155 lines
27 KiB
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155 lines
27 KiB
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<document id="8A61E96FF6416A48DEF346FF151909AD" ID-DOI="10.4467/16890027AP.14.016.1597" ID-ISSN="1689-0027" ID-Zenodo-Dep="10371261" IM.bibliography_approvedBy="felipe" IM.illustrations_approvedBy="felipe" IM.materialsCitations_approvedBy="felipe" IM.metadata_approvedBy="felipe" IM.tables_requiresApprovalFor="GgImagineBatch" IM.taxonomicNames_approvedBy="felipe" IM.treatments_approvedBy="felipe" checkinTime="1702473664736" checkinUser="tatiana" docAuthor="Jung, Jae Ho, Park, Kyung Min & Min, Gi Sik" docDate="2014" docId="03E487965D5FFFFEFF3A4FCB1A554658" docLanguage="en" docName="ActaProtozool.53.2.195-206.pdf" docOrigin="Acta Protozoologica 53 (2)" docSource="https://www.mendeley.com/catalogue/a3cffd2d-57a1-3cec-8819-13309dfcc513/" docStyle="DocumentStyle:64ABA4BEA387EE5C24A0DDEB32CC92E7.2:ActaProtozool.2014-.journal_article" docStyleId="64ABA4BEA387EE5C24A0DDEB32CC92E7" docStyleName="ActaProtozool.2014-.journal_article" docStyleVersion="2" docTitle="Pseudouroleptus jejuensis Jung & Park & Min 2014" docType="treatment" docVersion="2" lastPageNumber="201" masterDocId="FFDDFFEE5D59FFF8FF904A3B1F634009" masterDocTitle="Morphology and Molecular Phylogeny of Pseudouroleptus jejuensis nov. spec., a New Soil Ciliate (Ciliophora, Spirotrichea) from South Korea" masterLastPageNumber="206" masterPageNumber="195" pageNumber="201" updateTime="1702474269229" updateUser="ExternalLinkService" zenodo-license-document="CC-BY-4.0">
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<mods:title id="D00EB63E9F361B2DCAB16FAB4EC956CA">Morphology and Molecular Phylogeny of Pseudouroleptus jejuensis nov. spec., a New Soil Ciliate (Ciliophora, Spirotrichea) from South Korea</mods:title>
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<mods:namePart id="E3F0366D9159CC7E99C8664D4323EC21">Jung, Jae Ho</mods:namePart>
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<mods:namePart id="BDCEB7B314D8BFB97FEAC4FD8D2BC6A8">Park, Kyung Min</mods:namePart>
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<mods:namePart id="B1C2B533EC56854CFA5977CE278C18B2">Min, Gi Sik</mods:namePart>
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<mods:title id="614E7CAB60EDBBF7E6D5F4D807948E5F">Acta Protozoologica</mods:title>
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<mods:date id="8A4F405C501FDDE22068F97C2B7AF6CE">2014</mods:date>
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<mods:number id="EF58B884047412E5C4AC1CEC81981759">53</mods:number>
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<treatment id="03E487965D5FFFFEFF3A4FCB1A554658" ID-DOI="http://doi.org/10.5281/zenodo.10371238" ID-Zenodo-Dep="10371238" LSID="urn:lsid:plazi:treatment:03E487965D5FFFFEFF3A4FCB1A554658" httpUri="http://treatment.plazi.org/id/03E487965D5FFFFEFF3A4FCB1A554658" lastPageNumber="201" pageId="6" pageNumber="201">
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<subSubSection id="C357650B5D5FFFFEFF3A4FCB1D114600" box="[170,626,1519,1546]" pageId="6" pageNumber="201" type="nomenclature">
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<paragraph id="8BF236805D5FFFFEFF3A4FCB1D114600" blockId="6.[170,626,1519,1546]" box="[170,626,1519,1546]" pageId="6" pageNumber="201">
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<heading id="D0BA81EC5D5FFFFEFF3A4FCB1D114600" bold="true" box="[170,626,1519,1546]" fontSize="11" level="2" pageId="6" pageNumber="201" reason="4">
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<emphasis id="B939EA925D5FFFFEFF3A4FCB1D114600" bold="true" box="[170,626,1519,1546]" pageId="6" pageNumber="201">
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Ontogenesis of
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<taxonomicName id="4C4D4D035D5FFFFEFEF94FCB1E934603" authorityName="Jung & Park & Min" authorityYear="2014" box="[361,496,1520,1546]" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="jejuensis">
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<emphasis id="B939EA925D5FFFFEFEF94FCB1E934603" bold="true" box="[361,496,1520,1546]" italics="true" pageId="6" pageNumber="201">P. jejuensis</emphasis>
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</taxonomicName>
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(
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<figureCitation id="13762A055D5FFFFEFE6F4FD41D2F4603" box="[511,588,1519,1546]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Figs 4</figureCitation>
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,
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<figureCitation id="13762A055D5FFFFEFDC94FD41D0B4600" box="[601,616,1519,1545]" captionStart="Figs 5" captionStartId="8.[132,175,1604,1626]" captionTargetBox="[136,1458,226,1534]" captionTargetId="figure-6@8.[129,1467,223,1566]" captionTargetPageId="8" captionText="Figs 5A–D. Pseudouroleptus jejuensis, late (A, B) and post-dividers (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although they are still composed of dikinetids. A, B – dorsal (A) and ventral (B) views of late divider showing caudal cirri (arrows) and posteriorly migrating postperistomial cirrus (arrowheads). Note that the caudal cirri are not developed from dorsal kinety anlage 3. C, D – dorsal (C) and ventral (D) views of post-dividers. The two post-dividers were fixed from a single dividing cell im- mediately after the complete cell division. Some of parental dorsal bristles and cirri are still observed, and postperistomial (arrowheads) and caudal cirri (arrows) migrate forward to their final position. 3–5 – dorsal kineties 3–5. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371269" httpUri="https://zenodo.org/record/10371269/files/figure.png" pageId="6" pageNumber="201">5</figureCitation>
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)
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</emphasis>
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</heading>
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</paragraph>
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</subSubSection>
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<subSubSection id="C357650B5D5FFFFEFF3A4C201A554658" pageId="6" pageNumber="201" type="description">
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<paragraph id="8BF236805D5FFFFEFF3A4C201D704650" blockId="6.[132,779,1563,1945]" pageId="6" pageNumber="201">Some of dividers (i.e., middle, late, and post-dividers) were observed and described.</paragraph>
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<paragraph id="8BF236805D5FFFFEFF3A4C591E204790" blockId="6.[132,779,1563,1945]" pageId="6" pageNumber="201">
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<emphasis id="B939EA925D5FFFFEFF3A4C591EC34675" bold="true" box="[170,416,1634,1660]" pageId="6" pageNumber="201">Nuclear apparatus:</emphasis>
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Division of the nuclear apparatus proceeds as in most oxytrichids and urostylids (
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<bibRefCitation id="EFDC4B715D5FFFFEFF1C4C911E4A46CD" author="Berger H." box="[140,297,1706,1732]" pageId="6" pageNumber="201" pagination="1 - 1080" refId="ref4865" refString="Berger H. (1999) Monograph of the Oxytrichidae (Ciliophora, Hypotrichia). Monogr. Biol. 78: i - xii, 1 - 1080" type="journal article" year="1999">Berger 1999</bibRefCitation>
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, 2006). In mid-dividers, the macronuclear nodules fuse and become a single mass and micronuclei are inflated (
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<figureCitation id="13762A055D5FFFFEFE0D4CCB1D614702" box="[413,514,1776,1803]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Fig. 4A</figureCitation>
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). Next, the macronuclear mass divides twice and the inflated micronuclei become split and finish the division. The micronuclei always lie on the left of the macronuclear mass during the ontogenesis.
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</paragraph>
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<paragraph id="8BF236805D5FFFFEFCC64AE41B3D41E6" blockId="6.[816,1465,223,1617]" pageId="6" pageNumber="201">
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<emphasis id="B939EA925D5FFFFEFCC64AE41B4340F0" bold="true" box="[854,1056,223,249]" pageId="6" pageNumber="201">Oral apparatus:</emphasis>
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During the ontogenesis, the parental adoral membranelles are very likely inherited unchanged. In mid-dividers, the adoral membranelles of the opisthe form their definite structure and shape. The undulating membranes are still not separated in both the proter and opisthe. Next, the distal ends of adoral zones form arches like question mark. The undulating membranes become split.
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</paragraph>
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<paragraph id="8BF236805D5FFFFEFCC64BC31CA84323" blockId="6.[816,1465,223,1617]" pageId="6" pageNumber="201">
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<emphasis id="B939EA925D5FFFFEFCC64BC31B16421B" bold="true" box="[854,1141,504,530]" pageId="6" pageNumber="201">Ventral cirral pattern:</emphasis>
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In the mid-dividers, cirral anlagen I–VI are formed between right frontoventral row and adoral zone (
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<figureCitation id="13762A055D5FFFFEFBBF48051BEF4251" box="[1071,1164,574,600]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Fig. 4B</figureCitation>
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). Anterior portions of anlagen IV and VI are separated from the posterior portions. Left frontoventral row is very likely composed of these anterior portions of anlagen IV and VI, and entire anlage V. The rearmost cirrus of anlage IV migrates posteriorly below adoral zone (
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<figureCitation id="13762A055D5FFFFEFB6548D61A3A430E" box="[1269,1369,749,775]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Figs 4D</figureCitation>
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,
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<figureCitation id="13762A055D5FFFFEFAF748D61AD14301" box="[1383,1458,749,776]" captionStart="Figs 5" captionStartId="8.[132,175,1604,1626]" captionTargetBox="[136,1458,226,1534]" captionTargetId="figure-6@8.[129,1467,223,1566]" captionTargetPageId="8" captionText="Figs 5A–D. Pseudouroleptus jejuensis, late (A, B) and post-dividers (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although they are still composed of dikinetids. A, B – dorsal (A) and ventral (B) views of late divider showing caudal cirri (arrows) and posteriorly migrating postperistomial cirrus (arrowheads). Note that the caudal cirri are not developed from dorsal kinety anlage 3. C, D – dorsal (C) and ventral (D) views of post-dividers. The two post-dividers were fixed from a single dividing cell im- mediately after the complete cell division. Some of parental dorsal bristles and cirri are still observed, and postperistomial (arrowheads) and caudal cirri (arrows) migrate forward to their final position. 3–5 – dorsal kineties 3–5. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371269" httpUri="https://zenodo.org/record/10371269/files/figure.png" pageId="6" pageNumber="201">5B, D</figureCitation>
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, arrowheads).
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</paragraph>
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<paragraph id="8BF236805D5FFFFEFCC649081CB543BE" blockId="6.[816,1465,223,1617]" pageId="6" pageNumber="201">
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<emphasis id="B939EA925D5FFFFEFCC649081B0E4347" bold="true" box="[854,1133,819,846]" pageId="6" pageNumber="201">Marginal cirral rows:</emphasis>
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As usual the marginal cirral anlagen are developed within the parental rows and replace the parental structures. Dorsomarginal kineties are not found.
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</paragraph>
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<paragraph id="8BF236805D5FFFFEFCC649FB1BAC44C6" blockId="6.[816,1465,223,1617]" pageId="6" pageNumber="201">
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<emphasis id="B939EA925D5FFFFEFCC649FB1B4143D0" bold="true" box="[854,1058,959,986]" pageId="6" pageNumber="201">Dorsal ciliature:</emphasis>
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In the mid-dividers, the dorsal kineties 1–3 anlagen extend to the ends of the cell. Next, the kinety 3 anlage is split into three fragments, namely dorsal kineties 3–5 (
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<figureCitation id="13762A055D5FFFFEFB8E4E121B19444A" box="[1054,1146,1065,1091]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Fig. 4C</figureCitation>
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, double arrowheads). Caudal cirri are developed at the posterior portions of kineties 1, 2 anlagen only (
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<figureCitation id="13762A055D5FFFFEFBDD4E541BD24480" box="[1101,1201,1135,1161]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Figs 4C</figureCitation>
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,
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<figureCitation id="13762A055D5FFFFEFB514E541A6E4480" box="[1217,1293,1135,1162]" captionStart="Figs 5" captionStartId="8.[132,175,1604,1626]" captionTargetBox="[136,1458,226,1534]" captionTargetId="figure-6@8.[129,1467,223,1566]" captionTargetPageId="8" captionText="Figs 5A–D. Pseudouroleptus jejuensis, late (A, B) and post-dividers (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although they are still composed of dikinetids. A, B – dorsal (A) and ventral (B) views of late divider showing caudal cirri (arrows) and posteriorly migrating postperistomial cirrus (arrowheads). Note that the caudal cirri are not developed from dorsal kinety anlage 3. C, D – dorsal (C) and ventral (D) views of post-dividers. The two post-dividers were fixed from a single dividing cell im- mediately after the complete cell division. Some of parental dorsal bristles and cirri are still observed, and postperistomial (arrowheads) and caudal cirri (arrows) migrate forward to their final position. 3–5 – dorsal kineties 3–5. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371269" httpUri="https://zenodo.org/record/10371269/files/figure.png" pageId="6" pageNumber="201">5A, C</figureCitation>
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, arrows). The caudal cirri are not found from kinety 3 anlage, even in late and post-dividers (
|
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<figureCitation id="13762A055D5FFFFEFBAC4E8E1BA244C6" box="[1084,1217,1205,1232]" captionStart="Figs 5" captionStartId="8.[132,175,1604,1626]" captionTargetBox="[136,1458,226,1534]" captionTargetId="figure-6@8.[129,1467,223,1566]" captionTargetPageId="8" captionText="Figs 5A–D. Pseudouroleptus jejuensis, late (A, B) and post-dividers (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although they are still composed of dikinetids. A, B – dorsal (A) and ventral (B) views of late divider showing caudal cirri (arrows) and posteriorly migrating postperistomial cirrus (arrowheads). Note that the caudal cirri are not developed from dorsal kinety anlage 3. C, D – dorsal (C) and ventral (D) views of post-dividers. The two post-dividers were fixed from a single dividing cell im- mediately after the complete cell division. Some of parental dorsal bristles and cirri are still observed, and postperistomial (arrowheads) and caudal cirri (arrows) migrate forward to their final position. 3–5 – dorsal kineties 3–5. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371269" httpUri="https://zenodo.org/record/10371269/files/figure.png" pageId="6" pageNumber="201">Figs 5A, C</figureCitation>
|
||
).
|
||
</paragraph>
|
||
<paragraph id="8BF236805D5FFFFEFCC64EE31AD245CC" blockId="6.[816,1465,223,1617]" pageId="6" pageNumber="201">
|
||
<emphasis id="B939EA925D5FFFFEFCC64EE31B2244FB" bold="true" box="[854,1089,1240,1266]" pageId="6" pageNumber="201">Sequence analysis:</emphasis>
|
||
The SSU rRNA gene sequence of
|
||
<taxonomicName id="4C4D4D035D5FFFFEFCDF4EC71CB1451C" authorityName="Jung & Park & Min" authorityYear="2014" box="[847,978,1276,1301]" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="jejuensis">
|
||
<emphasis id="B939EA925D5FFFFEFCDF4EC71CB1451C" box="[847,978,1276,1301]" italics="true" pageId="6" pageNumber="201">P. jejuensis</emphasis>
|
||
</taxonomicName>
|
||
is 1,561 bp long and was deposited in the GenBank under accession number KF471024.
|
||
<taxonomicName id="4C4D4D035D5FFFFEFAE44F241B4C4552" authorityName="Jung & Park & Min" authorityYear="2014" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="jejuensis">
|
||
<emphasis id="B939EA925D5FFFFEFAE44F241B4C4552" italics="true" pageId="6" pageNumber="201">Pseudouroleptus jejuensis</emphasis>
|
||
</taxonomicName>
|
||
was clustered with
|
||
<taxonomicName id="4C4D4D035D5FFFFEFABB4F791C394576" authority="DQ" authorityName="DQ" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="caudatus">
|
||
<emphasis id="B939EA925D5FFFFEFABB4F791AD44552" box="[1323,1463,1345,1371]" italics="true" pageId="6" pageNumber="201">P. caudatus</emphasis>
|
||
DQ
|
||
</taxonomicName>
|
||
910904 and this clade was highly supported by all trees (NJ/ML/BI, 100/100/1.00) (
|
||
<figureCitation id="13762A055D5FFFFEFB2C4FB31A6545AB" box="[1212,1286,1416,1442]" captionStart="Figs 4" captionStartId="7.[125,168,1468,1490]" captionTargetBox="[127,1454,223,1416]" captionTargetId="figure-7@7.[123,1461,223,1456]" captionTargetPageId="7" captionText="Figs 4A–D. Pseudouroleptus jejuensis, middle (A, B) and late divider (C, D) after protargol impregnation. Note that the parental dorsal bristles are shown by single dots although still composed of dikinetids. The parental dorsal dikinetids become smaller and are less impregnated than newly developed one. A, B – dorsal (A) and ventral (B) views of middle divider showing dorsal kineties and cirral anlagen. C, D – dorsal (C) and ventral (D) views of late divider showing dorsal kinety 3 fragmentation (double arrowheads). Note that caudal cirri are developed at posterior end of kineties 1, 2 only (arrows). Postperistomial cirrus (arrowheads) is originated from the anlage IV and split from anterior part of the anlage. IV–VI – cirral anlagen IV–VI. Scale bars: 150 μm." figureDoi="http://doi.org/10.5281/zenodo.10371267" httpUri="https://zenodo.org/record/10371267/files/figure.png" pageId="6" pageNumber="201">Fig. 4</figureCitation>
|
||
). The K2P distance between
|
||
<taxonomicName id="4C4D4D035D5FFFFEFC4F4F901B0145CD" authorityName="Jung & Park & Min" authorityYear="2014" box="[991,1122,1451,1476]" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="jejuensis">
|
||
<emphasis id="B939EA925D5FFFFEFC4F4F901B0145CD" box="[991,1122,1451,1476]" italics="true" pageId="6" pageNumber="201">P. jejuensis</emphasis>
|
||
</taxonomicName>
|
||
and
|
||
<taxonomicName id="4C4D4D035D5FFFFEFB0B4F901A4145CC" box="[1179,1314,1451,1477]" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="caudatus">
|
||
<emphasis id="B939EA925D5FFFFEFB0B4F901A4145CC" box="[1179,1314,1451,1477]" italics="true" pageId="6" pageNumber="201">P. caudatus</emphasis>
|
||
</taxonomicName>
|
||
was 0.71%.
|
||
</paragraph>
|
||
<paragraph id="8BF236805D5FFFFEFCC64FF61A554658" blockId="6.[816,1465,223,1617]" pageId="6" pageNumber="201">
|
||
<emphasis id="B939EA925D5FFFFEFCC64FF61BED45E1" bold="true" box="[854,1166,1485,1512]" pageId="6" pageNumber="201">Occurrence and ecology:</emphasis>
|
||
As yet found only at the
|
||
<typeStatus id="54F688225D5FFFFEFCA14FCA1C074602" box="[817,868,1521,1547]" pageId="6" pageNumber="201">type</typeStatus>
|
||
locality of
|
||
<collectingRegion id="4989F8625D5FFFFEFC614FCA1B434602" box="[1009,1056,1521,1547]" country="South Korea" name="Jeju" pageId="6" pageNumber="201">Jeju</collectingRegion>
|
||
Island.
|
||
<taxonomicName id="4C4D4D035D5FFFFEFB154FCA1ADA4602" authorityName="Jung & Park & Min" authorityYear="2014" box="[1157,1465,1521,1547]" class="Hypotrichea" family="Oxytrichidae" genus="Pseudouroleptus" kingdom="Chromista" order="Oxytrichida" pageId="6" pageNumber="201" phylum="Ciliophora" rank="species" species="jejuensis">
|
||
<emphasis id="B939EA925D5FFFFEFB154FCA1ADA4602" box="[1157,1465,1521,1547]" italics="true" pageId="6" pageNumber="201">Pseudouroleptus jejuensis</emphasis>
|
||
</taxonomicName>
|
||
was isolated from a soil sample that was dark-brown coloured and covered with litter (
|
||
<taxonomicName id="4C4D4D035D5FFFFEFB284C0C1A4B4658" box="[1208,1320,1591,1617]" class="Magnoliopsida" family="Cannabaceae" genus="Celtis" kingdom="Plantae" order="Rosales" pageId="6" pageNumber="201" phylum="Tracheophyta" rank="species" species="undetermined">
|
||
<emphasis id="B939EA925D5FFFFEFB284C0C1B9F4658" box="[1208,1276,1591,1617]" italics="true" pageId="6" pageNumber="201">Celtis</emphasis>
|
||
sp.
|
||
</taxonomicName>
|
||
).
|
||
</paragraph>
|
||
</subSubSection>
|
||
</treatment>
|
||
</document> |