Loading...
HomeMy WebLinkAbout20000008 Ver 1_Mitigation Report_20080222• At,?LMG LAND MANAGEMENT GROUP INC. 7W Environmental Consultants February 21, 2008 TO: Ms. Joanne Steinhuis NC Division of Water Quality 127 Cardinal Drive Extension Wilmington, NC 28405 )00Lf 17116 2 2, 0 8 L' RE: Mason Inlet Relocation Project - Biological Monitoring Report: December 2006 (Year 5) Dear Joanne: On behalf of New Hanover County (NC), Land Management Group, Inc. (LMG) is providing the requested December 2006 (Year 5) Benthic Infaunal Report for the Mason Inlet Relocation Project. One (1) hard copy is enclosed for your review and use. Please include this as an addendum to the full report for Year 5 that was submitted in November 2007. Please contact our office if you need digital copies for distribution to other federal agencies reviewing the project. Should you have any questions or comments regarding the findings of this report, please feel free to contact me either by phone (910-452-0001) or by email at bmanninq(@Imqroup.net. r? U Sincerely, Land Management Group, l anning Environmental Scientist encl. 0 E R ('!?b R D M2. P MAR 1 3 2008 ,N^ STFJRMW,4TER BRANCt1. www.lmgroup.net • info@lmgroup.net • Phone: 910.452.0001 • Fax: 910.452.0060 3805 Wrightsville Ave., Suite 15, Wilmington, NC 28403 • P.O. Box 2522, Wilmington, NC 28402 Monitoring of benthic faunal communities associated with the Mason Inlet relocation project - 2006 sampling • Benthic Faunal Communities Benthic infauna is the community of organisms that live within the sedimentary environment or on the sediment surface, although organisms that live primarily on the sediment surface are referred to as "epi-benthic". In general when we refer to epi-fauna in the soft substrate community we are referring to the more motile crustaceans and fishes, especially juvenile finfish that may derive a significant portion of their diet from the benthos. Most benthic organisms tend to live 6 months to 1 year (although some taxa such as bivalves may live a number of years). These organisms also tend to have relatively low motility and once settled tend to move less than 5 meters over the course of their lives. Depending on environment and dominant taxa this community tends to respond relatively quickly to perturbations reflecting the average conditions at a location. The overall abundance of benthic organisms and the stability/resilience of the community can reveal much about the local environment and potential consequences to upper trophic groups. A community consistently dominated by disturbance oriented taxa may indicate persistent instability (either from actual sediment movement or potentially from deposition of material on the substrate surface) in the sedimentary environment. This study focuses on the subgroup of benthic fauna considered macrofauna within the size class of 500 microns (1000 microns= 1 millimeter) or greater. Most benthic organisms in this size class are heavily preyed upon by larger finfish and • crustaceans. One of the primary reasons for studying this group is that the benthic community provides a critical ecosystem role in transferring energy from algae and detritus that most infauna feed upon (although there are some predatory forms as well) to higher trophic levels. The other main reason for studying this group is based their close relationship with the sediment and various taxa will respond differently to acute and chronic disturbances of this habitat. Most tube forming taxa will thrive in more stable areas with limited rates of sedimentation. Free burrowing forms however require less compacted sediments and tend to dominate areas with greater sediment water content and greater amounts of organic materials. Most benthic environments are composed of a complex mosaic of sediment types influenced by local physical interactions, inputs from surrounding habitats and terrestrial environments, and biotic interactions. Monitoring of benthic fauna is an important part of many environmental studies, including beach dredge and fill operations and beach renourishment projects and marsh restoration projects because they provide a good indicator or both short and long term impacts and recovery. Sampling Design This report covers the 2006 sampling period for the post construction phase of the Mason Inlet relocation project. This project was initiated in 2001 with a set of preliminary samples collected in December 2001, prior to construction. The mason Inlet relocation was completed in 2002, with post construction sampling being conducted 2002-2006. The samples reported here represent four sediment sites (S1-S4) and two control sites (IV 1 and IV2) and three transects (MT2, MT4, and MT6) with three • positions (5, 150, 300) on each transect. Each position indicates the distance from the marsh edge. All samples for all sites were collected on a single day. The infaunal sampling reported here represents community composition four years following inlet relocation. All samples were collected at the same locations as previous samples to be consistent. It should be noted here that in the 2006 report several of the transect sites were marked as "old sites" however no such designation was indicated for the current report. Both the S and IV sites seem to be sand dominated based on the presence of Haustorid amphipods Neohaustorius schmitzi and the tanaid Lepidactylus dytisus these species tend to be more common on sand dominated shorelines although L. dytisus builds tubes and tends to associate with rhizomes. The marsh transect locations (MT2, MT4 and MT6) should have all been marsh interior samples although MT2-5 and MT4-5 contained the barnacle Chthamalus fragilus, that tend to be found on exposed hard substrate environments and Gemma gemma which is a small (2mm) brooding clam most commonly found on open sand flat and low energy sandy beach environments. There were four S subsites (S 1, S2, S3 and S4) and two IV sites (IV 1 and IV2). Each S and IV subsite was sampled with three replicate core samples. The MT transects consisted of three replicate core samples taken at each of three distances from the marsh edge (5, 150, and 300 feet into the marsh) on each transect (though the exact edge location varied somewhat over time with erosion or accretion). Infaunal samples were collected using standard benthic cores, 10 cm diameter x 15 cm deep. All samples were fixed in 10% buffered formalin (formaldehyde derivative) • solution with rose Bengal dye added and later transferred to a 50% isoproponol preservative for storage and processing. Samples were sieved through a 500 micron screen to remove fine sediments and aid processing. All organisms retained were separated from the remaining sediment and vegetative material using light microscopes and identified to the lowest possible taxonomic level (generally species). As part of our standard quality control and quality assurance procedures, identifications are subject to verification and a subset of sorted samples are rechecked to ensure removal of all organisms. All newly identified species and those that could not be identified to the species level are sent to authorities for clarification. Diversity was calculated using the Shannon Weiner Diversity Index. 2006 Community Description A total of 51 taxa were collected during the 2006 sampling period (Arachnids and terrestrial insects are excluded from this count as are harpacticoid copepods and nematodes that are generally too small to be retained on a 500 micron mesh but are probably present in the samples due to the amount organic material and not representative of accurate densities. Polychaetes (segmented worms) were represented by 16 taxa (the highest number of taxa among any group sampled), insects were represented by 8 taxa, while amphipods were represented by 5 taxa and bivalves by 3 taxa (Table 1 to Table 5). Gastropods were poorly represented, with most specimens lumped into the gastropods sp classification, because of small size (> lmm) and poor condition. Overall the most r? U numerous taxa were Hargeria rapax (Tanaid), Capitella Capitata (polychaete) and tubificid (Oligochaete). • The two sets of sand sites were characterized by lower species richness and lower diversity (Table 5). Only 6 taxa were collected from the IV sites, while 9 were collected from the S sites. This is a slight decline in species richness from the 2005 sampling period. The S and IV sites were both dominated by the amphipod Neohaustorius schmitzi although this is mainly due to the relatively high density of amphipods in station S3 and IV 1. By and large most taxa present in the S and IV sites were represented by single individuals. In general two of the marsh transect sites (MT2 and MT4) were characterized by higher species richness, greater mean abundances and slightly higher diversity measurements than the sand dominated sites. A total of 26 taxa were collected from the MT2 sites and 30 taxa from MT4 sites while only 14 taxa were collected from the MT6 sites. Species richness has declined in the MT6 consistently over the last three years. The dominant taxa at MT2 were Capitella capitata and Tubificidae sp. (Table 2) MT4 was dominated by Capitella capitata, Dasyhelea sp., Hargeria rapax, and Tubificidae sp. (Table 3). Densities of species in MT6 were overall low with no clear dominant species (Table 4) . Diversity takes into account both total abundance and relative proportion of each taxa to the total abundance. For a typical back marsh area along the southeastern coast of the United States a diversity that approaches or exceeds 1.0 would be considered is good. As seen in previous sampling periods diversity at both marsh transect and sand sites tended to be relatively low. However diversity showed slight increases in 2006 over 2005 for 4 of the 6 sites in the S and IV stations and at 6 or 9 sites for the transects. Highest diversity was calculated for MT2-5 (H'=1.03) and lowest diversity was calculated for the sand sites S3 and S4 (H'=0.30), due to low species richness and evenness (Table 1). • N r-+ N O r3"'+ O U • N N s., U U N U ai U Oy.., 7-? U 'C 73 9 cn cd U U cl 'C 3~ U • H 0 0 M M M M O O O O O O O O O O O O O O O O O ?t 01 ? ? O? N d: O O O O N ? O M t? M M O? M M ?O M M? O M O O O O O O O O O O O O- 0 0 0 ?t d N N T NT d 0 0 M OO? 0 0 0 M M ? [? ?"? M M M M M O \D O M M M O O O O O O O O N O O O -+ -? O O O ?t ? ? --? -+ M 01 01 d' ? M 0 r-- M M M O O O \O O O O O -- O -4 O- 0 0 O O O O O O O M M M M M M O O O O (= O O O O O O O O O O O O O O v) d i M ?D M M r+ N M O O O O O O O O O N O O ? -+ O O O ? w CS «3 ti Q to (4) y Cl??' N O Q ?_ bq c cz (u u C) O cG B3 Cl a) ?? O N b 'C L-a -.. ?" ct a) • a? N E-"+ U N cd 110. U U O, N U U Q, cd O U cl cd M "0 rl cd N U Cd b N U H N N N N O ? O .- -? M M O M M M ? (? M M N M M M O? ?O O O M 0 0 0 0 0 0 0 0 0 0 O O N O O N O M r-+ O ? ? ? N M N ? O O O O M O O `O M M O O O ?O O O O O O O O O O O O O O O O O -- O N O? O O vi O O O O N N O O .- O ` ? N M M M l? l? M [? [? ?"? M M M \O l0 M \O \O O O O O N O O N O O O O O O O O O O O O O M O 0 0 _U ? H o 'c Ln o =y ti ¢' Q, Q, Q o o a o C4 o, k ct Cs a? Ln Zs sy v a c? •O O N O h13 Ct Qj) -,z 43 2 rz M c., bp N 4 ?S„ ti p p ti p°j CS • • a? N H U U O O ?N kf) O M oo N 01) M N M M M O 00 01 -? O ? M M ?"? "? l? ? O M ? ? M M O O \O O M M ? O O O O M 01 ^-+ 0 0 N O O O O O O N M -+ N N U U Okr) d U ? N ? M M O O O O O O O O l? O O O O O N O 0 0 0 0 O U s., n ct CN N N M "Cl ? O O O ? H O O ? U ?"'"? M M ? O O ? F-? O O O O 0 0 0 0 0 0 0 •--? O? 0 0 0 ? O "cs ?. •O ¢ ti CS U O U p?j 'C7 ' O C's SZ co? L, 'd ° o a? o s ? o w • H U U Cd 40. U U U U U cd U O cd 7? O Cd cn 'C3 cd U U U M U H r. O O M .--+ tT. ? \p l? M O M M ?'•? ? ? ,? M M O O 01 O -? O O O O O O O O O O O O O O M O O O O N?c O\ : 00110N O N r` It O d ?O 00 N ct B O O 4 O M ?d M M M V? OM N M M "I? M O d M 0 0 6 M M M M M M O `O M O M O 't CD CD 0CD 0 Do MOO D"T 00V.) OOC? O "o OO ?t 01 a1 [? N M kn N 00 00 ' 'T O -- ` ? O N O ? \O " M M M M M M ? O M M M M M ? N O O r••? -+ O -+ 0 0 0 0 0 0 0 0 0 0 N O O O O O K U ti O (z ' ? oy In O Ln O f1 ? Q cd ?. ^a O Sl ) ? O O O ^ CS N coo U ? Q, O O O ? . N "? Ct U ? O ?1 U 45 O rn O ti z cn Z O O N N +b U O Do ? O0.' ? ? ? • ? ? U O N -Z ? U p q O d p b rz _ •? Ci Ci .= O _ O O Ci cd O U Z • ? ??asuuuuuv UgQg WWryQ7Q7Q7x? ? 4 • U U r.+ U N • U U N U cd U s? O U s., c? 'C a3 Cd 'O N U cd cz cd N b O U M U H /-I d• n ? o o l? ? O l? M M M N ?O M M ? M O O O O O 00 0 0 0 O O O O O O O N n ? M 00 N 00 N -- 0 0 0 0 01 d 00 O O? M M O O M B M O M M ? .--i ?: O O O O O O N O 0 0 0 -y O O N M O d' O O ? 00 O O t} 0 0 O ? M M ?"? M M l? l? ? M M O M M ?O ?O O O O O O O 00 O - O O O O O O O O O O N ? U Q, ? O Q cC y O O ¢ 1,0 ? rz N ? ti4 q O O , cn • ,? cn ;3 Q.) O .. R w C6 ti 'C 'C GA ,_ O S., N ?l N ? O S-' ? Z O Z ? Z! U yams ,0 E cd Oa , D A • a ? C / ] ? [? [? H H ? c: a? V) A .0 ? M O M O M y? O O O O O O O O O O O -+ O O O O -- O O O O O O M 4° N U s. 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 U ct U s-, O U - - 'C kr) ? O O -d /? O O O O O O O O O O O O O O O O O O O O O O O O r. M U k U c?C .? ¢' C-n ti O cn c O , CS ¢ Ci b S Q" Q y b?4 O C's CS Q, O Ct ti R. O O O Q" a cy o3 A - o o O ? o a a; l - ?z ti o? p , ° ° ? > m z N C,3 n , -lz ? o o o ' to o ?zj z Cd H ? r VD a i • 4 W W UUUUUU ° UgQgW W rz Cd (Z ip 1? C7 Q7 Q U ? ??N • a? H U U Cd 40, N U V) U U U U cd N O N ^d Cd 'C cd Cd "C7 cd N U "d cd N b O U _U f-? n H M O O M N ^? 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 I ? O 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 d. d. O O M M M M O O O O O O O O O O O O O O O O O O O O ? cd U S'+ U ?? U O N l? 41 jz m Q) p Z O sue, O b0 Table 5. Diversity and species richness by site for 2004, 2005 and 2006. Diversity is calculated using Shannon Weiner index. Diversity is a measurement of species evenness that incorporates relative abundance of individual species at a given site as well as the number of species present. Species Richness represents the total number of taxa present. Species richness presented here includes higher taxonomic groups for specimens that were incomplete and for juveniles specimens that could not be reliably identified to lower species level. Site Mean Total Abundance Diversity Species Richness 2004 2005 2006 2004 2005 2006 2004 2005 2006 IV 1 4.0 8.33 19.67 0.184 0.286 0.36 4 3 3 IV 2 12.33 0.33 4.11 0.278 0 0.48 6 1 3 S 1 2.0 106.33 24.0 0.244 0.503 0.39 2 5 8 S2 15.33 16.0 6.33 0.573 0.613 0.77 6 8 8 S3 302.67 11.0 19.0 0.376 0.734 0.30 16 8 7 S4 13.33 6.67 0.67 0.346 0.077 0.30 6 5 2 MT2 5 50.33 25.0 23.56 0.628 0.908 1.03 20 14 17 MT2150 184.0 99.0 22.33 0.86 0.953 0.76 21 22 11 MT2 300 34.67 109.0 103.33 0.586 0.732 0.86 17 21 18 MT4 5 76.0 105.0 55.33 0.729 0.6 0.80 20 14 16 MT4150 111.33 180.67 271.33 0.382 0.63 0.94 13 13 22 MT4 300 141.67 112.0 163.33 0.51 0.858 0.53 21 20 12 MT6 5 10.0 4.0 1.67 0.277 0.559 0.58 7 4 4 MT6150 21.3 7.0 1.33 0.531 0.682 0.43 13 6 3 MT6 300 12.0 187.75 11.0 0.653 0.258 0.79 10 17 8 C