Hi Ken,
Thanks for your reply. It is different for each species, so I will give some examples below:
Hypsipetes philippinus (Common species) - Philippine Bulbul
130 sites
Maximum number of observations per site: 3
Mean number of observations per site: 3
Sites with at least one detection: 114
Tabulation of y observations:
0 1 2 3 4 5 6 7 8
163 72 62 41 28 12 7 3 2
It has stable K if I exclude the random effect. Abundance estimate was 12.18 per 50m-radius point count. This is a bit high, but it not outrageously so.
Elegant Tit (common species)
130 sites
Maximum number of observations per site: 3
Mean number of observations per site: 3
Sites with at least one detection: 28
Tabulation of y observations:
0 1 2 3
359 20 7 4
(this is what the raw data looks like; just a subset)
A B C
0 0 1
0 0 2
0 0 0
0 0 0
0 0 1
1 0 0
0 0 0
1 0 0
3 1 0
2 0 0
0 0 0
0 0 0
0 0 0
0 0 0
0 0 3
mod = pcount(~ timesun ~ scale(forest_pland500) + scale(ED500) , K=300, umf, mixture="P")
This one did not stabilize with increasing K despite changing the mixture, the covariates, and random effect (removal/addition). Average abundance was estimated as 25 individuals per point (K=300), which is unrealistically high. However, the effect of the two covariates are consistent (i.e., not changing significance (0.05 threshold) and direction of the relationship) even if K is increased up to 2000.
From what I understand, changing the abundance covariates expectedly affects the intercept / estimate. Since I am using pcount() for hypothesis testing (not to get abundance estimates for the sites), I restricted the models to only have 2 covars (%forest and Edge density). This simple model with two explanatory var obviously is not enough to explain the variation in the data, could this be causing the unusually high intercepts?
Thank you for looking into this!
Jelaine