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TABLE 3 in Eight legs, two wings, one life for scientific research-celebrating the 80 birthday of Prof. Dr Jochen Martens
<p><b>TABLE 3:</b> Taxa honouring Jochen Martens until now (in alphabetical order within higher taxa, genera underlined). Total: 11 genera, 219 species, 1 subspecies [=231 taxa]</p><table><tbody><tr><th><b>ARACHNIDA</b></th><th>† <i>Mesobunus martensi</i> Huang, Selden & Dunlop 2009</th></tr></tbody><tbody><tr><th><b>Acari [2 species]</b></th><td><i>Metaphalangium martensi</i> Mitov, Perkovsky & Dunlop 2021</td></tr><tr><th><i>Malgacheliodes martensi</i> Ermilov, Hogo-Coetzee &</th><td><i>Phalangium martensi</i> Snegovaya, Cokendolpher & Zamani</td></tr><tr><th>Khaustov 2021</th><td>2021</td></tr><tr><th><i>Plonaphacarus martensi</i> Niedbala 2014</th><td><i>Pseudopachylus martensi</i> Kury 2006</td></tr><tr><th></th><td><i>Sabacon martensi</i> Tsurusaki & Song 1993</td></tr><tr><th><b>Araneae [29 species, 4 genera]</b></th><td><i>Sinonychia martensi</i> Zhang & Derkarabetian 2021</td></tr><tr><th><i>Agyneta martensi</i> Tanasevitch 2006</th><td><i>Spinopilar jocheni</i> Kury & Araujo 2021</td></tr><tr><th><i>Artema martensi</i> Huber 2021</th><td><i>Spinopilar magistralis</i> Kury & Araujo 2021</td></tr><tr><th><i>Belisana martensi</i> Yao & Li 2013</th><td><i>Spinopilar martialis</i> Kury & Araujo 2021</td></tr><tr><th><i>Brignoliella martensi</i> Brignoli 1972</th><td><i>Stenostygnus martensi</i> Mamani, Porto, Iglesias & Perez-</td></tr><tr><th><i>Camptoscaphiella martensi</i> Baehr 2010</th><td>Gonzalez 2021</td></tr><tr><th><i>Chalcoscirtus martensi</i> Zabka 1980</th><td><i>Texella martensi</i> Ubick 2021</td></tr><tr><th><i>Conothele martensi</i> Decae, Schwendinger &</th><td><i>Trogulus martensi</i> Chemini 1983</td></tr><tr><th>Hongpadharakiree 2021</th><td><i>Umbopilio martensi</i> Klimes 2006</td></tr><tr><th><i>Ctenus martensi</i> Jäger 2012</th><td></td></tr><tr><th><i>Dysdera martensi</i> Dunin 1991</th><td><b>Pseudoscorpiones [3 species]</b></td></tr><tr><th>† <i>Furcembolus martensi</i> Jiang & Li 2021</th><td><i>Ceriochernes martensi</i> Beier 1974</td></tr><tr><th><i>Harpactea martensi</i> Dunin 1991</th><td><i>Dactylochelifer martensi</i> Dashdamirov 2006</td></tr><tr><th><i>Hersilia martensi</i> Baehr 1993</th><td><i>Stenohya martensi</i> Schawaller 1987</td></tr><tr><th><i>Himalafurca martensi</i> Tanasevitch 2021</th><td></td></tr><tr><th><i>Himalaphantes martensi</i> Thaler 1987</th><td><b>Scorpiones [2 species]</b></td></tr><tr><th><i>Himalayana martensi</i> Grismado 2014</th><td><i>Ananteris martensi</i> Lourenço 2021</td></tr><tr><th><i>Himalcoeolotes martensi</i> Wang 2002</th><td><i>Himalayotityobuthus martensi</i> Lourenço 1997</td></tr><tr><th><i>Himalmartensus</i> Wang & Zhu 2008</th><td></td></tr><tr><th><i>Himalmartensus martensi</i> Wang & Zhu 2008</th><td><b>AVES [1 subspecies]</b></td></tr><tr><th><i>Iardinis martensi</i> Brignoli 1978</th><td><i>Parus (Periparus) ater martensi</i> Eck 1998</td></tr><tr><th><i>Leptonetela martensi</i> Zhu & Li 2021</th><td></td></tr><tr><th><i>Malinella martensi</i> Ono 1983</th><td><b>CRUSTACEA</b></td></tr><tr><th><i>Martensikara</i> Jäger 2021</th><td><b>Amphipoda [1 species]</b></td></tr><tr><th><i>Martensikara</i> <i>jocheni</i> Jäger 2021</th><td><i>Gammarus martensi</i> Hou & Li 2004</td></tr><tr><th><i>Martensinus</i> Wunderlich 1973</th><td></td></tr><tr><th><i>Martensopoda</i> Jäger 2006</th><td><b>Copepoda</b> <b>[1 species]</b></td></tr><tr><th><i>Mughiphantes martensi</i> Tanasevitch 2006</th><td><i>Parbatocamptus jochenmartensi</i> Dumont & Maas 1988</td></tr><tr><th><i>Pardosa martensi</i> Buchar 1978</th><td></td></tr><tr><th><i>Pseudopoda martensi</i> Jäger 2001</th><td><b>Isopoda [2 species]</b></td></tr><tr><th>† <i>Spatiator martensi</i> Wunderlich 2006</th><td><i>Pseudorthometopon martensi</i> Schmalfuss 1986</td></tr><tr><th><i>Suffasia martensi</i> Ono 2006</th><td><i>Rennelloscia martensi</i> Vandel 1973</td></tr><tr><th><i>Synagelides martensi</i> Bohdanowicz 1987</th><td></td></tr><tr><th><i>Walckenaeria martensi</i> Wunderlich 1972</th><td><b>INSECTA</b></td></tr><tr><th><i>Xysticus martensi</i> Ono 1978</th><td><b>Archaeognatha [1 species]</b></td></tr><tr><th></th><td><i>Machilontus martensi</i> Sturm 1990</td></tr><tr><th><b>Opiliones [22 species, 3 genera]</b></th><td></td></tr><tr><th><i>Anarthrotarsus martensi</i> Šilhavý 1967</th><td><b>Coleoptera [110 species, 1 genus]</b></td></tr><tr><th><i>Caucnemastoma martensi</i> Snegovaya 2011</th><td><i>Agathidium martensi</i> Angelini & De Marzo 1983</td></tr><tr><th><i>Cyphophthalmus martensi</i> Karaman 2009</th><td><i>Agathidium martensianum</i> Angelini & De Marzo 1994</td></tr><tr><th><i>Euphalangium martensi</i> Das & Bastawade 2006</th><td><i>Amara martensi</i> Hieke 1981</td></tr><tr><th><i>Fissiphallius martensi</i> Pinto-da-Rocha 2004</th><td><i>Amaurodera martensi</i> Coiffait 1982</td></tr><tr><th><i>Homolophus martensi</i> Staręga 1986</th><td><i>Amerizus martensi</i> Queinnec & Perreau 2002</td></tr><tr><th><i>Jime praecursor</i> Villareal, Kury & Colmenares 2021</th><td><i>Anisotoma martensi</i> Angelini & De Marzo 1994</td></tr><tr><th><i>Marayniocus martensi</i> Acosta 2006</th><td><i>Aphodius (Plagiogonus) martensi</i> Stebnicka 1986</td></tr><tr><th><i>Martensiellus</i> Schwendinger 2006</th><td><i>Aphthonaria martensi</i> Medvedev 1990</td></tr><tr><th><i>Martensolasma</i> Shear 2006</th><td><i>Apophylia martensi</i> Bezdĕk 2003</td></tr><tr><th><i>Martensolasma jocheni</i> Shear 2006</th><td><i>Atheta (Microdota) martensiella</i> Pace 1987</td></tr><tr><th><i>Martensopsalis</i> Giribet & Baker 2021</th><td><i>Augyles martensi</i> (Mascagni 1990)</td></tr><tr><th><i>Bacanius martensi</i> Gomy 1992</th><td><i>Nodina martensi</i> Medvedev 1992</td></tr><tr><th><i>Baeocera martensi</i> Löbl 1992</th><td><i>Nothochodaeus martensi</i> Huchet 2020</td></tr><tr><th><i>Blabs martensi</i> Skopin 1978</th><td><i>Oncosomechusa martensi</i> Pace 1987</td></tr><tr><th><i>Calathus martensi</i> Schmidt 1999</th><td><i>Oomorphoides martensi</i> Medvedev 1990</td></tr><tr><th><i>Calosoma davidi martensi</i> Paulus 1971</th><td><i>Oxypoda martensi</i> Pace 1984</td></tr><tr><th><i>Catops martensi</i> Perreau 1992</th><td><i>Paederidus martensi</i> Coiffait 1982</td></tr><tr><th><i>Cephennodes martensi</i> Jaloszyński 2017</th><td><i>Pelioptera martensi</i> Pace 1987</td></tr><tr><th><i>Cephennodes paramartensi</i> Jaloszyński 2017</th><td><i>Pelioptera martensianum</i> Pace 1987</td></tr><tr><th><i>Coelostoma martensi</i> Hebauer 2002</th><td><i>Penia martensi</i> Schimmel & Platia 1991</td></tr><tr><th><i>Conapion martensi</i> Korotyaev 1987</th><td><i>Phacophallus martensi</i> Bordoni 2002</td></tr><tr><th><i>Conapium martensi</i> Korotyaev 1987</th><td><i>Placusa martensi</i> Pace 1987</td></tr><tr><th><i>Corticaria martensi</i> Johnson 1977</th><td><i>Platydema martensi</i> Schawaller 1994</td></tr><tr><th><i>Cryptophagus martensi</i> Sen Gupta 1980</th><td><i>Pseudoplandria martensi</i> Pace 1987</td></tr><tr><th><i>Cychropsis martensi</i> Heinz 1994</th><td><i>Pterostichus martensi</i> Straneo 1977</td></tr><tr><th><i>Dermestes undulatus martensi</i> Kalik</th><td><i>Punicealis martensi</i> Kasantsev 1993</td></tr><tr><th><i>Dianous martensi</i> De Rougemont 1983</th><td><i>Pyrrhalta martensi</i> Medvedev & Sprecher-Uebersax 1999</td></tr><tr><th><i>Dima martensi</i> Schimmel & Platia 1991</th><td><i>Quedius (Microsaurus) martensi</i> Smetana 1975</td></tr><tr><th><i>Edaphus martensi</i> Puthz 1987</th><td><i>Scydmaenus martensi</i> Franz 1971</td></tr><tr><th><i>Elaphropus martensi</i> Baehr 2016</th><td><i>Scydmaenus paramartensis</i> Franz 1971</td></tr><tr><th><i>Emmelostiba martensiana</i> Pace 1987</th><td><i>Scymnus martensi</i> Canepari 1997</td></tr><tr><th><i>Encephalus (Ophnebioidea) martensi</i> Pace 1987</th><td><i>Silesis martensi</i> Platia & Schimmel 1991</td></tr><tr><th><i>Epuraea martensi</i> Kirejtshuk 1989</th><td><i>Silpha martensi</i> Emetz & Schawaller 1975</td></tr><tr><th><i>Euconnus (Napochus) martensis</i> Franz 1971</th><td><i>Someira martensi</i> Bordoni 2002</td></tr><tr><th><i>Euconnus martensianus</i> Franz 1971</th><td><i>Stenaesthetus martensi</i> Puthz 1987</td></tr><tr><th><i>Euconnus paramartensianus</i> Franz 1985</th><td><i>Stenus martensi</i> Puthz 1983</td></tr><tr><th><i>Eusphalerum martensi</i> Zanetti 2003</th><td><i>Stenus martensianus</i> Puthz 2013</td></tr><tr><th><i>Falsopodabrus martensi</i> Wittmer 1979</th><td><i>Strongylium martensi</i> Masumoto & Schawaller 2010</td></tr><tr><th><i>Freudeia martensi</i> Kaszab 1977</th><td><i>Tachinus (Tachinoderus) martensi</i> Coiffait 1982</td></tr><tr><th><i>Gabrius martensi</i> Schillhammer 1997</th><td><i>Tachyporus martensi</i> Coiffait 1982</td></tr><tr><th><i>Geotrupes martensi</i> Krikken 1981</th><td><i>Taizonia martensi</i> Medvedev 1984</td></tr><tr><th><i>Gonocephalum martensi</i> Kaszab 1977</th><td><i>Taumacera martensi</i> (Medvedev 1990)</td></tr><tr><th><i>Gunvorita martensi</i> Casale 1985</th><td><i>Thoracostrongylus martensi</i> Coiffait 1982</td></tr><tr><th><i>Hydaticus martensi</i> Wewalka 1972</th><td><i>Thyreocephalus jocheni</i> Bordoni 2002</td></tr><tr><th><i>Hydraena martensi</i> Skale & Jäch 2009</th><td><i>Tiruka martensi</i> Queinnec & Perreau 2002</td></tr><tr><th><i>Hydroporus martensi</i> Brancucci 1981</th><td><i>Tomoderus martensi</i> Uhmann 1982</td></tr><tr><th><i>Ischalia martensi</i> Paulus 1971</th><td><i>Trechus martensi</i> Deuve & Hodebert 1991</td></tr><tr><th><i>Isomira martensi</i> Novák 2014</th><td><i>Trichoglossina martensi</i> Pace 1987</td></tr><tr><th><i>Labidostomis martensi</i> Medvedev 1983</th><td><i>Trichotichnus martensi</i> Kataev & Schmidt 2017</td></tr><tr><th><i>Laemoglyptus martensi</i> Kazentsev 2009</th><td><i>Tropimenelytron martensianum</i> Pace 1987</td></tr><tr><th><i>Laemostenus (Antisphodrus) martensi</i> Casale 1980</th><td><i>Xanthalia martensi</i> Merkl 1991</td></tr><tr><th><i>Laemostenus (Pristonychus) martensianum</i> Casale 1988</th><td><i>Xantholinus martensi</i> Bordoni 1983</td></tr><tr><th><i>Laena jocheni</i> Schawaller 2006</th><td><i>Zabrus martensi</i> Freude 1986</td></tr><tr><th><i>Laena martensi</i> Kaszab 1973</th><td><b>Dermaptera [2 species]</b></td></tr><tr><th><i>Lederina martensi</i> Nikitsky 1994</th><td><i>Aborolabis martensi</i> Brindle 1987</td></tr><tr><th><i>Leptusa (Drepanoleptusa) martensi</i> Pace 1987</th><td><i>Allodahlia martensi</i> Brindle 1974</td></tr><tr><th><i>Limnobaris martensi</i> Korotyaev 2014</th></tr><tr><th><i>Liogluta martensi</i> Pace 1987</th><td><b>Diptera [1 species]</b></td></tr><tr><th><i>Martensomela</i> Medvedev 1984</th><td><i>Dixa martensi</i> Wagner 1983</td></tr><tr><th><i>Megarthrus martensi</i> Coiffait 1982</th><td></td></tr><tr><th><i>Melanotus martensi</i> Platia & Schimmel 2001</th><td><b>Ephemeroptera [2 species]</b></td></tr><tr><th><i>Microscydmus martensi</i> Franz 1971</th><td><i>Caenis martensi</i> Malzacher 2018</td></tr><tr><th><i>Microserica martensi</i> Ahrens 1998</th><td><i>Iron martensi</i> Braasch 1981</td></tr><tr><th><i>Monolepta martensi</i> Medvedev 1992</th><td></td></tr><tr><th><i>Myrmecopora martensi</i> Pace 1984</th><td><b>Heteroptera</b> <b>[7 species]</b></td></tr><tr><th><i>Nacerdes martensi</i> Švihla 1973</th><td><i>Bengalaria martensi</i> Vásárhelyi 1986</td></tr><tr><th><i>Nebria martensi</i> Huber & Schmidt 2012</th><td><i>Geovelia martensi</i> Zimmermann 1984</td></tr><tr><th><i>Nepalota martensi</i> Pace 1987</th><td><i>Kokeshia martensi</i> Štys 1985</td></tr><tr><th><i>Niphadonyx martensi</i> Zherichin 1987</th><td><i>Lygus martensi</i> Aglyamzyanov 2003</td></tr><tr><th><i>Orius (Heterorius) martensi</i> Péricart 1987</th><td></td></tr><tr><th><i>Phorticus martensi</i> Kerzhner 1992</th><td><b>Diplopoda [21 species, 3 genera]</b></td></tr><tr><th><i>Thaicoris martensi</i> Péricart 2000</th><td><i>Albanoglomus martensi</i> Golovatch 1981</td></tr><tr><th></th><td><i>Beronodesmoides martensi</i> Golovatch 2016</td></tr><tr><th><b>Hymenoptera [2 species]</b></th><td><i>Beronodesmus martensi</i> Golovatch et al. 2016</td></tr><tr><th><i>Myrmica martensi</i> Radchenko & Elmes 1998</th><td><i>Epanerchodus martensi</i> Golovatch 2014</td></tr><tr><th><i>Psithyrus (Eopsithyrus) martensi</i> Tkalcu 1974</th><td><i>Gonobelus martensi</i> Golovatch 2013</td></tr><tr><th></th><td><i>Hedinomorpha martensi</i> Golovatch 2014</td></tr><tr><th><b>Odonata [1 species]</b></th><td><i>Hedinomorpha martensorum</i> Golovatch 2021</td></tr><tr><th><i>Orthetrum martensi</i> Asahina 1978</th><td><i>Kelempekia martensi</i> Strasser 1974</td></tr><tr><th></th><td><i>Kophosphaera martensi</i> Wesener 2015</td></tr><tr><th><b>Orthoptera [1 species]</b></th><td><i>Martenseya</i> Shear 2021</td></tr><tr><th><i>Formosatettix martensi</i> Ingrisch 2001</th><td><i>Martensodesmus</i> Golovatch 1987</td></tr><tr><th></th><td><i>Martensosoma</i> Golovatch 1992</td></tr><tr><th><b>Psocoptera [2 species]</b></th><td><i>Nepalmatoiulus martensi</i> Enghoff 1987</td></tr><tr><th><i>Caecilius martensi</i> New 1983</th><td><i>Nepalotretus martensi</i> Golovatch 1987</td></tr><tr><th><i>Psococerastis martensi</i> New 1987</th><td><i>Nopoiulus (Paranopoiulus) martensi</i> Enghoff 1984</td></tr><tr><th></th><td><i>Ommatoiulus martensi</i> Mauriès 1969</td></tr><tr><th><b>Siphonaptera [1 species]</b></th><td><i>Pacidesmus martensi</i> Golovatch & Geoffroy 2006</td></tr><tr><th><i>Ctenophyllus martensi</i> Smit 1974</th><td><i>Paranedyopus martensi</i> Golovatch 1990</td></tr><tr><th></th><td><i>Persedicus martensi</i> Mauriès 1982</td></tr><tr><th><b>MOLLUSCA</b></th><td><i>Polydesmus mediterraneus martensi</i> Strasser 1967</td></tr><tr><th><b>Gastropoda [3 species]</b></th><td><i>Riukiaria martensi</i> Golovatch 2014</td></tr><tr><th><i>Bathyptychia martensi</i> Nordsieck 2001</th><td><i>Sholaphilus martensi</i> Golovatch 1986</td></tr><tr><th><i>Montiphaedusa martensiana</i> Nordsieck 1973</th><td><i>Tetracentrosternus martensi</i> Golovatch 2016</td></tr><tr><th><i>Quadriplicata lederi martensi</i> Nordsieck 1984</th><td><i>Tianella martensi</i> Shear 1979</td></tr><tr><th>MYRIAPODA</th><td><b>Pauropoda [1 species]</b></td></tr><tr><th><b>Chilopoda [2 species]</b></th><td><i>Sphaeropauropus martensi</i> Scheller 2000</td></tr><tr><th><i>Lithobius (Ezembius) martensi</i> Eason 1989</th><td></td></tr><tr><th><i>Otostigmus (Otostigmus) martensi</i> Lewis 1992</th></tr></tbody></table>
Linked collectors and determiners for: FURB - Herbário Dr. Roberto Miguel Klein.
Natural history specimen data linked to collectors and determiners held within, "FURB - Herbário Dr. Roberto Miguel Klein". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/b9a43c60-d2b6-445c-9362-2db65465c963">https://bionomia.net/dataset/b9a43c60-d2b6-445c-9362-2db65465c963</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/b9a43c60-d2b6-445c-9362-2db65465c963">https://gbif.org/dataset/b9a43c60-d2b6-445c-9362-2db65465c963</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Specimen based records and geographic locations of carabid beetles (Coleoptera) collected mainly by Dr. Kazuo Tanaka.
Natural history specimen data linked to collectors and determiners held within, "Specimen based records and geographic locations of carabid beetles (Coleoptera) collected mainly by Dr. Kazuo Tanaka". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/4407f212-7285-4d59-b3c8-cda206bb4657">https://bionomia.net/dataset/4407f212-7285-4d59-b3c8-cda206bb4657</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/4407f212-7285-4d59-b3c8-cda206bb4657">https://gbif.org/dataset/4407f212-7285-4d59-b3c8-cda206bb4657</a>. Formatted as a Frictionless Data package.
Photograph captions A from: Spence J, Kavanaugh D, Maddison DR, Boyd O, Brandmayr P, Garner B, Maveety S, Mosquera D, Moore W, Riley K, Shorthouse J, Sims L, Steiner W, Swing K, Turin H, Zamorano LS, Penev L (2021) Memories of Terry Erwin. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 1001-1036. https://doi.org/10.3897/zookeys.1044.68648
Photograph captions A Photograph captions. A Floating back to the Estación de Biodiversidad Tiputini, Orellana, Ecuador on the Rio Tiputini after a morning of collecting in the blackwater swamp upstream of the station, 30 June 2017 B Terry Erwin aspirating small carabids (Meotachys and Oxydrepanus) from leaf litter, Sendero Chichico, 21 June 2017. Photographs: O. Boyd.
Photograph caption from: Spence J, Kavanaugh D, Maddison DR, Boyd O, Brandmayr P, Garner B, Maveety S, Mosquera D, Moore W, Riley K, Shorthouse J, Sims L, Steiner W, Swing K, Turin H, Zamorano LS, Penev L (2021) Memories of Terry Erwin. In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 1001-1036. https://doi.org/10.3897/zookeys.1044.68648
Photograph caption Photograph caption. Galls induced by the cynipid Diplolepis polita found at the George Lake Field Station and associated species a Maturing galls on the leaves of Rosa acicularisb Larva of D. polita in dissected gall c Larvae of the inquiline Periclistus pirata that had structurally modified a gall after killing the inducer dEurytoma longavena, one of five species of parasitoids that attack gall inhabitants, ovipositing in a gall of D. polita. e) Larva of E. longavena after it had consumed larvae of gall inhabitants and gall tissues.
Supplementary material 1 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Images of Phersita convexa Sloane type series to accompany
Supplementary material 2 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Data file used for cladistic analysis of Theprisa and closely related moriomorphine genera
Figure 9 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 9 Distributional records for Theprisa spp.: T. otway (black circle); T. convexa (black square); T. montana (white circle).
Figure 7 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 7 Female reproductive tract of Theprisa spp., ventral view AT. otwayBT. convexaCT. montanaDT. australis. Abbreviations: bc, bursa copulatrix; co, common oviduct; dgd, defensive gland efferent duct; gc, gonocoxa; hg, hindgut; hs, helminthoid sclerite; sd, spermathecal duct; sg, spermathecal gland; sgd, spermathecal gland duct; sgs, spermathecal gland stem; sp, spermatheca; v, vagina. Scale bars: 0.50 mm.
Figure 8 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 8 Left gonocoxa, ventral view of Theprisa spp., ventral view AT. otwayBT. convexaCT. montanaDT. australisET. darlingtoni. Abbreviations: afs, apical fringe seta(e) of gonocoxite 1; ans, apical nematiform setae; des, dorsal ensiform seta; gc1, basal gonocoxite 1; gc2, apical gonocoxite 2; les, lateral ensiform setae; r, ramus.
Figure 5 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 5 Parameres of male aedeagus for Theprisa spp., outside lateral view. Right paramere shown above left paramere AT. otwayBT. convexaCT. montanaDT. australisET. darlingtoni. Abbreviations: lp, left paramere; rp, right paramere.
Figure 4 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 4 Male aedeagus internal sac in everted condition for Theprisa spp. AT. otway, right view BT. convexaCT. montanaDT. australisET. darlingtoni. Abbreviations: fl, flagellum; mf, microtrichial field; rp, right paramere. Scale bars: 0.5 mm
Figure 3 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 3 Male aedeagus including parameres of Theprisa spp., right, or anatomically ventral view AT. otwayBT. convexaCT. montanaDT. australisET. darlingtoni. Abbreviations: ad, apical divot; af, apical face; fl, flagellum; lp, left paramere; mf, microtrichial field; rp, right paramere.
Figure 6 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 6 Structures associated with abdominal segments VIII and IX for Theprisa spp., dorsal view AT. otwayBT. convexaCT. montanaDT. australisET. darlingtoni. Abbreviations: VIII, antecostal apodeme of abdominal segment VIII; IX, antecostal apodeme of abdominal segment IX; sp, spiracle of segment VIII; t, tergite of segment IX. Scale bars: 0.5 mm.
Figure 6 from: Maddison DR, Porch N (2021) A preliminary phylogeny and review of the genus Tasmanitachoides, with descriptions of two new species (Coleoptera, Carabidae, Bembidarenini). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 153-196. https://doi.org/10.3897/zookeys.1044.62253
Figure 6 Majority rule consensus tree of maximum likelihood bootstrap trees for the concatenated matrix of all gene fragments. Numbers on branches indicate the percentage of bootstrap replicates containing that clade. Outgroups not depicted.
Figure 2 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 2 Dorsal habitus illustrations of Theprisa spp.; range of standardized body lengths indicated AT. australis male BT. darlingtoni, female.
Figure 11 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 11 Female reproductive tract of Theprisa darlingtoni, ventral view; scale bar = 0.50 mm. Abbreviations: bc, bursa copulatrix; co, common oviduct; gc, gonocoxa; hg, hindgut; hs, helminthoid sclerite; sd, spermathecal duct; sg, spermathecal gland; sgd, spermathecal gland duct; sgs, spermathecal gland stem; sp, spermatheca; v, vagina.
Figure 12 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 12 Strict consensus of two equally parsimonious, 380-step cladograms including Theprisa spp. and cladistically neighboring moriomorphine taxa of the subtribe Tropopterina (see text); consensus cladogram length 382 steps, CI = 0.43, RI = 0.66. Character numbers are shown above cladogram edges, character states below. Cladogram root placed so tree topology is compatible with the more inclusive cladogram of Liebherr (2020: fig. 1). Filled squares represent unique state transformations on cladogram, open squares indicate state transformations that occur more than once on cladogram. Clades of this analysis previously recovered in Liebherr (2020) are indicated by pointers numbered 1; the clade subtended by Pterogmus reported in Liebherr (2019) indicated by the pointer numbered 2. Decay indices (i.e., Bremer Support values) shown beneath cladogram edges for all internal edges of the cladogram. Geographic distributions of species are indicated by abbreviations following species epithets: EOZ, southeastern Australia; i.e., A. C. T., New South Wales and Victoria; NNZ, North Island, New Zealand; NZ, New Zealand; SNZ, South Island, New Zealand; QOZ, Queensland; Tas, Tasmania; WOZ, Western Australia
Figure 10 from: Liebherr JK, Porch N, Shaw M, Sinclair BE, Maddison DR (2021) Systematic revision of the trans-Bassian moriomorphine genus Theprisa Moore (Coleoptera, Carabidae). In: Spence J, Casale A, Assmann T, Liebherr JК, Penev L (Eds) Systematic Zoology and Biodiversity Science: A tribute to Terry Erwin (1940-2020). ZooKeys 1044: 339-373. https://doi.org/10.3897/zookeys.1044.62335
Figure 10 Distributional records for Theprisa spp.: T. australis (circle); T. darlingtoni (square).
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