![]() |
Leaves of Dicranella hilariana have a thick midrib and square to rectangular cells. |
Essays, botanical travelogues, and other resources provided for students, instructors and anyone else seeking a deeper understanding of the nature of plants. Proceed below for recent posts or go to the Table of Contents (in the column to the right) for an organized list of topics.
Thursday, August 24, 2017
Mosses of Central Florida 27. Dicranella hilariana
Dicranella hilariana (Montagne) Mitten (Dicranaceae) is typically found on moist, clay banks, but appears to have adapted also to the disturbed slopes of phosphate mine pits and may be partially covered with sand. From the related genus Dicranum, Dicranella species differ mainly in their smaller size, shorter leaves, and lack of inflated (alar) cells at the base of the leaf. Like the other genera in this family, the leaf has a massive midrib, and the cells are squarish to rectangular.
From the two other species of Dicranella occurring in central Florida, D. hilariana differs primarily in the shape of its capsules, which are erect, symmetrical, and smooth, and in the color of the capsule stalks, which are yellow but may become somewhat reddish as they age. In D. varia the capsules are asymmetrical, somewhat bent to the side, and borne on red stalks. In D. heteromalla, the stalks are yellowish, but the capsules are nodding and conspicuously furrowed.
Monday, August 21, 2017
Mosses of Central Florida 26. Dicranum condensatum
Dicranum condensatum Hedwig (Dicranaceae) grows in sandy soil throughout Florida, sometimes forming deep cushions made up of long, mostly dead stems and leaves, with green tips. The leaves along the stem are of the same size and shape and are produced indefinitely, in contrast with the related species Campylopus surinamensis. It does produce spores, but apparently only rarely in our area.
Like all members of the family, the midrib (costa) of the leaf is massive, but not as broad as in Campylopus, occupying only 1/10 to 1/5 the width of the leaf in the lower part. Leaves are mostly 3.5-4.5 mm long, and more or less curled or twisted at their tips when dry. Cells are angular squarish near the tip, becoming more elongate toward the base, and distinctly larger and empty at the base (alar cells).
Two other species of Dicranum are found in Florida, but not as common or widespread. D. scoparium is found in humus, rotting stumps, tree bases, and has short-sinuous leaf cells. D. flagellare, found only in north Florida, has specialized whip-like branches with short, scale-like leaves pressed to the stem that arise from the axils of ordinary leaves. The related Dicranella has much shorter leaves. Ditrichum pallidum (Ditrichaceae) is sometimes confused with Dicranum. It grows in similar habitats, but typically has much longer leaves on shorter stems, resembling tiny clumps of grass.
A well-established clump of Dicranum condensatum nearly 6 cm deep. Only the leaves in the top centimeter or so were alive when this specimen was collected ( Lassiter 2077, USF) |
![]() |
Leaf cells of D. condensatum are squarish-rectangular in the upper part, and the margins of the leaf are toothed. |
Like all members of the family, the midrib (costa) of the leaf is massive, but not as broad as in Campylopus, occupying only 1/10 to 1/5 the width of the leaf in the lower part. Leaves are mostly 3.5-4.5 mm long, and more or less curled or twisted at their tips when dry. Cells are angular squarish near the tip, becoming more elongate toward the base, and distinctly larger and empty at the base (alar cells).
Leaves are twisted-curled when dry. |
Tuesday, August 15, 2017
Mosses of Central Florida 25. Campylopus surinamensis
Campylopus surinamensis Müller Hal. (Dicranaceae) is a hardy, desiccation-tolerant moss found in the dry, sandy soil of the Pine Flatwoods and dry roadsides. Synonyms include C. donnelli and C. gracilicaulis. From other members of its family, it is typically distinguished by the habit of producing shoots with two forms of leaves. Along the lower parts of the shoot, the leaves are small, widely spaced and pressed against the stem. In the upper part of the shoot, leaves are longer, and crowded into a distinct tuft. It apparently does not produce spores anywhere in North America, but reproduces asexually by means of small, hooked leaves produced in the axils of the main leaves.
The leaves are dominated by the massive midribs, that occupy about a third or more of the leaf width at the base, and nearly all of the leaf in the middle and upward into the prolonged tip. Other members of the family have still massive, but narrower, midribs, occupying less than a third of the leaf width at the base. The upper parts of the leaves are toothed along the margins. Leaf cells in the narrow blade region are squarish to irregular, becoming larger and more rectangular at the base. Leaves are somewhat curved but stiff when dry, not curled.
![]() |
As a colony of Campylopus surinamensis develops, some shoots form as short rosettes, but later shoots elevate their rosettes atop sparsely foliated stems. Photo of Essig 20090209-1 (USF) |
The leaves are dominated by the massive midribs, that occupy about a third or more of the leaf width at the base, and nearly all of the leaf in the middle and upward into the prolonged tip. Other members of the family have still massive, but narrower, midribs, occupying less than a third of the leaf width at the base. The upper parts of the leaves are toothed along the margins. Leaf cells in the narrow blade region are squarish to irregular, becoming larger and more rectangular at the base. Leaves are somewhat curved but stiff when dry, not curled.
![]() |
The leaves of Campylopus species are dominated by their massive midribs. |
Tuesday, August 8, 2017
Families Matter
You probably remember from introductory biology course, that the official way of naming a species is the binomial ("two-name") system. Each species name is composed of the genus name and the specific epithet. For example, Quercus alba is the name for the white oak. Quercus is the genus, which contains a number of other species of oaks, and alba is the specific epithet that refers exclusively to this one species.
In almost all scientific communication and labeling practices, however, a third identification tag, the family name, is added - e.g. Quercus alba (Fagaceae). This greatly increases the utility and comprehensibility of the naming system.
The binomial system itself evolved from a fundamental human instinct to recognize categories of things, and specific types within those categories. Before Linnaeus established the formalized latin system that gave us Quercus alba, there were "white oaks, red oaks, etc. (and the equivalent in various other languages), just as there were John Smith, William Smith, etc. Referring to just a "white" or "John," or "William," doesn't tell us much at all.
The binomial gives some context to a name, and helps us interpret new information. If someone describes a new species, Quercus antarctica (hypothetical) for example, we immediately know that it is another species of oak. We can predict that it will be a woody tree or shrub with simple leaves, and that it produces acorns. The family name adds another layer of recognition and predictiveness.
Suppose, for example, someone comes into the room raving about the spectacular specimen of Trigonobalanus doichangensis she'd seen at a botanical garden in Singapore. I myself would have stared blankly at her, having no idea what that gibberish stood for. But then she tells me that Trigonobalanus is a genus in the family Fagaceae. A big light bulb turns on in my head. Fagaceae is the family to which Quercus belongs, along with Castanea (chestnuts), Fagus (beeches), and several other genera. Suddenly I have an approximate idea of what this plant is.
The family name is therefore extremely valuable for recognizing, characterizing, identifying, labeling, storing, retrieving, and providing relationship context for plant specimens. Sometimes it is of more value than the genus name for providing a rough idea of what a plant is and where it fits in relationship to other plants, as in the Trigonobalanus example above. This requires, of course, some knowledge of plant families. Learning the characteristics of families is a routine part of studying plant taxonomy, but will also be highly useful to anyone with an interest in plants. Even the use of common names like "the orchid family" or the "iris family," etc., will be helpful when communicating with a lay audience.
The taxonomic system is a hierarchy of taxonomic categories, or taxa. Genus and family are two levels of taxa. Theoretically, we could also append the names of higher categories, like orders, classes, phyla, etc. You will find those in textbooks, but for everyday use, they would amount to information overload. We can refer casually to important higher categories, like angiosperms, gymnosperms, green algae, etc., without really worrying about their technical names or their rank (their level within the hierarchy).
Familly names for plants have been standardized with the "aceae" ending, which is attached to the name of the first named genus in the family The Asteraceae (sunflowers, etc.) gets its name from the genus Aster. So you'll know when you're seeing a family name. Some older names were different, ending in "ae," and using a descriptive term instead of a genus name as the base. The old name for the Asteraceae was the "Compositae," referring to the composite or compound nature of the flower heads. You will still see these type of names in the older literature. Some of the other common ones are "Palmae" (for Arecaceae), "Gramineae" (for Poaceae), "Leguminosae" (for Fabaceae), "Labiatae" (for Lamiaceae), "Crucferae" (for Brassicaceae) and "Umbelliferae" (for Apiaceae).
The point(s) of these remarks are several:
In almost all scientific communication and labeling practices, however, a third identification tag, the family name, is added - e.g. Quercus alba (Fagaceae). This greatly increases the utility and comprehensibility of the naming system.
The binomial system itself evolved from a fundamental human instinct to recognize categories of things, and specific types within those categories. Before Linnaeus established the formalized latin system that gave us Quercus alba, there were "white oaks, red oaks, etc. (and the equivalent in various other languages), just as there were John Smith, William Smith, etc. Referring to just a "white" or "John," or "William," doesn't tell us much at all.
The binomial gives some context to a name, and helps us interpret new information. If someone describes a new species, Quercus antarctica (hypothetical) for example, we immediately know that it is another species of oak. We can predict that it will be a woody tree or shrub with simple leaves, and that it produces acorns. The family name adds another layer of recognition and predictiveness.
Suppose, for example, someone comes into the room raving about the spectacular specimen of Trigonobalanus doichangensis she'd seen at a botanical garden in Singapore. I myself would have stared blankly at her, having no idea what that gibberish stood for. But then she tells me that Trigonobalanus is a genus in the family Fagaceae. A big light bulb turns on in my head. Fagaceae is the family to which Quercus belongs, along with Castanea (chestnuts), Fagus (beeches), and several other genera. Suddenly I have an approximate idea of what this plant is.
The family name is therefore extremely valuable for recognizing, characterizing, identifying, labeling, storing, retrieving, and providing relationship context for plant specimens. Sometimes it is of more value than the genus name for providing a rough idea of what a plant is and where it fits in relationship to other plants, as in the Trigonobalanus example above. This requires, of course, some knowledge of plant families. Learning the characteristics of families is a routine part of studying plant taxonomy, but will also be highly useful to anyone with an interest in plants. Even the use of common names like "the orchid family" or the "iris family," etc., will be helpful when communicating with a lay audience.
The taxonomic system is a hierarchy of taxonomic categories, or taxa. Genus and family are two levels of taxa. Theoretically, we could also append the names of higher categories, like orders, classes, phyla, etc. You will find those in textbooks, but for everyday use, they would amount to information overload. We can refer casually to important higher categories, like angiosperms, gymnosperms, green algae, etc., without really worrying about their technical names or their rank (their level within the hierarchy).
Familly names for plants have been standardized with the "aceae" ending, which is attached to the name of the first named genus in the family The Asteraceae (sunflowers, etc.) gets its name from the genus Aster. So you'll know when you're seeing a family name. Some older names were different, ending in "ae," and using a descriptive term instead of a genus name as the base. The old name for the Asteraceae was the "Compositae," referring to the composite or compound nature of the flower heads. You will still see these type of names in the older literature. Some of the other common ones are "Palmae" (for Arecaceae), "Gramineae" (for Poaceae), "Leguminosae" (for Fabaceae), "Labiatae" (for Lamiaceae), "Crucferae" (for Brassicaceae) and "Umbelliferae" (for Apiaceae).
The point(s) of these remarks are several:
1. For botany instructors and students, learning the characteristics of the plant families that occur in your area, and using plant family names when labeling or referencing specimens, has a huge practical value.
2. When identifying plants, recognizing the family narrows down your search and allows you to skip over what is usually the most difficult part of a taxonomic key.
3. Referencing the plant family when writing or talking about plants puts them into a context of relationship. The taxonomic system is not an arbitrary set of names, but reflects the natural evolutionary relationships among plants.
2. When identifying plants, recognizing the family narrows down your search and allows you to skip over what is usually the most difficult part of a taxonomic key.
3. Referencing the plant family when writing or talking about plants puts them into a context of relationship. The taxonomic system is not an arbitrary set of names, but reflects the natural evolutionary relationships among plants.
4. For practicing taxonomists, we need to keep in mind the practical value of maintaining a manageable number of stable families with meaningful, recognizable, distinguishing characteristics. That's not always easy, given the directive of modern phylogenetic taxonomy to reorganize plant diversity into strictly monophyletic taxa, which often requires splitting of old familiar families into smaller units, or lumping familiar families into larger families with more diverse characteristics.
Thursday, July 20, 2017
Mosses of Central Florida 24. Anomodon minor
Anomodon minor has creeping primary stems with short, scale-like leaves and semi-erect branches with larger, tongue-shaped leaves. Photo from dried herbarium specimen: Merner s.n. 15 June 1979 (USF) |
![]() |
Capsules of Anomodon minor are erect (unbent) and symmetrical.
Photo courtesy Robert A. Klips, Ohio Moss and Lichen Association.
|
Within the Anomodontaceae, Anomodon is distinguished from the only other genus, Herpetineuron, by the shape and other features of the leaves. In Herpetineuron, leaves gradually taper to a point and the cells are smooth, without papillae. Three other species of Anomodon occur in Florida. A. tristis appears to form thinner mats, occurs higher up on tree trunks, and is found only in the northern part of the state. A. attenuatus forms denser mats, with more frequently branched stems that lay more-or-less flat, and taper at the ends with increasingly smaller leaves. In A. rostratus, leaves are long and taper to a fine, hair-like point.
Leaves of Anomodon minor are elongate, tongue-shaped and with a rounded tip with small hard point. Cells are tiny, roundish and equipped with papillae. Lighter streak in the center is the midrib. |
Thursday, July 6, 2017
Mosses of Central Florida 23. Hygroamblystegium varium
Hygroamblystegium varium (Hedw.) Mönk.(Amblystegiaceae) is another moss frequently found in aquatic habitats in central Florida, along with Leptodictyum, Fontinalis, and species of Fissidens. Its leaves are shorter and spread more 3-dimensionally around the stem than those in Lepidodictyum, and the stems branch more frequently. Fontinalis is easily distinguished from these genera as its leaves lack a midrib altogether. The leaf cells in Fontinalis are also more elongate and curved, and the stalks of the sporangia (capsules) are extremely short. Fissidens, of course, is easily recognized by the smaller secondary leaves attached at each node with the main leaves. Like Amblystegium and Leptodictyum, which are in the same family, the capsules of Hygroamblystegium are erect, but slightly curved, and arise from short stems along the creeping main stems.
The family Amblystegiaceae is one of many moss families in taxonomic flux. Even the treatment in Flora North America (FNA) is self-proclaimed to be tentative, with the treatment of genera and species still controversial and unsettled. Hygroamblystegium and Amblystegium, each containing only one recognixed species, are weakly separated, and sometimes combined into a single genus. The principal differences noted in FNA are that the leaves of Amblystegium are smaller than those of Hygroamblystegium and the midrib is weaker, and that the plants lack paraphyllia (extra leaf-like or thread-like appendages between leaves). Amblystegium is also said to be always terrestrial, while Hygroamblystegium is often (but not always!) aquatic. By this definition it appears that Amblystegium serpens is found only in north Florida, and reports from central Florida need to be investigated.
In herbaria, Hygroamblystegium varium is more likely to be filed under Amblystegium, and it might be best to leave them there until the taxonomic dust settles. Some other species have been recognized, including Hygroamblystegium tenax, H. fluviatale, H. humile, H. trichopodium, and H. noterophilum, but it seems clear that these are all just variants of the aptly named H. varium.
![]() |
Leaf cells of Hygroamblystegium are short-rectangular or sometimes more elongate. |
A lucky shot of the tip of the capsule of Hygroamblystegium varium. |
Friday, May 19, 2017
Mosses of Central Florida 22. Leptodictyum riparium
Leptodictyum riparium (Hedw.) Warnst. (Amblystegiaceae) is the most common aquatic moss in central Florida. It is commonly found growing submerged on rocks along rivers, typically in thick mats, or exposed on rocks or tree bases close to water. Other aquatic mosses include some forms of Hygroamblystegium varium, and two species of Fissidens, which are much less common. Aquatic species of Sphagnum are confined to north Florida. Amblystegium serpens may be in our area, but voucher specimens need to be verified.
Leptodictyum is distinguished from other aquatic mosses by its long, straight, sparsely branched stems, with leaves extending stiffly from the sides of the stem (in more or less one plane). The leaves remain more or less stiff when dry, by may be somewhat rumpled. It rarely produces sporophytes in our area. Hygroamblystegium has shorter, more branched stems that tend to be more curved when dry, and shorter, more triangular leaves distributed uniformly around the stem. It is also more often found with sporophytes. Species of Fissidens are distinguished by their doubled leaves.
The leaves have a distinct midrib, and the leaf cells are generally elongate with thin, inconspicuous walls. Sporangia, when present, are somewhat curved and asymmetric, but none have been found among the specimens at USF.
Leptodictyum occurs in thick underwater mats. The stems are long, straight and sparsely branched. The leaves are spread stiffly in one plane, even when dry. From Franck 3314 (USF). |
Leptodictyum is distinguished from other aquatic mosses by its long, straight, sparsely branched stems, with leaves extending stiffly from the sides of the stem (in more or less one plane). The leaves remain more or less stiff when dry, by may be somewhat rumpled. It rarely produces sporophytes in our area. Hygroamblystegium has shorter, more branched stems that tend to be more curved when dry, and shorter, more triangular leaves distributed uniformly around the stem. It is also more often found with sporophytes. Species of Fissidens are distinguished by their doubled leaves.
The leaves of Leptodictyum have a distinct midrib, but which does not quite reach the tip. From Franck 3314 (USF) |
The leaves have a distinct midrib, and the leaf cells are generally elongate with thin, inconspicuous walls. Sporangia, when present, are somewhat curved and asymmetric, but none have been found among the specimens at USF.
The leaf cells are somewhat elongate and tapered at the ends, but do not stand out sharply under the microscope. From Lassiter et al 559 (USF) |
Subscribe to:
Posts (Atom)