Brachionus leydigii Cohn, 1862

Common Name: A rotifer

Synonyms and Other Names:

Brachionus quadratus Rousselet, 1889, Brachionus reticulatus Kertész, 1894, Brachionus quadratus rotundus Rousselet, 1907, Brachionus quadratus tridentatus Zernov, 1901



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Identification: Brachionus leydigii is a nearly square rotifer, with a body divided into three dorsal, ventral, and basal plates. The anterior dorsal margin has six spines of nearly equal length, with median spines slightly longer and curving somewhat ventrally. Small spines are usually present at the joint of the dorsal and basal plates. A large circular or club shaped foot opening is visible on the dorsal surface. The body wall of B. leydigii is firm and slightly raised toward the center (Leasi 2012).


Size: Total length 220–280 µm; maximum width 165 µm


Native Range: Neotropical, Afrotropical, Australian, Oriental, and Palearctic biogeographical regions (Segers 2007; Nandini et al. 2016).


This species is not currently in the Great Lakes region but may be elsewhere in the US. See the point map for details.

Ecology: Rotifers live mainly among aquatic vegetation in the littoral zone of lakes, ponds, rivers, canals, pools, and other small water bodies. Due to the absence of respiratory organs, this species uses its entire body surface to respire and is therefore unable to live in anaerobic conditions (Sládecek 1983). Most communities contain 50 to 500 individuals per liter, with the densest population reported in unpolluted water reaching 5,800 individuals per liter (Smith 2001). Brachionus ledygii filter feeds on small material such as bacteria and detritus and is able to selectively filter particles by size with a corona of cilia surrounding its mouth (Wallace 2002). Experiments on the rotifer composition among different lake types suggest that Brachionus spp. thrive primarily in eutrophic environments and are largely absent from oligotrophic and mesotrophic areas (Maemets 1983, Sládecek 1983; Sarma et al. 2019). Brachionus leydgii showed preference for high chlorophyll a and total phosphorus concentrations in the Scheldt river basin (France/Germany) (Le Coz et al. 2018).

With large population sizes and high turnover rates, rotifers are significant contributors to lake food webs (Herzig 1987; Starkweather 1987; Walz 1997). Additionally, rotifers are the first food of fish fry and are eaten by a variety of invertebrate predators, leading to the assimilation of their energy into higher trophic levels (Wallace 2002). Rotifers may also play a role in microplankton community structure, although the magnitude of their importance is unknown (Arndt 1993; Berninger et al. 1993; Rublee 1998). The study of rotifer population dynamics is challenging, as annual species abundance across a variety of habitats can vary greatly (Herzig 1987).

Rotifers’ annual reproductive cycle involves both sexual and asexual stages. The asexual phase involves amictic (parthenogenic) females who produce mitic haploid eggs in autumn, from which males hatch without fertilization. Males typically only live for a few hours, dying immediately after reproduction (Sládecek 1983). The sexual phase results in resting stage “winter eggs” that develop with a thick protective cover resistant to desiccation and extreme thermal conditions (Clement and Wurdak 1991, Sládecek 1983, Wurdak et al. 1978). After production, these diapausing eggs sink to the sediment where they can remain viable for several decades (Marcus et al. 1994; Kotani et al. 2001). When favorable conditions return, eggs complete their development; however, a fraction will remain viable and accumulate in the sediment, forming resting egg banks (Garcia-Roger et al. 2005). These egg banks may help to ensure survival through unfavorable environmental conditions as well as possibly act as a dispersal device (Templeton and Levin 1979; Fryer 1996; Hairston 1996, 1998; Ortells et al. 2000; Garcia-Roger et al. 2005). Anoxia or low oxygen levels in the sediment, however, may lead to low viability of diapausing eggs (Uye et al. 1984; Lutz et al. 1994).


Means of Introduction: Brachionus leydigii has a high probability of introduction to the Great Lakes (Confidence level: High).

Potential pathway of introduction: Shipping (Ballast sediment)

Brachionus ledygii has been identified as having high probability of introduction to the Great Lakes via residual ballast sediment, where its resting stage is able to survive high salinities during ballast water exchange (Bailey et al. 2004, 2005a, 2005b; Johengen et al. 2005). In a survey of the ballast water of 35 different vessels entering the Great Lakes, this species was found hatched from diapausing eggs in residual ballast sediment in four of the ships. Additionally, it was isolated from the sediment of those ships with a mean density of 3 individuals/40 g sediment (Bailey et al. 2005a; Johengen et al. 2005). It is likely that these resting stages are deposited by reproducing females taken in with ballast water rather than being brought in with disturbed sediments. Diapausing eggs present in sediment can pose an invasion risk if they are discharged during ballast operations or if they hatch during a voyage and the young rotifers are subsequently introduced during vessel deballasting (Gray and MacIsaac 2010). Of the 76 distinct taxa with a resting stage identified in this survey, Brachionus spp. were the most common and abundant of the Great Lakes non-natives (Bailey et al. 2005a). Brachionus spp. are a predominant component of the planktonic community in the lower Rhine River, a region where ballast is commonly taken for ships entering the Great Lakes (van Dijk and van Zanten 2005). However, this primarily freshwater species is less abundant in other ballast loading regions such as the Baltic Sea and coastal areas with high salinity (Viitasalo et al. 1995).

In more recent studies conducted since the 2006 (Canadian bound vessels) and 2008 (U.S. bound vessels) expansion of mandatory ballast flushing regulations to vessels with unpumpable ballast tank residuals, however, B. leydigii has been identified as having a significantly lower probability of introduction (Government of Canada 2006; Briski et al. 2010; Gray and MacIsaac 2010). Brachionus leydigii was not observed in ballast sediment collected in 2007 and 2008 from 19 ballast tanks of 17 randomly selected Great Lakes bound ships originating from European, South American, and Atlantic ports (i.e. after the new regulations were in place) (Briski et al. 2010). Furthermore, in situ hatching studies suggest that fewer than 1% of diapausing invertebrate eggs will hatch and become available for introduction. The likelihood of this species entering the Great Lakes is therefore reduced as compared to species that may become resuspended in ballast water (Johengen et al. 2005). Additionally, Santagata et al. (2008) report a 100% mortality rate for rotifers exposed to full strength seawater for one hour in both empty-refill and flow-through treatments.


Status: Unknown.

Only one specimen of Brachionus leydigii has been collected in Lake Erie to date (USEPA 2017; Connolly et al. 2018). Although only a single individual was collected, rotifer reproductive biology includes an asexual reproductive stage and diapausing eggs (see Ecology section above). In order to be considered an established species a reproducing population must be present within the basin. A reproducing population is inferred from multiple discoveries of adult and juvenile life stages over at least two consecutive years.

Brachionus leydigii has a moderate probability for establishment if introduced to the Great Lakes (Confidence level: Moderate).

This species produces a resting stage consisting of a three-layered diapausing egg that is protected from external stressors, such as desiccation and temperature extremes, until conditions become favorable and a viable individual hatches (Wurdak et al. 1978; Sládecek 1983; Clement and Wurdak 1991). This reproductive strategy leads B. ledygii to having high Great Lakes invasion potential, as diapausing eggs can be resistant to short term salinity exposure, are not easily flushed from ballast tanks, and have the potential for in situ hatching during a transoceanic voyage (Bailey et al. 2004, 2005a, 2005b, 2006; Gray et al. 2005; Gray and MacIsaac 2010). However, viability of similarly resistant diapausing copepods and cladoceran eggs is low under conditions of low oxygen or anoxia (Uye 1980; Uye et al. 1984; Carvalho and Wolf 1989).

Branchionus leydigii is distributed globally and present in a variety of physical and environmental conditions. Bailey et al. (2005a) and Johengen et al. (2005) reported this species as having a habitat match to the Great Lakes, able to hatch in a 0 ppt salinity medium. Additionally, because B. leydigii thrives in primarily eutrophic conditions, the central and western basins of Lake Erie may provide suitable habitat due to their high eutrophication potential (Summers 2001). Johengen et al. (2005) report observing one B. leydigii individual in an upper-wing ballast tank of a surveyed vessel, leading the authors to suggest that this may have been the result of a previous transoceanic ballast introduction to Hamilton Harbor, as residual sediments generally do not accumulate in upper-wing tanks. Because only a single individual was recorded, the status of establishment cannot be determined, but this finding may indicate that B. leydigii has been introduced previously to this location (Johengen et al. 2005).


Great Lakes Impacts:
Summary of species impacts derived from literature review. Click on an icon to find out more...

Beneficial

There is little or no evidence to support that Brachionus leydigii has the potential for significant environmental impacts if introduced to the Great Lakes.

While rotifers tend to be significant contributors to food web structure due to high abundances and rapid turnover rates, there is no species specific information currently available on the trophic effect of introduced populations of B. ledygii. In addition, approximately 275 species of rotifers have already been reported in the Great Lakes, and it is unlikely that the addition of a single species will lead to any new significant environmental impacts. This species has not been reported to affect native populations genetically in this review. However, there are numerous Brachionus spp. native to the Great Lakes but the potential for hybridization is unknown.

There is little or no evidence to support that Brachionus leydigii has the potential for significant socio-economic impacts if introduced to the Great Lakes.

As a group, introduced rotifers are not known to generate significant socio-economic impacts (O'Connor et al. 2008), and there are currently no reports of this species leading to negative impact in introduced areas.

There is little or no evidence to support that Brachionus leydigii has the potential for significant beneficial effects if introduced to the Great Lakes.

Rotifers have been widely used as a bioindicator species in pollution monitoring, and due to their sensitivity to pollutants and ease of culture, they have become important tools in ecotoxicological testing (Wallace 2002). However, there is no evidence supporting that B. leydigii will offer any advantage as an ecological indicator as compared to rotifers already present in the Great Lakes.


Management: Regulations (pertaining to the Great Lakes)

There are no known regulations for this species.*

*Ballast water regulations applicable to this species are currently in place to prevent the introduction of nonindigenous species to the Great Lakes via shipping. See Title 33: Code of Federal Regulations, Part 151, Subparts C and D (33 CFR 151 C) for the most recent federal ballast water regulations applying to the Great Lakes and Hudson River.

Note: Check federal, state/provincial, and local regulations for the most up-to-date information.

Control

Biological
There are no known biological control methods for this species.

Physical
There are no known biological control methods for this species

Chemical
There are no chemical control methods for this species.

Note: Check state/provincial and local regulations for the most up-to-date information regarding permits for control methods. Follow all label instructions.


References (click for full reference list)


Author: Baker, E., K. Dettloff and A. Fusaro


Contributing Agencies:
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Revision Date: 9/30/2021


Citation for this information:
Baker, E., K. Dettloff and A. Fusaro, 2024, Brachionus leydigii Cohn, 1862: U.S. Geological Survey, Nonindigenous Aquatic Species Database, Gainesville, FL, and NOAA Great Lakes Aquatic Nonindigenous Species Information System, Ann Arbor, MI, https://nas.er.usgs.gov/queries/greatlakes/FactSheet.aspx?Species_ID=3201&Potential=Y&Type=2&HUCNumber=DGreatLakes, Revision Date: 9/30/2021, Access Date: 4/26/2024

This information is preliminary or provisional and is subject to revision. It is being provided to meet the need for timely best science. The information has not received final approval by the U.S. Geological Survey (USGS) and is provided on the condition that neither the USGS nor the U.S. Government shall be held liable for any damages resulting from the authorized or unauthorized use of the information.