Abstract:Abstract. Two phylogenies of Morpho butterfl ies were previously published, founded on morphological data analysis. These phylogenies shared similarities but also several differences. In the present study we used partial sequences of the CO1 and Cyt b mitochondrial genes to infer the phylogenetic relationships between the subgenera. From the ten subgenera previously described, seven are shown to be monophyletic: Iphimedeia, Laurschwartzia, Iphixibia, Megamede, Grasseia, Balachowskyna and Deyrollia. Although no… Show more
“…This study showed that CO I gene alone was not enough to produce synapomorphies on each node but this gene was able to show a good support for a certain closely-related species. Previous study showed the mitochondrial gene CO I was very useful when combined with Cytochrome b to resolve the relationships in the genus Morpho (Nymphalidae) (Cassildé et al, 2012), or when combined with CO II in the genus Papilio (Caterino and Sperling, 1999). In addition, the combination of the CO I and EF-1α increased resolution and supports most of the phylogenetic relationships suggested by separate analysis of Ectoedemia s. str.…”
Many species of Lymantria are important forestry pests, including L. dispar which is well known distributed from Asia to North America as an invasive species. Like of most other genera of moths, the systematic of this genus is still in dispute, especially on the monophyly and the relationship within this genus due to the fact that genus is very large and varied. This genus was morphologically defined only by a single aphomorphy. To clarify the monophyly of the genus Lymantria, to reveal the phylogenetic relationship among the Indonesian species, and to establish the genetic characters of Indonesian Lymantria, we analyzed 9 species of Indonesian Lymantria involving 33 other species distributed around the world based on nucleotide sequence variation across a 516-bp region in the CO I gene. The results showed that the base composition of this region was a high A+T biased (C: 0.3333). The results also showed that the monophyly of Lymantria was not supported by bootstrap tests at any tree building methods. Indonesian species was distributed into four different groups but the relationship among them was still in dispute. It indicates that relationships among the basal nodes (groups) proposed here were least valid due to the fact that the number of species may not be enough to represent the real number of species in the nature. Moreover CO I gene sequences alone were not able to resolve their relationships at the basal nodes. More investigations were needed by including more species and other genes that the more conserved.
“…This study showed that CO I gene alone was not enough to produce synapomorphies on each node but this gene was able to show a good support for a certain closely-related species. Previous study showed the mitochondrial gene CO I was very useful when combined with Cytochrome b to resolve the relationships in the genus Morpho (Nymphalidae) (Cassildé et al, 2012), or when combined with CO II in the genus Papilio (Caterino and Sperling, 1999). In addition, the combination of the CO I and EF-1α increased resolution and supports most of the phylogenetic relationships suggested by separate analysis of Ectoedemia s. str.…”
Many species of Lymantria are important forestry pests, including L. dispar which is well known distributed from Asia to North America as an invasive species. Like of most other genera of moths, the systematic of this genus is still in dispute, especially on the monophyly and the relationship within this genus due to the fact that genus is very large and varied. This genus was morphologically defined only by a single aphomorphy. To clarify the monophyly of the genus Lymantria, to reveal the phylogenetic relationship among the Indonesian species, and to establish the genetic characters of Indonesian Lymantria, we analyzed 9 species of Indonesian Lymantria involving 33 other species distributed around the world based on nucleotide sequence variation across a 516-bp region in the CO I gene. The results showed that the base composition of this region was a high A+T biased (C: 0.3333). The results also showed that the monophyly of Lymantria was not supported by bootstrap tests at any tree building methods. Indonesian species was distributed into four different groups but the relationship among them was still in dispute. It indicates that relationships among the basal nodes (groups) proposed here were least valid due to the fact that the number of species may not be enough to represent the real number of species in the nature. Moreover CO I gene sequences alone were not able to resolve their relationships at the basal nodes. More investigations were needed by including more species and other genes that the more conserved.
“…We selected 119 sequences from two previously published datasets (Cassildé et al. ; Penz et al. ) and complemented this dataset with 24 additional nuclear sequences (see Supporting Information S1).…”
Section: Methodsmentioning
confidence: 99%
“…Although the genus has received recent attention to resolve phylogenetic relationships (Penz and DeVries ; Cassildé et al. , ; Penz et al. ; Blandin and Purser ), a completely resolved phylogenetic tree is still lacking.…”
Butterfly wings harbor highly diverse phenotypes and are involved in many functions. Wing size and shape result from interactions between adaptive processes, phylogenetic history, and developmental constraints, which are complex to disentangle. Here, we focus on the genus Morpho (Nymphalidae: Satyrinae, 30 species), which presents a high diversity of sizes, shapes, and color patterns. First, we generate a comprehensive molecular phylogeny of these 30 species. Next, using 911 collection specimens, we quantify the variation of wing size and shape across species, to assess the importance of shared ancestry, microhabitat use, and sexual selection in the evolution of the wings. While accounting for phylogenetic and allometric effects, we detect a significant difference in wing shape but not size among microhabitats. Fore and hindwings covary at the individual and species levels, and the covariation differs among microhabitats. However, the microhabitat structure in covariation disappears when phylogenetic relationships are taken into account. Our results demonstrate that microhabitat has driven wing shape evolution, although it has not strongly affected forewing and hindwing integration. We also found that sexual dimorphism of forewing shape and color pattern are coupled, suggesting a common selective force.
“…Penz & DeVries (2002) hypothesized that all species with larvae that feed on monocotyledonous plants represented early branches of the Morpho phylogeny, implying a single evolutionary switch to eudicot‐feeding. In contrast, the analysis by Cassildé et al (2010) implied a pattern of host plant use where eudicot‐feeding habits evolved once and was subsequently reversed. Forest species of Morpho are known to have distinct vertical distributions where the males of some glide at or above the forest canopy level, and others fly at lower strata.…”
This study compiles previously published morphological, colour and behavioural characters and includes new DNA sequence data for eight markers (one mitochondrial and seven nuclear) to re‐evaluate phylogenetic relationships and estimate times of divergence for Morpho butterflies using parsimony and Bayesian methods. We note an effect of missing data on phylogenetic inference and calculations of Partitioned Bremer Support. Morphology and DNA trees were moderately congruent, and the combined analyses of all data included elements of both sources. Both morphology and DNA support the monophyly of Morpho and the early separation of the sister pair M. marcus plus M. eugenia, but trees from different data sources are congruent mostly at derived nodes, and differ at several internal nodes. The analyses of combined data indicate that Morpho is composed of four clades each of which include one or more previously proposed subgenera. The subgenera Pessonia and Morpho were not monophyletic, and to address this issue we propose that Pessonia, syn.nov. be subsumed within Morpho. The ancestor of Morpho probably arose during the Oligocene, and most diversification seems to have occurred during the late Miocene. S‐DIVA analysis suggests eastern Andean region as the ancestral area for Morpho, and that the South American Atlantic Forest was colonized multiple times.
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