Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa,Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence

The morphology and morphogenesis of a new marine hypotrichous ciliate Pseudoamphisiella elongata sp. nov. isolated from mussel‐farming waters near Qingdao, China, are described based on living and protargol‐impregnated specimens. Morphologically, the new species can be distinguished from its known congeners by its elongate body shape, narrow oral field, having fewer dorsal kineties and caudal cirri, more marginal cirri, and differentiated pretransverse cirri. The identification as a new species is firmly supported by the sequences of the small subunit ribosomal rRNA (SSU rRNA) gene, compared with other known Pseudoamphisiella species, and the phylogenetic analysis. The morphogenetic characteristics can be summarized as follows: (1) the parental adoral zone of membranelles and undulating membranes are entirely rebuilt by the oral primordium, which develops de novo in the outermost region of the cortex; (2) the oral primordium in the opisthe and the frontoventral–transverse (FVT) anlagen in both dividers are formed independently on the cell surface; (3) an ‘extra’ marginal anlage originates to the right of the right marginal anlage, and develops into two or three ‘extra’ marginal cirri; (4) the FVT anlagen develop in the primary mode, and the last FVT streak contributes two migratory cirri (frontoterminal cirri), which are probably resorbed; (5) the right marginal anlagen in both dividers occur close together, independent of the old structure. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 231–243.     

Morphogenesis of the freshwater ciliate Neokeronopsis spectabilis (Kahl 1932) Warren et al., 2002, based on a China population (Ciliophora: Urostylidae)

The morphogenesis of the stichotrichous ciliate, Neokeronopsis spectabilis, collected from a freshwater pond near Harbin, north China, was observed following protargol impregnation. The overall morphogenetic events are characterized by: (1) the new oral primordium originates in association with the transverse cirri; (2) the proter's undulating membrane anlage is formed following the dedifferentiation of the parental endoral and paroral membranes, while the old adoral zone of membranelles is retained; (3) the fronto-ventral-transverse cirral anlagen originate independently on the right of the proter's undulating membrane anlage; (4) the left and right marginal cirri are derived from new anlagen that originate within the old marginal rows; (5) the generation of the dorsal kineties is of the "two-group-mode" with fragmentation and hence an oxytrichid pattern; and (6) similar to that in oxytrichids, the caudal cirri are formed at the posterior ends of the rightmost and two leftmost kineties of the group 1. Some new morphological data for N. spectabilis are also presented and the systematic position of the genus Neokeronopsis is briefly discussed. We conclude that its position among the urostylids is peripheral and that it very likely represents an intermediate form between the oxytrichids and urostylids.     

Divisional morphogenesis in the marine ciliate, Hemigastrostyla enigmatica (Dragesco & Dragesco-Kernéis, 1986) and redefinition of the genus Hemigastrostyla Song & Wilbert, 1997 (Protozoa, Ciliophora)

Morphogenetic events during the division of the marine hypotrichous ciliate, Hemigastrostyla enigmatica (Dragesco & Dragesco-Kernéis, 1986) Song & Wilbert, 1997 are described. The morphogenesis is characterized by:(1) 5 frontoventral-transverse cirral anlagen develop into 8 frontal, 5 ventral and 5 transverse cirri after Oxytricha-pattern;(2) there may be 6 FVT-anlagen in some individuals giving rise to more cirri which, however, will be resorbed after division;(3) anlage of the right marginal row at least in the opisthe occurs de novo right to the parental structures instead of within them;(4) according to the origin, the two extra ventral cirri right to transverse ones are not ventral or transverse cirri, which are from the retained old structure;(5) dorsal kineties originate from one group of DK-anlagen in both dividers with, very uniquely, an additional fragmentation of DK1, and(6) oral primordia will be formed in both dividing parts, from which the newly-built membranelles in the proter replace the posterior part of the parental AZM with a particular 'piecing together mode.Some features during the morphogenesis (e.g. variable number of cirral anlagen, presence of primary primordia, the mode of rebuilding of the proter's adoral zone of membranelles, origin of dorsal kineties and caudal cirri etc.) indicate that the genus Hemigastrostyla might present a intermediate form between oxytrichids and other related higher taxa. Based on our new observations, an improved diagnosis for genus Hemigastrostyla is given: marine or brackish water Oxytrichidae with slightly to conspicuously cephalized body shape; mostly 8–10 frontal, 5 ventral, 5 transverse and two to several extra ventral cirri to the right of the transverse ones, which are from the retained parental structure; caudal cirri present.     

Morphogenesis in the marine spirotrichous ciliate Apokeronopsis crassa (Claparède & Lachmann, 1858) n. comb. (Ciliophora: Stichotrichia), with the establishment of a new genus, Apokeronopsis n. g., and redefinition of the genus Thigmokeronopsis

Morphogenetic events during the division of the marine spirotrichous ciliate, Apokeronopsis crassa (Claparède & Lachmann 1858) n. comb. were investigated. Compared with members of the well-known genera Thigmokeronopsis, Uroleptopsis, and Pseudokeronopsis, A. crassa has one row of buccal cirri, high number of transverse cirri, clearly separated midventral rows, lacks thigmotactic cirri and a gap in adoral zone, its undulating membranes (UMs) anlage forms one cirrus and marginal rows and dorsal kineties form apokinetally during division. All these characteristics indicate that this organism represents a new taxon at the generic level, and hence a new genus is suggested, Apokeronopsis n. g. It is defined as thus: Pseudokeronopsidae with Pseudokeronopsis-like bicorona of frontal cirri and one marginal row on each side; one row of two or more buccal cirri in ordinary position; two midventral rows distinctly separated, hence of cirri that are not in a typical zig-zag pattern; high number of transverse cirri, caudal cirri absent, and frontoterminal cirri present; thigmotactic cirri absent, many macronuclear nodules fuse into many masses as well as marginal and dorsal kineties form apokinetally during morphogenesis. At the same time, the genus ThigmokeronopsisWicklow, 1981 is redefined, and one new combination, Apokeronopsis antarctica (Petz, 1995) n. comb. is proposed. The morphogenetic events of A. crassa are characterized as follows: (1) In the proter, the adoral zone of membranelles and UMs are completely renewed by the oral primordium. The UM anlage is formed apokinetally on the dorsal wall of the buccal cavity and is hence clearly separated from the frontoventral-transverse (FVT) cirral anlagen in the proter. (2) Frontoventral-transverse cirral anlagen are generated de novo in the outermost region of the cortex to the right of the old UMs. (3) A row of buccal cirri arises from FVT cirral streak I. (4) The marginal rows and dorsal kineties originate de novo in both dividers; no caudal cirri are formed. (5) The last FVT-streak contributes two frontoterminal cirri. (6) The many macronuclear nodules fuse into many masses (about 50 segments) during division, unlike a singular or branched mass as described in other urostylids.     

The Cortical Morphogenetic Cycle Associated with Cell Division in Diophrys Dujardin, 1841 (Ciliophora,Hypotrichida)1

Morphogenesis of cell division was investigated in Diophrys scutum, D. oligothrix, and D. appendiculata utilizing both light microscopy of living and stained specimens and SEM of preserved specimens. The cortical morphogenetic pattern of Diophrys is similar to that of other members of the family Euplotidae. The opisthe oral primordium, which develops in a subsurface pouch, forms posterior to the parental buccal cavity. The proter inherits the parental adoral zone of membranelles (AZM) apparently unchanged. The endoral membrane forms to the right of the posterior end of the AZM in the proter, in association with the developing AZM in the opisthe. The paroral cirrus and membrane develop from a single streak that first appears along the right edge of the buccal cavity in the proter to the right of the developing buccal structures of the opisthe. Frontal and transverse cirri develop in both proter and opisthe from five separate cirral primordia that form to the right of the buccal cavity. Left marginal cirri do not develop in association with the corresponding parental structures. Kinetosomes formed within the opisthe oral primordium, or kinetosomes that were part of any parental ciliary structure, do not appear to become part of any developing paroral structures, frontal, transverse, or left marginal cirri. Speciation within the genus Diophrys and evolution of the family Euplotidae as they relate to the morphogenesis of cortical structure are discussed.     

变藓棘毛虫的形态学重描述及细胞发生学研究

通过活体观察和蛋白银染色法对采自青岛沙滩半咸水的变藓棘毛虫Sterkiella histriomuscorum(纤毛门, 腹毛目)进行了形态学及细胞发生学研究。该种群形态学与前人报道的土壤及淡水种群基本一致: 虫体近长椭圆形, 活体大小约(100-160) m (40-75) m; 无皮层颗粒; 2938片口小膜; 额棘毛3根; 额腹棘毛4根; 口后腹棘毛3根; 横前腹棘毛2根; 横棘毛3-5根; 左右缘棘毛列分别由17-23、20-24根棘毛组成; 6列背触毛; 2枚大核。其主要发生学特征如下: (1)老口围带完全保留, 老波动膜解体重建; 后仔虫口原基独立发生; (2)额腹横棘毛为5原基次级发生式, 部分原基来自老棘毛解体, 以2:3:3:4:4方式分化为新棘毛; (3)缘棘毛原基产生于老结构中, 并向两极延伸逐渐形成前后仔虫的新结构; (4)背触毛发生为典型Oxytricha模式; (5)大核在发生过程中完全融合。研究对首次在半咸水生境中发现的变藓棘毛虫种群进行了活体形态学和纤毛图式描述, 补充了显微照片、性状统计数据及发生过程的细节信息。       

Divisional Morphogenesis in Amphisiellides illuvialis N. Sp., Paramphisiella caudata (Hemberger) and Hemiamphisiella terricola Foissner, and Redefinition of the Amphisiellidae (Ciliophora, Hypotrichida)

ABSTRACT. Classification of hypotrich ciliates is bewildering, possibly due to many unrecognized convergencies and the lack of detailed ontogenetic data in most species. A puzzling case are hypotrichs which have an obliquely extending "median cirral row" on the ventral surface between the right and left marginal cirral row. Such species are often assigned to the poorly defined family Amphisiellidae. However, we show by a comparative analysis of the divisional morphogenesis of three amphisiellid morphotypes and by a reevaluation of literature data that a median cirral row can be formed by at least four non-homologous processes. These data are used to define the "amphisiellid median cirral row/'(a row containing all or most cirri from at least two rightmost anlagen, arranged one behind the other during cytokinesis), to redefine the Amphisiellidae (Euhypotrichina with an amphisiellid median cirral row of which the anterior segment is formed by cirri of the rightmost ventral anlage and the posterior segment by cirri of the second ventral anlage from right; a middle segment may be formed by neighboring anlagen), and to improve the diagnoses of the seven genera assigned by us to this family. Attempts to reconstruct the evolution within the Amphisiellidae failed, in spite of the detailed morphological and ontogenetic data available. We thus conclude that such data, although highly valuable, are insufficient to light up the supergeneric phylogeny of hypotrich ciliates. For this, molecular markers and investigations of the morphogenetic processes at electron microscopic level appear indispensable.     

Morphology,Morphogenesis and Small Subunit rRNA Gene Sequence of a Soil Hypotrichous Ciliate,Perisincirra paucicirrata (Ciliophora,Kahliellidae), from the Shoreline of the Yellow River,North China

The morphology, morphogenesis, and 18S rRNA gene sequence of a soil hypotrichous ciliate Perisincirra paucicirrata, isolated from north China, were investigated. Perisincirra paucicirrata differs from its congeners in: (1) having a body length to width ratio in vivo of 4:1, (2) its adoral zone occupying between 15% and 25% of the total body length, and (3) the presence of two parabuccal cirri, three left (with 10–16 cirri each) and two right marginal rows (with 14–24 cirri each), and three dorsal kineties. Our study offers a first attempt to begin to map the morphogenetic processes of the genus, which are mainly characterised by the following: the formation of four frontal ventral transverse anlagens for each daughter cell, with the proter's anlage I originating from the reorganised anterior part of the parental paroral; the paroral and endoral anlage developed from the reorganised old endoral and do not contribute the first frontal cirrus; the frontoventral transverse anlage I contributing the left frontal cirrus; anlage II generating the middle frontal and the buccal cirri; anlage III developing the right frontal cirrus and the anterior parabuccal cirrus; and anlage IV contributing the posterior parabuccal cirrus. As an additional contribution, we judge that the inner one or the two right rows of P. kahli and P. longicirrata are marginal rows. Phylogenetic analysis based on SSU rDNA sequences suggests that Perisincirra is related to sporadotrichids, but provides no credible evidence for its taxonomic position.     

Morphology,ontogeny, and molecular phylogeny of two novel bakuellid-like hypotrichs (Ciliophora: Hypotrichia), with establishment of two new genera

The morphology, ontogeny and molecular phylogeny of Apobakuella fusca gen. n., sp. n. and Parabistichella variabilis gen. n., sp. n., from south China were investigated. Apobakuella fusca, brown colored, demonstrates bakuellid-like infraciliature, and a similar ontogenesis as the genus Bakuella. It is argued, however, that this species represents a novel genus, Apobakuella, which is characterized by two or more marginal rows on the right, several buccal and parabuccal cirri, and lack of frontoterminal and caudal cirri. Phylogenetic analysis based on SSU rRNA gene sequences supports the close relationship of Apobakuella with Neobakuella and Diaxonella within the core Urostylida. By contrast, Parabistichella variabilis has a dominant frontoventral row, few midventral pairs, a long midventral row, and one marginal row on each side. Its morphogenesis exhibits: (1) partial reorganization of the parental adoral membranelles; (2) over six frontoventral-transverse cirri anlagen; (3) intrakinetal development of the midventral row; and (4) very likely, formation of the frontoventral row from the midventral row anlage. Both the morphological characteristics and the SSU rRNA gene sequences suggest that it is incertae sedis among the basal hypotrichs. Further investigation of key taxa with additional molecular markers is required to reveal a better understanding on the phylogeny of Parabistichella.     

Morphology and Molecular Phylogeny of a New Hypotrich Ciliate,Pseudourostyla guizhouensis sp. nov. from Southern China,with Notes on a Chinese Population of Hemicycliostyla franzi (Foissner, 1987) Paiva et al., 2012 (Ciliophora,Hypotricha)

The morphology and molecular phylogeny of a soil hypotrich ciliate, Pseudourostyla guizhouensis sp. nov., collected from southern China, were investigated. Pseudourostyla guizhouensis sp. nov. has an elongate elliptical body measuring 180–310 × 65–85 μm in vivo; invariably two right and three or four left marginal rows; six or seven dorsal kineties; adoral zone consisting of 57–70 membranelles; 12–16 frontal cirri, one buccal cirrus, 13–20 midventral pairs, two frontoterminal cirri, two pretransverse cirri, and five to seven transverse cirri. Morphogenesis during physiological regeneration indicates that the marginal rows of each side originate from a common anlage that differentiates into several rows. Molecular phylogenetic analysis based on SSU rDNA sequence data reveals that P. guizhouensis sp. nov. clusters with the type species P. cristata (Jerka‐Dziadosz, 1964) Borror, 1972 and that the genus Pseudourostyla is monophyletic. The morphological characters of another soil hypotrich ciliate, Hemicycliostyla franzi (Foissner, 1987) Paiva et al., 2012, are also described based on a Chinese (Guizhou) population.     

The morphology and morphogenesis of a marine ciliate,Epiclintes auricularis rarisetus nov. sspec. (Ciliophora,Epiclintidae), from the Yellow Sea

The morphology and morphogenesis of a marine ciliate, Epiclintes auricularis rarisetus nov. sspec., collected from Qingdao, northern China were studied on live and protargol-impregnated specimens. This isolate can be recognized by its elongate, contractile and tripartite body with a size of 200-400×20-40 μm in vivo, about 30 ventrally located adoral membranelles, short undulating membranes, 2-3 frontal and 10-18 transverse cirri as well as 8-9 fronto-midventral rows, 22-31 left and 35-54 right marginal cirri, but no caudal cirri, invariably 3 dorsal kineties, of which kineties 1 and 3 link together anteriorly, 24-70 macronuclear nodules, marine habitat, and contribution of almost all frontal-midventral transverse cirral anlagen (FVT anlagen) to the formation of fronto-midventral rows. In its divisional morphogenesis, this species demonstrates some features rarely if ever found in any other urostyloids, e.g. partial replacement of the old adoral zone of membranelles, de novo formation of the oral primordium and the anlagen for marginal rows and dorsal kineties, contribution of almost all FVT anlagen to the transverse cirri, lack of frontoterminal cirri. In addition, its morphogenesis appears to differ in detail from that of E. auricularis auricularis nov. stat., based on published data. These remarkable morphogenetic traits of Epiclintes suggests a questionable systematic position for this genus in the Urostyloidea, therefore, further researches are urgently needed.     

Cortical structure in non-dividing and dividing Diophrys japonica spec. nov. (Ciliophora, Euplotida) with notes on morphological variation

The morphology and morphogenesis of Diophrys japonica spec. nov., isolated from the Mie Port, Nagasaki, Japan, were investigated from life and following impregnation with protargol. The new species is recognized by the following characters: Body elliptical in outline and slightly greyish to yellowish in color; size in vivo about 80-120 x 50-70 microm; pellicle flexible, with underlying granules densely arranged in lines; ciliature comprising about 30-46 adoral membranelles, 4-7 frontal, 1-4 ventral and 4-7 transverse cirri, always 1 left marginal and 3 caudal cirri, and 4 dorsal kineties; usually two macronuclear nodules; fragment kinety with 2-5 dikinetids; marine habitat. The main morphogenetic events are: (1) the opisthe's oral primordium develops de novo in a subsurface pouch near the left transverse cirri; (2) the proter retains the parental AZM except for reorganization of some proximal membranelles; (3) cirral anlagen for the frontal, ventral and transverse cirri in both dividers develop separately from the oral primordium or parental cirri, and are derived from the separation of primary primordia that originate de novo; (4) the anlagen for the left marginal cirrus and fragment kinety also form de novo and separately; (5) dorsal kinety anlagen occur within the parental structures at mid-body and posterior end of the cell, of which the right-most one contributes three caudal cirri from its posterior portion. Based on available ontogenetic data, the author proposes that the numbers of left marginal and caudal cirri can be regarded as reliable characters for species identification, while the numbers of frontal, ventral and transverse cirri are not consistent enough for species distinction. A key to the eleven adequately known species of Diophrys is presented.     

Morphogenesis of a unique pseudourostylid ciliate,Trichototaxis songi (Ciliophora,Urostylida)

Divisional morphogenesis in the freshwater spirotrichous ciliate, Trichototaxis songi Chen et al., 2007, was investigated. The main morphogenetic events are characterised as follows: (1) the parental oral apparatus is completely renewed by the independently formed oral primordium in the proter; (2) the oral primordium in the opisthe is formed on the cell surface; (3) several left cirri of the midventral pairs participate in the formation of the oral primordium in the opisthe; (4) FVT-anlage I forms the leftmost pair of the bicorona; (5) the macronuclear nodules fuse into many masses rather than a single or branched mass as described in most pseudokeronopsids; and (6) usually, two marginal anlagen develop within each left marginal row separately. However, the number of left marginal anlagen is highly variable, even differing between the proter and opisthe of the same divider. The increase in the number of left marginal anlagen is by de novo generation of small anlagen to the left of the intrakinetal left marginal anlage, whereas the decrease in number is by resorption of the old marginal row(s). We posit that Trichototaxis is an intermediate form between the Pseudourostylidae and Pseudokeronopsidae as it shares morphogenetic features with both. Additionally, as in Uroleptopsis (Uroleptopsis), FVT-anlage I forms the leftmost pair of the bicorona in Trichototaxis indicating these genera may be closely related.     

Morphology,morphogenesis and molecular phylogeny of a new marine ciliate,Trichototaxis marina n. sp. (Ciliophora,Urostylida)

The live morphology, infraciliature and morphogenesis of a new urostylid ciliate, Trichototaxis marina n. sp., collected from coastal water in Qingdao, China, were studied based on the observations of live and silver stained specimens. The new species is characterised as follows: body very flexible and contractile, slight to brick-reddish in colour due to irregularly-shaped, brick-red pigments; ca. 70 adoral membranelles; about 17 frontal cirri arranged in a bicorona; average 67 midventral pairs, the right base of each pair being conspicuously larger than the left base; five to seven transverse cirri; constantly two frontoterminal, one buccal and two pretransverse ventral cirri; two or three left marginal rows; right and innermost left marginal rows with 56–92 and 66–106 cirri, respectively; six bipolar dorsal kineties; more than 100 macronuclear nodules. The characteristic morphogenetic feature in T. marina is the development of the left marginal rows, that is, only one left marginal row is newly built the other one or two being retained from the parental cell. Phylogenetic analyses based on small subunit ribosomal gene sequence data reveal a close relationship of T. marina with members of family Pseudokeronopsidae.     

Morphology and morphogenesis of a new oxytrichid ciliate,Notohymena limus n. sp. (Ciliophora,Oxytrichidae) from Delhi,India

The morphology and morphogenesis of a new oxytrichid ciliate, Notohymena limus n. sp. were studied in vivo and after protargol impregnation. The new ciliate was isolated from the sewage sludge at Delhi Jal Board Sewage Treatment Plant located at Rithala, Delhi, India, using the non-flooded Petri dish method. N. limus n. sp. is characterized as follows: flexible dorsoventrally flattened ellipsoidal body; Notohymena-pattern undulating membranes; adoral zone of membranelles (AZM) occupied about 39% of the body length, and consists of around 26 membranelles; large and deep buccal cavity; colorless subpellicular granules present in groups and arranged around the bases of dorsal bristles; 4 macronuclear nodules; 2 micronuclei; 18 fronto-ventral-transverse (FVT) cirri in typical Oxytricha-pattern; 6 dorsal rows of bristles; 3 caudal cirri; about 16 right and 15 left marginal cirri; N. limus n. sp. is a new species on the basis of the combination of morphological, morphometric and morphogenetic characteristic features.     

Redescription of a poorly known marine ciliate, Leptoamphisiella vermis Gruber, 1888 n. g., n. comb. (ciliophora, stichotrichia, pseudoamphisiellidae), from the Yellow Sea, China

Leptoamphisiella vermisGruber, 1888 n. g., n. comb. (basionym Epiclintes vermisGruber, 1888) is an extraordinarily large and worm-like marine stichotrichous ciliate. Based on a population isolated recently from coastal waters of Qingdao, China, the living morphology and infraciliature are redescribed and its taxonomic position is defined. Accordingly, a new diagnosis for this species is suggested: large, marine Leptoamphisiella with a conspicuous layer of pellicular alveoli; 400-1000 microm x 40-70 microm in vivo; body band-like, highly flexible; about 40 membranelles; always three frontal and two buccal cirri; 52-80 transverse cirri (TC) extending to the posterior end of the buccal field; 57-79 left midventral and 44-62 right midventral cirri; 62-102 cirri in left and 63-91 cirri in right marginal rows (MR); 9-13 dorsal kineties that extend the full body length; about 100 macronuclear nodules and 5-13 micronuclei. The diagnosis for the new genus is as follows: vermiform Pseudoamphisiellidae with strongly contractile body, differentiated frontal, buccal, and highly developed TC; two remarkably separated midventral rows; one MR on each side of the body; frontoterminal and caudal cirri absent. Leptoamphisiella vermis n. comb. is fixed as the type species of the new genus.     

Description of a mirror-image doublet from a Brazilian strain of Gastrostyla setifera (Engelmann, 1862) Kent, 1882 (Ciliophora: Stichotrichia)

The present work describes a mirror-image doublet morph found in a Brazilian strain of the stichotrich ciliate Gastrostyla setifera (Engelmann, 1862) Kent, 1882, obtained from a sample of water and sediment from an urban freshwater stream in the city of Juiz de Fora (Minas Gerais, Brazil). The doublet measured 63 x 49 microm, and had two components where the right one has upside-down arranged adoral membranelles with a set of small oblique membranelles at its proximal (posterior) end. The fronto-ventral-transverse ciliature comprised 34 cirri, mostly related to the left component, as well as two marginal rows. On the dorsal surface there were eight dorsal kineties and six caudal cirri. Dorsomarginal kineties were lacking. The macronucleus comprised one irregular-shaped transverse nodule and two smaller roughly ellipsoid longitudinal nodules.     

多核织毛虫─新种,无性生殖周期中的形态及形态发生

本新种的典型特征为:表膜较薄但不弯曲,无表膜下颗粒;区别于该属其它种的最突出特点是具有多个大核(5.4±1.4);背触毛6列,在第3-4列之间具有一些额外散在的背触毛.口围由42.3±2.2片小膜组成;额、腹、横、尾棘毛恒为:5:5:3结构;本新种的形态发生结果与该属其它种类相同,6列新背触毛原基分别来源于背部的3列老背触毛和腹部的老右缘棘毛,在第3及第4列新背触毛列之间可见新出现并散在的几根背触毛.