Monday, June 15, 2015

Mosses of Central Florida 14. Hyophiladelphus agrarius

This specimen of Hyophiladelphus was
found growing on imported red pumice used
in a landscaping in Pinellas County
(Essig 20120818-1 USF).  In Florida, it is
typically found on limestone.
[For other mosses in this series, see the Table of Contents]

Hyophiladelphus agrarius (Hedw.) R. H. Zander (Pottiaceae) is one of many Florida mosses that is found only on limestone or other calcareous materials.  The single species in this genus is found throughout the southeastern United States, from Texas to South Carolina, and throughout tropical America.  It has at times been included in the related genus Barbula, but differs in its more compact, rosette-like shoots, and the lack of papillae (small, hard, round bumps) on the leaves.  Another related genus, Tortella, has a distinctive V-shaped pattern of clear cells at the base of the leaf, by which it can be distinguished.

All of these genera, and a few others in the family, have long, hair-like teeth, twisted around the opening of the capsule.

A colony of Hyophiladelphus, dried out at the time of the
photograph, occupies pockets in the eroded surface of a limestone
boulder. (Essig 20150402-2, USF)
Hyophiladelphus shoots are upright rosettes. The broad leaves
are nearly flat when hydrated, and have prominent, thick
midrib.  The shoots are green to dark green, or almost blackish
when dry. (Lewis 20061028-1, USF)

The long, hair-like teeth  (peristome) 
around the mouth of the capusle are 
twisted around each other. 
(Essig 20060931-1, USF)

At the base of the leaf, the cells are greatly enlarged, more or less rectangular,
and sometimes brownish. (Essig 20150527-2, USAF)
Cells in the upper part of the leaf are compact and roughly
squarrish to rectangular. (Essig 20120818-1, USF)
When dry, the leaves of Hyophiladelphus roll into a curved, tube-like configuration.  In these old capsules the long, twisted
peristome teeth have mostly fallen off. (Essig20150404-2, USF)

Wednesday, June 3, 2015

Minding your stems and crowns

[The following essay is re-posted, with some minor revisions, from one I did for the Oxford University Press blog.  The OUP site features pieces done by authors of OUP books.  I encourage you to check this interesting site.]

Since evolution became the primary framework for biological thought, we have been fascinated, sometimes obsessed, with the origins of things.  Darwin himself was puzzled by the seemingly sudden appearance of the angiosperms (flowering plants) in the fossil record.  In that mid-Cretaceous debut, they seemed to be already diversified into modern families, with no evidence of what came before them.  This was Darwin’s famous “abominable mystery.”

Birds arose around the same time, but for them we have a detailed fossil record documenting the evolution of their feathers, wings, and specialized skeletal features.   For plants, there is still a huge gap between living angiosperms and fossil groups that might be related to them, but we do have tools for whittling away at the mystery.   

Figure 1.  The angiosperm stem group consists of extinct 
seed plants that branched off after the common ancestor
 with other living seed plants (the gymnosperms), but before 
the common ancestor of known angiosperms (the crown group). 
The distinctive features of the angiosperms evolved in the
stem group. Source: modified from Wikimedia Commons, 
licensed by Creative Commons.
The “top-down” approach uses modern methods of DNA-based phylogenetic analysis to build accurate trees of the living angiosperms, identify the most archaic taxa among them, and from their characteristics make predictions about their common ancestor.  By definition, the living members of a group of organisms, their common ancestor, and any extinct species, or “dead ends,” among them, constitute a “crown group” (Fig. 1).

The “bottom up” approach analyzes the available fossil record, to identify which extinct species might be most closely related to the crown group, and which of their structures might have been transformed into the characteristic features of the crown group.  In the angiosperms, this means particularly the  flower parts.  The extinct organisms leading up to the crown group are referred to as the “stem group,”  which, by definition, extends backwards to an earlier ancestor shared with the next most closely related group of living organisms.

For example, the closest living relatives of birds are the crocodilians, and the bird stem group includes all of the dinosaurs (!).  That may sound like the tail wagging the dog (we can alternately call birds a subgroup of dinosaurs), but it is during the long line of dinosaurian ancestry that we see the evolution of feathers, wings, and flight, along with other features shared by birds and dinosaurs but not found in crocodilians.  Similarly, the stem group of amphibians is where fish turned into land animals, and the stem group of reptiles is where amphibians turned into reptiles, with advanced (amniotic) eggs that could be laid on land.  The stem groups are where all the fun is!

Figure 2. Like this modern Anemone, the first 
true flowers consisted of tepals, stamens, 
and a central cluster of carpels.
But who were the “dinosaurs” of the angiosperm story?  The stem group of the angiosperms goes back some 300 million years to where it split from the ancestor of the living gymnosperms – conifers, cycads, etc. (the “crocodilians” of the angiosperm story) (Fig. 1).   The common ancestor of both gymnosperms and angiosperms, which lived some 300 million years ago, was some kind of seed fern, a plant that bore seeds and pollen on its leaves.    The first full flowers, which may have come into existence around 140 million years ago were bisexual, with distinctive closed carpels, flattened stamens with 4 pollen sacs, and embryonic seeds (ovules) that were “bent” and contained by a double envelope (integument) (Figs. 2 and 3).  The plants that might tell how, why, and where ancient leafy structures were transformed into these distinctive organs are not only extinct, but also largely missing from the fossil record. 

Among known members of the angiosperm stem group, one bright spot lies within the extinct order Caytoniales.  Some phylogenetic analyses of fossil Mesozoic seed plants reveal this group to be the most closely related to the angiosperms.  This supports an older hypothesis promoted by evolutionary botanist G. L. Stebbins that the peculiar bent angiosperm ovule was derived from the seed-bearing cupule of the Caytoniales (Fig. 3).  Known members of the Caytoniales, however, provide little information about the evolution of modern stamens and carpels. 
Figure 3. The bent ovule with a double integument 
characteristic of the angiosperms (C) may have 
evolved from the seed-bearing cupules of the
 Caytoniales (A), as the number of ovules within 
was reduced to one (B). Source: redrawn after 
Brown, 1935, The Plant Kingdom, Ginn & Co., 
Boston and New York, with permission.

Why should there be a gap in the crucial part of the record?  The various Mesozoic seed ferns left a fair number of fossils; why not those leading up to the first angiosperms?  Aside from the lower fossilization rate of plants in general, it may be that the pre- and proto-angiosperms evolved in habitats where fossilization was particularly unlikely.  For Stebbins and others, that habitat was semi-arid subtropical uplands.  Stebbins felt that the patchy physical environment and seasonal, marginally sufficient rainfall in such environments provided the maximum stimulation for evolution of new growth forms, and in particular for the short reproductive cycle that is characteristic of the angiosperms.  Such environments are the primary hotbeds (“cradles”) of angiosperm innovation and diversity today, while wet tropical forests serve more as refugia or “museums” for archaic angiosperms. 

The study by Taylor Feild and his colleagues in 2004, which included analysis of the anatomy, physiology, and ecology of archaic living angiosperms, resulted in a very different hypothesis about the crown group ancestor: that it was adapted to disturbed areas and stream margins in dark, damp forests, where there might be similar pressures for a more rapid reproductive cycle.  Who was right?

The answer depends on our reference point.   The top-down approach defines the nature of the crown group ancestor, while the bottom-up approach makes hypotheses about adaptive events along the long stem lineage.  Angiosperm precursors in the stem group may very well have lived in a variety of habitats, including upland, semi-arid habitats prior to moving into damp, disturbed habitats.

The accumulation of the distinctive features of the angiosperms probably took millions of years, paralleling the progression from feathered dinosaur to true birds.  In fact, if we designate the first plant with closed carpels as the first angiosperm (“hidden seeds”), and if other standard features of the flower evolved either before or after that, then “angiosperms” and “flowering plants” are not exactly synonymous.  And the crown group ancestor refers to a still later reference point!   The crown group ancestor was not the first angiosperm, just as there were true birds prior to the bird crown group ancestor.  All we can say for sure is that it was a successful angiosperm, with all the standard floral features in place, and that it proliferated at the expense of other early angiosperms. 

Therefore, when postulating the origins of groups of plants, we must be careful to mind our stems and crowns!