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Online Supplementary Material for Seasonality, the Latitudinal Gradient of Diversity, and Eocene Insects
S. Bruce Archibald, William H. Bossert, David. R. Greenwood, and Brian D. Farrell
Online material includes:
Analysis of ichneumon wasp specimens Online Figure 1 Online Table 1
Analysis of Plecia specimens Online Figure 2
Comparisons of climatic estimation methods Online Table 2
Online Table 3: General compositions of McAbee, Harvard Forest and La Selva samples Online literature cited Online Table 4: Specimen / species compositions of samples
1
Analysis of ichneumon Wasp Specimens Size was not used in determination of ichneumonid wings to species due to its range within individuals of a species and sexual dimorphism, except in the extreme case of specimen 1988. Wings were grouped into six major groups (A-F) based on the shape of the “areolet”, the first Rs cell, a small cell in the centre of the forewing (online fig. 1). They were then categorized within each of these groups by combinations of three wing characters, and then further separated by comparisons of ratios of character measurements between the fossil specimens and in known, extant species.
Separation to groups
Abscissa numbers refer to those defined in online fig. 1D. Group A: areolet triangular, or sub-triangular; abscissa 1 meets abscissa 3 (no or
very short abscissa 2); abscissa 3 meets abscissa 5 (no abscissa 4); Group B: areolet as in Group A, but open, i.e., abscissa 3 space empty or very
weak; Group C: areolet sub-triangular; but abscissa 4 present (Group A: absent), short
relative to length of abscissa 3; abscissa 4 parallel or subparallel with abscissa 1; abscissa 1 meets abscissa 3 (no or very short abscissa 2);
Group D: as in Group C, but areolet open, i.e., abscissa 3 space empty or very weak;
Group E: areolet diamond-shaped: four-sided or slightly five-sided (if a short length of abscissa 2 present between abscissa 1 and abscissa 3), no side less than half length of other (other than brief length of abscissa 2, if present, as above);
Group F: areolet distinctly pentagonal: all five abscissae distinctly present (two abutting sides may be aligned).
Within these “areolet groups”, specimens were separated to subgroups by differing combinations of states of the following characters.
Character 1: 2m-cu: A) distinctly curved or B) rather straight; Character 2: crossvein cu-a: joins Cu: A) at, or B) distad branching of M+Cu to
M and Cu; Character 3: cu-a joins A: A) at a distinct angle, or B) perpendicular or closely so
to A.
Separation to species Within subgroups, specimens that shared the same states of characters 1-3 were
evaluated further with ratios of measurements of wing characters. Twelve measurements (A-L) of forewing characters were taken from camera lucida drawings of each fossil. Ratios of pairs of the measurements were used to control for intra-specific size differences (individual and by sexual dimorphism). These were compared with inter- and intra-specific variation in known species, taken from photographs of forewings of 96 specimens of 9 extant species (pinned specimens, MCZ) in three genera of three subfamilies. These were: Pterocormus annulatorius (n = 9), P. bucculentus (n = 4), P. centrator (n = 10); Compsocrypyus texensis (n = 7), C. resolutus (n = 6), C. melanostigmus (n = 18); Coccygomimus semirufus (n = 8), C. sumichrasti (n = 21), C. tomyris (n = 23).
2
Within extant species, the average value of each ratio within that species was taken, and its standard deviation within the species was determined. Within each species, no specimens were separated by more than two standard deviations, and all individuals species differed by more than two standard deviations between them. For a given ratio, the coefficient of variation, the ratio of standard deviation divided by the mean was constant within and differed consistently between species over all species examined.
Three ratios, together, separated all extant species, and were compared in the fossil specimens: L/C, D/C, and J/K. These ratios in part describe the shapes of cells 2R1 and 2M.
Specimens were grouped for a given ratio-character if they did not differ by more than three times the coefficient of variation for that ratio times their mean value, and were considered to have a species-level difference for that character if the difference between their values was greater than that amount. All those specimens were included in the same species that are within three standard deviations of any member of the species group, i.e., two may differ by more, but a third that is intermediate and differs from neither by more than three the set amount bound those two together.
3
Online Figure 1: Forewing of Pterocormus centrator with characters of Ichneumonidae mentioned in the text. (A), (B) measurements taken. (C) cells Ar (areolet), 2M, and 2R1 in italics; veins M+Cu, Cu and A; crossveins cu-a and 2m-cu. (D) veins and crossveins surrounding the areolet; circled numbers, see text. (A)–(C) to scale, 5 mm; (D) to scale, 1 mm.
Online Table 1 WING CHARACTER DATA USED FOR ICHNEUMONID SPECIES DEFINITIONS
4
C
har.
C
har.
C
har.
L
/C
D
/C
J/
K
num
ber
Gro
up S
peci
es
1 2
3 G
roup
L
/C
min
m
ax
Gro
up
D/C
m
in
max
G
roup
J/
K
min
m
ax
2107
A
sp
. 1
A
? ?
AA
1 0.
82
0.77
0.
87
AA
1 0.
44
0.34
0.
54
AA
1 2.
13
1.72
2.
54
1927
A
sp
. 1
A
? ?
AA
1 0.
82
0.76
0.
87
AA
1 0.
53
0.4
0.66
A
A1
2.77
2.
24
3.31
66
8 A
sp
. 1
A
A
A
AA
1 0.
8 0.
75
0.85
A
A1
0.6
0.46
0.
74
AA
1 2.
57
2.08
3.
07
2433
A
sp
. 2
A
A
A
AA
2 0.
89
0.83
0.
95
AA
1 0.
57
0.44
0.
71
AA
1 2.
8 2.
26
3.34
28
20
A
sp. 3
A
A
B
A
A3
0.97
0.
91
1.03
A
A1
0.45
0.
34
0.55
A
A2
3.69
2.
98
4.4
2023
A
sp
. 4
A
B
B
AA
3 1.
03
0.96
1.
1 A
A1
0.42
0.
32
0.52
A
A3
4.54
3.
67
5.42
14
6 A
sp
. 5
B
A
A
AB
1 0.
85
0.79
0.
9 A
B1
0.45
0.
34
0.55
A
B1
2.73
2.
2 3.
25
2200
A
sp
. 6
B
A
A
AB
2 0.
92
0.86
0.
99
AB
1 0.
62
0.48
0.
77
AB
1 2.
26
1.82
2.
69
2848
A
sp
. 7
B
A
A
AB
3 0.
98
0.91
1.
04
AB
1 0.
55
0.42
0.
68
AB
2 4.
04
3.26
4.
82
2416
B
sp
. 1
A
? ?
B1
0.95
0.
89
1.02
B
1 0.
57
0.43
0.
7 B
1 2.
65
2.14
3.
16
2859
B
sp
. 2
A
A
A
? ?
? ?
B2
3.9
378
B
sp. 3
B
B
B
B
2 0.
86
0.81
0.
92
B1
0.62
0.
47
0.77
B
1 2.
29
1.85
2.
73
684
C
sp. 1
A
A
A
C
AA
A1
0.79
0.
74
0.84
C
AA
A1
0.67
0.
51
0.83
C
AA
A1
2.31
1.
87
2.76
56
3 C
sp
. 1
A
A
A
CA
AA
1 0.
85
0.79
0.
91
CA
AA
1 0.
57
0.43
0.
7 C
AA
A1
2.65
2.
14
3.16
21
55
C
sp. 1
A
A
A
C
AA
A1
0.83
0.
78
0.89
C
AA
A1
0.54
0.
41
0.67
C
AA
A1
2.65
2.
14
3.16
27
83
C
sp. 1
A
A
A
C
AA
A1
0.8
0.75
0.
86
CA
AA
1 0.
54
0.41
0.
67
CA
AA
1 2.
67
2.15
3.
18
2106
C
sp
. 1
A
A
A
CA
AA
1 0.
8 0.
75
0.85
C
AA
A1
0.54
0.
41
0.67
C
AA
A1
2.6
2.1
3.11
30
04
C
sp. 1
A
A
A
C
AA
A1
0.82
0.
76
0.87
C
AA
A1
0.51
0.
39
0.63
C
AA
A1
2.24
1.
81
2.68
25
58
C
sp. 1
A
A
A
C
AA
A1
0.83
0.
78
0.89
C
AA
A1
0.57
0.
43
0.7
CA
AA
1 2.
46
1.99
2.
93
2097
C
sp
. 1
A
A
A
CA
AA
1 0.
86
0.8
0.91
C
AA
A1
0.51
0.
39
0.63
C
AA
A1
2.63
2.
12
3.14
21
56
C
sp. 1
A
A
A
C
AA
A1
0.86
0.
8 0.
92
CA
AA
1 0.
45
0.35
0.
56
CA
AA
1 3.
22
2.6
3.84
11
39
C
sp. 1
A
A
A
C
AA
A1
0.9
0.84
0.
96
CA
AA
1 0.
58
0.44
0.
71
CA
AA
1 2.
73
2.2
3.25
22
58
C
sp. 1
?
A
A
CA
AA
1 0.
77
0.72
0.
82
CA
AA
1 0.
54
0.41
0.
67
CA
AA
1 2.
3 1.
85
2.74
22
14
C
sp. 2
A
A
B
C
AA
B1
0.93
0.
87
0.99
C
AA
B1
0.47
0.
36
0.58
C
AA
B1
2.4
1.94
2.
86
138
C
sp. 3
A
A
B
C
AA
B2
0.98
0.
92
1.05
C
AA
B1
0.48
0.
37
0.6
CA
AB
2 3
2.42
3.
58
110
C
sp. 4
A
B
B
C
AB
B1
0.8
0.74
0.
85
CA
BB
1 0.
52
0.39
0.
64
? ?
2263
C
sp
. 5
A
B
B
CA
BB
2 0.
94
0.88
1
CA
BB
1 0.
48
0.37
0.
6 C
AB
B1
2.55
2.
06
3.04
39
4 C
sp
. 6
B
A
A
CB
AA
1 0.
84
0.79
0.
9 C
BA
A1
0.44
0.
33
0.54
C
BA
A1
2.75
2.
22
3.28
24
44
C
sp. 7
B
A
A
C
BA
A1
0.85
0.
79
0.91
C
BA
A1
0.48
0.
37
0.59
C
BA
A2
2.18
1.
76
2.6
638
C
sp. 8
B
A
B
C
BA
B1
0.87
0.
81
0.93
C
BA
B1
0.46
0.
35
0.57
C
BA
B1
3 2.
42
3.58
5
2839
C
sp
. 9
B
A
B
CB
AB
1 0.
87
0.81
0.
92
CB
AB
1 0.
5 0.
38
0.62
C
BA
B2
3.47
2.
8 4.
14
2953
C
sp
. 9
B
A
B
? ?
? ?
CB
AB
2 3.
06
2.47
3.
66
3001
C
sp
. 10
B
B
A
0.
91
0.85
0.
97
0.
6 0.
46
0.74
2.46
1.
99
2.94
76
7 D
sp
. 1
A
A
B
DA
AB
1 0.
82
0.76
0.
87
DA
AB
1 0.
52
0.4
0.65
D
AA
B1
2.56
2.
07
3.05
20
96
D
sp. 1
A
A
B
D
AA
B1
0.82
0.
76
0.87
D
AA
B1
0.48
0.
37
0.6
DA
AB
1 2.
74
2.21
3.
27
412
D
sp. 2
A
A
B
D
AA
B2
0.91
0.
85
0.97
D
AA
B1
0.55
0.
42
0.67
D
AA
B1
2.96
2.
39
3.53
19
88
D
sp. 3
B
A
A
D
BA
A1
0.87
0.
81
0.93
D
BA
A1
0.42
0.
32
0.52
D
BA
A1
2.29
1.
85
2.73
27
10
D
sp. 4
B
A
A
? D
BA
A1
0.82
0.
76
0.87
D
BA
A1
0.48
0.
36
0.59
D
BA
A1
2.3
1.85
2.
74
2110
D
sp
. 5
B
A
A
DB
AA
1 0.
81
0.75
0.
86
DB
AA
2 0.
62
0.47
0.
76
DB
AA
1 2.
42
1.96
2.
89
349
D
sp. 6
B
A
A
D
BA
A1
0.87
0.
82
0.93
D
BA
A1
0.44
0.
34
0.55
D
BA
A2
3.03
2.
45
3.61
24
17
D
sp. 7
B
A
B
D
BA
B1
0.95
0.
89
1.02
D
BA
B1
0.45
0.
35
0.56
?
?
2499
E
sp. 1
A
B
B
1 0.
93
1.07
0.44
0.
34
0.55
3.39
2.
74
4.05
14
0 E
sp. 2
B
B
B
1.06
0.
99
1.13
0.58
0.
44
0.72
?
60
5 F
sp. 1
A
A
A
0.76
0.
71
0.81
0.56
0.
42
0.69
?
29
75
F sp
. 2
A
A
B
FAA
B1
0.98
0.
92
1.05
FA
AB
1 0.
46
0.35
0.
57
FAA
B1
3.1
2.5
3.69
21
09
F sp
. 3
A
A
B
FAA
B2
0.85
0.
8 0.
91
FAA
B1
0.56
0.
43
0.7
FAA
B2
2.12
1.
71
2.53
24
28
F sp
. 4
B
A
A
0.
84
0.78
0.
89
0.
52
0.39
0.
64
2.
31
1.86
2.
75
2551
F
sp. 5
?
B
B
? ?
? ?
?
6
Analysis of Plecia Specimens
March flies, species of the genus Plecia (Diptera: Bibionidae: Pleciinae), are the most common insects at most Okanagan Highlands localities, and comprise about a quarter of this fossil assemblage. Handlirsch (1910) defined twenty species in the British Columbia Eocene, a number Cockerell (1925: p. 12) called “scandalous”. Rice (1959) revised these, added another two species, and placed two in Penthetria, the sister taxon to Plecia, which has very similar wings.
Unfortunately, none of these authors provided diagnoses for these species, as was the custom then. Intraspecific variation in wing morphology as illustrated by Rice appears larger than differences between many species pairs. Although they are common fossils, no species determinations for Okanagan Highlands Plecia (or Penthetria) specimens have been subsequently published. Wilson (1977: p. 1146) noted that assignment of these bibionid specimens to species is “extremely difficult”, and suggested that further revision of the Okanagan Highlands Bibionidae is necessary.
The approach taken here was similar to that taken for the Ichneumonidae. Twenty-three characters were measured on each wing (A-W, online fig. 2) of 129 well-preserved specimens out of 335 total. To control for size differences in intra-specific variation and sexual dimorphism, only ratios of these were used, yielding 23*22/2 = 253 possible distinct ratios. Unfortunately, many fossil specimens are incomplete in some portion, precluding some measurements.
To establish intra- and inter-specific variation in these ratios to compare among the fossils, 53 specimens of 5 extant species of Plecia were examined and measured (males and females): P. nearctica (n = 20), P. americana (n = 4), P. ephippium (n = 8), P. plagiata (n = 13), and P. collaris (n = 8); and 18 further specimens of the pleciine Penthetria heteroptera.
To establish if there was sexual dimorphism in the ratios themselves, which would hinder their use in species identification, the sum of squares of a ratio about its mean was partitioned into the between sex and within sex components, as in an analysis of variance. A ratio was rejected if the between sex component was more than 20% of the total.
Of the 253 possible measurement ratios, only 69 were sufficiently non-dimorphic to appear useful. Of these 69, many were highly correlated; hence, using all of them added nothing to our discrimination that a much smaller subset could achieve. A set of ratios were identified, which were not sexually dimorphic, which were not significantly correlated, which had a relatively small variance within an extant species, yet which had a much larger variance over the fossil specimens. They are: A/W, E/U, C/P, K/M, B/J, N/Q, T/W, R/U, I/O, Q/V, and A/F.
These ratios are highly diagnostic for the modern species. Linear Discriminant analysis using them split individual pairs of the 5 extant species perfectly, with Mahalonobis D2 values all in excess of 18. This is not helpful with regards to the fossils specimens, as the goal is not to assign them to modern species. It does suggest, however, that the ratios could be useful, with the caveat that only a subset are available in many due to partial preservation. No small subset of these ten ratios (two or three) reliably separates all of the extant species.
7
A Principal Components Analysis was done on the ten ratios over the extant species sample. The first two principal components explained about 90% of the total variance over the extant species. Unfortunately, projecting the data matrix for the extant species on these two main components did not separate the species.
Returning to the full set of 69 non-dimorphic ratios, variance of individual ratios between species was examined. Between each pair of extant species, with one notable exception, there was no overlap in ratio values for at least five of the ratios and at least one ratio in which the mean difference between the species was at least 0.33 times the average mean over the two species. This compares to the within species coefficient of variation, in which the standard deviation in any ratio was never more than about 17% of the mean, usually less than 10%. The exception to this result is the comparison of P. nearctica and P. collaris, which had overlap in all 69 of the non-dimorphic ratios. Despite this one failure, it seemed that a possible rule for grouping specimens into species was to pair specimens that did not differ in any one ratio by more than 30% of the mean value for that ratio in the two species. When this rule is applied to the aggregate 56 specimens of the five extant species, only 32/56 = .57% were assigned to their known species group correctly. A major error was assigning five of the P. collaris to the P. nearctica group. The number of specimens assigned to a single specimen group was 18/56, yielding a total of 22 “species” groups instead of the known 5 species. This increased the logarithmic Shannon species diversity index from 1.49 to 2.17, an error that seems intolerable. This amounts to an increase in the number of “effective” species taking relative abundance into consideration from 4.44 to 8.76. When this rule was applied to the fossil Plecia specimens 128 of the unknown specimens were assigned to 1 species and 1 specimen to a second species.
A rather arbitrary examination was done on the effect of reducing the difference required in any one ratio for separating a pair of specimens into two species, while adding a requirement that the average difference between the specimens over all of the ratios for which they have data in common. When two specimens were considered conspecific that do not differ by more than 34% of the mean of any one ratio, but split when the average relative difference (difference divided by the mean for the two specimens) over all ratios in common, the Shannon’s species diversity index was 1.49, exactly the known value. However, about 40% of the specimens were categorized incorrectly as to known species. Applying this mixed rule to the fossil specimens changed nothing. The result was two species with nearly all of the specimens in one species. Of course, this could be the correct categorization of the fossils, but the method for achieving it is very ad hoc, and cannot be accepted.
By the inability to obtain reliable species determinations for these fossil Plecia on the basis of these wing measurements, they were excluded.
8
Online Figure 2: Plecia nearctica wing, female. (A) habitus, (B) measurements taken on Plecia and Penthetria specimens; both to scale, 2 mm.
9
Comparison of Climatic Estimation Methods Online Table 2
COMPARISONS OF WEATHER STATION DATA AND PALEOCLIMATE EVALUATION METHODS. –––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– site N LMP MAT(obs) MAT(LMA) error N MAT(NLR) error LS 40 75% 25.8 21.6 2.0 28 20.7 ±3.3 HF 27 16.7% 7.2 7.3 1.8 33 9.1 ±3.6 Mc 21 29.2% – 10.7 2.5 34 13.5 ±2.5
site N CMMT(obs) CMMT(NLR) error LS 28 24.7 16.7 ±4.7 HF 33 -7.4 -1.4 ±9.1 Mc 35 – 5.8 ±2.0
site N MAP(obs) MAP(NLR) error LS 29 396 126 ±34 HF 33 107 111 ±45 Mc 35 – 108 ±36 –––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– NOTE. —Abbreviations: mean annual temperature (MAT), coldest month mean temperature (CMMT) and mean annual precipitation (MAP), observed weather station data (obs) and nearest living relative (NLR) and leaf margin analysis (LMA). Data from La Selva (LS), Costa Rica; Harvard Forest (HF), Massachusetts, USA; Eocene McAbee (Mc), British Columbia, Canada. N is the number of leaves (LMA) or taxa (NLR) used; LMP is the percent entire margined (non-toothed) woody dicot leaves. MAT and CMMT in °C and MAP in cm/year.
For comparative value, the paleoclimatic estimation methods employed to evaluate
McAbee climate (LMA and NLR) were done for Harvard Forest and La Selva, and results were compared with observed on-site weather station data. Harvard Forest LMA was calculated based on LMP data from Royer et al. (Royer et al. 2005), and La Selva on a new leaf collection. NLR was based on Harvard Forest online taxon lists (Harvard Forest 2006), and La Selva on determinations of the leaf collection by Orlando Vargas and Jose Gonzalez.
The LMA MAT for Harvard Forest, Massachusetts was accurate, with the mean value within 0.4º C of the observed weather station value. The mean value of the NLR estimate of MAT for Harvard Forest was about two degrees high, but with error values accurately reflected observed MAT. CMMT (NLR only) gave the Harvard Forest observed value, but only within the large error values. At La Selva, however, CMMT was underestimated, slightly inflating its prediction of seasonality there. MAP by NLR (only) gave a quite accurate prediction of the observed annual precipitation at Harvard Forest, but was less successful at La Selva, where it was underestimated by more than a third. CMMT and MAP are difficult to estimate using either proxy, with large errors and under-estimation a common outcome when calibrated using modern sites. The lower than
10
observed MAT and CMMT NLR estimates for La Selva are due in part to the inclusion in the calculation of genera of Lauraceae and some other taxa (e.g., Aquifoliaceae, Clethraceae, and Symplocaceae) that are typical of higher elevation forests. The presence of tree taxa in the La Selva forests that are typical of cooler upland forests is thought to be due to the ever-wet and cloudy character of the climate (Gentry 1990; Hammel 1990). The inconsistencies reported here between observed and estimated MAP are similar to those reported in other studies, and may reflect many plant taxa responding to precipitation as a threshold or stepped response, rather than as a linear response (Greenwood 2001; Burnham et al. 2005).
Online Table 3
GENERAL COMPOSITIONS OF MCABEE, LA SELVA, AND HARVARD FOREST SAMPLES
Taxon total total to spp __spp._________ McAbee Sample
Fossil insects 1417 – – Identifiable to order 1286 390 279 Diptera 487 45 38 Nematocera 463 27 23 Mycetophilidae 28 11 10 Tipulomorpha 40 14 11 Bibionidae (Plecia) 335 – – Trichoseridae? 2 2 2 incertae sedis 58 – – Brachycera 20 14 12 Syrphidae 8 7 6 incertae sedis 12 7 6 incertae sedis 4 4 3 Hemiptera 403 128 74
Auchenorrhyncha 306 90 55 Heteroptera 91 35 16 Sternorrhyncha 6 3 3
Hymenoptera 194 99 83 Symphyta 34 27 25 Siricidae 1 1 1 Cimbicidae 6 5 4 Tenthredinidae 26 21 20 Apocrita 160 72 58 Diapriidae 1 1 1 Proctotrupidae 2 2 2 Proctotrupoidea in. sed. 1 1 1 Ichneumonidae 86 48 34 Braconidae 6 2 2 Figitidae 2 1 1 Chrysidoidea in. sed. 1 1 1
11
Vespidae 2 2 2 Formicidae 13 6 6 Sphecidae (s.l.) 3 3 3 Apocrita in. sed. 44 5 5 Coleoptera 86 54 49 Mecoptera 23 19 8 Bittacidae 6 5 4 Dinopanorpidae 7 6 2 Unnamed fam. 7 7 1 Panorpidae 1 1 1 incertae sedis 2 – – Trichoptera 21 18 7 Blattodea 19 – – Neuroptera 17 15 11 Osmylidae 5 4 3 Hemerobiidae 3 3 3 Chrysopidae 8 7 4 incertae sedis 1 1 1 Ephemeroptera 14 – – Orthoptera 10 6 5 Ensifera 5 4 3 Prophalangopsidae 3 2 2
Tettigoniidae 2 2 1 Caelifera 3 2 2
incerate sedis 3 2 2 incerate sedis 2 – – Isoptera 6 3 1 Hodotermitidae 3 3 1 incerate sedis 3 – – Dermaptera 3 – – Odonata 3 3 3 Zygoptera 2 2 2 Megapodagrionidae 1 1 1 incertae sedis 1 1 1 Anisoptera 1 1 1 Aeshnidae 1 1 1
La Selva Sample Total 3717 1110 Diptera 981 245
Nematocera 253 72 Brachycera 728 173 Hemiptera 705 176 Sternorrhyncha 6 3 Auchenorrhyncha 618 136
12
Heteroptera 81 37 Hymenoptera 1203 320 Symphyta 18 5 Apocrtia 1185 315 Coleoptera 751 328 Trichoptera 3 3 Blattodea 1 1 Neuroptera 3 2 Ephemeroptera 1 1 Psocoptera 15 7 Orthoptera 48 23 Caelifera 23 10 Ensifera 25 13 Isoptera 1 1 Mantodea 4 2 Dermaptera 1 1
Harvard Forest Sample
Total 1938 660 Diptera 771 178 Nematocera 257 49 Brachycera 514 129 Hemiptera 76 28 Sternorrhyncha 5 2 Auchenorrhyncha 67 22 Heteroptera 4 4 Hymenoptera 745 373 Symphyta 31 8 Apocrtia 714 365 Coleoptera 262 54 Trichoptera 41 12 Blattodea 1 1 Neuroptera 5 2 Psocoptera 6 4 Orthoptera 17 1 Caelifera 17 1 Odonata 14 7 Note: —For details of sample compositions, see online Table 4. See Archibald (2007) for photographs and / or drawings of all McAbee specimens.
Online literature cited Archibald, S. B. 2007. Climate and species diversity: The Eocene Okanagan Highlands
insect view, vol. 1. PhD thesis, Harvard University, Cambridge, MA. Burnham, R. J., B. Ellis and K. R. Johnson. 2005. Modern tropical forest taphonomy:
does high biodiversity affect paleoclimatic interpretations? Palaios 20:439–451.
13
Cockerell, T. D. A. 1925. Tertiary insects from Kudia River, Maritime province, Siberia. Proceedings of the United States National Museum 68(2606), article 5.
Gentry, A. H. 1990. Floristic similarities and differences between Southern Central America and Upper and Central Amazonia. Pp. 141–160 in A. H. Gentry, ed. Four Neotropical Rainforests. Yale University Press, New Haven.
Greenwood, D. R. 2001. Climate - wood and leaves. Pp. 480–483 in D. E. G. Briggs and P. R. Crowther, eds. Palaeobiology II. Blackwell Scientific, London.
Hammel, B. 1990. The distribution of diversity among families, genera and habitat types in the La Selva flora. Pp. 75–84 in A. H. Gentry, ed. Four Neotropical Rainforests. Yale University Press, New Haven.
Handlirsch, A. 1910. Canadian Fossil Insects. Contributions to Canadian paleontology Vol. II, Part III. Memoir 12-P, Geological Survey Branch, Canada Department of Mines, Ottawa, Ontario.
Rice, H. M. A. 1959. Fossil Bibionidae (Diptera) from British Columbia. Geological Survey of Canada Bulletin 55.
Royer, D. L., P. Wilf, D. A. Janesko, E. A. Kowalski and D. L. Dilcher. 2005. Correlations of climate and plant ecology to leaf size and shape: potential proxies for the fossil record. American Journal of Botany 92:1141–1151.
Wilson, M. V. H. 1977. New records of insect families from the freshwater middle Eocene of British Columbia. Canadian Journal of Earth Sciences 14:1139–1155.
14
Onl
ine
Tabl
e 4
Sam
ple
Com
posi
tions
McA
bee
Sam
ple
Col
eopt
era
num
ber
Supe
rfam
ilyFa
mily
Gro
upSp
ecie
sQ
uant
.28
29in
certa
e se
dis
ince
rtae
sedi
sA
sp. 1
216
6in
certa
e se
dis
ince
rtae
sedi
sA
sp. 1
164
ince
rtae
sedi
sin
certa
e se
dis
Asp
. 22
2266
ince
rtae
sedi
sin
certa
e se
dis
Asp
. 220
25in
certa
e se
dis
ince
rtae
sedi
sA
sp. 3
112
51in
certa
e se
dis
ince
rtae
sedi
sA
sp. 4
120
20in
certa
e se
dis
ince
rtae
sedi
sA
sp. 5
124
56in
certa
e se
dis
ince
rtae
sedi
sA
sp. 6
113
0in
certa
e se
dis
ince
rtae
sedi
sB
sp. 1
112
46in
certa
e se
dis
ince
rtae
sedi
sB
sp. 2
117
46C
hrys
omel
oide
aCer
amby
cida
eC
sp. 1
198
2Te
nebr
iono
idea
Mor
delli
dae
Dsp
. 11
2400
Ela
tero
idea
cf.C
anth
arid
ae
Esp
. 11
2076
Sca
raba
eoid
eaP
assa
lidae
Fsp
. 11
2707
Ela
tero
idea
cf. E
late
ridae
Gsp
. 11
181
Ela
tero
idea
cf. E
late
ridae
Gsp
. 21
2963
Ela
tero
idea
cf. E
late
ridae
Gsp
. 31
2235
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 11
2280
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 21
249
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 31
600
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 41
1150
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 51
332
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 61
1902
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 71
77in
certa
e se
dis
ince
rtae
sedi
sH
sp. 8
129
57in
certa
e se
dis
ince
rtae
sedi
sH
sp. 9
1
15
2650
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 10
1N
Nin
certa
e se
dis
ince
rtae
sedi
sH
sp. 1
11
562
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 12
178
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 13
115
13in
certa
e se
dis
ince
rtae
sedi
sH
sp. 1
41
2230
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 15
161
5in
certa
e se
dis
ince
rtae
sedi
sH
sp. 1
61
2446
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 17
125
39in
certa
e se
dis
ince
rtae
sedi
sH
sp. 1
81
2719
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 19
126
53in
certa
e se
dis
ince
rtae
sedi
sH
sp. 2
01
405
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 21
121
91in
certa
e se
dis
ince
rtae
sedi
sH
sp. 2
21
2652
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 23
115
16in
certa
e se
dis
ince
rtae
sedi
sH
sp. 2
41
1327
ince
rtae
sedi
sin
certa
e se
dis
Hsp
. 25
127
5in
certa
e se
dis
ince
rtae
sedi
sH
sp. 2
61
100
ince
rtae
sedi
sin
certa
e se
dis
Isp
. 11
83in
certa
e se
dis
ince
rtae
sedi
sI
sp. 2
117
87in
certa
e se
dis
ince
rtae
sedi
sI
sp. 3
123
83in
certa
e se
dis
ince
rtae
sedi
sI
sp. 4
134
7in
certa
e se
dis
ince
rtae
sedi
sI
sp. 5
155
2C
uped
oide
aC
uped
idae
Jsp
. 11
418
Chr
ysom
eloi
deaC
hrys
omel
idae
Ksp
. 12
637
Chr
ysom
eloi
deaC
hrys
omel
idae
Ksp
. 159
6C
urcu
liono
idea
Cur
culio
nida
eL
sp. 1
1
16
La S
elva
Sam
ple
Col
eopt
era
Trap
Supe
rfam
ilyFa
mily
Spec
ies
T1M
13T1
W2
T2W
2T3W
2T4
W2
T5W
2T6
W2
HTW
2A
RB
tota
lC
arab
oide
aC
arab
idae
sp.1
11
Car
aboi
dea
Car
abid
aesp
.21
1C
arab
oide
aC
arab
idae
sp.3
11
2C
arab
oide
aC
arab
idae
sp.4
11
Car
aboi
dea
Cic
inde
lidae
sp. 1
11
13
Car
aboi
dea
Cic
inde
lidae
sp. 2
33
Car
aboi
dea
Dyt
isci
dae
sp. 1
66
Car
aboi
dea
Dyt
isci
dae
sp. 2
11
Hyd
roph
iloid
eaH
ydro
phili
dae
sp. 1
11
22
6S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
11
11
4S
taph
ylin
oide
aS
taph
ylin
idae
sp. 2
22
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 31
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 4
31
4S
taph
ylin
oide
aS
taph
ylin
idae
sp. 5
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 61
12
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 71
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 8
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 91
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
01
11
3S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
11
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
21
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
31
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
41
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
51
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
61
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
71
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 1
81
12
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 19
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 20
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 21
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 22
11
17
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 23
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 24
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 25
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 26
11
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 27
11
2S
taph
ylin
oide
aS
taph
ylin
idae
sp. 2
81
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 2
91
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
01
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
11
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
21
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
33
3S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
41
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
51
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
61
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 3
71
1S
taph
ylin
oide
aS
caph
idiid
aesp
. 11
1S
cara
baeo
idea
Sca
raba
eida
esp
. 11
1S
cara
baeo
idea
Sca
raba
eida
esp
. 21
1S
cara
baeo
idea
Cer
atoc
anth
idaes
p. 1
12
3S
cara
baeo
idea
Cer
atoc
anth
idaes
p. 2
11
Bup
rest
oide
aB
upre
stid
aesp
. 11
12
Bup
rest
oide
aB
upre
stid
aesp
. 21
1B
upre
stoi
dea
Bup
rest
idae
sp. 3
11
Bup
rest
oide
aB
upre
stid
aesp
. 41
1B
upre
stoi
dea
Bup
rest
idae
sp. 5
11
Bup
rest
oide
aB
upre
stid
aesp
. 61
1B
yrrh
oide
aP
tilod
acty
lidae
sp. 1
22
Byr
rhoi
dea
Ptil
odac
tylid
aesp
. 21
1B
yrrh
oide
aP
tilod
acty
lidae
sp. 3
11
Byr
rhoi
dea
Ptil
odac
tylid
aesp
. 41
1B
yrrh
oide
aP
tilod
acty
lidae
sp. 5
11
Byr
rhoi
dea
Ptil
odac
tylid
aesp
. 63
31
7B
yrrh
oide
aP
tilod
acty
lidae
sp. 7
11
Ela
tero
idea
Ela
terid
aesp
.12
2E
late
roid
eaE
late
ridae
sp.2
11
Ela
tero
idea
Ela
terid
aesp
.31
1
18
Ela
tero
idea
Ela
terid
aesp
.41
1E
late
roid
eaE
late
ridae
sp.5
11
13
Ela
tero
idea
Ela
terid
aesp
.61
1E
late
roid
eaE
late
ridae
sp.7
13
26
Ela
tero
idea
Ela
terid
aesp
.81
12
Ela
tero
idea
Ela
terid
aesp
.91
1E
late
roid
eaE
late
ridae
sp.1
01
1E
late
roid
eaE
late
ridae
sp.1
11
1E
late
roid
eaE
late
ridae
sp.1
21
1E
late
roid
eaE
late
ridae
sp.1
31
1E
late
roid
eaE
late
ridae
sp.1
41
1E
late
roid
eaE
late
ridae
sp.1
51
1E
late
roid
eaE
late
ridae
sp.1
61
1E
late
roid
eaE
late
ridae
sp.1
71
1E
late
roid
eaE
late
ridae
sp.1
81
1E
late
roid
eaLy
cida
esp
. 11
1E
late
roid
eaLy
cida
esp
. 21
1E
late
roid
eaLy
cida
esp
. 31
1E
late
roid
eaLy
cida
esp
. 41
1E
late
roid
eaLy
cida
esp
. 51
14
28
Ela
tero
idea
Lyci
dae
sp. 6
11
Ela
tero
idea
Lyci
dae
sp. 7
11
Ela
tero
idea
Lyci
dae
sp. 8
11
Ela
tero
idea
Lyci
dae
sp. 9
11
Ela
tero
idea
Lyci
dae
sp. 1
01
1E
late
roid
eaLy
cida
esp
. 11
31
59
18E
late
roid
eaLy
cida
esp
. 12
11
Ela
tero
idea
Lyci
dae
sp. 1
31
1E
late
roid
eaLy
cida
esp
. 14
11
Ela
tero
idea
Lyci
dae
sp. 1
52
2E
late
roid
eaLy
cida
esp
. 16
11
Ela
tero
idea
Lam
pyrid
aesp
. 11
12
Ela
tero
idea
Lam
pyrid
aesp
. 21
1E
late
roid
eaLa
mpy
ridae
sp. 3
21
3E
late
roid
eaLa
mpy
ridae
sp. 4
11
Ela
tero
idea
Lam
pyrid
aesp
. 51
1
19
Ela
tero
idea
Lam
pyrid
aesp
. 61
1E
late
roid
eaLa
mpy
ridae
sp. 7
11
Ela
tero
idea
Lam
pyrid
aesp
. 82
2E
late
roid
eaLa
mpy
ridae
sp. 9
88
Ela
tero
idea
Lam
pyrid
aesp
. 10
11
Ela
tero
idea
Lam
pyrid
aesp
. 11
11
2E
late
roid
eaLa
mpy
ridae
sp. 1
23
3E
late
roid
eaLa
mpy
ridae
sp. 1
31
1C
ucuj
oide
aC
ucuj
idae
sp. 1
11
Cuc
ujoi
dea
Lang
uirii
dae
sp. 1
11
2C
ucuj
oide
aLa
ngui
riida
esp
. 21
23
Cuc
ujoi
dea
Lang
uirii
dae
sp. 3
51
12
21
12C
ucuj
oide
aN
itidu
lidae
sp. 1
63
114
31
28C
ucuj
oide
aN
itidu
lidae
sp. 2
22
11
12
32
14C
ucuj
oide
aN
itidu
lidae
sp. 3
11
24
Cuc
ujoi
dea
Niti
dulid
aesp
. 41
1C
ucuj
oide
aN
itidu
lidae
sp. 5
21
3C
ucuj
oide
aN
itidu
lidae
sp. 6
11
Cuc
ujoi
dea
Niti
dulid
aesp
. 71
1C
ucuj
oide
aN
itidu
lidae
sp. 8
44
Cuc
ujoi
dea
Niti
dulid
aesp
. 91
1C
ucuj
oide
aN
itidu
lidae
sp. 1
01
1C
ucuj
oide
aN
itidu
lidae
sp. 1
11
1C
ucuj
oide
aN
itidu
lidae
sp. 1
21
1C
ucuj
oide
aE
roty
lidae
sp. 1
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 21
56
Cuc
ujoi
dea
Ero
tylid
aesp
. 31
12
Cuc
ujoi
dea
Ero
tylid
aesp
. 41
1C
ucuj
oide
aE
roty
lidae
sp. 5
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 61
1C
ucuj
oide
aE
roty
lidae
sp. 7
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 81
1C
ucuj
oide
aE
roty
lidae
sp. 9
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 10
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 11
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 12
22
20
Cuc
ujoi
dea
Ero
tylid
aesp
. 13
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 14
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 15
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 16
77
Cuc
ujoi
dea
Ero
tylid
aesp
. 17
11
Cuc
ujoi
dea
Ero
tylid
aesp
. 18
11
Cuc
ujoi
dea
Sph
indi
dae
sp. 1
21
3C
ucuj
oide
aB
iphy
llida
esp
. 11
1C
ucuj
oide
aC
occi
nelli
dae
sp. 1
11
2C
ucuj
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aC
occi
nelli
dae
sp. 2
11
Lym
exyl
oide
aLy
mex
ylid
aesp
. 11
1Te
nebr
iono
idea
Mor
delli
dae
sp. 1
11
Tene
brio
noid
eaM
orde
llida
esp
. 21
1Te
nebr
iono
idea
Mor
delli
dae
sp. 3
11
2Te
nebr
iono
idea
Mor
delli
dae
sp. 4
11
13
Tene
brio
noid
eaM
orde
llida
esp
. 51
1Te
nebr
iono
idea
Mor
delli
dae
sp. 6
21
3Te
nebr
iono
idea
Mor
delli
dae
sp. 7
11
24
Tene
brio
noid
eaM
orde
llida
esp
. 81
1Te
nebr
iono
idea
Col
ydiid
aesp
. 11
1Te
nebr
iono
idea
Tene
brio
nida
esp
. 11
1C
hrys
omel
oide
aCer
amby
cida
esp
. 11
1C
hrys
omel
oide
aCer
amby
cida
esp
. 21
1C
hrys
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oide
aCer
amby
cida
esp
. 31
1C
hrys
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aCer
amby
cida
esp
. 41
1C
hrys
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aCer
amby
cida
esp
. 51
1C
hrys
omel
oide
aCer
amby
cida
esp
. 61
23
Chr
ysom
eloi
deaC
eram
byci
dae
sp. 7
11
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 11
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 22
13
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 3
14
5C
hrys
omel
oide
aChr
ysom
elid
aesp
. 41
21
4C
hrys
omel
oide
aChr
ysom
elid
aesp
. 51
32
6C
hrys
omel
oide
aChr
ysom
elid
aesp
. 62
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 71
1
21
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 9
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 1
01
11
3C
hrys
omel
oide
aChr
ysom
elid
aesp
. 11
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 1
21
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 13
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 1
41
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 15
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 1
61
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 17
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 1
81
12
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 1
91
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 20
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 2
11
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 22
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 2
31
110
12C
hrys
omel
oide
aChr
ysom
elid
aesp
. 24
21
3C
hrys
omel
oide
aChr
ysom
elid
aesp
. 25
22
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 2
61
15
7C
hrys
omel
oide
aChr
ysom
elid
aesp
. 27
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 2
82
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 29
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 3
01
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 31
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 3
21
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 33
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 3
41
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 35
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 3
63
61
10C
hrys
omel
oide
aChr
ysom
elid
aesp
. 37
11
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 38
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 3
92
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 40
41
5C
hrys
omel
oide
aChr
ysom
elid
aesp
. 41
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 4
21
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 43
11
22
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 4
41
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 45
12
3C
hrys
omel
oide
aChr
ysom
elid
aesp
. 46
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 4
71
23
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 4
81
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 49
22
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 5
01
2122
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 5
11
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 52
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 5
33
34
31
14C
hrys
omel
oide
aChr
ysom
elid
aesp
. 54
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 5
53
14
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 5
61
12
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 5
71
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 58
71
16
65
26C
hrys
omel
oide
aChr
ysom
elid
aesp
. 59
22
4C
hrys
omel
oide
aChr
ysom
elid
aesp
. 60
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 6
11
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 62
23
5C
hrys
omel
oide
aChr
ysom
elid
aesp
. 63
11
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 64
11
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 65
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 6
61
12
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 6
71
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 68
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 6
92
13
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 7
01
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 71
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 7
21
12
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 7
31
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 74
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 7
51
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 76
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 7
71
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 78
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 7
91
1
23
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
02
2C
hrys
omel
oide
aChr
ysom
elid
aesp
. 81
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
27
32
315
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
33
3C
hrys
omel
oide
aChr
ysom
elid
aesp
. 84
33
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
51
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 86
11
Chr
ysom
eloi
deaC
hrys
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idae
sp. 8
73
14
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
81
23
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 8
91
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 90
11
Chr
ysom
eloi
deaC
hrys
omel
idae
sp. 9
11
1C
hrys
omel
oide
aChr
ysom
elid
aesp
. 92
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 1
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 2
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 3
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 4
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 5
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 6
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 7
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 8
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 9
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 1
01
1C
urcu
liono
idea
Cur
culio
nida
esp
. 11
11
2C
urcu
liono
idea
Cur
culio
nida
esp
. 12
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 1
31
1C
urcu
liono
idea
Cur
culio
nida
esp
. 14
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 1
51
1C
urcu
liono
idea
Cur
culio
nida
esp
. 16
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 1
71
1C
urcu
liono
idea
Cur
culio
nida
esp
. 18
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 1
91
1C
urcu
liono
idea
Cur
culio
nida
esp
. 20
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 2
11
12
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 2
21
23
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 2
31
1
24
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 2
41
1C
urcu
liono
idea
Cur
culio
nida
esp
. 25
21
22
7C
urcu
liono
idea
Cur
culio
nida
esp
. 26
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 2
71
71
9C
urcu
liono
idea
Cur
culio
nida
esp
. 28
71
8C
urcu
liono
idea
Cur
culio
nida
esp
. 29
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 3
01
12
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 3
11
1C
urcu
liono
idea
Cur
culio
nida
esp
. 32
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 3
31
1C
urcu
liono
idea
Cur
culio
nida
esp
. 34
12
3C
urcu
liono
idea
Cur
culio
nida
esp
. 35
55
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 3
61
11
92
14C
urcu
liono
idea
Cur
culio
nida
esp
. 37
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 3
81
31
41
10C
urcu
liono
idea
Cur
culio
nida
esp
. 39
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 4
01
12
4C
urcu
liono
idea
Cur
culio
nida
esp
. 41
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 4
21
173
21C
urcu
liono
idea
Cur
culio
nida
esp
. 43
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 4
41
1C
urcu
liono
idea
Cur
culio
nida
esp
. 45
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 4
61
1C
urcu
liono
idea
Cur
culio
nida
esp
. 47
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 4
81
1C
urcu
liono
idea
Cur
culio
nida
esp
. 49
12
3C
urcu
liono
idea
Cur
culio
nida
esp
. 50
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 5
11
1C
urcu
liono
idea
Cur
culio
nida
esp
. 52
11
13
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 5
31
12
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 5
41
1C
urcu
liono
idea
Cur
culio
nida
esp
. 55
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 5
61
1C
urcu
liono
idea
Cur
culio
nida
esp
. 57
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 5
81
1C
urcu
liono
idea
Cur
culio
nida
esp
. 59
11
25
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 6
01
1C
urcu
liono
idea
Cur
culio
nida
esp
. 61
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 6
21
1C
urcu
liono
idea
Cur
culio
nida
esp
. 63
11
Cur
culio
noid
eaC
urcu
lioni
dae
sp. 6
41
1C
urcu
liono
idea
Sco
lytid
aesp
. 13
21
6C
urcu
liono
idea
Sco
lytid
aesp
. 22
2C
urcu
liono
idea
Sco
lytid
aesp
. 31
1C
urcu
liono
idea
Sco
lytid
aesp
. 41
1C
urcu
liono
idea
Sco
lytid
aesp
. 51
1
26
Har
vard
For
est S
ampl
e
Col
eopt
era
Supe
rfam
ilyFa
mily
Spec
ies
6/25
/05
8/16
/04
tota
lC
arab
oide
aC
arab
idae
sp. 1
11
Car
aboi
dea
Car
abid
aesp
. 21
1S
taph
ylin
oide
aS
ilphi
dae
sp. 1
22
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 11
1S
taph
ylin
oide
aS
taph
ylin
idae
sp. 2
55
Sta
phyl
inoi
dea
Sta
phyl
inid
aesp
. 316
16S
taph
ylin
oide
aS
caph
idiid
aesp
. 11
1S
taph
ylin
oide
aLe
ptod
irida
esp
. 11
1E
ucin
etoi
dea
Sci
rtida
e sp
. 12
2E
ucin
etoi
dea
Sci
rtida
e sp
. 221
21E
ucin
etoi
dea
Sci
rtida
esp
. 38
8E
ucin
etoi
dea
Sci
rtida
esp
. 415
217
Sca
raba
eoid
eaS
cara
bida
esp
. 11
1B
upre
stoi
dea
Bup
rest
idae
sp. 1
11
Bup
rest
oide
aB
upre
stid
aesp
. 21
1E
late
roid
eaTh
rosc
idae
sp. 1
11
Ela
tero
idea
Thro
scid
aesp
. 23
912
Ela
tero
idea
Thro
scid
aesp
. 349
49E
late
roid
eaE
late
ridae
sp. 1
31
4E
late
roid
eaE
late
ridae
sp. 2
11
Ela
tero
idea
Ela
terid
aesp
. 33
3E
late
roid
eaLy
cida
esp
. 14
4E
late
roid
eaLa
mpy
ridae
sp. 1
22
Ela
tero
idea
Lam
pyrid
aesp
. 24
4E
late
roid
eaLa
mpy
ridae
sp. 3
11
Ela
tero
idea
Can
thar
idae
sp. 1
11
Ela
tero
idea
Can
thar
idae
sp. 2
11
Ela
tero
idea
Can
thar
idae
sp. 3
2626
Bos
trich
oide
aA
nobi
idae
sp. 1
11
Bos
trich
oide
aA
nobi
idae
sp. 2
11
Cle
oide
aC
lerid
aesp
. 11
1
27
Cle
oide
aC
lerid
aesp
. 21
1C
leoi
dea
Cle
ridae
sp. 3
22
Cle
oide
aC
lerid
aesp
. 44
4C
ucuj
oide
aE
roty
lidae
sp. 1
11
Cuc
ujoi
dea
End
omyc
hida
esp
. 11
1C
ucuj
oide
aC
occi
nelli
dae
sp. 1
18
9C
ucuj
oide
aC
occi
nelli
dae
sp. 2
22
Tene
brio
noid
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11
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11
36
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rtae
sedi
ssp
. 20
119
75S
ymph
yta
Tent
hred
inoi
dea
Cim
bici
dae
Cim
bici
nae
sp. 1
111
39S
ymph
yta
Tent
hred
inoi
dea
Cim
bici
dae
Cim
bici
nae
sp. 2
124
18S
ymph
yta
Tent
hred
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dea
Cim
bici
dae
Cor
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r Pac
hylo
stic
tinae
sp. 3
153
0S
ymph
yta
Tent
hred
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Cim
bici
dae
ince
rtae
sedi
ssp
. 42
2990
Sym
phyt
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certa
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dis
sp. 4
228
Apo
crtia
Pro
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certa
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dis
sp. 1
129
02A
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148
5A
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172
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certa
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sp. 1
1
40
2107
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
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ince
rtae
sedi
sA
sp. 1
319
27A
pocr
tiaIc
hneu
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Asp
. 166
8A
pocr
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Asp
. 124
33A
pocr
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certa
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dis
Asp
. 21
2820
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sA
sp. 3
120
23A
pocr
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hneu
mon
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aIch
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certa
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dis
Asp
. 41
146
Apo
crtia
Ichn
eum
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deaI
chne
umon
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ince
rtae
sedi
sA
sp. 5
122
00A
pocr
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hneu
mon
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neum
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certa
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dis
Asp
. 61
2848
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
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ince
rtae
sedi
sA
sp. 7
124
16A
pocr
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hneu
mon
oide
aIch
neum
onid
aein
certa
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dis
Bsp
. 11
2859
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sB
sp. 2
137
8A
pocr
tiaIc
hneu
mon
oide
aIch
neum
onid
aein
certa
e se
dis
Bsp
. 31
684
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sC
sp. 1
1156
3A
pocr
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hneu
mon
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certa
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dis
Csp
. 121
55A
pocr
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hneu
mon
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certa
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dis
Csp
. 127
83A
pocr
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hneu
mon
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certa
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Csp
. 121
06A
pocr
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Csp
. 130
04A
pocr
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hneu
mon
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Csp
. 125
58A
pocr
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Csp
. 120
97A
pocr
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Csp
. 121
56A
pocr
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mon
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Csp
. 111
39A
pocr
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Csp
. 122
58A
pocr
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Csp
. 122
14A
pocr
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hneu
mon
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certa
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dis
Csp
. 21
138
Apo
crtia
Ichn
eum
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deaI
chne
umon
idae
ince
rtae
sedi
sC
sp. 3
111
0A
pocr
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hneu
mon
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aIch
neum
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certa
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dis
Csp
. 41
2263
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sC
sp. 5
139
4A
pocr
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hneu
mon
oide
aIch
neum
onid
aein
certa
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dis
Csp
. 61
2444
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sC
sp. 7
163
8A
pocr
tiaIc
hneu
mon
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neum
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certa
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dis
Csp
. 81
2839
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sC
sp. 9
229
53A
pocr
tiaIc
hneu
mon
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aIch
neum
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certa
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Csp
. 930
01A
pocr
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hneu
mon
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Csp
. 10
176
7A
pocr
tiaIc
hneu
mon
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dis
Dsp
. 12
2096
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sD
sp. 1
412
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sD
sp. 2
1
41
1988
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sD
sp. 3
127
10A
pocr
tiaIc
hneu
mon
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certa
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dis
Dsp
. 41
2110
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sD
sp. 5
134
9A
pocr
tiaIc
hneu
mon
oide
aIch
neum
onid
aein
certa
e se
dis
Dsp
. 61
2417
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sD
sp. 7
124
99A
pocr
tiaIc
hneu
mon
oide
aIch
neum
onid
aein
certa
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dis
Esp
. 11
140
Apo
crtia
Ichn
eum
onoi
deaI
chne
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ince
rtae
sedi
sE
sp. 2
160
5A
pocr
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hneu
mon
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aIch
neum
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aein
certa
e se
dis
Fsp
. 11
2975
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sF
sp. 2
121
09A
pocr
tiaIc
hneu
mon
oide
aIch
neum
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aein
certa
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dis
Fsp
. 31
2428
Apo
crtia
Ichn
eum
onoi
deaI
chne
umon
idae
ince
rtae
sedi
sF
sp. 4
125
51A
pocr
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hneu
mon
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aIch
neum
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certa
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dis
Fsp
. 51
1963
Apo
crtia
Ichn
eum
onoi
deaB
raco
nida
ein
certa
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dis
sp. 1
141
9A
pocr
tiaIc
hneu
mon
oide
aBra
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dae
ince
rtae
sedi
ssp
. 21
507
Apo
crtia
Cyn
ipoi
dea
Figi
tidae
ince
rtae
sedi
ssp
. 11
225
Apo
crtia
Chr
ysid
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ain
certa
e se
dis
ince
rtae
sedi
ssp
. 11
592
Apo
crtia
Vesp
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aVe
spid
aesp
. 11
1094
Apo
crtia
Vesp
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aVe
spid
aesp
. 21
376
Apo
crtia
Vesp
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aFo
rmic
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sp. 1
139
0A
pocr
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spoi
dea
Form
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2292
Apo
crtia
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121
11A
pocr
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128
32A
pocr
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2996
Apo
crtia
Vesp
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aFo
rmic
idae
sp. 6
140
3A
pocr
tiaS
phec
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phec
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rtae
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ssp
. 11
526
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crtia
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certa
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sp. 2
124
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pocr
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rtae
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2988
Apo
crtia
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rtae
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ince
rtae
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ssp
. 11
383
Apo
crtia
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rtae
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sin
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rtae
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ssp
. 21
545
Apo
crtia
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rtae
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dis
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rtae
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ssp
. 31
418
Apo
crtia
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rtae
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ssp
. 41
2994
Apo
crtia
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42
La S
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Sam
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21
25
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29
14A
pocr
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11
13
Apo
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3A
pocr
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pocr
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11
Apo
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11
Apo
crita
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41
5A
pocr
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25
Apo
crita
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11
Apo
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11
Apo
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11
Apo
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sp. 7
11
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sp. 8
11
Apo
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11
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01
1A
pocr
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11
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21
12
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31
12
Apo
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sp. 1
42
13
6A
pocr
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. 15
11
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sp. 1
63
3A
pocr
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. 17
11
Apo
crita
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sp. 1
81
1A
pocr
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. 19
33
43
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crita
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1A
pocr
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11
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crita
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1A
pocr
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11
2A
pocr
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11
Apo
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Cha
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lcid
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sp. 1
11
Apo
crita
Cha
lcid
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lcid
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lcid
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chym
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sp. 2
21
3A
pocr
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halc
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. 11
1A
pocr
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halc
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. 22
2A
pocr
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. 32
2A
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. 41
1A
pocr
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. 51
1A
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. 61
1A
pocr
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halc
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. 71
1A
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. 81
1A
pocr
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halc
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. 91
1A
pocr
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52
7A
pocr
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. 11
11
Apo
crita
Cha
lcid
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21
1A
pocr
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. 13
11
Apo
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41
1A
pocr
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11
Apo
crita
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sp. 1
64
15
Apo
crita
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lcid
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lcid
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sp. 1
71
1A
pocr
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, 18
11
Apo
crita
Cha
lcid
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lcid
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Con
ura
sp, 1
91
1A
pocr
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11
Apo
crita
Cha
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sp. 1
11
Apo
crita
Cha
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32
157
128
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44
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35
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11
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41
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61
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55
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71
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81
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21
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11
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Apo
crita
Ichn
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Bra
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ogad
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1A
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ogad
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1A
pocr
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ogad
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1A
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ogad
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. 71
1A
pocr
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1A
pocr
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. 91
1A
pocr
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11
Apo
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Ichn
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11
Apo
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Ichn
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Bra
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31
1A
pocr
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mon
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11
Apo
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Ichn
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Bra
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Rog
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sp. 1
51
1A
pocr
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mon
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11
Apo
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Ichn
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Bra
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71
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11
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Chr
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sp. 2
22
15
Apo
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Chr
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11
Apo
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Chr
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11
Apo
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Chr
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sp. 5
11
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Chr
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mph
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sp. 6
11
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Chr
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mph
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sp. 7
11
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crita
Chr
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mph
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sp. 8
22
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crita
Chr
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aeP
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cera
sp. 1
11
2A
pocr
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hrys
idoi
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lidae
Pris
toce
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Pris
toce
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. 21
1A
pocr
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hrys
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deaB
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lidae
Pris
toce
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Pse
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12
Apo
crita
Chr
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sp. 2
11
Apo
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Chr
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ssp
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1A
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Bak
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llasp
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hrys
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lidae
Epy
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Bak
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llasp
. 21
1A
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lidae
Epy
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Epy
rissp
. 11
1A
pocr
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lidae
Epy
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Epy
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. 22
11
12
7A
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1
49
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11
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sp. 3
11
Apo
crita
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phia
sp. 1
11
Apo
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Vesp
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sp. 2
12
25
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illin
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phut
asp
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1A
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Mut
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sp. 2
11
Apo
crita
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mat
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palo
som
asp
. 11
1A
pocr
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Pom
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sp. 1
11
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Vesp
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lidae
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sp. 1
11
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crita
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lidae
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sina
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geni
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sp. 2
11
2A
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11
13
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lidae
Pep
sina
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. 11
1A
pocr
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dea
Pom
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Ano
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. 11
13
5A
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Pom
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Epi
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nsp
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1A
pocr
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Pom
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Poe
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ssp. 1
11
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Pom
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. 11
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Pom
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Prio
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. 21
1A
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Pom
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12
Apo
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Vesp
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umen
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Mon
tezu
mia
sp. 1
11
Apo
crita
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spid
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olis
tinae
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1A
pocr
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Vesp
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. 31
1A
pocr
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sp. 1
11
35
Apo
crita
Apo
idea
Sph
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phec
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Chl
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nsp
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1A
pocr
itaA
poid
eaS
phec
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Sph
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phex
sp. 1
11
Apo
crita
Apo
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Cra
bron
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phre
doni
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nulu
ssp
. 11
1A
pocr
itaA
poid
eaC
rabr
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emph
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nina
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sp. 1
11
Apo
crita
Apo
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Cra
bron
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Cra
bron
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asp
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1A
pocr
itaA
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rabr
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sp. 1
11
Apo
crita
Apo
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Cra
bron
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Cra
bron
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Tryp
oxyl
onsp
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12
Apo
crita
Apo
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Cra
bron
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Cra
bron
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Tryp
oxyl
onsp
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12
50
Apo
crita
Apo
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Cra
bron
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Cra
bron
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Tryp
oxyl
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1A
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sp. 1
13
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nopl
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11
12
Apo
crita
Apo
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Hal
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alic
tinae
Lasi
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sp. 2
33
Apo
crita
Apo
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Hal
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aeH
alic
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Lasi
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ssum
sp. 3
11
Apo
crita
Apo
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Hal
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alic
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Aug
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sp. 1
11
Apo
crita
Apo
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Hal
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alic
tinae
Aug
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lasp
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1A
pocr
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sp. 1
11
Apo
crita
Apo
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Api
dae
Xyl
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Cer
atin
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. 11
1A
pocr
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sp. 1
11
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Apo
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nae
Par
tam
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sp. 1
11
Apo
crita
Apo
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dae
Api
nae
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sp. A
11
Apo
crita
Apo
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Api
dae
Api
nae
Trig
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sp. B
11
Apo
crita
Apo
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Api
dae
Api
nae
Trig
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sp. C
11
Apo
crita
Vesp
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12
Apo
crita
Vesp
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icin
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arat
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sp. 1
12
3A
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sp. 1
11
Apo
crita
Vesp
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ptog
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sp. 1
61
7A
pocr
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spoi
dea
Form
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oner
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Lept
ogen
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1A
pocr
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spoi
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Form
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oner
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Pac
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23
6A
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Form
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Form
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23
Apo
crita
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crita
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Apo
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Apo
crita
Vesp
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Myr
mic
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Apt
eros
tigm
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. 21
1
51
Apo
crita
Vesp
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rmic
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Myr
mic
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Meg
alom
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Form
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sp. 2
22
Apo
crita
Vesp
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mic
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alom
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Form
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213
Apo
crita
Vesp
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Myr
mic
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Phe
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12
Apo
crita
Vesp
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Myr
mic
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Apo
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Apo
crita
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Apo
crita
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Apo
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sp. 5
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Apo
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sp. 7
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pocr
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Apo
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Pro
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110
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2A
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53
Apo
crita
Pro
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5A
pocr
itaIc
hneu
mon
oide
aB
raco
nida
eR
ogad
inae
?sp
. 31
01
Apo
crita
Ichn
eum
onoi
dea
Bra
coni
dae
Rog
adin
ae?
sp. 4
10
1A
pocr
itaIc
hneu
mon
oide
aB
raco
nida
eR
ogad
inae
?sp
. 51
01
Apo
crita
Ichn
eum
onoi
dea
Bra
coni
dae
Rog
adin
ae?
sp. 6
01
1A
pocr
itaIc
hneu
mon
oide
aB
raco
nida
eR
ogad
inae
?sp
. 70
22
Apo
crita
Ichn
eum
onoi
dea
Bra
coni
dae
Rog
adin
ae?
sp. 8
01
1A
pocr
itaC
hrys
idoi
dea
Bet
hylid
aeP
risto
cerin
aeP
seud
isob
rach
iuma
shm
eadi
02
2A
pocr
itaC
hrys
idoi
dea
Bet
hylid
aeE
pyrin
aeA
nise
pyris
subv
iola
ceus
01
1A
pocr
itaC
hrys
idoi
dea
Chr
ysid
idae
Chr
ysid
inae
Chr
ysis
nitid
ula
22
4
61
Apo
crita
Chr
ysid
oide
aC
hrys
idid
aeC
hrys
idin
aeC
hrys
issp
11
01
Apo
crita
Chr
ysid
oide
aD
ryin
idae
Ant
eoni
nae
Lonc
hodr
yini
ssp
. 1
20
2A
pocr
itaC
hrys
idoi
dea
Dry
inid
aeG
onat
otop
inae
??
sp. 2
10
1A
pocr
itaVe
spoi
dea
Mut
illid
aeM
yrm
osin
aeM
yrm
osa
unic
olor
01
1A
pocr
itaVe
spoi
dea
Mut
illid
aeM
utill
inae
Eph
uta
sp. 1
01
1A
pocr
itaVe
spoi
dea
Pom
pilid
aeP
epsi
nae
Dip
ogon
papa
go0
11
Apo
crita
Vesp
oide
aP
ompi
lidae
Pep
sina
eD
ipog
onpu
lchr
ipen
nis
24
6A
pocr
itaVe
spoi
dea
Pom
pilid
aeP
epsi
nae
Dip
ogon
sayi
03
3A
pocr
itaVe
spoi
dea
Pom
pilid
aeP
epsi
nae
Prio
cnem
isge
rman
a0
11
Apo
crita
Vesp
oide
aP
ompi
lidae
Pep
sina
eP
riocn
emis
hest
ia0
11
Apo
crita
Vesp
oide
aP
ompi
lidae
Pep
sina
eP
riocn
emis
min
orat
a1
01
Apo
crita
Vesp
oide
aP
ompi
lidae
Pep
sina
eA
uplo
pus
caer
ules
cens
10
1A
pocr
itaVe
spoi
dea
Pom
pilid
aeP
epsi
nae
Aup
lopu
sm
ellip
es0
22
Apo
crita
Vesp
oide
aP
ompi
lidae
Pep
sina
eA
geni
ella
nora
ta0
2222
Apo
crita
Vesp
oide
aP
ompi
lidae
Pom
plin
aeA
nopl
ius
sp. 1
10
1A
pocr
itaVe
spoi
dea
Pom
pilid
aeP
ompl
inae
Ara
chno
spila
arct
us0
22
Apo
crita
Vesp
oide
aP
ompi
lidae
Pom
plin
aeE
pisy
ron
bigu
ttatu
s1
01
Apo
crita
Vesp
oide
aP
ompi
lidae
Pom
plin
aeE
vage
tes
asig
nus
01
1A
pocr
itaVe
spoi
dea
Pom
pilid
aeP
ompl
inae
Eva
gete
spa
rvus
01
1A
pocr
itaVe
spoi
dea
Vesp
idae
Eum
enin
aeA
ncis
troce
rus
cats
kill
12
3A
pocr
itaVe
spoi
dea
Vesp
idae
Eum
enin
aeS
ymm
orph
usca
nade
nsis
60
6A
pocr
itaVe
spoi
dea
Vesp
idae
Vesp
inae
Vesp
ula
cons
obrin
a0
11
Apo
crita
Vesp
oide
aVe
spid
aeVe
spin
aeVe
spul
am
acul
ifron
s1
01
Apo
crita
Vesp
oide
aVe
spid
aeVe
spin
aeVe
spul
asp
. 10
11
Apo
crita
Vesp
oide
aVe
spid
aeVe
spin
aeD
olic
hove
spul
am
acul
ata
10
1A
pocr
itaVe
spoi
dea
Form
icid
aeD
olic
hode
rinae
Tapi
nom
ase
ssile
10
1A
pocr
itaVe
spoi
dea
Form
icid
aeFo
rmic
inae
Cam
pono
tus
nova
ebor
acen
sis
01
1A
pocr
itaVe
spoi
dea
Form
icid
aeM
yrm
icin
aeM
yrm
ica
punc
tiven
tris
01
1A
pocr
itaA
poid
eaC
rabr
onid
aeP
emph
redo
nina
eM
imum
esa
sp. 1
10
1A
pocr
itaA
poid
eaC
rabr
onid
aeP
emph
redo
nina
eP
senu
lus
sp. 1
31
4A
pocr
itaA
poid
eaC
rabr
onid
aeP
emph
redo
nina
eP
senu
lus
sp. 2
10
1A
pocr
itaA
poid
eaC
rabr
onid
aeP
emph
redo
nina
eP
assa
loec
ussp
. 13
03
Apo
crita
Apo
idea
Cra
bron
idae
Pem
phre
doni
nae
Pem
phre
don
sp. 1
11
2A
pocr
itaA
poid
eaC
rabr
onid
aeP
emph
redo
nina
eS
pilo
men
aba
rber
i0
22
Apo
crita
Apo
idea
Cra
bron
idae
Pem
phre
doni
nae
Stig
mus
frate
rnus
02
2
62
Apo
crita
Apo
idea
Cra
bron
idae
Pem
phre
doni
nae
Stig
mus
fulv
ipes
01
1A
pocr
itaA
poid
eaC
rabr
onid
aeC
rabr
onin
aeN
itela
sp. 1
02
2A
pocr
itaA
poid
eaC
rabr
onid
aeC
rabr
onin
aeTr
ypox
ylon
sp. 1
02
2A
pocr
itaA
poid
eaC
rabr
onid
aeC
rabr
onin
aeTr
ypox
ylon
sp. 2
02
2A
pocr
itaA
poid
eaC
rabr
onid
aeC
rabr
onin
aeTr
ypox
ylon
sp. 3
40
4A
pocr
itaA
poid
eaC
rabr
onid
aeC
rabr
onin
aeC
ross
ocer
ussp
. 11
12
Apo
crita
Apo
idea
Cra
bron
idae
Cra
bron
inae
Ect
emni
ussp
. 11
12
Apo
crita
Apo
idea
Cra
bron
idae
Cra
bron
inae
Rho
palu
mco
arct
atum
01
1A
pocr
itaA
poid
eaC
rabr
onid
aeC
rabr
onin
aeR
hopa
lum
rufig
aste
r2
13
Apo
crita
Apo
idea
Col
letid
aeH
ylae
inae
Hyl
aeus
sp. 1
10
1A
pocr
itaA
poid
eaA
ndre
nida
eA
ndre
nina
eA
ndre
nasp
. 11
01
Apo
crita
Apo
idea
And
reni
dae
And
reni
nae
And
rena
sp. 2
10
1A
pocr
itaA
poid
eaA
ndre
nida
eA
ndre
nina
eA
ndre
nasp
. 32
02
Apo
crita
Apo
idea
And
reni
dae
And
reni
nae
And
rena
vici
na1
01
Apo
crita
Apo
idea
Hal
ictid
aeH
alic
tinae
Aga
post
emon
sp. 1
01
1A
pocr
itaA
poid
eaH
alic
tidae
Hal
ictin
aeLa
siog
loss
umsp
. 11
01
Apo
crita
Apo
idea
Hal
ictid
aeH
alic
tinae
L. (D
ialic
tus)
sp. 1
35
8A
pocr
itaA
poid
eaH
alic
tidae
Hal
ictin
aeL.
(Dia
lictu
s)sp
. 21
01
Apo
crita
Apo
idea
Hal
ictid
aeH
alic
tinae
Sph
ecod
essp
. 10
11
Apo
crita
Apo
idea
Hal
ictid
aeH
alic
tinae
Aug
ochl
ora
pura
10
1A
pocr
itaA
poid
eaM
elitt
idae
Mel
ittin
aeM
elitt
asp
. 11
01
Apo
crita
Apo
idea
Meg
achi
lidae
Meg
achi
linae
Her
iade
ssp
. 11
01
Apo
crita
Apo
idea
Api
dae
Nom
adin
aeN
omad
asp
. 11
01
Apo
crita
Apo
idea
Api
dae
Api
nae
Bom
bus
bim
acul
atus
01
1A
pocr
itaA
poid
eaA
pida
eA
pina
eB
ombu
sim
patie
ns1
01
Apo
crita
Apo
idea
Api
dae
Api
nae
Bom
bus
tern
ariu
s1
01
Apo
crita
Apo
idea
Api
dae
Api
nae
Bom
bus
vaga
ns8
19
63
McA
bee
Sam
ple
Dip
tera
num
ber
Subo
rder
Fam
ilyG
enus
Spec
ies
Qua
nt.
1991
Nem
atoc
era
Tipu
lidae
sp. 1
124
60N
emat
ocer
aTi
pulid
aesp
. 22
1933
Nem
atoc
era
Tipu
lidae
sp. 2
2154
Nem
atoc
era
Tipu
lidae
sp. 3
146
Nem
atoc
era
Tipu
lidae
sp. 4
229
86N
emat
ocer
aTi
pulid
aesp
. 411
34N
emat
ocer
aTi
pulid
aesp
. 52
1350
Nem
atoc
era
Tipu
lidae
sp. 5
2372
Nem
atoc
era
Lim
oniid
aesp
. 11
2405
Nem
atoc
era
Lim
oniid
aesp
. 21
288
Nem
atoc
era
Lim
oniid
aesp
. 31
2160
Nem
atoc
era
Cyl
indr
otom
idae
sp. 1
125
36N
emat
ocer
aC
ylin
drot
omid
aesp
. 21
673
Nem
atoc
era
Tipu
lom
orph
a in
. sed
.sp
. 11
1979
Nem
atoc
era
Myc
etop
hilid
aesp
. 11
2219
Nem
atoc
era
Myc
etop
hilid
aesp
. 21
2390
Nem
atoc
era
Myc
etop
hilid
aesp
. 31
2021
Nem
atoc
era
Myc
etop
hilid
aesp
. 42
399
Nem
atoc
era
Myc
etop
hilid
aesp
. 411
24N
emat
ocer
aM
ycet
ophi
lidae
sp. 5
127
17N
emat
ocer
aM
ycet
ophi
lidae
sp. 6
152
1N
emat
ocer
aM
ycet
ophi
lidae
sp. 7
150
6N
emat
ocer
aM
ycet
ophi
lidae
sp. 8
125
55N
emat
ocer
aM
ycet
ophi
lidae
sp. 9
161
7N
emat
ocer
aM
ycet
ophi
lidae
sp. 1
01
694
Nem
atoc
era
Tric
hoce
ridae
sp
. 11
1237
Nem
atoc
era
Tric
hoce
ridae
?sp
. 21
2995
Bra
chyc
era
Syr
phid
aesp
. 11
1210
Bra
chyc
era
Syr
phid
aesp
. 21
2777
Bra
chyc
era
Syr
phid
aesp
. 32
2578
Bra
chyc
era
Syr
phid
aesp
. 3
64
2276
Bra
chyc
era
Syr
phid
aesp
. 41
1064
Bra
chyc
era
Syr
phid
aesp
. 51
1982
Bra
chyc
era
Syr
phid
aesp
. 61
575
Bra
chyc
era
ince
rtae
sedi
ssp
. 11
135
Bra
chyc
era
ince
rtae
sedi
ssp
. 22
45B
rach
ycer
a in
certa
e se
dis
sp. 2
1091
Bra
chyc
era
ince
rtae
sedi
ssp
. 31
184
Bra
chyc
era
ince
rtae
sedi
ssp
. 41
588
Bra
chyc
era
ince
rtae
sedi
ssp
. 51
1247
Bra
chyc
era
ince
rtae
sedi
ssp
. 61
1092
ince
rtae
sedi
since
rtae
sedi
ssp
. 11
207
ince
rtae
sedi
since
rtae
sedi
ssp
. 21
2600
ince
rtae
sedi
since
rtae
sedi
ssp
. 32
2826
ince
rtae
sedi
since
rtae
sedi
ssp
. 3
65
La S
elva
Sam
ple
Dip
tera
Trap
Subo
rder
Fam
ilySp
ecie
sT1M
13T1
W2
T2W
2T3
W2
T4W
2T5
W2
T6W
2H
TW2
AR
Bto
tal
Nem
atoc
era
Tipu
lidae
sp. 1
11
21
22
9N
emat
ocer
aTi
pulid
aesp
. 21
1N
emat
ocer
aTi
pulid
aesp
. 32
13
14
112
Nem
atoc
era
Tipu
lidae
sp. 4
54
11
26
120
Nem
atoc
era
Tipu
lidae
sp. 5
11
2N
emat
ocer
aTi
pulid
aesp
. 62
2N
emat
ocer
aTi
pulid
aesp
. 71
12
Nem
atoc
era
Tipu
lidae
sp. 8
41
16
Nem
atoc
era
Tipu
lidae
sp. 9
31
26
Nem
atoc
era
Tipu
lidae
sp. 1
01
1N
emat
ocer
aTi
pulid
aesp
. 11
21
21
21
35
118
Nem
atoc
era
Tipu
lidae
sp. 1
22
13
Nem
atoc
era
Tipu
lidae
sp. 1
32
2N
emat
ocer
aTi
pulid
aesp
. 14
11
Nem
atoc
era
Tipu
lidae
sp. 1
51
14
6N
emat
ocer
aTi
pulid
aesp
. 16
12
3N
emat
ocer
aTi
pulid
aesp
. 17
11
Nem
atoc
era
Tipu
lidae
sp. 1
82
2N
emat
ocer
aTi
pulid
aesp
. 19
11
Nem
atoc
era
Tipu
lidae
sp. 2
01
1N
emat
ocer
aTi
pulid
aesp
. 21
11
2N
emat
ocer
aTi
pulid
aesp
. 22
33
6N
emat
ocer
aTi
pulid
aesp
. 23
54
210
45
333
Nem
atoc
era
Tipu
lidae
sp. 2
41
1N
emat
ocer
aTi
pulid
aesp
. 25
11
Nem
atoc
era
Tipu
lidae
sp. 2
61
1N
emat
ocer
aTi
pulid
aesp
. 27
11
Nem
atoc
era
Tipu
lidae
sp. 2
81
11
3N
emat
ocer
aTi
pulid
aesp
. 29
11
Nem
atoc
era
Tipu
lidae
sp. 3
01
1N
emat
ocer
aTi
pulid
aesp
. 31
11
66
Nem
atoc
era
Tipu
lidae
sp. 3
21
1N
emat
ocer
aTi
pulid
aesp
. 33
11
Nem
atoc
era
Tipu
lidae
sp. 3
41
1N
emat
ocer
aTi
pulid
aesp
. 35
11
Nem
atoc
era
Tipu
lidae
sp. 3
61
1N
emat
ocer
aTi
pulid
aesp
. 37
11
2N
emat
ocer
aTi
pulid
aesp
. 38
11
2N
emat
ocer
aTi
pulid
aesp
. 39
11
Nem
atoc
era
Tipu
lidae
sp. 4
01
1N
emat
ocer
aTi
pulid
aesp
. 41
11
Nem
atoc
era
Tipu
lidae
sp. 4
21
11
3N
emat
ocer
aTi
pulid
aesp
. 43
11
24
Nem
atoc
era
Tipu
lidae
sp. 4
41
1N
emat
ocer
aTi
pulid
aesp
. 45
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 11
12
Nem
atoc
era
Myc
etop
hilid
aesp
. 22
2N
emat
ocer
aM
ycet
ophi
lidae
sp. 3
11
2N
emat
ocer
aM
ycet
ophi
lidae
sp. 4
11
2N
emat
ocer
aM
ycet
ophi
lidae
sp. 5
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 61
1N
emat
ocer
aM
ycet
ophi
lidae
sp. 7
31
4N
emat
ocer
aM
ycet
ophi
lidae
sp. 8
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 91
1N
emat
ocer
aM
ycet
ophi
lidae
sp. 1
02
2N
emat
ocer
aM
ycet
ophi
lidae
sp. 1
11
12
Nem
atoc
era
Myc
etop
hilid
aesp
. 12
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 13
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 14
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 15
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 16
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 17
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 18
81
11
11N
emat
ocer
aM
ycet
ophi
lidae
sp. 1
97
11
9N
emat
ocer
aM
ycet
ophi
lidae
sp. 2
04
11
6N
emat
ocer
aM
ycet
ophi
lidae
sp. 2
13
3
67
Nem
atoc
era
Myc
etop
hilid
aesp
. 22
11
13
Nem
atoc
era
Myc
etop
hilid
aesp
. 23
21
14
Nem
atoc
era
Myc
etop
hilid
aesp
. 24
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 25
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 26
11
Nem
atoc
era
Myc
etop
hilid
aesp
. 27
14
31
44
17B
rach
ycer
aTa
bani
dae
sp. 1
13
11
17
Bra
chyc
era
Taba
nida
esp
. 21
12
Bra
chyc
era
Taba
nida
esp
. 31
1B
rach
ycer
aTa
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chyc
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esp
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Bra
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esp
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aTh
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11
Bra
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Asi
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11
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11
Bra
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Asi
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11
Bra
chyc
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Dol
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24
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10B
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esp
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. 31
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33
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esp
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17
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Bra
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Dol
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Bra
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Bra
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11
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Dol
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32
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Bra
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Dol
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Bra
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Dol
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Dol
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11
Bra
chyc
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Dol
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01
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esp
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22
Bra
chyc
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Dol
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dae
sp. 3
22
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esp
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11
Bra
chyc
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Dol
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dae
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41
1B
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hopo
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esp
. 35
11
Bra
chyc
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Pip
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319
123
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Pip
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12
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11
Bra
chyc
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Syr
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12
Bra
chyc
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Syr
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. 22
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11
Bra
chyc
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Syr
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11
Bra
chyc
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Syr
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Syr
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11
15
Bra
chyc
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Syr
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. 91
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11
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141
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ciom
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11
Bra
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Laux
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aLa
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11
Bra
chyc
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Laux
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. 31
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aLa
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70
Bra
chyc
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Psi
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chyc
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Ric
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6B
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. 21
12
Bra
chyc
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22
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. 41
23
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chyc
era
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11
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1B
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52
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11
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chyc
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11
Bra
chyc
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esp
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15
Bra
chyc
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Mic
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esp
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1B
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11
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chyc
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chyc
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Ast
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chyc
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Eph
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23
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chyc
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Dro
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. 13
25
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chyc
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. 21
1B
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chyc
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chyc
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. 27
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114
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arco
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sp. 5
33
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53
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11
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11
Bra
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11
Bra
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21
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61
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11
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91
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01
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11
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21
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chin
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Har
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40
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50
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chyc
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Bra
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sp. 1
80
22
Bra
chyc
era
Dol
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dae
sp. 1
90
66
Bra
chyc
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Asi
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105
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era
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. 40
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chyc
era
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sp. 5
01
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. 60
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chyc
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sp. 1
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. 21
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Bra
chyc
era
Pip
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lidae
sp. 3
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214
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32
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826
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sp. 8
01
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41
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Bra
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Syr
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. 15
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sp. 1
61
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Bra
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Syr
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sp. 1
81
01
Bra
chyc
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Syr
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. 19
10
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sp. 2
01
01
Bra
chyc
era
Con
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. 10
22
Bra
chyc
era
Sci
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10
1B
rach
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aS
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. 20
11
Bra
chyc
era
Laux
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Bra
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Lonc
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11
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Teph
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11
Bra
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Mic
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11
Bra
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Clu
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11
Bra
chyc
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Aul
acig
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dae
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01
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sp. 1
01
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aC
hlor
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01
Bra
chyc
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Sca
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20
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Bra
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Cal
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sp. 1
01
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aC
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. 20
11
Bra
chyc
era
Cal
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ridae
sp. 3
01
1B
rach
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aS
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phag
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sp. 1
10
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aS
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sp. 2
10
1B
rach
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aS
arco
phag
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sp. 3
10
1B
rach
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aS
arco
phag
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sp. 4
15
6B
rach
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aS
arco
phag
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sp. 5
11
2B
rach
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aS
arco
phag
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sp. 6
90
9B
rach
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aS
arco
phag
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sp. 7
36
9B
rach
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aS
arco
phag
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sp. 8
10
1B
rach
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aS
arco
phag
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sp. 9
10
1
77
Bra
chyc
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Sar
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aesp
. 10
36
9B
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aS
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12
810
Bra
chyc
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Sar
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aesp
. 12
11
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rach
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aS
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30
1010
Bra
chyc
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Sar
coph
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aesp
. 14
10
1B
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aS
arco
phag
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sp. 1
53
03
Bra
chyc
era
Sar
coph
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aesp
. 16
617
23B
rach
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aS
arco
phag
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sp. 1
71
01
Bra
chyc
era
Sar
coph
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aesp
. 18
01
1B
rach
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aS
arco
phag
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sp. 1
90
11
Bra
chyc
era
Sar
coph
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aesp
. 20
01
1B
rach
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aS
arco
phag
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sp. 2
10
55
Bra
chyc
era
Sar
coph
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aesp
. 22
03
3B
rach
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aS
arco
phag
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sp. 2
30
22
Bra
chyc
era
Sar
coph
agid
aesp
. 24
01
1B
rach
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aS
arco
phag
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50
11
Bra
chyc
era
Sar
coph
agid
aesp
. 26
02
2B
rach
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aS
arco
phag
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sp. 2
70
11
Bra
chyc
era
Sar
coph
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aesp
. 28
02
2B
rach
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aS
arco
phag
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sp. 2
90
11
Bra
chyc
era
Sar
coph
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. 30
01
1B
rach
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aS
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phag
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10
11
Bra
chyc
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. 32
01
1B
rach
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aS
arco
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11
Bra
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Tach
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03
Bra
chyc
era
Tach
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. 21
01
Bra
chyc
era
Tach
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. 32
35
Bra
chyc
era
Tach
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02
Bra
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era
Tach
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02
Bra
chyc
era
Tach
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01
Bra
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era
Tach
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. 71
01
Bra
chyc
era
Tach
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. 81
01
Bra
chyc
era
Tach
inid
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. 91
01
Bra
chyc
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. 10
02
2B
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aTa
chin
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sp. 1
10
33
78
Bra
chyc
era
Tach
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aesp
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05
5B
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aTa
chin
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sp. 1
30
11
Bra
chyc
era
Tach
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. 14
01
1B
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aTa
chin
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sp. 1
50
11
Bra
chyc
era
Tach
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. 16
01
1B
rach
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aTa
chin
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sp. 1
70
11
Bra
chyc
era
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02
2
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McA
bee
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ple
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ber
Subo
rder
Fam
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Spec
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Qua
nt.
Mec
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ra20
26B
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sp.1
111
27B
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sp.2
229
91B
ittac
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sp.2
1924
Bitt
acid
aesp
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2500
Bitt
acid
aesp
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2837
Din
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dae
Din
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9D
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sp.1
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sp.1
1745
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2273
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Tric
hopt
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certa
e se
dis
sp. 1
957
2in
certa
e se
dis
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1123
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ssp
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33in
certa
e se
dis
sp. 1
2954
ince
rtae
sedi
ssp
. 111
26in
certa
e se
dis
sp. 1
2100
ince
rtae
sedi
ssp
. 123
92in
certa
e se
dis
sp. 1
2666
ince
rtae
sedi
ssp
. 132
8in
certa
e se
dis
sp. 2
1
80
490
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rtae
sedi
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. 33
450
ince
rtae
sedi
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. 319
22in
certa
e se
dis
sp. 3
646
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. 41
1163
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rtae
sedi
ssp
. 52
2825
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sedi
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. 522
24in
certa
e se
dis
sp. 6
119
26in
certa
e se
dis
sp. 7
1
25O
smyl
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sp.1
212
20O
smyl
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sp.1
159
Osm
ylid
aesp
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2851
Osm
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651
Hem
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sp.1
119
87H
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2716
Hem
erob
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sp.3
127
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hrys
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1121
Chr
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sp.1
2763
Chr
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sp.1
983
Chr
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sp.2
124
3C
hrys
opid
aesp
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2190
Chr
ysop
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sp.3
2189
Chr
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sp.4
127
90in
certa
e se
dis
sp.1
1
Ort
hopt
era
3003
Ens
ifera
Tetti
goni
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327
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162
3E
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alan
gops
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in. s
edis
sp. 2
126
5C
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rtae
sedi
sin
. sed
issp
. 11
679
Cae
lifer
ain
certa
e se
dis
in. s
edis
sp. 2
1
Isop
tera
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ropt
era
81
664
Hod
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miti
dae
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. 13
633
Hod
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dae
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142
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gopt
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rtae
sedi
ssp
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105
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sopt
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82
La S
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Sam
ple
Trap
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tal
Tric
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1
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diss
p. 1
11
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ropt
era
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11
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p. 1
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mer
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11
Psoc
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dissp
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23
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rtae
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certa
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23
Ort
hopt
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Cae
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dae
sp. 1
22
Cae
lifer
aTe
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dae
sp. 2
15
17
Cae
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11
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rtae
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11
12
Cae
lifer
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11
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Cae
lifer
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p. 3
11
Cae
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11
Cae
lifer
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11
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ince
rtae
sedi
ssp.
61
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sedi
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71
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14
Ens
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dae
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11
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esp
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11
3E
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dae
sp. 4
11
Ens
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esp
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12
8E
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dae
sp. 6
11
24
Ens
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esp
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raG
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dae
sp. 8
11
Ens
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esp
. 91
1E
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niid
aesp
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. 21
1E
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aesp
. 31
1E
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1
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tera
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sedi
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tode
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11
13
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rtae
sedi
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21
1
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map
tera
Ince
rtae
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ssp.
11
1
84
Har
vard
For
est S
ampl
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rder
Fam
ilySp
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Tric
hopt
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omat
idaesp
. 10
1010
Glo
ssos
omat
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. 23
03
Glo
ssos
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. 31
01
Glo
ssos
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03
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10
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21
01
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p. 3
10
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. 10
11
Lept
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idae
sp. 2
10
1H
ydro
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sp. 1
110
11H
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dae
sp. 2
10
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Dip
seud
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dae
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7
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ttode
ain
certa
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dis
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01
1
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aesp
. 12
24
Hem
erob
iidae
sp. 1
10
1
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opte
rain
certa
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dis
sp. 1
10
1in
certa
e se
dis
sp. 2
20
2in
certa
e se
dis
sp. 3
20
2in
certa
e se
dis
sp. 4
10
1
Ort
hopt
era
Cae
lifer
aA
crid
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sp. 1
017
17
85
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nata
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pter
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grio
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10
11
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pter
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23
03
Zygo
pter
aC
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esp.
33
03
Zygo
pter
aLe
stid
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44
Zygo
pter
aLe
stid
aesp
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01
Zygo
pter
aLe
stid
aesp
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11
Ani
sopt
era
Libe
llulid
aesp
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11
86
