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Witch-hazel family, of shrubs and small trees, in the order Saxifragales
The Hamamelidaceae are distinguishable from other families in the Saxifragales due to the range of floral characteristics that are generally uniform though all genera. Uniform characteristics include stipules borne on stems with leaves often 2-ranked. Genera usually have a two carpelgynoecium, although some species show variation. Other characteristics include a multicellular stigma, with shallow papillae or ridges.
Anther structure and the modes of opening are considered to be one of the most important features in the systematics and evolution of hamamelids. The anthers in Hamamelids are on average shorter than in other families in the Saxifragales. The anther valve openings are unique pleismorphic features that contrast with the simple longitudinal slits of the anthers in the upper Hamamelidae where the pollen is predominantly wind-driven.
The three types of anthers found in the Hamamelidaceae are:
Type 1) The theca (or sheath of anther) opens like a window with two wings; a common anther type.
Type 2) There is one valve opening to reveal two pollen sacs. Five genera in the Hamamelidoideae subfamily, confined to the Southern Hemisphere (Trichcladus, Dicoryphe, Ostrearia, Neostrearia, Noahdendron) are known to have this anther type.
Type 3) One valve opens a wing of anther tissue towards the center of the flower revealing one pollen sac. The two genera, Exbucklandia and Hamamelis is known to have this anther type.
Plants of the Hamamelidaceae have sticky pollen, which may have influenced the type of pollination that is seen in this family. Pollination is predominantly via insects or wind. However, the insect-pollinated genus Disanthus has been known to wind-pollinate (although inefficiently) in the event pollinators do not visit its flowers. The genus Rhodoleia is unique because it is bird-pollinated.
The pollen structure in the lower Hamamelidae is relatively uniform. The pollen patterns are tricolpate with reticulate exines.
The petals of the Hamamelidaceae are generally narrow and ribbon-like. The exceptions are the genera Corylopsis and Rhodoleia, which have spathulate or circular-like petals.
The flowers of Hamamelidaceae are mostly bisexual with perianth parts, which mature to fruits arranged in spikes, racemes or nonglobose heads.
The anemophilous groups within the Hamamelidaceae are often andromonoecious. Self-incompatibility is common, but self-compatibility occurs in some genera such as Hamamelis.
Cynomorium (Cynomoriaceae) remains unplaced within this tree
The infrafamilial classification of the Hamamelidaceae has been controversial, and has undergone a number of revisions based on morphology, the best known of which are those of Harms (1930) and Endress (1989).
The relationships between Exbucklandioideae and the other subfamilies have proven controversial. The unresolved monophyly of Exbucklandioideae and the clades of Disanthoideae, Rhodoleioideae, Exbucklandioideae or even Mytilarioideae being a sister clade to Hamamelidoideae may have been a result of differing DNA methodologies researchers have used to produce phylogenetic trees and the inclusion or exclusion of certain genera used as outgroups in their analyses. However, the sister relationship of Disanthoideae and Hamamelidoideae has been well supported, although some researchers do not support this. Strong support for making Altingioideae a family has been recognized by textbooks and the Angiosperm Phylogeny Group. Research continues to resolve the deep relationships of the subfamilies within the Hamamelidaceae by incorporating whole or fragmentary fossil evidence.
Hamamelidaceae contains 27-30 genera and 80-140 species distributed among five to six subfamilies. The subfamilies are Exbucklandioideae, Rhodoleioideae, Mytilarioideae, Disanthoideae, Hamamelidoideae, and Altingioideae, which has been elevated to a family Altingiaceae in some recent treatments. Many of the subfamilies are monotypic and the majority of the species lie within the Hamamelidoideae, which has 22 genera.
The long-standing question of whether Altingioideae should be a separate family has been assessed and supported by morphological and molecular phylogenetic studies.
The resulting subfamilial structure was eventually resolved in a series of molecular studies in the late 1990s, resulting in five distinct subfamilies, the majority of the genera residing in the nominative subfamily, Hamamelidoideae:
The relatively large size of subfamily Hamamelidoideae and its further subdivision into tribes has also been a matter of study and controversy. Six tribes are now recognized. The revised structure has greatly reduced Hamamelideae to a monotypic taxon, which had previously been further divided into subtribes:
The Hamamelidaceae were widely distributed in the Northern Hemisphere during the Upper Cretaceous and early Tertiary.Quaternary glaciation across the Northern Hemisphere caused the extinction of numerous species and the restricted distribution of others. Hamamelidaceae were completely obliterated from Europe along with numerous other genera of plants that were unable to escape the ice sheets due to geography (the Mediterranean Sea and Alps forming barriers that did not exist in North America and Asia)
The largest subfamily, the Hamamelidoideae, is now distributed in North America and western and eastern Asia. The Hamamelidoideae subtribe Dicoryphinae is now restricted to the African (including Madagascar and Comores) and Australian continents.
Disanthoideae and Rhodoleioideae are now restricted to southern China and the Caucasus region. Mytilarioideae is restricted to eastern Asia. Altingioideae is now restricted to eastern Asia and western Asia and North America between central Mexico and Belize.
^ abcdefghJudd, W.S., Campbell, C.S., Kellogg, E.A., Stevens, P.F. & Donoghue, M.J. 2010. "Plant Systematics: A Phylogenetic Approach, 3rd ed.". In [eds.], Plant Systematics: A Phylogenetic Approach, 3rd ed. In [eds.]. Sinauer Associates, Inc., Massachusetts.
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^ abQiu, Y.-L.; et al. (1998). "Phylogenetics of the Hamamelidae and their allies: parsimony analyses of nucleotide sequences of the plastid gene rbcL". International Journal of Plant Sciences. 159 (6): 891-905. doi:10.1086/297611.
^ abcMagallon, S.; Herendeen, P.S. & Crane, P.R. (2001). "Androdecidua endressii gen. et sp. nov., from the Late Cretaceous of Georgia (United States): Further Floral Diversity in Hamamelidoideae (Hamamelidaceae)". International Journal of Plant Sciences. 162 (4): 963-983. doi:10.1086/320770.
^Chang, H.T. (1979). "Hamamelidaceae". Flora Reipublicae Popularis Sinicae. 35: 36-116.
^ abMagallon, S. (2007). "From fossils to molecules: Phylogeny and the core eudicot floral groundplan in Hamamelidoideae (Hamamelidaceae, Saxifragales)". Systematic Botany. 32 (2): 317-347. doi:10.1600/036364407781179617. S2CID85920898.
^Huang, G.L. (1986). "Comparative anatomical studies on the woods of the Hamamelidaceae in China". Sunyatsenia. 1: 24-26.
^ abPan, K.-Y.; Lu, A.-M. & Wen, J. (1990). "Characters of Leaf Epidermis in Hamamelidaceae (s. l.)". Sunyatsenia. 28: 10-26.