A Multiterminal
Stretch Receptor, Chordotonal Organ and Hair Plate at the
Metathoracic Wing-hinge of Manduca sexta
(Lepidoptera: Sphingidae): Unraveling the Mystery of the
Noctuid Moth Ear B Cell
Jayne E. Yack,
G.G. Scudder, & James Fullard 1
1 Department of Biology, Erindale College,
University of Toronto
3359 Mississauga Rd. N., Mississauga, Ontario, Canada L5L 1C6
Home page:
http://www.erin.utoronto.ca/~w3full/
Email:
jfullard@credit.erin.utoronto.ca
Abstract
The present study aims to shed
light on the evolutionary origin of the B cell: a sensory element
of unknown function in the noctuid moth ear. Peripheral
projections of the metathoracic nerve IIIN1b1, homologue of the
noctuid moth tympanic nerve, are described in the atympanate moth
Manduca sexta on the basis of dissections with the aid of Janus
Green B, and intracellular tracer dyes Lucifer yellow and cobalt
lysine. A large multiterminal (Type II) neuron, attaching to
membranous cuticle ventral to the hind wing axillary cord, was
discovered. This cell appears to be homologous to the B cell in
the noctuid moth ear. Recordings from the IIIN1b1 nerve in M.
sexta reveal a continuous train of large, uniform spikes, presumed
to originate from the multiterminal cell. This unit increases its
rate of firing in response to hind wing elevation, suggesting that
it functions as a stretch receptor monitoring wing movements
during flight. Also identified in the tympanic nerve homologue,
and closely associated with the multiterminal cell, were a
chordotonal organ and hair plate.
The chordotonal organ consists of
a proximal scolopidial region, and a distal strand which attaches
to the sclerotized epimeron slightly medial to the multiterminal
cell. This simple chordotonal organ, having three uniterminal
(Type I) sensory cells, is homologous to the auditory cells of the
noctuid moth ear. The significance of these receptors as
proprioceptors in M. Sexta, and as evolutionary precursors to the
noctuid moth ear, is discussed.
NEED FIGURES
Fig. 1a-c Diagrams illustrating
the location of the metathoracic wing-hinge sensory complex in
Manduca sexta. a: Left lateral view of M. Sexta. An arrow marks
the general location of the wing-hinge receptor complex, as
illustrated in c. Scale bar: 1 cm. b: Left half of the metathorax
viewed from the midline showing the principle branches of nerve
root IIIN1 with surrounding nerves and musculature. The first
branch of IIIN1b (IIIN1b1) takes a lateral course between the
dorsoventral and dorsolongitudinal musculature where it innervates
the wing-hinge sensory cells. dl, dorsolongitudinal muscle; dv,
dorsoventral muscle; Sc, scutum; Scl, scutellum. Scale bar: 2 mm.
c: Posterior view of the left, descaled metathorax with parts of
the cuticle, musculature and tracheal tissue removed to reveal the
wing-hinge receptor complex. The stretch receptor attaches to the
membranous region (stippled) ventral to the axillary cord. The
strand of the chordotonal organ attaches to the sclerotized
cuticle of the epimeron in a slightly ventral position to the
stretch receptor. AxC, axillary cord; CO, chordotonal organ; dl,
dorsolongitudinal muscle; HW, hind wing; HP, hair plate; Sa,
subalar sclerite; Sc, scutum; Scl, scutellum; SR, multiterminal
stretch receptor. Scale bar: 500 mm
Copyright:
This document is composed of unpublished material
by Jayne E. Yack, James Fullard, and G.G. Scudder.
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