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Earthworm (Lumbricidae) survey of North Dakota fields
placed in the U.S.
Conservation Reserve Program
1/1/2003
Journal of Soil and Water
Conservation
By R. A. Utter
Twenty-three field sites in North
Dakota, where highly erodible soil is placed under
permanent vegetation in the U.S. Conservation Reserve Program (CRP) from five
to eight years, were surveyed for the presence or absence of earthworms. Soils
were sampled to determine chemical and physical properties, and soil cores were
collected to estimate earthworm populations. Earthworm species identified at 12
CRP sites were Aporrectodea tuberculata (Eisen), Aporrectodec trapezoids
(Duges), Aporrectodea caliginosa (Savigny), Dendrobaena octaedra (Savigny), and
Lumbricus rubellus (Hoffmeister). Sites with earthworms were associated with
organic matter levels of greater than 2.5%. Sand content of the 11 sites
without earthworms averaged 67% ([+ or -]13), and the soil usually contained
what appeared to be sharp shiny crystals or grains that might not be ideal for
earthworm survival. Dendrobaena octaedra and Lumbricus rubellus were found at
sites with the highest soil organic matter and nitrate-N levels plus low sa nd
percent. Soil P, K, pH and EC levels were not related to the presence or
absence of earthworms in these CRP sites. Total earthworm population estimates
from five CRP sites averaged 6.3 million [ha.sup.*1] ([+ or -]4.7), with
adults, juveniles, and cocoons at 0.6 ([+ or -]0.4), 4.5 ([+ or -]3.1), and 1.2
([+ or -]2.0) million [ha.sup.*1], respectively. Earthworm populations along a
90-meter transect from the edge of the CRP field were similar when averaged
over the five sites. An estimate of population at the other seven earthworm
sites was not possible because environmental stress as earthworms tended to
migrate only to areas in the field where taproot plant species were located.
The presence of wetlands or tree habitat in these CRP fields could not be used
as criteria for determining the presence of earthworms.
Keywords: Aporrectodea, Conservation Reserve Program, CRP, earthworms,
Lumbricidae, soil properties
Some soils in the United
States have been degrading at a rapid rate
because of serious soil erosion problems and loss of organic matter, usually
through extensive tillage practices. These poor soil-conservation practices
have reduced the quality of the soil by changing the chemical, physical, or
biological conditions in the soil and have raised water-quality concerns. The
Conservation Reserve Program (CRP) in the United States, one provision of the
Food Security Act of 1985, was established to address such concerns. This
program emphasizes removing from production cultivated fields with soils that
were highly erodible and placing them under permanent vegetation (mainly grass)
for at least 10 years. CRP, with slight modifications, has continued as part of
the 1990 Food, Agriculture, Conservation, and Trade Act (FACTA) and the 1996
Federal Agriculture Improvement and Reform Act (FAIR). States in the Northern Great Plains have placed a large number of acres
under CRP. North Dakota
has enrolled more than 3.1 million acres (CAST 1990). It is estimated that the
CRP initiative has decreased net erosion in the United States by 650 million tons
per year (CAST 1990), thus improving water quality. The long-term impact that
CRP can have on improving the quality of the soil for placement back into
production is being evaluated. Baer et al. (2000) reported that long-term
enrollment had a greater impact on some soil chemical and physical properties
than did short-term enrollment. Karlen et al. (1999) reported that several
soil-quality indicators were improved by placing cropland into perennial grass
in Iowa, Minnesota,
North Dakota, and Washington. They indicated that soil
biological indicators were changed more than soil chemical or physical
properties. Deibert (1997) proposed that the health of the soil could be
determined by measuring earthworm populations because their presence or absence
is influenced by agricultural management practices.
Although earthworm research is limited in the Northern
Great Plains, some believe that most species found in this area
were introduced from other countries because the native species did not survive
the last glaciation. This hypothesis was first proposed by Heimburger (1914)
and expanded by Gates (1970). Lee (1985) later summarized research to support
this belief in a chapter on earthworm dispersal. Barley (1961) was one of the
first researchers to describe the importance of earthworms to agricultural land.
Buckerfield (1992), Deibert and Utter (1994), and Kladivko and Timmenga (1990)
related the different soil-management practices (residue management or tillage
system, crop rotation, and the presence or absence of legumes) to earthworm
populations.
Earthworm distributions and species in the Northern
Great Plains may also be controlled by annual precipitation that
ranges from 25 cm (10 in) in the west to 50 cm (20 in) in the east. A recent
survey in this precipitation range, with pictures of earthworm species and
their distribution was presented by Utter et al. (1995a). Although Edwards
(1998) edited a book on current earthworm research, little information has been
reported on earthworm populations in fields that have been converted to CRP.
The survey reported in this paper was designed to determine: (1) which
earthworm species are present in CRP fields and (2) what impact placing fields
in CRP has on earthworm populations, particularly in relation to differences in
chemical and physical properties of the soil, position in the landscape, and
presence or absence of other habitat such as wetlands or trees.
Methods and Materials
Twenty--three field sites were selected in six counties of North Dakota with the largest acreages of
CRP land. Site information variables--including mapped soil series from the
most recent soil survey, site habitats (presence or absence of wetlands or
trees), landscape positions and aspect, year placed in CRP, previous crops
grown on the field, and current plant species in the CRP field--were recorded.
Soil samples from the 0 to 15 cm (0 to 6 in) depth were collected with a shovel
from 15 to 20 areas, selected at random, to represent the field at each site
(Franzen and Cihacek 1998). Samples at each site were combined in a bucket and
mixed, and sub-samples were placed in separate, marked, 2 qt plastic
containers, one container for each site. Sample containers with soil were
placed in a cooler, returned to the lab, air-dried, and ground to pass a 2 mm
sieve. Soil analyses, including organic matter (OM),
nitrate N, phosphorus (P), potassium (K), 1:1 pH, and electrical conductivity
(EC) were determined at the ND SU Soil Testing Lab using standard analytical
procedures Brown 1998). Part-icle-size analysis (sand, silt, clay) was
determined by the hydrometer method (Gee and Bauder 1986). Each field site was
initially surveyed once in 1994 for the presence or absence of earthworms
during April, May or June. Soil was extracted to 30 cm (12 in) depth with a
spade (shovel) at random locations across the field and examined. A positive
site indicated that earthworms were found somewhere in the CRP field, while a
negative site indicated no earthworms were found anywhere in the CRP field or
in adjacent trees, wetlands, or grass areas along the road ditches. When
earthworms were present, the adults were placed in labeled plastic bags
containing soil, which were placed in a cooler with ice for storage. Earthworm
samples were returned to the laboratory fixed with 10% formalin, and later
identified using a guide by Schwert (1990).
Based on previous research, the authors found that a core method provided
better estimates of earthworm populations because both small juveniles and
cocoons could be included in the total population. Also the standard formalin
method (Raw 1960) did not work well in some soils, especially clays, and the
researchers wanted to limit exposure to the hazardous chemical formalin. Thus,
intact soil cores were taken to make earthworm population estimates. Based on
the initial sampling described previously, cores were only taken at those sites
where the authors, based on experience, felt adequate earthworms were present
throughout the field. Single cores were taken along a transect at 30 m
intervals from the edge of the field. The transect was located at least 50 m
from any trees or wetland areas in the field, A 20 cm (8 in) diameter by 15 cm
(6 in) deep metal irrigation pipe was pounded into the soil. The core, with
soil and earthworms, was extracted and placed in a plastic mesh bag inside a plastic
bucket for storag e and transport. Landscape position and aspect of each core
was recorded because previous research suggested that location on the landscape
might influence populations. Soil from each core was hand-sorted to collect
earthworms. Subsequently, the sorted soil was washed over a 1 mm sieve to
recover cocoons and juvenile earthworms missed during hand-sorting. Number of
adults (recognizable from genital markings such as clitellum), juveniles (no
genital markings), and cocoons were counted and recorded. The estimated
reproductive capacity of the adult earthworms, found at sampling time, was
determined by summing the number of cocoons plus juveniles.
Averages, analysis of variance (ANOVA), and simple or multiple correlations
were performed on the data using SAS procedures (Freund and Littell 1981).
Standard deviations (SD) are provided for variable averages. Significant
differences among means or significant correlations were determined at the 0.05
level of probability Analyses were performed on either all 23 sites combined or
by a grouping of CRP sites (12 positive and 11 negative earthworm sites). The
three core distances along the transect were considered replications in the
five sites for populations estimates. Multiple correlations analysis included
soil properties (sand, silt, clay, OM, P, K,
pH, EC), habitat (trees, wetlands), and earthworm species (number of species,
A. tuberculata, A. trapezoides, A, caliginosa, Dendrobaena octaedra, L.
rubellus).
Results and Discussion
The location of each CRP earthworm sampling site within the state of North Dakota and mean
annual precipitation (Ramirez 1973) is depicted in Figure 1. Specific site
number, year established, plant species present, and previous crops for each
CRP site are summarized in Table 1. Previous crops rotated on the sites before
placing the land into CRP included wheat (Triticum aestivum L.), barley
(Hordeum vulgare L.), durum (Triticum turgidum L.), oats (Avena sativa L.), rye
(Secale cereale L.), sunflower (Helianthus annuus L.), corn (Zea mays L.),
soybean (Glycine max Merrill), dry edible bean (Phaseolus vulgaris L.), potato
(Solanum tuberosum L.), and summer fallow. The three predominant crops
previously found at nearly all CRP sites, in considering a four-year rotation, included
small grain at 50% of the time followed by fallow (20%) and sunflower (16%).
Plant species seeded on the CRP fields included tall wheat grass (Agropyron
elongatum), smooth brome grass (Bromus inermis, crested wheat grass (Agropyron
deser torum), alfalfa (Medicago sativa L.), slender wheat grass (Agropyron
trachycaulum), sweet clover (Melilotus officianalis Lam.), western wheat grass
(Agropyron smithu), intermediate wheat grass (Agropyron intermedium), pubescent
wheat grass (Agropyron trichophorum), and switch grass (Panicum virgatum).
Plant cover on the CRP sites was mainly grass with smooth brome (17 sites) and
slender wheat (9 sites) the main grasses that sometimes included intermittent
legumes plants such as alfalfa (19 sites) and sweet clover (13 sites). Weeds
species identified on some, but not all, of the sites included dandelion
(Taraxacum officinale), quackgrass (Agropyron repens), yellow goats beard
(Tragopogon pratensis), purple coneflower (Brauneria angustifolia, curled dock
(Rumex crispus), prickly lettuce (Lactuca virosa) and Canada thistle (Cirsium
arvense).
Soil properties for each site are listed in Table 2 with both the positive
and negative earthworm sites indicated. Particle-size analysis indicated that
sand content ranged from 8% to 81%, silt 6% to 45%, and clay 10% to 48%. The
average sand content was 60% ([+ or -]18) with both silt and clay fractions at
20% ([+ or -]10). A separation into positive (12 sites) and negative (11 sites)
earthworm sites indicated that, generally, sites with less than 60% sand
contained earthworms, while those exceeding 60% sand were absent of earthworms.
The average sand content (53%) for soils with earthworms places the textural
class in the loam or sandy clay loam category, while average sand content (67%)
on the sites with no earthworms places the texture as sandy loam. Some specific
site exceptions occurred, which we believe were related to soil particle
shapes. When earthworms were absent in the soil, we observed a portion of the
soil particles were shiny with what appeared to be distinct sharp flat edges.
We speculate tha t these sharp particles would be harmful when passing through
the earthworm gut or that their outer skin might be damaged as they moved
through the soil. Thus earthworms would tend to avoid or not survive in these
soils, and any introduced earthworms would not survive for long or reproduce
under these conditions. Lee (1985) cited several instances where
coarse-textured particles affected earthworm species and distribution in New Zealand and Egypt. The four positive earthworm
sites (sites 3, 14, 17, 23) with sand content greater than 60% had no
observable sharp soil particles. The exact nature of these sharp particles, or
crystal grains, and their effect on earthworms requires further investigation.
Only a few significant correlations (n = 12 and P < 0.05) were found
between earthworm numbers and soil particle size. A negative correlation (r =
-0.74) occurred between increased sand content and both Dendrobaena octaedra
and Lumbricus rubellus, with a subsequent positive correlation based on
increased silt (r = +0.77) and clay (r = +0.56) content. This is not surprising
because these two species are usually associated with high soil water content,
which occurs in soils with higher silt and clay content. Nordstrom and Rundgren
(1974) found a positive correlation between earthworm abundance (L. rubellus
and A. caliginosa) and clay content at depths below 20 cm (8 in) but pointed
out that this may be because of increased soil water at the lower depths as a
result of increased clay content.
The OM content of the soils from all CRP
sites ranged from 0.9% to 5.3% with an average of 3.2% ([+ or -]0.9). Although
more OM tends to encourage earthworm development as a result of more available
food, an OM content exceeding 2.5% was
adequate to support earthworms in these CRP sites. Those sites without
earthworms and with more than 2.5% OM were either associated with the presence
of sharp soil particles, previously discussed, or no earthworm source was
available or introduced as a result of human activity (earthworms transported
with soil attached to plant roots, tillage implements, or dumping earthworms
left after fishing). Nitrate-N (all sites) ranged from 1 to 14 ppm, P from 3 to
40 ppm, and K from 100 to 605 ppm. Although the average OM, nitrate N, P, and K
amounts on the sites with earthworms (12 sites) were higher than those with no
earthworms (11 sites), no significant correlations were obtained among earth
worms and P or K. Positive correlations, higher OM (r = +0.63) and nitrate-N (r
= +0.87), w ere found between these two variables and the presence of both
Dendrobaena octaedra and L. rubellus. A positive correlation was found between
the number of earthworm species found and higher nitrate N levels (r = +0.70).
The pH levels across all sites ranged from 6.2 to 7.9 with similar values or
soils with or without earthworms and little relationship between pH and the
presence or absence of earthworms. EC values, except at two sites, were usually
less than 1.0 mmhos/cm with a range of 0.16 to 2.30. High EC values were
positively correlated with both Dendrobaena octaedra and Lumbricus rubellus
species (r = +0.87). Lower average EC values in soils no earthworms would be
expected because these sites also have higher sand content, which would allow
easier leaching of salts to below the 15 cm sample depth.
Different species of earthworm were found at each CRP site (Table 3).
Thirteen sites contained trees, but only eight of these sites contained
earthworms. These earthworm species were probably introduced via the roots or
soil when the trees were established in the field. The five tree sites without
earthworms suggest that earthworms were never present or that any introduced
earthworms did not survive either because of dry soil conditions or the sharp
soil particles. The presence of earthworms on four sites without ;rees, three
with wetlands, indicates that the earthworms were transported to the field from
another area by tillage implements or carried by water or birds. A. caliginosa,
Dendrobaena octaedra and L. rubeilus were found at only one site. This is not
surprising as these three species were reported in only a few areas in a North Dakota earthworm survey by Utter et al. (1995b).
The main earthworm species, A. tuberculata and A. trapezoids, occurred at 10
and 5 sites, respectively. These two species were identified by Utter et al.
(1992) as the predominant earthworm species in North
Dakota cultivated fields, shelterbelts and prairie grasses.
In seven of the positive earthworm sites, the presence or number of
earthworms was very low across the field. This may be related to either the dry
soil conditions associated with low precipitation or the depletion of soil
water caused by dense vegetative growth. Earthworms, to survive at these sites,
tended to migrate or concentrate only in the field near plants with tap roots,
including alfalfa, sweet clover, dandelion, goats beard, and prickly lettuce.
Evidently the food materials or root exudates and/or moisture or nutrients
sustained the earthworms during these environmental stress periods. This may
offer a clue to sampling for earthworms under stress conditions. These same low
earthworm number CRP sites were checked in subsequent years, but the numbers
recovered still remained low.
Estimates of populations at five positive earthworm sites are presented in
Table 4. Populations of cocoons, juveniles, adults and total earthworms varied
with CRP site. High or low populations did not appear to be related to
landscape position or aspect, as distance that the core was taken from the edge
of the field showed no significant difference among populations. The adult
population (range 0 to 1.5 million) averaged about 640,000 [ha.sup.-1] ([+ or
-] 39,000). These populations are smaller than adult populations reported under
grass, trees, or reduced-tillage systems by other research in North
Dakota and Canada
(Utter and Deibert 1998, Clapperton et al. 1997). The reproductive capacity of
earthworms in soils under CRP with an adequate food supply, surface cover, and
soil water is well-demonstrated in these sites. The average number of cocoons
approached 1.2 million [ha.sup.-1], while the number of juveniles was about 4.5
million [ha.sup.-1]. Total reproduction (sum of cocoons plus juveniles) ranged
from a low of 925,000 [ha.sup.-1] (site 9 upper slope), where adult population
was also low at about 300,000 [ha.sup.-1], to a high of more than 1.8 million
[ha.sup.-1] (site 7 midslope) where the adult population exceeded 1.5 million
[ha.sup.-1]. The average earthworm reproduction exceeded 5.7 million
[ha.sup.-1], or about 9 cocoons plus juveniles for every adult earthworm. The
average total earthworm population at these five sites approached 6.4 million
[ha.sup.-1] with a range of 1.2 million (site 9 upper slope) to almost 20
million [ha.sup.-1] (site 7 midslope). When the population data were averaged
over all five sites, no significant differences were found for cocoons,
juveniles, adults, or total earthworm populations among sample core distance
from the edge of the field. These results were not expected, as previous
unpublished population surveys by the authors on no-till and organic fields
suggested that the lower landscape positions contained higher populations than
the upper slopes because of greater soil water. The effect of landscape
position on earthworm populations warrants further investigation in CRP fields.
Summary and Conclusion
Our survey provides information on the distribution and population of
earthworm species in CRP fields in North Dakota,
a dryland area of the Northern Great Plains
region. This information will provide a better understanding of the
distribution and population of earthworm species in various agroecosystems such
as CRP that was designated as a research imperative by Edwards et al. (1995).
Our results also provide some initial information on the relationships of
earthworms to texture (particle size), selected chemical soil properties,
landscape position, and other habitat in CRP fields. The predominant earthworm
specie found at the CRP sites was A. tuberculata, located at 10 of the 12
sites. Multiple species were found at only five sites. About 80% of the soils
sampled for earthworms in this survey were sandy loam or sandy clay loam
texture. Texture, or at least sand content, did not appear to be the
determining factor for the presence or absence of earthworms as earthworms were
found in 12 of 23 CRP sites with s and content that ranged from 8% to 74%.
However, sites with no earthworms usually had sand content above 60% sand and
sharp soil grains or crystals that would not be conducive for earthworm
survival. An OM content of 2.6% or more was
measured on all earthworm sites. Five sites without earthworms contained soil OM levels below 2.6%. Although the average [NO.sub.3]-N,
P, K, pH, and EC levels in the soil were higher in positive compared with
negative earthworm sites, little relationship was found among these chemical
soil properties and the presence or absence of earthworms. The presence of tree
or wetland habitat was not a good indicator of positive earthworms in the CRP
sites in this survey. Wetland areas in the CRP field without trees but with
earthworms suggest that the earthworms were previously transported to the field
from another area, either by tillage implements, water erosion, or birds.
Earthworm populations measured at five sites for cocoons, juveniles, and adults
averaged about 1.19 million [ha.sup. -1], 4.54 million [ha.sup.-1], and 0.64
million [ha.sup.-1], respectively On seven earthworm sites, earthworms were
only found where they tended to migrate because of environmental stress.
Estimates of populations at these sites, based on the core method of sampling,
would be unreliable. Insight is given in this survey for sampling earthworms
under environmental stress conditions, often exhibited under dense vegetation
in CRP fields, low precipitation, and course-textured soils that would normally
have low water-holding capacity.
Table 1
North Dakota CRP earthworm sampling sites, year established, plant
species, and previous crop information.
Year CRP plant CRP species Previous
Site established present + crops +
1 1987 SB,IW sg-fa
2 1987 SW,SB,AL cn-sg-db-cn
3 1987 SB,CW,SW,AL,SC sg-sg-sf
4 1986 SB sf-sg-db-sg
5 1986 CW,SC,SB,AL sg-sf-sg-fa
6 1986 TW,SB,AL sg-db-sg-po
7 1989 IW,CW,AL sg-fa
8 1988 WW,SB,AL sg-fa
9 1986 SW,CW,SC,SB,AL sg-sg-fa
10 1988 SB,AL,SC sg-sg-sf
11 1987 SW,SB,AL sf-cn
12 1989 SB,AL,SC sg-cn-sf-cn
13 1987 SB,AL,SC sg-cn-sf-sg
14 1986 IW,CW,AL,SC sg-sg-sf
15 1988 SB,AL sg-fa
16 1987 PW,TW,SW,AL,SC sg-fa-sf
17 1988 SW fa-sg-sg
18 1987 IW,SB sg-sg-sf
19 1987 IW,TW,AL,SC sg-sg-sf
20 1987 IW,TW,SC,AL fa-sf-sg
21 1987 SW,WW,IW,PW,WH,AL,SC sg-sg-fa
22 1986 SW,IW,AL,SC fa-sf-sg-cn
23 1986 TW,SW,SB,AL,SC sg-sf-fa
+ Plant species: TW = tall wheat grass; SB = smooth brome grass; CW =
crested wheat grass; AL = alfalfa; SW = slender wheat grass; SC = sweet
clover; WW = western wheat grass; IW = intermediate wheat grass; PW =
pubescent wheat grass; WH = switch grass.
++ Previous crops rotated before CRP: sg = small grain (wheat, barley,
durum, oats, rye); sf = sunflower; fa = summer fallow; cn = corn; sb =
soybean; db = dry edible bean; po = potato.
Table 2
North Dakota CRP earthworm sampling sites, mapped soil series, particle
sizes, and various chemical properties in the 0-15 cm (6-inch) soil
depth.
Organic
Mapped Sand Silt Clay Matter
soil
Site + series %
1 Lihen 77 6 17 1.9
2 Embden 81 9 11 2.3
3 + Arvilla 74 16 10 3.6
4 + Inkster 53 21 27 4.0
5 + Inkster 31 21 48 4.5
6 + Bearden 8 45 46 5.3
7 + Belfleld 56 18 26 2.7
8 Beisigi 63 15 22 2.4
9 + Shambo 51 25 24 3.3
10 Barnes 36 32 33 4.6
11 Renshaw 62 21 17 3.2
12 Arvilla 80 7 13 1.9
13 Arvilla 62 24 14 3.4
14 + Calvin 73 16 11 2.6
15 Arvilla 62 19 19 2.6
16 Arvilla 63 17 20 2.7
17 + Wyndmere 73 13 14 2.6
18 Fossum 81 9 10 1.8
19 Karlsruhe 72 13 15 2.8
20 + Barnes 41 32 27 4.0
21 + Sioux 59 27 14 4.1
22 + Swenoda 53 28 19 3.7
23 + Fossum 64 22 14 2.8
Average 60 20 20 3.2
SD ++ 18 10 10 0.9
Average (positive) 53 24 23 3.6
SD ++ 19 9 13 0.8
Average (negative) 67 16 17 2.7
SD ++ 13 8 6 0.8
NO3-N P K pH EC
Site + ppm 1:1 mmhos/cm
1 4 7 280 7.8 0.20
2 1 12 210 6.9 0.16
3 + 4 9 170 7.3 0.23
4 + 3 40 605 6.2 0.25
5 + 2 19 340 6.2 0.30
6 + 14 8 210 7.7 2.30
7 + 6 16 500 7.6 0.40
8 7 9 280 6.8 0.25
9 + 4 7 275 7.6 0.37
10 3 4 515 7.8 0.45
11 6 4 100 7.7 0.25
12 1 4 160 7.4 0.18
13 1 8 125 6.8 0.18
14 + 1 3 200 7.3 0.19
15 2 3 200 7.8 0.25
16 3 7 220 7.0 0.20
17 + 6 4 265 8.0 0.25
18 1 5 100 7.8 0.18
19 1 8 270 7.9 0.50
20 + 5 8 390 6.9 0.31
21 + 5 17 340 7.1 0.30
22 + 4 6 365 7.7 1.35
23 + 6 11 330 7.4 0.32
4 9 280 7.3 0.41
3 8 131 0.5 0.48
Average (positive) 5 12 332 7.2 0.55
SD ++ 3 10 126 0.6 0.63
Average (negative) 3 6 224 7.4 0.25
SD ++ 2 3 118 0.4 0.11
+ Number followed by a + indicates a site testing positive for
earthworms.
++ Standard deviation.
Table 3
North Dakota CRP earthworm sampling sites, Lumbricidae specie, and
habitat information.
Species
Aporrectodea Aporrectodea Aporrectodea Dendrobaena
Site + callginosa tuberculata trapezoides octaedra
1 0 + 0 0 0
2 0 0 0 0
3+ 0 X X 0
4+ 0 X 0 0
5+ 0 X 0 0
6+ 0 X 0 X
7+ 0 X 0 0
8 0 0 0 0
9+ 0 X X 0
10 0 0 0 0
11 0 0 0 0
12 0 0 0 0
13 0 0 0 0
14+ 0 X 0 0
15 0 0 0 0
16 0 0 0 0
17+ 0 X X 0
18 0 0 0 0
19 0 0 0 0
20+ X X 0 0
21+ 0 0 X 0
22+ 0 0 X 0
23+ 0 X 0 0
Specie Other habitat
persent
Lumbricus
Site + rubellus Wetlands Trees
1 0 0 0
2 0 0 X
3+ 0 0 X
4+ 0 0 X
5+ 0 X X
6+ X 0 X
7+ 0 X X
8 0 0 0
9+ 0 X 0
10 0 X 0
11 0 0 X
12 0 0 X
13 0 0 0
14+ 0 0 X
15 0 X 0
16 0 0 0
17+ 0 0 X
18 0 X X
19 0 X X
20+ 0 X 0
21+ 0 0 0
22+ 0 X 0
23+ 0 0 X
+ Number followed by a + indicates a site testing positive for
earthworms.
+ Code: 0 = specie or habitat not present at site; X = specie or habitat
present at site.
Table 4
North Dakota CRP earthworm sites, sampling dates, core distances,
landscape position-aspects, and Lumbricidae populations.
Core Landscape Cocoons +
Sample distance + position
Site date in meters and aspect million
[ha.sup.-1)
6 5/18/94 30 Nearly flat-South 3.084 (ss)
60 Nearly flat-South 0.308
90 Nearly flat-South 0.617
Average 1.336
7 6/21/94 30 Lower slope-East 1.233
60 Mid slope-East 8.017
90 Upper slope-East 0.925
Average 3.392
9 6/22/94 30 Upper slope-South 0.308
60 Mid slope-South 1.542
90 Lower slope-South 0.000
Average 0.617
17 4/19/94 30 Upper slope-West 0.308
60 Mid slope-West 0.617
90 Lower slope-West 0.617
Average 0.514
23 5/24/94 30 Lower slope-North 0.308
60 Mid slope-North 0.000
90 Upper slope-North 0.000
Average 0.103
Average 30 1.048
60 2.097
90 0.432
Average 1.192
SD (n) 2.048
Core Juveniles Adults Total
Sample distance +
Site date in meters million [ha.sup.-1)
6 5/18/94 30 4.009 0.308 7.401
60 1.542 0.308 2.158
90 4.317 0.617 5.551
Average 3.289 0.411 5.036
7 6/21/94 30 7.092 0.617 8.942
60 10.176 1.542 19.735
90 4.009 0.925 5.859
Average 7.092 1.028 11.512
9 6/22/94 30 0.617 0.308 1.233
60 1.850 0.925 4.317
90 2.158 0.000 2.158
Average 1.542 0.411 2.570
17 4/19/94 30 1.850 0.617 2.775
60 2.467 0.617 3.701
90 10.176 0.617 11.410
Average 4.831 0.617 5.961
23 5/24/94 30 8.017 0.308 8.633
60 4.934 0.617 5.551
90 4.934 123.3 6.167
Average 5.961 0.719 6.784
Average 30 4.317 0.432 5.797
60 4.194 0.802 7.092
90 5.119 0.678 6.229
Average 4.543 0.637 6.373
SD (n) 3.069 0.394 4.664
+ Distance the soil core was taken from the CRP field edge.
++ Cocoons = number of cocoons with one or more viable embryos; juvenile
= small earthworms with no recognizable genital markings; adults =
earthworms with either genital markings or developed citellum; Total =
sum of cocoons+ juveniles+adults.
(ss) Value time 100 equals the number of earthworms found in one square
meter.
[n] Standard deviation.
Acknowledgements
The authors would like to thank the North Dakota
cooperators for allowing their CRP fields to be sampled and those specific
personnel at the Carrington Research/Extension Center or Natural Resource
Conservation Service who helped in some part to locate sites and/or provide
general site information.
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Edward J. Deibert is a professor and
Rodney A. Utter is a research specialist with the Soil Science Department at
North Dakota State University in Fargo, North Dakota.
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