What follows are preliminary results of an investigation of the 2019-2021 MAM data to assess relationships between invasive carp densities and body condition (relative weight) of invasive carp as well as native, abundant planktivores. The goal of these analyses are to determine the value of MAM for assessing the impact of invasive carp, and by extension, invasive carp harvest on the native fish community.
Based on our conversation, it would seem we have two major hypotheses:
1. invasive carp density is inversely correlated with
invasive carp body condition
2. invasive carp density is inversely correlated with body
condition of native planktivores, putatively due to competition for
consumptive resources
It would seem there is one offshoot hypothesis from this work
directly applicable to management:
3. If a relationship exists between invasive carp desnity and
native planktivore body condition, can one predict with any useful
precision the density of invasive carp from native fish body condition
metrics?
To attack this question immediately, I’m using the available MAM data that is complete and QAQC’d, which is inclusive of 2019-2021. I plan to clean and organize the majority of the 2022 MAM data, but I currently lack some unknown quantity of jarred fish as well as all of La Grange.
I may eventually incorporate LTEF data, which I should have shortly, although I’m unsure how I want to use this data alongside MAM data since LTEF may not be collected in the same design-based methodology that allows for annual pool-wide estimates based on proportions of available and sampled environmental strata in each pool.
I’m limiting the analysis of invasive carp to just Silver carp and Grass carp, as they represent the vast majority of individuals in the system during these years. Hereby, when I say ‘Invasive carp’ I mean Silver and Grass carp combined.| SPECIES_CODE | n | percent |
|---|---|---|
| BHCP | 38 | 0.05 |
| GSCP | 20416 | 24.56 |
| SVCP | 62671 | 75.39 |
Per our conversation, I’m also limiting the analysis to adult Invasive carp. The LTRMP life history database uses 193mm as the cutoff for Silver carp adults and 200mm for Grass carp adults, and after analysing the MAM data I’ve bumped it up to 200mm for our combined grouping of both spp.
Because relative body weight is my choice metric for body condition, I’m eliminating any fish that weren’t measured exactly for both length and weight. I’m using strata weights to compile designed-based, annual, pool-wide estimates for Invasive carp daytime electrofishing catch, both in terms of number of fish (CPUE) and biomass (kgPUE). I’m only using Period 3 fish for both body condition and pool-wide abundance estimates because the majority of P1/P2 fish are not directly weighed and I don’t want to rely on modeled weights when the goal is to compare actual weights to model predictions (i.e. relative weight)
One could also apply strata weights to the fish, and may be data-driven reasons to do so in some pools, as both length and length’s relationship to weight seem to vary significantly by strata in certain pools. This seems to be true for both SVCP and a couple native planktivore’s. However, these trends seem pool-specific, not universal, with some strata high in some pools and low in others. See breakdowns for both Invasive carp spp. and Gizzard shad below.
Although these may be statistically significant differences, the fact that trends aren’t universal across pools makes me less convinced that correcting body condition by strata weights is going to solve some big issue here. If we’re ignoring size differences among strata, we can then lump in LTEF size data or maybe even commercial harvest size data alongside the MAM size data and not worry that LTEF/harvest is “oversampling” MCB fishes. If it’s not IRBS or fisheries-in-general convention to strata-weight the fish sizes as well as the abundance, my choice would be to ignore the size and condition differences between strata and lump everything together.
For now, I’m just going to analyze the MAM data because that’s what I had on hand to start and am most familiar with. This only provides 3 years of data but eliminates issues of biased abundance from pool-wide MAM abundance estimates and mostly-MCB LTEF abundance estimates. I haven’t modeled the differences in abundances among strata, but I think it’s safe to assume those are likely different. More on that later…
Finally, here’s my attempt at answering our first question. I’m modeling using the formula abundance estimate ~ body condition to test for correlations, but I’m plotting the data on the opposite axes because it seems a more intuitive cause-and-effect, to me at least. For body condition, I’m using the LTRM life history database’s length-weight relationship parameters for Silver carp even though I’m modeling both Silver and Grass carp, but the parameters are very similar for both species.
First I’ll plot abundance estimates by pool and year, to get a sense of the abundance data we’re using.
Note the large standard error bars on the Starved Rock CPUE values. This may be important later, so below I’ll also plot the average of the Variance, Standard Error of the Mean, and Coefficients of Variation for each pool’s annual CPUE estimates. You’ll notice that Starved Rock has much higher Variance and SEM than other pools, but a lower CV.
Now the plots that test our first hypothesis, in the style of Coulter
et al. (2018):
As it stands with just MAM data from 2019-2021, a generalized linear mixed model using Pool as a random effect shows a significant relationship between Invasive carp relative weight and number of Invasive carp well with Invasive carp biomass. I’m posting the model summary using number of fish below, because it seemed to have a better model fit. Including Year as an effect did not improve model fit for either variable.
## Generalized linear mixed model fit by maximum likelihood (Laplace
## Approximation) [glmerMod]
## Family: Gamma ( log )
## Formula: n_weighted_mean ~ mean_weight_r + (1 | POOL_REACH)
## Data: modeling_data
##
## AIC BIC logLik deviance df.resid
## 41.2 44.3 -16.6 33.2 12
##
## Scaled residuals:
## Min 1Q Median 3Q Max
## -0.9305 -0.7228 0.1862 0.4895 1.4440
##
## Random effects:
## Groups Name Variance Std.Dev.
## POOL_REACH (Intercept) 0.7591 0.8713
## Residual 0.2590 0.5089
## Number of obs: 16, groups: POOL_REACH, 6
##
## Fixed effects:
## Estimate Std. Error t value Pr(>|z|)
## (Intercept) 13.259 4.850 2.734 0.00626 **
## mean_weight_r -12.753 4.448 -2.867 0.00414 **
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## Correlation of Fixed Effects:
## (Intr)
## mean_wght_r -0.993
I think there good evidence to suggest a relationship between Invasive carp body condition and Invasive carp abundance here, even though it’s difficult to visualize due to the random effect at play. For that, we can plot GLM predictions, which give me a sense that, even though it’s a significant relationship, the confidence intervals are wide making any predictions of abundance from body weight rather uninformative. The model is an exceptionally poor fit for three points, all belonging to Starved Rock pool. We should discuss if you think there is a biological or methodological reason for this.
## $mean_weight_r