Apiomorpha nookara Mills, MacDonald, Rigby & Cook, sp. n

Autor: Mills, Penelope J., Macdonald, Melanie L., Rigby, Lisa M., Cook, Lyn G.
Rok vydání: 2011
Předmět:
DOI: 10.5281/zenodo.6189281
Popis: Apiomorpha nookara Mills, MacDonald, Rigby & Cook sp. n. Holotype female, ex. Eucalyptus racemosa, Australia, New South Wales, Arakoon Road, Arakoon, S 30 �� 53 ��� 29.6, E 153 ��04���06.1���, 26.xii. 2008, L. G. Cook, code LGC01098. To be deposited in the Australian National Insect Collection, Canberra along with its associated gall. Additional material of the holotype specimen (LGC01098) includes gut and ovary tissue stored at - 70 ��C in the School of Biological Sciences at The University of Queensland (Australia) and genomic DNA stored at - 20 ��C at the same institution (both labeled LGC01098); holotype material also includes DNA sequence data: partial 18 S SSU rDNA (Genbank accession: JN 863287), partial 28 S LSU rDNA (Genbank accession: JN 863288) and partial COI (Genbank accession: JN 863289). Paratypes: 2 slide-mounted females from collection LGC00343 (labeled f 1 and f 2), ex. E. racemosa, Australia, New South Wales, near South West Rocks, S 30 �� 53 ��� 25 ���, E 153 ��04��� 16 ���, 22.v. 2005, L. G. Cook. 1 slide-mounted female from collection LGC00820, ex. E. racemosa, Australia, New South Wales, corner of Bruce Field Street and Keith Andrews Avenue, South West Rocks, S 30 �� 54 ���05.5���, E 153 ��02��� 10.7 ���, 31.xii. 2007, L. G. Cook. Adult female (Fig. 1). Description based on four whole adult females (slide mounted material: LGC00343 f 1, LGC00343 f 2, LGC00820, LGC01098) and one partial female (slide-mounted: LGC00309). Body. 5���8 mm long, 3���5 mm wide. Abdomen tapered to anal lobes. Integument mostly membranous in young adult females but moderately to heavily sclerotised in older specimens. Abdominal segment VIII longer ventrally than dorsally. Antenna. 5 segmented, but segmentation often indistinct, 140���170 ��m long; with 2���4 pegs (fleshy setae) (18��� 45 ��m long) and 1 coeloconic peg (10 ��m long) on apical segment; 5���7 trichoid setae (10���46 ��m long) present on other segments as follows: I 4���5 (mostly 4), II 0, III 0���3 (mostly 1), IV 0���1 (mostly 1). Labium. 121���140 ��m long, 111���130 ��m wide. Clypeolabral shield. 157���210 ��m long, 125���150 ��m wide. Spiracles. Typical trilabiate type, as per A. minor species group of Gullan (1984). Mesothoracic spiracles 200��� 277 ��m long, 106���142 ��m wide, metathoracic spiracles 200���300 ��m long, 120���173 ��m wide. Legs. Sparse trichoid setae scattered on all segments. Forelegs shortest (344���493 ��m), mid legs (571���730 ��m) shorter than hind legs (875���951 ��m). Hind coxa and hind femur with high density of pustules, evenly spread across dorsal and ventral surfaces. Claw distinct on all legs in young adult females, indistinct in older females. Anal ring. Invaginated (although not clear on all specimens), 105���161 ��m in diameter, slightly concealed by a sclerotised shield, with 16���20 ring setae, each 105���320 ��m long. Anal lobes. Lightly to moderately sclerotised, 380���480 ��m long. Tapering apically and apices slightly divergent. Each apex distinctly bifurcate, with terminating subequal spine-like processes 10���25 ��m long, lying in the dorso-ventral plane. Trichoid setae 90���350 ��m long, mostly restricted to the ventral and outer surfaces of lobes, with 1 long (340 ��m) robust trichoid seta (most broken on specimens examined) originating ventrally from near apex of anal lobes. Venter. Multilocular disc pores (with 5���11 loculi, but predominantly 7 and 9); clustered around mouth, but sparsely distributed from head (H) to AVII inclusive; no pores present on AVIII. Trichoid setae (16���353 ��m long) densest and most robust on AVIII and anal lobes; setae become sparser anteriorly. Vulva. Intersegmental between AVI and AVII. Dorsum. Spine-like setae in irregular rows as follows: H���TI and TII (0), TIII (2 or 3), AI (1���4), AII (4���6), AIII (3���9), AIV (3���15), AV (6���12), AVI (6���15), AVII (7���11). Multilocular disc pores (5���11 loculi, predominantly 7 and 9) sparse, mostly in a band towards the anterior margin on segments TII���AVI, although several can be found posteriorly, scattered on AVII. No multilocular disc pores on AVIII. Gall of adult female (Figs 2���4). Description based on 15 galls of adult females, including collections LGC01098, LGC00343, LGC00820, LGC00309, LGC00305 and LGC00716. Host, localities and number of adult female galls measured for each code can be found in Table 1. LGC00309 E. racemosa S 30 �� 54 ��� 10 ��� E 153 ��02���07��� 1 1 LGC00343 E. racemosa S 30 �� 53 ��� 25 ��� E 153 ��04��� 16 ��� 2 2 LGC00716 E. racemosa S 30 �� 53 ��� 25 ��� E 153 ��04��� 16 ��� 0 1 LGC00820 E. racemosa S 30 �� 53 ��� 19 ��� E 153 ��04��� 23 ��� 1 9 LGC01098 E. racemosa S 30 �� 53 ��� 30 ��� E 153 ��04���06��� 1 1 Gall ovoid to ovo-cylindrical (Fig. 2���4), 9.1���14.5 mm long, 6.1���8.5 mm wide, attached to plant stem at gall base. Young galls red or green, turning brown or grey when older. Apex of gall blunt, 2.0��� 6.5 mm in diameter. Outer opening of gall irregular, 1���4 mm wide. Outer chamber 1.0���5.0 mm in diameter and 1.0���4.0 mm deep. Apical orifice of inner chamber (in which female resides) circular: 0.4���1.5 mm in diameter. Inner chamber similar in shape to that of adult female: 5.2���8.7 mm long and 3.1 ���5.0 mm in diameter. Gall of adult male (Fig. 5). Only a single gall of an adult male has been found (collection LGC00343). It is small and tubular, 6 mm long, 2 mm wide, flared at the apical opening and was found on a leaf. Six galls of immature males were also collected from leaves of the same plant. Phylogenetic relationships (Fig. 6). Analysis of the mtDNA COII region (Fig. 6) suggests that A. nookara is closely related to A. minor. Although there is little support for most relationships within Apiomorpha using this gene region (Fig. 6), there was strong bootstrap support for a sister relationship between A. minor (2 n= 84 form) and A. nookara (BS= 99 in MP, 82 in ML). Apiomorpha nookara is also morphologically similar to members of the A. minor species group (A. minor, A. sessilis and A. annulata), and using Gullan's (1984) key to adult females for A. nookara leads to the final couplet separating A. sessilis and A. annulata. Given the phylogenetic results and the morphological similarity, we place A. nookara in the A. minor species group. Karyotype (Figs 7���10). Both individuals karyotyped (LGC00309 and LGC01098), and their embryos, had a diploid chromosome number of 2 n= 6. This karyotype has not been previously reported for specimens from the A. minor species-group, which have counts ranging between 2 n= 4 to 2 n= 84 (Cook 2000; Mills & Cook 2010). Diagnosis. The biological species concept (Mayr 1942) was used to delimit A. nookara, with morphological and karyotypic characters assessed to determine whether there is likely reproductive isolation between this population and other populations or species of Apiomorpha. The two-chambered gall of the adult female of A. nookara clearly distinguishes the species from all other described species of Apiomorpha. Only one other described species (A. variabilis) has two cavities within the gall, but the galls of adult females of A. variabilis are much larger (23���50 mm long, 21���34 mm wide) than the small galls induced by females of A. nookara (9���14.5 mm long). Furthermore, the galls of A. nookara are ovoid to ovo-cylindrical rather than pyriform like those of A. variabilis. The adult female of A. variabilis is also different from A. nookara. Most strikingly, A. variabilis has many more spine-like setae than A. nookara on abdominal segments AIII-AV. Apiomorpha variabilis: 14���32 (AIII), 17���27 (AIV), 15���24 (AV). Apiomorpha nookara: 3���9 (AIII), 3���15 (AIV), 6���12 (AV). The number of spine-like setae on individuals of A. nookara also differs from that of the three species within the A. minor species-group (A. minor, A. sessilis and A. annulata) (Gullan, 1984). Adult females of A. nookara differ from those of A. minor in having no spine-like setae on segment TII, and in having fewer spine-like setae on most of the other dorsal segments. Apiomorpha minor: 4���47 (TIII), 9-59 (AII), 14���58 (AIII), 17���45 (AV), 18���50 (AVI), 12-37 (AVII). Apiomorpha nookara: 2���3 (TIII), 4���6 (AII), 3���9 (AIII), 6���12 (AV), 6���15 (AVI), 7���11 (AVII). Apiomorpha nookara also has multilocular disc pores on the anterior edge of AVII, which are absent on adult females of A. minor. Adult females of A. nookara differ from adult females of A. sessilis in having no spine-like setae on TII, and having fewer spine-like setae on dorsal segments TIII, AII-AIII, AV and AVII. Apiomorpha sessilis: 6���14 (TIII), 9��� 16 (AII), 11���18 (AIII), 14���18 (AV), 13���18 (AVII). Apiomorpha nookara: 2���3 (TIII), 4���6 (AII), 3���9 (AIII), 6���12 (AV), 7���11 (AVII). In addition, the spine-like setae dorsally on AVII in adult female A. nookara are elongated and sharp (Fig. 11), whereas those of A. sessilis are short and blunt (Fig. 12). Adult females of A. nookara differ from those of A. annulata in having elongated sharp spines dorsally on AVI- AVII (Fig. 11) (A. annulata has short, blunt spines on these two segments, similar to those found on AVII in adult females of A. sessilis), and in having fewer spine-like setae on AI and AIII. Apiomorpha annulata: 5���14 (AI), 12��� 19 (AIII). Apiomorpha nookara: 1���4 (AI), 3���9 (AIII). Apiomorpha nookara also differs in having multilocular disc pores on the anterior edge of AVII (A. annulata has none), and antennae that are five-segmented rather than foursegmented in A. annulata (which can be observed more clearly in younger, less-sclerotised adult females). Host-plant associations and geographic distribution. Apiomorpha nookara has been found only on E. racemosa, the narrow-leaved scribbly gum (Eucalyptus subgen. Eucalyptus sect. Cineraceae, ser. Psathyroxylon; sensu Brooker 2000). Prior to the synonymies recognised by Pfeil and Henwood (2004), the populations of scribbly gum from which A. nookara has been collected were known as E. signata F. Muell. Eucalyptus racemosa (sensu Pfeil and Henwood 2004) is widespread across New South Wales and Queensland (Australia), but is confined to woodland or dry sclerophyll forests on sandy and swampy flats (PlantNET 2011). Given that the host is widespread, it is possible that A. nookara might have a broader distribution than that currently recognised. Etymology. The species epithet " nookara " is the reverse spelling of the location where the first live specimens were seen���Arakoon Conservation Park near South West Rocks (NSW), and the name of the road along which the holotype specimen (LGC01098) was collected. The name also was chosen because none of the 41 previously described species of Apiomorpha begins with the letter "n". The name should be treated as an indeclinable noun.
Published as part of Mills, Penelope J., Macdonald, Melanie L., Rigby, Lisa M. & Cook, Lyn G., 2011, A recently discovered species of Apiomorpha R��bsaamen (Hemiptera: Coccoidea: Eriococcidae) with unusual gall morphology, pp. 55-63 in Zootaxa 3093 on pages 57-62, DOI: 10.5281/zenodo.279076
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