Length-Weight Relationships, Age and Growth, and Body Condition of the Spottail Shiner [Notropis hudsonius) (Clinton 1824) in the Western Basin of Lake Erie.
The family Cyprinidae consists of minnows and carp and is the largest family of freshwater fishes in the world (Nelson 2006). Minnows are essential to energy transfer from lower to upper trophic levels by converting nutrients from zooplankton and aquatic insects to the broader food web (Hartman et al. 1992). Understanding the rates of growth and relationships between weight and length are essential to life history and population age structure. Accurately modeling aquatic ecosystem function depends on information that can be acquired through simple and cost effective techniques (Froese 2006).
The Spottail Shiner, Notropis hudsonius is common along the Atlantic coast, from the Altamaha drainage in Georgia north to the Connecticut and Thames drainages, throughout most of the St. Lawrence and Great Lakes basin and southern part of the Hudson Bay, north and west throughout Canada to the western border of Alberta near the mouth of the Mackenzie River (Scott and Grossman 1973; Lee et al. 1980; Page and Burr 1991). Within the United States, the range extends southeast from northeastern Montana, North Dakota, eastern South Dakota, to southern Illinois including Minnesota, Michigan, Iowa, northern Indiana, and northern Ohio (Trautman 1981; Becker 1983; Page and Burr 1991; Stauffer et al. 1995; Simon 2011).
This study investigated the relationship between length and weight in Spottail Shiner to understand growth patterns based on gender with respect to habitat. In addition, the sex ratio and length frequency distribution was used to predict age structure. Both length and weight relationships are useful in comparing different populations and evaluating ecological patterns. Lake Erie individuals were collected from coastal habitats in the Western Basin and were compared to tributary populations. The purpose of this study was to determine patterns in gender growth differences, and specific correlations between two measures of length (i.e., total length [[L.sub.T]] and standard length [[L.sub.S]]) and weight ([M.sub.B]) based on gender. Differences in growth were assessed to find whether differences between Spottail Shiner populations in the Western Basin were associated with coastal habitats compared to tributary habitats. Lastly, the growth range and age structure of individuals from the Bass Islands were compared to other populations in the Great Lakes region.
MATERIALS AND METHODS
The Laurentian Great Lakes encompass one-fifth of the available freshwater in the world (Steffen et al. 2014). Lake Erie is globally the tenth largest lake and stores about two percent of the total volume of all of the Great Lakes (FWPCA 1968; Munawar et al. 1999). Lake Erie is the shallowest, most southern, and the most productive of the Great Lakes (Michalak et al. 2013). It has three separate basins, the western, central, and eastern basins, with depth increasing in an easterly direction (FWPCA 1968). This study was conducted in the Western Basin near the Bass Island Archipelago (in the area contained within lat 41.737198 N, lon -82.877068 W; lat 41.714358 N, lon -82.768781 W; lat 41.583450 N, lon -82.889107 W; and lat 41.591534 N, lon -82.825972 W), which is comprised of 31 islands in Ottawa County, Ohio. The study area has five major tributaries that include the Maumee (lat 41.700961 N, lon -83.413353 W), Sandusky (lat 41.472058 N, lon -82.704037 W), Huron (lat 41.394587 N, lon -82.552474 W), Portage (lat 41.515670 N, lon -82.956786 W), and Vermillion (lat 42.424544 N, lon -82.364765 W) rivers.
All study data was collected in the Western Basin of Lake Erie during daylight hours using a variety of gears and techniques to reduce bias. Studies were collected for a variety of purposes as part of investigations of the Bass Island region. Individual Spottail Shiner were collected from coastal and tributary habitats. Individuals used in the current study were collected during ichthyological investigations primarily during the spawning season (June-July). Sex ratios, length-frequency distribution, and length and weight relationships were based on 529 individuals from tributary, coastal, and open water habitats. Lot collections are part of the permanent collection of the Museum of Biodiversity, ET. Stone Laboratory, The Ohio State University and are housed at Gibraltar Island.
Individual fish were randomly subsampled from site-specific collection lots and blotted dry to remove excess moisture prior to wet weighing using a Sartorius balance with a resolution of 1 [micro]g (Middleton et al. 2013). Residual weights were adjusted from the wet weight to provide [M.sub.B]. Due to the precision of the balance used in the analysis, it was impractical to measure live individuals or to attempt to weigh fish in the field. Fish were anesthetized in MS222 and fixed in 10 percent formalin. Fish used in the laboratory analysis were soaked in water just prior to being measured. The relationship between freshly preserved individuals was tested to verify weight accuracy. Fish shrinkage was stable after seven days after which lengths and weights were measured. Shrinkage was less than five percent of the true weight of live individuals; however, it is recognized that data might not completely reflect the length-weight relationships of live individuals. Length and weight of all specimens had similar treatment, so it is assumed equal effects in specimen response based on preservation. Individuals were blotted dry, and then weighed using an analytical balance. Gender was determined using a Zeiss dissection microscope. Male genitals were elongate, tube-shaped and associated with modified scales and resided within a shallow trough just posterior the anus and anterior the anal fin origin, while the female genitals were broader at the base and narrow at the distal edge for egg deposition. Length measurements included standard length ([L.sub.s]) and total length ([L.sub.T]), which were measured using digital calipers to the nearest 0.01 mm. The [L.sub.s] was measured from the tip of the snout, horizontally, to the posterior tip of the notochord at the hypural plate, while [L.sub.T]was measured from the tip of the snout, horizontally, to the tip of the depressed caudal fin (Hubbs et al. 2004). All measurements were based on the standard procedure described in Hubbs et al. (2004). Age groups of individual Spottail Shiner were determined using length frequency distribution analysis (Nielson and Johnson 1983).
Log normalized length and weight were graphed using a best fit trend line and the results were evaluated using simple linear regression. To determine the role of sex and habitat in growth of Spottail Shiner, an Analysis of Covariance (ANCOVA) (STATISITICA 11.0) was done to compare [M.sub.B] and length, i.e., [L.sub.s] and [L.sub.T] between males and females, and between tributary and coastal waters. Habitat class was assessed to determine size effect, by separating populations into tributary and coastal shoreline groups. An F-test was used to compare body weight [M.sub.B] and length ([L.sub.s] and [L.sub.T]) for males and females, between weight or length between males and females, or if there was a significant difference between the males in tributary compared to coastal habitats (Sokal and Rohlf 2011). Spottail Shiner age groups were determined by sex using length-frequency distribution analysis (Nielsen and Johnson 1983). A two-way Analysis of Variance (ANOVA) (Sokal and Rohlf 2011) was used to determine if there were significant differences in the size distributions of age class between males and females. A chi-squared test was used to determine if there was any significant difference in the sex ratio between males and females in the random subsample. A two-way Analysis of Variance (F-test) was used to determine if there were significant differences in tributary males and females compared to coastal males and females.
Spottail Shiner populations from the coastal shorelines of Bass Islands, the open water of the Bass Islands, Portage River, and Terwilliger's Pond in the Western Basin of Lake Erie were studied to determine length-weight relationships (n = 529). We examined 1556 individuals from 26 sites around the Western Basin (see Supplemental Materials for list of sites) of Lake Erie and 529 individuals were randomly subsampled based on coastal, open water, and tributary habitats. Spottail Shiner individuals from the Western Basin had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.0902x-5.2289, [R.sup.2] = 0.995, Fig. 1) and a positive correlation between log normalized [L.sub.s] and [M.sub.B] (y = 3.1397x-5.0501, [R.sup.2] = 0.996, Fig. 1).
Male individuals had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.0984x-5.2465, [R.sup.2] = 0.995, Fig. 1) and a significant positive correlation between log normalized [L.sub.s] and [M.sub.B] (y = 3.1551x-5.0775, [R.sup.2]= 0.996, Fig. 1). Male individuals collected in tributaries had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.2211x-5.5001, [R.sup.2] = 0.983, Fig. 2) and a positive correlation between log normalized [L.sub.s] and [M.sub.B] (y = 3.1796x-5.134l, [R.sup.2] = 0.988, Fig. 2). Male individuals collected in coastal water had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.1052x-5.2521, [R.sup.2]= 0.995, Fig. 2) and a positive correlation between log normalized [L.sub.s].and [M.sub.B](y = 3.l6l21x-5.0852, [R.sup.2]= 0.996, Fig. 2).
Female Spottail Shiner had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.078x-5.2034, [R.sup.2] = 0.995, Fig. 1) and a positive correlation between log normalized [L.sub.s] and [M.sub.B] (y = 3.1338x-5.0393, [R.sup.2] = 0.996, Fig. 1). Female individuals collected in tributaries had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.0367x-5.1356, [R.sup.2] = 0.966, Fig. 3) and a positive correlation between log normalized [L.sub.s] and [M.sub.B] (y = 3.1236x-5.028, [R.sup.2] = 0.987, Fig. 3). Female individuals collected in coastal waters had a positive correlation between log normalized [L.sub.T] and [M.sub.B] (y = 3.08x-5.2055, [R.sup.2] = 0.995, Fig. 3) and a positive correlation between log normalized [L.sub.s].and [M.sub.B](y = 3.135x-5.0402, [R.sup.2]= 0.997, Fig. 3).
There was a stable sex ratio of 1:1 for males and females. Males were not significantly different compared to females for either [L.sub.T] or [L.sub.s] (F-test = 1.020, df = 260, 267, p-value = 0.437). Male and female individuals did not have a significant difference in [M.sub.B] (F-test = 1.067, df = 260, 267, p-value = 0.304). Tributary male individuals [L.sub.T].was significantly different from coastal water male [L.sub.T] (F-test = 0.347, df = 64, 196, p-value = < 0.001). Male Spottail Shiner in tributary areas had a significantly different [L.sub.T] compared to coastal water male Spottail Shiner (F-test = 0.361, df = 64, 196, p-value = <0.001). Male Spottail Shiner [M.sub.B] in tributary areas was not significantly different from coastal water male [M.sub.B] (F-test = 0.784, df = 64, 196, p-value = 0.129). Tributary female individuals [L.sub.T]. was significantly different from coastal water female [L.sub.T] (F-test = 0.174, df = 33, 225, p-value = < 0.001). Female Spottail Shiner in tributary areas had a significantly different [L.sub.s] compared to coastal water female Spottail Shiner (F-test = 0.174, df = 33, 225, p-value = <0.001). Female Spottail Shiner [M.sub.B] in tributary areas were significantly different from coastal water female [M.sub.B] (F-test = 0.239, df = 33, 225, p-value = <0.001). Tributary individuals were significantly different than coastal individuals (F-test = 0.346, df = 65, 202, p = < 0.001).
Length frequency distributions of males and females show the differences in [L.sub.T] Male age I individuals ranged from 12-54, age II individuals ranged from 57-99, and age III individuals ranged from 99-132 (Fig. 4b). Female age I individuals ranged from 12-48, age II individuals ranged from 53-102, and age III individuals ranged from 102-129 (Fig. 4a). The tributary and coastal females had the same age classes as all females (Fig. 4c), while male coastal individuals had the same age classes as all males (Fig. 4d).
Carlander (1969) reviewed previous studies that analyzed the length and weight relationship of the Spottail Shiner. Populations in previous studies within the Midwestern United States included Ohio (Wells and House 1974; Trautman 1981), Iowa (McCann 1959), New York (Werner 1980), Pennsylvania (Cooper 1983), Minnesota (Carlander 1943; Smith and Kramer 1964), Michigan (Wells and House 1974), Maryland (Elser 1961), Virginia (Jenkins and Burkhead 1994), Wisconsin (Becker 1983), Alabama (Alabama Department of Conservation 1958), and Canada (Peer 1966; Scott and Crossman 1973). We compare our information to other Great Lakes and Midwestern North American populations (Table 1). No latitudinal gradient was observed within the range of Spottail Shiner, and a positive relationship was observed between age and weight (Carlander 1969; Wells and House 1974). Gender based differential growth was observed with females tending to be larger than males based on mean [L.sub.T] (Wells and House 1974). The positive regression analysis relationships of Spottail Shiner show that they exhibit indeterminate growth. Positive correlations exist between length and weight and show that a significant, positive relationship between age and length, as well as age and weight, existed for Western Basin Lake Erie populations. This is a similar result as reported by Wells and House (1974), which studied a Western Basin Lake Erie population near Sandusky.
Significant differences in [L.sub.T] and [M.sub.B] were not expected in tributary compared to coastal habitats. We hypothesized that due to lack of isolation from one another and ability to migrate freely that growth would not have been significantly different; however, F-test analyses found that there was a significant difference for males between tributary and coastal habitats. Females were expected to have increased weights compared to males due to the timing of the study; however, no difference in weight was exhibited. Spottail Shiner spawning occurs throughout its range throughout June and July (Becker 1983); therefore, females would be increasing in weight as vitellogenesis of ova occurs (Campbell and MacCrimmon 1970). Congruous with the preferred spawning habitat of Spottail Shiner includes bottom substrates composed of gravel and sand, which should have increased the likelihood of spawning males and large females being collected (Dickson 2008). Based on the b-factor in the logarithmic relationship between length and weight, Spottail Shiner individuals exhibited positive allometric growth. However, the b-value for females was lower. All age studies found that females were slightly larger than males, but were not significantly different in length of males and females, or in weights between males and females. Thus, female individuals were growing slightly faster in length than gaining weight. Potential explanations might be that the metabolic energy needed to yolk ova in females caused a decrease in expected weight. This pattern may be due to a lack of forage, or even density related feeding mechanisms caused by the large schools of individuals.
Bass Island region individuals exhibited less growth than statewide individuals during age I, but there was insufficient information for statewide comparison of individuals for ages II and III. Compared to other populations within the Spottail Shiner range, individuals in the Bass Island region of Lake Erie continue to show a trend of lower lengths at age I, but at ages II and III, the lengths are consistent with other areas within the range (Table 1).
The importance of understanding basic length-weight, age and growth, and condition factors of members of the family Cyprinidae is critical for determining the trophic structure of a dynamic system, such as Lake Erie. Although population dynamics of cyprinids have not been well studied, the high economic significance of a balanced minnow foundation in the food web is critical for stability in the Western Basin (Hubbs et al. 2004). Spottail Shiner populations may reflect changing conditions and can serve as an early warning indicator of Lake Erie fish assemblage stability. They are extremely important commercially since they support a large baitfish industry and can serve as a dominant food source for top predator, whole body carnivores (Hubbs et al. 2004). Changing conditions in the Spottail Shiner population may reflect future large-scale effects potentially caused by hypoxia, climate change, or harmful algal blooms (Munawar et al. 1999; Michalak et al. 2013).
OHIO: Ottawa Co. Lake Erie, Schoolhouse Bay, off Lutz Point, Trawl #2, Middle Bass Island, Put-in-Bay Twp., 41.0114403N -82.7845333W, VII:8:2011, TP Simon & EEOB 621 (N = 1 ); Lake Erie, 1.3 km off Catawba Island, ODNR Trawl #021, Catawba Island, Put-In-Bay Twp., 41.5602000N -82.8557000W, VI:27:2011, TP Simon & EEOB 621 (N = 5 ); Lake Erie, Fox's Marsh, Middle Bass Island, Put-In-Bay Twp., 41.2866700N -82.6426000W, VII:7:2003, CL Smith, D Kane, and EEOB 621, (N = 17 ); Lake Erie, Honey Point, North Bass Island, Put-In-Bay Twp., 41.3022700N -82.3431810W, VII:29:2011, TP Simon & EEOB 621 (N = 41 ); Lake Erie, Schoolhouse Bay, off Lutz Point, Trawl #2, Middle Bass Island, Put-In-Bay Twp., 41.6856333N -82.7847667W, VII:8:2011, TP Simon & EEOB 621 (N = 3 ); Lake Erie, East Pointe, 2.5 mi E Put-In-Bay Twp., 41.6653700N -82.7964000W, VII:25:2014, TP Simon & EEOB 5930 (N = 13); Lake Erie, Northeast Beach, 0.6 mi N Put-In-Bay, Gibraltar Island, 41.6584580N -82.8191030W, VL262015, TP Simon & EEOB5930 (N = 1 ); Lake Erie, Perry Monument Beach, 0.5 mi E Put in Bay, South Bass Island, Put-In-Bay Twp. 41.6527660N -82.8126230W, VI:24:2015, TP Simon & EEOB5930 (N = 165 ); Terwilliger's Pond, Bayview Avenue, 0.3 mi W Put-In-Bay, South Bass Island, Put-In-Bay Twp., 41.6566500N -82.8269550W, VI:25:1966, MB Trautman (N = 13 ); Lake Erie, School-house Bay Trawl, Middle Bass Island, Put-In-Bay Twp., 41.6950000N -82.7963330W, VII:9:2010, TP Simon & EEOB 621 (N = 5[lj); Lake Erie, Perry Monument Beach, 0.1 mi NW Put-In-Bay, South Bass Island, 41.2866700N -82.6426000W, VI:29:1992, TM Berra & EEOB 621 (N = 18); Lake Erie, South Bass State Park, 2 mi S Put-In-Bay, South Bass Island, Put-In-Bay Twp., 41.6432760N -82.8377550W, VI:24:2015, TP Simon & EEOB 5930 (N = 12 ); Lake Erie, Alligator Bar, SW Gibraltar Island, South Bass Island, Put-In-Bay Twp., 41.6573148N -82.8229398W, VII:2:2010, TP Simon & EEOB 621 (N = 1); Lake Erie, School-house Bay, Mid-bay Trawl, Middle Bass Island, Put-In-Bay Twp., 41.6867167N -82.7963167W, VII:9:2010, TP Simon & EEOB 621 (N = 2); Lake Erie, East Pointe Beach, 1.2 mi E Put-In-Bay, South Bass Island, Put-In-Bay Twp., 41.6656130N -82.7958310W, VI:24:2015, TP Simon & EEOB 5930 (N = 40); Lake Erie, Manilla Bay, North Bass Island, Put-In-Bay Twp., 41.7128310N -82.8308130W, VIII:31:1967, MB Trautman (N = 620 ); Lake Erie, Put-In-Bay, South Bass Island, Put-In-Bay Twp., 41.6558280N -82.8245020W, VILL1987, Ross (N = 55 ); Lake Erie, School-house Bay, Mid-bay trawl, Middle Bass Island, Put-In-Bay Twp., 41.6886167N -82.7844500W, VH:9:2010, TP Simon & EEOB 621 (N = 5 ); Portage River, OH SR 51 Bridge, Elmore, Elmore Twp., 41.6562660N -82.8272260W, VI:27:1980, Ross (N = 13 ); Lake Erie, East North Bass Island, Put-In-Bay Twp., 41.2809000N -82.1699100W, VII:5:2004, N Ultrup (N = 203 ); Lake Erie, Fox's Marsh, North Bass Island, Put-In-Bay Twp., 41.7119444N -82.8319444W, VII:8:2002, CL Smith and EEOB 621 (N = 4 ); Lake Erie, SE Shore to East Pointe, North Bass Island, Put-In-Bay Twp., 41.7075640N -82.8105000W, VII: 12:2010, TP Simon & EEOB 621 (N = 1 ); Portage River, OH SR 51 Bridge, Elmore, Elmore Twp., 41.4766600N -82.9532000W, VTI:7:2011, TP Simon & EEOB 621 (N = 1 [l]);Terwilliger's Pond, Bayview Avenue, 0.2 mi W Put-In-Bay, South Bass Island, Put-In-Bay Twp., 41.6562660N -82.8272260W, VII:8:2011, TP Simon & EEOB 621 (N = 3 ); Lake Erie (N = 21 ); Lake Erie, South Bass Island, Put-In-Bay Twp., VI:23:1966, Ichthyology Class (N = 292 ).
This study was supported by The Ohio State University, Franz T Stone Laboratory, Ohio Sea Grant, The Thomas Langlois foundation, and The Friends of Stone Lab through generous donation.
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ELIZABETH IGNASIAK (1), ZACHARY STEFFENSMEIER, ELLEN WARFIELD and FELICIA BRATTI, Franz T. Stone Laboratory, The Ohio State University, Put-in-Bay, OH, USA, and THOMAS P. SIMON, School of Public and Environmental Affairs, Indiana University, Bloomington, IN, USA.
(1) Address correspondence to Elizabeth M. Ignasiak, 8427 Muirland Dr., Broadview Heights, OH 44147. Email: firstname.lastname@example.org
Table 1 Comparison of Spottail Shiner age and growth relationships based on literature from the Great Lakes region and Midwestern United States Mean LT Range (mm) Location Age 0 Age I Age II Age III Age IV Canda (Saskatchewan) Nemeiben Lake -- 38 61 84 -- Crooked Lake -- 46 69 91 -- Iowa Clear Lake 39.3 76.7 98.2 107.9 -- Michigan Kalamazoo River Male -- 54 79 93 106 Female -- 56 80 94 105 Lake Michigan Male -- 62 95 108 116 Female -- 63 97 114 123 Minnesota (Statewide) 23-51 41-66 64-84 84-94 -- Lake of the Woods 48 66 89 -- -- Lower Red Lake Male -- 56 85 100 103 Female -- 58 90 106 113 Ohio (Statewide) 51-76 64-84 -- -- -- Lake Erie (Western Basin) Male -- 76 101 125 -- Female -- 78 108 135 -- Lake Erie, Bass Islands(July) Male -- 32 82 112 -- Female -- 30 82 114 -- Wisconsin Sugar Creek 63 96 109 120 124 Mean LT Range (mm) Location Age V Study Canda (Saskatchewan) Nemeiben Lake -- Peer (1966) Crooked Lake -- Peer (1966) Iowa Clear Lake -- McCann(1959) Michigan Kalamazoo River Wells and House (1974) Male Female Lake Michigan -- Wells and House (1974) Male 129 Female 131 Minnesota (Statewide) -- Carlander(1943) Lake of the Woods -- Carlander(1943) Lower Red Lake Smith and Kramer (1964) Male -- Female -- Ohio (Statewide) -- Trautman (1981) Lake Erie (Western Basin) Wells and House (1974) Male -- Female -- Lake Erie, Bass Islands(July) Current Study Male -- Female -- Wisconsin Sugar Creek -- Becker (1983)
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|Author:||Ignasiak, Elizabeth; Steffensmeier, Zachary; Warfield, Ellen; Bratti, Felicia; Simon, Thomas P.|
|Publication:||The Ohio Journal of Science|
|Date:||Dec 1, 2017|
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