Locating a mate in 3D: the case of Temora longicornis

Using laser optics to illuminate high-resolution video-recordings, we revealed behavioural mechanisms through which males of the calanoid copepod speciesTemora longicornis locate females. Males ofT. longicornis swam at signi¢cantly faster speeds than females along more sinuous routes, possibly re£ecting adaptations to increase encounter with females. Upon approaching within 2mm (i.e. two body lengths) of a female’s swimming path, males accelerated to signi¢cantly higher pursuit speeds. Pursuit trajectories closely traced the trajectories of females, suggesting that males were following detectable trails created by swimming females. Males ofT. longicornis detected female trails up to at least 10-s old, and tracked trails for distances exceeding13 cm, or 130 body lengths. Females were positioned up to 34.2mm away from males (i.e. reactive distance) when males initiated ‘mate-tracking’. It was always the males of T. longicornis that detected and pursued mates. In rare events, males pursued other males. Behavioural £exibility was exhibited by males during mate-tracking. Males generally tracked the trails of ‘cruising’ (i.e. fast-swimming) females with high accuracy, while the pursuits of ‘hovering’ (i.e. slow-swimming) females often included ‘casting’ behaviour, in which males performed sharp turns in zigzag patterns within localized volumes.This casting by males suggested that hovering females create more dispersed trails than cruising females. Casting behaviour also was initiated by males near locations where females had hopped, suggesting that rapid movements by females disrupt the continuity of their trails. Males were ine⁄cient at choosing initial tracking directions, following trails in the incorrect direction in 27 of the 67 (40%) mating pursuits observed. Males usually attempted to correct misguided pursuits by ‘back-tracking’ along trails in the correct direction. Males were observed to detect and track their own previous trajectories without females present, suggesting the possibility that males follow their own trails during back-tracking. Observations of males tracking their own trails and the trails of other males bring into question the speci¢city of trails as a mechanism promoting reproductive isolation among co-occurring planktonic copepods.

[1]  M. Murano,et al.  Mating behavior of the marine copepodOithona davisae , 1988 .

[2]  B. Frost,et al.  Chemical Communication in the Marine Planktonic Copepods Calanus Pacificus and Pseudocalanus Sp , 1976 .

[3]  C. S. Holling The functional response of invertebrate predators to prey density , 1966 .

[4]  John J. Videler,et al.  Swimming behaviour of developmental stages of the calanoid copepod Temora longicornis at different food concentrations , 1995 .

[5]  M. Youngbluth,et al.  Mating behavior in three species of Pseudodiaptomus (Copepoda: Calanoida) , 1983 .

[6]  J. Fornshell,et al.  Population structure and swarm formation of the cyclopoid copepod Dioithona oculata near mangrove cays , 1991 .

[7]  J. Strickler,et al.  Calanoid Copepods, Feeding Currents, and the Role of Gravity , 1982, Science.

[8]  J. Gerritsen,et al.  Encounter Probabilities and Community Structure in Zooplankton: a Mathematical Model , 1977 .

[9]  Norman A. Slade,et al.  Apparent Size as the Determinant of Prey Selection by Bluegill Sunfish (Lepomis Macrochirus) , 1976 .

[10]  P. Tiselius,et al.  Foraging behaviour of six calanoid copepods: observations and hydrodynamic analysis , 1990 .

[11]  D. J. Hall,et al.  Optimal Foraging and the Size Selection of Prey by the Bluegill Sunfish (Lepomis Macrochirus) , 1974 .

[12]  S. Katona EVIDENCE FOR SEX PHEROMONES IN PLANKTONIC COPEPODS , 1973 .

[13]  W. Peterson,et al.  Seasonal contrasts in the diel vertical distribution, feeding behavior, and grazing impact of the copepod Temora longicornis in Long Island Sound , 1993 .

[14]  J. Videler,et al.  The trade-off between feeding, mate seeking and predator avoidance in copepods: behavioural responses to chemical cues , 1996 .

[15]  Jr Strickler,et al.  Matched spatial filters in long working distance microscopy of phase objects , 1999 .

[16]  J. Yen,et al.  Advertisement and concealment in the plankton: what makes a copepod hydrodynamically conspicuous? , 1996 .

[17]  E. Buskey Swimming pattern as an indicator of the roles of copepod sensory systems in the recognition of food , 1984 .

[18]  G. Boxshall,et al.  Functional Significance of the Sexual Dimorphism in the Cephalic Appendages of Euchaeta Rimana Bradford , 1997 .

[19]  C. S. Holling Some Characteristics of Simple Types of Predation and Parasitism , 1959, The Canadian Entomologist.

[20]  W. Peterson Abundance, age structure and in situ egg production rates of the copepod Temora longicornis in Long Island Sound, New York , 1985 .