Early flowering plants are thought to have been woody species restricted to warm habitats. This lineage has since radiated into almost every climate, with manifold growth forms. As angiosperms spread and climate changed, they evolved mechanisms to cope with episodic freezing. To explore the evolution of traits underpinning the ability to persist in freezing conditions, we assembled a large species-level database of growth habit (woody or herbaceous; 49,064 species), as well as leaf phenology (evergreen or deciduous), diameter of hydraulic conduits (that is, xylem vessels and tracheids) and climate occupancies (exposure to freezing). To model the evolution of species' traits and climate occupancies, we combined these data with an unparalleled dated molecular phylogeny (32,223 species) for land plants. Here we show that woody clades successfully moved into freezing-prone environments by either possessing transport networks of small safe conduits and/or shutting down hydraulic function by dropping leaves during freezing. Herbaceous species largely avoided freezing periods by senescing cheaply constructed aboveground tissue. Growth habit has long been considered labile, but we find that growth habit was less labile than climate occupancy. Additionally, freezing environments were largely filled by lineages that had already become herbs or, when remaining woody, already had small conduits (that is, the trait evolved before the climate occupancy). By contrast, most deciduous woody lineages had an evolutionary shift to seasonally shedding their leaves only after exposure to freezing (that is, the climate occupancy evolved before the trait). For angiosperms to inhabit novel cold environments they had to gain new structural and functional trait solutions; our results suggest that many of these solutions were probably acquired before their foray into the cold.

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We examined seed-mass variation in 39 species (46 populations) of plants in eastern-central Illinois, USA. The coefficient of variation of seed mass commonly exceeded 20%. Significant variation in mean seed mass occurred among conspecific plants in most species sampled (by hierarchical ANOVA), averaging 38% of total variance. For most species, within-plant variation was the larger component of total variance, averaging 62% of total variance. Variation in seed mass among fruits within crops was significant in most species tested. We conclude that variation in seed mass among and within plants is widespread and common. There was little evidence of trade-offs between number of seeds and mean or variance of seed mass, and little correlational evidence of local competition for maternal resources. No consistent ecological (dispersal mode and growth form) correlates of variance of seed mass were evident.

Trumpet creeper is self‐incompatible and bears long, tubular, orange flowers from June to September. Flowering peaks rapidly, then declines and continues at low levels for several weeks. The initial burst of flowering may attract pollinators that return even during subsequent reduced flowering. Most flowers open before noon and nectar production totals 110 μl of 26% sucrose equivalents per flower, an exceptionally high production for a temperate zone plant. Production ceases within 20–30 hr of flower opening, but corollas persist for several days and may serve to attract pollinators. Effective pollination reduces the period of stigma receptivity and speeds closing of stigma lobes. Only 1–9% of flowers produced mature fruits at four sites in Illinois and Missouri. Roughly 400 pollen grains had to be deposited on a receptive stigma to cause fruit development beyond an initial period of high abortion. At two sites, 17% and 89% of stigmas received over 400 pollen grains. Assuming 50% of deposited grains were from the same plant, fruit production at one site was clearly pollinator limited, that at the second site may have been. Ruby‐throated Hummingbirds (Archilochus colubris) deposited ten times as much pollen per stigma per visit as honeybees (Apis mellifera) and bumblebees (Bombus spp.). Fruit set was highest where rubythroat visitation was most frequent. Trumpet creeper appears primarily adapted for hummingbird pollination, but can also be adequately pollinated by honeybees and bumblebees. This is one of the first attempts to relate pollen‐depositing capabilities of pollinators of any plant to pollen requirements for fruit production. Several characteristics suggest that trumpet creeper may be adapted to pollination at low densities (often called traplining) in its presumed original, woodland, habitat.