The neotropical freshwater family Potamotrygonidae appears to be the only stingray group that has radiated in a non‐marine environment. To assess the affinities of potamotrygonids to other rays, a phylogenetic analysis was undertaken using 39 morphological characters from 18 stingray groups. The single tree produced (CI = 0.80, RI = 0.88) suggests that neotropical freshwater rays are a monophyletic group, and that within Potamotrygonidae, Paratrygon is basal to a clade composed of Plesiotrygon and Potamotrygon. The sister group to potamotrygonids was determined to be amphi‐American Himantura—these taxa share synapomorphies of the ventral mandibular musculature and the hyomandibular/mandibular articulation. The topology suggests that potamotrygonids are derived from a freshwater‐invading ancestor that was distributed along the northern coast of South America (Pacific and Caribbean) prior to the emergence of the isthmus of Panama. This hypothesis conflicts with parasite‐based biogeographic scenarios of a stricdy Pacific origin for potamotrygonids. General systematic results concerning urolophids, dasyatids, and pelagic myliobatoid stingrays are also discussed.

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Freshwater habitats make up only ∼0.01% of available aquatic habitat and yet harbor 40% of all fish species, whereas marine habitats comprise >99% of available aquatic habitat and have only 60% of fish species. One possible explanation for this pattern is that diversification rates are higher in freshwater habitats than in marine habitats. We investigated diversification in marine and freshwater lineages in the New World silverside fish clade Menidiinae (Teleostei, Atherinopsidae). Using a time-calibrated phylogeny and a state-dependent speciation-extinction framework, we determined the frequency and timing of habitat transitions in Menidiinae and tested for differences in diversification parameters between marine and freshwater lineages. We found that Menidiinae is an ancestrally marine lineage that independently colonized freshwater habitats four times followed by three reversals to the marine environment. Our state-dependent diversification analyses showed that freshwater lineages have higher speciation and extinction rates than marine lineages. Net diversification rates were higher (but not significant) in freshwater than marine

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One of the most remarkable types of migration found in animals is diadromy, a life-history behaviour in which individuals move between oceans and freshwater habitats for feeding and reproduction. Diadromous fishes include iconic species such as salmon, eels and shad, and have long fascinated biologists because they undergo extraordinary physiological and behavioural modifications to survive in very different habitats. However, the evolutionary origins of diadromy remain poorly understood. Here, we examine the widely accepted productivity hypothesis, which states that differences in productivity between marine and freshwater biomes determine the origins of the different modes of diadromy. Specifically, the productivity hypothesis predicts that anadromous lineages should evolve in temperate areas from freshwater ancestors and catadromous lineages should evolve in tropical areas from marine ancestors. To test this, we generated a time-calibrated phylogeny for Clupeiformes (herrings, anchovies, sardines and allies), an ecologically and economically important group that includes high diversity of diadromous species. Our results do not support the productivity hypothesis. Instead we find that the different modes of diadromy do not have predictable ancestry based on latitude, and that predation, competition and geological history may be at least as important as productivity in determining the origins of diadromy.