Increased autumn productivity permits temperate trees to compensate for spring frost damage.

Climate warming is leading to earlier budburst and therefore an increased risk of spring frost injury to young leaves. But to what extent are second-cohort leaves, which trees put out after leaf-killing frosts, able to compensate incurred losses? To investigate whether second-cohort leaves behave differently from first-cohort leaves, we exposed saplings of beech (Fagus sylvatica), oak (Quercus robur), and honeysuckle (Lonicera xylosteum) to experimental treatments mimicking either a warm spring or a warm spring with a leaf-killing frost. Refoliation took 48, 43, and 36 d for beech, oak and honeysuckle, respectively. In beech and oak, autumn Chl content and photosynthesis rates were higher in second- than in first-cohort leaves, senescence in second-cohort leaves occurred c. 2-wk-later, and autumn bud growth in beech was elevated 66% in frost-damaged plants compared with the warm spring treatment. No differences in autumn phenology and growth were observed for honeysuckle. Overall, in beech and oak, delayed Chl breakdown in second-cohort leaves mitigated 31% and 25%, respectively, of the deficit in growing-season length incurred by spring frost damage. These results reveal an unexpected ability of second-cohort leaves of beech and oak to compensate for spring frost damage, and demonstrate that long-lived trees vary their autumnal phenology depending on preceding productivity.

Clock-dated phylogeny for 48% of the 700 species of Crotalaria (Fabaceae-Papilionoideae) resolves sections worldwide and implies conserved flower and leaf traits throughout its pantropical range.

BACKGROUND: With some 700 species, the pantropical Crotalaria is among the angiosperm's largest genera. We sampled 48% of the species from all sections (and representatives of the 15 remaining Crotalarieae genera) for nuclear and plastid DNA markers to infer changes in climate niches, flower morphology, leaf type, and chromosome numbers. RESULTS: Crotalaria is monophyletic and most closely related to African Bolusia (five species) from which it diverged 23 to 30 Ma ago. Ancestral state reconstructions reveal that leaf and flower types are conserved in large clades and that leaf type is uncorrelated to climate as assessed with phylogenetically-informed analyses that related compound vs. simple leaves to the mean values of four Bioclim parameters for 183 species with good occurrence data. Most species occur in open habitats <1000 m alt., and trifoliolate leaves are the ancestral condition, from which unifoliolate and simple leaves each evolved a few times, the former predominantly in humid, the latter mainly in dry climates. Based on chromosome counts for 36% of the 338 sequenced species, most polyploids are tetraploid and belong to a neotropical clade. CONCLUSIONS: An unexpected finding of our study is that in Crotalaria, simple leaves predominate in humid climates and compound leaves in dry climates, which points to a different adaptive value of these morphologies, regardless of whether these two leaf types evolved rarely or frequently in our focal group.

Chromosome number reduction in the sister clade of Carica papaya with concomitant genome size doubling.

PREMISE OF THE STUDY: Caricaceae include six genera and 34 species, among them papaya, a model species in plant sex chromosome research. The family was held to have a conserved karyotype with 2n = 18 chromosomes, an assumption based on few counts. We examined the karyotypes and genome size of species from all genera to test for possible cytogenetic variation. METHODS: We used fluorescent in situ hybridization using standard telomere, 5S, and 45S rDNA probes. New and published data were combined with a phylogeny, molecular clock dating, and C values (available for ∼50% of the species) to reconstruct genome evolution. KEY RESULTS: The African genus Cylicomorpha, which is sister to the remaining Caricaceae (all neotropical), has 2n = 18, as do the species in two other genera. A Mexican clade of five species that includes papaya, however, has 2n = 18 (papaya), 2n = 16 (Horovitzia cnidoscoloides), and 2n = 14 (Jarilla caudata and J. heterophylla; third Jarilla not counted), with the phylogeny indicating that the dysploidy events occurred ∼16.6 and ∼5.5 million years ago and that Jarilla underwent genome size doubling (∼450 to 830-920 Mbp/haploid genome). Pericentromeric interstitial telomere repeats occur in both Jarilla adjacent to 5S rDNA sites, and the variability of 5S rDNA sites across all genera is high. CONCLUSIONS: On the basis of outgroup comparison, 2n = 18 is the ancestral number, and repeated chromosomal fusions with simultaneous genome size increase as a result of repetitive elements accumulating near centromeres characterize the papaya clade. These results have implications for ongoing genome assemblies in Caricaceae.