A phylogenetic study on genera of Cidariini from the Holarctic and the Indo-Australian areas (Lepidoptera: Geometridae: Larentiinae)

A cladistic analysis of forty-one species, belonging to ten genera, of the Cidariini sensu Herbulot from the Holarctic and the Indo-Australian areas, was performed using seventy-seven characters including larval and pupal data. Eight most parsimonious cladograms were found (length 398, CI 0.30, RI 0.70). The monophyly of the Cidariini is demonstrated, using selected species of Xanthorhoini sensu Herbulot as the outgroup. The relationships among the genera are as follows: ( Ecliptopera ( Eulithis ( Cidaria (( Plemyria ( Chloroclysta , Dysstroma ))(( Thera , Pennithera ) ( Heterothera ))))). This result suggests some taxonomic changes: Dysstroma Hübner, stat. rev. and Chloroclysta Hübner stat. rev. are sister taxa; Heterothera Inoue stat. rev. includes Viidaleppia Inoue, syn.n., Heterothera firmata (Hübner) comb.n. is transferred from Pennithera Viidalepp to Heterothera sensu lato . The results of confirmation and incongruence tests suggest that the characters from adult and immature stages exhibit the same evolutionary pattern. Thus the phylogeny derived from the combined data matrix does not give a misleading conclusion, even though there are many missing states in the larval data set.     

Intra- and interspecific sex-pheromone communication in the genus Yponomeuta

ABSTRACT. Male behaviour in pheromone attraction was observed in a wind tunnel for eight species of the genus Yponomeuta Latreille. Interspecific responses and the effect of some combinations of female pheromones were also investigated. The results show that the species Yponomeuta cagnagellus (Hübner), Y. malinellus Zeller, Y. rorellus (Hübner) and Y. plumbellus (Den. & Schiff.) are isolated by the specificity of their female pheromones. The other four species, Y. evonymellus (L.), Y. padellus (L.), Y. irrorellus (Hübner) and Y. vigintipunctatus (Retz.), exhibited interspecific pheromone attraction.     

Phylogenetic relationships of Acronictinae with discussion of the abdominal courtship brush in Noctuidae (Lepidoptera)

We present results of an eight‐gene molecular study of the subfamily Acronictinae and related Noctuidae. Amphipyrinae are recovered as sister to Acronictinae, but with weak support – not surprisingly, the content of the two subfamilies has often been mixed in classifications. Balsinae, previously placed near Acronictinae or within Noctuinae, is recovered within an unresolved polytomy of Cuculliinae, Eustrotiinae, Raphiinae and Dilobinae. Gerbathodes Warren, Moma Hübner and Nacna Fletcher are excluded from Acronictinae. Three genera recently transferred into the subfamily – Cerma Hübner, Chloronycta Schmidt & Anweiler and Comachara Franclemont – are confirmed as acronictines. Lophonycta Sugi (the type genus of Lophonyctinae) is returned to the Acronictinae. Sinocharis Püngeler, formerly considered to be Acontiinae or as the basis of its own subfamily Sinocharinae, is nested within early diverging Acronictinae genera. Both subfamilies are formally synonymized: i.e. Lophonyctinae syn.n. and Sinocharinae syn.n. Nine acronictine genus‐level taxa were found to nest within the nominate genus Acronicta Ochsenheimer: Eogena Guenée, Hyboma Hübner, Hylonycta Sugi, Jocheaera Hübner, Oxicesta Hübner, Simyra Ochsenheimer, Subacronicta Kozhanchikov, Triaena Hübner, and Viminia Chapman. Eogena, Oxicesta, and Simyra, currently treated as valid genera, nest within terminal clades of the genus Acronicta and are here subsumed within the genus: Eogena syn.n. , Oxicesta syn.n. and Simyra syn.n. Four well‐supported species groups within Acronicta are identified: the alni clade, the leporina clade, the nervosa clade and the psi clade. While many previous treatments have stated explicitly that Acronictinae lack abdominal scent brushes, or excluded genera with brushes from the subfamily, we show that well‐developed brushes are present in three early diverging acronictine genera: Cerma, Lophonycta, and Sinocharis. We illustrate and describe the brushes of all three genera, and briefly review the taxonomic distribution of the anterior abdominal courtship brushes in Noctuidae, emphasizing the labile evolutionary distribution of these structures.     

Impact of (Z)-7-dodecenol and turbulence on pheromone-mediated flight manoeuvres of male Trichoplusia ni

Abstract. Turbulence and chemical noise are two factors which may influence pheromone-mediated flight manoeuvres of a moth in natural habitats. In this study, the effects of turbulence and the behavioural antagonist (Z)-7-dodecenol on flight manoeuvres of male Trichoplusia ni (Hübner) were evaluated in a wind tunnel. Male moths increase airspeed and course angles when turbulence is increased. This leads to significant increases in the length of flight tracks, but significant reductions in the time taken to reach a pheromone source. In less disturbed pheromone plumes, distributions of course angles and track angles of male T.ni show a prominent peak centred about 0° relative to the upwind direction, indicating that moths can temporarily steer directly upwind toward a pheromone source.
When (Z)-7-dodecenol is released 10 cm upwind of a pheromone source to form an overlapping plume downwind, course angles, airspeeds and ground-speeds of male T.ni are reduced significantly compared with those in uncon-taminated pheromone plumes. This results in a longer flight time to reach a pheromone source. The decrease in flight speed would decrease the rate of contact with filaments, and thereby perhaps allow the moth to detect uncon-taminated pheromone filaments independently from filaments containing the behavioural antagonist.     

Evolution of ecological traits and wing morphology in Hemileuca (Saturniidae) based on a two-gene phylogeny

We present a molecular phylogeny for the genus Hemileuca (Saturniidae), based on 624 bp of mitochondrial cytochrome oxidase I (COI) and 932 bp of the nuclear gene elongation factor 1 alpha (EF1alpha). Combined analysis of both gene sequences increased resolution and supported most of the phylogenetic relationships suggested by separate analysis of each gene. However, a maximum parsimony (MP) model for just COI sequence from one sample of most taxa produced a phylogeny incongruent with EF1alpha and combined dataset analyses under either MP or ML models. Time of year and time of day during which adult moths fly corresponded strongly with the phylogeny. Although most Hemileuca are diurnal, ancestral Hemileuca probably were nocturnal, fall-flying insects. The two-gene molecular phylogeny suggests that wing morphology is frequently homoplastic. There was no correlation between the primary larval hostplants and phylogenetic placement of taxa. No phylogenetic pattern of specialization was evident for single hostplant families across the genus. Our results suggest that phenological behavioral characters may be more conserved than the wing morphology characters that are more commonly used to infer phylogenetic relationships in Lepidoptera. Inclusion of a molecular component in the re-evaluation of systematic data is likely to alter prior assumptions of phylogenetic relationships in groups where such potentially homoplastic characters have been used.     

A phylogeographical analysis of the bemisia tabaci species complex based on mitochondrial DNA markers

Mitochondrial 16S ( approximately 550 bp) and cytochrome oxidase I (COI) ( approximately 700 bp) sequences were utilized as markers to reconstruct a phylogeography for representative populations or biotypes of Bemisia tabaci. 16S sequences exhibited less divergence than COI sequences. Of the 429 characters examined for COI sequences, 185 sites were invariant, 244 were variable and 108 were informative. COI sequence identities yielded distances ranging from less than 1% to greater than 17%. Whitefly 16S sequences of 456 characters were analysed which consisted of 298 invariant sites, 158 variable sites and 53 informative sites. Phylogenetic analyses conducted by maximum parsimony, maximum-likelihood and neighbour-joining methods yielded almost identical phylogenetic reconstructions of trees that separated whiteflies based on geographical origin. The 16S and COI sequence data indicate that the B-biotype originated in the Old World (Europe, Asia and Africa) and is most closely related to B-like variants from Israel and Yemen, with the next closest relative being a biotype from Sudan. These data confirm the biochemical, genetic and behavioural polymorphisms described previously for B. tabaci. The consideration of all global variants of B. tabaci as a highly cryptic group of sibling species is argued.     

Cladistic analysis of the Neotropical butterfly genus Adelpha (Lepidoptera: Nymphalidae), with comments on the subtribal classification of Limenitidini

Abstract.  A two-stage cladistic analysis of 114 characters from adult and immature stage morphology provided phylogenetic hypotheses for the diverse Neotropical nymphalid butterfly genus Adelpha Hübner. Higher-level cladistic relationships were inferred for thirty Adelpha species and twenty other species of Limenitidini, confirming the monophyly of Adelpha as currently conceived and indicating several montane Asian species as potential sister taxa for the genus. Cladistic relationships between all eighty-five Adelpha species were then inferred using three outgroup combinations. Basal and terminal nodes were reasonably resolved and supported, but a low proportion of non-wing pattern characters resulted in weak resolution and support in the middle of the tree. The most basal members of Adelpha feed on the temperate or montane plant family Caprifoliaceae, suggesting that a switch from this family early in the evolutionary history was important in subsequent diversification into tropical lowland habitats. The cladograms confirm suspicions of earlier authors that dorsal mimetic wing patterns have convergently evolved a number of times in Adelpha . The subtribal classification of Limenitidini is discussed and both Lebadea (from Parthenina) and Neptina are transferred to Limenitidina, whereas Cymothoe , Bhagadatta and Pseudoneptis (all formerly Limenitidina) are regarded as incertae sedis .     

A phylogenetic analysis of the Neotropical riodinid butterfly genera Juditha, Lemonias, Thisbe and Uraneis, with a revision of Juditha (Lepidoptera: Riodinidae: Nymphidiini)

Abstract. A cladistic analysis is presented for all twenty-four species in the Neotropical riodinid butterfly genera Juditha Hemming, Lemonias Hübner, Thisbe Hübner and Uraneis Bates based on sixty-nine characters of male and female morphology and external facies, and utilizing Audre domina Bates as the outgroup. All characters are illustrated. The analysis confirms the monophyly of Juditha and Uraneis , but indicates that Lemonias is polyphyletic and Thisbe is paraphyletic with respect to Uraneis , leading us to synonymize Uraneis with Thisbe (syn.n.). Juditha is found to be the sister clade to true Lemonias + ( Thisbe + Uraneis ). A revision of Juditha is presented which includes discussions on the taxonomy, biology and distribution of its species, and illustrations of the adults and male and female genitalia of all taxa and the early stages of an exemplar, J. caucana . Eight species are recognized in Juditha , including two, J. naza and J. inambari , which are described as new. The following new generic combinations are made: rubigo Bates is transferred from Juditha to Pachythone Bates; agave Godman & Salvin and leucogonia Stichel are transferred from Lemonias to Pseudonymphidia Callaghan; ochracea Mengel, theodora Godman and albofasciata Godman are transferred from Audre Hemming to Lemonias; fenestrella Lathy is transferred from Thisbe to Synargis Hübner; hyalina Butler, ucubis Hewitson and incubus Hall, Lamas & Willmott are transferred from Uraneis to Thisbe; and odites Cramer (= phylleus Auctt.) is transferred from Synargis to Juditha (comb.n.).     

A review of the moth tribe Palyadini with the description of a new genus (Geometridae: Ennominae)

The tribe Palyadini Guenée is revised at the generic level. It includes about 115 described species, and occurs in tropical America with representatives from Florida to Argentina. There are six genera: Palyas Guenée, Phrygionis Hübner, Pityeja Herrich-Schäffer, Argyrotome Warren, Opisthoxia Hübner, and a new genus Ophthalmoblysis. Ophthalmophora Guenée and Argyroplutodes Warren are treated as junior synonyms of Opisthoxia. Checklists of the species-group names in each genus are included.     

Taxonomy of the Cidariini (Lepidoptera, Geometridae) in Korea (I)

ABSTRACT Among forty species of the Korean Cidariini, a tribe of Larentiinae (Lepidoptera, Geometridae), nineteen species of ten genera are revised: Ecliptopera Warren, Lampropteryx Stephens, Eustroma Hübner, Eveeliptopera Inoue, Lobogonodes Bastelberger, Hysterura Warren, Sibatania Inoue, Eulithis Hiibner, Gandaritis Moore, and Electrophaes Prout. The diagnostic characters and monophyly of each genus are provided. Figures of adults including male and female genitalia, and distribution maps in Korea are also provided.     

Molecular systematics of the order anaspidea based on mitochondrial DNA sequence (12S, 16S, and COI)

Fragments from three mitochondrial genes (12S, 16S, and COI) were sequenced to reconstruct a molecular phylogeny of the opisthobranch order Anaspidea. The molecular phylogeny supports the placement of the genus Akera, a taxon previously regarded by some authors as a cephalaspidean, within the Anaspidea. Incongruence between the molecular data and the classifications based on morphology suggests that some of the taxonomic characters (i.e., shell, parapodia fusion) traditionally used for the classification of sea hares must be reevaluated, since they may be homoplastic. The ancestral nature of Notarchus based on the molecular evidence suggests that homoplasy may be an explanation for the morphological resemblance of this species to the more derived sea hares with highly fused parapodia and concentrated nerve ganglia. Finally, examples are given of how comparative studies of the evolution of learning mechanisms in the anaspidean clade will benefit from the phylogenetic hypothesis presented in this paper.     

THE CLADISTICS OF AMAURIS BUTTERFLIES: CONGRUENCE, CONSENSUS AND TOTAL EVIDENCE

Abstract— Two data sets for 10 species of African milkweed butterflies (Nymphalidae, Danainae: one Danaus , two Tirumala , seven Amauris ) have been analysed cladistically, separately and in combination. One data set comprised 32 morphological characters, the other comprised 68 chemical compounds from male scent organs. Analysed separately, the two data sets produced six similar but non-identical minimum-length solutions. Analysed together, the combined data set of 100 characters produced a single minimum-length tree, identical to one of the three solutions for the morphological data set. The combined data produced a more informative result than congruence comparisons based on strict or combinable component consensus analysis. These results, together with re-analysis of a morphological data set for all 15 species of Amauris (which produced 12 minimum-length solutions), permit increased resolution of the existing classification of this Afrotropical genus, including the formal recognition of two subgenera, Amauris ( Amauris ) Hübner, and Amauris ( Amaura ) Geyer ( stat. rev. ). The fit of uniquely derived, unreversed chemical characters to the tree raises the possibility that stepwise additive evolution of semiochemicals may have occurred during cladogenesis of these mimetic butterflies. The implications for chemoecology and speciation are briefly discussed.     

The age and phylogeny of wood boring weevils and the origin of subsociality

A large proportion of the hyperdiverse weevils are wood boring and many of these taxa have subsocial family structures. The origin and relationship between certain wood boring weevil taxa has been problematic to solve and hypotheses on their phylogenies change substantially between different studies. We aimed at testing the phylogenetic position and monophyly of the most prominent wood boring taxa Scolytinae, Platypodinae and Cossoninae, including a range of weevil outgroups with either the herbivorous or wood boring habit. Many putatively intergrading taxa were included in a broad phylogenetic analysis for the first time in this study, such as Schedlarius, Mecopelmus, Coptonotus, Dactylipalpus, Coptocorynus and allied Araucariini taxa, Dobionus, Psepholax, Amorphocerus-Porthetes, and some peculiar wood boring Conoderini with bark beetle behaviour. Data analyses were based on 128 morphological characters, rDNA nucleotides from the D2-D3 segment of 28S, and nucleotides and amino acids from the protein encoding gene fragments of CAD, ArgK, EF-1α and COI. Although the results varied for some of the groups between various data sets and analyses, one may conclude the following from this study: Scolytinae and Platypodinae are likely sister lineages most closely related to Coptonotus; Cossoninae is monophyletic (including Araucariini) and more distantly related to Scolytinae; Amorphocerini is not part of Cossoninae and Psepholax may belong to Cryptorhynchini. Likelihood estimation of ancestral state reconstruction of subsociality indicated five or six origins as a conservative estimate. Overall the phylogenetic results were quite dependent on morphological data and we conclude that more genetic loci must be sampled to improve phylogenetic resolution. However, some results such as the derived position of Scolytinae were consistent between morphological and molecular data. A revised time estimation of the origin of Curculionidae and various subfamily groups were made using the recently updated fossil age of Scolytinae (100 Ma), which had a significant influence on node age estimates.     

The evolution of social behaviour in Blaberid cockroaches with diverse habitats and social systems: phylogenetic analysis of behavioural sequences

The adequacy and utility of behavioural characters in phylogenetics is widely acknowledged, especially for stereotyped behaviours. However, the most common behaviours are not stereotyped, and these are usually seen as inappropriate or more difficult to analyze in a phylogenetic context. A few methods have been proposed to deal with such data, although they have never been tested on samples larger than six species, which limits their evolutionary interest. In the present study, we perform behavioural observations on 13 cockroach species and derive behavioural phylogenetic characters with the successive event‐pairing method. We combine these characters with morphological and molecular data (approximately 6800 bp) in a phylogenetic study of 41 species. We then reconstruct ancestral states of the behavioural data to study evolution of social behaviour in these insects with regard to their social systems (i.e. solitary, gregarious, and subsocial) and diversity of habitat choice. We report for the first time that nonstereotyped behavioural data are adequate for phylogenetic analyses: they are no more homoplastic than traditional data, and support several phylogenetic relationships that we discuss. From an evolutionary perspective, we show that the solitary species Thanatophyllum akinetum does not display original behavioural interactions, suggesting phylogenetic inertia of interactive behaviours despite a radical change in social structure. Conversely, the subsocial species Parasphaeria boleiriana shows original behavioural interactions, which could result from its peculiar social system or habitat. We conclude that phylogenetic approaches in studies of behaviour are useful for deciphering evolution of behaviour and discriminating between its different modalities, even for nonstereotyped characters. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 111 , 58–77.     

Exposure to fenitrothion causes malfunctions of Spodoptera exigua Hübn. (Lep., Noctuidae) eggs

A long-term exposition of Spodoptera exigua (Hübner) larvae to fenitrothion caused abnormalities in egg structure. When examined under a scanning electron microscope, the eggs revealed diminutions and cracks around the micropylar and aeropylar region. The damage was proportional to the concentration of the insecticide. The observed changes may be one of the reasons for the decreased survival of populations exposed to fenitrothion.     

Phylogenetic utility and comparative morphology of the composite scale brushes in male phycitine moths (Lepidoptera, Pyralidae)

Male pyralid moths in the subfamily of Phycitinae are known to possess composite scale brush structures associated with the 8th abdominal sternite, but the histology and the structural morphology of these organs have not been adequately explored. As such, the phylogenetic utility of these structures is unknown. We examine the pre-genitalic abdominal histology of male Dioryctria reniculelloides (Pyralidae: Phycitinae) associated with the composite scale brushes, as well as structural morphology within the genus Dioryctria and two closely related genera. The composite scale brushes are composed of fused scales. The musculature associated with the base of sternum 8 shows considerable modification compared to previously described Lepidoptera. Complex glandular tissue was also found associated with the scale brush structures, suggesting secretory function. Phylogenetic utility of ultrastructure and gross morphology was examined for major Dioryctria species groups. Many characters were homoplasious, but several supported the monophyly of the genus, as well as some internal relationships. In conclusion, the combination of ultrastructural, gross morphological and histological characters can be a rich source of information for elucidating a range of evolutionary relationships within the subfamily.     

Phylogenetic analysis of the genus Cheilosia (Diptera, Syrphidae) using mitochondrial COI sequence data

The genus Cheilosia is one of the most diverse and speciose genera of Syrphidae (Diptera). The phylogenetic relationships of the hoverfly genus Cheilosia was investigated for the first time using molecular data. The mitochondrial protein-coding gene cytochrome c oxidase subunit I (COI) was chosen for sequencing; 1341 characters were obtained for 24 ingroup taxa and these were analyzed with parsimony. The monophyly of the genus Cheilosia was well supported. Current taxonomic division of Cheilosia into two subgenera (sg. Nigrocheilosia and sg. Neocheilosia) and most nonformalized species groups based on morphology were supported by the monophyletic groups identified in the molecular analysis. The phylogenetic informativeness of COI in resolving the subtribal relationships within the tribe Cheilosiini remains ambiguous.     

Molecular identification of three Ompok species using mitochondrial COI gene

A DNA-based barcode identification system that is applicable to all animal species will provide a simple, universal tool for the identification of fish species. The barcode system is based on sequence diversity in subunit 1 cytochrome c oxidase (COI) gene. Identification and characterization of fish species based on morphological characters are sometimes found to be erroneous and environmentally affected. There are no studies on the genus Ompok in India at molecular level and species identification of the Ompok is usually carried out through morphological features. A total of 106 samples from three species Ompok pabda, O. pabo and O. bimaculatus were collected from eight sampling sites of seven Indian rivers. One hundred and six sequences were generated from COI region of three Ompok species and 21 haplotypes were observed. The sequence analysis of COI gene revealed three genetically distinct Ompok species and exhibited identical phylogenetic resolution among them. The partial COI gene sequence can be used as a diagnostic molecular marker for identification and resolution of taxonomic ambiguity of Ompok species.     

Preference for bedding material in Syrian hamsters

This study aimed to determine whether Syrian (golden) hamsters, Mesocricetus auratus, prefer certain bedding materials and whether bedding material can affect paw condition, body weight gain and wheel-running activity. In a first experiment, 26 male hamsters had access to two connected cages, each cage containing a different bedding material (either pine shavings, aspen shavings, corn cob or wood pellets). In a second experiment, 14 male hamsters had access to four connected cages that contained the different bedding materials and also a piece of paper towel to serve as nest material. In a third experiment, 30 male hamsters were each placed in a single cage, 10 of them with pine shavings, 10 with aspen shavings and 10 with corn cob, and they were monitored for 50 days. Significant preferences in the first experiment were: pine shavings over aspen shavings, corn cob over wood pellets, pine shavings over corn cob and aspen shavings over wood pellets (aspen shavings versus corn cob was not tested). However, there was no significant preference expressed in the second experiment, suggesting that the general preference for shavings in the first experiment was based on bedding material suitability as a nesting material. No significant effect of bedding material on paw condition, body weight gain and wheel-running activity was detected. None of the four bedding materials tested in this study can be judged to be inappropriate in the short term if nesting material is added to the cage and if the litter is changed regularly.     

A phylogenetic approach to the evolution of fish behaviour

Summary WHAT HAVE WE LEARNED?As I indicated in the introduction, this is a non-traditional review. I have not asked What generalizations can we draw about the evolution of fish behaviour based upon information gleaned from phylogenetically based studies? Instead, I have presented detailed discussions of those studies. The reason for this approach is quite simple: if all studies in such a wide area of investigation can be discussed at length in one relatively short paper, then the database is not large enough to warrant the move from information collection to information synthesis. The purpose of this review, then, has been to capture the enthusiasm of the phylogenetically orientated fish ethologists and to highlight their discoveries, in the hopes that this will stimulate further research. If successful, the next review of phylogeny and the evolution of fish behaviour will follow a more familiar pathway.Although the database does not allow us to draw generalizations about the evolution of specific behavioural characters in fishes, the studies to date have uncovered a number of more general evolutionary insights. First, phylogenetic conservatism is evident at all levels of analysis, from the muscle activity patterns that underlie behavioural characters (Lauder 1986; Westneat and Wainwright, 1989; Westneat 1991; Wainwright and Lauder, 1992) through foraging preferences (Winterbottom and McLennan, 1993) and egg deposition strategies (Johnston and Page, 1992) to parental care (Stiassney and Gerstner, 1992). This conservatism forms the backbone against which the appearance of novel behaviours (apomorphies) can be highlighted. Each species' behavioural repertoire is thus a unique combination of very old (plesiomorphic), relatively old (synapomorphic) and recently derived (autapomorphic) characters. Second, phylogenetic analysis has allowed us to investigate models of behavioural evolution that were constructed from a variety of microevolutionary fitness parameters. The macroevolutionary patterns have corroborated some parts of those models (transition from biparental to female-only care: Gross and Sargent, 1985; Stiassney and Gerstner, 1992; transition from fresh water to anadromy: Gross et al., 1988; Stearley, 1992) and highlighted other parts of the models that would benefit from a re-examination of the basic assumptions (transition from biparental or female-only to male-only care: Gross and Sargent, 1985; Stiassney and Gerstner, 1992). Third, expanding our evolutionary perspective to include clades of organisms has allowed researchers to formulate new theories of behavioural evolution incroporating information about the patterns of character origin and diversification as well as information about character maintenance (Ryan, 1900a; Ryan and Rand, 1990; Ryan et al., 1990a). And finally, examination of macroevolutionary correlations between the origin and diversification of behavioural characters has allowed us to make predictions about the forces influencing the evolution of those characters that can then be tested experimentally (McLennan et al., 1988; Basolo, 1990a,b, 1991; McLennan, 1991). The studies presented in this paper have spanned a wide theoretical arena. They have revealed a number of interesting insights about the evolution of behaviour, and in so doing, have demonstrated the hybrid vigour of a research programme based upon integrating phylogeny and experimental ethology, phylogeny and functional morphology, and phylogeny and behavioural ecology. The question to be answered now is:WHERE DO WE GO FROM HERE?If this fledgling research programme is to remain vigorous, we need to do two things. First, channels of communication must be re-opened between systematists and ethologists. Specifically, we need to encourage systematists to construct robust phylogenetic trees for groups of fish that either have already been well studied behaviourally and ecologically, or would be of interest to ethologists if a phylogeny existed (the belontiids, poeciliids, and rivulines come to mind, to name just a few). In the absence of such critical information, behavioural ecologists are faced with the option of investigating their ethological data based upon trees reconstructed from old classification schemes or phenograms, neither of which produces a robust phylogenetic hypothesis of genealogy. Researchers who have opted for this approach preface their investigations with the caveat that the analysis and conclusions are only preliminary because of the unsatisfactory nature of the phylogenetic hypotheses available to them. The importance of a preliminary analysis cannot be understimated for researchers who are frustrated by their inability to apply the phylogenetic approach to their burgeoning data sets. It is, however, critical to remember that a preliminary analysis can, at best, produce only tentative results. If the data themselves are both incomplete and ambiguous, this will compound the problems arising from the absence of a rigorous phylogenetic framework, which will produce a confusing picture of behavioural evolution. It is also important to realize that even the most robust phylogenetic tree is still only a hypothesis of genealogical relationships, a hypothesis that may change with the discovery of new data.Second, links must be forged between comparative ethology and behavioural ecology. All of the examples discussed in this paper uncovered a phylogenetic component in patterns of behavioural origin and diversification. The discovery of this phylogenetic influence, however, is only the first step in developing a comprehensive evolutionary picture because phylogenetic patterns can tell us very little about the processes underlying those patterns. In order to explore questions of process, we must incorporate information about the fitness parameters of behavioural characters into our evolutionary picture. For example, optimizing such parameters onto a phylogenetic tree may allow us to investigate whether there are any macroevolutionary correlations between the origin and divergence of a behaviour and a change in one (or more) of the fitness components. We must also incorporate information about the genetic, developmental and physiological control of behaviour into our comparative framework (Brooks and McLennan, 1991; Willis et al., 1991; Lauder et al., 1993). This is perhaps the most neglected aspect of comparative ethology and will thus be the most difficult to remedy. Details of the genetic and developmental systems underlying behaviour are known for only a handful of taxa and for only a handful of behaviours within those taxa. The physiological control of behaviour is better studied, but has yet to be placed within a phylogenetic context (but see e.g. Stearley, 1992, for an example of the insights that can be gained from such a study). The results of such a multilevel approach will be a more robust estimate of the relative roles for the effects of both phylogenetic heritage and environmental factors in the evolution of behaviour in fishes.