Rapateaceae and Bromeliaceae each have a center of diversity in South America and a single species native to a sandstone area in west Africa that abutted the Guayana Shield in northern South America before the Atlantic rifted. They thus provide ideal material for examining the potential role of vicariance versus long-distance dispersal in creating amphiatlantic disjunctions. Analyses based on ndhF sequence variation indicate that Rapateaceae and Bromeliaceae are each monophyletic and underwent crown radiation around 41 and 23 Ma, respectively. Both exhibit clocklike sequence evolution, with bromeliads evolving roughly one-third more slowly than rapateads. Among rapateads, the divergence of west African Maschalocephalus dinklagei from its closest South American relatives implies that Maschalocephalus resulted via long-distance dispersal 7 Ma, not ancient continental drift; only its sandstone habitat is vicariant. Rapateads arose first at low elevations in the Guayana Shield; the earliest divergent genera are widespread along riverine corridors there and, to a lesser extent, in Amazonia and the Brazilian Shield. Speciation at small spatial scales accelerated 15 Ma with the invasion of high-elevation, insular habitats atop tepuis. Among bromeliads, Pitcairnia feliciana diverges little from its congeners and appears to be the product of long-distance dispersal ca. 12 Ma. Brocchinia/Ayensua and then Lindmania are sister to all other bromeliads, indicating that the Guayana Shield was also the cradle of the bromeliads. Three lineages form an unresolved trichotomy representing all other bromeliads: (1) Tillandsioideae, (2) Hechtia, and (3) a large clade including remaining genera of Pitcairnioideae and all Bromelioideae. The last includes a clade of pitcairnioid genera endemic to the Guayana and Brazilian Shields; a xeric group (Abromeitiella/Deuterocohnia/Dyckia/Encholirium/Fosterella) from southern South America and the southern Andes, sister to Pitcairnia; and Andean Puya, sister to Bromelioideae, with many of the latter native to the Brazilian Shield. Both Rapateaceae and Bromeliaceae appear to have arisen at low elevations in the Guayana Shield, experienced accelerated speciation after invading dissected mountainous terrain, and undergone long-distance dispersal to west Africa recently. Bromeliad acquisition of key adaptations to drought (e.g., CAM photosynthesis, tank habit, tillandsioid leaf trichomes) 17 Ma appears to have coincided with and help cause the centripetal invasion of drier, more seasonal regions beyond the Guayana Shield, resulting in a wider familial range and dominance of the epiphytic adaptive zone. Geology, past and present climate, and proximity to South America help account for both families occurring in nearly the same area of Africa. We present a new classification for Rapateaceae, including a new tribe Stegolepideae, a new subfamily Monotremoideae, and revisions to tribe Saxofridericieae and subfamily Rapateoideae.

To address the composition of the urticalean rosids, the relationships of the component families (maximally Cannabaceae, Cecropiaceae, Celtidaceae, Moraceae, Ulmaceae, and Urticaceae) and analyze evolution of morphological characters, we analyzed sequence variation for a large sampling of these families and various rosid outgroups using rbcL, trnL-F, and ndhF plastid regions. Urticalean rosids are derived out of a lineage including Barbeyaceae, Dirachmaceae, Elaeagnaceae, and Rhamnaceae, with Rosaceae less closely related; thus, they are imbedded within Rosales. Ulmaceae are the sister to all remaining families. Cannabaceae are derived out of a subclade of Celtidaceae; this expanded family should be called Cannabaceae. Cecropiaceae are derived within Urticaceae and are polyphyletic with Poikilospermum derived elsewhere within Urticaceae; this expanded family should be called Urticaceae. Monophyletic Moraceae are sister to this expanded Urticaceae. Support for these relationships comes from a number of morphological characters (floral sexuality, presence or absence of hypanthium, stamen type and dehiscence, pollen pore number, ovule position, and embryo alignment) and chromosome numbers. Most fruit types, in terms of ecological dispersal, are derived independently multiple times and are strongly correlated with habitat.

To examine relationships and test previous sectional delimitations within Fuchsia, this study used parsimony and maximum likelihood analyses with nuclear ITS and chloroplast trnL-F and rpl16 sequence data for 37 taxa representing all sections of Fuchsia and four outgroup taxa. Results support previous sectional delimitations, except for F. verrucosa, which is related to a Central American clade rather than to section Fuchsia and is described here as a new section Verrucosa. The basal relationships within Fuchsia are poorly resolved, suggesting an initial rapid diversification of the genus. Among the species sampled, there is strong support for a single South Pacific lineage, a southern South American/southern Brazilian lineage, a tropical Andean lineage, and one or two Central American and Mexican lineages. There is no clear support for an austral origin of the genus, as previously proposed, which is more consistent with Fuchsia's sister group relationship with the boreal Circaea. An ultrametric molecular clock analysis (all minimal dates) places the split between Fuchsia and Circaea at 41 million years ago (mya), with the diversification of the modern-day lineages of Fuchsia beginning at 31 mya. The South Pacific Fuchsia lineage branches off around 30 mya, consistent with fossil records from Australia and New Zealand. The large Andean section Fuchsia began to diversify around 22 mya, preceded by the divergence of the Caribbean F. triphylla at 25 mya. The Brazilian members of section Quelusia separated from the southern Andean F. magellanica around 13 mya, and the ancestor of the Tahitian F. cyrtandroides split off from the New Zealand species of section Skinnera approximately 8 mya.

The reproductive strategies of frogs are highly diverse, but analysis of these strategies in a phylogenetic context has lagged behind other taxa. Here we investigate associations between aspects of parental care and egg size in a phylogenetic context. We obtained data on egg size and parental care strategies in various species of frogs from the scientific literature. We developed a phylogenetic supertree of frogs by combining the results of multiple phylogenetic analyses using matrix representation parsimony. We used phylogenetic pairwise comparisons to investigate the correlation between various forms of parental care and egg size across the order Anura. We also investigated correlations between tadpole carnivory and egg size, and phytotelm breeding and egg size. We also investigated the association of egg size with several environmental factors. Parental care, male parental care, direct development, stream breeding and montane breeding habitats were all associated with large egg size. Female care (in species with trophic egg feeding), carnivory, use of small pools (phytotelmata) and use of temporary pools were not associated with egg size.