Nealeurodicus altissimus (Quaintance) Quaintance, 2004
publication ID |
https://doi.org/ 10.5281/zenodo.158856 |
DOI |
https://doi.org/10.5281/zenodo.5659558 |
persistent identifier |
https://treatment.plazi.org/id/FD3C627A-FF94-FFB5-FF40-FD46FEF1FB50 |
treatment provided by |
Plazi |
scientific name |
Nealeurodicus altissimus (Quaintance) |
status |
comb. nov. |
Nealeurodicus altissimus (Quaintance) View in CoL comb. nov.
( Figs 33, 99–101, 128)
Aleurodes altissima Quaintance, 1900: 20 –21. Syntypes, Mexico [examined]. Aleurodicus altissimus (Quaintance) Cockerell, 1902: 280
Aleurodicus (Metaleurodicus) altissimus ( Quaintance) Quaintance & Baker, 1913: 73 Metaleurodicus altissimus (Quaintance) Bondar, 1923a: 81
Radialeurodicus altissimus (Quaintance) Baker, 1937: 608 .
Ceraleurodicus altissimus (Quaintance) Mound & Halsey, 1978: 238 View in CoL .
DISTRIBUTION. Neotropical Region — Belize, Colombia, Costa Rica, Mexico, Nicaragua, Panamá, Venezuela.
COMMENTS. N. altissimus is principally defined by the following suite of puparial characters: a row of typically 15 pairs of long outer submarginal setae present ( Fig. 33); the cephalic and third abdominal pairs of compound pores are of unique structure (Figs 100, 101), the small main pore (12–20 µ m diameter) featuring a 3spoked central opening, surrounded by an array of widerimmed bright simple pores; each of abdominal segments IV–VII bearing a pair of elongate compound pores that present laterally to the viewer (Fig. 99), each about 12–16 µ m in diameter; abdominal segment VIII with a pair of compound pores similar in diameter to those on segments IV–VII, but not elongate, presenting axially to the viewer; more mature puparia are rendered highly visible by secretions of characteristic spiky form (Fig. 128) which can become opaquely white but younger, actively feeding, individuals are often extremely cryptic.
There is evidence to suggest that N. altissimus comprises a complex of very closelyrelated species. The axial processes of the compound pores on abdominal segments IV– VII differ substantially between populations. In some samples, each process is truncate, hardly extending beyond the pore mouth (Fig. 99b); in others, the process is simply somewhat longer, but sometimes (notably on Inga species) the axial process of each compound pore is acute and swordlike, more than doubling the overall length of the structure (Fig. 99a). There is substantial variation in the degree and nature of puparial cuticular pigmentation, affecting the appearance of many of the simple pores, but pigmentation alone is unlikely to be a useful character (see generic discussion, above). The density of distribution of the dorsal disc simple pores, the degree of tubercle development in the outer submargin, and the position of the compound pores on abdominal segment VIII, relative to those on segment VII, also vary. Pupariaassociated adults are only available for two samples, and yet one significant difference is apparent between them: females of a population from Inga possess a distinct cluster of bright pores on each side of the vasiform orifice, but such pores are entirely wanting in females from Canavalia cf. oxyphylla . Once again, investigation of puparia and associated adults from a wider variety of populations is desirable.
N. altissimus sensu lato is one of the most abundant members of the Aleurodicinae in the CFR, and is common elsewhere in Central America. Baker (1937) proposed a new species, N. ingae , for a member of the altissimus group that has much broader compound pores on abdominal segments IV–VII, but specimens matching this nominal species have not been found amongst several samples taken from Inga in Belize. The limited available material, collected elsewhere in Central America and identified as N. ingae , also reveals variation in compound pore size.
To judge from the BMNH collection and the results of this study, N. altissimus sensu lato displays a clear preference for fabaceous [legume] hosts although, curiously, host plant data available to Mound & Halsey (1978) did not include any legumes at all. Indeed, material present in BMNH has all been collected from Fabaceae — in the genera Canavalia , Cassia , Erythrina , Inga, Loncohcarpus , Machaerium , and from one unidentified legume.
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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Nealeurodicus altissimus (Quaintance)
John H. Martin 2004 |
Ceraleurodicus altissimus (Quaintance) Mound & Halsey, 1978 : 238
Mound 1978: 238 |
Radialeurodicus altissimus (Quaintance) Baker , 1937 : 608
Baker 1937: 608 |
Aleurodicus (Metaleurodicus) altissimus ( Quaintance) Quaintance & Baker , 1913 : 73
Bondar 1923: 81 |
Quaintance 1913: 73 |
Aleurodes altissima
Cockerell 1902: 280 |
Quaintance 1900: 20 |