identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
039F879CFFCC2227FF5BF9CAFA6062E9.text	039F879CFFCC2227FF5BF9CAFA6062E9.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Molineus lotoris	<div><p>Molineus lotoris n. sp.</p><p>(Fig. 1, A–J)</p><p>Type host. Procyonidae: Procyon lotor L., Raccoon.</p><p>Type locality. Motozintla, Chiapas State, Mexico, 15°22’ 00’’N latitude, 92°15’00’’ W longitude.</p><p>Type specimens. Holotype, male (CNHE 9238); allotype, female (CNHE 9774); paratypes, 3 females, 1 male (CNHE 9309).</p><p>Site of infection. Stomach.</p><p>Prevalence and intensity. 1 of 1 raccoon infected with 11 worms.</p><p>Etymology. The species epithet refers to the specific name of the host.</p><p>Description. Nematodes of medium size, body not coiled. Females greater than males. Prominent and globular cephalic vesicle present, terminating in several transverse striations (Fig. 1A). Lips absent; in apical view, 6 externolabial, and 4 cephalic papillae and 2 small amphids present (Fig. 1B). Deirids not observed. Cervical groove absent. Excretory pore opening at mid-length of claviform esophagus (Fig. 1A). Males with symmetrical caudal bursa type 2–1–2 (Fig. 1C). Females didelphic and amphidelphic (Fig. 1D). Cuticle with fine, transverse striations. Synlophe composed of uninterrupted ridges. Number of ridges variable in both sexes and at body regions. Synlophe studied in one male and two females. Cuticular ridges begin immediately after the cephalic vesicle and terminate anterior to the anus or cloaca. Ridges orientated perpendicularly to body surface. At anterior level of females, two lateral ridges of the synlophe run closely, protruding from the rest of the ridges. Number of ridges in males: 11 just posterior to cephalic vesicle (Fig. 1E), 17 at mid-body level (Fig. 1F), and 24 at posterior end (Fig. 1G); in females, number of ridges 19–20 just posterior to cephalic vesicle (Fig. 1H), 17–21 at mid-body level (Fig. 1I), and 17 at posterior region (Fig. 1J).</p><p>Male. Body 2.12 (1.8–2.41 ± 0.30, n=4) length by 0.05 (0.04–0.06 ± 0.005, n=4) maximum width. Cephalic vesicle 0.36 (0.34–0.39 ± 0.02, n=3) long by 0.12 (0.15–0.28 ± 0.1, n=3) wide at anterior end. Distance from anterior end to excretory pore 0.11 (0.10–0.12 ± 0.02, n=4) and to nerve ring 0.12 (0.12–0.14 ± 0.07, n=4). Esophagus 0.13 (0.12–0.16 ± 0.02, n=4) by 0.014 (0.013–0.015 ± 0.001, n=4) in maximum width. The bursa is symmetrical, covered ventrally by minute spine-like structures. The bursal ray pattern is of type 2–1–2. Rays 2 and 3 separate near base, run separately, and reach bursal margin. Rays 4 diverges at base from other lateral rays, deflected ventral, approximately l/2 length of other lateral rays. Rays 5 and 6 diverge close to base, are parallel, and reach bursal margin. Rays 8 originates approximately 1/3 of distance from base of dorsal ray, directed dorsolaterally, not reaching bursal margin. Dorsal ray thick, divided into 2 long primary branches. Each one of these, in turn, forks again into rays 9 and 10. Rays 10 distinctly bifid. External branch (rays 9) longer, curving ventrally. Spicules complex, base of handle with thickenings; equal in size, 0.10 (0.099–0.115 ± 0.008, n=4) long; blade divided approximately at 1/2 distance from proximal end into external and internal processes. Internal process slender, ending in globular swelling. External process terminating in point. Gubernaculum 0.048 (0.043– 0.052 ± 0.004, n=3) long; crosier-like, curving ventrally, with ventral projection and slight anterior protrusion (Fig. 1C). Distal end terminates bluntly.</p><p>Female. Worms 2.91 (2.46–3.36 ± 0.31, n=7) long by 0.066 (0.006–0.071 ± 0.003, n=7) in maximum width, at the vulva level, tapering at both ends. Cephalic vesicle 0.043 (0.039–0.047 ± 0.002, n=7) long by 0.034 (0.032– 0.039 ± 0.003, n=7) wide. Distance to nerve ring and excretory pore from anterior end, 0.168 (0.162–0.175 ± 0.004, n=6) and 0.144 (0.143–0.147 ± 0.002, n=5), respectively. Esophagus 0.622 (0.318–0.327 ± 0.003, n=7) long by 0.023 (0.019–0.028 ± 0.002, n=7) in maximum width. Didelphic and amphidelphic; vulva located 0.58 (0.47– 0.66 ± 0.069, n=7) from caudal extremity, in the posterior sixth of the body. Vagina vera 0.023 (0.017–0.026 ± 0.003, n=7) long, vestibule 0.073 (0.065–0.078 ± 0.005, n=7) long. Anterior ovejector 0.12 (0.11–0.12 ± 0.003, n=7) long [vestibule, 0.073 (0.065–0.078 ± 0.005, n=7); infundibulum, 0.018 (0.013–0.21 ± 0.004, n=7); sphincter, 0.023 (0.021–0.028 ± 0.003, n=7)]; posterior ovejector 0.025 (0.021–0.032 ± 0.004, n=7) long [vestibule, 0.073 (0.049–0.084 ± 0.016, n=7); infundibulum, 0.022 (0.019–0.026 ± 0.002, n=7); sphincter, 0.025 (0.021–0.032 ± 0.004, n=7)]. Eggs in anterior uterine branch: 17 (12–25 ± 4.6, n=7); eggs in the posterior uterine branch: 8 (6–10 ± 1.64, n=7); embryonated, elliptical 0.037 (0.030–0.049 ± 0.006, n=10) long by 0.022 (0.019–0.023 ± 0.002, n=10) wide, forming a single row in the uterus. Anus without lips, 0.063 (0.052–0.075 ± 0.009, n=7) from posterior end. Body terminating in a sharp spine 0.008 (0.006–0.013 ± 0.002, n=6) long.</p><p>Remarks. Up to now, 27 species of the genus Molineus have been described around the world (Durette-Desset et al. 1981; Platt &amp; Pence 1981; Wu &amp; Zhang 1984; Durette-Desset &amp; Pesson 1987; Durette-Desset &amp; Corvione 1988; Durette-Desset et al. 2000a, b, 2001): 12 from the Neotropical, 3 from the Ethiopian, 5 from the Oriental, 4 from the Palearctic, and 3 from the Nearctic Realms. Most of the 27 species are parasites of Mammalia ( Carnivora 22 species, Primates 4), and only one species associated with Squamata has been collected ( M. inexpectatus Durette-Desset, Guerrero &amp; Boyer, 2000). A mix of morphological traits is diagnostic for Molineus lotoris n. sp.: 1) presence of a prominent and globular cephalic vesicle; 2) spicules length &lt;0.14 (0.10), with 2 terminal processes and 3) males with 17 synlophe ridges at mid-body region.</p><p>The new species described in the present study can be differentiated from 20 of the 27 species contained in the genus by having 2 instead of 3 terminal processes in the spicules. Among species having 3 terminal processes in the spicules, M. inexpectatus, M. inglisi Durette-Desset &amp; Pesson, 1987, M. midas Durette-Desset &amp; Corvione, 1998, M. springsmithi Inglis &amp; Ogden, 1965 and M. vexillarius Dunn, 1961 are distinguished from the Mexican species because males of those species have a smaller number of synlophe ridges at mid-body level (14, 10–12, 14, NEW MOLINEUS IN MEXICO Zootaxa 4320 (2) © 2017 Magnolia Press · 393 11–15, vs 17, respectively) (Dunn 1961; Inglis &amp; Ogden 1965; Durette-Desset &amp; Corvione 1998; Durette-Desset et al. 2000b); in contrast, M. patens (Dujardin, 1845) Petrov, 1928 and M. genettae Cameron, 1927 are differentiated from M. lotoris because they have a greater number of these structures (40 ridges in both species vs 17 in the new one) (Travassos 1937; Durette-Desset &amp; Pesson 1987). Three other species can be separated from the new species described herein, because its spicules are longer than those of M. lotoris (0.099–0.115): M. nasuae Lent &amp; Freitas, 1938 (0.119–0.184), M. petrovi Durette-Desset &amp; Pesson, 1987 (0.154–0.175) and M. sichuanensis Wu &amp; Zhang, 1984 (0.132–0.159) (Petrov 1928; Lent &amp; Freitas 1938; Wu et al. 1984). The Palearctic distribution of M. legerae Durette-Desset &amp; Pesson, 1987 and the Nearctic distribution of M. mustelae Schmidt, 1965 as well as the greater body size of males (about twice the size of the Mexican species, i.e., 5.6–7 and 4.2–6 vs 1.8–2.41, respectively) allows distinguishing these 2 species from the new species described herein (Schmidt 1965; Durette-Desset &amp; Pesson 1987). Molineus europeaus Zunker, 1929 and M. torulosus (Molin, 1861) have a larger size of body (8.5 and 7.9–9.7, respectively) and spicules (0.145 and 0.172–0.180, respectively), than M. lotoris (1.8–2.41 and 0.099– 0.115, respectively). In addition, M. europaeus is distributed in the Palearctic Realm, while M. lotoris is a Neotropical species, and M. torulosus parasitizes primates and the new species carnivores (Zunker 1929; Durette- Desset et al. 2001).</p><p>Molineus major Cameron, 1936, Molineus pardalis Cameron, 1936 and M. planicipitis (Cameron, 1928) Travassos, 1937 differ from M. lotoris n. sp. by having the dorsal lobe separated from lateral lobes while in the new species, the dorsal lobe is merged with the contour of the bursa. In addition, the size of body of M. major (5–5.5) and M. planicipitis (4.3) is greater than that of M. lotoris n. sp. (1.8–2.41) and spicules and gubernaculum of M. pardalis are smaller (0.075 and 0.037) than in the new species (0.10 and 0.048, respectively) (Cameron 1936; Travassos, 1937). Finally, the body of males and females of M. barbaris Cameron, 1936 (3.4 and 4.1), M. cati Durette-Desset, Boomker &amp; Malan, 2000 (5.1 and 5.7), and M. samueli Platt &amp; Pence, 1981 (8–11.8 and 12.1– 13.6), is larger than the body of both sexes of M. lotoris (1.8–2.41 and 2.6–3, respectively), and the rays 9 are shorter than the dorsal ray in M. barbaris and M. cati instead of larger as in the new species (Cameron 1936; Durette-Desset et al. 2000a). In addition, M. samueli differs from M. lotoris by having 52 vs 17 synlophe ridges at mid-body level, respectively (Platt &amp; Pence 1981).</p><p>The remaining 7 species have 2 terminal processes in the spicules as in M. lotoris n. sp.; nonetheless, the length of body and the size of spicules are greater in males of M. brachyurus Costa &amp; Freitas, 1967 (5.8–6.9 and 0.205–0.217) and M. cynictis Leroux, 1933 (5.5 and 0.184) than in the new species (1.8–2.41 and 0.099–0.115); in addition, the dorsal lobe of M. lotoris n. sp. is merged with the lateral lobes, while it is distinct in the 2 former species (Leroux 1933; Costa &amp; Freitas 1967). Molineus barbatus Chandler, 1942 can be separated from the Mexican species because the body size of males is almost twice that of M. lotoris (4.3–4.7 vs 1.8–2.41, respectively); further, males of M. barbatus have 24–28 ridges in the synlophe (Chandler 1942) and males of the new species have 17 in mid-body region. The presence of a globular cephalic vesicle in the new species enables differentiation from M. asiaticus Tubangui &amp; Masilugnan, 1937, M. felineus Cameron, 1923 and M. paraensis Travassos, 1937, which have a cylindrical cephalic vesicle. In addition, these 3 species have the dorsal lobe distinct from lateral lobes (Travassos 1937; Tubangui &amp; Masilugnan 1937) and the latter 2 possess a smaller number of ridges in the synlophe than M. lotoris n. sp. (12–14 and 14, vs 17, respectively). Spicules of the new species are complex, with the internal process slender, ending in a globular swelling, while in M. asiaticus the spicules terminate in 2 needlelike processes (Tubangui &amp; Masilugnan 1937).</p><p>Molineus lotoris n. sp. most closely resembles M. elegans (Travassos, 1921), particularly because both species have a globular cephalic vesicle. However, M. elegans has a cervical groove (absent in the new species), the body of males as well as spicule length are slightly greater in M. elegans (2.9–3.5 and 0.120–0.134 vs 1.8–2.41 and 0.099–0.115, respectively) and their bursa is trilobed (instead of having lobes merged as in M. lotoris). In addition, number of synlophe ridges in M. elegans is smaller than in M. lotoris (12 vs 17, respectively) (see Travassos 1937).</p></div>	https://treatment.plazi.org/id/039F879CFFCC2227FF5BF9CAFA6062E9	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Mata-López, Rosario	Mata-López, Rosario (2017): A new species of Molineus (Nematoda: Molineidae) parasite of Procyon lotor (Mammalia: Carnivora) in Mexico with a taxonomic key for the species of the genus. Zootaxa 4320 (2): 391-400, DOI: 10.11646/zootaxa.4320.2.12
039F879CFFC5222AFF5BFC25FCEF63DF.text	039F879CFFC5222AFF5BFC25FCEF63DF.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Molineus Cameron 1923	<div><p>Taxonomic key for the species included in Molineus distributed worldwide</p><p>1 Spicules with 2 terminal processes........................................................................ 2</p><p>- Spicules with 3 terminal processes........................................................................ 9</p><p>2 Length of spicules&gt; 0.160.............................................................................. 3</p><p>- Length of spicules &lt;0.140.............................................................................. 4</p><p>3 Spicules with distal end of internal process tri-digitated.......................... M. brachyurus Costa &amp; Freitas, 1967 Host: Chrysocyon brachyurus (Carnivora); Neotropical Realm</p><p>- Spicules with distal end of internal process terminating in point............................ M. cynictis (Leroux, 1933) Host: Cynictis penicillata ( Carnivora); Ethiopian Realm</p><p>4 Synlophe ridges&gt;14................................................................................... 5</p><p>- Synlophe ridges &lt;14................................................................................... 7</p><p>5 Spicules with a conspicuous medially-directed barb anteriorly............................ M. barbatus Chandler, 1942 Host: Procyon lotor (Carnivora); Nearctic Realm</p><p>- Spicules without a conspicuous medially-directed barb anteriorly................................................ 6</p><p>6 Spicules complex, with the internal process slender, ending in globular swelling........................ M. lotoris n. sp. Host: Procyon lotor (Carnivora); Neotropical Realm</p><p>- Spicules simple, terminating in 2 needlelike processes...................... M. asiaticus Tubangui &amp; Masilugnan, 1937 Host: Paradoxurus hermaphroditus (Carnivora); Oriental Realm</p><p>7 Spicules with 1 straight process and other ending in hook......... M. elegans (Travassos, 1921) Travassos &amp; Darriba, 1929 Host: Saimiri sciureus (Primates); Neotropical Realm</p><p>- Spicules with both processes with straight distal ends........................................................ 8</p><p>8 Bursa not distinctly divided into lobes................................................ M. felineus Cameron, 1923 Host: Puma yagouaroundi (Carnivora); Neotropical Realm</p><p>- Bursa distinctly divided into lobes................................................. M. paraensis Travassos, 1937 Host: Potos flavus (Carnivora); Neotropical Realm</p><p>9 Terminal processes of spicules similar in length............................................................. 10</p><p>- Terminal processes of spicules different in length........................................................... 14</p><p>10 Length of spicules &lt;0.1................................... M. inexpectatus Durette-Desset, Guerrero &amp; Boyer, 2000 Host: Lachesis muta (Squamata); Neotropical Realm</p><p>- Length of spicules&gt; 0.12.............................................................................. 11</p><p>11 Dorsal lobe not differentiated from the lateral lobes...................................... M. europaeus Zunker, 1928 Host: Mustela putorius (Carnivora); Palearctic Realm</p><p>- Dorsal lobe differentiated from the lateral lobes............................................................. 12</p><p>12 Length of spicules&gt; 0.17.......................................................... M. torulosus (Molin, 1861) Host: Cebus capucinus (Primates); Neotropical Realm</p><p>- Length of spicules &lt;0.14.............................................................................. 13 13 Point of interno-dorsal process of spicules hammer-shaped................... M. midas Durette-Desset &amp; Corvione, 1998 Host: Saguinus midas (Primates); Neotropical Realm</p><p>- Terminal processes of spicules ending in point............................................ M. major Cameron, 1936 Host: Eira Barbara (Carnivora); Neotropical Realm</p><p>14 Spicules with two large and one short processes............................................................ 15</p><p>- Spicules with two short and one large processes........................................................... 19</p><p>15 Dorsal ray shorter than rays 4................................................... M. planicipitis (Cameron, 1928) Host: Prionailurus planiceps (Carnivora); Oriental Realm</p><p>- Dorsal ray larger or similar in length than rays 4............................................................ 16</p><p>16 Terminal processes of spicules not fused nor enveloped by a membrane..................... M. barbaris Cameron, 1936 Host: Eira barbara (Carnivora); Neotropical Realm</p><p>- Terminal processes of spicules fused or enveloped by a membrane.............................................. 17</p><p>17 Terminal processes of spicules enveloped by a membrane................ M. cati Durette-Desset, Boomker &amp; Malan, 2000 Host: Felis catus (Carnivora); Ethiopian Realm</p><p>- Terminal processes of spicules fused..................................................................... 18</p><p>18 Rays 9 bifurcate.................................................................. M. mustelae Schmidt, 1965 Host: Mustela frenata (Carnivora); Nearctic Realm</p><p>- Rays 9 entire................................................................ M. nasuae Lent &amp; Freitas, 1938 Host: Nasua narica (Carnivora); Neotropical Realm</p><p>19 Synlophe ridges&gt; 20.................................................................................. 20</p><p>- Synlophe ridges &lt;20.................................................................................. 23</p><p>20 Synlophe ridges 20–24..................................................... M. sichuanensis Wu &amp; Zhang, 1984 Host: Ailurus fulgens (Carnivora); Oriental Realm</p><p>- Synlophe ridges&gt; 40.................................................................................. 21</p><p>21 Synlophe ridges 52........................................................... M. samueli Platt &amp; Pence, 1981 Host: Taxidea taxus (Carnivora); Nearctic Realm</p><p>- Synlophe ridges 40................................................................................... 22</p><p>22 Length of spicules&gt; 0.200....................................................... M. genettae (Cameron, 1927) Host: Genetta genetta (Carnivora); Ethiopian Realm</p><p>- Length of spicules &lt;200........................................................... M.patens (Dujardin, 1845) Host: Mustela nivalis (Carnivora); Palearctic Realm</p><p>23 Length of spicules 0.154-0.175......................................... M. petrovi Durette-Desset &amp; Pesson, 1987 Host: Mustela sibirica (Carnivora); Palearctic Realm</p><p>- Length of spicules &lt;0.140............................................................................. 24</p><p>24 Length of gubernaculum 0.1............................................ M. legerae Durette-Desset &amp; Pesson, 1987 Host: Vulpes vulpes ( Carnivora); Palearctic Realm</p><p>- Length of gubernaculum &lt;0.07......................................................................... 25</p><p>25 Gubernaculum hooked anteriorly........................................... M. springsmithi Inglis &amp; Ogden, 1965 Host: Prionailurus bengalensis (Carnivora); Oriental Realm</p><p>- Gubernaculum not as above............................................................................ 26</p><p>26 Medio-internal terminal processes of spicules ending barbed............................... M. vexillarius Dunn, 1961 Host: Saguinus nigricollis (Primates); Neotropical Realm</p><p>- Terminal processes of spicules ending in point.............................................................. 27</p><p>27 Synlophe ridges 10-12.................................................. M. inglisi Durette-Desett &amp; Pesson, 1987 Host: Prionailurus bengalensis (Carnivora); Oriental Realm</p><p>- Synlophe ridges 16............................................................... M. pardalis Cameron, 1936 Host: Leopardus pardalis (Carnivora); Neotropical Realm</p></div>	https://treatment.plazi.org/id/039F879CFFC5222AFF5BFC25FCEF63DF	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		MagnoliaPress via Plazi	Mata-López, Rosario	Mata-López, Rosario (2017): A new species of Molineus (Nematoda: Molineidae) parasite of Procyon lotor (Mammalia: Carnivora) in Mexico with a taxonomic key for the species of the genus. Zootaxa 4320 (2): 391-400, DOI: 10.11646/zootaxa.4320.2.12
