{"id":32730,"date":"2021-08-12T11:11:46","date_gmt":"2021-08-12T09:11:46","guid":{"rendered":"https:\/\/opistobranquis.info\/?p=32730"},"modified":"2021-08-12T11:18:58","modified_gmt":"2021-08-12T09:18:58","slug":"noves-tecniques-moleculars-de-determinacio-taxonomica-en-heterobranchia","status":"publish","type":"post","link":"https:\/\/opistobranquis.info\/ca\/noves-tecniques-moleculars-de-determinacio-taxonomica-en-heterobranchia\/","title":{"rendered":"Noves t\u00e8cniques moleculars de determinaci\u00f3 taxon\u00f2mica en Heterobranchia"},"content":{"rendered":"<p>L&#8217;\u00fas de t\u00e8cniques moleculars per a investigar la hist\u00f2ria evolutiva dels grups animals i definir llinatges monofil\u00e8tics s&#8217;ha expandit exponencialment en les \u00faltimes d\u00e8cades, convertint-se en un dels passos essencials per aconseguir una bona taxonomia integrativa.<\/p>\n<p>La taxonomia integrativa \u00e9s un camp en constant evoluci\u00f3 basat en estudis multidisciplinaris que combinen diferents tipus de car\u00e0cters informatius que poguessin ser diagn\u00f2stics en diferents nivells taxon\u00f2mics i que sovint s&#8217;utilitzen per dilucidar les reconstruccions filogen\u00e8tiques que s&#8217;entenien malament en el passat. Aix\u00ed, la sistem\u00e0tica de molts t\u00e0xons s&#8217;ha resolt recentment mitjan\u00e7ant la combinaci\u00f3 de dades moleculars, ecol\u00f2giques, de comportament, morfol\u00f2giques i qu\u00edmiques (Ekimova et al., 2015; Fern\u00e1ndez-Vilert et al., 2021; Furfaro et al., 2018; Furfaro et al., 2021; Goodheart et al., 2018; Padula et al., 2016; Schillo et al., 2019).<\/p>\n<p>Pel que fa a l&#8217;an\u00e0lisi molecular, cont\u00ednuament s&#8217;estan buscant nous marcadors gen\u00e8tics que puguin ser diagn\u00f2stics a diferents nivells taxon\u00f2mics i que es puguin sumar als ja existents. L&#8217;ADN mitocondrial (ADNmt) \u00e9s, en la majoria dels casos, la millor eina per diferenciar els nivells taxon\u00f2mics m\u00e9s baixos, com ara esp\u00e8cies i g\u00e8neres, aix\u00ed com per investigar la diversitat cr\u00edptica i esdeveniments d&#8217;especiaci\u00f3 recents (Furfaro et al., 2021; Pola et al., 2007; Pola et al., 2012; Furfaro et al., 2016), per\u00f2 tamb\u00e9 t\u00e9 certes limitacions que es presenten en forma d&#8217;errors. Per evitar aquests errors se solen incloure marcadors nuclears en les an\u00e0lisis, per\u00f2 aquests s\u00f3n poc o gens informatius en els nivells taxon\u00f2mics inferiors (Furfaro et al., 2021; Furfaro et al., 2016b; Gali\u00e0-Camps et al., 2020).<\/p>\n<h4>L&#8217;estudi dels heterobranquis marins<\/h4>\n<p>En els heterobranquios marins (Mollusca, Gastropoda) la hist\u00f2ria evolutiva, quan s&#8217;estudia a nivell familia, es reconstrueix utilitzant principalment tres marcadors moleculars: dos gens mitocondrials, part de la subunitat I de la citocrom-oxidasa (COI) i part del ribosoma subunitat 16S, aix\u00ed com el gen nuclear histona 3 (H3). Mitjan\u00e7ant aquests marcadors s&#8217;ha aclarit la sistem\u00e0tica de diverses fam\u00edlies de heterobranquis i s&#8217;han resolt i corregit resultats erronis derivats d&#8217;estudis morfol\u00f2gics previs (Ekimova et al., 2015; Padula et al., 2016; Fern\u00e1ndez-Vilert et al., 2021) .<\/p>\n<p>Per\u00f2 resulta que la seq\u00fc\u00e8ncia prim\u00e0ria d&#8217;algunes regions de l&#8217;ARNr mitocondrial \u00e9s hipervariable i dif\u00edcil d&#8217;alinear entre esp\u00e8cies semblants. Aquesta hipervariabilidad d&#8217;ARNr tamb\u00e9 passa amb l&#8217;ARN 16S ribos\u00f2mic mitocondrial (ARNr 16S), utilitzat com a marcador cl\u00e0ssic, que es plega en diferents dominis i stem-loops (en catal\u00e0 es coneixen com a &#8220;tija en bucle&#8221;), un tipus d&#8217;estructures que s&#8217;origina quan dues regions d&#8217;una mateixa cadena, generalment amb una seq\u00fc\u00e8ncia de nucle\u00f2tids complement\u00e0ria si la llegim en sentits oposats, s&#8217;aparella base a base per formar una doble h\u00e8lix (o tija) que acaba en un bucle de bases desaparellades.<\/p>\n<div id=\"attachment_32732\" style=\"width: 910px\" class=\"wp-caption aligncenter\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-32732\" data-attachment-id=\"32732\" data-permalink=\"https:\/\/opistobranquis.info\/ca\/noves-tecniques-moleculars-de-determinacio-taxonomica-en-heterobranchia\/1280px-stem-loop-svg\/\" data-orig-file=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?fit=1280%2C872&amp;ssl=1\" data-orig-size=\"1280,872\" data-comments-opened=\"0\" data-image-title=\"Stem-loop\" data-image-description=\"\" data-image-caption=\"&lt;p&gt;Un ejemplo de una secuencia de ARN que producir\u00eda una estructura en horquilla o tallo-bucle es la siguiente:&lt;br \/&gt;\nAC&lt;strong&gt;GUGCCACG&lt;\/strong&gt;AUUCAA&lt;strong&gt;CGUGGCAC&lt;\/strong&gt;AG&lt;br \/&gt;\nEn esta secuencia, los nucle\u00f3tidos en negrita, que son complementarios, se emparejar\u00edan formando el tallo, y la secuencia central no complementaria formar\u00eda el bucle. Fuente: Wikipedia&lt;\/p&gt;\n\" data-large-file=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?fit=900%2C613&amp;ssl=1\" class=\"size-large wp-image-32732\" src=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?resize=900%2C613&#038;ssl=1\" alt=\"\" width=\"900\" height=\"613\" srcset=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?resize=1024%2C698&amp;ssl=1 1024w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?resize=300%2C204&amp;ssl=1 300w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?resize=150%2C102&amp;ssl=1 150w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/1280px-Stem-loop.svg_.png?w=1280&amp;ssl=1 1280w\" sizes=\"auto, (max-width: 900px) 100vw, 900px\" \/><p id=\"caption-attachment-32732\" class=\"wp-caption-text\">Un exemple d&#8217;una seq\u00fc\u00e8ncia d&#8217;ARN que produiria una estructura de tija en bucle \u00e9s la seg\u00fcent:<br \/>AC<strong>GUGCCACG<\/strong>AUUCAA<strong>CGUGGCAC<\/strong>AG<br \/>En aquesta seq\u00fc\u00e8ncia, els nucle\u00f2tids en <strong>negreta<\/strong>, que son complementaris, s&#8217;emparellarien formant la tija, i la seq\u00fc\u00e8ncia central no complementaria formaria el bucle. Font: Wikipedia<\/p><\/div>\n<p>Quan els alineaments basats en les seq\u00fc\u00e8ncies prim\u00e0ries no s\u00f3n f\u00e0cils d&#8217;aconseguir, \u00e9s una pr\u00e0ctica comuna i suggerida eliminar aquestes porcions per estabilitzar el senyal filogen\u00e8tica, de fet hi ha programes espec\u00edfics que ajuden a tallar aquestes regions hipervariables, per exemple, el programa GBlocks (Castresana, 2000; Talavera &amp; Castresana, 2007). L&#8217;eliminaci\u00f3 d&#8217;aquestes regions d&#8217;alineaci\u00f3 poc fiables del conjunt de dades \u00e9s promoguda per diversos treballs influents destinats a demostrar la millora del suport estad\u00edstic de les an\u00e0lisis filogen\u00e8tics quan es talla l&#8217;aleatorietat en les alineacions de seq\u00fc\u00e8ncia (K\u00fcck et al., 2010; Privman et al., 2012). No obstant aix\u00f2, aquesta pr\u00e0ctica significa que, inevitablement, algunes regions molt informatives, font de car\u00e0cters diagn\u00f2stics, sovint no es tenen en compte.<\/p>\n<p>La informaci\u00f3 derivada de l&#8217;estructura plegada de l&#8217;ARNr 16S no s&#8217;ha utilitzat fins ara en mol\u00b7luscs, a excepci\u00f3 de dos treballs de Furfaro et al. (2016b; 2016c), en els quals es va utilitzar aquest marcador gen\u00e8tic amb un parell de llimacs marins simp\u00e0trics i en els quals es va reportar una diversitat estructural 2D de l&#8217;ARNr 16S, principalment utilitzant les tiges en bucle L7 altament variable i L13 (Lydeard et a l&#8217; ., 2000), el que demostra que la informaci\u00f3 de les estructures secund\u00e0ries de l&#8217;ARN \u00e9s una valuosa eina de diagn\u00f2stic addicional per a la taxonomia integrativa i per a la delimitaci\u00f3 d&#8217;esp\u00e8cies (Furfaro et al., 2016b; 2016c).<\/p>\n<h4>El cas dels Myrrhinidae<\/h4>\n<p>En aquesta l\u00ednia Furfaro &amp; Mariottini (2021) han utilitzat la comparaci\u00f3 dels resultats de les an\u00e0lisis filogen\u00e8tics d&#8217;un conjunt de dades concatenades (el gen H3 nuclear i els marcadors mitocondrials COI i 16S), per investigar la sistem\u00e0tica a un nivell taxon\u00f2mic superior al nivell d&#8217;esp\u00e8cie. En particular, es va utilitzar com a cas d&#8217;estudi un clade polifil\u00e8tic (Furfaro &amp; Mariottini, 2020) compost per quatre g\u00e8neres classificats dins la fam\u00edlia Myrrhinidae Bergh, 1905: <em>Dondice<\/em> Marcus Er. 1958 (4 esp\u00e8cies); <em>Godiva<\/em> Macnae, 1954 (4 esp\u00e8cies); <em>Hermissenda<\/em> Bergh, 1879 (3 esp\u00e8cies) i <em>Phyllodesmium<\/em> Ehrenberg, 1831 (27 esp\u00e8cies). Van triar aquesta fam\u00edlia com a exemple per investigar la capacitat de les an\u00e0lisis d&#8217;estructura de plegat 2D de donar informaci\u00f3 \u00fatil sobre la sistem\u00e0tica d&#8217;aquest grup d&#8217;animals mitjan\u00e7ant l&#8217;observaci\u00f3 de caracter\u00edstiques morfol\u00f2giques i moleculars. L&#8217;elecci\u00f3 va estar basada en la peculiaritat dels g\u00e8neres involucrats, les seves hist\u00f2ries filogen\u00e8tiques no resoltes i la seva estrat\u00e8gia defensiva \u00fanica: la capacitat de autotomizar els cerata si se&#8217;ls molesta.<\/p>\n<p>Despr\u00e9s d&#8217;una an\u00e0lisi de l&#8217;estructura de tija en bucle de la mol\u00e8cula d&#8217;ARNr 16S, es va triar la tija-bucle L7 espec\u00edfica i altament variable com la m\u00e9s divergent i informativa per a aquest grup i es va revelar que era diagn\u00f2stica per a discriminar inequ\u00edvocament diferents estructures d&#8217;ARNr 16S. Aquest enfocament, basat en la descripci\u00f3 de la &#8220;morfologia molecular&#8221; d&#8217;aquesta regi\u00f3 molt variable de l&#8217;ARNr 16S mitocondrial (Furfaro et al., 2016b), pot considerar-se com una eina addicional per a la delimitaci\u00f3 d&#8217;esp\u00e8cies i la taxonomia integradora en heterobranquis i, m\u00e9s generalment, en els mol\u00b7luscs marins.<\/p>\n<div id=\"attachment_32733\" style=\"width: 682px\" class=\"wp-caption aligncenter\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-32733\" data-attachment-id=\"32733\" data-permalink=\"https:\/\/opistobranquis.info\/ca\/noves-tecniques-moleculars-de-determinacio-taxonomica-en-heterobranchia\/fig3\/\" data-orig-file=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/fig3.jpg?fit=672%2C637&amp;ssl=1\" data-orig-size=\"672,637\" data-comments-opened=\"0\" data-image-title=\"fig3\" data-image-description=\"\" data-image-caption=\"\" data-large-file=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/fig3.jpg?fit=672%2C637&amp;ssl=1\" class=\"wp-image-32733 size-full\" src=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/fig3.jpg?resize=672%2C637&#038;ssl=1\" alt=\"\" width=\"672\" height=\"637\" srcset=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/fig3.jpg?w=672&amp;ssl=1 672w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/fig3.jpg?resize=300%2C284&amp;ssl=1 300w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2021\/08\/fig3.jpg?resize=150%2C142&amp;ssl=1 150w\" sizes=\"auto, (max-width: 672px) 100vw, 672px\" \/><p id=\"caption-attachment-32733\" class=\"wp-caption-text\">Font:\u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0 \u00a0Furfaro &amp; Mariottini (2021)<\/p><\/div>\n<p>Els resultats van confirmar la validesa dels g\u00e8neres <em>Godiva<\/em>, <em>Hermissenda<\/em> i <em>Phyllodesmium<\/em> com es concebien tradicionalment, per\u00f2 tamb\u00e9 els van portar a proposar excloure <em>Dondice banyulensis<\/em> del g\u00e8nere <em>Dondice<\/em> i assignar-la com a esp\u00e8cie tipus d&#8217;un nou g\u00e8nere <em>Nemesis<\/em> gen. nov. No obstant aix\u00f2, la pres\u00e8ncia d&#8217;un hom\u00f2nim major, que t\u00e9 prioritat sobre el recentment declarat <em>Nemesis<\/em> Furfaro &amp; Mariottini, 2021, va anul\u00b7lar aquest \u00faltim nom de g\u00e8nere i va invocar la necessitat d&#8217;un nom de reempla\u00e7ament d&#8217;acord amb les regles de la ICZN. Per tant els autors van proposar <em>Nemesignis<\/em> com el nou nom de reempla\u00e7ament (Furfaro &amp; Mariottini, 2021b) en virtut de l&#8217;article 60.3 de la ICZN i, en conseq\u00fc\u00e8ncia, <em>Nemesignis banyulensis<\/em> (Portmann &amp; Sandmeier, 1960) com a la seva esp\u00e8cie tipus.<\/p>\n<div id=\"attachment_31095\" style=\"width: 910px\" class=\"wp-caption aligncenter\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-31095\" data-attachment-id=\"31095\" data-permalink=\"https:\/\/opistobranquis.info\/ca\/guia\/nudibranchia\/aeolidioidea\/nemesignis-banyulensis\/dondice-banyulensis-by-miquel-pontes-mpg_4610\/\" data-orig-file=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?fit=1280%2C850&amp;ssl=1\" data-orig-size=\"1280,850\" data-comments-opened=\"0\" data-image-title=\"Nemesignis banyulensis by Miquel Pontes\" data-image-description=\"&lt;p&gt;Nemesignis banyulensis by Miquel Pontes&lt;\/p&gt;\n\" data-image-caption=\"&lt;p&gt;Nemesignis banyulensis by Miquel Pontes&lt;\/p&gt;\n\" data-large-file=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?fit=900%2C598&amp;ssl=1\" class=\"size-large wp-image-31095\" src=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?resize=900%2C598&#038;ssl=1\" alt=\"Nemesignis banyulensis by Miquel Pontes\" width=\"900\" height=\"598\" srcset=\"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?resize=1024%2C680&amp;ssl=1 1024w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?resize=300%2C199&amp;ssl=1 300w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?resize=150%2C100&amp;ssl=1 150w, https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?w=1280&amp;ssl=1 1280w\" sizes=\"auto, (max-width: 900px) 100vw, 900px\" \/><p id=\"caption-attachment-31095\" class=\"wp-caption-text\"><em>Nemesignis banyulensis<\/em> per Miquel Pontes<\/p><\/div>\n<p>A m\u00e9s, el g\u00e8nere monoespec\u00edfic <em>Nanuca<\/em> <span style=\"font-family: Ubuntu;\">(anteriorment classificat dins la familia Facelinidae) <\/span>es sinonimitzava amb el g\u00e8nere <em>Dondice<\/em> i, en conseq\u00fc\u00e8ncia, el tax\u00f3 <em>Nanuca sebastiani<\/em> passava a dir-se <em>Dondice sebastiani<\/em> comb. nov. dins la familia Myrrhinidae. No obstant aix\u00f2, com <em>Nanuca<\/em> Er. Marcus, 1957 t\u00e9 prioritat sobre <em>Dondice<\/em> Er. Marcus, 1958, va resultar que les esp\u00e8cies d&#8217;aquest clade <em>Dondice<\/em> s&#8217;han de classificar sota <em>Nanuca<\/em>, quedant aix\u00ed: <em>Nanuca galaxiana<\/em> (Millen &amp; Hermosillo, 2012), <em>N. occidentalis<\/em> (Engel, 1925), <em>N. parguerensis<\/em> (Brandon i Cutress, 1985) i <em>N . trainitoi<\/em> (Furfaro &amp; Mariottini, 2020).<\/p>\n<h4>Conclusions<\/h4>\n<p>L&#8217;enfocament &#8220;morfol\u00f2gic molecular&#8221; de l&#8217;ARNr 16S va revelar ser una eina taxon\u00f2mica poderosa per delimitar tant a nivell d&#8217;esp\u00e8cie com de g\u00e8nere i va ser una forma \u00fatil de recuperar informaci\u00f3 que generalment es perd en les an\u00e0lisis filogen\u00e8tiques. Esperem veure aviat nous treballs emprant aquesta interessant metodologia.<\/p>\n<h4>Refer\u00e8ncies<\/h4>\n<ul>\n<li>Castresana, J. (2000) Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol. Biol. Evol., 17: 540\u2212552<\/li>\n<li>Ekimova, I., Korshunova, T., Schepetov, D., Neretina, T., Sanamyan, N. &amp; Martynov, A. (2015) Integrative systematics of northern and Arctic nudibranchs of the genus Dendronotus (Mollusca, Gastropoda), with descriptions of three new species. Zool. J. Linn. Soc., 173: 841\u2013886<\/li>\n<li>Fern\u00e1ndez-Vilert, R., Giribet, G., Salvador, X. &amp; Moles, J. (2021) Assessing the systematics of Tylodinidae in the Mediterranean Sea and Eastern Atlantic Ocean: Resurrecting Tylodina rafinesquii Philippi, 1836 (Heterobranchia: Umbraculida). J. Molluscan Stud. , 87: eyaa031<\/li>\n<li>Furfaro, G., Modica, M.V., Oliverio, M. &amp; Mariottini, P. (2016) A DNA-barcoding approach to the phenotypic diversity of Mediterranean species of Felimare Ev. Marcus &amp; Er. Marcus, 1967 (Mollusca: Gastropoda), with a preliminary phylogenetic analysis. Ital. J. Zool., 83: 195\u2013207\u00a0 DOI:<a href=\"https:\/\/doi.org\/10.1080\/11250003.2016.1150525\">10.1080\/11250003.2016.1150525<\/a>.<\/li>\n<li>Furfaro, G., Picton, B., Martynov, A. &amp; Mariottini, P. (2016b) Diaphorodoris alba Portmann &amp; Sandmeier, 1960 is a valid species: Molecular and morphological comparison with D. luteocincta (M. Sars, 1870). Zootaxa, 4193: 304\u2013316.<\/li>\n<li>Furfaro, G., Mariottini, P., Modica, M.V., Trainito, E., Doneddu, M. &amp; Oliverio, M. (2016c) Sympatric sibling species: The case of Caloria elegans and Facelina quatrefagesi (Gastropoda: Nudibranchia). Sci. Mar., 80: 511\u2013520<\/li>\n<li>Furfaro, G., Salvi, D., Mancini, E. &amp; Mariottini, P. (2018) A multilocus view on Mediterranean aeolid nudibranchs (Mollusca): Systematics and cryptic diversity of Flabellinidae and Piseinotecidae. Mol. Phylogenetic Evol., 118: 13\u201322, DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.ympev.2017.09.001\">10.1016\/j.ympev.2017.09.001<\/a><\/li>\n<li>Furfaro, G. &amp; Mariottini, P. (2020) A new Dondice Marcus Er. 1958 (Gastropoda: Nudibranchia) from the Mediterranean Sea reveals interesting insights into the phylogenetic history of a group of Facelinidae taxa. Zootaxa, 477731: 1\u201322<\/li>\n<li>Furfaro, G., Salvi, D., Trainito, E., Vitale, F. &amp; Mariottini, P. (2021) When morphology does not match phylogeny: The puzzling case of two sibling nudibranchs (Gastropoda). Zool. Scr. 2021, 1\u201316, DOI: <a href=\"https:\/\/doi.org\/10.1111\/zsc.12484\">10.1111\/zsc.12484<\/a>.<\/li>\n<li>Furfaro, G. &amp; Mariottini, P. (2021) Looking at the Nudibranch Family Myrrhinidae (Gastropoda, Heterobranchia) from a Mitochondrial \u20182D Folding Structure\u2019 Point of View. <em>Life<\/em> 11: 583. DOI: <a href=\"https:\/\/doi.org\/10.3390\/life11060583\">10.3390\/life11060583<\/a><\/li>\n<li>Furfaro, G. &amp; Mariottini, P. (2021b) <em>Nemesignis<\/em>, a replacement name for <em>Nemesis<\/em> Furfaro &amp; Mariottini, 2021 (Mollusca, Gastropoda, Myrrhinidae), preoccupied by <em>Nemesis<\/em> Risso, 1826 (Crustacea, Copepoda). <em>Life<\/em> 11: 809. DOI: <a href=\"https:\/\/doi.org\/10.3390\/life11080809\">10.3390\/life11080809<\/a><\/li>\n<li>Gali\u00e0-Camps, C., Carmona, L., Cabrito, A. &amp; Ballesteros, M. (2020) Double trouble. A cryptic first record of Berghia marinae Carmona, Pola, Gosliner &amp; Cervera, 2014 in the Mediterranean Sea. Mediterr. Mar. Sci., 21: 191\u2013200, DOI: <a href=\"https:\/\/doi.org\/10.12681\/Mms.20026\">10.12681\/Mms.20026<\/a>.<\/li>\n<li>Goodheart, J.A., Bleidi\u00dfel, S., Schillo, D., Strong, E., Ayres, D.L., Preisfeld, A., Collins, A.G., Cummings, M.P. &amp; W\u00e4gele, H. (2018) Comparative morphology and evolution of the cnidosac in Cladobranchia (Gastropoda: Heterobranchia: Nudibranchia). Front. Zool. , 15: 1\u201318<\/li>\n<li>K\u00fcck, P., Meusemann, K., Dambach, J., Thormann, B., von Reumont, B.M., W\u00e4gele, J.W.; &amp; Misof, B. (2010) Parametric and non-parametric masking of randomness in sequence alignments can be improved and leads to better resolved trees. Front. Zool., 7: 1\u201312<\/li>\n<li>Lydeard, C., Holznagel, W.E., Schnare, M.N. &amp; Gutell, R.R. (2000) Phylogenetic analysis of molluscan mitochondrial LSU rDNA sequences and secondary structures. Mol. Phylogenetics Evol., 15: 83\u2212102<\/li>\n<li>Martynov, A., Mehrotra, R., Chavanich, S., Nakano, R., Kashio, S., Lundin, K. &amp; Korshunova, T. (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia). ZooKeys, 818: 89<\/li>\n<li>Padula, V., Bahia, J., St\u00f6ger, I., Camacho-Garc\u00eda, Y., Malaquias, M.A.E., Cervera, J.L. &amp; Schr\u00f6dl, M. (2016) A test of color-based taxonomy in nudibranchs: Molecular phylogeny and species delimitation of the Felimida clenchi (Mollusca: Chromodorididae) species complex. Mol. Phylogenetics Evol. , 103: 215\u2013229<\/li>\n<li>Pola, M., Cervera, J.L. &amp; Gosliner, T.M. (2007) Phylogenetic relationships of Nembrothinae (Mollusca: Doridacea: Polyceridae) inferred from morphology and mitochondrial DNA. Mol. Phylogenetics Evol., 43: 726\u2013742.<\/li>\n<li>Pola, M., Camacho-Gar\u00eda, Y.E. &amp; Gosliner, T.M. (2012) Molecular data illuminate cryptic nudibranch species: The evolution of the Scyllaeidae (Nudibranchia: Dendronotina) with a revision of Notobryon. Zool. J. Linn. Soc., 165: 311\u2013336.<\/li>\n<li>Privman, E., Penn, O. &amp; Pupko, T. (2012) Improving the performance of positive selection inference by filtering unreliable alignment regions. Mol. Biol. Evol., 29: 1\u22125.<\/li>\n<li>Schillo, D., Wipfler, B., Undap, N., Papu, A., Boehringer, N., Eisenbarth, J.H. &amp; W\u00e4gele, H. (2019) Description of a new Moridilla species from North Sulawesi, Indonesia (Mollusca: Nudibranchia: Aeolidioidea)\u2014Based on MicroCT, histological and molecular analyses. Zootaxa, 4652: 265\u2013295<\/li>\n<li>Talavera, G. &amp; Castresana, J. (2007) Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst. Biol., 56: 564\u2212577<\/li>\n<\/ul>\n<p><p><strong>Citeu aquest article com: <\/strong><\/p><div style=\"display: block; background: #444444; padding: 10px 30px 10px 10px; border-radius: 5px; line-height: 18px;\"><p class=\"citacio\"><b>Pontes, Miquel<\/b> (2025) <em>\"Noves t\u00e8cniques moleculars de determinaci\u00f3 taxon\u00f2mica en Heterobranchia\"<\/em> a <em>OPK-Opistobranquis<\/em>. Publicat: 12\/08\/2021. Accedit: 27\/07\/2026. Disponible a (<a href=https:\/\/opistobranquis.info\/ca\/?p=32730>https:\/\/opistobranquis.info\/ca\/?p=32730<\/a>)<\/p><p><\/p><\/div><p><\/p><\/p>","protected":false},"excerpt":{"rendered":"<p>L&#8217;\u00fas de t\u00e8cniques moleculars per investigar la hist\u00f2ria evolutiva de grups animals i definir llinatges monofil\u00e8tics s&#8217;ha expandit exponencialment en les \u00faltimes d\u00e8cades, convertint-se en un dels passos essencials per aconseguir una bona taxonomia integrativa.<\/p>\n<p class=\"continue-reading-button\"> <a class=\"continue-reading-link\" href=\"https:\/\/opistobranquis.info\/ca\/noves-tecniques-moleculars-de-determinacio-taxonomica-en-heterobranchia\/\">Continua llegint<i class=\"crycon-right-dir\"><\/i><\/a><\/p>\n","protected":false},"author":5,"featured_media":31095,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[347,1304],"tags":[1436,1437,1438,1439,1440,1441,1442,1443,1444,1445,1409,1446,1447],"class_list":["post-32730","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-articles","category-biologia","tag-16s","tag-2d-rna-barcoding","tag-dondice","tag-genetica","tag-heterobranquios","tag-horquilla","tag-morfologia-molecular","tag-myrrhinidae","tag-nemesignis","tag-nidibranquios","tag-nudibranchia","tag-stem-loops","tag-tallo-bucle"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"https:\/\/i0.wp.com\/opistobranquis.info\/wp-content\/uploads\/2020\/12\/Dondice-banyulensis-by-Miquel-Pontes-MPG_4610.jpg?fit=1280%2C850&ssl=1","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/posts\/32730","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/comments?post=32730"}],"version-history":[{"count":10,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/posts\/32730\/revisions"}],"predecessor-version":[{"id":32742,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/posts\/32730\/revisions\/32742"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/media\/31095"}],"wp:attachment":[{"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/media?parent=32730"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/categories?post=32730"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/opistobranquis.info\/ca\/wp-json\/wp\/v2\/tags?post=32730"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}