Overview

Distribution

Localities documented in Tropicos sources

Salvinia minima Baker:
Argentina (South America)
Belize (Mesoamerica)
Bolivia (South America)
Brazil (South America)
Colombia (South America)
Costa Rica (Mesoamerica)
Ecuador (South America)
El Salvador (Mesoamerica)
French Guiana (South America)
Guatemala (Mesoamerica)
Honduras (Mesoamerica)
Mexico (Mesoamerica)
Nicaragua (Mesoamerica)
Panama (Mesoamerica)
Peru (South America)
Paraguay (South America)
Uruguay (South America)
United States (North America)
Caribbean (Caribbean)
Venezuela (South America)

Note: This information is based on publications available through Tropicos and may not represent the entire distribution. Tropicos does not categorize distributions as native or non-native.
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Physical Description

Morphology

Description

Plants deep green, ± elongate. Stems to ca. 6 cm; hairs dark. Leaves 1--1.5 cm. Blades of floating leaves almost round to elliptic, obtuse or notched at tip, rounded to cordate at base, abaxially (facing upward) with stiff hairs, with 4 separated branches (i.e., not fused at their tips), adaxially (facing into water) brown and pubescent with slender unbranched hairs. Venation obscure, areolate, but tips of veins free, ending short of margins. Sporocarps in clusters of 4--8, proximal sporocarps with up to 25 megasporangia, distal sporocarps with numerous microsporangia.
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Ecology

Habitat

Depth range based on 6 specimens in 1 taxon.

Environmental ranges
  Depth range (m): 2 - 2
 
Note: this information has not been validated. Check this *note*. Your feedback is most welcome.

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Molecular Biology and Genetics

Molecular Biology

Barcode data: Salvinia minima

The following is a representative barcode sequence, the centroid of all available sequences for this species.


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Statistics of barcoding coverage: Salvinia minima

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 1
Specimens with Barcodes: 1
Species With Barcodes: 1
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Conservation

Conservation Status

National NatureServe Conservation Status

United States

Rounded National Status Rank: NNR - Unranked

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NatureServe Conservation Status

Rounded Global Status Rank: G5 - Secure

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Wikipedia

Salvinia minima


Salvinia minima is a species of aquatic, floating fern that grows on the surface of still waterways.[1] It is usually referred to as common salvinia or water spangles'. Salvinia minima is native to South America and was introduced to the United States in the 1920s-1930s.[2] It is classified as an invasive species internationally and can be detrimental to native habitats.[3] This species is similar to but should not be confused with giant salvinia, Salvinia molesta.

Physical description[edit]

The leaves of Salvinia minima are small and oval in shape, ranging from 0.4 to 2 centimeters in length.[1] Each rhizome of the fern floats close to the surface and has a joined set of leaves that branch off horizontally.[1] The leaves grow in joined sets of three, with two leaves floating on the surface and one leaf dissected, hanging underneath.[4] This species is rootless but the dissected leaves that hang down act as root-like structures and are longer than the floating leaves.[4] Fine white hairs grow uniformly on the leaf surface and serve to repel water. The hairs grow close together in groups of four, bending out and touching together at their top ends to form a whisk or eggbeater-like shape. There are longer brown hairs present on the underside of leaves as well.[5] Leaves range from bright green to brown in color, often browning with age and in sunlight.[1]

Growth[edit]

Salvinia minima undergoes three unique stages of growth. In the primary (initial) stage, a single bud or a small number of buds of the fern are introduced to an environment. In this stage, the leaves will lie flat on the surface of the water. In the secondary stage, the ferns have been growing and multiplying and the leaves will begin to curl upward. In the tertiary (final) stage, the individual ferns will become much more dense and appear as mats on top of the water. The leaves may be almost vertical in this stage because of crowding.[6]

Salvina minima can be found in dense mats when it reaches the tertiary stage of growth

Reproduction[edit]

Reproduction in Salvinia minima occurs asexually through fragmentation. Though sporocarps, spore-producing sacs, may be present on the leaves of this species, Salvinia minima is thought to be sterile and can only reproduce asexually. Any part of a rhizome that buds or breaks off can form another daughter plant. Since fragmentation can occur continuously, Salvinia minima often shows exponential growth. Buds and rhizome fragments can also remain dormant for periods of time when growth is less favorable.[1]

Habitat[edit]

Salvinia minima commonly grows on the surface of still or slow-moving freshwater areas, such as lakes, ponds, and canals. It can tolerate water salinity of up to 4 to 7 parts per thousand (ppt) (or 1.003-1.005 SG) and also inhabits brackish water, including swamps, marshes, and wetlands. This species can also be found in backyard ponds and private lakes and can be purchased in states where it is not prohibited as a noxious plant.[1]

Invasive status[edit]

Though Salvinia minima is indigenous to Central and South America, it has been introduced to parts of the United States, where it is considered a non-indigenous invasive species. It was first noted in the U.S. in St. John's river in eastern Florida. It is thought to have been transported there by shipping boats in the late 1920s or early 1930s.[1] S. minima quickly expanded its range throughout Florida and then expanded westward and northward in the United States. It spreads to new habitats on the bottoms of boats, in ship ballast tanks, through flooding waterways, or can be carried by birds or other animals. S. minima currently has a range that spreads across the southeast from Florida to New Mexico as well as some northern states, including New York, Massachusetts, New Jersey, and Maryland. It is also present in Puerto Rico.[7] S. minima is listed as a noxious plant in Texas, where it is prohibited from being owned and transported.[7][8]

Effect on native habitats[edit]

When introduced to a new environment, Salvinia minima can quickly reproduce and form expansive mats on the top of waterways. Its presence and speedy reproduction can out-compete and inhibit the growth of native water plants. Mats of S. minima can block sunlight from entering the water, which suppresses the growth of underwater plants that photosynthesize, resulting in less dissolved oxygen in the water. This can lead to fish kills. Waterfowl species that feed on either fish or native aquatic plants can also be affected by a lack of food. In bayou and swamp areas specifically, S. minima is known to out-compete the floating aquatic plant duckweed (Lemnoideae). Duckweed is a relatively benign plant that is rich in protein and serves as a common source of food for many fish and bird species in its ecosystem.[9] S. minima, however, has no known nutritional value.[10] The result of an invasion of S. minima on native habitats can be a serious threat to native species and overall biodiversity. As such, S. minima is considered an invasive species and is described on the Global Invasive Species Database.[1][6]

S. minima can be a nuisance to recreational watercraft, especially kayaks and canoes, in areas where it grows densely. It can also have adverse affects on crawfish farming, rice farming, and other commercial activities that occur in waterways where it is present.[6]

Management efforts[edit]

In order to protect native environments, efforts to eradicate or contain the spread of Salvinia minima have been attempted. Management tactics include various methods and research studies that have shown a range of effectiveness.

Mechanical control[edit]

Mechanical methods include the physical removal of S. minima from areas where it is established. This can include raking the surface of the water or seining the plants off with large nets. Mechanical methods have proven mostly ineffective because it can be difficult to maneuver equipment in small waterways, and any fragments left behind will regrow.[8]

Chemical control[edit]

Chemical herbicides that have been used with the best success on S. minima include the ingredients fluridone, imazamox, and penoxsulam. Some of these herbicides kill S. minima more successfully when a surfactant is added to make the chemicals stick to the surface of the leaves. Though herbicides are effective in controlling S. minima, they can have adverse effects. Herbicides can kill or cause harm to native organisms that are not the intended target. Also, if a large area of S. minima is sprayed with an herbicide all at once, the dead plant matter will sink into the water and decompose, which can deplete oxygen in the water and result in fish kills. Smaller sections can be sprayed at a time to combat this side effect.[8]

It is impractical to treat very large bodies of water with herbicides as any fragments that do not die will regrow quickly. The cost of herbicides is high, from $198 to $297 per hectare. Chemical means are overall a less desirable method of control because of the side effects and cost.[6]

Biological control[edit]

Biological control methods involve the introduction of another species in order to contain the spread of an invasive species. This method aims to bring more balance back to an ecosystem that has been invaded by weakening the invasive organism so it has fewer competitive advantages, as well as decreasing or containing the invasive species' population.[11]

Biological control efforts for S. minima have been centered around the tiny salvinia weevil, Cyrtobagous salviniae. This weevil is native to South America. It was introduced accidentally in Florida, a state in which salvinia is widespread but considered manageable. The manageable level of salvinia species, both S. minima and Salvinia molesta (giant salvinia), is thought to be caused by the presence of these weevils, which live and feed on the salvinia leaves.[2]

Since the discovery of the weevils, research has been conducted on the effects of weevils in different habitats of S. minima. In 2005-2006, a research group from Louisiana State University (LSU) introduced salvinia weevils into Gramercy, LA, where S. minima is present. The salvinia weevils were collected from Florida and kept in greenhouses on the LSU campus in Baton Rouge. In the study, the effects of the weevils on S. minima were compared to the effects of the salvinia stem-borer moth, Samea multiplicalis. The stem-borer moth is a species native to the southern United States and is known to feed on other salvinia species in the same genus. Both the moth and the weevil feed on salvinia plants and control its spread. The study had four treatments: the weevil alone, the moth larvae alone, the weevil and moth larvae combined, and a control group. Each group was placed in a 1-m2 poyvinylchloride (PVC) pipe frame that was placed over a section of S. minima in a waterway in Gramercy. There were four replicates of each treatment. Each month during the research, S. minima plant mass was collected from each treatment square and then measured to find the dry weight of the plant. Data were compiled into bar charts to compare the effects of the four treatments over time. The results of this study found that the three treatments all had a significant effect in decreasing the amount of S. minima in an area when compared to the control group, though none of the three experimental treatments were statistically better than the other two. From June to October 2006, the average biomass of S. minima in the treatment groups was 100-375 grams, whereas the average biomass of S. minima in the control frames was 450-600 grams. The salvinia stem-borer moth is native to the United States and presents no threat to the environment. There are also no known negative impacts of introducing the non-indigenous salvinia weevils to the environment, as they feed exclusively on S. minima and S. molesta.[6]

The lack of detrimental effects makes biological control methods the most promising in the long-term management of S. minima. Research studies and control efforts are ongoing.

See also[edit]

References[edit]

  1. ^ a b c d e f g h "Salvinia minima." Global Invasive Species Database. Edited 4 Oct 2010. http://www.issg.org/database/species/ecology.asp?si=570&fr=1&sts=&lang=EN
  2. ^ a b Jacono, C.C., Davern, T.R., Center, T.D. (2001) "The Adventive Status of Salvinia minima and S. molesta in the Southern United States and the Related Distribution of the Weevil Cyrtobagous salviniae." Castenea. 66:214-226. http://fl.biology.usgs.gov/posters/Nonindigenous/Status_of_Salvinia/status_of_salvinia.html
  3. ^ "Common Salvinia." Louisiana Invasive Species. Tulane/Xavier Center for Bioenvironmental Research. Edited 2010. http://is.cbr.tulane.edu/Species_CommonSalvinia.html
  4. ^ a b Salvinia minima. Center for Aquatic and Invasive Plants. University of Florida. http://plants.ifas.ufl.edu/node/395
  5. ^ Kaufman, S.R.; Kaufman, W. (2007). Invasive Plants: Guide to Identification and the Impacts and Control of Common North American Species. Stackpole Books: Mechanicsburg, PA. Pg 439-441.
  6. ^ a b c d e Tewari, S. and Johnson, S (2011). “Impact of two herbivores, Samea multiplicalis (Lepidoptera: Crambidae) and Cyrtobagous salviniae (Coleoptera: Curculionidae), on Salvinia minima in south Louisiana.” Journal of Aquatic Plant Management 49: 36-43. http://apms.org/wp/wp-content/uploads/2012/10/v49p36.pdf
  7. ^ a b "Salvinia minima." PLANTS database. United States Department of Agriculture. http://plants.usda.gov/java/profile?symbol=SAMI7#
  8. ^ a b c "Common salvinia management options." Texas A&M AgriLife Extension, Wildlife and Fisheries Sciences. http://aquaplant.tamu.edu/management-options/common-salvinia/
  9. ^ Cross, J.W. (2002). "The Charms of Duckweed." http://www.mobot.org/jwcross/duckweed/duckweed.htm
  10. ^ "Common salvinia description." Texas A&M AgriLife Extension, Wildlife and Fisheries Sciences. http://aquaplant.tamu.edu/plant-identification/alphabetical-index/common-salvinia/
  11. ^ "Biological control." Plant Management in Florida Waters. http://plants.ifas.ufl.edu/manage/control-methods/biological-control#Salvinia
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Notes

Comments

A report of Salvinia minima from Minnesota has not been confirmed. 

 The following names have been variously misapplied to plants in the flora area: Salvinia auriculata Aublet; Salvinia natans (Linnaeus) Allioni; Salvinia rotundifolia Willdenow.

The name Salvinia auriculata has been misapplied to species in the United States. Salvinia auriculata differs from S . minima in the arrangement of the hairs on the abaxial leaf surface. Those in S . minima are free, while those of S . auriculata (and several other species) are joined at their tips, the hairs resembling an "egg beater." This rather obvious feature is sometimes difficult to assess in herbarium specimens because the hairs are often curled or shriveled into a brownish knot, or have been broken and lost entirely, or never develop. Careful searches must be made to locate intact hairs for identification. Although no previous reports of other species in North America have been verified, these species could be easily overlooked. Salvinia molesta D. S. Mitchell, for example, is in cultivation in Columbia County, Florida, and represents a candidate for escape. Species of Salvinia are known to escape in various regions (G. R. Proctor 1985).

I have seen only three fertile specimens of Salvinia minima , all from Florida, two collected in April and the third collected in November. As with Azolla , collectors should make every effort to locate fertile plants.

Material of Salvinia natans (Linnaeus) Allioni has been misidentified as S . rotundifolia (M. L. Fernald 1950), and as such, might be mistakenly attributed to S . minima . In North America, the name S . natans appears to have been applied only to an 1886 collection from Perry County, Missouri (J. A. Steyermark 1963). This application may have been correct because the collection is outside the greater part of the range of S . minima , at a latitude consistent with S . natans from Europe and Asia, and the population was reportedly an escape from cultivation (J. A. Steyermark 1963).

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