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79

DENVER MUSEUM OF NATURE & SCIENCE

REPORTS

|

No. 3, July 2, 2016

20

th

International Congress of Arachnology

release lines as they move in their webs. Some crucial

aspects of tarsal morphology were elegantly documented

long ago by E. Nielsen. Several recent advances on the

behavioral side have been made possible by video recordings

of behavior. The spider’s legs routinely follow each other in

various behavioral contexts, thus economizing on the

exploratory behavior needed by more posterior legs to locate

new lines. The short-distance searching movements made

by a following leg are asymmetrical (prolateral for legs I

and II, retrolateral for legs III and IV), and these orienta-

tions are appropriate to allow their asymmetrically placed

median claws and serrate accessory setae to contact and

grasp the lines that they encounter. And the tarsus itself (or,

less likely its claw) is routinely twisted on its longitudinal

axis to bring the median claw into a position perpendicu-

lar to the line, thus allowing the claw to clamp even those

lines that are parallel to the spider’s longitudinal axis.

Keywords: behavior, functional morphology, web spiders

Student - oral presentation

Control of signal alignment during the

dynamic courtship display of a salticid

*Sebastian A. Echeverri, Nathan I. Morehouse, Daniel B.

Zurek

Department of Biological Sciences, University of Pitts-

burgh, 4249 5th Avenue, Pittsburgh, PA 15260, USA

sae53@pitt.edu

Signals are often directional, meaning that they are best

perceived from certain angles. Likewise, sensory systems

often have directional biases. Thus, alignment of directional

signals and directional sensors may often be critical for

effective communication. However, we know little about

how animals establish and maintain alignment during

signaling. We analyzed the dynamic courtship dances of the

jumping spider

Habronattus pyrrithrix

to better under-

stand how often alignment is achieved, and who is primarily

responsible (i.e. male, female, or both). In this species,

courtship consists of distinct long- and short-range phases.

Males produce a forward-facing visual display that includes

color, pattern, and movement. Females view this display

with two types of eyes: color sensitive principal eyes with

narrow fields of view, and colorblind secondary eyes with

wide fields of view. The combined inputs of these eyes create

a visual field where colors and fine patterns of male displays

can only be perceived by a female if the male is in front of

her. We recorded relative positions and orientations of both

actors throughout courtship to evaluate how consistently

male displays are aligned with the female principal field of

view, and who is responsible. Males always oriented their

displays toward the female. When females were free to move,

male displays were only consistently aligned with female

color vision during the short range phase. When female

position was fixed, signal alignment consistently occurred

during both courtship phases, and maximal alignment

during the short range phase occurred for a greater propor-

tion of time. This suggests that normal female movements

may reduce communication efficacy. In addition, when

tethered females were rotated to face away, males rarely

repositioned themselves to re-align their display. Thus,

although signal alignment is a function of both sexes, males

may rely on females for effective communication.

Keywords: communication efficacy, courtship signaling,

signaling behavior, Salticidae

Oral presentation

Revision of

Misumessus

(Araneae: Thomis-

idae), with observations on crab spider

epigynal hoods

G. B. Edwards

Florida State Collection of Arthropods, 1911 SW 34th

Street Gainesville, FL 32608 USA

gb.edwards@freshfromflorida.com

The previously monotypic genus

Misumessus

, type species

M. oblongus

(Keyserling, 1880), is found to consist of

at least seven species distributed throughout most of

North America, all of Central America, Bermuda, and the

Greater and Lesser Antilles. Species are distinguished in

the males primarily by the position of the embolus base

and the length of the filamentous end of the embolus,

with the embolus curling around the tegulum more than

360 degrees. In the females, differences are more subtle,

but length and shape of the median epigynal piece, and

differences in face morphology detail, can distinguish

them. In addition, four of the species have other distinctive