Gonatopus bartletti, Olmi, 1984, Olmi, 1984
publication ID |
https://doi.org/10.11646/zootaxa.1226.1.2 |
DOI |
https://doi.org/10.5281/zenodo.15602749 |
persistent identifier |
https://treatment.plazi.org/id/03E2D444-0650-363A-A050-2007573FAB8A |
treatment provided by |
Felipe |
scientific name |
Gonatopus bartletti |
status |
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The postembryonic development of G. bartletti includes four larval instars: three immature and one mature instar.
Egg ( Figs 1–3 View FIGURES 1–6 )
Eggs (Figs 2,3) are small, kidneyshaped, smooth, with little brown area at their anterior pole and without conspicuous structures on their surface when observed with optical microscope. At hatching, chorion is ruptured, breaking into pieces; fragments remain attached to cuticle of larva in some cases.
Remarks. Females of Gonatopus bartletti parasitize adults of Dalbulus maidis , laying their eggs into the intersegmental membranes of the host’s abdomen ( Fig. 1 View FIGURES 1–6 ).
First instar ( Fig. 4 View FIGURES 1–6 )
Length: 0.50–0.60 mm; width: 0.34–0.46mm.
Larva very small, with two anterior white kidneyshaped cephalic vesicles. Colour changing from whitish at hatching to light brown; posterior body region only slightly bent in ventral direction and protruding outside the host; body with ventral tubercle ( Fig. 4 View FIGURES 1–6 ), probably serving to anchor parasite in host’s body (see Barret et al. 1965).
Indistinct segmentation present ( Fig. 4 View FIGURES 1–6 ); respiratory system has nine (one thoracic and eight abdominal) pairs of lateral spiracles.
Remarks. After the larva has completed its growth, it moults and its exuvia remains attached to the body of the following instar, as in other species of Gonatopodinae .
Second instar ( Fig. 5 View FIGURES 1–6 )
Length: 0.68–0.90 mm; width: 0.42–0.60mm.
Remarks. This instar differs from the first one by an increase in size, a sturdy integument and the presence of the first instar exuvia ( Fig. 5 View FIGURES 1–6 ).
Third instar ( Fig. 6 View FIGURES 1–6 )
Length: 0.92–1.16 mm; width: 0.48–0.58mm.
Remarks. The main characters distinguishing this instar from the previous ones are its size and the presence of two exuviae (relating to 1 st and 2 nd instar), which cover it partially ( Fig. 6 View FIGURES 1–6 ).
Mature larva ( Figs 7–22 View FIGURES 7–11 View FIGURES 12–17 View FIGURES 18–21 View FIGURE 22 )
Length: 1.64–3.44 mm; width: 0.80–0.96 mm.
Larva apodous, creamy white yellowish, with typical facies of mature Gonatopodinae larvae.
Head capsule longer than wide, well sclerotized with its posterior part retracted under 1 st thoracic segment ( Fig.14 View FIGURES 12–17 ). Antennae very simple, reduced to two small elliptical pits, both with two small conical sensilla medially ( Figs 15 View FIGURES 12–17 , 22 View FIGURE 22 ); one sensory bristle present medially to each antenna ( Fig. 22 View FIGURE 22 ). Near base of each mandible is peculiar subrectangular heavily sclerotized and dark pigmented area, with lensshaped quite transparent protuberance in its anterolateral angle (its ultrastructure and function are under investigation) ( Figs 9 View FIGURES 7–11 , 16 View FIGURES 12–17 , 22 View FIGURE 22 ); one pair of small sensory pores and one sensory bristle present in each of those areas ( Fig. 22 View FIGURE 22 ). Frontoclypeal suture indistinct. Frontoclypeus with one pair of sensory pores and two pairs of sensory bristles ( Figs 14 View FIGURES 12–17 , 22 View FIGURE 22 ); anterior margin of clypeus concave. Labrum large, dorsally convex, apically rounded. On its dorsal surface, from proximal to distal margin, one pair of sensory pores, row of 7–8 sensory bristles placed semicircularly in preapical position, and numerous irregularly distributed apical sensory bristles ( Figs 14, 17 View FIGURES 12–17 , 18 View FIGURES 18–21 , 22 View FIGURE 22 ). Epipharynx without peculiar structures. Mandible strongly sclerotized, unidentate ( Fig.22 View FIGURE 22 ). Each mandible with broad base, narrow and medially curved apical portion and dorsal subproximal sensory bristle. Maxilla ( Fig. 18 View FIGURES 18–21 ) weakly sclerotized, each with maxillary palpus, three sensory bristles arranged in semicircle near base of palpus and two other ones placed ventrolaterally in its proximal region. Maxillary palpi subcylindrical ( Figs 18, 19 View FIGURES 18–21 ). Each palpus with apical area delimitated by cuticular edge with four sensilla of different size and shape: two uniarticulated, small and coneshaped and two biarticulated consisting of long cylindrical basal and small coneshaped apical article; in subapical position one medially placed sensory bristle and laterally large sensory pit present ( Fig. 19 View FIGURES 18–21 ). Labium weakly sclerotized, consisting of postmentum and the median lobe ( Figs 18, 20 View FIGURES 18–21 ). The median lobe, formed by prementum and hypopharynx ( Buyckx, 1948), bears spinneret distally and labial palpi subapically. Three pairs of sensory bristles are arranged in semicircle in proximity of base of each palpus. Labial palpi ( Fig. 21 View FIGURES 18–21 ) broad and well defined, similar in structure to maxillary palpi, each with proximal large sensorial pit and four distal sensilla structurally similar to those of maxillary palpi. The spinneret opens apically by transverse slit ( Fig. 20 View FIGURES 18–21 ).
Thorax and abdomen with indistinct segmentation ( Figs 7, 8 View FIGURES 7–11 ), with some sparse minute bristles. Tracheal system with nine pairs of spiracles (one pair of large thoracic spiracles and eight pairs of small abdominal ones located on first eight abdominal segments) ( Figs 8 View FIGURES 7–11 , 12, 13 View FIGURES 12–17 ).
Remarks. The mature larva feeds on the internal organs of the host. Having killed the host, the larva emerges into the open and builds its cocoon in a suitable place, often on a maize leaf ( Fig. 11 View FIGURES 7–11 ). The whitish subovoidal cocoon consists of a double wall ( Fig. 10 View FIGURES 7–11 ).
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.
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