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The following fish species did not appear to be hosts:
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3. Potential hosts for Lampsilis radiata luteola (Lamarck, 1819)
Laboratory infections have identified the following potential hosts (* - previously identified as a host in other studies):
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The following fish species did not appear to be hosts:
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SURFIN FOR CLAMS
Leigh Ann McDougal
USDA Forest Service, Southern Region Freshwater Mollusk
Coordinator
110 Southpark Drive, Blacksburg, VA 24060
540-552-4641
l.mcdougal@juno.com.
I'm pretty much a novice at finding my way around the internet but for other beginners I thought I would list some of the freshwater mussel resources that I was able to find on the world wide web. I haven't tried to list individual researcher's home pages because there are so many of them.
Listservers
UNIO - Focuses on freshwater unionid mussels. To subscribe send an e-mail message to Majordomo@lists.umbc.edu The first line of text should contain the following statement: subscribe UNIO your e-mail address
MOLLUSCA - Includes marine and paleontological as well as freshwater. To subscribe, send an e-mail message to listproc@ucmpl.berkely.edu In the body of the message type: subscribe mollusca your name
CONCH-L - Shell collectors. Send a message to listserv@uga.cc.uga.edu In the body of the message type: subscribe conch-l your name
SHELLFISH - Probably mostly marine mollusks? Send message to to shellfish-request@kenyon.edu In the body of the message type: subscribe
Web Pages
1. Illinois Natural History Survey Mollusk Collection - this page includes links to many other mussel resources including; the Triannual Unionid Report, mussel researchers list, symposium proceedings, Field Guide to Freshwater Mussels of the Midwest, systematic research collections list, and of course a lot of stuff about IL. http://www.inhs.uiuc.edu/cbd/collections/mollusk.html
2. Mollia - logistic information about malacology, info about meetings, on-line collections databases, Unitas Malacologica newsletter and other links. http://www.ucmp.berkeley.edu/mologis/mollia.html
3. Species Accounts, US Fish and Wildlife Service, Divs of
Endangered Species, Region 4 - has a lot of SE US mussel species
accounts from the Red Book. Region 4 page:
http://www.fws.gov/~r4eao/
US Fish and Wildlife Service Endangered Species home page:
http://www.fws.gov/~r9endspp/endspp.html
4. Former Category 2 Candidate species. http://ucmp1.berkely.edu/barryr/cat2.html
5. Questions about Mussels. http://www-personal.umich.edu/~rsherman/questions.html
6. University of Michigan, Museum of Zoology Mollusk Publications. http://www.ummz.lsa.umich.edu/mollusks/pub.html
7. American Malacological Union 1997 meeting - paper abstracts. http://ucmp1.berkeley.edu/mologis/meeting.html
8. Conchologists of America (COA) sponsor a bunch of different web pages. They have the same address except the ending is different for each. http://coa.acnatsci.org/conchnet/ (add the rest of the address listed for each)
- Freshwater mussel references: uniorefs.html
- Mussel collecting in Kansas: couch995.html
- Freshwater mussel articles: acfwmus1.html
- New species: adunew-f.html
9. Some Recent Publications on Adult and Juvenile Unionid Mussels. http://www.wfu.edu/users.dimock/muss.html
10. Alabama Molluska, Freshwater Species. http://fly.hiwaay.net/~dwills/mussels/alafuwspl.html
8. Rhode Island Freshwater Clams and Mussels. http://brooktrout.geo.uri.edu/riseagrant/clams_fs.html
9. Montana Freshwater Mussels. http://rivers.oscs.montana.edu/dlg/aim/mollusca/sum2.html
Spectaclecase (Cumberlandia monodonta) host(s) still elusive
Cindy Lee and Mark Hove
Univ. of Minnesota Dept. of Fisheries & Wildlife
1980 Folwell Ave., St. Paul, MN 55108
(612) 624-3019
leexO444@maroon.tc.umn.edu
mh@fw.umn.edu
The host requirements of Cumberlandia monodonta, a federally listed species (Category 2), have not been determined. We are working with Chris Barnhart, Andrew Roberts, and Frank Riusech at SW Missouri State University, and Richard Neves and Michelle Steg at Virginia Polytechnic Institute and State University to determine suitable host(s) for this species.
Twenty-three fish species and the mudpuppy were exposed to glochidia this spring at the University of Minnesota Glochidial metamorphosis was not observed for any of the species tested (Table 1).
Table 1. Species exposed to Cumberlandia monodonta glochidia
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A number of interesting observations were made this spring on the conglutinates and the way they were released. As previously observed under laboratory conditions, the unusually shaped conglutinates released by this species (Knudsen and Hove 1997) are accompanied by a viscous, sticky, transparent, gelatinous material. This year divers observed C. monodonta releasing conglutinates in the St. Croix Rivar. Soon after divers removed a flat stone that covered a large group of C. monodonta they began to release conglutinates. Conglutinates were arranged along the length of a transparent, gelatinous strand; approximately 0.6 m in length. Another behavior witnessed in the field and the laboratory was the propensity for gravid females to release their conglutinates at the same time.
It's interesting to note that Cyclonaias tuberculata will also produce a large gelatinous conglutinate; 10 cm long in static water and possibly 20 cm long in a light current. Perhaps the strategy of producing "super-conglutinates" like those constructed by Lampsilis perovalis is more widely employed than previously thought. Funding was provided by the Minnesota Dept. of Natural Resources, Natural Heritage and Nongame Research Program, and University of Minnesota Undergrad. Research Opportunities Program. We gratefully thank Dave Heath, Ron Benjamen, and Mark Endris of the WI Dept. of Natural Resources for their underwater observations while collecting gravid mussels.
Literature Cited
Knudsen K. A. and M. C. Hove. 1997. Spectaclecase (Cumberlandia monodonta) conglutinates unique, host(s) elusive. Triannual Unionid Report. 11: 2.
Host fish suitability studies and host attracting behaviors of Tritogonia verrucosa, the pistolgrip
Jennifer E. Kurth and Mark C. Hove
University of Minnesota, Department of Fisheries & Wildlife
1980 Folwell Avenue
St. Paul, MN 55108
(612) 624-3019
kurt0007@tc.umn.edu
mh@fw.umn.edu
Eleven fish species were exposed to T. verrucosa glochidia released by females collected from the St. Croix River at Interstate State Park Minnesota (Table 1). While none of the species facilitated metamorphosis of glochidia into juveniles, glochidia on the 3 year old black bullheads and yellow bullheads grew significantly. Although yellow bullheads can serve as suitable hosts for T. verrucosa glochidia (Pepi and Hove 1997), juveniles were not observed during this study. Flathead catfish have also been reported as suitable hosts for T. verrucosa (Howells, 1996). Unfortunately, our flathead catfish died due to mechanical problems before metamorphosis was observed.
Table 1. Fishes exposed to T. verrucosa glochidia
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Funding was provided by the Minnesota Dept. of Natural Resources, Natural Heritage and Nongame Research Program, and University of Minnesota, Undergraduate Research Opportunities Program. We gratefully thank Dave Heath, Ron Benjamen, and Mark Endris of the Wisconsin Dept. of Natural Resources for their underwater observations while collecting gravid mussels.
Literature Cited
Howells, R. G. 1996. Pistolgrip and Gulf Mapleleaf hosts. Info-Mussel Newsletter. 4(3): 3.
Pepi, V. E. and M. C. Hove. 1997. Suitable fish hosts and mantle display behavior of Tritogonia verrucosa. Triannual Unionid Report. 11: 3.
Title of Study: REPRODUCTION IN A FRESHWATER UNIONID (MOLLUSCA: BIVALVIA) COMMUNITY DOWNSTREAM OF CAVE RUN RESERVOIR IN THE LICKING RIVER AT MOORES FERRY, KENTUCKY
Name: Stephen Eugene McMurray
Date of Degree: May, 1997
Institution: Eastern Kentucky University
Location: Richmond, Kentucky
Pages in Thesis: 120
Candidate for the Degree of: Master of Science
Major Field: Biology (Applied Ecology)
Scope of Study: The objective of this study was to determine why recruitment had ceased or had been dramatically decreased in the diverse unionid community at Moores Ferry, Bath County, Kentucky, and to compare it with a unionid community 159 kilometers downstream at Butler, Pendleton County, Kentucky, which was thought to be healthy. It was hypothesized that the loss of recruitment in the Moores Ferry bed was the result of Cave Run Reservoir, located approximately 35.4 km upstream.
Findings and Conclusions: A total of 20 unionid glochidia were collected by drift nets, compared to 235 juvenile Corbicula fluminea. Six of the fish collected from Moores Ferry and none of those collected from Butler had infestations of glochidia. Only 10.1% of the unionids observed from Moores Ferry and only 13.5% of those observed from Butler had their gills modified as marsupia. Histological examination revealed that the sex ratios for Actinonaias ligamentina and Elliptio dilatata at Moores Ferry and A. ligamentina at Butler did not differ significantly from 1:1. The sex ratio for E. dilatata at Butler was statistically different from 1:1. One of the A. ligamentina from Moores Ferry was found to be hermaphroditic. Most of the males from both sites had more than one cell type of spermatogenesis present in their testes, and usually the most advanced type present dominated the acini. Spermatids were most common in E. dilatata and sperm morulae and spermatids were most common in A. ligamentina from Moores Ferry. Spermatids and spermatozoa were observed in E. dilatata and spermatocytes, spermatids, and spermatozoa were observed in A. ligamentina from Butler. Oogonia, oocytes, and ova were observed in the ovarian alveoli of female E. dilatata from Butler. Oogonia were round to oval, up to 40 ~m in diameter, and were usually embedded in the alveolar wall. Oocytes were oval to tear drop or balloon shaped, 50 to 150 ~m in diameter, and were attached to the alveolar wall by a cytoplasmic stalk. Ova were round to oval in shape, 65 to 165 ~m in diameter, and were usually free in the lumen of the alveoli. Most of the E. dilatata from Moores Ferry were in the second stage of oogenesis (oocytes), while the first stage of oogenesis (oogonia) was predominantly found at Butler. Most of the females of A. ligamentina and E. dilatata from Moores Ferry had empty marsupia. Most of the female A. ligamentina from Butler had mature glochidia in the marsupia. For E. dilatata, however, most of the females had empty marsupia. Post-impoundment water temperatures for the Licking River at Farmers, Kentucky, were significantly lower than preimpoundment temperatures for the months of May through July. There was no significant decrease in temperature for the month of August and a significant increase in water temperature for the month of September. The average monthly discharge increased from pre- to post-impoundment periods for the months of June through September and decreased during the month of May. Even though there were no significant differences in discharge and only significant decreases in temperature for a few months, the impacts of these changes were still important. The average monthly discharge and temperature at Moores Ferry may not have been as important as the spikes of discharge and decreases in temperature caused by releases of hypolimnionic water from Cave Run Reservoir. These data clearly showed that these releases had impacted the downstream faunas. Based on these data, it was recommended in order to ameliorate the combined effects of discharge and temperature that: 1) the individual spikes of discharge be reduced; and 2) the water for discharge be epilimnionic or mixed to produce a warmer discharge. Further study at Butler needs to be completed to determine the impacts to, and assess the current health of, this community.
Identification of host fishes for Lampsilis altilis and Villosa vibex
Wendell R. Haag, Melvin L. Warren, Jr., and Mahala Shillingsford
USDA Forest Service, Southern Research Station, Forest Hydrology
Lab
1000 Front Street Oxford, MS 38655
601-234-2744.
We have completed laboratory host identification trials for Lampsilis altilis and Villosa vibex. Gravid females of these two species were collected in March 1997 from Shoal Creek (Coosa River drainage) in Talladega National Forest, northeastern Alabama. Methods followed closely those of Zale and Neves (1982). All trials were conducted at 19oC. Host fishes are species that produced live juvenile mussels; non-hosts are species that rejected all glochidia without producing juveniles. Marginal hosts are species that carried glochidia for extended periods but produced no juveniles, only inactive juveniles, or extremely low numbers of active juveniles (<5).
Lampsilis altilis
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Villosa vibex
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Zale, A.V. and R.J. Neves. 1982. Canadian Journal of Zoology 60:2535-2542.
Confirmation of Lampsilis altilis as a superconglutinate producer
Wendell R. Haag1, April Hargus2, and Melvin L. Warren, Jr. 1
1 USDA Forest Service, Southern Research Station, Forest Hydrology Lab, 1000 Front Street, Oxford, MS 38655. 601-234-2744.
2 USDA Forest Service, National Forests in Alabama, 2946 Chestnut St., Montgomery, AL 36107.
As of this year, three North American unionid species (Lampsilis perovalis, L. subangulata, and L. australis) had been confirmed as producing superconglutinates, a large, minnow-shaped conglutinate containing the entire glochidial contents of both gravid gills and tethered to the female mussel by a hollow mucus strand (Haag et al. 1995; O'Brien et al. 1997). In addition, Lampsilis altilis, endemic to the Coosa and Tallapoosa River drainages in Alabama, Georgia, and Tennessee, was suspected to produce superconglutinates, based on having gravid gill morphology similar to that of confirmed superconglutinate producers (P. Hartfield, USFWS, Jackson, MS, personal communication). However, this behavior had never been observed in L. altilis.
On March 11, 1997 (water temp. = 18oC), we surveyed for mussels in Shoal Creek, a Coosa River tributary in Talladega National Forest, northeastern Alabama. We found one female Lampsilis altilis releasing a superconglutinate. The female was perched upright with about one-half of her shell exposed above the substrate and trailing a mucous strand about 40 cm in length. In addition, we found one female perched upright in sand trailing a short segment of a mucous strand (suggesting that the superconglutinate had been torn off), and two detached superconglutinates were found snagged on twigs in the stream. In addition to using superconglutinates, L. altilis appears to also employ the host attraction strategy of other species of Lampsilis. On this same date, we found six gravid female L. altilis displaying mantle flaps characteristic of non-superconglutinate producing species of Lampsilis. The mantle flaps were pigmented with a dusky gray stripe on the outer surface, a row of black spots on the inside surface? and a distinct eyespot on the posterior-most end. The flaps were pulsated in a manner similar to the behavior of L. cardium. All of the displaying females had fully gravid gills visible through the shell aperture, but none showed any sign of producing superconglutinates. The one female found producing a superconglutinate was not displaying mantle flaps, but the flaps, complete with eyespots, could be seen lying retracted, anterior to the siphons. These observations bring the total number of known superconglutinate producers to four, with two species in the Mobile Basin (L. altilis and L. perovalis), one in the Escambia/Choctawhatchee system (L. australis), and one in the Apalachicola/Ochlockonee system (L. subangulata). No other species are known to have the unusual marsupial morphology characteristic of these species, thus, superconglutinate production may be unique to these four taxa. Other superconglutinate producers have modified mantle margins that may be rhythmically undulated during the breeding season (Hartfield and Butler 1997). However, these mantle flaps are greatly reduced relative to the typical Lampsilis condition and the "display" is inconspicuous and probably does not serve to attract a host. Lampsilis altilis is unique among these four species in having and displaying a well-developed lure-like mantle flap in addition to producing a superconglutinate. This suggests that the presence of well-developed mantle flaps such as those of L. altilis may represent the basal condition for this group, mantle flap lures having been lost in the other three species along with increased specialization for infecting host fishes by superconglutinate production. However, additional characters are needed to test this hypothesis.
Literature cited
Haag, W.R., R.S. Butler, and P.D. Hartfield. 1995. Freshwater Biology 34:471-476.
Hartfield, P.D. and R.S. Butler. 1997. pp. 11-14, in K.S. Cummings, A.C. Buchanan, C.A. Mayer, and T.J. Naimo (editors). Conservation and management of freshwater mussels II: Initiatives for the future. Proceedings of a UMRCC symposium, 16-18 October 1995, St. Louis, Missouri. Upper Mississippi River Conservation Committee, Rock Island, Illinois.
O'Brien, C.A., J. Brim-Box, and A. Daniels. 1997. (Abstract). p.291, in K.S. Cummings, A.C. Buchanan, C.A. Mayer, and T.J. Naimo (editors). Conservation and management of freshwater mussels II: Initiatives for the future. Proceedings of a UMRCC symposium, 16-18 October 1995, St. Louis, Missouri. Upper Mississippi River Conservation Committee, Rock Island, Illinois.
Biological Checklist of the Kemptville Creek Drainage Basin
Frederick W. Schueler
RR#2 Oxford Station, Ontario, Canada
bckcdb@istar.ca
(613)258-3107
Another Year Surveying the Distribution Of Unionids in Eastern Ontario. I have continued the survey of the Unionids of eastern & central Ontario I began with support from the Ministry of Natural Resources in 1995 (Schueler, 1996. A Survey of the Unionid mussels of the Rideau and lower Ottawa drainages (in Ontario). Triannual Unionid Report 9:5). The commonest species have or are hybrid populations. Some lower Ottawa River Elliptio appear intermediate between the widespread E. complanata & E. dilatata (historically known from the vicinity of Montreal). Anodonta (=Pyganodon) grandis and A. cataracta seem to intergrade (while A. grandis-like shells predominate, I found A. cataracta-like shells at the outlet of Fawn Lake, Mississippi drainage, and Higley Lake & Lyn Creek, Leeds Co). Lampsilis (r.) radiata and L. (r.) siliquoidea seem to hybridize freely throughout the area. These three "common species," or complexes, are represented at most sites that I sampled. I am unsure of the taxonomic status of diverse Lampsilis that resemble L. ovata.
In southern Renfrew Co., despite high water, in May 1996, I found the common species at several sites with, at Lake Dore, Strophitus undulatus, at Muskrat River/Hwy 17, Lasmigona compressa, and at Black Bay, Calabogie Lake, Lampsilis cf ovata. In Lanark Co, the Mississippi River from Almonte to Blakeney has the most diverse fauna in the area, with the common species, L. cf ovata, Lasmigona costata, Ligumia recta, & Alasmidonta marginata. Upstream of the falls at Almonte S. undulatus was at three sites, L. compressa at two headwater sites, Anodontoides ferussacianus in Bolton Creek, a shell of L. costata in the main river at Glen Isle, but only 1-3 of the common species at 16 other sites.
In Ottawa-Carleton Region, the upper Jock River supports the common species, Strophitus undulatus, Anodontoides ferussacianus, and Lasmigona compressa. The Rideau River lock-bypass rapids at Andrewsville (where no Dreissena were seen in 1996) contain large old Lasmigona costata & Ligumia recta, and many Lampsilis radiata (a 154 mm L. radiata shell is the largest known from E. Ont.). Downstream, in Ottawa, below Hogsback Falls (one of the historically richest Unionid sites in the area), water was startlingly clear and the bottom covered with lst-yr Dreissena in September 1996. In June, 1997, shells of dead Dreissena formed 30 cm deep drifts, water was more turbid, and though there were many mussels they did not pave the bottom. In 1996 L. radiata were crowded with Dreissena: in the substrate as if killed in situ, freshly dead on the surface, or bearded with Dreissena but still alive. In 1997 there were only a very few living L. radiata & E. complanata, and shells of L. costata & Ligumia recta.
At Spenserville, Grenville Co, the only clear rocky stretch of the South Nation River supports the common species, Strophitus undulatus & Lasmigona compressa. I found Leptodea fragilis in the South Nation near its muddy mouth at the Ottawa River (first fresh modern E. Ont. specimens). Along the Ottawa River from Hudson to Pointe Fortune, Quebec, Elliptio complanata predominates, and while many shells are heavy and diverse in shape and colour, none were clearly E. dilatata. Sites along the St Lawrence River ail had many Dreissena and shells of the common species (mostly E. complanata & L. radiata), but no living Unionids (Leeds Co: St Lawrence Pk in Brockville & Halsteads Bay, Grenville Co: Claybank Bay, Maitland, & Windmill Battle Pk).
A brief (August, 1996) visit to streams draining the Oak Ridges Moraine north of Lake Ontario (records plotted in Metcalfe-Smith, et al., 1997. Biodiversity of Freshwater mussels in the Lower Great Lakes Drainage Basin. NWRI Contribution 97-90), found very few Unionids. Strophitus undulatus was the only Mollusc in Bowmanville Creek at Hampton. At Garden Hill a large Lasmigona costata was the only Unionid in a rocky riffle below a milldam. In Cold Creek, at Orland (a clear pasture creek sampled at a bridge riffle), Elliptio & Lampsilis were absent, but S. undulatus, Anodontoides ferussacianus, & Lasmigona compressa were present. First-year Dreissena were widespread in lakes and locks of the Trent Canal system, but were not evident at the Trent River (7 km SSW Campbellford), where the common species were found with L. costata & Ligumia recta (mostly old clams in rubble on limestone bedrock), Lampsilis cf ovata, Alasmidonta undulata (first L. Ontario drainage record, a few old shells), Villosa iris, A. ferussacianus, & S. undulatus. The introduced crayfish Orconectes rusticus was so abundant here that it was hard to imagine that any juvenile Unionid could survive.
THE 1995 AND 1996 EVALUATION OF A UNIONID MOLLUSK POPULATION AFTER A 1994 TRANSLOCATION PROJECT: THE WOLF RIVER, N OF SHIOCTON, WI.
HAVLIK, MARIAN E.
Malacological Consultants
1603 Mississippi Street, La Crosse, WI 54601-4969
Phone/Fax: 608-782-7958
E-mail: havlikme@aol.com
A unionid translocation was done August 1994, at STH 54 bridge, Wolf River, Shiocton, WI. Our 1993 preliminary survey (20-0.25 m2 samples required) showed a mean density of 3.0/m2 with threatened Tritogonia verrucosa (Raf. 1820) at 13.33% (0.4/m2). 17 species (957 specimens) were collected at bridge (2.46/m2). All were marked or numbered on both valves, including 124 T. verrucosa (12.96%, 0.318/m2, 3-31 years, 9 juveniles, 58 males and 57 females). Per WDNR permit, 10 T. verrucosawere placed in each of 3-1.0 m2 replicates. Translocation habitat was limited. Unionids were placed 0.3 m apart in an area 2.0 m X 100 m, along the rock/ sand interface, upstream and downstream of replicates. Several T. verrucosa were found at the translocation site which was marked at treeline with orange plastic survey stakes; replicates were similarly marked underwater. In 1995 we sampled the downstream half of site, and 2 replicates. Of 87 unionids, 49 were hash marked, 12 numbered, and 26 unmarked. Only one 27 year old hash marked unionid was dead (98.4% survival). Mean density was 5.08/m2 for marked, and 2.17/m2 for unmarked shells. Replicate #2 included 4 T. verrucosa, 1 Ligumia recta, 1 hash-marked, and 3 unmarked unionids. Replicate #3 included 3 T. verrucosa and 5 unmarked shells. 4 numbered T. verrucosa were recovered from 40-0.25 m2 quadrats. T. verrucosa were found clumped in several areas. Actinonaias l. carinata (Barnes, 1823) were buried up to 2 inches under sand. Divers only found 3 stakes marking replicates (in riprap); others were either buried or washed away. Replicates were again marked. In 1996 we sampled the upstream half of the site, and all 3 replicates. Of 92 mussels found, 55 were alive and 37 dead; 32 were hash marked, 14 numbered, and 46 unmarked. 5 hash marked and 2 numbered mussels were dead (84.8% survival). Mean density was 3.0/m2 for marked and 1.23/m2 for unmarked mussels (mean 4.23/m2). Recovered from replicate #1 were 6 T. verrucosa, 6 hash-marked and 5 unmarked mussels; from replicate #2 were 3 T. verrucosa (#48 dead), and 6 unmarked mussels; and from replicate #3 were 3 T. verrucosa (#34 dead) and 4 unmarked mussels. 2 numbered T. verrucosa were recovered from 40-0.25 m2 quadrats. 0f the 52-0.25 m2 quadrats, 19 were negative, including 2 in replicate #2. No empty mussels were fresh-dead. Most marked mussels continued to be found near the rock riprap/sand interface. Divers only found 3 stakes (in riprap) marking replicates. The channelward stakes were either not found, buried in sand, or washed away. Our results show that careful quick handling of mussels out of water give an acceptable survival rate 2 years post-project. The mortality of marked mussels did not appear to be associated with this translocation because 100% of the unmarked mussels were found alive in 1995, whereas only 35.6% of the unmarked mussels ware found alive in l996. This indicates that unusual relocation efforts are generally unnecessary, however we recommend hand planting of special status mussels when habitat is restricted in width.
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