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Pilot  Study  to  Evaluate  the 
Practicality  of  Aquatic  Ecosystem 

Monitoring 
in  Small  Agricultural  Streams  in  Alberta 


/dlbcrla 

Environment 


Digitized  by  the  Internet  Archive 

in  2015 


https://archive.org/details/pilotstudytoevalOOande 


Pilot  Study  to  Evaluate  the  Practicality  of  Aquatic 
Ecosystem  Monitoring  in  Small  Agricultural 

Streams  in  Alberta 


Prepared  by: 


A.-M.  Anderson,  R.  Casey,  J.  Willis,  and  S.  Manchur 


Environmental  Assurance 
Alberta  Environment 


March  2009 


W0901 


ISBN:  978-0-7785-8106-2  (Printed  Edition) 

ISBN:  978-0-7785-8107-9  (On-Line  Edition) 

Web  Site:  http://environment.gov.ab.ca/info/home.asp 


Any  comments,  questions,  or  suggestions  regarding  the  content  of  this  document  may 
be  directed  to: 

Water  Policy  Branch 
Alberta  Environment 
7th  Floor,  Oxbridge  Place 
9820-  106th  Street 
Edmonton,  Alberta  T5K  2J6 
Phone:  (780)427-2654 
Fax:  (780)422-6712 


Additional  copies  of  this  document  may  be  obtained  by  contacting: 

Information  Centre 
Alberta  Environment 
Main  Floor,  Oxbridge  Place 
9820 -  106th  Street 
Edmonton,  Alberta  T5K  2J6 
Phone:  (780)427-2700 
Fax:  (780)422-4086 
Email:  env.infocent@gov.ab.ca 


EXECUTIVE  SUMMARY 


Monitoring,  evaluation  and  reporting  on  aquatic  ecosystem  health  are  implicit 
requirements  of  the  government  of  Alberta  Water  for  Life  commitment  to  assure  "healthy 
aquatic  ecosystems  "  (HAE).  In  addition  to  water  quality  monitoring,  an  increasing 
amount  of  monitoring  of  sediment  quality  and  biological  communities  has  occurred  in 
recent  years  on  major  rivers,  but  comparable  monitoring  efforts  on  small  streams  have 
been  very  limited. 

A  pilot  study  was  conducted  on  three  streams  from  an  existing  water  quality  network  of 
agricultural  streams  (i.e.,  the  Alberta  Environmentally  Sustainable  Agriculture  or  AESA 
network)  to  evaluate  the  feasibility  and  practicality  of  including  sediment  and  non-fish 
biota  monitoring.  In  fall  2006  AESA  sampling  locations  on  Rose  Creek,  the  Blindman 
River  and  Strawberry  Creek  were  sampled  for  benthic  invertebrates  (kick  nets),  epilithic 
and  planktonic  algae  (community  analysis  and  chlorophyll-a)  and  bottom  sediments 
(nutrients  and  particle  size)  Field  measurements  and  observations  were  taken  of  basic 
water  quality  parameters,  hydrometric  features,  and  reach,  stream  and  bank 
characteristics. 

The  three  watersheds  are  located  in  different,  although  adjacent  ecoregions,  and  they  are 
farmed  with  a  different  level  of  intensity.  The  Rose  Creek  site  is  more  erosional  in 
nature,  and  has  lower  dissolved  nutrient  levels  and  higher  flows  than  the  Blindman  River 
and  especially  Strawberry  Creek.  Riparian  damage  due  to  cattle  access  was  particularly 
evident  at  the  Blindman  River  site. 

Sampling  of  biological  communities  and  sediments  from  small  streams  proved  to  be 
feasible  and  practical.  However,  sampling  techniques  and  the  type  of  field  information 
differ  significantly  from  those  routinely  obtained  from  larger  provincial  rivers.  Therefore 
it  would  be  important  to  invest  in  staff  training  if  stream  sampling  was  to  be  carried  out 
routinely. 

Benthic  invertebrate  and  epilithic  algal  communities  comprised  many  taxonomic  groups 
for  which  ecological  requirements  and  responses  to  various  forms  of  disturbance  are 
fairly  well  understood.  The  distribution  of  such  organisms  has  been  used  elsewhere  to 
develop  indicators  which  in  turn  have  been  used  to  assess  the  'health'  or  'integrity'  of 
aquatic  ecosystems.  Even  at  the  scale  of  this  pilot  study  it  was  possible  to  note 
differences  in  biological  communities  among  streams  that  were  linked  to  the  degree  of 
eutrophication  (e.g.,  nutrient  levels  and  dissolved  oxygen  conditions),  and  physical 
habitat  characteristics  and  disturbance.  Phytoplankton  communities  were  not  very 
diverse  and  appeared  to  have  less  potential  for  future  monitoring  programs. 

One  of  the  difficulties  in  assessing  aquatic  ecosystem  health  in  Alberta  lies  in  defining 
'healthy'  aquatic  ecosystems.  One  approach  is  to  use  'natural  or  least  impacted' 
conditions,  to  define  'background'  or  'reference  conditions'  and  use  these  as  a  depiction 
of  healthy  conditions,  for  a  given  eco-region.  To  capture  variability  within  an  ecoregion, 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  » 
in  Alberta 


researchers  advocate  sampling  about  20  carefully  selected  sites  for  2  to  3  years.  Applied 
to  Alberta,  80  streams  would  have  to  be  sampled  to  cover  the  four  main  ecoregions  with 
agricultural  activity.  The  effort  is  substantial,  but  would  allow  the  description  of 
expectations  of  'healthy'  conditions,  which  in  turn  would  enable  the  definition  of  bio- 
criteria.  Such  information  is  basic  to  health  assessments  of  agricultural  streams  and 
similar  streams  influenced  by  other  types  of  human  activities  (e.g.,  forestry,  mining, 
urban  development). 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams 
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iii 


TABLE  OF  CONTENTS 


EXECUTIVE  SUMMARY  II 

LIST  OF  TABLES  VI 

LIST  OF  FIGURES  VI 

LIST  OF  APPENDICES  VI 

ACKNOWLEDGEMENTS  VII 

1.0       BACKGROUND  1 

2.0       OBJECTIVES  2 

3.0       METHODS  3 

3.1  SAMPLING  SITES  3 

3.2  SAMPLING  METHODS  5 

3. 2. 1  Field  Measurements  5 

3. 2. 2  Benthic  Invertebrates  5 

3. 2. 3  Epilithic  Algae  5 

3.2.4  Phytoplankton  6 

3.2.5  Sediment  6 

3.3  SAMPLE  PROCESSING  METHODS  6 

3. 3. 1  Benthic  Invertebrate  Samples  6 

3.3.2  Epilithic  and  Plankton  Algal  Taxonomy,  and  Chlorophyll-a 
Analyses  7 

3.3.3  Sediment  Chemistry  8 

3.4  DATA  ANALYSIS  8 

4.0       RESULTS  AND  DISCUSSION  10 

4.1  GENERAL  SITE  DESCRIPTION  10 

4.2  PRACTICAL  CONSIDERATIONS  ABOUT  THE  PILOT 
SAMPLING  10 

4.3  SEDIMENT  ANALYSES  1 1 

4.4  BENTHIC  INVERTEBRATES  1 2 

4.5  EPILITHIC  ALGAE  16 

4.6  PHYTOPLANKTON  21 

5.0       GENERAL  DISCUSSION  24 


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5.1  SUITABILITY  AND  PRACTICALITY  OF  MONITORING 
TECHNIQUES  24 

5.2  SELECTION  OF  POTENTIAL  INDICATORS  OF  HEALTH  24 

5.3  CONSIDERATIONS  FOR  FUTURE  AEH  MONITORING  OF 
AGRICULTURAL  STREAMS  25 

6.0       LITERATURE  CITED  28 

6.1  GENERAL  LITERATURE  28 

6.2  TAXONOMIC  REFERENCES:  BENTHIC  INVERTEBRATES  31 

6.3  TAXONOMIC  REFERENCES:  ALGAE  35 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams 
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V 


LIST  OF  TABLES 

Table  1          Summary  of  background  information  on  the  three  AESA  streams  selected 
for  the  pilot  study  3 

Table  2  Sediment  particle  size  and  nutrient  levels   1 2 

LIST  OF  FIGURES 

Figure  1         Agricultural  watersheds  monitored  under  the  Alberta  Environmentally 

Sustainable  Agriculture  (AES A)  program  4 

Figure  2         Benthic  invertebrate  data  for  three  agricultural  streams   14 

Figure  3         Epilithic  algae:  major  taxonomic  groups  in  agricultural  streams  17 

Figure  4         Epilithic  algal  counts,  biomass,  chlorophyll-a  and  number  of  species  in 

agricultural  streams  18 

Figure  5         Diatom  metrics  for  monitoring  eutrophication  in  agricultural  streams  (after 
Potapova  and  Charles,  2007)  20 

Figure  6         Planktonic  algal  counts,  biomass,  chlorophyll-a,  and  number  of  species.  22 

Figure  7         Planktonic  algae:  Major  taxonomic  groups  in  agricultural  streams  23 

LIST  OF  APPENDICES 

Appendix  1     Summary  of  field  observations  39 

Appendix  2     Benthic  invertebrate  community  composition  recorded  in  three 

agricultural  streams  in  2006  42 

Appendix  3     Benthic  invertebrate  community  composition  recorded  in  three 

agricultural  streams  in  2006  52 

Appendix  4     Phytoplankton  density  (number  of  units/L)  and  biomass  (milligram/m3)  in 
agricultural  streams  (2006)   55 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  vi 
in  Alberta 


ACKNOWLEDGEMENTS 


Water  for  Life,  Aquatic  Ecosystem  Health  working  group  provided  funding  to  process 
sediment  and  biological  samples. 

Epilithic  chlorophyll-*?  and  sediment  chemistry  samples  were  analyzed  at  the  Analytical 
Chemistry  Laboratory  of  the  Alberta  Research  Council  in  Vegreville  under  supervision  of 
Frank  Skinner.  Dr.  Michael  Agbeti  (Bio-Limno  Research  &  Consulting  Inc.)  Halifax, 
Nova  Scotia  identified  and  enumerated  epilithic  algae.  William  J.  Anderson,  Spruce 
Grove,  Alberta  sorted,  identified  and  enumerated  benthic  invertebrates. 

Mary  Raven  finalized  figures  and  tables  and  formatted  the  report. 

T.  Hebben  and  R.  Zurawell  (Alberta  Environment)  provided  valuable  comments  on  the 
algal  monitoring  and  L.R.  Noton  (Alberta  Environment)  reviewed  the  report. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  vii 
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1.0  BACKGROUND 


Monitoring,  evaluation  and  reporting  on  aquatic  ecosystem  health  are  required  to  assure 
the  Government  of  Alberta  Water  for  Life  (WFL)  commitment  of  "healthy  aquatic 
ecosystems.  "  Healthy  aquatic  ecosystems  (HAE)  can  be  defined  as  functioning  and 
diverse  systems  of  biological  communities  (primary  producers,  invertebrates  and 
vertebrates)  interacting  with  an  adequate  chemical  (water  and  sediment  quality)  and 
physical  environment  (hydrology,  channel  processes,  riparian  zones)  (e.g.,  Whitford 
2005). 

In  Alberta,  provincial-scale  monitoring  of  aquatic  ecosystem  health  (AEH)  has  focused 
primarily  on  surface  water  quality  of  rivers  and  lakes.  Expansion  of  provincial  networks 
and  programs  to  include  sediment  quality  and  non-fish  biota  (e.g.,  benthic  invertebrates, 
and  other  aquatic  biota)  of  rivers,  streams,  lakes  and  wetlands  is  required  to  support  WFL 
goals.  The  development  of  such  monitoring  programs  requires  selection  of  practical  and 
efficacious  sampling  methods,  sample  processing  and  data  management  procedures,  and 
appropriate  indicators  of  aquatic  ecosystem  health. 

Monitoring,  evaluating  and  reporting  on  the  diverse  range  of  aquatic  ecosystems  and 
human  influences  on  a  provincial  scale  represent  a  complex  and  costly  undertaking.  To 
maximize  efficiencies  and  control  costs,  North  South  Consulting  Inc.  et  al  (2007) 
recommend  building  on  existing  monitoring  networks,  which  already  provide  information 
on  some  AEH  components. 

The  Alberta  Environmentally  Sustainable  Agriculture  (AESA)  stream  water  quality 
sampling  program  has  involved  monitoring  of  23  streams  and  was  designed  to  document 
the  effects  of  agriculture  on  stream  water  quality  over  time.  The  AESA  network 
comprised  streams  selected  based  on  similarities  in  soils  and  landscapes  attributes  of  their 
watersheds  and  the  range  of  agricultural  intensities  and  practices  in  these  watersheds 
(Anderson  et  al.  1999).  The  AESA  program  focused  on  surface  water  quality  indicators 
known  to  be  influenced  by  agricultural  intensity  (e.g.,  nutrients,  pesticides,  bacteria)  (e.g., 
Anderson  et  al.1998),  but  did  not  include  other  measures  of  AEH. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  1 
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2.0  OBJECTIVES 


The  intent  of  this  small  pilot  project  was  to  scope  the  feasibility  of  adding  sediment  and 
non-fish  biota  to  AESA  stream  monitoring  and  to  make  a  preliminary  evaluation  of  the 
data. 

Specific  objectives  were  to: 

•  Test  the  suitability  and  practicality  of  monitoring  techniques  at  a  few  sites; 

•  Provide  some  preliminary  information  for  sediment  chemistry  and  biological 
communities; 

•  Produce  recommendations  for  future  AEH  monitoring  of  agricultural  streams. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams 
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2 


3.0  METHODS 


3.1         Sampling  Sites 

The  pilot  study,  which  took  place  in  August  -  September  2006,  focussed  on  three 
agricultural  streams:  Strawberry  Creek  and  the  Blindman  River  in  the  Boreal  Transition 
ecoregion  and  Rose  Creek  in  the  Western  Alberta  Upland.  The  original  classification  of 
agricultural  intensity  relied  on  1991  Statistics  Canada  census  data  (Anderson  et  al.  1998) 
data  pertaining  to  chemical  and  fertilizer  expenses  and  manure  production  and  the 
drainage  basins  spanned  the  range  of  agricultural  intensity:  'low"  (Rose  Creek), 
"moderate"  (Blindman  River)  and  "high"  (Strawberry)  (Table  1,  Figure  1).  Census  data 
from  1996,  2001  and  2006  indicate  that  agricultural  intensity  in  the  Blindman  River 
drainage  basin  has  fluctuated  between  "medium"  and  "high",  while  that  in  Strawberry 
Creek  has  fluctuated  between  "high"  and  "medium"  (Lorenz  et  al.,  2008(  draft). 
Blindman  retains  a  "medium"  rating,  but  Strawberry  Creek  is  now  also  rated  as 
"medium".  Nutrient  levels,  particularly  dissolved  nutrients,  for  the  period  of  record 
(Table  1)  are  generally  lowest  in  Rose  and  highest  in  Strawberry  Creek,  a  situation  which 
has  been  documented  in  every  year  of  monitoring  (e.g.,  Anderson  et  al.  1998,  Anderson 
1997,  1998,  Carle  2001,  Depoe  and  Westbrook  2003,  Depoe,  2004,  Depoe  2006  a,b, 
Lorenz  et  al.,  2008(  draft). 

Sampling  of  sediments  and  biological  community  took  place  near  the  Water  Survey  of 
Canada  gauging  station  which  has  also  been  the  marker  for  the  water  quality  sampling 
sites. 


Table  1        Summary  of  background  information  on  the  three  AESA  streams 
selected  for  the  pilot  study 


ROSE  CREEK 


BLINDMAN  RIVER      STRAWBERRY  CREEK 


Drainage  basin  size  (km2) 

559 

353 

592 

Ecoregion 

Western  Alberta  Upland 

Boreal  Transition 

Boreal  Transition 

Major  watershed 

North  Saskatchewan  River 

Red  Deer  River 

North  Saskatchewan  River 

Agricultural  Intensity 

Anderson  et  al.  (1999)  based  on  1991  census 

Low 

Medium 

High 

Lorenz  and  Depoe(2009). ('average'  of  1996,  2001,2006  census) 

Low 

Medium 

Medium 

Mean  daily  discharge  2006  (cms) 


1.372 


0.559 


0.326 


Nutrient  Concentrations  (mg/L  )  (Lorenz  et  al.  draft) 

Nutrient  data  from  1995  to  2006 

Minimum-Median-Maximum 

Minimum-Median-Maximum 

Minimum-Median-Maximum 

TP 

0.062  0.234  0.955 

0.136  0.297  0.536 

0.189   0.692  1.249 

TDP 

0.018  0.030  0.058 

0.058  0.152  0.338 

0.047   0.0127  0.319 

TN 

0.900   1.332  2.551 

1.305   1.973  3.495 

1.186  3.296  4.628 

TKN 

0.862   1.276  2.453 

1.079   1.702  2.857 

0.894   2.516  3.203 

(N02"+N03")-N 

0.011   0.016  0.036 

0.032   0.130  0.271 

0.136   0.367  0.859 

(NH4+)-N 

0.023  0.054  0.084 

0.061    0.227  0.560 

0.075  0.387  0.756 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  3 
in  Alberta 


AESA  Stream  Survey 
Watershed  Locations 

Watershed 
City  # 

L.  Hines  Creek 

2.  Grande  Prairie  Creek 

3.  Klesknn  Drain 

4.  Paddle  River 

5.  Wabash  Creek 

6.  Tomahawk  Creek 

7.  Strawberry  Creek 

8.  Buffalo  Creek 

9.  Stretton  Creek 

10.  Blindman  River 

1 1 .  Rose  Creek 

12.  Ha\  nes  Creek 

13.  Three  hills  Creek 

14.  Ray  Creek 

15.  Renwick  Creek 

16.  Crowfoot  Creek 

17.  New  West  Coulee 

18.  Drain  S-6 

19.  Battersea  Drain 

20.  Prairie  Blood  Coulee 

21.  Trout  Creek 

22.  Meadow  Creek 

23.  Willow  Creek 


Watershed  Type 

Irrigation  Stream 
Low  Agricultural  Intensity 
Moderate  Agricultural  Intensity  f£> 
High  Agricultural  Intensity  ^ 


>23 
Grande  Prairie 


Edmonton 


11 


©10 

J2 


Calgary 


16 


23 

.21 


J7 


•19  «18 


22  • 

20 


Lethhridge 


Figure  1       Agricultural  watersheds  monitored  under  the  Alberta 

Environmentally  Sustainable  Agriculture  (AESA)  program 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams 
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4 


3.2         Sampling  Methods 


3. 2. 1  Field  Measurements 

Field  measurements  and  observations,  based  on  Barbour  et  al.  1999,  Jones  et  al.  2004, 
and  Stambaugh  et  al.  2006  protocols  were  carried  out  at  each  site.  The  sampling  reach 
was  defined  as  6  times  bank  full  width,  and  three  transects  were  established:  Transect 
(Tl)  at  the  lower  (downstream)  end  of  the  reach,  T2  in  the  middle  and  T3  at  the  upper 
(upstream)  end.  Wetted  width,  bank  full  width,  depth,  mean  flow  velocity  were 
measured  along  each  transect;  instantaneous  discharge  was  estimated  from  these 
measurements.  Multi-probe  readings  of  DO,  percent  DO  saturation,  conductivity,  pH  and 
temperature  were  recorded  along  five  points  on  Tl .  Water  samples  were  collected  from 
that  reach.  Reach  characteristics  such  as  stream  nature  (i.e.,  riffle,  run,  pool  or  pool/back 
eddy),  %  macrophyte  coverage  and  dominant  taxa,  substrate  composition  (e.g.,  %  cobble, 
gravel,  sand  based  on  visual  estimates)  and  substrate  embeddedness  were  recorded  for 
each  transect.  Bank  characteristics  such  as  bank  stability,  degree  of  undercutting, 
dominant  riparian  vegetation  and  terrestrial  canopy  cover  were  recorded  for  a  1 0  m  strip 
centered  on  each  transect.  A  summary  of  field  observations  recorded  during  the  pilot  is 
provided  in  Appendix  1 . 

3.2.2  Benthic  Invertebrates 

D-frame  kick  nets  were  used  to  collect  invertebrates.  One-minute  kick  samples  were 
collected  at  each  of  the  three  transects  for  the  study  reach.  Sampling  was  carried  out  by 
kicking  the  substrate,  and  moving  in  an  upstream  direction  across  the  channel  while 
sweeping  the  net  over  the  disturbed  substrate.  If  the  net  appeared  to  clog,  sampling  was 
interrupted;  the  net  emptied  and  sampling  resumed  for  the  remainder  of  the  time.  The 
three  one-minute  transect  samples  were  combined  to  form  one  composite  sample  per 
study  reach.  Although  most  of  Alberta  Environment's  (AENV)  benthic  invertebrate 
monitoring  of  large  rivers  has  relied  on  nets  of  210  u.m  mesh  size,  rapid  assessment 
procedures  which  are  popular  in  some  Canadian  and  US  monitoring  programs  of  smaller 
streams  (e.g.,  Jones  et  al.  2004)  use  much  coarser  mesh  sizes.  To  evaluate  the  relative 
merits  of  invertebrate  data  obtained  with  different  mesh  sizes,  two  sets  of  nets  (210  urn 
and  400  u.m  mesh  size)  were  used  at  each  site. 

Samples  were  transferred  to  plastic  bags  and  preserved  with  buffered  formaldehyde 
shortly  after  collection.  Three  replicate  samples  were  collected  with  each  net  at  the 
Blindman  River  site  to  describe  variability.  Each  replicate  consisted  of  three  one-minute 
kicks  collected  along  each  transect  and  pooled  to  form  a  composite  sample. 

3.2.3  Epilithic  Algae 

Epilithic  algae  for  chlorophyll-a  determination  were  scraped  from  rocks  using  the 
template  method  (Alberta  Environment  2006).  Scrapings  from  a  4  cm2  template  were 
taken  from  each  of  three  rocks  taken  to  form  a  replicate  sample.  A  replicate  sample  was 
generated  along  each  transect,  yielding  three  replicates  per  reach.  Algal  material  was 
placed  on  a  GF/C  filter,  sprinkled  with  MgC03,  and  then  wrapped  in  aluminum  foil,  kept 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  5 
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on  ice  until  return  to  the  field  office  and  then  frozen.  Triplicate  samples  (two  additional 
replicates  per  transect)  were  taken  at  the  Blindman  River  site  for  QA/QC  purposes. 

Epilithic  algae  for  taxonomic  analysis  were  also  obtained  using  the  template  method,  but 
in  this  case  scrapings  (4  cm  /scraping)  from  nine  rocks  (three  per  transect)  were 
combined  to  form  one  composite  sample.  The  sample  was  preserved  with  Lugol's 
solution  and  five  drops  of  formaldehyde.  Additional  samples  (three  replicates,  collected 
as  described)  were  obtained  from  the  Blindman  River  to  describe  variability  in  taxonomic 
data. 

3.2.4  Phytoplankton 

Water  was  collected  from  five  cross  channel  points  along  the  lower  (Tl)  transect  and 
pooled  in  a  carboy.  The  sample  was  well  mixed  and  poured  off  into  1L  dark  Nalgene 
containers  for  Ch\-a  analysis  and  100  mL  phytoplankton  jars.  Ch\-a  samples  were 
filtered  on  GF/C  filters  in  the  laboratory;  MgC03  was  sprinkled  on  the  filter  before 
freezing. 

Phytoplankton  samples  for  taxonomic  analysis  were  preserved  in  the  field  with  Lugol's 
solution  and  a  few  drops  of  formaldehyde.  Two  additional  samples  were  poured  off  from 
cross  sectional  composite  samples  collected  sequentially  (over  a  period  of  approximately 
half  an  hour)  at  the  Blindman  River  site  to  assess  variability  over  time. 

3.2.5  Sediment 

One  composite  sediment  sample  per  site  was  collected  from  depositional  areas  along  the 
three  transects,  using  the  'spoon  method'  as  described  in  Alberta  Environment  (2006). 
These  composite  samples,  destined  for  particle  size  and  nutrient  analyses,  were  stored  in 
plastic  bags  and  kept  cool  until  delivery  to  the  analytical  laboratory. 

3.3         Sample  Processing  Methods 

3. 3.1       Ben  thic  In  vertebra  te  Samples 

The  zoobenthic  samples  were  washed  over  a  2,  and  a  0.210  mm  sieve.  The  coarse 
fraction  was  sorted  in  its  entirety;  the  material  washed  onto  the  fine  sieve  was  sub- 
sampled  using  a  Marchant  Box  (Marchant  1989).  A  minimum  of  500  organisms  were 
sorted,  or  at  least  three  of  the  100  cells  in  the  Marchant  Box  were  processed.  This  was 
needed  to  obtain  a  minimum  level  of  precision  deemed  necessary  for  the  (sub)sampling 
invertebrates  (see  Elliott  1977,  Wrona  et  al.  1982).  All  invertebrates  were  sorted  under  a 
dissecting  microscope  (magnification  range  6  to  50X). 

Specimens  were  identified  to  genus  or  species  where  possible,  according  to  Edmunds  et 
al  (1976),  Wiggins  (1977),  Merritt  and  Cummins  (1996),  Clifford  (1991),  Thorp  and 
Covich  (2001),  and  others  using  the  most  current  taxonomic  designations  available  (See 
Taxonomic  References) 

Benthic  Invertebrate  taxonomic  analyses  are  presented  in  Appendix  2. 

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3.3.2       Epilithic  and  Plankton  Algal  Taxonomy,  and  Chlorophyll-a 
Analyses 

Chlorophyll-^  was  determined  fluorometrically  after  acetone  extraction  at  the  Analytical 
Chemistry  Laboratory,  Alberta  Research  Council,  Vegreville.  Phaeophytin-a,  a 
degradation  product  of  chlorophyll  was  measured  in  epilithic  samples.  Results  are 
reported  as  mg/m2  for  epilithic  samples  and  mg/m3  for  plankton  samples. 

Non-diatoms  (soft  algae)  and  diatoms  were  analyzed  separately.  Depending  on  their 
concentration,  non-diatoms  samples  were  diluted  first.  To  determine  the  appropriate 
dilution,  the  original  samples  were  screened  to  assess  the  densities  of  algae  and  non-algal 
matter  (debris  and  particulate  matter).  Aliquots  of  the  appropriately  diluted  samples  were 
allowed  to  settle  overnight  in  sedimentation  chambers  following  Utermohrs  procedure 
described  in  Lund  et  al.  (1958).  Algal  units  were  counted  from  a  minimum  of  four 
transects  on  a  Zeiss  Axiovert  40  CFL  inverted  microscope.  Counting  units  were 
individual  cells,  filaments,  or  colonies  depending  on  the  organization  of  the  algae.  Both 
diatoms  and  non-diatoms  were  counted.  For  soft  algae,  between  250  and  300  units  were 
counted  at  500X  magnification;  a  number  transects  were  scanned  at  250X  for  larger 
algae.  For  diatoms,  a  minimum  of  250  was  set  as  the  target.  At  this  stage,  diatoms  were 
not  identified  to  species  or  genus,  but  recorded  as  "diatoms",  and  were  later  identified  to 
species  from  prepared  slides. 

Preparation  of  diatom  slides  consisted  of  digesting  sub-samples  using  concentrated  nitric 
acid  and  hydrogen  peroxide  and  washing  several  times  (by  centrifuging)  with  distilled 
water.  A  few  drops  of  the  diatom  slurry  were  placed  on  a  cover  slip  and  allowed  to 
evaporate  overnight.  Once  dry,  the  diatoms  were  mounted  in  Naphrax  and  identified 
using  1000  to  1500  X  magnifications  (under  oil  immersion)  on  a  Zeiss  Axioskop  40 
compound  microscope.  A  minimum  of  500  diatom  frustules  were  counted  on  each  slide. 
The  diatom  counts  on  the  slides  were  converted  to  density  based  on  the  number  of 
transects  covered  during  the  fresh  (Utermohl)  counts. 

Biomass  was  calculated  from  recorded  abundance  and  specific  biovolume  estimates, 
based  on  geometric  shapes  (Rott  1981),  assuming  a  specific  gravity  of  one.  The 
biovolume  (mm3/m3  fresh  weight)  of  each  species  was  estimated  from  the  average 
dimensions  of  10  to  15  individuals.  The  biovolumes  of  colonial  taxa  were  based  on  the 
number  of  individuals  in  a  colony.  All  calculations  for  cell  concentration  (units/cm  )  and 
biomass  (|ug/cm  )  were  performed  with  Hamilton's  (1990)  computer  program. 

Taxonomic  identifications  of  soft  algae  were  based  primarily  on  Anton  and  Duthie 
(1981),  Entwisle  et  al.  (2007),  Findlay  and  Kling  (1976),  Huber-Pestalozzi  (1961,  1972, 
1982,  1983),  Tikkanen  (1986),  Prescott  (1982),  Whitford  and  Schumacher  (1984), 
Starmach  (1985),  Komarek  &  Anagnostidis  (1998,  2005),  and  Wehr  and  Sheath  (2003). 
Diatom  identifications  were  based  primarily  on  the  following  texts  and  supplemented 
with  other  publications:  Krammer  and  Lange-Bertalot  (1986,  1988,  1991a,b),  Reavie  and 
Smol  (1998),  Cumming  et  al.  (1995),  Bahls  (2004),  Camburn  and  Charles  (2000),  Fallu 
et  al.  (2000),  Patrick  and  Reimer  (1966,  1975),  Siver  and  Kling  (1997),  and  Siver  et  al 
(2005). 


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Results  of  epilithic  and  plankton  algal  community  data  are  shown  in  Appendix  3  and  4, 
respectively. 

3.3.3       Sediment  Chemistry 

Particle  size,  organic  carbon,  total  nitrogen  (as  TKN)  and  total  phosphorus  were  analyzed 
in  sediments  collected  at  each  site.  Method  descriptions  are  outlined  below. 

Total  Phosphorus:  the  sediment  sample  is  digested  with  sulfuric  acid,  potassium  sulphate 
and  a  mercury  catalyst  at  360°C.  All  phosphorus  species  are  converted  to  phosphate 
which  is  determined  colorimetrically  in  an  automated  system  by  the  molybdate-antimony 
tartrate-ascorbic  acid  method. 

Total  Kjeldahl  Nitrogen:  sediment  sample  is  digested  with  sulfuric  acid,  potassium 
sulphate  and  a  mercury  catalyst  at  360°C.  Organic  nitrogen  is  converted  to  ammonia, 
which  is  determined  colorimetrically  in  an  automated  system  by  the  phenate  method. 

Organic  Carbon  in  sediments  is  determined  by  the  difference  between  total  carbon  and 
inorganic  carbon.  Total  carbon  in  sediments  is  obtained  by  placing  a  known  amount  of 
sample  in  a  crucible  and  combusting  the  sample  at  950°C.  The  carbon  dioxide  formed  is 
measured  in  an  infrared  cell.  Inorganic  carbon  in  sediment  samples  is  obtained  by 
acidifying  a  known  amount  of  sample  with  excess  sulphuric  acid.  The  evolved  CO2  is 
trapped  in  sodium  hydroxide.  The  partial  alkalinity  of  samples  is  compared  to  CaC03 
standards  to  determine  total  carbonate  and  inorganic  carbon. 

Particle  size  distribution  in  sediments  is  measured  using  the  hydrometer  method  and  is 
based  on  M.R.  Carter  (1993)  as  described  in  Soils  Sampling  and  methods  of  Analysis, 
507:509.  Lewis  Publishers. 

3.4         Data  Analysis 

This  small  dataset  did  not  lend  itself  to  statistical  analyses  (e.g.,  comparison  among  sites). 
Therefore,  evaluation  of  results  relied  primarily  on  visual  appraisal  of  graphs  and  tables. 
Simple  metrics  were  calculated;  these  included  taxonomic  diversity  (i.e.,  number  of 
major  taxonomic  groups,  genera,  or  individual  taxa)  and  absolute  and  proportional 
(percent)  abundance  and  biomass  (algae,  only)  at  various  taxonomic  levels.  An  extensive 
exploration  of  merits  of  a  broad  range  of  'metrics'  was  not  justified  here  because  of  the 
limited  data  set. 

However,  the  applicability  of  recent  work  by  Potapova  and  Charles  (2007),  involving  the 
development  of  a  nutrient  preference  index  for  diatoms,  was  tested  with  the  diatom  data 
from  this  pilot  study.  The  authors  compiled  an  indicator  species  list  by  defining  the 
nutrient  preference  range  for  riverine  diatom  species  in  the  United  States  based  on 
species  distribution  and  nutrient  data.  Data  used  in  this  process  are  those  from  the  U.S. 
Geological  Survey  National  Water  Quality  Assessment  program.  Species  which  had  the 
highest  mean  relative  abundance  and  frequency  of  occurrence  at  TP<10  uL"1  were 
designated  as  'low  TP  or  LP',  those  with  TP  >100  uL1  as  'high  TP  or  HP',  those  with 

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TN<  0.2  mgL"1  were  designated  as  Mow  TN  or  LN\  those  with  TP  >3  mgL"1  as  'high  TN 
or  HN'.  A  high  index  value  indicates  that  species  which  thrive  under  high  nutrient 
conditions  prevail,  and  vice  versa. 

Indices  for  total  phosphorus  (P-preference  index)  and  total  nitrogen  (N-preference  index) 
indicators  were  calculated  as: 

P-Preference  index  =  1QHP 

HP+LP 

N-  Preference  index  =  1QHN 

HN+LN 

The  indices  for  our  stream  data  were  calculated  using  species  abundance  data.  In 
addition,  absolute  and  relative  abundance  of  species  with  high,  low,  and  unclassified 
nutrient  preferences  were  graphed.  'Unclassified'  species  were  those  which  did  not 
appear  or  did  not  receive  a  rating  in  Potapova  and  Charles  (2007). 


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4.0    RESULTS  AND  DISCUSSION 


4.1  General  Site  Description 

As  mentioned  earlier  (Table  1),  the  three  watersheds  are  located  in  different  ecoregions 
and  they  drain  lands  that  are  farmed  with  different  intensity.  In  part  as  a  result  of  these 
different  features,  there  were  some  important  site-specific  differences  which  would  be 
expected  to  influence  biological  communities. 

The  Rose  Creek  site  had  mostly  erosional  substrate  (cobble,  gravel)  with  small 
depositional  patches  (sand  and  fines);  at  the  time  of  sampling  there  was  measurable  flow 
(Appendix  1).  The  Blindman  River  held  both  types  of  habitat,  although  depositional 
substrate  was  dominant  at  the  sampling  site.  There  was  some  flow  at  the  site,  but  it  was 
not  measurable.  The  Strawberry  Creek  site  was  dominated  by  depositional  substrates  and 
there  was  no  flow  at  the  time  of  sampling. 

At  the  time  of  sampling  water  was  well  oxygenated,  alkaline,  and  conductivity  ranged 
from  316  jj.S.cm"1  in  Rose  Creek  to  611  jiS.cm"1  in  Strawberry  Creek.  Macrophytes  were 
present  at  all  sites,  but  they  were  abundant  (25-50%  coverage)  at  only  one  transect  on 
Strawberry  Creek.  Bank  stability  was  considerably  affected  by  uncontrolled  access  of 
cattle  to  the  Blindman  River.  Livestock  trails  were  visible,  but  to  a  much  lesser  extent  at 
the  Rose  Creek  site.  Strawberry  Creek  had  unstable  banks,  including  some  steep  banks 
with  no  vegetation  and  erodable  soils;  there  was  no  evidence  of  cattle  activity  at  this  site. 

Riparian  cover  at  Rose  Creek  was  comprised  of  sedges,  shrubs,  deciduous  and  coniferous 
trees,  and  a  relatively  small  amount  of  bare  soil.  At  the  Blindman  River  site  grasses, 
sedges  and  shrubs  dominated  along  with  bare  soil  especially  where  cattle  accessed  the 
stream.  Strawberry  Creek  had  a  mix  of  grass,  sedges  and  shrubs  with  some  deciduous 
trees.  Terrestrial  canopy  cover  over  the  wetted  area  was  low  at  all  sites.  A  beaver  dam 
was  present  about  1 00  m  upstream  of  the  upper  transect  on  the  Blindman  River,  and 
about  1  km  downstream  of  the  lower  transect  on  Strawberry  Creek.  No  beaver  dams 
were  observed  in  the  immediate  vicinity  of  the  Rose  Creek  site. 

4.2  Practical  Considerations  about  the  Pilot  Sampling 

Following  are  general  observations  regarding  time  commitment,  training  requirement, 
and  suitability/practicality  of  sampling  techniques. 

It  took  each  of  three  staff  approximately  6,  7  and  9  hours  to  perform  field  data  and 
sample  collections  at  Rose  Cr.,  Strawberry  Cr.,  and  the  Blindman  River,  respectively. 
Time  estimates  for  this  pilot  study  are  probably  in  excess  of  what  would  be  required  if 
sampling  was  part  of  routine  monitoring.  Note  that  the  Blindman  River,  which  took  the 
greatest  amount  of  time,  involved  much  additional  sampling  (triplicate  sampling  of 
benthic  invertebrates  and  algae). 

Field  measurements  such  as  GPS  readings,  hydrometric  measurements,  and  multi-probe 
readings  require  familiarity  with  equipment  and  procedures,  but  was  otherwise  easy  to 

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standardize.  The  documentation  of  the  various  reach  and  bank  characteristics  was 
somewhat  more  difficult  to  standardize  because  it  involves  visual  observations  and 
qualitative  measures. 

Collection  of  benthic  invertebrates  with  kick  nets  was  the  most  practical  approach 
considering  the  wide  range  of  variability  in  depth,  substrate  type  and  flow  conditions 
expected  in  streams  across  Alberta.  Both  kick  nets  (210  and  400  |Jm  mesh  size) 
performed  well  in  Rose  Creek  which  had  coarse  substrates.  Clogging  of  the  nets  with 
fines  was  an  issue  in  the  Blindman  River  and  Strawberry  Creek  which  are  more 
depositional  in  nature.  Kick  nets  only  allow  qualitative  sampling  (i.e.,  not  quantitative). 
Fixed-time  sampling  (3  minutes  per  sample  in  this  pilot  study)  is  one  way  of 
standardizing  the  samples.  However,  additional  factors  need  to  be  standardized  among 
sites,  samplers,  and  over  time  to  achieve  reasonably  consistent  sampling.  These  include 
the  intensity  of  kicking,  the  velocity  with  which  the  net  is  swept  back  and  forth,  and  the 
sampler's  travel  speed.  Staff  training  and  reliance  on  experienced  staff  are  critical  in  the 
collection  of  samples  that  can  be  compared  over  time  and  among  sites. 

Suitable  rocks  for  epilithic  algae  sampling  were  eventually  found  at  all  3  stream  sites. 
However,  the  time  involved  in  finding  rocks  was  greatest  at  the  Strawberry  Creek  site 
which  was  more  depositional  in  nature  than  the  two  other  sites.  Alternative  sampling 
approaches  are  needed  to  sample  sandy  or  muddy  sites  devoid  of  rocks.  The  use  of  a 
small  (2.5  cm  diameter)  core  is  currently  being  tested  to  sample  such  fine-grained 
substrates. 

Sampling  of  water  quality,  including  phytoplankton  and  sediments  was  straightforward  at 
all  sites. 

If  sampling  of  AEH  indicators  in  small  streams  were  to  become  part  of  a  regular 
program,  staff  training  and  consistent  involvement  of  experienced  staff  would  be  critical 
in  achieving  consistency  in  site  assessments  and  acquisition  of  standardized  samples. 
Based  on  the  experience  of  this  pilot  study  it  is  estimated  that  sampling  of  water, 
sediments,  benthic  invertebrates  (one  kick  net),  epilithic  algae  and  conducting  the  field 
measurements  would  require  a  minimum  of  2  to  3  hours  from  a  well-trained  crew  of 
three. 

4.3         Sediment  Analyses 

Sediment  analyses  are  summarized  in  Table  2.  Particle  size  distribution  illustrates  some 
of  the  habitat  differences  described  earlier.  Sediment  collected  from  Rose  Creek  was 
mostly  sandy,  whereas  sediment  from  the  other  two  sites  also  contained  a  substantial 
amount  of  silt  and  clay.  Organic  carbon  was  low  at  all  sites. 


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Table  2        Sediment  particle  size  and  nutrient  levels 


Rose  Creek 

Blindman  River 

Strawberry  Creek 

Sand  % 

98 

66 

73 

Silt  % 

<1 

17 

13 

Clay  % 

2 

17 

15 

Organic  Carbon  % 

<0.8 

<0.8 

0.8 

Inorganic  Carbon  % 

0.4 

1.8 

1.6 

Total  Carbon  % 

0.6 

2.3 

2.4 

Sediment  TKN  mg/kg 

259 

1860 

939 

Sediment  TP  mg/kg 

504 

842 

541 

Consistent  with  the  substrate  type  and  level  of  agricultural  intensity,  Rose  Creek  had  the 
lowest  levels  of  total  phosphorus  and  nitrogen.  Blindman  River  sediments  had  the 
highest  levels  of  nutrients,  along  with  the  highest  percentage  of  silt  and  clay. 

4.4         Benthic  Invertebrates 

Comparison  of  sites 

Benthic  invertebrates  were  abundant  and  diverse  in  the  three  streams  (Appendix  2).  In 
total,  128  taxa  belonging  to  a  wide  variety  of  invertebrate  taxonomic  groups  were 
recorded  (e.g.,  Turbellaria,  Nematoda,  Oligochaeta,  Hirudinea,  Cladocera,  Copepoda, 
Ostracoda,  Amphipoda,  Ephemeroptera,  Plecoptera,  Trichoptera,  Diptera,  Hemiptera, 
Coleoptera,  Odonata,  Mollusca,  and  Acari).  Based  on  collections  with  both  nets,  the 
number  of  invertebrates  was  lower  in  Rose  Creek  than  in  Strawberry  Creek  and  the 
Blindman  River,  in  particular.  However,  taxonomic  diversity  was  greater  in  Rose  Creek 
and  the  Blindman  River  than  in  Strawberry  Creek  (Figure  2  a,  b,  and  e);  this  trend  is 
likely  related  to  differences  in  substrate  sampled  in  the  three  streams  (Appendix  1). 

The  invertebrates  collected  with  the  210  um  net  at  the  Rose  Creek  site  were  dominated 
numerically  by  Chironomidae,  Trichoptera,  Ephemeroptera  and  Oligochaeta;  other 
groups  such  as  Plecoptera  and  small  crustaceans  (Cladocera,  Copepoda,  Ostracoda)  were 
also  well  represented  (Figure  2  d  and  e).  Ephemeroptera,  Plecoptera,  and  Trichoptera, 
often  referred  to  as  "EPT"  are,  for  the  most  part,  typical  inhabitants  of  erosional 
substrates,  and  relatively  good  water  quality,  and  they  were  most  abundant  and  diverse  in 
Rose  Creek  (Figure  2  c).  Another  typical  inhabitant  of  hard  bottom  erosional  substrates 
only  encountered  in  Rose  Creek  was  the  mollusc  Ferrissia  rivularis  (Appendix  2). 
Despite  the  dominance  of  erosional  species,  some  typical  inhabitants  of  depositional 
substrates  included  the  burrowing  mayfly  Ephemera  and  small  numbers  of  Ilyocryptus 
sordidus,  a  benthic  cladoceran  with  special  adaptations  (haemoglobin)  to  low  dissolved 
oxygen  levels  (Appendix  2). 

The  fauna  from  the  Blindman  River  and  Strawberry  Creek  site  was  dominated  by  small 
crustaceans,  Oligochaeta,  and  Chironomidae.  Although  some  of  the  crustaceans  are 
planktonic  (e.g.,  Daphnia,  Chydorus,  cyclopoid  copepods),  the  typically  benthic 
Ilyocryptus  sordidus  was  abundant  at  these  sites.  Amphipoda  {Hyallella  azteca  and 

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Gammarus  lacustris)  were  fairly  abundant  in  the  Blindman  River,  but  they  occurred  in 
low  numbers  in  Strawberry  Creek.  Ephemeroptera  and  Trichoptera  were  present  at  the 
Blindman  River  and  Strawberry  Creek  sites  although  they  were  less  diverse  and  abundant 
than  in  Rose  Creek.  Leptophlebiidae  were  the  only  Trichoptera  found  at  the  Strawberry 
Creek  site.  No  Plecoptera  were  found  in  the  Blindman  River  or  Strawberry  Creek. 

The  fauna  from  Rose  Creek  was  indicative  of  a  well  oxygenated,  erosional  habitat  with 
moderate  nutrient  levels;  whereas  the  fauna  from  the  Blindman  River  site  suggested  a 
mixed  habitat,  potentially  with  areas  of  low  dissolved  oxygen  and  generally  with  higher 
nutrient  levels.  Substrate,  flow  and  dissolved  oxygen  conditions  appeared  to  be  even 
more  restrictive  in  Strawberry  Creek. 

Although  the  variability  in  the  number  of  benthic  invertebrates  in  the  Blindman  River 
replicates  was  large,  particularly  in  the  210  |um  mesh  kick  samples,  the  total  number  of 
taxonomic  groups  per  sample  and  the  relative  contribution  of  major  taxonomic  groups  to 
total  numbers  were  less  variable  (Figure  2).  This  is  relevant  as  it  suggests  that  the 
manner  in  which  kick  samples  were  collected  provided  a  repeatable  indication  of  the 
invertebrate  community  composition. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  13 
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a.  Total  Numbers 


250000 
200000 
150000 


S  100000 


50000 
0 


♦  210  ym 
m  400  [im 


1  2  3 

1=Rose,  2=Blindman,  3=Strawberry 


c.%EPT 


♦  210|jm 
■  400  urn 


1  2  3 

1=Rose,  2=Blindman,  3=Straw berry 


b.  Total  Number  of  Taxa 


80 
70 
60 
50 
40 
30 
20 
10 
0 


♦  210  urn 
■  400  urn 


1  2  3 

1=Rose,  2=Blindman,  3=Strawberry 


Note  three  replicate  samples  collected  in  the  Blindman  River 


80 

70 

60 

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x 

«j 

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6 

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10 


d.  No.  Taxa  Per  Major  Taxonomic  Group  (210  urn) 


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□  Amphipoda 

□  Diptera 

□  Chironomidae 

■  Plecoptera 

□  Trichptera 

□  Ephemera  ptera 

■  Oligochaeta 

□  Small  crustaceans 


f.  No.  Taxa  Per  Major  Taxonomic  Group  (400  urn) 


□  Others 

■  Mollusca 

■  Coleoptera 

□  Amphipoda 

■  Diptera 

□  Chironomidae 

■  Plecoptera 

□  Trichptera 

□  Ephemera  ptera 

■  Oligochaeta 

□  Small  crustaceans 


e.  Percent  Contribution  of  Major  Taxonomic 
Groups  to  Total  Numbers  (210  urn  kick  samples) 


□  Others 

■  M  ollusca 

■  Coleoptera 

□  Amphipoda 

■  Diptera 

□  Chironomidae 

■  Plecoptera 

□  Trichptera 

□  Ephemera  ptera 

■  Oligochaeta 

□  Small  crustaceans 


100% 
80% 

c 
o 

1  60% 

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|  40% 
O 

20% 


g.  Percent  Contribution  of  Major  Taxonomic 
Groups  to  Total  Numbers  (400  urn  kick  samples) 


0% 


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■  Diptera 

□  Chironomidae 

■  Plecoptera 

□  Trichptera 

□  Ephemera  ptera 

■  Oligochaeta 

□  Small  crustaceans 


Figure  2      Benthic  invertebrate  data  for  three  agricultural  streams 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  14 
in  Alberta 


Comparison  of  samples  collected  with  the  210  and  400  um  kick  samples 
Differences  among  sites  were  consistent  in  samples  collected  with  the  210  or  400  um 
kick  net.  However,  as  could  be  expected,  total  counts  in  the  2 1 0  um  nets  were 
consistently  higher,  or  much  higher,  than  in  the  corresponding  400  um.  The  difference  in 
taxonomic  diversity  between  nets  was  not  as  pronounced,  but  samples  collected  with  the 
finer  net  had  2  to  6  additional  species,  compared  to  those  collected  with  the  coarse  net 
(Figure  2  a  and  b,  Appendix  2). 

Overall  abundance  and  taxonomic  diversity  were  lower  in  400  um  kick  samples,  but  not 
all  taxonomic  groups  were  affected  in  the  same  way  (Appendix  2): 

•  Many  of  the  small  crustaceans  are  small  enough  that  they  could  pass  through  the 
400  um  mesh.  As  a  result  their  number  and  diversity  were  considerably  lower  in 
the  coarse  kick  net  samples.  With  the  exception  of  Simnocephalus,  a  rather  large 
cladoceran,  small  crustaceans  would  have  been  missed  altogether  at  the  Rose 
Creek  site  with  the  400  urn  mesh  kick  sampler. 

•  Interestingly,  some  molluscs  (e.g.,  Valvatidae,  Pisidium  and  Sphaeridae),  were 
more  numerous  in  the  400  than  210  |um  kick  samples. 

•  Furthermore,  some  invertebrates  were  encountered  only  in  the  400  um  kick 
samples.  These  include  the  caddis  flies  Argaylea  (Blindman),  and  Mystacides  and 
Amphicosmoecus  (Rose  Creek)  and  the  stoneflies  Pteronarcys  and  Perlodidae 
(Rose  Creek). 

The  differences  in  results  between  the  two  nets  are  likely  due  to  the  greater  filtering 
capacity  of  the  coarse  net.  The  fine  net  clogs  up  faster  and  once  this  happens  organisms 
can  escape  actively,  or  they  can  easily  be  washed  away  with  water  that  does  not  pass 
through  the  net  anymore. 

Considering  that  general  faunal  differences  among  sites  remained  consistent  regardless  of 
the  net  used  (i.e.,  interpretation  of  the  data  would  have  been  similar),  there  are  some 
advantages  in  using  the  coarse  net.  These  include  dealing  with  samples  that  have 
somewhat  fewer,  but  larger  organisms  and  the  fact  that  the  response  to  environmental 
disturbance  of  many  larger  organisms  is  often  better  understood  that  that  of  small 
crustaceans. 

In  a  comparison  of  Bow  River  benthic  invertebrate  samples  collected  with  Neill  cylinder 
and  the  same  two  kick  nets  as  in  this  study,  Saffran  and  Anderson  (2009)  also  noted  the 
similarity  in  general  longitudinal  patterns  obtained  regardless  of  sampler,  or  mesh  size 
used.  However,  because  there  is  a  historical  invertebrate  database  that  relied  on  Neill 
samples,  and  also  because  of  advantages  offered  by  routinely  replicated  Neill  cylinder 
samples  in  statistical  significance  testing,  recommendations  were  made  to  continue  using 
Neill  samplers  in  large  provincial  rivers. 

There  is  no  historical  database  for  benthic  invertebrates  in  agricultural  streams  and, 
hence,  considering  their  apparent  advantages,  the  use  of  400um  kick  nets,  could  be 
recommended  in  future  sampling  of  small  streams.  Substrate  can  vary  considerably  in 
agricultural  streams  and  kick  nets  could  be  used  in  erosional  or  depositional  type 
substrates  where  Ekman  grabs  and  Neill  cylinders,  respectively,  would  not  be  suitable. 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  15 
in  Alberta 


4.5         Epilithic  Algae 


Epilithic  algae  formed  diverse  species  associations  at  the  three  sites.  Diatoms 
(Bacillariophyceae)  were  the  most  diverse  group  with  a  total  record  of  85  different  taxa 
belonging  to  25  genera.  Chlorophytes  (Chlorophyceae)  with  27  different  taxa  (12  genera) 
were  the  second  most  diverse,  followed  by  Cyanobacteria  with  15  different  taxa  (11 
genera).  Xanthophyceae  and  Dinophyceae  were  minor  groups  in  terms  of  taxonomic 
diversity  (one  taxon  each),  abundance  and  biomass  (Figure  3,  Appendix  3). 

Cell  counts  and  biomass  were  greatest  in  Strawberry  Creek  (Figure  4  a,  b)  and  taxonomic 
diversity  was  lowest  in  Rose  Creek  (Figure  4  c).  Diatoms  and  Cyanobacteria  contributed 
most  to  cell  counts  and  biomass,  but  the  chlorophytes  Spirogyra  sp.  and  Cladophora  sp. 
were  important  biomass  contributors  in  one  of  the  replicates  taken  at  the  Blindman  River 
site  and  at  the  Strawberry  Creek  site,  respectively  (Figure  3  a,  b,  d,  Appendix  3). 
Dominant  diatoms  in  terms  of  biomass  contribution  were  Cocconeis  pediculus, 
Cocconeis  placentula  (Rose  Creek),  Cocconeis  placentuala  (Blindman  River), 
Mastogloia  smithii  and  Rhopalodia  gibba  (Strawberry  Creek).  Gloeotrichia 
(Cyanobacteria)  and  Cladophora  sp.  and  Pediastrum  boryanum  (Chlorophyceae) 
dominated  the  biomass  at  Strawberry  Creek  (Appendix  3). 

Replicates  (each  consisting  of  scraping  from  3  rocks  taken  from  each  of  the  3  transects) 
taken  at  the  Blindman  River  site  show  that  there  are  differences  in  the  diversity,  cell 
counts  and  calculated  biomass  (Figure  3),  although  the  same  major  groups  account  for 
most  of  the  abundance  and  diversity  (Figure  4).  The  largest  differences  among  the  three 
replicates  occur  in  biomass  estimates  and  are  due  to  the  importance  of  one 
Chlorophyceae  taxon  {Spirogyra  sp.)  in  one  of  the  replicates  and  not  the  other  (Figure  3 
d,  Appendix  3).  These  differences  are  indicative  of  natural  spatial  heterogeneity,  and 
QA/QC  samples  need  to  be  incorporated  in  further  stream  sampling  to  verify  how 
representative  composite  samples  (3  rocks  from  each  of  3  transects)  are  of  the  sampled 
stream  reach. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams 
in  Alberta 


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Chlorophyll  levels  varied  substantially  among  the  three  replicate  samples  collected  at 
each  site  and  this  illustrates  the  variability  among  transects  (Figure  4d).  In  contrast  with 
biomass  estimates  based  on  cell  volumes  (Figure  4  b),  chlorophyll-^/  levels,  which  also 
are  an  indicator  of  biomass,  were  highest  at  the  Blindman  site  and  they  were  rather 
similar  between  Rose  and  Strawberry  creeks  (Figure  4  d).  Based  on  biomass  calculated 
from  cell  volumes,  Strawberry  Creek  had  the  highest  biomass,  but  not  based  on 
Chlorophyll-a.  The  difference  may  be  due  to  the  dominance  of  Gloeotrichia  at  the  site. 
Gloeotrichia  forms  mucilaginous  colonies  which  can  become  very  abundant  and  coat  the 
substrate  with  a  thick  mucilaginous  film.  The  chlorophyll-a  content,  however,  may  be 
rather  low  as  phycobilins,  rather  than  chlorophyll-a,  tend  to  be  the  dominant 
photosynthetic  pigment  in  cyanobacteria.  Hence,  taxonomic  information  is  an  insightful 
complement  to  chlorophyll-a  measurements  and  contributes  to  a  better  understanding  of 
biomass  patterns  in  epilithic  communities. 

The  relationship  between  diatom  distribution  and  water  quality  is  better  documented  than 
that  of  soft  bodied  algae  (Potapova  2005),  and  diatoms  are  widely  used  to  monitor  river 
conditions  in  the  United  States  and  Europe  (Potapova  and  Charles  2007,  Tison  et  al. 
2005). 

Nutrient  preference  classes  and  N  and  P  preference  indices  derived  by  Potapova  and 
Charles  (2007)  were  applied,  to  determine  if  diatom  metrics  could  be  used  to  differentiate 
among  agricultural  streams  (Figure  5).  This  is  one  way  in  which  relationships  between 
nutrient  levels  and  diatom  species  composition  can  be  established  in  agricultural  streams. 
Rose  Creek  had  a  lower  index  value  for  P  (Figure  5  a)  and  N  (Figure  5b)  than  the 
Blindman  River  and  Strawberry  Creek.  In  Strawberry  Creek,  and  especially  the 
Blindman  River,  species  with  high  nutrient  preference  were  considerably  more  abundant 
than  species  with  low  nutrient  preference  (Figure  5  c  to  d).  In  Rose  Creek,  numeric 
contributions  of  diatoms  with  high  and  low  nutrient  preferences  were  equivalent. 

Total  nutrient  concentrations  in  our  agricultural  streams  are  rather  high  compared  to  the 
threshold  ranges  defined  by  Potopova  and  Charles  (2007)  (Table  1).  For  TP  and  TN  the 
three  pilot  streams  would  all  fall  in  the  high  nutrient  range.  If  dissolved  nutrients  were 
considered,  Rose  Creek  would  fit  in  an  intermediate  range  for  TDP,  while  the  Blindman 
River  and  Strawberry  Creek  still  fit  in  the  'high'  range.  All  streams  would  fall  in  the 
intermediate  range  for  dissolved  nitrogen.  The  differences  among  sites  in  nutrient 
preferences  of  diatoms  are  consistent  with  the  differences  in  nutrient  levels  observed  in 
water  and  sediments.  This  suggests  that  diatoms  may  be  potential  indicators  of  the 
trophic  status  of  agricultural  streams. 

As  noted  by  Potapova  and  Charles  (2007),  metrics  derived  from  diatom-nutrient 
relationships  tend  to  be  more  useful  when  they  are  derived  from,  and  employed  in 
regional-scale  studies  rather  than  continental  or  intercontinental  studies.  As  more 
epilithic  algal  taxonomy  information  is  associated  with  water  quality  information,  it  will 
become  possible  to  refine  such  metrics  for  Alberta. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  19 
in  Alberta 


a.  Diatom  Index  Based  on  TP  Preference 


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Figure  5      Diatom  metrics  for  monitoring  eutrophication  in  agricultural 
streams  (after  Potapova  and  Charles,  2007) 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  20 
in  Alberta 


4.6  Phytoplankton 


A  total  of  50  individual  taxa,  comprising  35  different  genera  were  recorded  in 
phytoplankton  samples.  These  include  Cyanobacteria  (5  taxa,  5  genera),  Chlorophyceae 
(16  taxa,  12  genera),  Chrysophyceae  (5  taxa,  3  genera),  Cryptophyceae  (8  taxa,  3  genera), 
Euglenophyceae  (3  taxa,  3  genera),  Dinophyceae  (3  taxa,  1  genus),  and  Bacillariophyceae 
(Diatoms:  10  taxa,  9  genera)  (Appendix  4).  The  algal  classes  Chrysophyceae, 
Cryptophyceae  and  Euglenophyceae  which  occurred  in  plankton  were  not  found  in  the 
epilithic  algal  samples  (Appendix  3). 

The  three  replicates  collected  sequentially  at  the  lower  transect  in  the  Blindman  River 
showed  a  lot  of  variability  in  terms  of  cell  counts,  biomass,  taxonomic  diversity  (taxa  and 
genera)  and  specific  taxonomic  compositions  (Figures  6  and  7).  The  degree  of  variability 
observed  at  the  Blindman  site  encompassed  the  range  of  variability  observed  at  the  three 
sites.  On  average,  cell  counts,  biomass  and  diversity  were  slightly  higher  at  the 
Blindman  site,  but  chlorophyll-a  content  (single  sample)  was  noticeably  higher  (Figure 
6).  The  high  degree  of  variability  observed  in  phytoplankton  replicates  from  the 
Blindman  site  may  be  an  indication  of  heterogeneity  in  phytoplankton  communities  of 
small  streams.  If  this  is  the  case,  composite  samples  taken  along  the  sampling  reach 
would  likely  be  better  indicators  of  site  conditions  than  single  grab  samples. 

Cryptophytes  and  Euglenophytes  were  numerically  abundant  at  all  sites  (Figure  7). 
Chlorophytes  contributed  most  to  the  biomass  and  diversity  of  Rose  Creek,  and  they  were 
diverse  and  important  contributors  to  the  biomass  in  one  of  the  Blindman  replicates,  but 
not  the  others.  Chlorophytes  were  poorly  represented  at  the  Strawberry  Creek  site  where 
Cyanobacteria  were  more  abundant  and  diverse  and  contributed  more  to  the  biomass  than 
at  any  other  site.  Cyanobacteria  were  not  recorded  in  the  phytoplankton  from  Rose 
Creek.  Although  diatoms  were  present  at  all  sites,  their  abundance,  biomass  and  diversity 
was  rather  low,  especially  compared  to  their  importance  in  epilithic  algal  samples. 

Individual  species  which  were  important  biomass  contributors  at  Rose  Creek  were 
Mougeotia  (Chlorophyceae)  and  Cocconeis  (Bacillariophyceae).  Cryptomonas  marsonii 
and  Rhodomonas  minuta  (Cryptophyceae)  and  Euglena  minuta  were  important  at 
Strawberry  Creek.  At  the  Blindman  River  site,  Chlamidomonas  (Chlorophyceae), 
Cryptomonas  erosa,  Cryptomonas  reflexa  and  Rhodomonas  minuta  (Cryptophyceae)  and 
Euglena  minuta  (Euglenophyta)  contributed  substantially  to  the  biomass  of  each  of  the 
three  replicates.  Other  species  were  important  in  only  one  or  two  of  the  Blindman  River 
replicates  (e.g.,  Cocconeis,  Cryptomonas  erosa,  unidentified  Chrysophytes,  Pediastrum 
boryanum,  and  Microspord). 

The  diversity  of  diatoms  in  phytoplankton  samples  was  far  too  low  to  attempt  to  calculate 
Potapova  and  Charles'  nutrient  indices,  or  to  relate  diatom  nutrient  preferences  to  trophic 
status. 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  21 
in  Alberta 


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5.0    GENERAL  DISCUSSION 


5.1  Suitability  and  Practicality  of  Monitoring  Techniques 

The  pilot  study  has  illustrated  the  practicality  of  collecting  biological  communities  and 
sediments  from  small  Alberta  streams. 

•  Kick  net  samples  collected  with  a  400  urn  mesh  offer  some  advantages  over  those 
collected  with  the  210  um  and  would  be  recommended  for  further  sampling  of 
small  streams. 

•  Sediment  and  epilithic  algal  sampling  procedures  described  in  AENV  (2006)  were 
appropriate  for  agricultural  streams.  However,  rocks  suitable  for  epilithic  algal 
sampling  are  often  difficult  to  find  in  streams  where  depositional  habitats  prevail. 
The  use  of  alternate  sampling  methods  needs  to  be  investigated  further  (e.g., 
"mini  core"  sampler). 

•  A  critical  goal  of  future  sampling  should  be  to  ensure  that  samples  and  field 
information  are  collected  in  a  consistent  manner  by  experienced  staff  so  that  data 
are  comparable  over  time  and  among  sites.  Although  this  is  a  general  requirement 
of  any  sampling  program,  it  applies  particularly  to  AEH-related  sampling 
components  that  are  qualitative  or  semi-quantitative,  or  that  rely,  to  some  extent, 
on  value  judgement  (e.g.,  benthic  invertebrate  kick  samples,  field  observations  of 
bank  and  reach  characteristics).  Sampling  protocols  need  to  be  developed  and 
included  in  the  field  manual,  and  staff  training  ensured. 

5.2  Selection  of  Potential  Indicators  of  Health 

Benthic  invertebrate  and  algal  communities  were  diverse  and  abundant  and  offer  good 
potential  for  further  monitoring,  along  with  water  and  sediment  quality.  Involvement  of 
trained  field  staff  and  diverse  scientific  expertise  through  the  full  monitoring,  evaluation, 
and  reporting  process  is  important.  This  expertise  should  complement  and  build  on 
existing  information  when  appropriate.  Examples  of  existing  information  for  benthic 
invertebrate  and  algal  groups  include: 

•  Benthic  invertebrates  have  been  used  widely  to  document  the  ecological  "health" 
or  "integrity"  of  surface  waters  and  they  have  been  used  extensively  in 
biomonitoring  programs  (e.g.,  Klemm  et  al.  2003,  Wright  et  al.  1995,  Sylvestre  et 
al.  2005).  Ecological  requirements  and  responses  to  various  forms  of  disturbance, 
such  as  nutrient  enrichment  and  toxicity,  are  relatively  well  understood  (e.g., 
Hilsenhoff  1987,  1988,  Mandaville,  2002,  Carlisle  et  al.  2007).  Biological  criteria 
have  been  developed  for  many  states  in  the  U.S.  (e.g.,  Younos  2002).  There  is 
obvious  benefit  to  including  benthic  invertebrates  in  future  biological  monitoring 
of  small  streams.  The  composition  and  abundance  of  aquatic  communities,  such 
as  benthic  invertebrates,  integrate  changes  in  the  chemical  and  physical 
environment,  unlike  water  quality  samples  which  represent  conditions  at  the  time 
of  sampling. 

•  In  addition,  algal  growth  on  bottom  substrates  is  a  very  useful  measure  of  the 
influences  of  nutrient  enrichment  in  streams.  For  example,  diatoms  have  also 
been  widely  used  to  assess  various  stressors  on  water  quality  (e.g.,  NAWQA  data 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  24 
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set  used  in  Potapova  and  Charles  2005),  species  specific  responses  to  nutrient 
enrichment,  acidification,  and  discharge  alterations  have  been  documented  and 
many  indices  have  been  developed  to  summarize  responses  to  environmental 
changes  (e.g.,  Soininen  2004,Potapova  and  Charles  2005,  Tison  et  al  2005). 
Some  researchers  believe  that  diatoms  are  a  more  sensitive  indicator  to  nutrient 
enrichment  than  benthic  invertebrates  (Steinberg  and  Schiefele  1988).  The  wealth 
of  species-specific  ecological  information  and  the  numeric  and  taxonomic 
dominance  of  diatoms  in  our  epilithic  algal  samples,  flags  this  group,  in 
association  with  other  epilithic  algal  species,  as  a  potentially  powerful  biological 
indicator  of  eutrophication  in  small  streams.  This  along  with  the  relative  ease  to 
standardize  collection  and,  compared  to  benthic  invertebrates,  more  moderate 
sample  processing  cost  makes  epilithic  algal  communities  a  top  candidate  for 
further  monitoring  in  small  streams. 

•  In  contrast,  phytoplankton  communities  were  the  least  diverse  and  most  variable 
in  terms  of  abundance  and  diversity.  Diatoms  were  a  relatively  minor  element  of 
the  phytoplankton  associations,  which  were  dominated  by  so-called  "soft  algae". 
Although  soft  algae  are  routinely  monitored,  their  taxonomy  and  ecological 
requirements  are  not  as  well  known  (Potapova  2005).  The  phytoplankton  species 
composition  in  our  samples  could  be  influenced,  in  part,  by  the  time  of  year 
samples  were  collected  (e.g.,  diatoms  would  likely  be  more  abundant  and  diverse 
in  spring  e.g.,  Gamier  et  al.  1995).  Overall  phytoplankton  in  this  pilot  study 
appeared  to  yield  less  easily  interpretable  information  than  either  benthic 
invertebrates  or  epilithic  algae. 

Information  on  sediment  quality  is  needed  to  establish  baseline  conditions  and  further 
sampling  of  sediments  in  agricultural  streams  is  recommended.  There  is  a  need  to 
evaluate  variables  closely  associated  with  agricultural  activities,  such  as  pesticides, 
pharmaceuticals  and  feed  additives  used  in  the  livestock  industry.  In  some  cases,  the 
evaluation  of  sediment  quality  data  is  hampered  by  the  limited  number  of  effects 
guidelines  or  thresholds  to  assess  the  significance  of  contaminant  detections. 

5.3         Considerations  for  Future  AEH  Monitoring  of  Agricultural  Streams 

Currently,  one  of  the  difficulties  in  assessing  AEH  in  Alberta  lies  in  defining  the 
characteristics  of  'healthy'  aquatic  ecosystems.  Considerable  progress  has  been  made  in 
the  United  States  over  the  last  20  years  to  narrow  down  the  concepts  of  biological 
"health"  or  'integrity'.  Following  are  key  references  extracted  from  Davis  and  Simon 
(1995): 

•  Biological  integrity  is  defined  as  ". .  .the  ability  of  an  aquatic  ecosystem  to  support 
and  maintain  a  balanced,  adaptive  community  of  organisms  having  a  species 
composition,  diversity,  and  functional  organization  comparable  to  natural  habitats 
of  a  region"  (Karr  and  Dudley  1981). 

•  It  is  recognized  that  entirely  natural  or  unimpaired  habitats  may  no  longer  exist, 
but  an  estimate  of  expected  biological  integrity  in  surface  waters  can  be  based 
upon  "least  impacted  conditions"  or  "reference  conditions". 

•  Least  impacted  reference  conditions  form  the  basis  for  developing  biological 
goals,  or  biological  criteria. 


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The  regional  scale  that  is  used  to  define  biological  criteria  may  vary  among  water  body 
types,  but  ecoregions  have  been  favoured  for  small  to  medium-sized  streams  by  many 
researchers  and  agencies  (e.g.  Omernik  1995,  Stoddard  2005,  Tison  2005).  Various 
stream  types  may  exist  within  an  ecoregion  and  in  order  to  maximise  the  relevance  of 
reference  conditions,  it  is  useful  to  classify  streams  based  on  natural  hydrological  features 
(e.g.,  stream  order,  drainage  basin  size,  discharge  patterns,  contributing  areas),  and  man- 
made  features,  in  this  case  mostly  related  to  non  point  sources  (e.g.,  land  use  in  watershed 
and  along  riparian  areas,  road  crossings). 

According  to  Hughes  (1995),  the  number  of  reference  sites  needed  to  characterize 
reference  conditions  is  a  function  of  regional  variability  and  size,  the  desired  level  of 
detectable  change,  resources  and  study  objectives.  Hughes  proposed  that  20  randomly 
selected  sites  from  candidate  reference  sites  in  a  given  region  provide  a  reasonable 
estimate  of  reference  conditions.  These  selected  sites  could  be  subdivided  in  groups  that 
account  for  different  stream  types. 

The  next  and  essential  step  is  to  acquire  sufficient  biological  information  from  reference 
sites  and  match  it  with  relevant  chemical  and  physical  characteristics  of  streams  and 
watersheds.  Such  dataset  would  form  the  basis  for  developing  biological  criteria. 
Biocriteria  may  differ  in  nature,  and,  or  numerical  value  depending  on  the  ecoregion  and 
type  of  stream  (e.g.,  biocriteria  based  on  Ephemeroptera,  Plecoptera  and  Trichoptera  may 
be  relevant  in  Foothill  stream,  but  not  grassland  streams  where  diversity  and  abundance 
of  these  groups  is  low). 

Following  are  some  key  implications  for  the  development  of  an  AEH  monitoring 
program  on  agricultural  streams  in  Alberta. 

•  The  AESA  stream  network  offers  a  reasonable  foundation  in  the  sense  that  the  23 
streams  were  selected  from  major  ecoregions  where  agriculture  is  an  important 
land  use;  streams  were  ranked  according  to  agricultural  intensity  in  their  basins. 
There  is  a  historical  water  quality  database  spanning  a  period  of  8  to  13  years, 
depending  on  the  stream.  Surface  water  quality  sampling  was  interrupted  for  all 
but  8  streams  in  2008  and  water  quality  sampling  would  need  to  resume. 

•  In  order  to  define  background  conditions  it  would  be  necessary  to  expand  the 
network.  Considering  that  most  of  the  network  encompasses  4  ecoregions  this 
could  imply  that  a  minimum  of  80  (20  times  4)  streams  would  need  to  be  selected 
and  monitored  to  establish  reference  conditions.  In  some  instances  it  may  be 
possible  to  select  streams  that  are  'minimally'  impacted,  but  in  others,  such  as 
grassland  streams  in  central  Alberta,  or  irrigation  canals,  the  goal  may  be  simply 
to  define  current  baseline  conditions.  Establishing  background  conditions  can 
require  several  years.  Rosenberg  et  al.  (1999)  sampled  219  sites  over  a  three  year 
period  to  establish  reference  conditions  for  benthic  invertebrate  monitoring  in  the 
Fraser  River  catchment  in  British  Columbia. 

•  Frequency  and  intensity  of  monitoring  would  be  high  initially  (e.g.,  many  streams 
over  a  period  of  2  to  3  years).  Later  on  monitoring  could  be  reduced  to  a  selection 
of  representative  streams  (e.g.,  the  established  AESA  network,  every  5  years). 
Periodic  validation  of  a  selection  of  reference  sites  would  be  useful  to  account  for 
temporal  variability. 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  26 
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•  Timing  of  sampling  would  be  particularly  critical  in  ephemeral  streams  of 
grassland  and  Parkland  regions  where  late  spring  may  be  the  only  time  with 
flowing  water  and  established  biological  communities.  Sampling  in  Foothills  and 
Boreal  plain  streams  could  likely  be  postponed  to  early  summer. 

Although  the  financial  commitment  to  such  monitoring  program  is  large,  it  is  one  of  the 
realities  of  meaningful  monitoring  and  reporting  on  aquatic  ecosystem  health.  In  this 
case,  strong  baseline  information  would  be  established  and  biocriteria  could  be  developed 
to  report  periodically  on  aquatic  ecosystem  health  of  agricultural  streams. 

It  is  expected  that  the  value  of  biomonitoring  of  agricultural  streams  would  extend  well 
beyond  periodic  reporting  on  aquatic  ecosystem  health  of  these  streams. 

•  Establishing  reference  conditions  for  a  variety  of  streams  would  be  very  helpful  to 
assess  effects  of  other  land  uses  (e.g.,  forestry  or  urban  development). 

•  Another  major  application  of  biomonitoring  information  could  be  the  assessment 
of  the  effectiveness  of  beneficial  management  practices,  including  riparian 
conditions,  on  aquatic  ecosystem  health  (e.g.,  if  nutrient  control  measures  on  land 
are  effective  one  would  expect  to  see  corresponding  changes  in  epilithic  algal  and 
benthic  invertebrate  communities). 

•  As  nutrient  and  diatom  association  datasets  for  Alberta  streams  and  rivers  are 
expanded,  the  possibility  would  exist  to  validate  nutrient  tolerance  ranges  (e.g.,  as 
defined  by  Potapova  and  Charles  2007)  for  the  range  of  regional  conditions  in 
Alberta,  thereby  refining  the  value  of  diatoms  in  the  assessment  of  stream 
eutrophication  in  Alberta. 

•  Preference  ranges  for  other  species  groups  could  also  be  investigated  with 
associated  data  sets  (e.g.,  Carlisle  et  al.  2007  investigated  the  influence  of  water 
quality  on  benthic  invertebrate  distribution). 


Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  27 
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6.0    LITERATURE  CITED 


6.1         General  Literature 

Alberta  Environment.  2006.  Aquatic  Ecosystems  Field  Sampling  Protocols. 

Environmental  Monitoring  and  Evaluation  Branch,  Environmental  Assurance 
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Anderson,  A.-M.  1998.  Water  quality  Monitoring  program  1997.  Annual  Technical 

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Anderson,  A.-M.  2000.  Water  quality  Monitoring  program  1998.  Annual  Technical 

Report.  Water  quality  monitoring  of  agricultural  streams  and  lakes.  Prepared  for 
the  AESA  Water  Quality  Committee.  Published  by  Alberta  Agriculture,  Food  and 
Rural  Development,  Edmonton,  AB. 

Anderson,  A.-M.,  D.O.  Trew,  R.D.  Neilson,  N.D.  MacAlpine,  and  R.  Borg.  1998. 

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Anderson,  A.-M.,  S.E.  Cooke  and  N.MacAlpine  1999.  Watershed  selection  for  AESA 
stream  monitoring  program.  Alberta  Environmentally  Sustainable  Agriculture, 
Resource  Monitoring,  Water  Quality.  159  p. 

Barbour,  M.T.,  J.  Gerritsen,  B.D.  Snyder,  and  J.B.  Stribling.  1999.  Rapid  Bioassessment 
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Carle,  N.  2001.  Water  Quality  Monitoring  Program  2000.  Annual  Technical  Report: 

Water  Quality  Monitoring  of  Small  Streams  in  Agricultural  Areas.  Prepared  for 
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Rural  Development,  Edmonton,  AB. 

Carlisle,  D.M.,  M.R.  Meador,  S.R.  Moulton  II,  P.  M.  Ruhl.  2007.  Estimation  and 

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Davis,  W.D.  and  T.  P.  Simon.  Eds.  1995.  Biological  Assessment  and  Criteria  tools  for 
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Depoe,  S.  2006a.  Water  Quality  Monitoring  Program  2004.  Annual  Technical  Report: 
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Depoe,  S.  2006b.  Water  Quality  Monitoring  Program  2003.  Annual  Technical  Report: 
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Depoe,  S.  and  C.J.Westbrook,  2003.  Water  Quality  Monitoring  Program  2001.  Annual 
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modeling.  Limnol.  Oceanogr.  40(4)  750-765. 

Hilsenhoff,  W.L.  1987.  An  improved  biotic  index  of  organic  stream  pollution.  Great 
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Hilsenhoff,  W.L.  1988.  Rapid  field  assessment  of  organic  pollution  with  a  family-level 
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Jacques  Whitford.  2005.  Scope  of  work  for  the  initiatl  Assessment  of  aquatic  ecosystem 
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Jones,  C.  Somers,  K.M.  Craig,  B.  and  Reynoldson,  T.  2004.  Ontario  Benthos 

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Steinberg,  C.  and  S.  Schiefele.  1988.  Biological  indication  of  trophy  and  pollution  of 
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Stoddard,  J.L.  2005.  Use  of  ecological  regions  in  aquatic  assessments  of  ecological 
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Sylvestre,  S.  2004.  Invertebrate  Biomonitoring  Field  and  Laboratory  Manual  for  running 
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Sylvestre,  S.  M.  Fluegel  and  T.  Tuominen.  2005.  Benthic  invertebrate  assessment  of 

streams  in  the  Georgia  Basin  using  the  reference  condition  approach:  Expansion 
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Conservation  Branch.  Vancouver,  British  Columbia. 

Tison,  J.,  Y.-S.  Park,  M.  Coste,  J.G.  Wasson,  L.  Ector.  F.  Rimet  and  F.  Delmas.  2005. 

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on  the  French  hydrosystem  scale.  Water  Research  39:3 1 77-3 1 88. 

Wright,  LA.,  B.C.  Chessman,  P.G.  Fairweather  and  LJ.  Benson  L.J.  1995.  Measuring 
the  impact  of  sewage  effluent  on  the  macroinvertebrate  community  of  an  upland 
stream:  the  effect  of 


Wrona,  F.G.,  M.G.  Culp  and  R.W.  Davies.  1982.  Macroinvertebrate  subsampling:  A 
simplified  apparatus  and  approach.  Can.  J.  Fish.  Aquat.  Sci.  39:  1051-1054. 

Younos,  T.  (Ed.)  2002.  Advances  in  water  monitoring  research.  Lavoisier  Librairie.  230p 


6.2         Taxonomic  References:  Benthic  Invertebrates 

Alexander,  C.  P.  &  G.  W.  Byers.  1981.  Tipulidae.  Pp.  153-190.  IN:  Manual  of  Nearctic 
Diptera,  Vol  L  Research  Branch,  Agriculture  Canada.  Ottawa,  ON. 

Anonymous.  1997.  A  key  to  Cladocera  (Crustacea)  of  British  Columbia.  Resources 
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Anonymous.  2003.  Buglab  Key  to  Western  Baetidae  Nymphs. 

www.usu.edu/buglab/proiects/Western%20Baetidae%20Nymphs.pdf 


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Anonymous.  2003.  A  image-based  key  to  the  zooplankton  of  the  Northeast  (USA). 

Version  2.0.  Center  for  Freshwater  Biology,  Department  of  Zoology,  University 
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Anonymous.  2005.  The  Mayflies  of  North  America  (Mayfly  Central). 
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Bednarik,  A.  F.  &  W.  P.  McCafferty.  1979.  Biosystematic  revision  of  the  genus 

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Balcer,  M.  D.,  N.  L.  Korda  &  S.  I.  Dodson.  1984.  Zooplankton  of  the  Great  Lakes:  A 
guide  to  the  identification  and  ecology  of  the  common  crustacean  species. 
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Baumann,  R.W.,  A.R.  Gaufin,  and  R.F.  Surdick  1977.  The  stoneflies  (Plecoptera)  of  the 
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Brigham,  A.  R.,  W.  U.  Brigham  &  A.  Gnilka  (eds.).  1982.  Aquatic  insects  and 
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Brinkhurst,  R.  O.  1986.  Guide  to  the  freshwater  aquatic  microdile  oligochaetes  of  North 
America.  Department  of  Fisheries  and  Oceans:  Ottawa,  ON. 

Burian,  S.  K.  2001.  A  revision  of  the  genus  Leptophlebia  Westwood  in  North  America 
(Ephemeroptera:  Leptophlebiidae:  Leptophlebiinae).  Ohio  Biological  Survey 
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Cannings,  R.  A.  &  K.  M.  Stuart.  1977.  The  dragonflies  of  British  Columbia.  British 
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Clarke,  A.  H.  1981.  The  freshwater  mollusks  of  Canada.  National  Museum  of  Natural 
Sciences.  Ottawa,  ON. 

Clifford,  H.C.  1991.  Aquatic  Invertebrates  of  Alberta.  The  University  of  Alberta  Press. 
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Davies,  R.  W.  1971.  A  key  to  the  freshwater  Hirudinoidea  of  Canada.  J.  Fish.  Res.  Bd. 
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Dillon,  R.  T.,  Jr.  2006.  Key  to  freshwater  gastropods  of  the  Pacific  Northwest.  The 

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Dillon,  R.,  Jr.  no  date.  Freshwater  Mollusk  Conservation  Society  Committee  on  the 

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Edmunds,  G.  F.,  S.  L.  Jensen  &  L.  Brener.  1976.  The  mayflies  of  North  America. 
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Edmondson,  W.  T.  1959.  Fresh-water  biology  (2nd  ed.).  John  Wiley  &  Sons,  New  York, 
NY. 

Epler,  J.  H.  2001.  Identification  manual  for  the  larval  Chironomidae  (Diptera)  of  North 
and  South  Carolina.  A  guide  to  the  taxonomy  of  the  midges  of  the  southeastern 
United  States,  including  Florida.  Special  Publication  SJ2001-SP13.  North 
Carolina  Department  of  Environment  and  Natural  Resources,  Division  of  Water 
Quality,  Raleigh,  NC  and  St.  Johns  River  Water  Management  District.  Palatka, 
FL. 

Jacobus,  L.  &  R.  P.  Randolph.  2005.  Mayflies  in  Moscow:  Northwest  Ephemeroptera 
Nymphs.  Northwest  Biological  Assessment  Workshop.  University  of  Idaho. 
Moscow,  ID. 

Havel,  J.  &  R.  Rhodes  1998.  The  zooplankton  project.  Southwest  Missouri  State 
University,  http://science.smsu.edu/zooplankton/ 

Kathman,  R.  D.  &  R.  O.  Brinkhurst.  1999  (revised).  Guide  to  the  freshwater  oligochaetes 
of  North  America.  Aquatic  Resources  Center,  College  Grove,  TN. 

Klemm,  D.  J.  1985.  A  guide  to  the  freshwater  Annelida  (Polychaeta,  Naidid  and 
Tubificid  Oligochaeta,  and  Hirudinea  of  North  America).  Kendall/Hunt 
Publishing.  Dubuque,  IA. 

Korinek,  V.  1981.  Diaphanosoma  birgei  n.sp.  (Crustacea,  Cladocera).  A  new  species 
form  America  and  its  widely  distributed  subspecies  Diaphanosoma  birgei  ssp. 
Lacustris  n.ssp.  Can.  J.  Zool.  59:  1115-1121. 

Korinek,  V.  1987.  Revision  of  three  species  of  the  genus  Diaphanosoma  Fischer,  1850. 
Hydrobiologia  145:  35-45. 

Larson,  D.  J.;  Y.  Alarie  &  R.  E.  Roughly.  2000.  Predaceous  diving  beetles  (Coleoptera: 
Dytiscidae)  of  the  Neartic  region,  with  emphasis  on  the  fauna  of  Canada  and 
Alaska.  NRC  Press.  Ottawa,  ON. 

Lowen,  R.  G.  &  J.  F.  Flannagan.  1990.  The  nymph  and  male  of  Centroptilum  infrequens 
MCD  (Baetidae).  IN:  Mayflies  and  Stoneflies:  I.C.  Campbell  (ed.).  pp.  31 1-321. 
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Lowen,  R.  G.  &  J.  F.  Flannagan.  1991.  Four  Manitoba  species  of  Centroptilum  Eaton 
(Ephemeroptera:  Baetidae)  with  remarks  on  the  genus.  IN:  Overview  and 
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Lowen,  R.  G.  &  J.  F.  Flannagan.  1992.  Nymphs  and  imagoes  of  four  North  American 
species  of  Procloeon  Bengtsson  with  description  of  a  new  species 
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May,  M.L.  &  P.S.  Corbet.  2001.  Occurrence  and  taxonomic  significance  of  a  palpal 
spine  in  larvae  of  Enallagma  and  other  genera  (Odonata:  Coenagrionidae). 
International  J.  Odonatology  4(1):  41-49. 

Milligan,  M.  R.  1997.  Identification  manual  for  the  aquatic  oligochaeta  of  Florida. 
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McCafferty,  W.  P.  &  R.  D.  Waltz.  1990.  Revisionary  synopsis  of  the  Baetidae 

(Ephemeroptera)  of  North  and  Middle  America.  Trans.  Am.  Entomol.  Soc. 
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Merritt,  R.  W.  &  K.  W.  Cummins  (eds.)  1996.  An  introduction  to  the  aquatic  insects  of 
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Morihara,  D.  K.  &  W.  P.  McCafferty.  1979.  The  Baetis  larvae  of  North  America 
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Nimmo,  A.  P.  1965.  A  new  species  of  Psychoglypha  Ross  from  western  Canada,  with 
notes  on  several  other  species  of  Limnephilidae  (Trichoptera).  Can.  J.  Zool.  43: 
781-787. 

Pescador,  M.  L.  &  A.  K.  Rasmussen.  1995.  Identification  manual  for  the  caddisfly 

(Trichoptera)  of  Florida.  Department  of  Environmental  Protection,  Division  of 
Water  Facilities.  Tallahassee,  FL. 

Poirrier,  M.  A.  &  Y.  M.  Arceneaux.  1972.  Studies  on  southern  Sisyridae  (Spongilla- 
flies)  with  a  key  to  the  third-instar  larvae  and  additional  sponge-host  records. 
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Pupedis,  R.  J.  1980.  Generic  differences  among  new  world  Spongilla-fly  larvae  and  a 
description  of  the  female  of  Climacia  striata  (Neuroptera:  Sisyridae).  Psyche  87: 
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Ross,  H.  H.  1944.  The  caddisflies,  of  Trichoptera  of  Illinois.  Illinois  Natural  History 
Bulletin  23(1).  Urbana,  IL. 

Sawyer,  R.  T.  1972.  North  American  freshwater  leeches,  exclusive  of  the  Pisciolidae, 
with  a  key  to  all  species.  University  of  Illinois  Press.  Urbana,  IL. 

Smirnov,  N.  N.  1971.  Fauna  of  the  U.S.S.R.  crustacean,  Vol.  1(2):  Chydoridae.  Israel 
Program  for  Scientific  Translation.  Jerusalem,  Israel. 


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Smith,  D.  G.  2001.  Pennak's  freshwater  invertebrates  of  the  United  States  (4th  ed.).  New 
York:  John  Wiley  and  Sons,  Inc.  New  York,  NY. 

Stephenson,  J.  1972.  The  oligochaeta.  Wheldon  &  Wesley  Ltd.  New  York,  NY. 

Stewart,  K.  W.  &  B.  P.  Stark.  2002.  Nymphs  of  North  American  Stonefly  genera 
(Plecoptera)  (2nd  ed.).  The  Caddis  Press.  Columbus,  OH. 

Steyskal,  G.  C.  &  L.  V.  Knutson.  1981.  Empididae.  Pp.  607-624.  IN:  Manual  of 

Nearctic  Diptera,  Vol  1.  Research  Branch,  Agriculture  Canada.  Ottawa,  ON. 

Tennessen,  K.  2007.  Odonata  larvae  of  the  Pacific  Northwest  (An  identification 
Manual).  Watutoma,  WI. 

Teskey,  H.  J.  1981.  Key  to  the  Families— Larvae.  Pp.  125-147.  IN:  Manual  of  Nearctic 
Diptera,  Vol  1 .  Research  Branch,  Agriculture  Canada.  Ottawa,  ON. 

Thorp,  J.  H.  &  A.  P.  Covich.  2001.  Ecology  and  classification  of  North  American 
freshwater  invertebrates  (2n  ed.).  Academic  Press.  San  Diego,  CA. 

Usinger,  R.  L.  (ed.)  1956.  Aquatic  insects  of  California.  Berkeley:  University  of 
California  Press.  Berkeley,  CA. 

Waltz,  R.  D.  &  W.  P.  McCafferty.  1987.  New  genera  of  Baetidae  for  some  Nearctic 

species  previously  included  in  Baetis  Leach  (Ephemeroptera).  Ann.  Entomol.  Soc. 
Am.  80(5):  667-670. 

Wiersema,  N.  A.  1999.  Two  new  species  of  Procloeon  (Ephemeroptera:  Baetidae)  from 
Texas.  Ent.  News  110(1):  27-35. 

Wiederholm,  T.  (ed.).  1983.  Chironomidae  of  the  Holarctic  region:  Keys  and  diagnoses. 
Part  1:  Larvae.  Ent.  Scandinavica  Supplement  19. 

Wiggins,  G.  B.  1960.  A  preliminary  systematic  study  of  the  North  American  larvae  of 
the  caddisfly  family  Phryganeidae  (Trichoptera).  Can.  J.  Zool.  38:  1 153-1 170. 

Wiggins,  G.  B.  1996.  Larvae  of  the  North  American  Caddisfly  genera  (Trichoptera)  (2nd 
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Zimmerman,  J.  R.  1981.  A  revision  of  the  Colymbetes  of  North  America  (Dytisicidae). 
The  Coleopterists  Bui.  35(1):  1-52. 

6.3         Taxonomic  References:  Algae 

Anton,  A.  and  H.  C.  Duthie.  1981.  Use  of  cluster  analysis  in  the  systematics  of  the  algal 
genus  Cryptomonas.  Can  J.  Bot.  59:  992-1002. 


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Bahls,  L.  2004.  Northwest  Diatoms:  A  photographic  catalogue  of  species  in  the 

Montana  Diatom  Collection,  with  ecological  optima,  associates,  and  northern 
distribution  records  for  the  nine  northwestern  United  States. 

Camburn,  K.  and  D.  F.  Charles.  2000.  Diatoms  of  low-alkalinity  lakes  in  the 

northeastern  United  States.  The  Academy  of  Natural  Sciences  of  Philadelphia. 
152  pp. 

Cumming,  B.F.,  Wilson,  S.E.  and  J.P.  Smol.  1995.  Diatoms  from  British  Columbia 

(Canada)  lakes  and  their  relationship  to  salinity,  nutrients  and  other  limnological 
variables.  Bibliotheca  Diatomologica.  Band  3 1 .  J.  Cramer,  Berlin,  Stuttgart.  207 
pp. 

Entwisle,  T.  J.,  Skinner,  S.  Lewis,  S.  H.  and  H.J.  Foard.  2007.  Algae  of  Australia: 

Batrachospermales,  Thoreales,  Odeogoniales  and  Zygnemacae.  ABRS,  Caberra; 
CSIRO  Publishing,  Melbourne.  191  pp. 

Fallu,  M.-A,  N.  Allaire  and  R.  Pienitz.  2000  .  Freshwater  Diatoms  from  northern  Quebec 
and  Labrador  (Canada).  Bibliotheca  Diatomologica.  Band  45.  J.  Cramer,  Berlin, 
Stuttgart.  200  pp. 

Findlay,  D.  L.  and  H.  J.  Kling.  1976.  A  species  list  and  pictorial  reference  to  the 
phytoplankton  of  central  and  northern  Canada.  Fisheries  and  Environment 
Canada,  Fisheries  and  Marine  Service,  Manuscript  Report  No.  1503.  619  pp. 

Hamilton,  P.  1990  .  The  revised  edition  of  a  computerized  counter  for  plankton, 
periphyton  and  sediment  diatom  analysis.  Hydrobiologia.  194:  23-30. 

Huber-Pestalozzi,  G.  1961.  Das  phytoplankton  des  SiiPwassers.  Systematik  und 
Biologic  5  Teil,  Chlorophyceae  (Griinalgen),  Ordnung:  Volvocales  Die 
Binnengewaser  (Band  XVI).  -  E.  Schweizerbart'sche  Verlagsbuchhandlung 
(Nagele  u  Obermiller),  Stuttgart.  728  pp. 

Huber-Pestalozzi,  G.  1972.  Das  phytoplankton  des  SiiPwassers.  Systematik  und 

Biologic  6  Teil,  Chlorophyceae  (Griinalgen),  Ordnung:  Tetrasporales  von  B. 
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Huber-Pestalozzi,  G.  1982.  Das  phytoplankton  des  SiiPwassers.  Systematik  und 

Biologic  8  Teil,  1  Halfte.  Conjugatophyceae  Zygnematales  und  Desmidiales  von 
Kurt  Forster,  Pfronten/Allgau  Die  Binnengewaser  (Band  XVI).  -  E. 
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Huber-Pestalozzi,  G.  1983.  Das  phytoplankton  des  SiiPwassers.  Systematik  und 

Biologic  7  Teil,  1  Halfte.  Chlorophyceae  (Griinalgen),  Ordnung:  Chlorococcales 

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von  J.  Komarek  und  B.  Fott.  Die  Binnengewaser  (Band  XVI).  -  E. 
Schweizerbart'sche  Verlagsbuchhandlung  (Nagele  u  Obermiller),  Stuttgart.  1044 
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Juttner,  I.,  S.  Sharma,  B.M.  Dahal,  S.J.  Omerod,  P.J.  Chimonides  and  E.J.  Cox.  2003. 
Diatoms  as  indicators  of  stream  quality  in  the  Kathmandu  Valley  and  Middle 
Hills  of  Nepal  and  India.  Freshwater  Biol.  48:2065-2084. 

Komarek  J.  and  K.  Anagnostidis.  1998.  Cyanoprokaryota.  1.  Teil:  Chroococcales.  In: 
Ettl,  H.  et  al.  (eds.):  Suswasserflora  von  Mitteleuropa.  Begrundet  von  A.  Pascher. 
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Komarek  J.  and  K.  Anagnostidis.  2005.  Cyanoprokaryota.  2.  Teil:  Oscillatoriales. 

Suswasserflora  von  Mitteleuropa.  Founded  by  A.  Pascher.  Edited  by  Burkhard 
Biidel,  Lothar  Krientiz,  Georg  Gartner  and  Michael  Schagerl.  Volume  19/1 . 
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Krammer,  K.  and  H.  Lange-Bertalot.  1986.  Bacillariophyceae.  1.  Teil:  Naviculaceae.  In: 
Ettl,  H.  et  al.  (eds.):  Suswasserflora  von  Mitteleuropa.  Begrundet  von  A.  Pascher. 
Band  2/1.  Stuttgart- Jena.  876  pp. 

Krammer,  K.  and  H.  Lange-Bertalot.  1988.  Bacillariophyceae.  2  Teil:  Bacillariaceae, 
Epithemiaceae,  Surirellaceae.  In:  Ettl,  H.  et  al.  (eds.):  Suswasserflora  von 
Mitteleuropa.  Begrundet  von  A.  Pascher  Band  2/2.  Stuttgart- Jena.  596  pp. 

Krammer,  K.  and  H.  Lange-Bertalot.  1991a.  Bacillariophyceae.  3  Teil:  Centrales, 

Fragilariaceae,  Eunotiaceae.  Unter  Mitarbet  von  H.  Hakansson  &  M.  Norpel.  In: 
In:  Ettl,  H.  et  al.  (eds.):  Suswasserflora  von  Mitteleuropa.  Begrundet  von  A. 
Pascher  Band  2/3.  Stuttgart- Jena.  576  pp. 

Krammer,  K.  and  H.  Lange-Bertalot.  1991b.  Bacillariophyceae.  4  Teil:  Achnanthaceae 
Kritische  Erganzungen  zu  Navicula  (Lineolatae)  und  Gomphonema.  In:  Ettl,  H.  et 
al.  (eds.):  Suswasserflora  von  Mitteleuropa.  Band  2/4.  Stuttgart-Jena.  437  pp. 

Lund,  J.  W.  G.,  Kippling,  C.  and  E.  D.  le  Cren.  1958.  The  inverted  microscope  method 
of  estimating  algal  numbers  and  the  statistical  basis  for  the  estimation  by 
counting.  Hydrobiol.  11:144-170. 

Patrick,  R.  and  C.W.  Reimer.  1966.  The  Diatoms  of  the  United  States  Exclusive  of 
Alaska  and  Hawaii.  Vol.  1.  The  Academy  of  Natural  Sciences  of  Philadelphia. 
688  pp. 

Patrick,  R.  and  C.W.  Reimer.  1975.  The  Diatoms  of  the  United  States  Exclusive  of 
Alaska  and  Hawaii.  Vol.  2,  Part  1.  The  Academy  of  Natural  Sciences  of 
Philadelphia.  213  pp. 


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Prescott,  G.  W.  1982.  Algae  of  the  western  Great  Lakes.  Otto  Koeltz  Science 
Publishers.  977  pp. 

Reavie,  E.D.  and  J. P.  Smol.  1998.  Freshwater  diatoms  from  the  St.  Lawrence  River. 
Bibliotheca  Diatomologica.  Band  41.  J.  Cramer,  Berlin,  Stuttgart.  136  pp. 

Rott,  E.  1981.  Some  results  from  phytoplankton  counting  inter-calibrations.  Schweiz  Z. 
Hydrol.  24:  15-24. 

Siver,  P. A.  and  H.  Kling.  1997.  Morphological  observations  of  Aulacoseira  using 
scanning  microscopy.  Can.  J.  Bot.  75:1807-1835. 

Siver,  P.A.,  P.B.  Hamilton,  K.  Stachura-Suchoples  and  J.P.  Kociolek.  2005.  Diatoms  of 
North  America:  The  Freshwater  Flora  of  Cape  Cod,  Massachusetts,  USA. 
Iconographia  Diatomologica.  463  pp. 

Starmach,  K.  1985.  Chrysophyceae  und  Haptophyceae.  In:  Ettl,  H.  et  al.  (eds.): 
Siiswasserflora  von  Mitteleuropa.  Begriindet  von  A.  Pascher  Band  1 .  VEB 
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Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  38 
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Appendix  3  Epilithic  algal  community  composition  recorded  in  three 
agricultural  streams  in  2006 


Ollcdill  INdlllt;. 

Rose  Creek 

Blindman  R.  #1 

Blindman  R.  #2 

Blindman  R.  #3 

Strawberry  Creek 

Plato  QamnloH' 

30-Aug-06 

5-Sep-06 

5-Sep-06 

5-Sep-06 

31-Aug-06 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Bacilarriophyceae  (Diatoms) 

Achananthes  delicatula  (Kuetzing) 

Grunow 

0 

0 

9884 

3.203 

3503 

0.694 

4170 

1.52 

1786 

0.394 

Achnanthes  lanceolata  (Brebisson) 

Grunow 

5530 

0.553 

34596 

3.243 

17517 

1.752 

20854 

2.085 

7147 

0.715 

Achnanthes  minutissima  Kuetzing 

29496 

0.995 

98848 

5.931 

36202 

1.14 

46921 

2.628 

477070 

16.101 

Amphora  lybica  Ehrenberg 

0 

0 

0 

0 

2335 

0.2 

3128 

0.205 

0 

0 

Amphora  pediculus  (Kuetzing)  Grunow 

11061 

0.18 

29654 

0.483 

2335 

0.041 

8341 

0.116 

0 

0 

Amphipleura  pellucida  Kuetzing 

1843 

2.301 

9884 

8.224 

2335 

2.616 

0 

0 

17867 

18.861 

Caloneis  bacillum  (Grunow)  Cleve 

7374 

0.83 

9884 

0.68 

0 

0 

0 

0 

21441 

2.144 

Caloneis  sp 

0 

0 

0 

0 

0 

0 

0 

0 

1786 

0.335 

Cocconeis  pediculus  Ehrenberg 

36870 

117.883 

9884 

58.123 

9342 

54.935 

5213 

30.656 

0 

0 

Cocconeis  placentula  var  lineata 

(Ehrenberg)  Van  Heurck 

134575 

130.774 

242178 

102.926 

162328 

73.048 

120953 

51.405 

0 

0 

Craticula  halophila  (Grunow  et  Van  Heurck) 

D.  G.  Mann 

0 

0 

0 

0 

0 

0 

3128 

3.363 

0 

0 

Cyclotella  meneghiniana  Kuetzing 

0 

0 

9884 

15.9 

2335 

0.917 

8341 

5.661 

0 

0 

Cyclotella  ocellata  Pantocsek 

0 

0 

2471 

0.97 

0 

0 

0 

0 

0 

0 

Cymbella  microcephala  Grunow 

0 

0 

0 

0 

1167 

0.032 

0 

0 

121501 

3.313 

Cymbella  minuta  Hilse 

5530 

0.394 

0 

0 

0 

0 

0 

0 

8933 

0.468 

Cymbella  perpusilla  Cleve  Euler 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Cymbella  silesiaca  Bleisch  ex. 

Rabenhorst 

1843 

0.293 

0 

0 

0 

0 

0 

0 

1786 

0.299 

Cymbella  sinuata  Gregory 

0 

0 

0 

0 

5839 

0.214 

1042 

0.03 

0 

0 

Denticula  kuetzingii  Grunow 

0 

0 

0 

0 

0 

0 

0 

0 

35735 

8.041 

Denticula  subtilis  Grunow 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Diatoma  moniliformis  Kuetzing 

129045 

15.324 

0 

0 

0 

0 

0 

0 

0 

0 

Diatoma  tenuis  Agardh 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Diatoma  vulgaris  Bory 

0 

0 

0 

0 

0 

0 

0 

0 

7147 

12.865 

Didymosphaeria  geminata  (Lyngyb.)  M. 

Schmidt 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Diploneis  puella  (Schumann)  Cleve 

0 

0 

0 

0 

3503 

0.175 

2085 

0.13 

7147 

1.487 

Epithemia  adnata  (Kuetzing) 

Brebisson 

97705 

62.532 

7413 

7.414 

26860 

29.546 

6256 

6.256 

0 

0 

Epithemia  sorex  Kuetzing 

141949 

84.034 

39539 

31.632 

29195 

23.357 

18768 

15.015 

8933 

5.289 

Fragilaria  vaucheriae  (Kuetzing) 

Petersen 

14748 

1.062 

0 

0 

0 

0 

0 

0 

0 

0 

Gomphonema  acuminatum  Ehrenberg 

0 

0 

0 

0 

3503 

5.132 

0 

0 

1786 

4.544 

Gomphonema  augur  var  sphaeophorum 

(Ehrenberg)  Lange-Bertalot 

0 

0 

0 

0 

1167 

1.737 

0 

0 

0 

0 

Gomphonema  olivaceum  (Hornemann) 

Brebisson 

14748 

6.4 

32125 

29.046 

15181 

10.295 

9384 

5.154 

0 

0 

Gomphonema  parvulum  Kuetzing 

0 

0 

7413 

1.207 

4671 

0.95 

5213 

1.508 

0 

0 

Gomphonema  pumilum  (Grunow)  Reichardt 

&  Lange-Bertalot 

5530 

0.625 

0 

0 

2335 

0.264 

0 

0 

0 

0 

Gomphonema  sp 

0 

0 

4942 

0.559 

0 

0 

0 

0 

0 

0 

Hantzschia  amphioxys  (Ehrenberg) 

Grunow 

0 

0 

0 

0 

0 

0 

0 

0 

1786 

0.858 

Mastogloia  smithii  Thwaites  ex.  W.  Smith 

0 

0 

0 

0 

2335 

0.934 

0 

0 

112567 

92.868 

Melosira  varians  (Agardh) 

3687 

7.819 

0 

0 

0 

0 

0 

0 

0 

0 

Navicula  lanceolata  (Agardh)  Ehrenberg 

0 

0 

0 

0 

1167 

1.46 

0 

0 

0 

0 

Navicula  agrestis  Hustedt 

0 

0 

27183 

1.305 

1167 

0.065 

0 

0 

0 

0 

Navicula  bryophila  Petersen 

0 

0 

7413 

0.741 

0 

0 

0 

0 

0 

0 

Naviucula  capitatoradiata  Germain 

14748 

8.967 

2471 

1.463 

12846 

8.222 

3128 

2.407 

7147 

4.345 

Navicula  cincta  (Ehrenberg)  Ralfs 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Navicula  cryptocephala  Kuetzing 

3687 

2.124 

22240 

11.743 

29195 

10.729 

11469 

5.873 

1786 

0.7 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  52 
in  Alberta 


Appendix  3  Epilithic  algal  community  composition  recorded  in  three 
agricultural  streams  in  2006  (con't) 


Stream  Name: 

Rose  Creek 

Blindman  R.  #1 

Blindman  R.  #2 

Blindman  R.  #3 

Strawberry  Ck 

Date  Sampled: 

30-Aug-06 

5-Sep-06 

5-Sep-06 

5-Sep-06 

31-Aug-06 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Navicula  cryptotenella  (Lange-Bertalot) 

11061 

3.794 

24712 

3.089 

4671 

0.584 

12512 

2.477 

144729 

18091 

Navicula  capitata  Ehrenberg 

0 

0 

4942 

0.89 

0 

0 

0 

0 

0 

0 

Navicula  decussis  Oestrup 

5530 

2.212 

0 

0 

0 

0 

0 

0 

0 

0 

Navicula  gregaria  Donkin 

1843 

0.431 

7413 

1.668 

7006 

2.232 

3128 

0.958 

0 

0 

Navicula  margalithii  Lange-Bertalot 

14748 

18.435 

0 

0 

3503 

4.379 

0 

0 

0 

0 

Navicula  menisculus  Schumann 

1843 

0.361 

2471 

0.712 

0 

0 

1042 

0.255 

3573 

0.447 

Navicula  miniscula  Grunow 

1843 

0.115 

0 

0 

0 

0 

0 

0 

0 

0 

Navicula  notha  Wallace 

0 

0 

0 

0 

2335 

0.462 

0 

0 

0 

0 

Navicula  pseudanglica  Lange-Bertalot 

0 

0 

7413 

1.816 

3503 

1.277 

0 

0 

0 

0 

Navicula  pupula  Kuetzing 

0 

0 

2471 

0.909 

2335 

0.747 

1042 

0.367 

3573 

1.144 

Navicula  radiosa  Kuetzing 

1843 

3.595 

2471 

1.977 

0 

0 

1042 

1.825 

0 

0 

Navicula  schroeterii  Meister 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Navicula  sp 

0 

0 

4942 

0.712 

1167 

0.841 

0 

0 

3573 

2.001 

Navicula  subminiscula  Mangiun 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Navicula  subhamulata  Grunow 

0 

0 

4942 

0.463 

0 

0 

0 

0 

0 

0 

Navicula  veneta  Kuetzing 

3687 

0.461 

22240 

2.78 

7006 

0.963 

15640 

1.955 

8933 

1.117 

Navicula  viridula  (Kuetzing)  Ehrenberg 

0 

0 

4942 

19.928 

0 

0 

0 

0 

0 

0 

Nitzschia  acicularis  (Kuetzing)  W.  Smith 

0 

0 

0 

0 

2335 

0.654 

0 

0 

0 

0 

Nitzschia  calida  Grunow 

0 

0 

0 

0 

2335 

1.202 

0 

0 

0 

0 

Nitzschia  constricta  (Kuetzing)  Ralfs 

0 

0 

7413 

3.136 

14013 

5.928 

2085 

1.602 

0 

0 

Nitzschia  dissipata  (Hantzsch)  Grunow 

68209 

14.068 

29654 

7.414 

14013 

4.379 

9384 

2.346 

0 

0 

Nitzschia  fonticola  Grunow 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Nitzschia  frustulum  (Kuetzing)  Grunow 

3687 

0.461 

27183 

3.398 

12846 

1.445 

6256 

0.782 

58963 

7.37 

Nitzschia  gracilis  Hantzsch 

0 

0 

0 

0 

0 

0 

0 

0 

14294 

2.173 

Nitzschia  heufleriana  Grunow 

0 

0 

0 

0 

0 

0 

1042 

1.126 

0 

0 

Nitzschia  inconspicua  Grunow 

0 

0 

2471 

0.044 

0 

0 

0 

0 

0 

0 

Nitzschia  intermedia  Hantzsch 

0 

0 

4942 

8.896 

0 

0 

0 

0 

0 

0 

Navicula  levidensis  (W.  Smith)  Grunow 

0 

0 

7413 

15.43 

10510 

17.736 

2085 

0.547 

0 

0 

Nitzschia  linearis  (Agardh)  W.  Smith 

3687 

2.65 

0 

0 

0 

0 

2085 

5.339 

0 

0 

Nitzschia  palea  (Kuetzing)  W.  Smith 

0 

0 

44481 

9.452 

7006 

1.401 

4170 

0.667 

7147 

1.787 

Nitzschia  perminuta  Lange-Bertalot 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Nitzschia  paleacae  Grunow 

5530 

0.299 

69193 

6.366 

8174 

0.441 

17725 

1.702 

0 

0 

Nitzschia  recta  Hantzsch 

0 

0 

17298 

33.732 

5839 

3.285 

1042 

2.369 

0 

0 

Nitzschia  sinuata  vartabellaha  (Grunow) 

Grunow 

0 

0 

0 

0 

0 

0 

0 

0 

3573 

1.144 

Rhoicosphenia  abbreviata  (Agardh)  Lange- 

Bertalot 

0 

0 

17298 

2.815 

14013 

2.737 

10427 

1.867 

0 

0 

Rhopalodia  gibba  (Ehrenberg)  0.  Muller 

7374 

11.061 

0 

0 

3503 

6.131 

0 

0 

35735 

57.892 

Rhopalodia  musculus  (Ketzing)  0.  Muller 

0 

0 

0 

0 

0 

0 

0 

0 

3573 

0.643 

Stephanodiscus  minutulus  (Kuetzing)  Cleve 

&  Mueller 

0 

0 

12356 

2.484 

0 

0 

1042 

0.088 

0 

0 

Surirella  angusta  Kuetzing 

0 

0 

2471 

1.421 

3503 

4.557 

1042 

0.86 

0 

0 

Surirella  brebisonii  Krammer  &  Lange- 

Bertalot 

0 

0 

0 

0 

1167 

1.604 

0 

0 

0 

0 

Surirella  minuta  Brebisson 

0 

0 

0 

0 

1167 

0.338 

0 

0 

0 

0 

Synedra  ulna  (Nitzsch)  Ehr. 

1843 

3.54 

14827 

16.681 

3503 

3.09 

7298 

16.35 

1786 

3.431 

CYANOBACTERIA 

Anabaena  sp 

0 

0 

32125 

0.454 

61895 

2.074 

46921 

5.307 

0 

0 

Anabaenopsis  cunningtonii  R.  Taylor 

0 

0 

0 

0 

0 

0 

0 

0 

162597 

5.449 

Aphanocapsa  elachista  W.  &  G.S.  West 

0 

0 

0 

0 

0 

0 

0 

0 

142942 

2.021 

Chroococcus  limneticus  Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

7147 

0.808 

Gloeotrichia  sp 

175132 

46.216 

0 

0 

46713 

10.566 

62562 

14.151 

2287079 

517.325 

Leibleinia  sp 

0 

0 

284189 

3.571 

0 

0 

0 

0 

0 

0 

Merismopedia  elegans  A.  Braun 

0 

0 

0 

0 

0 

0 

0 

0 

50029 

1.677 

Mehsmopedia  glauca  (Ehrenberg) 

Naegeli 

0 

0 

158157 

28.404 

0 

0 

22939 

2.594 

0 

0 

Merismopedia  tenusissima  Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

25014 

0.105 

Oscillatoria  limnetica  Lemmerman 

9217 

0.116 

69193 

0.87 

0 

0 

0 

0 

35735 

0.449 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  53 
in  Alberta 


Appendix  3  Epilithic  algal  community  composition  recorded  in  three 
agricultural  streams  in  2006 


otlcdlll  Mdnlt; 

Rose  Creek 

Blindman  R.  #1 

Blindman  R.  #2 

Blindman  R.  #3 

Strawberry  Ck 

Date  Sampled: 

30-Aug-06 

5-Sep-06 

5-Sep-06 

5-Sep-06 

31-Aug-06 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Phormidium  sp1 

110610 

8.34 

331142 

24.968 

159992 

16.084 

1 32423 

13.313 

62537 

6.287 

Phormidium  sp2 

18435 

1 .853 

405278 

63.661 

64230 

14.529 

o 

0 

o 

o 

Planktolyngya  limnetica  Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

1786 

0.022 

Pseudanabaena  limnetica  Komarek 

0 

0 

0 

0 

0 

0 

0 

0 

o 

o 

Tolypothrix  sp 

36870 

14.826 

197697 

105.998 

23356 

7.191 

93843 

28.892 

955927 

216.226 

Ankistrodesmus  fasciculatus  (Lundb.)  Kom.- 

Legn. 

3687 

0.261 

0 

0 

0 

0 

0 

0 

0 

0 

Ankistrodesmus  gracilis  (Reinsch)  Kors. 

0 

0 

0 

0 

0 

0 

1042 

0.049 

0 

0 

Ankistrodesmus  spiralis  (Turner) 

Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

3573 

50.52 

Cladophora  sp 

0 

0 

0 

0 

4671 

15.849 

0 

0 

76831 

486.609 

Cosmarium  granatum  Brebisson 

0 

0 

0 

0 

0 

0 

0 

0 

3573 

28.98 

Cosmarium  meneghinii  Brebisson 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Cosmarium  sp 

0 

0 

0 

0 

0 

0 

0 

0 

5360 

24.699 

Elakatothrix  genevensis  (Reverdin) 

ninaaK 

3687 

0.139 

0 

0 

0 

0 

0 

0 

0 

0 

Monoraphidium  contortum  (Thuret) 

Komarkova-Legenerova 

0 

0 

0 

0 

2335 

0.077 

0 

0 

0 

0 

Monoraphidium  griff ithii  (Berkeley) 

Komarkova-Legenerova 

1843 

0.232 

0 

0 

0 

0 

0 

0 

21441 

0.909 

Monoraphidium  minutum  (Nag.) 

Komarkova-Legenerova 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Monoraphidium  pusillum  (Printz)  Kom- 

Legn. 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

iviougeoua  sp. 

0 

0 

0 

0 

0 

0 

0 

0 

17867 

37.82 

Oocystis  solitaria  Wittrock 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Pediastrum  boryanum  (Turpin)  Meneghini 

0 

0 

0 

0 

0 

0 

0 

0 

7147 

318.778 

Pediastrum  tetras  (Ehrenberg)  Ralfs 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Scenedesmus  acutiformis  Schroeder 

0 

0 

9884 

1.863 

28027 

4.403 

0 

0 

10720 

1.078 

Scenedesmus  acutus  Meyen 

0 

0 

19769 

1.987 

0 

0 

0 

0 

7147 

1.123 

Scenedesmus  bijuga  (Turp.)  Lagerheim 

0 

0 

0 

0 

9342 

1.223 

0 

0 

0 

0 

Scenedesmus  obliquus  (Turpin) 

Kuetzing 

0 

o 

0 

0 

0 

0 

o 

o 

0 

0 

Scenedesmus  opoliensis  P.  Richter 

o 

o 

0 

0 

0 

0 

8341 

1.118 

0 

0 

Scenedesmus  quadricauda  (Turpin) 

Brebisson 

0 

0 

0 

0 

0 

0 

4170 

1.957 

14294 

5.748 

Scenedesmus  sempervirens  Chodat 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Scenedesmus  sp 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Spirogyra  sp  Link 

0 

0 

0 

0 

4671 

126.795 

0 

0 

0 

0 

Stigeoclonium  sp 

0 

0 

0 

0 

0 

0 

0 

0 

0 

0 

Tatraedron  caudatum  (Corda)  Hansgirg 

0 

0 

0 

0 

0 

0 

0 

0 

1786 

0.936 

XANTHOPHYCEAE 

Characiopsis  sp 

0 

0 

0 

0 

2335 

0.235 

0 

0 

0 

0 

DINOPHYCEAE 

Gymnodinium  pusillum  (Penard) 

Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

1786 

8.981 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams 
in  Alberta 


54 


Appendix  4  Phytoplankton  density  (number  of  units/L)  and  biomass 
(milligram/m3)  in  agricultural  streams  (2006) 


Stream  Name: 
Date  Sampled: 

Rose  Creek 
30-Aug-06 

Blindman  R.  #1 
5-Sep-06 

Blindman  R.  #2 
6-Sep-06 

Blindman  R.  #3 
5-Sep-06 

Strawberry  Creek 
31-Aug-06 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density  Biomass 

CYANOBACTERIA 

Anabaenopsis  cunningtonii  R.  Taylor 

0 

0 

0 

0 

0 

0 

0 

0 

zodZd 

Cylindrospermum  sp 

0 

0 

0 

0 

0 

0 

12762 

3  248 

0 

0 

Merismopedia  tenusissima 
Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

12762 

2.165 

Oscillatoria  limnetica  Lemmerman 

0 

0 

12762 

2.245 

0 

0 

0 

0 

0 

0 

Snowella  lacustris  (Chodat)  Komarek  et 
Hindak 

0 

0 

0 

0 

0 

0 

0 

0 

12762 

25.661 

CHLOROPHYCEAE 

A n^ic^mWo cm/ /c  rimc'ili^  /Rt^inQph^ 
Aw  fniolf  UUtroi //L/o  yicJKslllo   \  r\cil  loL-i  l  / 

Kors. 

u 

u 

u 

O  1  uou 

1  DP.Q 

n 
u 

u 

0 

0 

Ankyra  judayi  (G.M.  Smith)  Fott 

0 

0 

12762 

0.301 

0 

0 

0 

0 

0 

0 

\^nianiyuufiiViiao  bp.  i 

12762 

1.069 

0 

0 

0 

0 

0 

0 

0 

0 

Chlamydomonas  sp.  2 

0 

0 

25525 

23.095 

76576 

69.285 

25525 

13.365 

0 

0 

Crucegenia  tetrapedia  (Kirchner)  W.  & 

O.O.  Vvobl 

0 

0 

12762 

1.711 

0 

0 

0 

0 

12762 

1.711 

(  »C#r»UC7iCl  *-✓/  Ut/OL/i  /t?i  i    IL.CI  l  II 1 1 .  ^  W.IVI. 

Smith 

1  97fi9 
I  Z  1  DZ 

u.ooo 

u 

u 

u 

u 

n 
u 

u 

0 

0 

IVIIlslUapUta  bp 

U 

u 

1  97R9 
I  c.  1  Oil 

u 

u 

u 

n 

0 

0 

IVIUI IUI  ajjl  IIUIUI 1 1  LfUl  ILUI  LUI II   \  \  \l\J\  &l ) 

Komarkova-Legenerova 

0 

0 

12762 

0.601 

0 

0 

0 

0 

u 

u 

Monoraphidium  griffithii  (Berkeley) 
Komarkova-Legenerova 

12762 

0.902 

0 

0 

0 

0 

0 

0 

o 

0 

Mougeotia  sp. 

12762 

357.249 

0 

0 

0 

0 

0 

0 

o 

o 

Oocystis  parva  W.  &  G.S.  West 

0 

0 

12762 

2.406 

0 

0 

0 

0 

0 

0 

Pediastrum  boryanum  (Turpin) 
Meneghini 

0 

0 

12762 

262.651 

0 

0 

0 

0 

0 

0 

Scenedesmus  acutiformis  Schroeder 

12762 

2.406 

0 

0 

0 

0 

12762 

0.481 

u 

u 

Scenedesmus  acutus  Meyen 

0 

0 

25525 

1.925 

12762 

5.132 

0 

0 

o 

0 

Scenedesmus  opoliensis  P.  Richter 

12762 

4.811 

0 

0 

0 

0 

0 

0 

0 

0 

Tetraedron  minimum  (A.  Braun) 
Hansgirg 

12762 

1 1 .547 

0 

0 

0 

0 

0 

0 

0 

0 

CHRYSOPHYCEAE 

Chromulina  sp. 

25525 

8.554 

0 

0 

63813 

21.384 

0 

0 

51050 

17.107 

Mallomonas  sp 

0 

0 

0 

0 

12762 

8.554 

0 

0 

n 

o 

Ochromonas  sp 

12762 

4.277 

25525 

8.554 

25525 

8.554 

0 

0 

4  ?77 

Unidentified  naked  Chrysophyte  sp 
(Ochromonas  1  Chromulina  )-large 

76576 

25.661 

140389 

52.725 

102101 

34.215 

76576 

30.793 

102101 

34.215 

Unidentified  naked  Chrysophyte  sp 
(Ochromonas  1  Chromulina  )-small 

25525 

0.214 

25525 

0.601 

38288 

0.902 

0 

0 

25525 

0.601 

CRYPTOPHYCEAE 

Cryptomonas  erosa  Ehrenberg 

0 

0 

12762 

6.843 

76576 

72.171 

0 

0 

0 

0 

Cryptomonas  marsonii  Skuja 

12762 

13.365 

38288 

40.095 

25525 

21.384 

38288 

102.644 

63813 

171.073 

Cyrptomonas  phaseolus  Skuja 

0 

0 

12762 

5.132 

0 

0 

0 

0 

0 

0 

Cryptomonas  reflexa  Skuja 

0 

0 

114864 

259.817 

63813 

125.097 

12762 

14.702 

0 

0 

Cryptomonas  rostratiformis  Skuja 

0 

0 

0 

0 

12762 

40.416 

0 

0 

0 

0 

Katablepharis  ovalis  Skuja 

0 

0 

51050 

4.277 

63813 

5.346 

0 

0 

12762 

0.855 

Rhodomonas  minuta  Skuja 

153152 

34.642 

625373 

141.456 

612610 

138.569 

408407 

92.379 

331830 

75.058 

Rhodomonas  minuta  var. 
nanoplanctonica  Skuja 

51050 

3.421 

63813 

4.277 

38288 

3.208 

38288 

2.566 

38288 

4.01 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  55 
in  Alberta 


Appendix  4  Phytoplankton  density  (number  of  units/L)  and  biomass 
(milligram/m3)  in  agricultural  streams  (2006) 


Stream  Name: 

Rose  Creek 

Blindman  R.  #1 

Blindman  R.  #2 

Blindman  R.  #3 

Strawberry  Creek 

Date  Sampled: 

30-Aug-06 

5-Sep-06 

6-Sep-06 

5-Sep-06 

31-Aug-06 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

Density 

Biomass 

EUGLENOPHYCEAE 

Euglena  cf.  minuta  Prescott 

293542 

157.387 

561559 

301.089 

472220 

253.188 

255254 

136.859 

204203 

109.487 

Euglena  sp 

0 

0 

0 

0 

12762 

57.737 

0 

0 

0 

0 

Phacus  sp 

0 

0 

0 

0 

0 

0 

12762 

21.384 

0 

0 

DINOPHYCEAE 

Gymnodinium  ordinatum  Skuja 

0 

0 

0 

0 

0 

0 

o 

o 

12762 

8.019 

Gymnodinium  pusillum  (Penard) 

Lemmermann 

0 

0 

0 

0 

0 

0 

0 

0 

12762 

34.054 

R&rn  i  ADinpuvrPAP  fniATniui^ 

DHUILLAKIUrn  Il/CME  ( U 3M  1  <JiV\0) 

Amphora  sp 

U 

u 

I Z  /  OZ 

O  A^'X 
Z.4  I  O 

U 

U 

U 

n 
U 

U 

U 

Navicula  sp 

O  1  UOU 

1  1  OA  R 

occon 
ZOOZD 

z.ooo 

1  T7CO 

-1  A  C77 

14.  Of  1 

Zo.4oD 

QQOQQ 

oozoo 

o.Zl 

Neidium  sp 

o 

0 

o 

0 

12762 

4.084 

o 

o 

o 

0 

Nitzschia  or  Fragilaria  sp 

0 

0 

25525 

1.723 

25525 

4.39 

0 

0 

0 

0 

Rhoicosphenia  abbreviata  (Agardh) 

Lange-Bertalot 

0 

0 

0 

0 

12762 

2.077 

0 

0 

0 

0 

Synedra  sp 

0 

0 

0 

0 

12762 

2.553 

0 

0 

12762 

1.149 

Centric  diatom 

12762 

1.283 

63813 

25.06 

38288 

15.036 

25525 

2.165 

0 

0 

Cocconeis  sp 

76576 

117.621 

38288 

68.612 

51050 

20.42 

76576 

44.012 

0 

0 

Diatoma  moniliformis  Kuetzing 

25525 

1.838 

0 

0 

0 

0 

0 

0 

0 

0 

Fragilaria  capucina  Desmazieres 

12762 

0.517 

0 

0 

0 

0 

0 

0 

0 

0 

Pilot  Study  to  Evaluate  the  Practicality  of  Biological  Monitoring  of  Small  Agricultural  Streams  56 
in  Alberta 


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