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ABSTRACT:
Infauna influence geoacoustic parameters in surficial marine sediments. To investigate these effects, an experiment
was conducted in natural sand-silt sediment in the northern Gulf of Mexico. In situ acoustic measurements of sedi-
ment sound speed, attenuation, and shear speed were performed, and sediment cores were collected from the upper
20 cm of the seabed. Laboratory measurements of sound speed and attenuation in the cores were conducted, after
which the core contents were analyzed for biological and physical properties. Since no model currently accounts for
the effects of infauna, a deviation from model predictions is expected. To assess the extent of this, acoustic measure-
ments were compared with the viscous grain shearing model from Buckingham [J. Acoust. Soc. Am. 122, 1486
(2007); J. Acoust. Soc. Am. 148, 962 (2020)], for which depth-dependent profiles of sediment porosity and mean
grain size measured from the cores were used as input parameters. Comparison of acoustic results with distributions
of infauna, worm tubes, and shell hash suggests biogenic impacts on acoustic variability and model accuracy are
2456 J. Acoust. Soc. Am. 152 (4), October 2022 0001-4966/2022/152(4)/2456/19/$30.00 C 2022 Acoustical Society of America
V
https://doi.org/10.1121/10.0014907
including bivalves and polychaetes, can capture fine sus- II. EXPERIMENT
pended particles, aggregate them, and deposit them as
A. Overview
fecal pellets on the sediment surface. Bioirrigation of bur-
rows transports oxygen to anoxic subsurface sediments, A field experiment was conducted during May 8–11,
creating sharp redox gradients and modifying sediment 2017, in Petit Bois Pass, a channel that lies approximately
chemistry.12 Increased cohesion by exopolymeric substan- ten miles off the northern Gulf of Mexico coast and in
ces (EPS) secreted by microbes and microalgae can con- between the barrier islands of Petit Bois Island, Mississippi
tribute to enhanced shear strength near the sediment to the west and Dauphin Island, Alabama to the east
surface;13 however, infaunal organisms can substantially (Fig. 1). A seabed lander with acoustic probes (Fig. 2) was
reduce the stabilizing effects of EPS through bioturba- deployed from the vessel (the R/V E. O. Wilson) to the sea-
tion.14 These combined effects can manifest as temporal bed surface to collect in situ measurements of sediment
and spatial variability in compressional and shear wave sound speed, sound attenuation, and shear speed within the
propagation parameters in the seabed surficial sedi- top 20 cm of the sediment, spanning the depth range within
ment,15–19 which can impact acoustic scattering from and the sediment in which infaunal activities are expected, gen-
propagation into the seabed.20–28 Further investigation is erally in approximately the top 10 cm.7 Diver cores were
needed to determine the effects of infauna on sound propa- collected from each measurement location to sample the
gation in ocean bottom sediments, which could better sediment’s physical properties (bulk density, porosity, and
inform sonar operation in various shallow-water applica- grain size distribution), the local infauna distribution, and
tions, as well as the use of acoustics for remote sensing of the biogenic features of shell hash and worm tubes. Prior to
benthic ecosystems.29–31 destructive sampling, the cores were vertically scanned with
A deficiency that exists in our present understanding of an acoustic core logger to provide additional sound speed
sediment acoustics is that predictive models do not explic- and attenuation measurements. Vertical gradients were
itly account for the physical impacts of volume heterogene- examined within two sites, as infauna are most abundant
ities (e.g., infauna bodies or burrows, worm tubes, or shell near the sediment-water interface, and the experiment tar-
hash) on geoacoustic properties.32–34 Part of this stems from geted sites with different communities, specifically higher
J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al. 2457
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FIG. 3. (Color online) CARL apparatus: (a) photograph of CARL set up in the laboratory benchtop and schematics of (b) transmission and (c) resonance
modes. Diagrams in (b) and (c) are adapted from Ref. 45 with permission from Gabriel R. Venegas. (C) Copyright 2019, Gabriel R. Venegas.
sediment, shell hash, and mucus that may increase attenua- pffiffiffiffiffiffiffiffiffi
cs =q
tion due to the scattering of acoustic energy;19 and Soft- cs ¼ 1=2 ; (3)
bodied, Soft-tube, Structuring (SSS) worms that build tubes Re ðixTÞn gs ðxÞ
of fine-grained sediment and mucus that may increase shear
strength but are unlikely to substantially increase scattering. and
Additional details about the diver core analyses are provided rffiffiffiffi
q 1=2
in supplementary material.44 as ¼ x Im ðixTÞn gs ðxÞ ; (4)
cs
FIG. 4. (Color online) Depth dependence of sediment physical properties measured from the 7.6-cm-diameter cores. Grain size fractions are gravel (circles),
Petit Bois Pass) was potentially influenced by the hydrody- group, which includes larger hard-bodied or hard-shelled
namic environment. Site 2 was near the western edge of the animals such as brittle stars, crustaceans, and mollusks that
pass and potentially less affected by current, and thereby burrow in the sediment. The body sizes of many of the
better able to retain finer grains near the seabed surface. For HNM animals were on the order of 1 cm or greater, thus
the grain size distributions here, the inclusive standard devi- they are potential acoustic scatterers at the upper end of the
ation was 1 < rI < 2:5, indicating poorly to very poorly acoustic frequencies used in this experiment.
sorted grain size distributions based on the descriptive ter- Another functional group of potential acoustic signifi-
minology of Folk and Ward,52 in contrast to sediment acous- cance at these sites was the soft-bodied, hard-tube, struc-
tic model assumptions of a well sorted distribution turing (SHS) group, which included hard-tube-building
characterized by the mean grain size. worms such as Owenia and Diopatra. These animals struc-
ture the sediment by building tubes made from shell frag-
B. Infauna, worm tubes, and shell hash ments, sediment, and mucus. Although the biomass of SHS
was lower than that of the hard-bodied group, the mass of
Because the distributions of the depth-integrated mass tubes was high, especially at Site 1, which had an approxi-
per surface area of infauna, worm tubes, and shell hash from mately six times greater median hard worm tube mass than
the cores at each site tend to have a great deal of spread and Site 2, primarily from the polychaete, Owenia fusiformis
contain several outliers, the results are reported in terms of (Table I). The diameter of the Owenia tubes ranged
median and interquartile range instead of mean and standard between 2 and 5 mm (2.6 6 1.0 mm at Site 1 and
deviation (Table I). For comparison, the depth-integrated 2.8 6 1.6 mm at Site 2, mean 6 standard deviation), but
mass per surface area was estimated from cores that were the tube can extend from above the surface down to
processed for sediment properties. Infauna, hard worm 5–10 cm depth; therefore, they are also good candidate
tubes, and shell hash represented approximately 0.02%, acoustic scatterers.
0.03%, and 0.3% of the mass per surface area of the overall The soft-bodied, soft tube, structuring (SSS) and soft-
seabed material, respectively. bodied, no tube, mixing (SNM) functional groups were also
The total infauna biomass per site was similar, with the present, although in small biomass quantities that were simi-
Site 1 median value being approximately 1.5 times greater lar between the sites. Thus, it is assumed that these animals
than Site 2. Most of the animal biomass at both sites fell had less potential influence on the sediment and, hence, the
into the hard-bodied, no tube, mixing (HNM) functional acoustics at these sites.
J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al. 2461
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TABLE I. Median (and interquartile range) of depth-integrated masses per relatively constant over the upper 20 cm (Fig. 5). For the
surface area of infauna, worm tubes, and shell hash at each site. For com- most part, there was approximately twice as much shell hash
parison, the depth-integrated mass of sediment per surface area at each site
is given. The depth integration spans the upper 20 cm, and all quantities are
at Site 1 than Site 2 over all depths, with the exception of
given in units of g m2. one high shell hash mass density value observed close to
20 cm from one core at Site 2.
Quantity Site 1 Site 2 Overall, Site 1 had more hard worm tubes, SHS func-
Total infauna 155.8 (191.2) 102.9 (52.6) tional group infauna, and shell hash than Site 2, but two sites
Hard-bodied, no tube, mixing (HNM) 119.7 (189.5) 104.5 (41.8) had similar overall amounts of infauna. Both sites had simi-
Soft-bodied, no tube, mixing (SNM) 4.3 (4.5) 2.1 (7.3) lar depth-dependence of infauna (negative gradient) and
Soft-bodied, hard tube, structuring (SHS) 6.3 (16.9) 0.6 (6.1) shell hash (no gradient). Finally, Site 1 had a higher mass of
Soft-bodied, soft tube, structuring (SSS) 7.3 (6.2) 10.4 (10.1) hard worm tubes near the surface than Site 2.
Hard worm tubes 370.6 (407.9) 63.7 (79.6)
Shell hash 2906.0 (117.6) 1527.3 (647.6) V. ACOUSTIC RESULTS
Sediment 698 103 681 103
Acoustic results are presented in this section from the in
situ field measurements and the laboratory CARL measure-
Site 1 had roughly twice as much mass per surface area ments. By combining the in situ and CARL data sets, the
of shell fragments present compared to Site 2 (Table I). Site acoustic behavior of the sediment can be examined over
1 also had larger fragments of shell hash, 3.5 6 1.6 mm at many decades of frequency, between 8 and 300 kHz for
Site 1 compared to 2.3 6 1.3 mm at Site 2 (mean 6 standard sound speed ratio, 60–300 kHz for attenuation, and
deviation). 0.2–0.9 kHz for shear speed.
Vertical profiles of infauna biomass density ninf (Fig. 5) Rather than simply presenting the measurements by
displayed negative vertical gradients at both sites, where themselves, they are compared with the VGS model to place
most of the infauna resided in the upper 7.5 cm of the sedi- the acoustic measurements in context with the measured
ment, 72% at Site 1 and 69% at Site 2. Thus, the infauna profiles of sediment bulk properties and grain size distribu-
tion. Therefore, the selection of model inputs is first dis-
FIG. 5. (Color online) Vertical profiles of the infauna, worm tube, shell hash mass density, and mean shell fragment size for Site 1 (circles) and Site 2 (dia-
monds). All measurements from each core collection location within each site are plotted to demonstrate the level of intra-site variability. Data from individ-
ual cores are connected by lines.
2462 J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al.
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X 2
physical parameters (b, qf, qs, Bf, Bs, H, d, and u), ten fixed E ¼ min Mðs0 ; fj Þ cð fj Þ ; (15)
0 s
constants (cp0 ; cs0 , b0, d0, u0, H0, qs0 , q0, n, and T), and the j
two viscoelastic time constants sp;s . All of the measurable
parameters can be obtained from either the literature or anal- where Mðs0 ; fj Þ is the modeled sound speed at the jth fre-
ysis of the sediment cores, pore fluid, or bottom water prop- quency for the value s0 of the viscoelastic time constant and
erties. Tabulated values for pore fluid density qf, grain cð fj Þ is the measured sound speed. After the best-fit value of
bulk modulus Bs, grain density qs, and H were taken from sp was found for each site, computed high-frequency values
the literature.2,40 Pore fluid bulk modulus was estimated of sound speed and shear speed well above the compres-
using the pore fluid density and mean measured bottom sional threshold frequency (ft;p ¼ 1=2psp ) were used to cal-
water sound speed, Bf ¼ qf c2f . For depth-dependent data- culate ss from Eq. (9).
model comparisons, vertical profiles of porosity b and mean The best-fit values of sp and ss for each site are listed in
grain size u averaged over the various core measurements Table III, and these parameters were then combined with
shown in Fig. 4 were directly input into the VGS model. vertical profiles of porosity and mean grain size from the
Although the grain size fraction varied with depth in the cores as inputs to the VGS model. Average vertical profiles
sediment, the predominate grain size classes were sand and were computed from the porosity and mean grain size data
silt; therefore, single values of qs, Bs, and H for quartz were shown in Fig. 4 and were used as direct inputs to the VGS
used. The fixed constants were given in previously pub- model to produce depth-dependent predictions of cp, ap, and
lished literature40 and are listed in Table II, and the visco- cs for comparison with the acoustic data. To calculate the
elastic time constants were determined by a fit to the depth-dependent compressional and shear moduli, each core
broadband sound speed ratio data. section was treated as a sediment layer, and the porosity,
The compressional viscoelastic time constant sp was grain size, and thickness of each section were input
obtained by fitting Eq. (1) to the broadband (8–300 kHz) directly into Eqs. (13) and (14). The depth-dependent VGS
combined in situ and CARL sound speed ratio data sets. models were then computed at the same frequencies as the
For this fit, the model was implemented with a homoge- in situ and high-frequency CARL measurements for direct
neous sediment with compressional and shear moduli comparison.
J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al. 2463
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grain size decreased and the porosity increased with increas- exceed the model predictions at shallower depths. Scatter in the
ing depth, leading to a predicted sound speed ratio profile high-frequency sound speed data at Site 2 encompasses the
with a negative gradient (i.e., sound speed decreases with range of depth-dependent VGS predictions; however, there is
depth). Site 2 had more uniform porosity and mean grain little correlation between the shallower measurements and
size profiles, thus the predicted sound speed increases with predictions.
depth (a positive sound speed gradient). Site 1 sound speed ratio decreased with sediment depth
The low-frequency sound speed data from CARL’s reso- (Fig. 7), which was more evident in the CARL measure-
nance mode (Fig. 6) represent the effective sound speed of the ments because the in situ measurements had much coarser
entire core averaged over the entire 20-cm measurement depth depth-resolution and did not extend closer to the interface
interval. The measured low-frequency sound speed ratios than 5 cm. As noted previously, this decrease in sound speed
tended to be less than unity, indicating that at low frequencies ratio with depth was in part due to the increase in porosity
the sediment was acoustically similar to mud at both sites, and and decrease in mean grain size with depth at this site. In
the low-frequency CARL measurements approached the depth- situ sound speed ratio measurements at Site 1 tend to be
averaged VGS low-frequency limits for each site. Similar to higher than the VGS model predictions by approximately
the VGS prediction, there was an increase in sound speed 2%–5%, and this difference is greatest at the lowest frequen-
between the low-frequency CARL measurements and the cies where the in situ measurements partially overlapped the
higher frequency in situ measurements, and sound speed vari- transition region predicted by the VGS model. Site 1 high-
ability was greatest in the high-frequency CARL measure- frequency CARL measurements in the 4–20 cm depth inter-
ments. The high-frequency sound speed values at Site 1 were val are in good agreement with the predicted sound speed
approximately 2.5% higher than those at Site 2. The deeper ratio profile; however, the measurements deviate from the
high-frequency CARL measurements from Site 1 agree better predicted sound speed ratio in the 1–4 cm interval closest to
with the deeper VGS-predicted sound speed ratios, but they the seabed surface, where the measured sound speed ratio
FIG. 6. (Color online) Comparison of measured sound speed ratio, attenuation, and shear speed with VGS model predictions for both sites. Data are repre-
sented by monochrome circles (LF CARL resonance mode sound speed ratio), variegated circles (HF CARL transmission mode sound speed ratio and atten-
uation), and variegated diamonds (in situ sound speed ratio, attenuation, and shear speed), where darker hued markers indicate shallow sediment depths and
the shading becomes lighter for increasing depth (in situ and HF CARL only). Vertical error bars indicate the measurement uncertainty. VGS model predic-
tions for depth-averaged porosity and mean grain size are short-dashed black lines, and the solid gray lines indicate VGS model predictions at depths
between 1 cm and 21 cm in 4-cm increments (darker represents shallower depths). Thinner, long-dashed lines in the bottom row are the depth-averaged VGS
shear speed prediction with ss ¼ 1.
2464 J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al.
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FIG. 7. (Color online) Comparison of measured and modeled sound speed ratio profiles for both sites. Vertical profiles for Site 1 are displayed on the top
row, Site 2 profiles are on the bottom row. Measurement frequency increases from left to right. For comparison with Fig. 6, the same variegated symbols are
used to represent in situ data (diamonds) and high-frequency CARL data (circles). The solid lines are the VGS model predictions using the average porosity
gradient steepens and the variability in the measurements k ¼ 1.23 for Site 2, revealing a departure from linear fre-
increases. In contrast, both the in situ and CARL sound quency dependence.
speed ratio measurements are in better agreement with the Based on the porosity and grain size vertical profile
VGS model at Site 2; however, variability in the measure- measurements from the cores, the VGS model predicts
ments is greatest at this site in the 1–4 cm interval CARL increasing attenuation with depth at both sites, in which the
measurements, as is the discrepancy between the data and attenuation at Site 1 is expected to double with increasing
the model. Finally, both in situ and high-frequency CARL depth in the 1–20 cm interval and increase by a factor of 2.3
data sets include measurements at a frequency of 100 kHz, in the same interval at Site 2 (Fig. 8). Note that the measured
and it should be noted that the data points from these differ- and predicted gradients do not change much across the
ent measurement systems overlap at this frequency. 60–300 kHz band for both sites, whereas the measurement-
model deviation increases with frequency. The in situ atten-
2. Attenuation uation measurements at both sites are over-predicted by the
VGS model by factors between 1.4 and 2.7, with larger
Below the threshold frequency ft;p , the VGS model pre- data-model deviation observed at the lowest frequencies.
dicts that the attenuation scales with frequency squared, High-frequency CARL measurements at both sites are in
whereas above the threshold frequency the attenuation is good agreement between 100 and 140 kHz below 4 cm,
expected to scale approximately linearly with frequency. although the model tended to under-predict the data above
The lowest frequency in situ attenuation measurements 4 cm. Like the sound speed profiles, the variability in the
(60 kHz) are just above the expected threshold so no data attenuation measurements is highest in the 1–4 cm interval.
are available for comparison with the predicted sub- As noted, before, the high-frequency CARL attenuation
threshold frequency dependence (Fig. 6). The attenuation measurements are under-predicted by the VGS model in the
data between 60 and 140 kHz roughly agree with the VGS 180–300 kHz band, and this disagreement occurs over a
prediction, although a good deal of variability is present in greater portion of the measurement depth-interval as the fre-
the data, which is not captured by the depth-dependent quency increases (Fig. 8). This is most apparent at 300 kHz,
model predictions. Above 180 kHz, the attenuation data where there is higher attenuation measured than predicted
appear to depart from the approximately linear frequency for most of the measurement depth interval. There is greater
dependence predicted by the VGS model. Indeed, compar- deviation between the attenuation measurements and model
ing the high-frequency CARL data above 180 kHz to a at Site 1, particularly at higher frequencies, which could be
power law fit, ap f k , we find that k ¼ 1.31 for Site 1 and influenced by the greater abundance of hard worm tubes at
J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al. 2465
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FIG. 8. (Color online) Comparison of measured and modeled attenuation profiles for both sites. For comparison with Fig. 6, the same variegated symbols
are used to represent in situ data (diamonds) and high-frequency CARL data (circles). The solid lines are the VGS model predictions using the average
porosity and mean grain size profiles as inputs. The confidence bounds on the model based on variability from the core data are too small to be visible in the
Site 1, which might have more of an effect as frequency speeds tend to skew roughly 50% lower than the best-fit
increases. model predicts on average, indicating the sediment is
slightly softer than is predicted by the VGS model based on
3. Shear speed the porosity and mean grain size inputs from the cores.
Values of shear speed measured at both sites range
VI. RELATING DATA-MODEL DEVIATION
between 10 and 40 m s1 (Figs. 6 and 9). The VGS model TO BIOLOGICAL PARAMETERS
shear speed prediction overlaps with the measurements at
the lower end of the 0.2–0.9 kHz band; however, the mea- In this section, relationships between the deviation from
sured shear speed displays little variation with either depth the acoustic data to the VGS model and infauna, worm tube,
or frequency, which is in disagreement with the model. Note and shell hash mass density profiles are examined to test the
that the shear threshold frequency, ft;s ¼ 1=2pss , is 1.7 kHz hypothesis that the infaunal community alters sediment
for Site 1 and 1.5 kHz for Site 2, placing the measurement acoustic properties. Although correlations between the data-
band in the transition regime where greater dispersion would model deviation and benthic parameters (e.g., sound speed
be expected. If the shear viscoelastic time constant is set to deviation vs infauna biomass density) are not necessarily an
ss ¼ 1, however, the resulting VGS model prediction indication of cause-and-effect relationship, such correlations
(dashed lines in Fig. 6) exceeds the data by more than a fac- or the lack of correlation are useful in establishing what
tor of two with no overlap between the model and data. It is parameter combinations might be important and could lead
worth noting that in other recent applications of the VGS to more directed future research. Some general data-model
model, the shear viscoelastic time constant is taken to either deviation metrics are introduced first, followed by results of
be infinite39,40 or orders magnitude larger than the best fit the correlation analysis focused on the high-frequency
values here;53,54 however, there have been very little shear CARL data.
wave data in those applications to justify otherwise. The
A. Data-model deviation metrics
predicted shear speed gradient displays an approximately
cubic-root power-law depth dependence (Fig. 9). The in situ To quantify the data-model deviation at each measure-
shear speed data tend to cluster around the mean measured ment frequency and depth, the following quantity dk;j is
shear speed of 25.3 m s1, which is close to the predicted defined:
shear speed at 0.2 kHz at both sites; however, the data-
model deviation increases as the frequency increases for the Dk;j Mk;j
dk;j ¼ ; (16)
entire measurement depth interval. The measured shear Mk;j
2466 J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al.
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FIG. 9. (Color online) Comparison of measured and modeled shear speed profiles for both sites. For comparison with Fig. 6 the same color-shaded symbols
are used to represent in situ data (diamonds). The solid lines are the VGS model predictions using the average porosity and mean grain size profiles as inputs,
and the gray-shaded area indicate the confidence bound the model based on variability from the core data. The thin dashed lines indicate the mean shear
speed over all of the measurements, 25.3 m s1.
measurements (5-cm steps in the 5–20 cm interval), provid- the data from both sites were combined to increase the num-
ing a more detailed description of the depth-dependence, ber of data points N, and the Pearson correlation coefficient
particularly in the uppermost layer of sediment. Only the r was computed. Additionally, p-values were computed for
high-frequency CARL data extend into the 1–4 cm depth each variable pair to assess whether the reported correlation
interval and having data in this interval is crucial for com- was statistically significant, using the p < 0.05 criterion.
parison with the worm tube mass and infauna biomass, since There was statistically significant positive correlation
this interval has the highest concentration of those quanti- between infauna biomass density and the cumulative data-
ties. The high-frequency CARL measurements extend to the model deviation for sound speed (r ¼ 0.32, N ¼ 76) and atten-
frequency band where a significant deviation of the mea- uation (r ¼ 0.42, N ¼ 78) (Fig. 11). The highest correlation
sured attenuation from the VGS model was observed was found between hard worm tube mass density and cumu-
(f > 180 kHz). Therefore, this data set is most useful in lative attenuation error (r ¼ 0.62, N ¼ 61), although this was
investigating whether the data-model deviation is correlated driven primarily by two samples from Site 1 with very high
with the presence of the infauna, worm tubes, or shell hash. worm tube density (Fig. 5). No significant correlation was
Only CARL data from the 15.2-cm cores were used for found between hard worm tube mass density and cumulative
this analysis since these cores provided the measurements of sound speed deviation or between shell hash mass density
infauna biomass, worm tubes, and shell hash. The high- and either sound speed or attenuation deviation.
frequency CARL sound speed and attenuation data were Correlation coefficients were also computed as a func-
sorted into bins that matched the 15.2-cm-diameter core sec- tion of frequency for the frequency-dependent data-model
tions so the two data sets could be compared. These bins deviation dcp and dap . Each correlation coefficient value
were in the following intervals: 0–2.5 cm, 2.5–7.5 cm, was obtained from data pairs spanning all available sedi-
7.5–12.5 cm, 12.5–17.5 cm, and 17.5–22.5 cm. ment depths, similar to the scatter plots shown in Fig. 11,
The acoustic variables considered in this analysis were but for each measurement frequency (Fig. 12). Correlation
the depth-dependent cumulative and frequency-dependent of sound speed deviation with infauna biomass density had
sound speed and attenuation data-model deviation values between r ¼ 0.3 and r ¼ 0.4 for the 140–300 kHz
(jDcp j; jDap j; dcp ; dap ), and the biologically related varia- band, whereas there was no significant correlation at any
bles considered were depth-dependent densities of infauna frequency between sound speed deviation and hard worm
biomass, hard worm tube mass, and shell hash mass tube mass density or shell hash mass density. For attenuation
(ninf ; ntube ; nsh ). For each acoustic-biological variable pair, data-model deviation, there was significant correlation with
2468 J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al.
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both infauna biomass and worm tube mass densities in the A deficiency of the data set is that there were only two
entire 100–300 kHz band (r > 0.5). sites, and they vary in more than two parameters. Therefore,
it is difficult to isolate the effects of the worm tubes, the
VII. DISCUSSION infauna themselves, specific functional groups, shell hash,
A. Spatial variability in biological and acoustic or gradients in grain size and porosity between the two sites
properties and which of these features result in higher variability and
model deviation. We note that the grain size and porosity
Although the two sites in this study were geographi- profiles are direct inputs to the VGS model; therefore, the
cally very close and both contained primarily silt and sand, depth-dependent heterogeneity in sediment type is captured
there were several key differences between the sites. Site 1 to some extent in the depth-dependent profiles of acoustic
had a gradient from sandy to siltier sediment with increas- parameters predicted by the model. Thus, by looking at
ing depth, whereas the sediment at Site 2 was more verti- where the data-model deviation is highest, we focus on bio-
cally mixed. Site 1 had nearly the same total infauna genic effects not accounted for by the model.
biomass as Site 2; however, the infaunal community at Site
1 exhibited a higher fraction of tube-building worms
(group SHS) and approximately eight times higher hard B. Depth-dependence of biological and acoustic
properties
worm tube density near the surface than Site 2, which is
notable because hard worm tubes have been shown to Comparison of the measured sound speed and attenua-
increase attenuation at acoustic frequencies greater than tion with the VGS model predictions indicated better overall
100 kHz.19 Also, noted, Site 1 had about twice as much data-model agreement at sediment depths greater than 5 cm
shell hash as Site 2. Consistent with our hypotheses, Site 1, below the sediment-water interface than in the near-surface
with greater biological activity, also had higher variability layer. Increased variability in the sound speed and attenua-
in acoustic properties and deviation from the acoustic tion measurements also occurred in the upper 1–4 cm of the
model. sediment at both sites. At both sites, most of the infaunal
J. Acoust. Soc. Am. 152 (4), October 2022 Lee et al. 2469
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(a) measurement of porosity from the cores, (b) the effect of and shell hash provide a unique data set for testing sediment
coupling between the in situ probes and the sediment on the acoustics models such as VGS or others and for evaluating
amplitude measurements, and (c) potential timing errors in potential reasons that the models fail. The increased data-
the time delay measurements. Further detail on the measure- model deviation for at high frequencies is particularly inter-
ment procedures and data analysis for all of the measured esting, as these are the frequencies at which we would
quantities are given in Ref. 44. expect inhomogeneities like infauna, tubes, and shell hash to
Regarding the porosity and bulk density measurements, have the largest effect.
evaluating water content from core samples is notoriously The low-frequency CARL resonance mode sound speed
difficult because manipulation of the sediment invariably measurements are consistent with the VGS model transition
involves loss of intergranular water; however, efforts were from high-frequency behavior to the Mallock-Wood sound speed
taken to minimize water loss during collection and labora- low-frequency limit, which is c0 =cf 0:985 for both sites. The
tory sampling of the cores.44 Furthermore, the expressions transition occurs at higher frequency (ft;p 26:5 kHz) than
used to derive porosity and bulk density from the water con- previously estimated for sand (ft;p 1:3 kHz)37,40 or mud
tent measurements did not rely on precise knowledge of the (ft;p < 100 Hz),40,53,54 as shown in Fig. 13. Furthermore, the
volume of the sediment samples, but rather on the wet and low-frequency shear speed measurements, with an average
dry weights of the samples, which were measured, and the value of approximately 25 m s1, are consistent with a shear
densities of the pore water and mineral grains, which are threshold frequency of ft;s 720 Hz, suggesting a softer sedi-
well known,2,44 thereby removing uncertainty contributed ment than would be predicted by lower values of ft;s that have
from the sample volume. been previously suggested for muddy sediment.40,53,54 In the
Another potential source of error in evaluating the data- VGS model, ft;p and ft;s are threshold frequencies above
model deviation could arise from inefficient coupling which the effects of pore fluid viscosity become negligible
between the in situ probes and sediment, particularly in the for compressional and shear waves, respectively. This can
top several centimeters of sediment where the sediment also be interpreted as a threshold wavelength kt, related to the
matrix is easily disturbed. Below 5 cm (the depth range of threshold frequencies via the wave speeds.38 For the sedi-
the in situ measurements), it was assumed that the loading ments here, kt 0:4 cm, which represents a much smaller
FIG. 13. (Color online) Comparison of VGS model predictions for three different values of viscoelastic time constant, corresponding to the fit-determined
values from the present case (sp ¼ 6 ls), sand (sp ¼ 0:12 ms), and mud (sp ¼ 0:01 s), with the data. For all curves shown here, the following depth- and
site- averaged parameters are used: b ¼ 0:62, u ¼ 59 lm, and d ¼ 0.1 m. The remaining model input parameters are given in Table II.
8
worm tubes, shell hash, or other inhomogeneities are present P. S. Meadows and J. Tait, “Modification of sediment permeability and
in the medium,33 and the measurements presented in this shear strength by two burrowing invertebrates,” Mar. Biol. 101, 75–82
paper are consistent with that notion. (1989).
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H. Murray, A. Meadows, and P. S. Meadows, “Biogeomorphological
Another finding of this work was that the VGS com- implications of microscale interactions between sediment geotechnics and
pressional viscoelastic time constant determined from the marine benthos: A review,” Geomorphology 47, 15–30 (2002).
10
data-model fit was inconsistent with previous estimates for A. K. Hannides, S. M. Dunn, and R. C. Aller, “Diffusion of organic and
either sand or mud, and hence the associated threshold fre- inorganic solutes through macrofaunal mucus secretions and tube linings
in marine sediments,” J. Mar. Res. 63, 957–981 (2005).
quency was much higher. There are two possible explana- 11
D. C. Rhoads and L. F. Boyer, “The effects of marine benthos on physical
tions for this inconsistency that are related to the infauna: properties of sediments: A successional perspective,” in Animal-Sediment
(1) the properties of the inter-granular pore fluid have been Relations: The Biogenic Alteration of Sediments, edited by P. L. McCall
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12
N. Volkenborn, L. Polerecky, S. Hedtkamp, J. Beusekom, and D. Beer,
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13
measurements indicated that the sediment at both sites was S. U. Gerbersdorf, R. Bittner, H. Lubarsky, W. Manz, and D. M.
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of the VGS model that did not include sufficiently small 14
E. Deckere, T. J. Tolhurst, and J. Brouwer, “Destabilization of cohesive
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