Appendix B. Comparison between logistic-exposure and apparent nest success; discussion and interpretation of nest survival as a function of haying data model.
TABLE B1. Apparent nest success (ANS) was generally noticeably higher than logistic-exposure (L-E) nest success in the Champlain Valley (New York, Vermont) 20022005. The potential number of failed nests missed is the number of nests needed to attain the model nest success results given that the number of fledged nests was the true number of fledged nests.
SPECIES |
TREATMENT |
YEAR |
FAILED |
FLEDGED |
TOTAL |
ANS |
ANS AVG |
L-E nest success |
L-E nest success AVG |
Bobolink |
GRAZED |
2003 |
15 |
8 |
23 |
0.35 |
0.34 |
0.20 |
0.21 |
|
|
2004 |
16 |
10 |
26 |
0.38 |
|
0.19 |
|
|
|
2005 |
3 |
4 |
7 |
0.57 |
|
0.22 |
|
|
EARLY |
2002 |
8 |
0 |
8 |
0.00 |
0.02 |
0.06 |
0.05 |
|
|
2003 |
10 |
0 |
10 |
0.00 |
|
0.06 |
|
|
|
2004 |
20 |
0 |
20 |
0.00 |
|
0.04 |
|
|
|
2005 |
2 |
1 |
3 |
0.33 |
|
0.04 |
|
|
MIDDLE |
2003 |
27 |
2 |
29 |
0.07 |
0.39 |
0.31 |
0.32 |
|
|
2004 |
16 |
7 |
23 |
0.30 |
|
0.29 |
|
|
|
2005 |
16 |
25 |
41 |
0.61 |
|
0.36 |
|
|
LATE |
2002 |
32 |
35 |
67 |
0.52 |
0.64 |
0.45 |
0.46 |
|
|
2003 |
7 |
19 |
26 |
0.73 |
|
0.48 |
|
|
|
2004 |
12 |
22 |
34 |
0.65 |
|
0.45 |
|
|
|
2005 |
5 |
22 |
27 |
0.81 |
|
0.47 |
|
Savannah Sparrow |
GRAZED |
2002 |
4 |
2 |
6 |
0.33 |
0.46 |
0.22 |
0.25 |
|
|
2003 |
13 |
15 |
28 |
0.54 |
|
0.26 |
|
|
|
2004 |
29 |
20 |
49 |
0.41 |
|
0.24 |
|
|
|
2005 |
15 |
16 |
31 |
0.52 |
|
0.28 |
|
|
EARLY |
2002 |
22 |
18 |
40 |
0.45 |
0.21 |
0.09 |
0.08 |
|
|
2003 |
33 |
15 |
48 |
0.31 |
|
0.10 |
|
|
|
2004 |
102 |
10 |
112 |
0.09 |
|
0.07 |
|
|
|
2005 |
54 |
7 |
61 |
0.11 |
|
0.06 |
|
|
MIDDLE |
2003 |
6 |
21 |
27 |
0.78 |
0.66 |
0.44 |
0.45 |
|
|
2004 |
11 |
14 |
25 |
0.56 |
|
0.41 |
|
|
|
2005 |
8 |
12 |
20 |
0.60 |
|
0.50 |
|
|
LATE |
2002 |
9 |
17 |
26 |
0.65 |
0.55 |
0.39 |
0.40 |
|
|
2003 |
16 |
25 |
41 |
0.61 |
|
0.41 |
|
|
|
2004 |
20 |
28 |
48 |
0.58 |
|
0.39 |
|
|
|
2005 |
16 |
6 |
22 |
0.27 |
|
0.41 |
|
Nest survival as a function of haying date
Nest survival was modeled as a function of the Z-transformed haying dates:
log-odds (y) = 2.6933+ 0.1782 (Z-transformed haying date)
(SE = 0.0248, 95% CI = 0.1297 – 0.2267).
This model fit much better than the intercept (null) model (Likelihood-ratio test:
= 53.5, df = 1, P < 0.00001). The positive slope of this equation illustrated that each delayed day of hay harvest increased log-odds (nest success) by 0.1782. Each delayed day of hay harvest also increased daily nest survival with a slight curvilinear trend. Nest success increased by 7% when hay harvest was delayed from the earliest observed haying date, 27 May, to the average haying date, 15 June. Daily nest success increased 0.00037% /day during this period. Within the ‘early’ and ‘middle’ groups, the average ‘early’ cut occurred on 3 June and the average ‘middle’ cut occurred on 27 June. Nest success increased 9.5% between these dates. Delayed hay harvest continued to have a positive effect on the rate in which daily nest success increased until 20 July.
|
FIG. B1. Increase in nest survival and nest success with each daily delay in hay harvest for savannah sparrows and Bobolinks in the Champlain Valley (New York, Vermont) 20022005. Nest survival was modeled as a function of the Z-transformed haying dates: log-odds (y) = 2.7064 + 0.1763 (Z-transformed haying date) (SE = 0.0248, 95% CI = 0.1276 – 0.2250). The greatest increases in daily nest survival occurred from 28 May to 6 June (+0.0009). These data should be interpreted cautiously, however, because delaying the first haying data from 26 May to 6 June is a statistical construct that has no biological value; such a delay will still result in zero reproduction. Within this early-haying period, 100% of all observed nests failed due to hayfield management. |