Praecantrix saxicola, Hegg & Morgan-Richards & Trewick, 2024
publication ID |
https://doi.org/ 10.5852/ejt.2024.971.2761 |
publication LSID |
lsid:zoobank.org:pub:F82472D1-595D-4DB7-A463-513B94BE85D9 |
persistent identifier |
https://treatment.plazi.org/id/03AF8780-FFB5-FF89-BE5D-559B5878F86B |
treatment provided by |
Plazi |
scientific name |
Praecantrix saxicola |
status |
gen. et sp. nov. |
Praecantrix saxicola gen. et sp. nov.
urn:lsid:zoobank.org:act:7888A528-5ABC-4CBA-AA33-4641DAA7CB26
Figs 3 View Fig , 9 View Fig , 10J View Fig , 12L View Fig , 13K View Fig , 16J–L View Fig , 19J–L View Fig , 23D View Fig
Diagnosis
The largest of the two species in the genus Praecantrix gen. nov. (body length 9 to 14 mm), it is characterised by sexual dimorphism, the females being larger than males, a pale grey colour throughout and a dense tomentum covering the whole insect. This is in contrast to Praecantrix silvatica gen. et sp. nov., which is glabrous and shiny, and has a clear, crisp line delimiting the white body under-parts from the dark dorsal regions.
In the western part of its distribution range, P. saxicola gen. et sp. nov. is sympatric with species of Pharmacus and with Notoplectron brewsterense . It is most easily differentiated from Pharmacus by its lighter coloration, smaller size and micro-habitat preferences, with Pharmacus being more often found in cracks in solid rock. Notoplectron brewsterense is stockier, with shorter legs, has articulated linear spines on the hind tibiae and is glabrous, whereas P. saxicola is covered in fine tomentum. Additionally, female Pharmacus and Notoplectron have a smooth upper valve of the ovipositor, whereas P. saxicola has an ovipositor serrated above in the distal third ( Fig. 19K–L View Fig ).
In Otago, P. saxicola gen. et sp. nov. is sympatric with Isoplectron pallidum . The latter species, however, prefers cracks or small pockets in solid rock, and (in spite of the name) has a darker body colour.
Etymology
The Latin noun ‘ saxum ’ means ‘stone’, ‘rock’; in the plural also ‘stony place’. The insect is a dweller of stony places.
Material examined (see also Supp. file 1: Table S12)
Holotype
NEW ZEALAND • ♂, adult; Mackenzie (MK), Mt Wakefield , Aoraki / Mt Cook NP; 43.71987° S, 170.12763° E; 1450 m a.s.l.; 13 May 2017; D. Hegg leg.; broken rocks on ridgeline; night search + insect net; NMNZ AI.071904. GoogleMaps
Paratype
NEW ZEALAND • 1 ♀, adult; Central Otago (CO), Mt St. Bathans ; 44.71826° S, 169.77104° E; 1650 m a.s.l.; 9 Mar. 2019; D. Hegg leg.; on rock bluffs; night search + insect net; GenBank: PP155085; NMNZ AI.071905 GoogleMaps .
Other material
NEW ZEALAND – Central Otago (CO) • 1 ♂, 1 ♀; Mt Kyeburn, Danseys Pass ; 44.95471° S, 170.30851° E; 1100 m a.s.l.; Dec. 2013; T. Jewell leg.; in scree among bluffs; GenBank: PP155088, PP155089; MPN CW2574 , CW2575 GoogleMaps • 3 ♂♂; same data as for preceding; MPN CW2572 , CW2573 , CW2576 GoogleMaps • 1 ♀; same data as for preceding; 16 Jan. 2017; D. Hegg leg.; night search + insect net; GenBank: PP155087; MPN CW3520 GoogleMaps • 1 ♀; Awakino Ski-field, St Marys Range ; 44.78° S, 170.31° E; 1800 m a.s.l.; 20 Apr. 1998; B. Sinclair leg.; in scree; MPN CW173 GoogleMaps • 1 ♂; same data as for paratype; GenBank: PP155086; MPN CW4317 GoogleMaps • 2 ♀♀; same data as for paratype; MPN CW4551 , CW4552 GoogleMaps • 3 nymphs; same data as for paratype; MPN CW4318 to CW4320 . – Mackenzie (MK) GoogleMaps • 1 ♂; Ahuriri River East Branch; 44.27917° S, 169.74279° E; 1720 m a.s.l.; 30 Apr. 2022; D. Hegg leg.; in scree among bluffs; night search + insect net; MPN CW5611 GoogleMaps • 1 ♀; same data as for preceding; MPN CW5612 GoogleMaps • 1 ♀; Mt Wakefield, Aoraki / Mt Cook NP; 43.70548° S, 170.12192° E; 1680 m a.s.l.; 12 Mar. 2016; D. Hegg leg.; on sparsely vegetated ground; night search; GenBank: PP155084; MPN CW2880 GoogleMaps • 1 ♂; Mt Wakefield, Aoraki / Mt Cook NP; 43.71063° S, 170.12445° E; 1750 m a.s.l.; 18 Mar. 2017; D. Hegg leg.; broken rocks on ridgeline; night search + insect net; MPN CW3540 GoogleMaps • 1 nymph; same data as for preceding; MPN CW3332 GoogleMaps • 1 ♀; same data as for preceding; 17 Apr. 2017; MPN CW3946 GoogleMaps • 1 nymph; same data as for preceding; MPN CW3947 GoogleMaps • 1 ♀; Mt Wakefield, Aoraki / Mt Cook NP; 43.71798° S, 170.12875° E; 1540 m a.s.l.; 13 May 2017; D. Hegg leg.; broken rocks on ridgeline; night search + insect net; MPN CW3517 GoogleMaps . – South Canterbury (SC) • 1 ♂; Fox Peak ; 43.84° S, 170.79 °E; 2000 m a.s.l.; 22 Feb. 2015; S. Trewick leg.; GenBank: PP155082; MPN CW2811 GoogleMaps • 1 ♀; same data as for preceding; GenBank: PP155083; MPN CW2812 GoogleMaps .
Description
MEASUREMENTS. See Table 1. Sexual dimorphism in body length, with females being nearly 25% larger than males.
HEAD. Vertex pale with four brown lines running from the fastigium to the anterior margin of the pronotum, two above the eyes and two near the centre. Grey patches behind the eyes. Eyes grey-green. Frons, clypeus and labrum pale, with two faint dark patches below the scapes of the antennae. Labial and maxillary palps pale. Scapes and pedicels pale; flagellum reddish-brown.
THORAX. Pronotum, mesonotum and metanotum grey with a pale median line, covered in fine tomentum ( Fig. 12L View Fig ).
LEGS. Sexual dimorphism present. The hind tibiae are about the same length as the body in females, 10% longer than the body in males. Since females are larger than males by approx. 25%, females have longer legs. Fore femora always unarmed at the apex. Mid femora armed with one retrolateral spine at the apex; prolateral apical spine absent. Hind femora armed with up to one prolateral and one to three retrolateral ventral linear spines, the retrolateral ones being larger. Fore and mid tibiae armed with two pairs of ventral linear spines, one pair of ventral apical spines and one pair of dorsal apical spines. Hind tibiae armed with about 26 dorsal linear spines (min 22, max 33) on both the anterior and the posterior edge. Hind tibiae armed at the apex with two ventral sub-apical spines, two ventral apical spines, two dorsal apical spines and two dorsal sub-apical spines; the dorsal apical spines are largest. First hind tarsal segment armed with two to seven dorsal linear spines; second hind tarsal segment occasionally armed with one dorsal linear spine.
ABDOMEN. All tergites covered in fine tomentum; grey with a pale median line running along the whole length of the body ( Fig. 12L View Fig ). Sternites pale.
MALE TERMINALIA. Same as in Praecantrix silvatica gen. et sp. nov., but with longer bristles on the two lobes at the apex of the subgenital plate ( Fig. 16J–L View Fig ). Cerci on average 15% of body length, covered in sparse, mostly short hair; conical in the basal half, tapering to a blunt tip in the distal half. Styli short and stumpy.
FEMALE TERMINALIA. Subgenital plate square, with two rounded lobes on the distal corners, not as pronounced as in Praecantrix silvatica gen. et sp. nov., covered with sparse hair at the apex ( Fig. 19J View Fig ). Ovipositor approximately 70% of body length; nearly straight and only weakly recurved upwards near the apex; lower valve with 5 to 7 teeth below at the apex; dorsal surface of upper valve finely serrated in distal third ( Fig. 19K–L View Fig ).
Distribution and habitat
A small alpine rhaphidophorid that inhabits the dry alpine regions east of the Southern Alps, in Central Otago and in the Mackenzie Country ( Fig. 10J View Fig ). It is predominantly found on scree slopes or boulder fields and is most easily recognised by the light grey or grey-brown body colour and grey-green eye colour. When disturbed, it jumps erratically up and down until it falls into a hole between rocks.
Unresolved taxa
We have one specimen ( Fig. 8 View Fig ) from old-growth forest in Ohakune (Taupō Region, North Island), which we have been unable to resolve (specimen code MPN CW5373; GenBank: PP155150; iNaturalist 73080453). This is a male nymph belonging to a taxon that appears to be sister to Isoplectron bicolor sp. nov. based on DNA analysis and on the numerous ventral linear spines on the hind femora. We have spent in excess of 20 nights searching for more specimens, in all four seasons, without any luck. Most likely, we are dealing with a cryptic tree canopy species, like I. bicolor . The latter is the taxon for which we have obtained the smallest sample size in this study; the one adult female we have been able to collect also took in excess of ten person nights searching.
It is likely that a dedicated tree canopy sampling approach will be required to capture this elusive insect. Methods that have been employed in similar forest habitats include fogging and branch clipping ( Ozanne 2005), even tree felling ( Otte & Alexander 1983: 397). We do not favour any of these methods since they are destructive and they are better suited to generic biodiversity monitoring than to targeting a specific insect, especially one that cannot even be located by sound. More realistic approaches may be liaising with road maintenance crews, who occasionally need to fell trees close to the road verge, or building a structure to access the canopy, e.g. a crane or a suspended walkway ( Ozanne 2005).
NMNZ |
Museum of New Zealand Te Papa Tongarewa |
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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