontal, one buccal<br />

<strong>and</strong> 4-7 transverse cirri; 9-13 pairs <strong>of</strong> midventral cirri<br />

distributed mostly in frontal area; 3-6 ventral rows with<br />

3-5 cirri each; consistently 3 dorsal kineties; numerous<br />

macronuclei; cortical granules grouped in short rows;<br />

one contractile vacuole in anterior 1/3 <strong>of</strong> cell.<br />

Morphological description. Body shape generally<br />

constant, length <strong>to</strong> width ratio about 3:1 with both ends<br />

well rounded; cell margins almost parallel with slight<br />

bulge in middle portion (Fig. 1). Buccal field about 1/3 <strong>to</strong><br />

2/5 body length (Fig. 1). Pellicle rigid, cortical granules<br />

colorless or slightly greenish when observed at low<br />

magnification, about 0.8 µm across, typically grouped<br />

<strong>to</strong>ge<strong>the</strong>r <strong>and</strong> sparsely arranged in short rows on both<br />

ventral <strong>and</strong> dorsal sides <strong>of</strong> cell (Figs 2, 3, 53). Cy<strong>to</strong>plasm<br />

colourless <strong>to</strong> grayish, usually containing numerous shiny<br />

globules (2-5 µm in diameter), which render <strong>the</strong> cell<br />

completely opaque. Food vacuoles large, usually several<br />

in number, <strong>and</strong> containing flagellate, small ciliates or<br />

bacteria. Contractile vacuole (CV) situated near left<br />

border about 1/3 <strong>to</strong> 2/5 <strong>of</strong> <strong>the</strong> way down <strong>the</strong> body (Figs<br />

1, 3). Pulsation interval ra<strong>the</strong>r long (up <strong>to</strong> 5 min). About<br />

50 ellipsoid macronuclear nodules, each ca 3-5 µm long<br />

<strong>and</strong> containing several large nucleoli; micronuclei globular,<br />

only recognized after protargol staining (Fig. 8).<br />

Locomotion moderately fast, crawling on substrate,<br />

sometimes jerking back <strong>and</strong> forth.<br />

Adoral zone <strong>of</strong> membranelles about 1/3 <strong>of</strong> cell length<br />

with distal end only slightly curved <strong>to</strong>wards right border.<br />

Bases <strong>of</strong> membranelles ca 7-8 µm in length. Cilia <strong>of</strong><br />

membranelles 15-20 µm long. Undulating membranes<br />

relatively long, slightly curved <strong>and</strong> noticeably crossed<br />

(Figs 4, 7).<br />

Somatic ciliature typical <strong>of</strong> genus. Three slightly<br />

enlarged, <strong>and</strong> one smaller, frontal cirrus arranged in<br />

anteriormost portion <strong>of</strong> frontal area; cirri about 20 µm<br />

long. One buccal cirrus near anterior 1/3 <strong>of</strong> undulating<br />

membranes (Fig. 4). Mostly 6 fron<strong>to</strong>terminal cirri relatively<br />

fine, located at anterior terminus <strong>of</strong> right marginal<br />

row (Figs 4, 7). Midventral rows composed <strong>of</strong> closely<br />

spaced oblique pairs <strong>of</strong> cirri <strong>and</strong> extending <strong>to</strong> about <strong>the</strong><br />

level <strong>of</strong> <strong>the</strong> cy<strong>to</strong>s<strong>to</strong>me (Fig. 7). Posterior <strong>to</strong> <strong>the</strong>se<br />

midventral rows are (usually) 4-5 ventral rows (arrows<br />

in Fig. 7) each with 3 <strong>to</strong> 5 cirri, which are also obliquely

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