dcsimg

Comprehensive Description

provided by Memoirs of the American Entomological Society
Blaberus craniifer Burmeister (Plate VIII, figures 6 and 7.)
183S. Bl[ubera] craniijera Burmeister, Handb. Ent., ii, abth. ii, pt. i. p. 516.
[Cuba.] 1839. Blahcra various Serxille, Hist. Nat. Ins., Orth., p. 78. (In part; 9.) [9,
Cuba.] 1857. Blatta {Blabera) atropos Guerin (not Blatta atropos of Stoll, 1 813), in Sagra,
Hist. Cuba., Anim. Artie, p. 333. [Havana, Cuba.]
1864. Blabera atropos Saussure (not Blatta atropos of Stoll, 1813), Mem. Hist. Nat. Mex., iv, p. 233. [o", 9 : Cuba; Hot coast of Mexico.]
1888. B{labera) atropos Bolivar {not Blatta atropos of Stoll, 1813), Mem. Soc. Zool. France, i. p. 133. ["Should be the most abundant species in Cuba."]
The present species shows near relationship to B. atropos (Stoll), ■■'-•' agreeing in the exceptionally dark general coloration of
32" Blaberus atropos (Stoll) 1813. [Blatta] atropos Stoll, Natuur. Afbeeld. Beschryv., Kakkerlakken, p. 4, Register p. 14, pi. Ild. fig. 8. (No locality given.)
1865. Bl[abera] fusca Brunner, Nouv. Syst. Blatt., p. 376. [9, Chile.]
1868. Blabera laticollis Walker, Cat. Blatt. Br. Mus., p. 5. [d", British Guiana.]
Brunner, in 1865, applied the name atropos to B. discoidalis or an extremely closely related species, and redescrihed the present insect as fusca. Walker's laticoUis is an evident synon'm, which name was placed under at'^opos (there, howeer, incliidmg craniifer) by Kirby in 1904.
The most striking features of the s[)ecies arc given al)oe. The concealed male genitalia are similar to those found in craniifer, but the surrounding soft median mantle has the free margin fringed dextrad with heavier chitinous teeth, showing distinct uncination,
the tegmina and wings, in the moderately large size (for the genus) and rather broad form. The confusion in the literature is in large part due to the fanciful death's-head marking, figured and described for atropos, and in that species situated on the mesonotum and metanotum. In the present species the dark pronotal spot bears pale markings, which afford an even more striking fanciful resemblance to the human eyes, nose and mouth, and failure to recognize the proper position of this marking in the two species has resulted in constant confusion.
The most striking features of difference between the species are as follows. In craniifer the male averages distinctly smaller than the female; with pronotum decidedly smaller, the length being contained in the width nearly 1.4 times in the male and 1.49 times in the female. The interocular space in the male is slightly less than, to slightly more than, half the interocellar width ; in the female slightly more than half, to slightly less than, the full interocellar width. The dark pronotal spot contains four pale markings suggesting the human eyes, nose and mouth, these very rarely in part obliterated. The tegmina are dark blackish brown with a prout's brown tinge, and have the proximal portions of the marginal and anal fields strikingly buffy, the extent of these markings variable and their distal margins extremely irregular but sharply defined; frequently, and particularly in the males, a large transverse suffusion of buffy is, to varying degrees, weakly indicated mesad on the tegmina.
while sinistrad these are further developed into relatively much larger chitinous processes, rounded distad, with surfaces shagreenous, the largest being situated proximad, which projection is apically irregularly bilobate.
Measurements {in millimeters)
Length Length Width Length Width
Cf of of of of of
body pronotum pronotum tegmen tegmen
Caparo, Trinidad. (8) 42.7-49.1 I3-3-I5-3 19 3-21-6 50.8-56.4 19.2-20
? Caparo, Trinidad. (14) 57-5«« 14-6-15.9 20,8-22.9 53-57-« 22-23
Specimens Examined: 27; 10 males and 17 females.
Diego Martin, Trinidad, VI, 20, 1915, (R. A. Wood; river estate), i 9 , [Hebard Cln.]. Caparo, Trinidad, VI, 1913, (^. M. Klages), 2c^, 3 9 , [A. N. S. P.]; VIII, 1913, (S. M. Klages), 8cf , 13 9 , [Hebard Cln.]. In atropos the difference in size of the sexes is much less apparent; the pronotum axerages only slightly smaller in the male, the length being contained in the width about 1.43 times in both sexes. The interocular space in the male is slightly more than half, to fully, the interocellar width; in the female slightly less than, to fully, the interocellar width. The dark pronotal spot is normally solid ; faint traces of a jjortion of the same type of marking as found so conspicuous in craiiiifer are apparent in rare examples. The tegmina are dark blackish brown with an argus brown tinge, the marginal fields are brownish Inifty, often suffused with darker distad ; the tegmina appear otherwise almost solid in coloration until spread, when the humeral trunk is found to be very dark, the anal field rather pale and the mesal portion of the tegmina rather darker than the other distal portions.
The female of B. varians of Serville is clearly this species; the male the same as his B. discoidalis.
In addition to the diagnostic features described above, the following features are found in the present species.
(Key West, Florida.) Head blackish brown in general coloration, eyes often paler, ocelli and soft portions of clypeus conspicuously buffy. Ocelli distinct; flattened surfaces of ocellar areas slanting mesad, so that the inner margins are raised slighthabove the flattened intervening portion of the face. Pronotum subelliptical, the cephalic and caudal margins almost equally con-ex, this slightly more pronounced mesad on both margins, the latero-caudal angles faintly indicated b"" a slightly greater convexity there of the caudal margin. Tegmina broad, broadly rounded distad, with apex mesal in position. Wings with anterior field decidedly suffused with brown, posterior field less suftused, all veins dark brown. Dorsal surface of abdomen in both sexes with seventh segment acute-angulate produced latero-caudad, with apices of productions blunt; eighth much narrower across abdomen and but slightly projecting beyond caudal margin of seventh, with small, rounded, latero-caudal projections; ninth still narrower across abdomen, with caudal margin straight. Supra-anal plate projecting and subciuadrate, moderateK^ bilobate. Cerci moderately slender, slightly incurved, tailoring distad to acute apex, with about se""enteen short joints; ])olished and slighth' conex aboe, strongh' conex and ^■ery hair>' lielow, with narrow, deep, lateral channels on external and distal portion of internal margins. Mesad in the anal chamber of the male, from above a soft surrounding mantle, a moderately stout, short, tapering, blunt^ chitinous projection extends caudad; the surrounding mantle having the free dorsal and distal margins fringed with minute, chitinous teeth. Dextrad of this organ, from a broad chitinous base, a stout subchitinous shaft is directed caudad curing
license
cc-by-nc-sa-3.0
bibliographic citation
Hebard, M. 1917. The Blattidae of North America. Memoirs of the American Entomological Society vol. 2. Philadelphia, USA

Death's head cockroach

provided by wikipedia EN

The death's head cockroach (Blaberus craniifer) is a species of cockroach belonging to the family Blaberidae. It is often confused with the discoid cockroach, Blaberus discoidalis, due to its similar appearance. It is distinguished by jet black cloak-like marking on its wings and a skull-shaped, amber/black marking on its pronotum. The name death's head comes from the markings on the top of the pronotum: "cranii", which is Latin for "of the head", and "fer", meaning "carry" or "carrier".[1] Due to their unique appearance and certain characteristics, they make an easy to care for pet or display insect for entomologists and hobbyists.

Distribution and habitat

B. craniifer is native to Mexico, the West Indies, and Central America. It has also been introduced into southern Florida in the United States.[2] They can be found on forest floors, hiding in leaf matter and rotting wood.[3]

Diet and predators

In their native habitats, B. craniifer will feed on any organic food source available, including leaf matter.[1] In captivity, it is recommended they are provided foods like fresh fruit and vegetables, wet dog food and moist cereal.[3] B. craniifer is potential prey for both invertebrates, such as spiders, mantids, centipedes, and parasitoid wasps, and vertebrate insectivorous animals, including fish, amphibians, reptiles, birds and mammals.[4]

Behaviour

In response to a predator approaching or after an attack, B. craniifer burrows itself into softer substrates when possible, using its head and pronotum, allowing the cockroach to hide.[4] Cockroaches are gregarious insects, meaning they often interact and associate with one another. B. craniifer secretes a volatile aggregative pheromone from the mandibular glands when engaging in gregarious behaviour.[5]

Physiology

Adults of B. craniifer have wings that possess pink flight muscles capable of supporting sustained flight. However, they generally only glide short distances.[6] Juveniles lack wings and prefer to burrow.

Cockroaches, including B. craniifer, are known to possess independent pulsatile circulatory organs within their antennae, also known as an antennal heart.[7]

It has been found that B. craniifer is capable of regenerating some of its tissues. B.craniifer can regenerate more proximal tissues and structures in a more distal amputation level on its leg after a distal part of the femur foreleg was transplanted to a proximal level of a hindleg tibia. This discovery concluded then that some insects are capable of regenerating certain tissues, and the most frequent type of regeneration in B. craniifer is intercalary regeneration.[8]

Reproduction and sexual dimorphism

B. craniifer are ovoviviparous cockroaches and mate once at a time. The act of mating begins with the female emitting a sex pheromone, which stimulates loco-motor activity in the male to approach the female.[9] While the female emits the sex pheromones from pygidial glands, which are located posteriorly on the abdomen,[10] she will also assume a calling posture. The male touches the female with his antennae to assess her as a sexual partner.[11] The male raises his wings and wingsheaths vertically and rotates 180 degrees.[9] The female turns and moves towards the males' abdominal tergites, where an aphrodisiac sex pheromone made exclusively by males is emitted through secretions. A close relationship is known to exist between the release of these pheromonal signals from specific glands and the corresponding behaviours of female calling posture and male wing raising.[10] The female licks these secretions while the male slides backwards underneath the female and hooks the edge of the subgenital plate with his phallomere. The female allows insertion by the male into the genital atrium by turning 180 degrees and opening the abdominal cavity.[9]

The spermatophore is made by the male inside the females' genital atrium, which is rejected by her multiple days later due to the secretions of her spermathecal glands. Several days later, an ootheca is laid and placed by the female into her brood sac. The gestation period for B. craniifer lasts 55 to 65 days. After this period, the ootheca is ejected and the larvae free themselves from the embryonic covering. During the preoviposition period and during gestation sexual receptivity of females is inhibited.[9]

Both sexes have fully developed wings, but can be distinguished in that the females have a much larger subgenital plate than the males.[12] While sexual dimorphism of the antennae is often seen in other cockroach species, such as Periplaneta americana, no antennal sexual dimorphism is apparent in B. craniifer.[13]

Citations

  1. ^ a b "Species Blaberus craniifer - Death's Head Cockroach - BugGuide.Net". bugguide.net. Retrieved 2019-11-29.
  2. ^ "Death's Head Cockroach". www.eol.org. Retrieved 2019-12-01.
  3. ^ a b EXOTIC-PETS.CO.UK. "Deaths Head Cockroach - Blaberus craniifer". www.exotic-pets.co.uk. Retrieved 2019-11-29.
  4. ^ a b Clark, Andrew J.; Triblehorn, Jeffrey D. (2014). "Mechanical properties of the cuticles of three cockroach species that differ in their wind-evoked escape behavior". PeerJ. 2: e501. doi:10.7717/peerj.501. ISSN 2167-8359. PMC 4121590. PMID 25101230.
  5. ^ Quennedey, André; Brossut, Rémy (1975-01-01). "Les glandes mandibulaires de Blaberus craniifer burm. (Dictyoptera, Blaberidae) developpement, structure et fonctionnement". Tissue and Cell. 7 (3): 503–517. doi:10.1016/0040-8166(75)90022-1. ISSN 0040-8166. PMID 1179412.
  6. ^ McGorry, Clare A.; Newman, Caroline N.; Triblehorn, Jeffrey D. (July 2014). "Neural responses from the wind-sensitive interneuron population in four cockroach species". Journal of Insect Physiology. 66: 59–70. doi:10.1016/j.jinsphys.2014.05.017. ISSN 1879-1611. PMC 4104545. PMID 24879967.
  7. ^ Pass, Günther (1985). "Gross and fine structure of the antennal circulatory organ in cockroaches (Blattodea, Insecta)". Journal of Morphology. 185 (2): 255–268. doi:10.1002/jmor.1051850210. ISSN 1097-4687. PMID 29976030. S2CID 49704623.
  8. ^ Bohn, Horst (1976-10-15). "Regeneration of proximal tissues from a more distal amputation level in the insect leg (Blaberus craniifer, Blattaria)". Developmental Biology. 53 (2): 285–293. doi:10.1016/0012-1606(76)90230-X. ISSN 0012-1606. PMID 992210.
  9. ^ a b c d Grillou, Huguette (1973-01-01). "A study of sexual receptivity in Blabera craniifer Burm. (Blattaria)". Journal of Insect Physiology. 19 (1): 173–193. doi:10.1016/0022-1910(73)90231-X. ISSN 0022-1910.
  10. ^ a b Sreng, Leam (2013-01-01). "Cockroach tergal glands producing female sex attractant pheromones and male aphrodisiacs in particular in the subfamily Blaberinae (Blattaria: Blaberidae)". European Journal of Entomology. 103 (4): 817–829. doi:10.14411/eje.2006.112. ISSN 1210-5759.
  11. ^ Abed, Dehbia; Tokro, Patrice; Farine, Jean-Pierre; Brossut, Rémy (1993-03-01). "Pheromones in Blattella germanica and Blaberus craniifer (Blaberoidea): Glandular source, morphology and analyses of pheromonally released behaviours". Chemoecology. 4 (1): 46–54. doi:10.1007/BF01245896. ISSN 1423-0445. S2CID 40600269.
  12. ^ Ross, Andrew J. (2012). "Testing decreasing variability of cockroach forewings through time using four Recent species: Blattella germanica, Polyphaga aegyptiaca, Shelfordella lateralis and Blaberus craniifer, with implications for the study of fossil cockroach forewings". Insect Science. 19 (2): 129–142. doi:10.1111/j.1744-7917.2011.01465.x. ISSN 1744-7917. S2CID 86327022.
  13. ^ Lambin, M. (1973). "[The antennal sensilla of some cockroaches with special reference to Blaberus craniifer (Burm.) (author's transl)]". Zeitschrift für Zellforschung und Mikroskopische Anatomie. 143 (2): 183–206. ISSN 0340-0336. PMID 4761511.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Death's head cockroach: Brief Summary

provided by wikipedia EN

The death's head cockroach (Blaberus craniifer) is a species of cockroach belonging to the family Blaberidae. It is often confused with the discoid cockroach, Blaberus discoidalis, due to its similar appearance. It is distinguished by jet black cloak-like marking on its wings and a skull-shaped, amber/black marking on its pronotum. The name death's head comes from the markings on the top of the pronotum: "cranii", which is Latin for "of the head", and "fer", meaning "carry" or "carrier". Due to their unique appearance and certain characteristics, they make an easy to care for pet or display insect for entomologists and hobbyists.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN