363 research outputs found
FIGURE 1 in Description of Panagrellus ulmi sp. n. (Rhabditida, Panagrolaimidae) from Iran, and comments on the species of the genus and its relatives
No full textFIGURE 1. Panagrellus ulmi sp. n. A: Neck. B: Anterior end. C: Lateral field. D: Female genital system. E: Female entire. F: Male entire. G–I: Spicule. J–L: Gubernaculum. M: Female posterior end. N: Male posterior end. O: Vulva in ventral view.Published as part of Abolafia, Joaquín, Alizadeh, Mehrdad & Khakvar, Reza, 2016, Description of Panagrellus ulmi sp. n. (Rhabditida, Panagrolaimidae) from Iran, and comments on the species of the genus and its relatives, pp. 245-267 in Zootaxa 4162 (2) on page 248, DOI: 10.11646/zootaxa.4162.2.3, http://zenodo.org/record/25615
Panagrellus ulmi Abolafia, Alizadeh & Khakvar, 2016, sp. n.
No full textPanagrellus ulmi sp. n. (Figs 1‒3) Material examined. Eleven females and ten males in good condition. Type locality and habitat. The species was collected inside wetwood cankers caused by Lelliottia nimipressuralis (Carter) (Enterobacteriaceae) on Ulmus glabra Hudson from the Bahman Boulevard, Tabriz, province of East Azerbaijan (Iran), at 1449 m altitude (38º 03' 43'' N; 46º 19' 48'' E). Type material. Eight females (holotype and paratypes) and seven males (paratypes) deposited in Departamento de Biología Animal, Biología Vegetal y Ecología, Universidad de Jaén, Spain; two females and two males (paratypes) deposited in Department of Plant Protection, University of Tabriz, 29 Bahman Blvd, Tabriz, Iran; and one female and one male (paratypes) deposited in the nematode collection of the Swedish Museum of Natural History, Stockholm (Sweden). Morphometrics. Listed in Table 1. Description. Adult: Nematodes of small size, 0.91‒1.22 mm long in females and 0.82‒1.18 mm long in males. Body cylindrical, tapering towards both ends. Habitus slightly ventrally curved after fixation. Cuticle with scarcely visible transverse striations or annuli, about 1 µm wide at mid-body. Lateral field with two wings or alae seen as three longitudinal incisures at mid-body, inconspicuous under LM. Lip region low, narrowing to distal end, with six small lips, more or less rounded, and oral opening surrounded by six acute liplets; six labial papillae located at the base of oral liplets and four cephalic papillae located at base of dorsal and ventral lips. Amphid openings small, slit-like, located at base of the lateral lips. Stoma panagrolaimoid; cheilostom without refractive rhabdia; gymnostom shorter than cheilostom, with straight refractive rhabdia; stegostom as long as cheilo-gymnostom, having funnel-shaped lumen in lateral view and walls with non-refractive rhabdia. Pharynx panagrolaimoid; pharyngeal corpus almost cylindrical with metacorpus not swollen; isthmus slender, 2.2‒2.8 times the corpus length; basal bulb ovoid, with valvular apparatus. Cardia conoid, surrounded by intestinal tissue. Intestine lacking distinct specialization, but a cardiac portion is differentiated at its anterior part slightly longer than the corresponding body width, with thinner walls. Nerve ring and hemizonid at 63‒74% of neck length, the former surrounding the anterior part of the isthmus. Excretory pore at 52‒68% of neck length, at level of metacorpus, difficult to observe in the most of specimens. Deirid not visible. Female: Reproductive system mono-prodelphic, located at right side of intestine; ovary very long without flexures, sometimes reaching the posterior part of the intestine; oocytes initially in two rows and posteriorly in only one; oviduct with thick walls, as long as the corresponding body diameter; uteri with very thin walls, 5.5‒11.2 times the corresponding body diameter long; uterine eggs usually present in different stages of development, frequently with well-developed juveniles; postvulval uterine sac long, 2.0‒3.4 times the corresponding body diameter, swollen and connected to the vagina by a short tubular part; vagina extending inwards obliquely 21‒41% of body diameter, surrounded by strong musculature. Vulva-anus distance 1.5‒2.1 times the tail length or 3.9‒6.6 times the corresponding body diameter. Rectum 1.0‒2.2 times as long as anal body diameter, with three glands. Tail elongate-conoid, narrower in posterior half. Phasmid at 34‒46% of tail length. Male: Reproductive system monorchic with ventrally reflexed testis. Tail elongate-conoid, narrower at its posterior third. Spicules curved ventrad, with manubrium rounded or ventrally hook-shaped, calamus very short and lamina ventrally bent with dorsal anterior hump, fork-like bifurcate tip and ventral wing. Gubernaculum ventrally bent, showing an anterior dorsal handle-like manubrium. Genital papillae arranged in two precloacal pairs, one adcloacal pair and five postcloacal pairs: two mid-subventral (sv1 and sv2), one subventral terminal (sv3), one mid-subdorsal (sd1) and one subdorsal terminal (sd2). Phasmid at 39‒46% of tail length, close to the terminal papillae. Diagnosis. Panagrellus ulmi sp. n. is characterized by its small size (0.91‒1.22 mm long in females and 0.82‒1.18 mm long in males), lateral field with three longitudinal incisures, lip region narrowing to distal end with six small lips and oral opening surrounded by six acute liplets, stoma with gymnostom shorter than cheilostom, cheilorhabdia not refrigent, gymnorhabdia refrigent, pharynx with metacorpus not swollen and isthmus slender, excretory pore at level of metacorpus, ovary very long without flexures, oviduct swollen, postvulval uterine sac long, 2.0‒3.4 times the corresponding body diameter, female and male tails elongate-conoid, spicules with rounded and ventrally bent manubrium and lamina with dorsal anterior hump and fork-like bifurcate tip, gubernaculum with anterior dorsal handle-like manubrium, postcloacal genital papillae five pairs, two anterior subventral, one anterior subdorsal at same level than the first subventral, one posterior subventral and one posterior subdorsal both at same level. Relationships. The new species resembles other species having slender spicules with bifurcate tips, including P. ceylonensis Hechler, 1971, P. dubius Sanwal, 1960, P. leperisini Massey, 1974, P. nepenthicola (Menzel, 1922) Goodey, 1945, P. redivivoides (Goodey, 1943) Goodey, 1945, P. redivivus (Linné, 1767) Goodey, 1945 and P. silusioides Tsalolikhin, 1965. It can be differentiated from all of these by its narrower lip region with liplets (vs wider with rounded lips lacking liplets). It can also be distinguished from P. ceylonensis by having a more anterior excretory pore position (at 52‒58% of neck length or at metacorpus level vs at 93% or at bulbus), shorter spicules (24‒32 µm long with large bifurcation at tip vs 87‒95 µm long with small bifurcation) and gubernaculum (12‒17 µm long vs 30‒34 µm long). From P. dubius by having a more anterior excretory pore position (vs at 60‒68% or at bulbus level), longer female tail (112‒144 µm, c’= 4.5‒6.5 vs 87 µm, c’= 3.4), smaller spicules (24‒32 µm vs 39‒45 µm) and gubernaculum (12‒17 µm vs 25‒36 µm). From P. leperisini by the more anterior position of the excretory pore (at 78% or at isthmus level), longer isthmus (corpus 2.2‒2.8 times the isthmus length vs 4.7 times), shorter spicules (vs 58 µm) and gubernaculum (vs 28 µm). From P. nepenthicola by its small body length (0.91‒1.22 vs 2.00‒2.88 µm in females and 0.82‒1.18 vs 1.36‒1.87 µm in males), slighly more anterior vulva position (V= 64‒68 vs 71‒77), smaller spicules (vs 59‒71 µm). From P. pycnus by having more anterior vulva position (vs 71‒77), different arrangement of genital papillae (sv1 and sv2 separate from each other and sd1 at same level than sv1 vs sv1 and sv2 together and sd1 more posterior), shorter spicules (vs 50‒70 µm and with small bifurcation at tip) and gubernaculum (vs 25‒27 µm). From P. redivivoides, the most similar species, by having longer isthmus (2.2‒2.8 times the isthmus length vs corpus 4.0‒10.4 times), spicules with large bifurcation (vs small) and different arrangement of genital papillae (vs sv1 and sv2 very close and sd1 posterior to sv2). From P. redivivus by its more anterior excretory pore position (vs at 73‒90% or at posterior part of isthmus), shorter male tail (76‒124 µm vs 100‒154 µm), shorter spicules (vs 36‒70 µm) and gubernaculum (18‒32 µm). From P. silusioides by its small body length (vs 2.20‒2.60 µm in females and 1.70‒2.10 µm in males), more anterior position of excretory pore (vs at 77% or at isthmus level). Etymology. The specific epithet references the tree where the nematode was found. Comments on the genus Panagrellus and its relatives. The genus Panagrellus Thorne, 1938 is a homogeneous taxon (Fig. 4 A‒N, Table 2) characterized by having a short gymnostom, long postvulval sac [P. pycnus was initially described by Thorne (1938) as lacking a postvulval sac but re-examination of the type material by Hechler (1971a) showed that it does have a postvulval sac although it was not illustrated] and spicules with bifurcate tip (see Stock & Nadler 2006). Most of the species present slender ventrally curved spicules with rounded or hook-like manubrium; only three species [P. dorsobidentatus (Rühm, 1956) Baker, 1962, P. ludwigi (de Man, 1910) Goodey, 1945 and P. ventrodentatus (Heindl-Mengert 1956) Baker, 1962] have robust, scarcely ventrally curved spicules with truncate manubrium. This genus shows morphological similarities with the genus Baujardia Bert, Tandingan De Ley, van Driessche, Segers & De Ley, 2003 (Fig. 4 O), mainly in the morphology of the postvulval sac (almost identical with the species examined here), spicule and gubernaculum morphology (especially those of P. ventrodentatus). This close relationship is also supported by molecular analysis (see phylogenetic tree in Bert et al., 2003). For this monotypic genus, Andrássy (2005) erected the subfamily Baujardinae based on the presence of lip region with cephalic setae and the slightly different structure of the stoma (longer and bearing denticles). However, these characters are not enough to maintain it separate from the subfamily Panagrellinae Andrássy, 1976. Accordingly, we propose Baujardinae as a junior synonym of Panagrellinae. On the other hand, the morphology of the spicule with bifurcate tip, frequent in Panagrellus, appears also in other species not belonging to this genus, as in Plectonchus hunti Stock, De Ley, De Ley, Mundo-Ocampo, Baldwin & Nadler, 2002. In fact, this species presents numerous characters disagreeing with the rest of the species included in the genus Plectonchus Fuchs, 1930, such as a shorter gymnostom than cheilostom (vs longer), more anterior vulva position (at 53‒77% of the body length vs more posterior, at 66‒80%, close to anus), offset sac-like spermatheca (vs not offset or absent), very short postvulval sac (one third of the corresponding body diameter vs absent), female and male tails plump conoid with acute mucro (vs conoid to conoid elongate, posteriorly constricted), spicules almost straight with lamina having slightly bifurcate tip (vs bent spicule with acute tip) and gubernaculum almost straight (vs slightly sigmoid). These differences suggest that this species does not belong to the genus Plectonchus. Although the morphology of the spicules, with slightly bifurcate tip, agrees with what is seen in Panagrellus, differences such as the presence of an offset sac-like spermatheca (vs not offset), postvulval sac length (very short, less than a half of the corresponding body diameter vs very long, ca 3 times its width), and in tail morphology (plump conoid vs elongate in both sexes) suggest otherwise. Alternatively, most of the morphological features agree well with those of species of the genus Panagrobelus Thorne, 1939 (Fig. 5 A‒E, Table 3), only differing in the lip morphology (lips grouped in pairs with secondary axils slightly expanded to oral opening vs lips with primary and secondary axils expanded in flap-like processes, the secondary ones larger). As can be observed, the morphology of P. hunti is intermediate between Panagrellus and Panagrobelus, while molecular analyses (see Nadler et al. 2006, Stock & Nadler, 2006) show that P. hunti is more related to Panagrobelus (P. stammeri) than to any studied Panagrellus species. Because of this, there do not appear to be enough differences to propose a new genus only for this species and we transfer it to the genus Panagrobelus as P. hunti (Stock, De Ley, De Ley, Mundo-Ocampo, Baldwin & Nadler, 2002) n. comb. The lip region of this species could be a plesiomorphic character state, where the small secondary axil process is homologous with the flap-like process (apomorphic) present in other species of Panagrobelus. On the other hand, the genus Plectonchus (Fig. 5 F‒O, Table 4) contains, after removing P. hunti, species mainly with large gymnostom, post-equatorial vulva (V= 66‒81), spicules with rounded manubrium and anteriorly bent lamina, and usually robust and sigmoid gubernaculum. The lip region, however, shows great variation. Agreeing with this pattern is Anguilluloides procerus (Weingärtner, 1953) Rühm, 1956 (Fig. 5 M), the only species of the genus Anguilluloides Rühm, 1956, distinguished from some species of the genus Plectonchus only by having a shorter gymnostom (see Andrássy 1984). This character state is also present in such Plectonchus species as P. cuniculari Fuchs, 1930 and P. longevulvus Khan, Hussain & Tahseen, 2012. For this reason, we consider there are not enough differences between these genera to maintain them as separate taxa, and we consider Anguilluloides a junior synonym of Plectonchus, and suggest that its only species be renamed as Plectonchus procerus (Weingärtner, 1953) n. comb. Diagnosis of Panagrellus (emended). Panagrolaimidae, Panagrellinae. Body slightly curved ventrally after fixation. Cuticle with fine annulations. Lateral field with two longitudinal wings. Lip region with six low lips, slightly separated and grouped in pairs, with primary and secondary axils similar in morphology. Amphids slit-like. Stoma with wide cheilo-gymnostom, cheilostom longer than gymnostom, only cheilostom with refringent rhabdia; stegostom variable in length, having narrow lumen. Pharyngeal corpus subcylindrical, without demarcation between pro- and metacorpus, not or only scarcely swollen; isthmus usually long and narrow; basal bulb rounded or pyriform with distinct valvular apparatus. Nerve ring encircling the isthmus. Excretory pore located anterior or posterior to nerve ring. Female reproductive system mono-prodelphic; ovary anterior to vulva, posteriorly reflexed and extending slightly past the vulva, sometimes reaching the rectum. Offset spermatheca absent. Post-vulval sac long, about 2 to 3.5 times the corresponding body diameter long. Vagina long, straight or slightly oblique, strongly muscular. Vulva slightly post-equatorial, rarely more posterior (V=53‒82), protruding, with the anterior lip slightly larger than the posterior. Female tail conoid elongate, ca 3‒7 times the anal body diameter with acute tip. Phasmids located at middle of tail. Male reproductive system monorchic; testis reflexed posteriorly. Male tail conoid, slightly ventrad curved, with narrower part after last papillae. Genital papillae three precloacal pairs, two subventral and one sublateral, four or five postcloacal pairs, and a single ventral papilla. Spicules paired and symmetrical, with rounded ventral bent manubrium, frequently hook-like, lamina with bifurcate tip and ventral velum present but inconspicuous. Gubernaculum slightly ventral curved. List of species. The genus Panagrellus currently includes 14 species (see Table 2): Type species: P. redivivus (Linné, 1767) Goodey, 1945 syn. Chaos redivivus Linné, 1767 syn. Anguillula rediviva (Linné, 1767) Stiles & Hassal, 1905 syn. Turbatrix redivivus (Linné, 1767) Peters, 1927 syn. Turbator redivivus (Linné, 1767) Goodey, 1943 syn. Vibrio anguillula Müller, 1773 syn. Vibrio glutinus Müller, 1783 syn. Vibrio anguillula glutinus Müller, 1783 syn. Gordius glutinus (Müller, 1783) Oken, 1815 syn. Anguillula glutina (Müller, 1783) Ehrenberg, 1838 syn. Rhabditis glutina (Müller, 1783) Dujardin, 1845 syn. Anguillula silusiae de Man, 1913 syn. Turbatrix silusiae (de Man, 1913) Peters, 1927 syn. Turbator siusiae (de Man, 1913) Goodey, 1943 syn. Panagrellus silusiae (de Man, 1913) Goodey, 1945 syn. Neocephalobus leucocephalus Steiner, 1936 syn. Turbator leucocephalus (Steiner, 1936) Goodey, 1943 syn. Panagrellus leucocephalus (Steiner, 1936) Goodey 1945 syn. Cephalobus parasiticus Sandground, 1939 Other species: P. ceylonensis Hechler, 1971 P. dorsobidentatus (Rühm, 1956) Baker, 1962 syn. Anguillula dorsobidentata Rühm, 1956 P. dubius Sanwal, 1960 P. filiformis (Sukul, 1971) Andrássy, 1984 syn. Tylorhabdus filiformis Sukul, 1971 P. japonicus (Yokoo & Ota, 1961) Andrássy, 1984 syn. Brevibucca japonica Yokoo & Ota, 1961 P. leperisini Massey, 1974 P. ludwigi (de Man, 1910) Goodey, 1945 (name corrected by Andrássy 2005) syn. Anguillula ludwigii de Man, 1910 syn. Turbatrix ludwigii (de Man, 1910) Peters, 1927 syn. Turbator ludwigi (de Man, 1910) Goodey, 1943 P. nepenthicola (Menzel, 1922) Goodey, 1945 syn. Anguillula nepenthicola Menzel, 1922 syn. Turbator nepenthicola (Menzel, 1922) Goodey, 1943 P. pycnus Thorne, 1938 P. redivivoides (Goodey, 1943) Goodey, 1945 syn. Turbator redivivoides Goodey, 1943 syn. Anguillula redivivoides (Goodey, 1943) Rühm, 1956 syn. Anguillula zymosiphila Brunold, 1950 syn. Panagrellus zymosiphilus (Brunold, 1950) Goodey, 1945 P. silusioides Tsalolikhin, 1965 P. ulmi sp. n. P. ventrodentatus (Heindl-Mengert, 1956) Baker, 1962 syn. Anguillula ventrodentata Heindl-Mengert, 1956 Species sex L a b c c̕ V Stoma Excretory pore/neck length lenght (%) or position ceylonensis 10♀♀ 1057—1530 24.0 (n=1) 5.5—8.0 7.7—10.8 4.7—5.6* 58— 81 11—14 93* 4♁♁ 1090—1180 27.0—29.0 5.3—6.1 7.3—9.7 4.7* - 13—14 bulbus dorsobidentatus ?♀♀ 880—924 17.2—18.3 5.9—6.0 11.0—11.1 2.6* 69 10—11? ?♁♁ 748—880 21.2—23.4 5.0—5.3 7.5—8.7 4.0* - 10—11? ludwigi ?♀♀ 780—945 18.6—22.5 4.8—5.9 5.9—6.8 4.6* 68—69 12 75* ?♁♁ 690—780 18.6—22.5 5.8—5.9 5.9—6.8 5.6* - 12 isthmus dubius ? ♀♀ 980—1200 25.1—30.7 5.4—6.0 9.2—9.5 3.4* 60—68?? ?♁♁ 760—1010 26.2—30.3 5.3—5.7 8.4—10.1 3.7* - 11* isthmus 8♁♁ 802—968 24.3—32.2 4.7—5.4 8.1—10.0? - 9—14? filiformis 1♁ 780 23.5 4.3 8.8 4.5* - 5.8* 70 isthmus japonicus 100♀♀ 878—1201 21.1—38.1 5.7* 6.7—12.6 5.5* 58—72? 55* 100♁♁ 696—1002 17.9—39.2 4.7* 7.7—12.2 3.5* -? metacorpus leperisini ? ♀♀ 820—970 22.3—24.8 5.6—5.8 6.9—8.2 5.4* 66—69 7* 78* ?♁♁ 740—920 22.0—25.0 6.0—6.3 8.2—8.4 2.8* - 7* isthmus ludwigi 20♀♀ 1090—1350 23.0—35.0 3.5—6.6 5.0—9.0 5.6—5.8* 68* 12 67* 9♁♁ 1000—1120 30.0—36.0 5.1—5.8 7.1—9.0 4.9—5.2* -? isthmus nepenthicola ? ♀♀ 2000—2400 28.0—35.0 5.6—5.8 9.0—10.0? 77?? ?♁♁ 1360—1600 30.0—45.0 4.0—5.0 12.0—15.0? -?? ?♀♀ 2300—2880 27.6—35.5 5.9—7.2 9.7—12.0? 76—82?? ?♁♁ 1360—1870 32.0—45.5 4.6—5.6 12.0—15.7 4.0* -?? pycnus ?♀♀ 1000—1400 18.0 8.0 8.5 4.7* 73?? ?♁♁ 800—1200 21.0 6.8 9.0 3.9* -?? ?♀♀ 1170—1410 16.0—22.0 6.1—8.0 8.0—10.0 6.0 71—77?? ?♁♁ 800—1200 21.0—27.0 5.7—7.4 8.0—10.0 3.5—4.0 -?? 12♀♀ 1170—1410 16.0—21.5 6.1—8.0 7.6—10.4 5.8* 71— 77 11—14? 15♁♁ 900—1222 20.6—26.9 5.7—7.4 7.9—10.4 4.1* - 10—13? redivivoides ?♀♀ 980—1700 17.0—24.0 5.0—8.0 8.0—10.0 5.2* 64—70?? ?♁♁ 810—1280 23.0—27.0 5.0—6.5 8.0—10.0 4.0* -?? zymosiphilus ?♀♀ 870—2170 13.6—33.1 5.4—10.3 6.0—12.9 4.8* 53—82 16* 57* ?♁♁ 730—1340 18.2—33.9 4.6—7.2 6.7—10.1 4.5* - 14* metacorpus 24♀♀ 942—1373 18.7—25.7 4.9—8.2 8.3—12.2 5.6* 62— 73 10—14? 28♁♁ 653—1098 17.3—32.7 4.6—6.1 7.9—11.8 2.9—3.3* - 9—13? ……continued on the next page Species sex L a b c c̕ V Stoma Excretory pore/neck length lenght (%) or position redivivus ?♀♀ 2560 30.0—35.0 10.0—12.0 12.0—15.0 4.6* 70* 14—15 79* silusiae ?♁♁ 1900 35.0—40.0 8.0—9.0 12.0—15.0 3.2* - 14—15 isthmus base silusiae 1♀ 2500??????? 1♁ 1700 21.8* 7.1* 9.7* 3.0* -? 73* isthmus leucocephalus ? ♀♀ 1000—1100 20.8—23.2 5.9—6.4 7.6—7.9? 66—67? 81*?♁♁ 900—940 27.0—32.0 4.9—5.5 7.4—9.7 4.1* -? isthmus base parasiticus ?♀♀ 900—1450 28.0* 7.5* 7.5* 4.8* 68* 17* 82*?♁♁ 780—1120??? 4.5* -? isthmus base?♀♀ 1040—1370?????? 76*?♁♁ 950—1240??? 5.3* - 11* isthmus?♀♀ 1015—1750 26.4—35.0 6.5—9.6 6.6—13.5 7.3* 57—80 7*??♁♁ 1190—1205 28.3—31.2 6.5—9.6? 4.2* -???♀♀ 1315—1515 21.6—29.1 6.5—6.9 8.7—10.7 4.7* 66— 68 12—14 90*?♁♁ 1125—1230 25.0—29.3 5.6—6.2 7.3—8.8 3.5* - 12—14 bulbus?♀♀ 1300—2100 21.0—31.0 6.0—9.2 8.0—12.0? 62— 70 12—16 ??♁♁ 1100—1840 22.0—35.0 5.9—8.3 8.0—11.0? - 12—16? silusiae ? ♀♀ ???????? 76♀♀ 1220—2090 19.0—31.2 5.7—9.2 7.2—11.6 7.0* 56—71 14—18? 75♁♁ 705—1806 21.0—35.4 4.1—8.3 6.9—11.5 4.6* - 9—17? leucocephalus 6♀♀ 840—1185? 5.0—6.8 7.4—8.6? 65— 71 9—12? 2♁♁ 870—867? 5.0—5.5 7.2—7.9? - 9—10??♀♀ 1110—2090 19.0—31.0 6.0—9.5 7.0—11.0 6.0—7.0 58—71???♁♁???? 4.2* -?? silusioides ? ♀♀ 2200—2600 21.0—29.0 8.7—9.6 11.0—13.0 6.2* 66—78? 77?♁♁ 1700—2100 25.0—38.0 6.6—8.3 9.0—13.0? -? isthmus sp. n. 11♀♀ 906—1217 18.3—30.3 4.3—5.7 7.4—9.4 4.5—6.5 64— 68 10—12 52—58 10♁♁ 817—1183 25.0—34.9 4.0—5.7 8.1—11.2 3.3—4.9 - 10—12 metacorpus ventrodentatus ? ♀♀ 847—1112 16.0—17.0 5.0—8.0 7.0—9.0 4.6* 63—74 6*??♁♁ 581—647 20.0—25.0 4.0 5.0—7.0 4.1* -?? ……continued on the next page Species Corpus/isthmus Postvulval sac/body Tail Vulva-anus/body width Country or Habitat Reference width or Spicules or Gubernaculum ceylonensis 2.5* 3.0* 138—139* 4.7* Sri Lanka Hechler (1971b) ? 87—95 143* 30—34 Latex exuding in rubber tree dorsobidentatus ? 2.8* 83—83 3.5* Germany Rühm (1956) ? 22—26 86—114 14—18 Frass of insects in oak ludwigi 3.1*? 105—140? Germany Rühm (1956) ? 23—24 98—116 14—17 Frass of insects in oak and beech dubius ?? 87*? Canada Sanwal (1960) ? 57—72 95* 25—36 Frass from mines of insects ? 39—45 85** 26—30 Sanwal̕s material re-examined Hechler (1971a) filiformis 2.3* 22 102* 14* India Sukul (1971) Thermal spring japonicus 3.4*, 5.5* 2.4* 86—140** 7.1* Japan Yokoo & Ota (1961) 3.8*
Application of Z-restriction-based Multi-criteria Choice to a Marketing Mix Problem
No full textAbstractIn this paper the method of solving Z-number valued multiobjective linear programming problem proposed in “R.A. Aliev, O.H. Huseynov, R.R. Aliyev, A.V. Alizadeh, The Arithmetic of Z-numbers. Theory and Applications. Singapore: World Scientific, 2015” is applied to solve a marketing mix problem. The method utilizes differential evolution optimization. The obtained results show validity and applicability of the proposed approach
The Effect of Life Skills Training on Social Health: A Case Study of 15- to 29-Year-Olds in Haji Abad City Mohammad Hassan Sharbatiyan[1], Samereh Alizadeh Khaneghahi[2] Received: 27/06/2017 Accepted: 13/03/2017
No full textThe Effect of Life Skills Training on Social Health: A Case Study of 15- to 29-Year-Olds in Haji Abad City Mohammad Hassan Sharbatiyan[1], Samereh Alizadeh Khaneghahi[2] Received: 27/06/2017 Accepted: 13/03/2017 Abstract The aim of this research is to investigate the effect of life skills on social health regarding theoretical foundations by Keyes (social health) and the Bandura social learning theory (life skills). The sample size was 368 persons who were selected through simple random sampling using a standardized questionnaire. The results have been analysed using the SPSS 22 software. T-Tests, Pearson correlation, regression and path analysis have been used to analyse the relationships between variables. The results indicate that the rate of youth social health was medium to high. Findings show a direct relationship between the dimensions of life skills and social health in the studied population. Also social health of youth is significant different depending on marital status, but not on gender. The regression results also indicate that among factors influencing health, the communication skill variable, beta=0.93, has the greatest direct impact on social health in the studied population. The findings of path analysis show that only the critical-creative thinking variable has a direct and indirect effect, other variables only have a direct effect on the participants. Results also indicate that measures of communication skill, rate of self-consciousness, decision making, excitement and creative thinking can explain up to 90 percent of the dependent variable. Keywords: Youth, Haji Abad, Social Health, Life Skills [1]. Corresponding Author Faculty Member at Department of Sociology. Payame NoorUniversity (PNU). (Corresponding Author). [email protected] [2]. Master of Social Science research, MazandaranUniversity. [email protected]
Adaptive Neural Signal Detection for Massive MIMO
No full textThesis: S.M. in Computer Science and Engineering, Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2019Cataloged from PDF version of thesis.Includes bibliographical references (pages 55-58).Massive Multiple-Input Multiple-Output (MIMO) is a key enabler for fifth generation (5G) cellular communication systems. Massive MIMO gives rise to challenging signal detection problems for which traditional detectors are either impractical or suffer from performance limitations. Recent work has proposed several learning approaches to MIMO detection with promising results on simple channel models (e.g., i.i.d. Gaussian entries). However, we find that the performance of these schemes degrades significantly in real-world scenarios in which the channels of different receivers are spatially correlated. The root of this poor performance is that these schemes either do not exploit the problem structure (requiring models with millions of training parameters), or are overly-constrained to mimic algorithms that require very specific assumptions about the channel matrix. We propose MMNet, a deep learning MIMO detection scheme that significantly outperforms existing approaches on realistic channel matrices with the same or lower computational complexity. MMNet's design builds on the theory of iterative soft-thresholding algorithms to identify the right degree of model complexity, and it uses a novel training algorithm that leverages temporal and frequency locality of channel matrices at a receiver to accelerate training. Together, these innovations allow MMNet to train online for every realization of the channel. On i.i.d. Gaussian channels, MMNet requires 2 orders of magnitude fewer operations than existing deep learning schemes but achieves near-optimal performance. On spatially-correlated realistic channels, MMNet achieves the same error rate as the next-best learning scheme (OAMPNet [1]) at 2.5dB lower Signal-to-Noise Ratio (SNR) and with at least lOx less computational complexity. MMNet is also 4-8dB better overall than a classic linear scheme like the minimum mean square error (MMSE) detector.by Mehrdad Khani Shirkoohi.S.M. in Computer Science and EngineeringS.M.inComputerScienceandEngineering Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Scienc
Knowledge Type Identification in API Documentation
No full text<p>This release contains the source code and instruction on how to obtain the dataset to reproduce the results presented in the following paper</p>
<pre><code>@inproceedings{FMM19,
title={On Using Machine Learning to Identify Knowledge in API Reference Documentation},
author={Fucci, Davide and M. Alizadeh B., Alireza and Maalej, Walid},
booktitle={27th ACM Joint European Software Engineering Conference and Symposium on the Foundations of Software Engineering},
pages={103--112},
year={2019},
doi={10.1145/3338906.3338943}
organization={IEEE}
}
</code></pre>
Feature Selection with Artificial Bee Colony Algorithm on Z-Alizadeh Sani Dataset
No full textInnovations in Intelligent Systems and Applications Conference (ASYU) -- OCT 04-06, 2018 -- Adana, TURKEYRelevant and irrelevant features compose data. Evaluation of these features is the fundamental task for classification and clustering processes and during this processes, irrelevant features induce obtaining false results. Likewise, due to the relevant features' direct effect on the processes, results can be more correct and stable. This also represents the aim of the feature selection process that tries to achieve as high as possible results with as small as possible feature selection subset. In this study, Artificial Bee Colony (ABC) algorithm based feature selection method is updated and employed on Z-Alizadeh Sani data set that consists of 56 features including the class attribute collected from 303 patients. 16 of the 56 features are selected by ABC based updated feature selection method. Also, accuracy and F-measure values are measured as 89.4% and 0.894 respectively, which are higher than the values produced by the raw dataset.CUKUROVA Univ,Yildiz Tech Univ,IEEE Turkey Sect,Cukurova Univ Comp Eng DeptScientific Research Projects Commission Unit of Adana Science and Technology University [18332001, 18103004]This study was supported by Scientific Research Projects Commission Unit of Adana Science and Technology University under Grant Number: 18332001 and Grant Number: 18103004. Please send all your correspondence to [email protected] which is the e-mail address of our Corresponding Author
Continuous Learning for Lightweight Machine Learning Inference at the Edge
No full textWith the proliferation of edge devices such as mobile phones, consumer robots, drones, wearables, and IoT devices, the generation of data at the edge of the internet network has been increasing exponentially. Machine Learning (ML) models, particularly Deep Neural Networks (DNNs), have the ability to process this data with remarkable accuracy. However, state-of-the-art ML models require substantial computational resources that edge devices typically lack, necessitating a shift to powerful servers in the cloud as hosts for these models. Running these models at the edge is desirable due to benefits such as low-latency results and adherence to data privacy constraints, but is limited by the available computational power and energy consumption of edge devices. Moreover, lightweight models designed for edge devices often exhibit a significant drop in accuracy. Continuous learning offers a potential solution by improving the accuracy of lightweight models by dynamically adapting them to specific scenes or narrow distributions of inputs, which is especially relevant since in practice, these models do not need to generalize to every possible sample from the distribution.
In this thesis, two key methods are introduced to tackle the challenges in continuous learning systems for edge devices: Model Streaming and Model Reuse. Model Streaming offloads the adaptation process to remote machines with greater computational capacity and updates only a critical subset of model parameters that significantly influence the lightweight model’s performance, reducing the bandwidth needed for model updates. Model Reuse uses an efficient DNN model to dynamically select a suitable lightweight model from a library of historical models designed for similar input distributions, boosting the scalability, responsiveness, and accuracy of continuous learning systems. These methods are applied to practical systems, including MMNet for adaptive neural signal detection in 5G cellular communication systems, AMS for real-time video inference on edge devices, SRVC for efficient video compression, and RECL for responsive, resource-efficient continuous learning for video analytics.
We show how continuous learning can significantly improve lightweight machine learning inference on edge devices. The proposed techniques effectively address the unique challenges posed by resource-constrained edge environments. Practical applications presented in the thesis, such as MMNet, AMS, SRVC, and RECL, demonstrate the real-world effectiveness of these methods. These innovations in continuous learning have the potential to reshape the landscape of edge computing by offering more accurate and adaptable inference capabilities, enabling efficient use of computational resources, reduced latency, and better energy efficiency.Ph.D
Review of Abbas Alizadeh, 'Chogha Mish, Volume 2: The Development of a Prehistoric Regional Center in Lowland Susiana, Southwestern Iran. Final Report on the Last Six Seasons of Excavations, 1972-1978'. Oriental Institute Publications 130 (Chicago 2008). Oriental Institute of the University of Chicago 395 Seiten mit Abbildungen; geb.; ISBN-13: 9781885923523 ISBN: 188592352X
No full textThis volume is the second and final monograph on the University of Chicago Oriental Institute excavations at the important multi-period site of Chogha Mish in the eastern Susiana Plain, Khuzestan, Iran. The first volume (henceforth CM Vol I) was authored by the excavators of the site, Pinhas Delougaz and Helene Kantor, although as the volume appeared after their deaths, Abbas Alizadeh played an important role as editor. CM Vol I appeared in 1996, and covered the first five seasons of excavations from 1961 - 1971. The second volume (henceforth CM Vol II) covers the last six seasons of excavations, from 1972-1978. CM Vol II is authored, rather than edited, by Abbas Alizadeh, and he is owed a debt of gratitude by all archaeologists interested in prehistoric Iran and Mesopotamia for bringing this material to print. As outlined in the Preface, the author and his collaborators faced numerous challenges in bringing this material to publication, and as Alizadeh noles with regret, the deaths of Oelougaz and Kantor represented not only a personal loss but also the loss of much information about the excavations themselves. Moreover, critical excavation documents including notebooks from the 10th and 11th seasons and all section drawings from the 6th-11th seasons were lost when the project dig house was destroyed. Finally, the chipped stone assemblage from the site has been lost and is therefore not reported on in the volume, and there is no chapter on the faunal remains, although the raw data on some 40,000 bones studied by Jane Wheeler Pires-Ferreira is presented in an appendix
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