Paracyphocrania major Hennemann, Conle & Suzuki, 2015
publication ID |
https://doi.org/ 10.11646/zootaxa.5073.1.1 |
publication LSID |
lsid:zoobank.org:pub:AA3269D1-CA2F-4528-BC9D-3A4C75D05BD9 |
DOI |
https://doi.org/10.5281/zenodo.10061731 |
persistent identifier |
https://treatment.plazi.org/id/03DB87EE-FFA9-9D0D-FF40-585BFD4BF7DE |
treatment provided by |
Plazi |
scientific name |
Paracyphocrania major Hennemann, Conle & Suzuki, 2015 |
status |
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Paracyphocrania major Hennemann, Conle & Suzuki, 2015 View in CoL
( Figs. 36–37 View FIGURE 36 View FIGURE 37 )
Paracyphocrania major Hennemann, Conle & Suzuki, 2015: 42 View in CoL , figs. 80–85, 128. HT, ♀: Indonesien: Peleng Island ( E of Sulawesi ), via Detani IX.2009 [ ZSMC, ex coll. SS] ; PT, ♀: Indonesien: Peleng Island ( E of Sulawesi ), via Detani IX.2009 [coll. SS]; PT, 3 eggs: Indonesien: Peleng Island ( E of Sulawesi ), via Detani IX.2009 [ ZSMC, ex coll. SS]; PT, 8 eggs: Indonesien: Peleng Island ( E of Sulawesi ), via Detani IX.2009 [coll. FH No. 0849-E, ex coll. SS]; PT, 10 eggs: Indonesien: Peleng Island ( E of Sulawesi ), via Detani IX.2009 [coll. SS] .
Conle & Hennemann, 2018: 117.
Further material examined [17 ♂♂, 7 ♀♀, eggs]: 2 ♂♂, 2 ♀♀: O-Sulawesi, Prov. Sulawesi Tengah, BanggaiInseln , W-Peleng Island , Buko District, Tinanasu, VIII.2010 [coll. FH, No’s 0849-1 to 4] ; 1 ♂: ex Zucht: M. Ortiz 2018 F1-Generation, Herkunft: W-Peleng, Buko District , Tataba, 2017 [coll. FH, No’s 0849-5] ; 2 ♂♂, 10 eggs: ex Zucht: M. Ortiz 2020, Herkunft: W-Peleng, Buko District , Tataba, 2017 [coll. FH, No’s 0849-6 to 7, E2]; 1 ♀, 4 ♂♂: O-Sulawesi, Prov. Sulawesi Tengah, Banggai-Inseln , W-Peleng Island, Buko District , btw. Tatendeng village and Eben village 400–550 m, IX.2011 [coll. FH, No’s 0849-8 to 12]; 4 ♀♀, 8 ♂♂: O-Sulawesi, Prov. Sulawesi Ten-gah, Banggai-Inseln , W-Peleng Island, Buko District , btw. Tatendeng village and Eben village 400–550 m, IX.2011 [ IMQC] .
Differential diagnosis: From the ♂♂ of the Sulawesian P. lativentris (Redtenbacher, 1908) these ♂♂ readily differ by the distinctly spinose mesonotum ( Figs. 36B–C View FIGURE 36 ; only with a few scattered tubercles in lativentris ) and more intense yellow to orange, wholistic coloured anal fan of the alae ( Fig. 36G View FIGURE 36 ; only with weakly defined grey markings in the outer and apical portions which fade towards the base of wing in lativentris ).
Description: The colouration is described from pictures of live wild and captive reared specimens.
♂ ( Fig. 36G View FIGURE 36 , 37A–B View FIGURE 37 ). Moderately sized Phasmatini (body length excluding cerci 91.0–106.0 mm) with a spinose mesothorax and long alae (53.0–61.0 mm). Colouration basically a mixture of green and tones of brown. Head, prothorax, front legs (except base of profemora), tarsi and cerci pale to mid creamish or greyish brown. Bases of profemora as well as mid and hind legs green. Mesonotum, meso- and metasternum apple green, mesopleurae ochre with a slight rosy hue, the metapleurae green with the lower portion coloured like mesopleurae. Abdomen greyish green, the terminal two segments with a slight brownish wash. Tegmina mid brown with the anterior margin broadly white and the basal portion apple green. Costal region of alae light brown with a slight greenish wash, the anterior margin white basally. Anal fan transparent dull yellow to orange and all over with several bold and fairly well defined angular dark grey markings ( Fig. 36G View FIGURE 36 ). Eyes ferrugineous. Antennae creamish mid brown dorsally and somewhat darker ventrally.
Head: Strongly globose, slightly longer than wide, the vertex convex and smooth, broadest just behind the eyes ( Figs 36B–C View FIGURE 36 ). Ocelli well developed and frons with a shallow oval impression. Eyes large, projecting hemispherically and their diameter contained almost 1.6x in length of genae. Antennae reaching to posterior margin of abdominal segment II ( Fig. 36G View FIGURE 36 ), densely setose and consisting of 26 antennomeres. Scapus compressed dorsoventrally, rectangular in dorsal aspect and almost 1.5x longer than wide ( Fig. 36C View FIGURE 36 ). Pedicellus short, cylindrical and less than half the length of scapus. III about 2x longer than pedicellus, IV–XIV very elongate and gradually increasing in length, the following gradually decreasing in length. XIV with a glossy and dark brown, node-like basal swelling dorsally.
Thorax: Pronotum considerably shorter and narrower than head, 1.5x longer than wide, slightly narrowed premedially and with the anterior half somewhat narrower than posterior portion ( Fig. 36C View FIGURE 36 ). Transverse median sulcus distinctly impressed, gently curved and spanning almost entire width of segment. Mesothorax about 3.6x longer than pronotum and parallel-sided with only the very posterior portion gently widened. Anterior ¾ of mesonotum unevenly armed with rather obtuse, conical spines of variable sizes, the lateral surfaces with a marginal row of granules ( Figs. 36B–C View FIGURE 36 ). Mesopleurae only with a few minute scattered granules ( Fig. 36B View FIGURE 36 ), the mesosternum obtusely tectinate longitudinally and set with a very few small irregularly disposed granules in posterior half. Metapleurae with 5–6 small granules along lower margin, metasternum smooth. Tegmina elongate-ovate and somewhat narrowed basally; in basal half with a fairly well developed, rounded central hump. Alae reaching about half way along abdominal segment VII ( Fig. 36G View FIGURE 36 ).
Abdomen: Median segment slightly shorter than metanotum. Segment II considerably longer then median segment, II–VI uniform in width, parallel-sided and almost uniform in length, on average 3.8x longer than wide. VII less than ¾ the length of VI, parallel-sided. VIII about 3/4 the length of VII and trapezoidal in dorsal aspect with posterior margin notably wider than anterior margin. IX roughly equal in length to VII and constricted medially. Anal segment strongly keeled and tectiform, the lateral surfaces roundly convex and the posterior margin sharply angular in lateral aspect, with the ventral corner slightly protruded and acute ( Fig. 36D View FIGURE 36 ); interior surface of posterior margin roundly swollen posteriorly and with a longitudinal bulge that is armed three black in-curving teeth. Cerci very large, foliaceous, strongly flattened laterally, almost 2x longer than anal segment and with the apex rather obtuse ( Figs. 36D–F View FIGURE 36 ). Poculum strongly convex, cup-shaped and with a fairly prominent, obtusely conical sub-basal projection ( Fig. 36D View FIGURE 36 ); the posterodorsal margin labiate and broadly rounded ( Fig. 36 F View FIGURE 36 ).
Legs: All moderately long and slender. Profemora about as long as head, pro- and mesothorax combined, mesofemora almost equal to combined length of pro- and mesothorax, metafemora reaching to posterior margin of abdominal segment IV. Bases of profemora strongly compressed and curved, the dorsal margins distinctly approaching each other with the anterior margin raised; all outer carinae sparsely serrate. Medioventral carina fairly indistinct and roughly midways on ventral surface of femur. All outer carinae of protibiae as well as mid and hind legs distinctly and acutely dentate; teeth however smaller and less in number on dorsal carinae. Probasitarsi elongate, unarmed and somewhat shorter than remaining tarsomeres combined. Meso- and metabasitarsi with the ventral carinae minutely dentate and little longer than following three tarsomeres combined.
Comments: The previously unknown ♂♂ are here described and illustrated for the first time. In addition to the usual green colour form also yellow ♀♀ occur in nature and in breeding stocks in Indonesia. Experiments on whether the rare yellow form only emerges from unfertilized eggs or also occurs in sexual stocks is on-going. Different colour morphs are known to occur in the related Indonesian Eurycnema versirubra Serville, 1838 . This species has a typical green or yellow versirubra morph with red ventral surfaces of the tegmina and alae in its natural habitat on the island of Timor. A versifasciata morph occurs in a turquoise or yellow colour form with yellow ventral surfaces of the tegmina and alae form exclusively in parthenogenetic cultures. The latter colour forms of the versifasciata morph appear to result from the loss of certain genes in parthenogenetic reproduction and the typical green colour and red undersides of the wings re-occur in the next generation if parthenogenetic ♀♀ are mated by ♂♂ ( Hennemann, Conle & Suzuki, 2015: 33):
Culture stock originating from Tataba has been imported to Europe by M. Ortiz ( France) in September of 2017 and the species is since successfully reared in captivity. Breeding appears to be modestly easy in large, well ventilated cages and high humidity. Salal ( Gaultheria shallon , Ericaceae ), oaks ( Quercus spp. , Fagaceae ), chestnut ( Castanea sativa , Fagaceae ) and bramble ( Rubus fruticosus , Rosaceae ) are frequently accepted as alternative food plant and also Eucalyptus (Myrtaceae) is occasionally accepted. In their natural habitats in Peleng, P. major is known to feed on cashew ( Anacardium occidentale , Anacardiaceae ), jackfruit ( Artocarpus heterophyllus , Moraceae ), guava ( Psidium guajava , Myrtaceae ) and avocado trees ( Persea spp. , Lauraceae ). Adult insects exhibit an active startle display if disturbed with both sexes frequently flashing their wings and walking away with the wings held open. While ♂♂ are capable of active flight and may fly off if disturbed ( Fig. 37B View FIGURE 37 ) and also used their flight ability to reach mates, ♀♀ are observed to be rather stationary and to leave the feeding branch only after complete defoliation (personal communication with H. Purwanto). Females produce an average of 10– 15 eggs per week and a total of 250– 300 eggs in a life time. The eggs are flicked away singularly by an abrupt movement of the abdomen. Fertilized eggs hatch after 4 months and unfertilized eggs take about 6 months to hatch if stored in moist conditions and at temperatures of 25–28°C (personal communication with H. Purwanto). The hatching rates in the first three generations of breeding in Europe have been very high and close to 100% (personal communication with M. Ortiz). At average temperatures of 25°C ♀♀ reach maturity after about 12 months, while ♂♂ develop slightly faster.
Distribution: Banggai Islands, Peleng (endemic).
ZSMC |
Germany, Muenchen [= Munich], Zoologische Staatssammlung |
SS |
Università di Sassari |
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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Paracyphocrania major Hennemann, Conle & Suzuki, 2015
Hennemann, Frank H. 2021 |
Paracyphocrania major
Hennemann, F. H. & Conle, O. V. & Suzuki, S. 2015: 42 |