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Page 1: S7-2.1 44.6 HIGHAM, T.E., DAY, S.W., WAINWRIGHT, P.C ... · PDF fileSixteen extinct rhinocerotoid taxa were then examined for osteologi- ... species. Unpalatable butterflies in general

S7-2.1HEYLAND, A., MOROZ, L.L.; [email protected]. The WhitneyLaboratory for Marine Bioscience, Saint Augustine, University of FloridaSEARCH FOR NEURONAL TRANSCRIPTS INVOLVED IN THEMETAMORPHIC TRANSITION OF THE SEA HARE APLYSIACALIFORNICA

Metamorphosis among many marine invertebrate species involves aradical transition from a larval to a juvenile/adult body plan that can occurin a remarkably short period of time. Metamorphic competence directlyprecedes this radical change in morphology and can best be described as thedevelopmental potential of a larva to undergo the radical transition inresponse to environmental signals. Such signals (i.e. settlement cues, sub-strate architecture, temperature, food etc.) are modulated via neuronal genenetworks. A metamorphic pattern with competence and a fast radical trans-formation evolved many times independently in animals and we hypothe-size that similar signaling modules have been co-opted for the regulation ofa) the development to competence and b) the interpretation and modula-tion of environmental signals. However the actual signaling architectureunderlying these processes is largely unknown for the majority of marineinvertebrate species. We used representative oligo-arrays constructed fromtranscripts obtained from the Aplysia californica (sea hare, Mollusca) centralnervous system to explore the following two questions: 1) What neuron spe-cific genes are expressed during development to metamorphic competence?2) What neuron specific genes are expressed immediately after settlement,i.e. upon exposure to specific environmental signals. We validated ourexpression analysis of specific neuropeptides, nuclear hormone receptors andchemoreceptor molecules using in situ hybridizations. SupportContributed By: NIH, NSF, & McKnight BR Foundation.

44.6HIGHAM, T.E., DAY, S.W., WAINWRIGHT, P.C.;[email protected]. University of California, Davis, Rochester Instituteof TechnologyCAN PEAK BUCCAL CAVITY PRESSURE BE USED TO PREDICTPEAK FLUID SPEED DURING SUCTION FEEDING IN FISHES?

Suction-feeding fish capture prey by rapidly expanding their buccalcavity, which generates a flow of water directed towards their mouth. A sub-ambient pressure inside the buccal cavity is associated with this expansion,and the magnitude of this pressure differs considerably among species of fishand within an individual. Although peak sub-ambient pressure is thoughtto be proportional to fluid speed squared by Bernoullis principle, no studyhas measured both pressure and fluid speed simultaneously. Thus, we quan-tified buccal pressure and fluid speed simultaneously during feeding in fourindividuals of largemouth bass, Micropterus salmoides. We measured pres-sure by inserting a transducer through the skull of the fish so that the tip ofthe transducer was flush with the dorsal surface of the buccal cavity. Wemeasured fluid speed using digital particle image velocimetry (DPIV). Alaser sheet was positioned on the mid-sagittal plane of the fish so that thefluid speed could be measured along a transect extending from the center ofthe fishs mouth. We found that peak pressure was significantly correlated

with the peak fluid speed (r2=0.61; P<0.01) of the same feeding. However,the magnitudes of the pressures were much greater (up to 5 times) thanthose estimated from the measured fluid speeds. We found that peak pres-sure preceded peak gape and peak fluid speed by an average of 14 ms and18 ms, respectively. Thus, although correlated, pressure is sub-maximal atthe time of peak fluid speed. In conclusion, a substantial amount of varia-tion in peak fluid speed cannot be explained by peak pressure, suggestingthat a mechanism other than pressure is being modulated by the fish inorder to alter fluid speed. Supported by NSF IOB-0444554.

45.5HIERONYMUS, T.L., WITMER, L.M.; [email protected]. OhioUniversity, AthensFROM ARMOR TO ANCHOR: CHARACTER EVOLUTION OFTHE SKIN AND HORNS OF RHINOS

Previous reconstructions of extinct rhinocerotid taxa have invokedthree separate patterns of nasal horns, but without specifying an explicit andmechanistic relationship between unpreserved soft tissues and available oste-ological correlates. New data on the anatomy and histology of rhinoceroshorn attachment allows a reevaluation of previous reconstructions and anassessment of character evolution in the dermis and epidermis that make upthese unique horns. Numerous osteological specimens of extant rhinocerosand taxa with similar dermal histology were examined to test a mechanistichypothesis of osteological correlate formation in relation to an epidermalhorn. Sixteen extinct rhinocerotoid taxa were then examined for osteologi-cal correlates indicative of derived dermal architecture and keratinous horns.The resulting character scores were optimized onto a composite phylogenyof Rhinocerotoidea. Based on the co-occurrence of these osteological corre-lates with other morphological features commonly associated with agonisticbehaviors, a phylogenetically independent pairwise comparison was con-ducted to determine the extent of character correlation among a diversearray of extant mammalian taxa. This study found a consistent osteologicalcorrelate of horn attachment related to mechanical epigenetic control ofbone growth. This correlate is separate from the correlate of derived dermalarchitecture that occurs elsewhere on the skull. The latter first appears at thebase of Rhinocerotidae in the Middle Eocene, while true horns do notappear until the Late Oligocene Early Miocene, and only within the crowngroup Rhinocerotini. Character correlations between the relevant soft tissuesand other features in many extant mammalian taxa provide a basis for recon-structions of behavior and ecology in extinct rhinocerotids.

52.1HILL, R.I.; [email protected]. University of California, BerkeleyMORPHOLOGY AND LOCOMOTOR MIMICRY IN ITHOMIINEBUTTERFLIES (NYMPHALIDAE)

Neotropical ithomiine butterflies (Nymphalidae) exhibit rampantconvergent evolution of color patterns. It is not uncommon in lowlandrainforest to find up to nine color patterns at a site, with several species from2-5 genera exhibiting each pattern. This color pattern convergence is anexcellent example of Müllerian mimicry involving mutually distastefulspecies. Unpalatable butterflies in general have associated kinematic andmorphological traits such as slow flight, low wing beat frequency and rear-ward displaced center of body mass. Mimicry among unpalatable butter-flies is known to extend to flight morphology and kinematics in Heliconiusbutterflies, but the generality of this locomotor mimicry has not been test-ed. Morphological measurements of 38 species of ithomiine butterfliesfrom an assemblage in eastern Ecuador containing eight mimetic color pat-terns, or mimicry rings, are used to examine whether locomotor mimicryexists in the ithomiines. Do species that share color pattern also share flightmorphology? Principal components and discriminant function analyses areused to assess which morphological traits best discriminate among mimicryrings. Comparative analyses using a molecular phylogeny are also used toexamine scaling relationships and morphological trait evolution.

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