ZooKeys 725: 17-29 (20 | 7) A peer-reviewed open-access journal doi: 10.3897/zookeys.725.20010 SHORT COMMUNICATION #ZooKey S http:/ /Z00 keys -pen soft.net Launched to accelerate biodiversity research Seeking quantitative morphological characters for species identification in soldiers of Puerto Rican Heterotermes (Dictyoptera, Blattaria, Termitoidae, Rhinotermitidae) Zachary H. Griebenow!”, Susan C. Jones', Tyler D. Eaton! | Department of Entomology, The Ohio State University, 2501 Carmack Rd., Columbus, OH, 43210-1065, USA 2. Department of Entomology & Nematology, University of California-Davis, 381A Briggs Hall, One Shields Ave., Davis, CA, 95616-5270, USA Corresponding author: Zachary H. Griebenow (zgriebenow@ucdavis.edu) Academic editor: P Stoev | Received 4 August 2017 | Accepted 21 November 2017 | Published 29 December 2017 Attp.//zoobank.org/E1E422E7-0017-4CD3-8828-7CFCDB672992 Citation: Griebenow ZH, Jones SC, Eaton TD (2017) Seeking quantitative morphological characters for species identification in soldiers of Puerto Rican Heterotermes (Dictyoptera, Blattaria, Termitoidae, Rhinotermitidae). ZooKeys 725: 17-29. https://doi.org/10.3897/zookeys.725.20010 Abstract Subterranean termites in the genus Heterotermes Froggatt (Rhinotermitidae: Heterotermitinae) are pan- tropical wood feeders capable of causing significant structural damage. The aim of this study was to inves- tigate soldier morphological attributes in three Puerto Rican species of Heterotermes previously identified by sequencing of two mitochondrial genes and attributed to Heterotermes tenuis (Hagen), H. convexino- tatus (Snyder) and H. cardini (Snyder). Soldiers (n = 156) were imaged and measured using the Auto- Montage image-stacking program. We demonstrated that Puerto Rican Heterotermes soldiers could not be identified to species level based upon seven morphometric indices or any combination thereof. Nor could differences in soldier head pilosity be used to discriminate species, in contrast to previous findings. How- ever, previously described characters of the soldier tergal setae were reported to be useful in discriminating H. tenuis from both of its Puerto Rican congeners. Keywords Caribbean, Heterotermes cardini, Heterotermes convexinotatus, Heterotermes tenuis, Morphometrics, taxonomy Copyright Zachary H. Griebenow et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 18 Zachary H. Griebenow et al. / ZooKeys 725: 17-29 (2017) Introduction Heterotermes Froggatt, 1897 (Rhinotermitidae: Heterotermitinae) is a pantropical genus of subterranean wood feeding termites (Constantino 2000). Seventeen spe- cies have been reported as pests that damage human structures (Scheffrahn and Su 2000). The Heterotermes fauna in the Caribbean Region (the Bahamas, Greater An- tilles, and Lesser Antilles) is thought to consist exclusively of pest species that have been introduced from the South American mainland (Constantino 1998, Evans et al. 2013). Caribbean Heterotermes are consequently of interest in that they are both invasive and economically significant. In the Caribbean Region, the Puerto Rican archipelago is situated at the eastern end of the Greater Antilles and is adjacent to the younger, actively volcanic Lesser Antilles, hence providing a biotic link to the South American mainland. Our understanding of Heterotermes species identity and distribution in the Carib- bean Region has fluctuated over time, with the species composition of the Heterotermes fauna in Puerto Rico and its associated islands being quite ambiguous. Snyder (1956) reported Heterotermes tenuis (Hagen, 1858) and Heterotermes convexinotatus (Snyder, 1924) from the archipelago, while Scheffrahn et al. (2003) left Puerto Rican Heter- otermes specimens unidentified to species level due to taxonomic uncertainty. Using a phylogenomic approach conjunct with some morphological and biogeographical data, Szalanski et al. (2004) concluded that Heterotermes cardini (Snyder, 1924) was present in the Caribbean Region in addition to H. tenuis and H. convexinotatus, along with one or more undescribed species. Three samples from Puerto Rico were included in their study, all identified as H. convexinotatus. In contrast, Eaton et al. (2016) reported H. tenuis, H. convexinotatus, and H. cardini in Puerto Rico based on molecular phy- logenies of two mitochondrial loci from 76 Puerto Rican samples, with morphological confirmation of species identification. Furthermore, their phylogenomic data provided strong evidence that the proposed undescribed Heterotermes (Szalanski et al. 2004) were consistent with H. cardini. Heterotermes soldiers from the Caribbean remain difficult to reliably distinguish due to non-robust diagnostic morphological characters: Snyder (1924) asserted that soldiers of the three species differed in cephalic and pronotal pilosity, body coloration, and rela- tive size. However, due to morphological ambiguity, Snyder (1924) suggested in his original descriptions of H. convexinotatus and H. cardini (the latter described from the Bahamas) that they might be synonymous with H. tenuis. Consequently, alates (winged reproductives) are essential for reliable species identification of those Heterotermes spp. putatively present in Puerto Rico (Snyder 1924; Szalanski et al. 2004; Eaton et al. 2016). Since alates are produced only seasonally, they are difficult to obtain and are seldom properly associated with their parent colonies. Therefore, robust soldier-based identification of Puerto Rican Heterotermes is of practical taxonomic interest. The purpose of our study was to measure morphometric parameters in the soldier caste from a comprehensive sample of the Puerto Rican Heterotermes fauna, and to de- termine what parameters, if any, were most useful in identifying Heterotermes to species Seeking quantitative morphological characters for species identification in soldiers... 19 level. Additionally, pilosity of the head capsule (Snyder 1924) and abdominal tergites of Heterotermes soldiers (Constantino 2000) were examined as diagnostic characters. The possibility of an additional, undescribed species of Heterotermes in the Caribbean Region (as per Szalanski et al. 2004) was also herein analyzed. Materials and methods Our study is supplementary to that of Eaton et al. (2016) in that it largely uses a sub- set of the same Puerto Rican Heterotermes samples (n = 60 of 76 samples). These were assigned to H. tenuis, H. convexinotatus, or H. cardini on the basis of their 16S rRNA and cytochrome oxidase subunit II (COI) phylogeny. Samples were collected by SC] from different locales on the main island of Puerto Rico and adjacent Culebra Island in 2002, 2004, 2006, or 2010. Each sample consisted of termites collected from a single access point in a given colony and placed in individual vials filled with absolute alcohol. In total, 156 individual soldiers were examined morphometrically (see Suppl. ma- terial 1), with 3 being selected, when available, from each sample, providing 40 speci- mens of H. tenuis, 55 H. convexinotatus, and 61 H. cardini. We investigated mandible length in combination with the same axis of the head capsule, along with head width (Figure 1), in order to provide additional commonality with the data presented in Constantino (2000) and Szalanski et al. (2004). In addition, multiple pronotal metrics (Figure 2) were examined, two of them novel to this study (see Suppl. material 1). A to- tal of three morphometric indices recommended by Roonwal (1969) for use in termite taxonomy were derived from a subset of these metrics (see Suppl. material 1). Cephalic setae were surveyed in 79 of the 156 soldiers, plus an additional 7 H. convexinotatus soldiers examined without morphometric analysis. Also, setae within a 300-um radius of the soldier fontanelle were censused in 66 of the 156 soldiers. A subset of 45 of the 156 soldiers was used for characterization of tergal setae. A Z16 APO stereomicroscope (Leica Microsystems, Buffalo Grove, USA) with a KY-570B camera (JVC, Wayne, USA) was used to image specimens for morphomet- ric analysis and examination of tergal setae, with images being stacked into montage microphotographs using Auto-Montage Pro software (ver. 5.01.0005, Synoptics Ltd., Cambridge, UK). We performed analyses of variance (ANOVA), discriminant analyses, and £-means cluster analyses on morphometric data using SPSS Statistics 24 (2016, International Business Machines, Armonk, USA). ‘The level of significance for all analyses was set at «=0.05. Based on the results of ANOVA, a discriminant analysis and three &-means cluster analyses were performed using all statistically significant parameters. Discrimi- nant analyses determine the efficacy of any array of variables in assigning group mem- bership (Green et al. 2008). k-means cluster analyses do not assume a priori assignments of specimens to groups, instead attempting to iteratively delineate groups de novo from the data given according to the number of groups provided by an a priori hypothesis. Our k-means 20 Zachary H. Griebenow et al. / ZooKeys 725: 17-29 (2017) Figure |. Cephalic metrics: AA' = maximum length of mandible; BB' = maximum width of head; CC' = length of head to lateral base of mandibles. Parallels used to delineate metrics (see Suppl. mate- rial 1) are marked in red. Figure 2. Pronotal metrics: AA'= maximum length of pronotum; BB' = maximum width of pro- notum; CC’ = depth of anterior pronotal notch; DD' = depth of posterior pronotal notch. Parallels are marked in black. cluster analyses specified 3, 4, and 2 morphometric-delineated groups within the sam- pled Heterotermes fauna. The first analysis was premised according to the conclusion of Eaton et al. (2016) that there are 3 valid Heterotermes spp. in the Puerto Rican archi- pelago. The second was premised according to the conclusion of Szalanski et al. (2004) that 4 Heterotermes spp. occur in the Caribbean Region. The third was premised ac- cording to the phylogenetic hypothesis that H. tenuis is sister to a clade including H. convexinotatus and H. cardini (Szalanski et al. 2004; Eaton et al. 2016): if this were Seeking quantitative morphological characters for species identification in soldiers... 21 the case, one would expect specimens to group into two clusters. It was not possible to delineate one or more metrics on a total of 40 specimens (5 H. tenuis, 8 H. convexino- tatus, and 27 H. cardini), so these were excluded from &-means cluster analysis. Results and discussion ANOVA concerning all parameters demonstrated that all but one of the metrics sur- veyed — the depth of the posterior pronotal notch, which was novel to this study — displayed statistically significant variation across all three species (Table 1). Only one of the three morphometric indices we derived — the head-mandible index (Roonwal 1969) — exhibited statistically significant variation across all three species (Table 1). Discriminant and &-means cluster analyses used only statistically significant param- eters. Of all 116 specimens with sufficient morphometric data for their inclusion in dis- criminant analysis, our discriminant analyses correctly classified 87.1% to species. Thus, while the majority of Puerto Rican Heterotermes with sufficient morphometric data could be accurately identified to species level using statistically significant morphometric pa- rameters, these data were not invariably reliable for that purpose; nor was this mode of identification concise given that a total of seven parameters was necessary. The results of morphometric 3- and 4-cluster analyses did not consistently conform to the phylogenetic hypotheses of Eaton et al. (2016) and Szalanski et al. (2004) for Caribbean Heterotermes, respectively, nor did any cluster analysis support placement of H. tenuis as a sister-group to the remaining two putative species of Heterotermes. Further- more, no morphometric consensus, novel or otherwise, could be made across all three k-means cluster analyses (Table 2). These results were likely influenced by the fact that many specimens (n = 40) provided insufficient data to be included in cluster analyses. We found short to medium-length (uniformly <100 «m) setae on the head capsules of all H. convexinotatus specimens examined with respect to this character, but pilosity of this species and 7. tenuis was comparable (Table 3). Furthermore, there was considerable overlap in head capsule pilosity among all three species (Table 4). Likewise, the area within a 300-um radius of the fontanelle of a subset of the 156 specimens displayed considerable overlap in seta quantity and no apparent pattern among all three species (Table 5). We therefore conclude that soldier head pilosity is not a reliable character for discriminating among Puerto Rican Heterotermes species, contrary to Snyder (1924). Although soldiers of all three Heterotermes species bore a distinct line of bristles (setae noticeably longer than surrounding setae) along the posterior margins of abdominal ter- gites (excluding the epiproct), only H. tenuis soldiers had a distinct row of long hairs on central tergal surfaces (Figure 3). In contrast, short setae (often <10 pm long) not arranged in distinct rows predominated on the central tergal surfaces of H. convexinotatus and H. cardini soldiers. These correspond to the “numerous microscopic hairs” described by Con- stantino (2000) on 4. convexinotatus tergites. Whereas Constantino (2000) did not com- pare the tergal pilosity of H. cardini to H. tenuis, we make a novel report that tergal seta distribution also can be used to distinguish H. tenuis soldiers from those of H. cardini. 22 Zachary H. Griebenow et al. / ZooKeys 725: 17-29 (2017) Table |. Results of an ANOVA assessing variation of select morphometric parameters. Parameters exhib- ited statistically significant differentiation if P<0.05. Parameter df F value P value Head capsule length 27: 36.089** 0.000 Mandible length 124 36.089** 0.000 Head width 126 pUWoo 0.000 Pronotum width 150 46.723** 0.000 Pronotum length 150 Ve kee ai 0.042 Depth of anterior pronotal notch 146 3.242** 0.000 Depth of posterior pronotal notch 122 42.885 0.826 Pronotal index 150 0.575 0.564 Head-mandible index 124 Gwe" 0.002 Head index IF 1.434 0.242 Table 2. Cluster membership under respective phylogenetic hypotheses. Insufficient morphometric data precluded analysis of 40 specimens. Cluster numeration was arbitrary. Distance was measured relative to computed cluster center. 2-Cluster Hypothesis 3-Cluster Hypothesis 4-Cluster Hypothesis ee Cluster__| Distance H. tenuis 2 253.54143 | 32.20008 a 46.50913 H. tenuis D: 326.77099 3 74.86261 3 53.2888 H. tenuis 2 354.21671 3 117.6952 i 93.6614 H. tenuis x 85.55526 y) 84.16529 2 81.85684 H. tenuis 2 312.57804 3 87.58546 3 83.58083 H. tenuis 2: 309.6662 a) 84.9422 3 85.65045 H. tenuis 2 256.37002 3 39.99476 3 37.3955 H. tenuis 2 234.62472 é) 81.46453 3 100.08422 H. tenuis 2 121.91754 2 103.66997 2 106.89786 H. tenuis 2 251.06997 ) 52.89946 3 68.95685 H. tenuis 2 314.68978 3 61.76796 a 41.12887 H. tenuis 1 160.0722 I 163.05486 1 163.73504 H. tenuis 3 85.69223 H. tenuis 3 58.86668 H. tenuis 3 62.79373 H. tenuis 2 169.0256 H. tenuis 2 113.2921 2 132.59409 ps 102.7966 H. tenuis 2 314.97147 =) 66.84973 3 43.15213 H. tenuis 2 108.07079 2 186.68133 pe 125.18157 H. tenuis ps 208.05716 3 109.93034 5) 128.41514 H. tenuis ep 310.24474 3 73.71241 3 55.89708 H. tenuis 2 124.9129 3 142.88123 2 146.78559 H. tenuis 2 380.73388 3 124.49842 3 9912555 H. tenuis 2 166.58084 3 234.09751 2 177.17161 H. tenuis 2 326.48907 3 68.58936 3 46.22216 H. tenuis 2 151.22401 2 67.91019 4 91.83434 Seeking quantitative morphological characters for species identification in soldiers... 23 2-Cluster Hypothesis 3-Cluster Hypothesis 4-Cluster Hypothesis ang Cluster__| Distance H. tenuis 4 43.17484 H. tenuis 4 102.5721 H. tenuis 4 69.74912 H. tenuis 4 65.41226 H. tenuis 1 301.11995 4 124.68136 H. tenuis 2 267.73784 157.77828 4 82.99303 H. tenuis 1 301.10911 206.37768 4 120, 7071-2. H. tenuis 2, 280.63396 180.37562 4 113.16429 H. tenuis 2 57.2989 166.99186 2 76.70921 H. convexinotatus 2 66.64623 162.67921 2 76.51109 H. convexinotatus D, 100.58655 74.61512 2: 87.54042 H. convexinotatus 2 45.53643 73.81509 2 30.55171 H. convexinotatus 1 92.8697 1 106.97731 1 109.89883 H.. convexinotatus i 42.58346 1 61.12458 1 66.23971 H.. convexinotatus 1 48.37568 1 72.47772 H.. convexinotatus 1 170.7652 1 201.95907 H.. convexinotatus 1 100.92468 1 134.78135 H.. convexinotatus 1 168.40471 H.. convexinotatus 1 161.85759 H.. convexinotatus 1 39.48472 1 65.59095 H.. convexinotatus 2 190.79254 4 74.07688 H.. convexinotatus 1 131.65924 1 165.14755 H.. convexinotatus 1 177.67905 H. convexinotatus ps 100.109 3 88.36581 2: 85.5312 H.. convexinotatus 2 256.96346 2 159.35016 4 111.01812 H. convexinotatus 1 63.17991 1 65.26824 1 67.17037 H. convexinotatus 1 172.68076 1 197.98883 1 201.96107 H.. convexinotatus 1 89.89609 1 79138937 1 79.56232 H.. convexinotatus 2 219.01414 2 121.76263 4 78.87236 H.. convexinotatus i 115.93995 1 116.1732 1 117.93494 H.. convexinotatus 1 61.6565 1 59:65379 1 39.16278 H.. convexinotatus 2 161.9857 2 71.84719 4 93.15414 H.. convexinotatus 2 168.94894 2 67.60631 4 72.92106 H. convexinotatus 2 72.73062 2 96.75358 2 55.58775 H.. convexinotatus 2 98.61692 Z 75.0215 H. convexinotatus 2 76.50752 H.. convexinotatus 2 109.20261 2 86.98483 H. convexinotatus 2 80.01889 H. convexinotatus 4 100.72459 H. convexinotatus 2 107.73092 2, 90.72008 H.. convexinotatus 2 156.36624 H. convexinotatus 3 130.77036 H.. convexinotatus 2 239.38575 4 99.8207 H. convexinotatus 2 92.55724 2 120.63307 2 7 E2226 1 H. convexinotatus 2 116.67981 2 53.59368 2 94.82665 24 Zachary H. Griebenow et al. / ZooKeys 725: 17-29 (2017) =e Clans Hypo Cluster__| Distance H. convexinotatus 4 102.7939 H.. convexinotatus 2 55.07361 2 164.29003 2. 72.06005 H. convexinotatus 2 88.91133 H. convexinotatus 2 94.07228 H.. convexinotatus 2 82.23475 2 103.79059 2: 65.28595 H. convexinotatus 2 160.4155 85.86284 4 111.32346 H.. convexinotatus 2; 89.50309 187.87274 2; 101.76863 H. convexinotatus 2, 167.55718 109.25237 4 137.91008 H. convexinotatus py 79.39547 121.25412 2 71.32581 H.. convexinotatus 2 124.51904 AT9: 70772 2 123.62927 H. convexinotatus D, 101.38499 44.47996 2 80.3574 H. cardini 1 50.62172 49.4603 1 52.54455 H. cardini 2 156.96056 72.06053 4 92.09658 H. cardini 2, 116.3222 68.96384 3 105.05938 H. cardini Z 133.27853 4 107.50376 H. cardini 49.75939 H. cardini 62.57799 H. cardini 4 151.5971 H. cardini 1 233.92987 4 131.26097 H. cardini 1 152.27189 1 118.84265 H. cardini 130.72768 H. cardini 95.34782 H. cardini 1 186.62386 4 204.59382 H. cardini 1 157.73427 1 153.65728 A. cardini 183.74985 15739795 1 154.03872 A. cardini 253:735398 198.98527 1 193.37452 A. cardini 74.31731 92.99662 1 96.63796 A. cardini 103.83294 105.39398 if 107.29047 A. cardini 217.06493 192.74338 1 189.6661 A. cardini 201.84888 171.83761 1 167.68972 A. cardini 238.91474 207.60536 1 203.09527 H. cardini 195.04476 163.03509 1 158.21636 H. cardini 150.4453 93.68494 4 126.39925 A. cardini 135.8617 70.67088 4 95337 Hcardini | __—2_———i|:'164.19757 |__| tases | 4 137.5087 H. cardini 4 155.38894 A. cardini 1 214.2815 H. cardini 1 269.8637 H. cardini 134.63763 H. cardini 4 61.65641 A. cardini 2 4 116.96033 H cardini sien ib f08603 A cardini yall aes H. cardini 1 66.89762 1 65.16361 1 66.45667 A. cardini 1 178.07806 1 183.42556 1 185.36444 Table 3. Summary statistics for cephalic seta counts. Number of soldiers | Number of samples H. convexinotatus 36 Species H.. tenuis H. cardini Average 18.6923 Seeking quantitative morphological characters for species identification in soldiers... 25 Standard error 2.48427 0.9818 0.85053 Table 4. Cephalic setae counts. Identifiers are as follows: sample #_year of collection_replicate_species. Identifier # of cephalic setae 67_10_01_tenuis 27 84_06_01_tenuis 26 84_06_02_tenuis pas 84_06_03_ tenuis 25 84_06_04_tenuis 29 84_06_05_tenuis 2 84_06_06_tenuis 10 84_06_07_tenuis 16 84_06_08_ tenuis 2D 84_06_09_tenuis 19 84_06_10_tenuis 26 84_06_11_tenuis 8 84_06_12 tenuis 8 235_04_01_convexinotatus 19 34_06_01_convexinotatus 13 66_06_01_convexinotatus 15 226 _04_01_convexinotatus 20 226_04_02_convexinotatus 13 226_04_03_convexinotatus eal 233_04_01_convexinotatus 27 233_04_02_ convexinotatus 17 233_04_03_convexinotatus 26 74_02_01_convexinotatus 18 74_02 02 convexinotatus 17 74_02_03_convexinotatus pal 64_02_01_convexinotatus 12 64_02 02 convexinotatus 19 64_02 03 _convexinotatus RS 257_04_01_convexinotatus 10 257_04_02_convexinotatus 23 257_04_03_convexinotatus 16 267_04_01_convexinotatus 16 267_04_02_convexinotatus 25 267_04_03_convexinotatus 25 258_04_01_convexinotatus 17 258 04 02 convexinotatus 24 258_04_03 convexinotatus 17 427 _04_01_convexinotatus 11 26 Zachary H. Griebenow et al. / ZooKeys 725: 17-29 (2017) Identifier # of cephalic setae 427 04_02_convexinotatus 14 427 _04_03_ convexinotatus 20 414 04 02 convexinotatus 2 404_04_01_convexinotatus 14 407_04_01_convexinotatus 7 407_04_02_convexinotatus 14 407_04_03_convexinotatus 5 407_04_04_convexinotatus 8 428 04 _01_convexinotatus 18 428 04 02 convexinotatus 16 428 04 03 convexinotatus 23 10_02_01 cardini 18 10_02 02 cardini 13 218_04_01_cardini 9 218 _04_02 cardini 11 218_04_03_cardini 6 22_02_01 cardini 15 22 02 02 cardini 19 22_02_03_cardini £9 222 04_01_cardini 15 222 04 02 cardini 14 222 _04_03_cardini 15 25_06_01_cardini 13 25_06_02 cardini 13 25_06_03_cardini 8 31_06_01_cardini 4 32 02 01 cardini 16 32 02 02 cardini 20 32_02_03_cardini 18 44 02 01 cardini 6 44 02 02 cardini 14 44 02 03 cardini 5 65_02_01_cardini 10 65_02 02 cardini 20 65_02_03_cardini 20 66_02_01_cardini 14 66_02_ 02 cardini 8 66_02_03_cardini 11 67_02_01_cardini 16 67_02_02 cardini pal 67_02_03_cardini 14 78_02_01_cardini 17 78 02 02 cardini 18 78_02_03_cardini 9 79_02_01_cardini s 79_02_02_cardini 20 79_02_03_cardini 26 79_02_04_cardini 18 Seeking quantitative morphological characters for species identification in soldiers... Wy, Table 5. Summary statistics for seta counts within a 300-um radius of the soldier fontanelle. Species Standard error H. tenuis a TT 0.190053 H.convexinotas | 5 | 5.666667 | 0.214214 H. cardini 38 4.230769 | 0.405096 Figure 3. Posterior abdominal tergites of H. tenuis. Rows of long setae on central tergal surfaces are circled. Conclusions Our findings demonstrated that examined morphometric characters of the soldier pro- notum and head could not reliably differentiate Heterotermes species in the Puerto Rican archipelago. These data did not provide any well-resolved distinction between the three putative species in question, such as is supported by rigorous phylogenomic investigation (Eaton et al. 2016). We also found that H. convexinotatus and H. cardini soldiers could not be unequivocally discriminated by cephalic seta counts, contrary to Snyder (1924). However, H. tenuis soldiers could be readily identified by means of tergal setal distribution, as reported by Constantino (2000). We furthermore report that soldier tergal seta distribution is useful to distinguish H. tenuis from H. cardini. Acknowledgements ‘This research was supported in part by State and Federal funds appropriated to the Ohio Ag- ricultural Research and Development Center, by USDA NIFA Hatch Project OHOO1170, 28 Zachary H. Griebenow et al. / ZooKeys 725: 17-29 (2017) and by Research Scholar Award funds disbursed by the Undergraduate Research Office of The Ohio State University. The authors would like to thank Abhijoy Saha for his statistical consulting services; Dr David Shetlar for his assistance proofreading application materials for the Research Scholar Award; Huayan Chen and Dr Hans Klompen for their assistance in the imaging process; and Alex Tyrpak, Kara Baker and Nina Bogart for their past and present aid and support at the Jones Laboratory. References Constantino R (1998) Catalog of the living termites of the New World (Insecta: Isoptera). Arquiv- os de Zoologia 35: 135-231. http://dx.doi.org/10.11606/issn.2176-7793.v35i2p 135-230 Constantino R (2000) Key to the soldiers of South American Heterotermes with a new species from Brazil (Isoptera: Rhinotermitidae). Insect Systematics and Evolution 31: 463-472. http://dx.doi.org/10.1163/187631200X00499 Eaton TD, Jones SC, Jenkins TM (2016) Genetic diversity of Puerto Rican Heterotermes (Isop- tera: Rhinotermitidae) revealed by phylogenetic analysis of two mitochondrial genes. Journal of Insect Science 16: 111. https://doi.org/10.1093/jisesa/iew099 Evans TA, Forschler BT, Grace JK (2013) Biology of invasive termites: a worldwide review. Annual Review of Entomology 58: 455-474. https://doi.org/10.1146/annurev-ento-120811-153554 Froggatt WW (1897) Australian Termitidae. Part II. Proceedings of the Linnaean Society of New South Wales, 21(4) [1896]: 510-552. [2 plates] Green SB, Salkind NJ, Akey TM (2008) Using SPSS for Windows and Macintosh: Analyzing and understanding data. Prentice Hall, Upper Saddle River, New Jersey, 458 pp. Hagen HA (1858) Monographie der Termiten. Linnaea Entomologica 12: i-iii, 4-342, 459. [3 plates] Roonwal ML (1969) Measurement of termites (Isoptera) for taxonomic purposes. Journal of the Zoological Society of India 21: 9-66. Scheffrahn RH, Su N-Y (2000) Featured creatures — West Indian subterranean termite. University of Florida — IFAS. http://entnemdept.ufl.edu/creatures/urban/termites/heterotermes.htm Scheffrahn RH, Jones SC, Krecek J, Chase JA, Mangold JR, Su N-Y (2003) Taxonomy, distribu- tion, and notes on the termites (Isoptera: Kalotermitidae, Rhinotermitidae, Termitidae) of Puerto Rico and the U.S. Virgin Islands. Annals of the Entomological Society of America 96: 181-201. https://doi.org/10.1603/0013-8746(2003)096[0181:TDANOT]2.0.CO;2 Snyder TE (1924) Descriptions of new species and hitherto unknown castes of termites from America and Hawaii. Proceedings of the U. S. National Museum 64: 1—40. [5 plates] https:// doi.org/10.5479/si.00963801.64-2496. 1 Snyder TE (1956) Termites of the West Indies, the Bahamas and Bermuda. Journal of Agriculture of the University of Puerto Rico 40: 189-202. Szalanski AL, Scheffrahn RH, Austin JW, Krecek J, Su N-Y (2004) Molecular phylogeny and biogeography of Heterotermes (Isoptera: Rhinotermitidae) in the West Indies. Annals of the Entomological Society of America 97: 556-566. https://doi.org/10.1603/0013- 8746(2004)097[0556:MPABOH]2.0.CO;2 Seeking quantitative morphological characters for species identification in soldiers... 29 Supplementary material | Definitions of soldier morphometric parameters Authors: Zachary H. Griebenow, Susan C. Jones, Tyler D. Eaton Data type: taxonomic metrics and indices. Explanation note: Definitions of all morphometric parameters utilized in this study, sensu Roonwal (1969). Copyright notice: This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0/). The Open Database License (ODDbL) is a license agreement intended to allow users to freely share, modify, and use this Dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited. Link: https://doi.org/10.3897/zookeys.725.20010.suppl1