Jay F. Bolin

Single-copy nuclear genes place haustorial Hydnoraceae within piperales and reveal a cretaceous origin of multiple parasitic angiosperm lineages.

Extreme haustorial parasites have long captured the interest of naturalists and scientists with their greatly reduced and highly specialized morphology. Along with the reduction or loss of photosynthesis, the plastid genome often decays as photosynthetic genes are released from selective constraint. This makes it challenging to use traditional plastid genes for parasitic plant phylogenetics, and has driven the search for alternative phylogenetic and molecular evolutionary markers. Thus, evolutionary studies, such as molecular clock-based age estimates, are not yet available for all parasitic lineages. In the present study, we extracted 14 nuclear single copy genes (nSCG) from Illumina transcriptome data from one of the “strangest plants in the world”, Hydnora visseri (Hydnoraceae). A ∼15,000 character molecular dataset, based on all three genomic compartments, shows the utility of nSCG for reconstructing phylogenetic relationships in parasitic lineages. A relaxed molecular clock approach with the same multi-locus dataset, revealed an ancient age of ∼91 MYA for Hydnoraceae. We then estimated the stem ages of all independently originated parasitic angiosperm lineages using a published dataset, which also revealed a Cretaceous origin for Balanophoraceae, Cynomoriaceae and Apodanthaceae. With the exception of Santalales, older parasite lineages tend to be more specialized with respect to trophic level and have lower species diversity. We thus propose the “temporal specialization hypothesis” (TSH) implementing multiple independent specialization processes over time during parasitic angiosperm evolution.

Pollination Biology of Hydnora africana Thunb. (Hydnoraceae) in Namibia: Brood‐Site Mimicry with Insect Imprisonment

Hydnora africana is a root holoparasite of southern Africa that emerges only to flower. The trimerous flowers of H. africana have androecial and gynoecial chambers and attract floral visitors with putrid odors emitted from prominent osmophores. We observed floral phenology and insect visitation for H. africana at two sites in southern Namibia and evaluated the insect imprisonment mechanism with beetle addition and pollen viability assays. Flowers are putatively protogynous for 3 d. We observed 18 floral visitors, including 10 coleopteran species imprisoned by the smooth inner surface of the androecial chamber. The hide beetle Dermestes maculatus (Tenebrionidae) accounted for 76.9% of the imprisoned insects, with a density of \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage[OT2,OT1]{fontenc} \newcommand\cyr{ \renewcommand\rmdefault{wncyr} \renewcommand\sfdefault{wncyss} \renewcommand\encodingdefault{OT2} \normalfont \selectfont} \DeclareTextFontCommand{\textcyr}{\cyr} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document} \landscape

Floral thermogenesis of three species of Hydnora (Hydnoraceae) in Africa.

2.2\pm 0.6

GENETIC DIVERSITY OF STRIGA AND IMPLICATIONS FOR CONTROL AND MODELING FUTURE DISTRIBUTIONS

\end{document} per flower. The D. maculatus addition experiment ( \documentclass{aastex} \usepackage{amsbsy} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{bm} \usepackage{mathrsfs} \usepackage{pifont} \usepackage{stmaryrd} \usepackage{textcomp} \usepackage{portland,xspace} \usepackage{amsmath,amsxtra} \usepackage[OT2,OT1]{fontenc} \newcommand\cyr{ \renewcommand\rmdefault{wncyr} \renewcommand\sfdefault{wncyss} \renewcommand\encodingdefault{OT2} \normalfont \selectfont} \DeclareTextFontCommand{\textcyr}{\cyr} \pagestyle{empty} \DeclareMathSizes{10}{9}{7}{6} \begin{document} \landscape

Nutritional and isotopic relationships of selected Bornean tropical mistletoe–host associations in Brunei Darussalam

n=9

Isotopic evidence of partial mycoheterotrophy in Burmannia coelestis (Burmanniaceae)

\end{document} ) clearly demonstrated imprisonment during the carpellate stage. Changes in the inner surfaces of the androecial chamber, stippling, and texturing allowed D. maculatus to escape after pollen release. More than 55.5% of the beetles escaped, dusted with pollen, within 3 d after pollen release. Pollen was still viable 3 d after pollen release. The beetle addition and pollen assays demonstrate the efficiency of the H. africana imprisonment mechanism.