Survey assessment of semi-pelagic Gadoids: the example of Walleye Pollock, Theragra chalcogramma, in the Eastern Bering Sea.
Karp, William A. ; Walters, Gary E.
Introduction
Direct assessment provides essential information for the management
of many marine fish stocks. Frequently, demersal stocks are assessed by
means of bottom trawl surveys, and pelagic stocks are assessed using
acoustic techniques together with some form of direct sampling such as
midwater trawling. Each approach has its own strengths and limitations
but these types of routine surveys provide critical information for many
stocks.
When a stock is semi-pelagic (or semi-demersal) in habit, however,
it is difficult to accomplish overall assessment with a single
technique, and it may be necessary to assess the pelagic and demersal
components independently. Because the biases associated with each
technique differ, difficulties may be encountered when attempting to
combine the data to produce a comprehensive estimate.
To address this problem, survey objectives should be evaluated. If
the assessment process requires a survey-based estimate of overall
abundance, problems associated with combining the two sets of data
require careful consideration. But if it is satisfactory to provide
indices of the abundance of certain portions of the stock, such as
specific age groups, it may be possible to consider the pelagic and
demersal assessments as independent sources of information, and problems
associated with combining data sets would then be of less concern.
The walleye pollock, Theragra chalcogramma, resource of the
continental shelf and slope of the Eastern Bering Sea (EBS) supports
major fisheries activities. The species is semipelagic and is generally
found in pelagic and demersal regions over bottom depths of 25--400 m,
although it does occur in the pelagic zones of deeper waters (Sample and
Bakkala, 1989). Greatest abundances are found along the outer
continental shelf over water depths of 100--300 m (Wespestad and Megrey,
1990). Scientists from the NMFS Alaska Fisheries Science Center (AFSC)
conduct the assessment of this stock. The demersal component of the
stock is assessed annually during a multi-species bottom trawl survey of
the EBS shelf. Smallscale surveys began in the early 1970's, and
the present survey coverage was first established in 1975 and has been
done annually since 1979. Also beginning in 1979, an expanded triennial bottom trawl survey has been conducted; this has covered a greater area
of the shelf and the waters of the upper continental slope. During the
triennial surveys, the pelagic component of the pollock stock has also
been assessed by means of an echo integration--midwater trawl (EIMWT)
survey.
In this paper we evaluate the methodology and results of the
pollock assessments conducted during the triennial surveys as an example
of semi-pelagic gadoid assessment. In considering the sources of bias,
we offer suggestions for research and changes in methodology which may
lead to improvements.
Methods
Detailed information on survey methodology was presented by Bakkala
and Wakabayashi (1985), Bakkala et al. (1985), Walters et al. (1988),
and Bakkala et al. (1992). Here we provide an overview of bottom trawl
and EIMWT techniques.
Bottom Trawling
Assessment of demersal pollock on the EBS shelf and slope is
conducted within the broader objectives of a multi-species bottom trawl
survey designed to assess the condition of stocks of several species.
Surveys are performed annually during the months of June, July, and
August when migratory activities are believed to be minimal. Every third
year a more comprehensive survey, covering a larger area of the shelf
and slope, is carried out. Details of the triennial survey design are
presented by Bakkala (1988) and an illustration of the area sampled is
presented in Figure 1.
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An Eastern otter trawl (type 83--112) with 900 kg steel V-doors has
been used for sampling since 1982 (Table 1). Previously, a similar but
smaller net, the 400 mesh Eastern trawl with 570 kg doors, was used.
Both trawls were constructed of the same mesh sizes (Table 1), however,
the 83--112 was rigged with 30 cm chain extensions on the footrope ends
to improve bottom tending characteristics.
[TABULAR DATA OMITTED]
Prior to 1988, trawl width (wingspread) measurements were made on
only a few tows made by any vessel with a given trawl. The averages of
the measured widths were then used for all tows within an annual survey
by that vessel and trawl. Beginning in 1988, the acquisition of
sufficient mensuration equipment allowed measurements for almost every
tow. Examination of these data revealed that trawl operating width is
primarily a function of the amount of trawl warp extended (Rose and
Walters, 1990). This analysis indicated mean widths-per-tow of 12--20 m
over bottom depths of 20--200 m. Warp extended over these depths ranged
from 90 to 550 m.
Time on the bottom and the distance fished for each haul were
determined from the time and location where the winch brakes were set to
the time and location of the beginning of haul back. Based on depth
readings from the trawl mensuration equipment, trawl settling time was
considered insignificant at depths encountered on the EBS shelf. The
locations of the vessel at the start and end of each haul were obtained
from LORAN C instruments. Biological information was obtained from the
catches so that biomass and population abundance could be estimated by
species, size, and age; catches greater than 1 metric ton (t) were
subsampled using procedures designed to ensure randomness (Hughes, 1976;
Bakkala et al., 1985).
Analytical procedures were described by Wakabayashi et al. (1985).
An area swept technique which incorporates the wingspread and distance
fished measurements described above, was used to develop biomass,
population, and size composition estimates (Alverson and Pereyra, 1969;
Doubleday and Rivard, 1981). Each catch was standardized into catch per
unit of area. The standardized catches within a stratum were then used
to estimate stratum biomass, and the stratum estimates were summed over
the entire area. Length-frequency data and age-length keys, developed
from fish sampled during the survey and aged from otoliths, were applied
to the data to provide stratum and overall survey estimates of size
composition and age composition.
Until 1990, the standardized catches of each species by each vessel
were compared using a Bayesian approach (Geisser and Eddy, 1979). If
significant differences between vessels were found for a particular
species, the catches of the least efficient vessel were adjusted to be
equivalent to catches from the most efficient vessel for that species by
the ratio of the mean catches per unit effort (CPUE). Because this
method was based on the estimation of a ratio, it was sensitive to
occasional large CPUE values. Beginning in 1990, a new method developed
by Kappenman(1) was used to compare the distribution of CPUE values
based on a power transformation and develop a scaling factor for
adjustment. This method has been applied to the time series of data back
through 1982.
Acoustic and Midwater Trawl Assessment
The acoustic method for pelagic stock assessment is based on the
principle of echo integration. An echo sounding system transmits
discrete pulses of sound into the water and waits for a period of time
to receive echoes from targets in the insonified volume of water. The
received echoes, in the form of voltages, are then fed into an echo
integrator which squares and sums the voltage samples. The output of the
echo integrator is proportional to the density of the fish insonified
(Dragesund and Olsen, 1965; Forbes and Nakken, 1972; Burczynski, 1982).
Conversion of relative to absolute biomass estimates is dependent
upon consistent system performance as monitored by calibration
procedures and information regarding the acoustic properties of the fish
in the form of mean acoustic target strength (TS). TS is dependent on
species, size, behavior, and, in some cases, depth. Since small changes
in mean TS can give rise to large errors in biomass estimation, direct
in situ measurement of TS is generally recommended (Ehrenberg, 1983;
Foote, 1991).
Techniques for the U.S. EIMWT surveys were described by Karp and
Traynor (1989) and Traynor and Nelson (1985). Additional details were
reported by Bakkala et al. (1985) and Walters et al. (1988). Transect
lines were surveyed by means of a scientific quality 38 Khz acoustic
system consisting of a transmitter, a towed transducer, a receiver, and
a computer based digital echo integrator. The acoustic system was
installed in a portable van that could be located on the deck of the
survey vessel. When conditions were suitable, in situ target strength
studies were conducted in order to collect target strength distribution
information for a range of fish sizes and behavioral patterns. Dual-beam
and split-beam techniques (Traynor and Ehrenberg, 1979) have been
employed for this purpose, although most data has been collected with a
split-beam system in recent years.
Since we do not yet have sufficient information to enable us to
apply field measurements of TS during analysis of survey data,
alternative approaches have been used as an interim measure. Before
1988, a TS value of -30 dB/kg was applied in the conversion of
integrator values to estimates of biomass; starting in 1988, however,
the empirical target strength/length relationship developed by Foote and
Traynor (1988) (TS = 20 log (Fork Length (cm)) - 66.0) has been employed
and has provided results which are generally consistent with in situ
measurements.
The acoustic system was calibrated before and after each survey.
The underwater acoustic calibration system available at the University
of Washington's Applied Physics Laboratory was employed to conduct
standard transmit and receive response and equivalent beam angle
measurements. Also, beginning in 1988, the standard target technique, as
described by Foote et al. (1987) was adopted and is now carried out in
situ to monitor system performance at intervals during each survey.
Midwater trawling was an integral part of each survey. A large
midwater trawl was used to collect biological samples when significant
echo sign was encountered during the acoustic transects. Midwater trawl
types and specifications have changed several times during the period
that these surveys have been conducted (Table 1). As indicated in the
table, different trawls were used for sampling juvenile and adult
pollock sign. The vertical opening of each net was monitored with a
netsonde. Towing speed in all surveys was approximately 1.5 m/sec.
Fishing was carried out on an opportunistic basis in order to
collect adequate samples from the different types of echo sign
encountered throughout the survey area. Since contamination with other
species occurred infrequently, the primary objective of this sampling
was to provide sufficient data for partitioning the acoustic estimates
of biomass by size and age, and developing size and age specific
population estimates. The information collected from these trawls was
not used to provide quantitative information on abundance. Catches were
processed in a manner similar to that described for the demersal trawl
surveys. Age composition was determined by means of age-length keys
obtained by analyzing otoliths taken from fish sampled randomly from
most catches.
All EIMWT triennial surveys have taken place in the summer, during
the same general time period as the bottom trawl surveys. In 1979 only
the outer portion of the shelf and the upper slope were surveyed
(Traynor and Nelson, 1985). In 1982 the entire shelf and upper slope
over bottom depths from about 40 to 500 m was surveyed with a zigzag
transect design (Bakkala et al., 1985). Subsequent surveys have covered
most of the shelf waters deeper than 50 m and the slope. Starting in
1985, equidistantly-spaced parallel transect survey designs (e.g., Fig.
2) have been employed (Walters et al., 1988; Bakkala et al., 1992).
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Results
Because the general objective of this contribution is to discuss
the methodology for overall pollock assessment in the EBS, this section
will concentrate on the types of information produced during the
triennial surveys. Results of the 1979, 1982, 1985, and 1988 triennial
shelf/slope surveys were reported by Bakkala and Wakabayashi (1985),
Bakkala et al. (1985), Walters et al. (1988), and Bakkala et al. (1992),
and the results of more detailed analysis of data from these surveys
were presented by Karp and Traynor (1989), Sample and Bakkala (1989),
and Traynor et al. (1990a). Results of the 1991 survey were not
available when this report was prepared. Rather than present detailed
figures of pollock distribution for each survey, the 1988 results are
provided as an example (Fig. 3--5). Similar figures for the preceding
triennial surveys were provided by Karp and Traynor (1989).
[CHART OMITTED]
The 1988 survey results indicated patterns of distribution similar
to those observed during previous triennial surveys. Taken
independently, neither the bottom trawl nor the EIMWT survey results
provide complete information on the horizontal distribution of pollock
(Fig. 3, 4). Most demersal pollock occurred in waters deeper than 100 m,
and few were found in trawls conducted in water shallower than 50 m.
Pelagic pollock were more abundant in waters deeper than 100 m.
Localized areas of high abundance generally occurred in the vicinity of
Unimak Pass and south of the Pribilof Islands, and overall pollock
abundance was usually higher to the north and west of the Pribilof
Islands than elsewhere (see Figure 1 for location of depth contours and
geographic sites). EIMWT surveys alone would not have documented the
presence of pollock in shallower waters of the continental shelf, but,
by combining the two types of survey data, it was possible to produce a
more comprehensive map of distribution which indicated the trend of
increasing overall abundance with depth (fig. 5).
Comparison of results from the four combined demersal trawl and
EIMWT surveys conducted over a 10-year period indicates substantial
differences in abundance and vertical distribution between years (Fig.
6). Differences in the age-specific proportions of pollock found in
midwater and on bottom are also apparent (Fig. 7,8). For example, the
proportion of 1 - and 2-year-old fish in midwater was much greater than
on bottom in 1979, whereas the proportion of age 1 fish on bottom
exceeded that in midwater in subsequent survey years; age 2 and 3 fish
were more abundant in midwater than on bottom during each survey, but
age 4 fish were more abundant demersally in 1979 and in midwater in
1982, 1985, and 1988. The proportion of fish older than 5 years assessed
by bottom trawl always exceeded the EIMWT derived proportion; this
supports the perception that demersal orientation is more common for
older fish (Fig. 9). The extremely strong 1978 year class undoubtedly
influenced the unusual vertical distribution of juvenile fish that was
observed in 1979. Our ability to track the progress of this year class
over a 10-year period has been greatly enhanced by the use of both
assessment methods. It is apparent that the variability of age-specific
distribution in the midwater and demersal zones, overlaid on the general
trend of increased demersal orientation with age, could not have been
adequately documented by one assessment method alone. In addition, this
combined assessment approach has enabled us to better document the
progression of the above average year classes of 1982 and 1984. Many of
the trends and patterns observed in the time series of data can be
reasonably attributed to differences in year class strength, overall
abundance, and recruitment to the shelf and slope stocks. Nevertheless,
it is likely that some of our perceptions have been influenced by biases
that are inherent in our survey techniques. For example, the total
abundance of the 1981 year class appeared to increase between 1982 and
1985. This suggests that this year class was not fuily available to
either (or both) surveys at age 1.
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Limitations
Biases of concern to scientists conducting these surveys can be
classified into three principal categories: those associated with
deficiencies in biological knowledge; those associated with fishing
gear, fish behavior, and the catching process; and those associated with
the technique of echo integration.
Biological Considerations
The category of biological knowledge includes migratory activities
and factors relating to stock identification. Detailed knowledge of
patterns of stock distribution in space and time is an essential
prerequisite for assessment survey design. Since these surveys have been
conducted over relatively short time periods, when EBS pollock are
believed to be in a nonmigratory feeding mode, horizontal migrations are
not considered to be a serious source of bias. However, assumptions
regarding the geographical distribution of the stock are based on
limited information and it is generally recognized that the stock
extends into unsurveyed areas of the western Bering Sea. Stock
identification is of particular concern with regard to the origin of
fish caught in the central Bering Sea and adjacent to Bogoslof Island (lat. 54[degrees]N, long. 168[degrees]W). The midwater and demersal
surveys have not always been synchronous. This is a potential source of
bias if significant migration does occur.
Vertical migration is also of some concern. The demersal trawl
surveys are conducted only during daylight hours to avoid possible
inconsistencies. EIMWT surveys have been carried out on a 24 hour per
day basis. Even though diel changes in vertical distribution are
apparent, it has been assumed that movement between the pelagic and
demersal zone is not significant and that possible biases are minimal
due to the short darkness period during the summer. Interannual changes
in vertical distribution have been observed and the resultant changes in
availability to each survey technique are a cause of serious concern.
Concerns regarding vessel avoidance, gear performance, and
interactions between gear and fish during bottom trawl surveys have
received a great deal of attention (Clark, 1979; Engas and Godo, 1986;
Koeller, 1991; Olsen, 1990; Ona and Godo, 1990; Wardle, 1986). The
development of instruments for monitoring some aspects of gear
performance has been of great importance in this context. Such equipment
is now used on a routine basis during EBS bottom trawl surveys (Rose and
Walters, 1990).
The estimates of wingspread used prior to 1988 introduced bias into
the pollock abundance assessment process because they did not account
for the effect of varying scope. These early estimates were based on
averages of small numbers of measurements taken in various locations,
and for each survey the mean wingspread for the net aboard each vessel
was used to estimate area swept. Work by Godo and Engas (1989) and Rose
and Walters (1990), among others, has demonstrated that trawl width
increases with scope. Most pollock are found in deeper water, where
scope lengths and, therefore, wingspreads are greater than average. Thus
for the greater proportion of pollock catches, net wingspread would have
been underestimated and biomass overestimated. Since juvenile pollock
are generally found in shallower waters than adults, it is likely that
this source of bias incorporates an age-specific component.
In the area-swept calculations, it is assumed that the effective
width of the net is equivalent to the wingspread. Work by Engas and Godo
(1989a) indicates that the effective width of a demersal trawl used for
sampling gadoids is related to fish size. In general, they demonstrated
that, as sweep length (distance between trawl doors and net) was
increased, catch rates of Atlantic cod, Gadus morhua, and haddock,
Melanogrammus aeglefinus, increased with increasing fish length. They
concluded that the herding effect is greater for larger fish. Loss of
small fish under the net, as observed by Engas and Godo (1989b) is
thought to be minimal in the EBS surveys because the net does not have
roller gear and is rigged to dig into the bottom slightly in order to
better sample crabs.
The second component of the area-swept estimate is distance
travelled along the bottom. Net contact with bottom does not occur until
after the winch brakes are set and the gear settles. The rate at which
the gear settles is influenced by winch and vessel speed, water
currents, depth, and net construction. At the end of the tow the net
does not lift off as soon as the winches are turned on. However, the
actual forward motion of the net across the bottom during haul back is
difficult to determine. Even if the exact distance were known, the
degree to which it is appropriate to correct for time off bottom is not
clear because of the confounding effect of species and size related
patterns of behavior. Beginning in 1993, new techniques will be used to
address this problem. By using a time-depth recorder fitted to the net
and Global Positioning System (GPS) navigation, exact time and position
of settling and lift off can be determined. Thus haul duration can be
measured and anomalous gear behavior identified. However, techniques are
not yet available for observing how well the gear stays in contact with
the bottom (bottom tending). There is also some concern that the area
swept is based on distance travelled rather than the quantity of water
passing through the net. Gear flowmeters are available to investigate
this issue but they have not yet been used during AFSC surveys.
The procedure for fishing power correction (FPC), or
standardization of observations to the most efficient vessel-gear
combination has also changed in recent years. The new technique is
considered to be more statistically appropriate than the method employed
previously. However, the FPC procedure considers only species-specific
effects and does not take size-specific factors into consideration.
Also, the decision to adjust area swept estimates to the most efficient
vessel-gear combination is based on the implicit assumption that
catchability cannot exceed unity.
Younger pollock tend to remain in the water column and older fish
are generally more demersally oriented. Several researchers (e.g.,
Olsen, 1990; Nunnallee(2)) have demonstrated that gadoids may dive in
response to perceived disturbance from vessels and/or trawls. This
behavior could lead to changes in relative availability to each
assessment method. Size specific differences in patterns of avoidance
are also likely. With the exception of 1979, the demersal survey biomass
estimate of age 1 fish has always been higher than that obtained by
EIMWT. Midwater estimates of age 2 and 3 pollock are generally higher
than in the demersal survey, but the reverse is true for most ages
greater than 3 in the majority of years. If the demersal trawl gear that
was introduced in 1982 sampled age 1 fish with greater efficiency than
before, this could partially explain the unusually high proportion of
age 1 fish observed by the EIMWT method in 1979. It should be noted,
however, that the 1978 year class was extremely large, and its midwater
abundance in 1979 was very high. The change in gear type has undoubtedly
compromised the integrity of the time series of data in a number of
ways. Unfortunately, however, limited resources and inclement weather
have precluded any meaningful comparison of the two trawl types.
Size and age composition of the midwater component of the stock is
estimated by applying the information obtained from midwater trawling to
the echo integration results. Thus, the degree to which the trawl
samples represent the actual composition of the echo sign is a
fundamental concern. The process of judging echograms and assigning
biological characteristics based on trawls is somewhat subjective. Hylen
et al.(3) believe the process of assigning biological characteristics to
be a principal source of error in the determination of size and species
specific acoustic abundance estimates (Aglen, 1989). Errors that result
from avoidance, selectivity, or herding will be reflected in the
size-and age-specific abundance estimates. Of particular concern are
size-specific phenomena such as selectivity, or differences in avoidance
reactions. The observations of Engas and Godo (1989b) regarding the
greater degree to which larger gadoids are herded into the path of a
bottom trawl are probably also applicable in the pelagic zone; one might
also expect greater escapement of small fish through the rope wings of
the midwater trawl. It is not known if the diving avoidance behavior observed by Nunnallee(2) occurs to a greater degree in larger fish, but
their stronger swimming abilities and greater stamina suggest this
possibility.
Echo Integration
Calibration is an essential component of a quantitative acoustic
assessment program. The system was calibrated frequently, and echo
sounder performance was monitored during the surveys.
Due to the limited dynamic range of the echo sounder and the need
to set an integration voltage threshold high enough to eliminate
extraneous noise, we undoubtedly obscured acoustic returns from low
density distributions of pollock during these surveys. The degree to
which this resulted in underestimation of abundance is unknown, but our
general observations of the pattern of pollock aggregation and
distribution suggest that this problem was not severe, especially since
the survey area is relatively shallow.
Before 1988, a constant average TS value was used in biomass
estimation calculations. Selection of too low a mean TS value would have
led to an overestimate of fish abundance; this would have been more
likely when smaller fish predominated, such as in 1979. This is because,
in general, the TS per unit weight for small fish is greater than for
large fish. The use of observed fish length compositions and the
empirical TS-length relationship of Foote and Traynor (1988) to compute
mean TS in 1988 makes some progress towards addressing the problem but
relies heavily on the assumption that the midwater trawl catches
accurately represent the size composition of the fish sampled
acoustically (further implications of this assumption are discussed
below). In the EBS, schools of juvenile fish are generally spatially
separate from schools of adults, so that the effects of selectivity may
be less severe in this context. Neither TS estimation technique has been
able to take into account behavioral and other factors that influence
fish target strength (Traynor et al., 1990b).
An accurate measure of the acoustic pulse width is essential if
biomass estimates are to be obtained by echo integration. The acoustic
pulse width provides one dimension of the computation used to determine
the amount of energy transmitted into the water. If uncorrected, an
erroneous assumption that the pulse width is too wide will lead an
underestimate of abundance. The reverse is also true. A computer program
was developed to sample the rectified voltage signal from individual
fish targets and calculate the effective integration pulse width
(Traynor and Nelson, 1985).
Sound energy decreases with distance from the transducer due to
spreading and attenuation. To compensate for this, echo sounder
receivers incorporate a time varied gain (TVG) amplifier and provide for
an estimate of attenuation due to absorption by seawater. The AFSC
acoustic system TVG function is measured using a computer program that
samples calibration oscillator signals at 1 m intervals. Deviations from
the theoretically correct TVG were determined and corrected as described
by Traynor and Nelson (1985). If uncorrected, deviations from the
theroetically correct TVG could lead to biased estimates of abundance.
Overcorrection (too much gain) would cause overestimation and
undercorrection would cause underestimation.
The acoustic system and operating procedures were designed to
minimize the effects of self noise. Self noise is the sum of noise
components contributed by the vessel and the electronic equipment. Since
low-noise, scientific quality instruments were used, the principal
potential source of self noise was the survey vessel. During these
surveys, vessel noise was minimized by selection of appropriate engine
speed and propeller pitch, and, on occasion, suspending survey
operations during inclement weather.
Reverberatory noise occurs when the transmitted sound pulse
intercepts bubbles or biological sound scatterers (i.e., organisms other
than the target species). In general, during the EBS surveys, most
ambient or reverberatory sources of noise were eliminated or reduced to
an insignificant level by setting an appropriate signal threshold and
eliminating data from nontarget species during data processing. It
should be noted, however, that the process of setting an appropriate
system threshold is one of compromise; setting a threshold high enough
to eliminate most extraneous noise will result in the elimination of
returns from fish, especially at low levels of density. The transducer
was generally towed deep enough to avoid near-surface noise from air
bubbles but no deeper than the shallowest expected occurrence of pollock
(Traynor et al., 1990b).
Separation of fish echoes from bottom echoes is subject to physical
and operational limitations. System parameters limit the absolute
ability of an echo sounder to separate near-bottom targets from the
bottom itself and fish in contact with the bottom cannot be assessed by
echo integration. Provided that echo integration is carried out in small
discrete depth intervals, it is usually possible to eliminate unwanted
bottom echoes from the data and include acoustic returns from fish
within a short distance (2--3 m) of the bottom. This procedure was
followed during AFSC data collection and analysis.
The methodology discussed above refers to the AFSC acoustic system
that was in use through the 1988 triennial survey. Beginning in 1991, a
new set of instruments, with improved stability, dynamic range, and
signal-to-noise ratio has been employed (Knudsen, 1990). The basic
methodology has not changed, but technical improvements have reduced the
potential impact of some of the aforementioned concerns.
Overall Estimates
All the aforementioned biases are of concern when combining the
results of the pelagic and demersal assessments. Each method is subject
to a series of biases and it is likely that combining the two sets of
estimates will exacerbate the effects. The basic assumption implicit in this procedure is that the effective sampling height of the bottom trawl
is 3 m, that all demersal fish are fully available only to the bottom
trawl, and all pelagic fish are fully available only to the acoustic
assessment. It is also assumed that all sizes of fish in each zone have
a catchability of unity to the respective assessment method. In the
preceding paragraphs we have presented evidence to suggest that these
assumptions may not be completely valid. For example, diving avoidance
behavior may increase the availability of pelagic fish to the demersal
trawl and reduce their availability to the pelagic trawl. This may
result in inaccuracies in both demersal and pelagic size and age
composition estimates. Godo and Wespestad (1990) postulate that this is
indeed the case, and that it led to substantial overestimation of older
fish in 1988, as indicated by a divergence of fishery based and survey
based estimates in that year. Their argument is plausible because it
considers the tendency of the bottom trawl to sample larger fish with
greater efficiency in the horizontal plane due to herding and in the
vertical plane due to diving avoidance behavior. The diving behavior
would probably also lead to an underestimate of the proportion of larger
fish in the pelagic region.
Preliminary results of the 1991 triennial survey add further weight
to this argument (Williamson)(4). With the new acoustic assessment
system, pelagic pollock biomass estimates covered the water column down
to 1.0 m off bottom. The preliminary pelagic biomass estimate was 2.1
million t and the preliminary bottom trawl estimate (covering the lower
3 m) was 5.0 million t. Extrapolation of the echo integration results to
the bottom increases the overall EIMWT estimate by a relatively small
amount. This suggests that the effective width of the bottom trawl is
considerably greater than the distance between wingtips and the
effective height is greater than 3 m.
As mentioned earlier, bottom trawl surveys are conducted during
daylight, while acoustic and midwater trawl sampling are carried out
during daylight and darkness. Much work has been done on the effect of
diel changes on fish behavior and assessment results throughout the
world (e.g., Engas and Soldal, 1992; Wardle, 1986; Woodhead, 1964) but
this phenomenon has not been investigated extensively with regard to
Bering Sea pollock assessment. The impact of these phenomena on survey
results can be substantial, and considerable research is called for. It
also seems reasonable to evaluate the manner in which survey data is
used to tune the fishery based analysis; perhaps the demersal and
pelagic estimates could be considered as independent estimates of the
condition of certain sets of age groups. Sample and Bakkala (1989)
demonstrated a highly significant regression when comparing bottom trawl
and cohort analysis estimates of age 4--9 pollock abundance for the
period 1979--86. Since the population ageing process is gradual, one
might expect the size dependent phenomena discussed above to have
influenced the annual bottom trawl (and triennial EIMWT) results
gradually over a period of years. If this had been the case, it might
have been apparent in the work of Sample and Bakkala (1989); it would be
interesting to extend their analysis with recently obtained data.
Toward Improved Assessments
As we recognize the various problems associated with bottom trawl
and EIMWT surveys we must address them in a systematic manner. In the
light of recent work carried out at AFSC and elsewhere, appropriate
research is being planned.
Relationships between net width and trawl warp determined by Rose
and Walters (1990) have been applied to the historic 83--112 trawl data
for which direct width measurements were not made. This enabled us to
make corrections in the area swept estimates and investigate the degree
of bias associated with assumptions regarding the horizontal opening of
the net. Biases leading to overestimates in the earlier analyses
(especially for trawls made in deeper water) were apparent in all but
one year. Overall, the magnitude of the bias was approximately 3%, a
value less than we originally expected. For species with predominantly
inshore, shallow-water distributions, underestimation biases were
indicated.
The CPUE values have now been used to reevaluate the FPC estimates
necessary to complete a new set of biomass estimates for the time
series. After applying these two sets of corrections, it will be
necessary to review the multi-year data set. It must be recognized that
these corrections will not account for all sources of error. For
example, if wingspread exceeds design limitations, changes in gear
performance can be expected. It has been argued that the FPC approach is
no more than an interim solution and will be eliminated when we better
understand fish behavior in relation to fishing gear and can take
significant phenomena into account in our assessment process (Munro(5)).
Research will be directed towards in situ monitoring of gear
performance and establishing techniques for maintaining performance
within design limitations. The work of Engas and Ona (1991) on the use
of restrictors for door spread shows promise in this regard.
The innovative approach to determining settling and haulback time
and distance fished described above will help reduce errors in area
swept calculations and enable us to better identify poor hauls. We are
also concerned with the problems of subsampling large catches and
interested in the recent work which investigated the advantages and
disadvantages of shorter tow durations (Godo et al., 1990).
Other problems in fishing gear technology are more difficult to
research and will require a major effort. It is essential that research
on gear design and fish behavior in relation to fishing gear be assigned
high priority if we are to understand and address the biases in our
survey estimates.
The data presented above suggest that larger pollock are more
demersally oriented but we are not sure of the extent to which this
perception is tainted by interactions between fish and sampling gear. We
are now able to collect continuous TS measurements through the water
column during the surveys. Provided that suitable target densities can
be encountered, and the single target selection algorithm is equally
effective through the range of depths sampled, we will be able to use TS
measurement data to examine possible trends in size with proximity to
the bottom. It should also be possible to design experiments to
investigate how such trends are influenced by the passage of a trawl.
Because of the influence of fish behavior on TS these types of
observations will have to be evaluated with caution.
The work of Engas and Godo (1989a) suggests that we must
investigate the effect of sweep length on the size (and species)
composition in our catches. This leads to a consideration of priorities.
Because the trawl survey is designed to assess a multispecies community,
it will probably never be possible to optimize the design with respect
to pollock. Since most of the species sampled by the bottom trawl are
truly demersal, perhaps we need to develop an alternate technique for
assessment of this semi-pelagic species. Regardless, it is essential
that we investigate the size and species-specific sampling efficiencies
of our sampling trawls.
We believe that it may be possible to develop the EIMWT technique
to produce satisfactory total water column estimates of pollock
abundance. Recent work on problems of near-bottom detection (Ona, 1988
(cited in Godo and Wespestad, 1990) and Mitson, 1983) suggests that it
may be possible to collect useful integration data very close to the
bottom and make appropriate corrections for regions of the acoustic beam
that are obscured in this near bottom region. While the physical
limitations have not changed, our understanding of the limitations has
improved, and newly developed tools for collecting and processing echo
integration data will make it easier for us to conduct research in this
area (Knudsen, 1990; Foote et al., 1991). It is important to bear in
mind that this approach will still require us to make assumptions about
fish distribution and behavior close to the bottom, and these
assumptions may be difficult to test.
We will still be faced with some questions regarding trawl sampling
biases when it comes to developing age specific abundance estimates.
This will become even more critical if we are to expand our EIMWT method
into the demersal zone. An alternative approach would involve using
acoustic measurements to investigate and document availability of
pollock to demersal gear. Much research remains to be done if we are to
develop effective techniques for combining biological information from
midwater and bottom trawls while accounting for the biases inherent in
the use of each type of gear.
The methods described above are designed to provide estimates of
absolute abundance. However, we have presented overwhelming evidence of
substantial bias in our survey results. This supports the argument that
survey results should be considered as indices of relative abundance
that have significance only as elements in a time series. Even under
this constraint, we must work under assumptions regarding the
consistency of bias which may be difficult to support.
Realistically, however, we must consider the manner in which survey
results are applied. Stock assessment models that are used to determine
allowable biological catch (ABC) levels for commercial fisheries require
a source of absolute abundance information. This can be obtained from
analysis of historic fisheries data or from survey results. Analysis of
fisheries data requires reliable time series of catch and effort
information and realistic estimates of natural mortality and terminal
fishing mortality rates.
For some fisheries, data are insufficient, and in other cases
assumptions regarding mortality rate estimation may be difficult to
support. This leaves us on the horns of a dilemma. Are we more willing
to accept the assumptions implicit in developing absolute abundance
estimates from survey data than those implicit in the analysis of
fishery data? The problem can be resolved by taking a pragmatic
approach, recognizing the limitations under which we are forced to work
and making best use of the data that is available. Inevitably we will
sometimes have no choice but to use survey results as measures of
absolute abundance. This serves only to emphasize the need for all
scientists involved in stock assessment to understand the limitations in
their data and investigate approaches to improving the quality of
information used in the stock assessment process.
Acknowledgments
We wish to acknowledge the advice of Arill Engas, David Somerton,
Jim Traynor, Mark Wilkins, and Russell Nelson in preparing this
document. This manuscript was originally presented at the 1991 statutory
meeting of the International Council for Exploration of the Sea in La
Rochelle, France.
(1)Kappenman, R. F. 1992. Estimation of the fishing power
correction factor. U.S. Dep. Commer., NOAA, Natl. Mar. Fish. Serv.,
Alaska Fish. Sci. Cent. Proc. Rep. 92--01, 10 p.
(2)Nunnallee, E. P. 1991. An investigation of the avoidance
reactions of Pacific whiting (Merluccius productus) demersal and
midwater trawl gear. Pap. pres. to Fish Capture Committee, Int. Counc.
Explor. Sea, C.M. 1991, paper/B:5, Session U.
(3)Hylen, A., O. Nakken, and K. Sunnana. 1986. The use of acoustic
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assessment, and management of gadoids from the North Pacific and
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Alaska Fish. Cent., Natl. Mar. Fish. Serv., NOAA, 7600 Sand Point Way
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(4)Williamson, N.J. NMFS Alaska Fisheries Science Center, 7600 Sand
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on recent stock assessments is provided in the 1993 stock assessment and
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Sea/Aleutian Islands, and it is available from the North Pacific Fishery
Management Council, P.O. Box 103136, Anchorage, AK 99510.
(5)Munro, P. NMFS Alaska Fisheries Science Center, 7600 Sand Point
Way N.E., Seattle, WA 98115. Personal commun.
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