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Sepsis cynipsea
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<h2 id="description">Description</h2> <p>These dung flies are black in color, and approximately 4–5 mm (0.16–0.20 in) long.<a class="footnote-ref" id="fnref:5" href="#fn:5"><sup>5</sup></a> They have two translucent wings that contain one dark spot near the tip of each. They look like ants, and often are difficult to identify without a microscope due to their appearance.<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> </p> <h2 id="distribution">Distribution</h2> <p><i>Sepsis cynipsea</i> dung flies are most commonly found in Europe. They prefer warm temperatures and can be more easily found from May to October in lower altitudes, and June to September in higher altitudes where the temperature is typically cooler.<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a> In higher altitudes, female flies have shorter lifespans, are smaller, and lay fewer clutches of eggs.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> They require fresh dung, primarily from cows and sheep, for reproduction.<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a> They also eat <a href="/facts/Nectarivory/DpaMFneX">nectar</a> which is a source of sugar.<a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> </p> <h3>Altitude effects</h3> <p><i>Sepsis cynipsea</i> dung flies are often found in regions with varying altitudes, such as the <a href="/facts/Swiss_Alps/4oUJF4jo">Swiss Alps</a>.<a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a> Out of the many different <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a> species that are found in these regions, <i>Sepsis cynipsea</i> flies prefer intermediate altitudes but are found at all altitudes where other species of dung flies are found.<a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a> In the areas where these fly species are prevalent, there is more species diversity at higher altitudes.<a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a> Higher altitude environments tend to be more variable, so species found at higher altitudes have to be better at adapting to environmental changes.<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a> However, <i>S. cynpisea</i> flies at different altitudes enter <a href="/facts/Diapause/y4fPYEjC">diapause</a> at the same time and stop producing eggs at the same time in the season.<a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a> </p> <h3>Temperature effects</h3> <p>The temperature during the larval phase of development impacts growth rates and final body size of <i>Sepsis cynipsea</i>.<a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a> <i>S. cynipsea</i> grow the best at intermediate temperatures compared to similar species.<a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a> However, in colder temperatures, <i>S. cynipsea</i> growth rates may increase so that they can reach adulthood before a cold season. Their growth rate also increases with warmer temperatures.<a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a> At 30 °C (86 °F), it takes approximately 7 days for <i>S. cynipsea</i> flies to mature from eggs to adults.<a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a> Resource availability, which can vary based on environmental conditions and competition with other species, also has an impact on the size of an adult body.<a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a> <i>S. cynipsea</i> primarily uses temperature to determine when to enter <a href="/facts/Diapause/y4fPYEjC">diapause</a>.<a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a> </p> <h3>Competition</h3> <p>Because <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a> flies are often found in the same regions, there can be competition between species, like from <i>S. neocynipsea</i> which also prefers fresh cow dung for reproduction. However, some fly species, like <i>S. duplicata</i> prefer dry and old cow dung; this is known as <a href="/facts/Niche_differentiation/FEptbJhd">niche differentiation</a>.<a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a> </p> <h2 id="mating">Mating</h2> <h3>Reproduction</h3> <p><i>Sepsis cynipsea</i> flies are most known for their mating practices that involve <a href="/facts/Sexual_conflict/fUQprV8R">sexual conflict</a>. Their mating habits have been extensively studied to better understand sexual selection, <a href="/facts/Mate_choice/rMjIUJaP">female choice</a>, and reluctance in mating.<a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a> <i>Sepsis cynipsea</i> flies require fresh dung to mate,<a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a> and they prefer dung that is less than one hour old.<a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a> Females land on the fresh dung, where large numbers of males are already waiting,<a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a> and ingest fresh dung. The females lay their eggs on the dung, and while they are laying their eggs, a male gets on top of the female and guards her.<a class="footnote-ref" id="fnref:27" href="#fn:27"><sup>27</sup></a> Males are not selective for females; they tend to mount the first female they encounter on the dung.<a class="footnote-ref" id="fnref:28" href="#fn:28"><sup>28</sup></a> However, this is not copulation. The eggs she is laying are fertilized from a previous mate.<a class="footnote-ref" id="fnref:29" href="#fn:29"><sup>29</sup></a> After she lays her eggs on the fresh dung, she and the male move to the grass that surrounds the dung pile, where they have the opportunity to mate, although most pairs do not, as the female successfully shakes the male off.<a class="footnote-ref" id="fnref:30" href="#fn:30"><sup>30</sup></a> If they do make genital contact and mate, the next eggs she lays will probably be his. When the eggs hatch and the larvae emerge, the larvae eat the dung and then leave.<a class="footnote-ref" id="fnref:31" href="#fn:31"><sup>31</sup></a> <i>S. cynipsea</i> flies have evolved to develop quickly so they avoid competition with other coprophagous organisms and before the dung dries up.<a class="footnote-ref" id="fnref:32" href="#fn:32"><sup>32</sup></a> </p> <h3>Sexual conflict</h3> <p>Female <i>Sepsis cynipsea</i> flies are larger than the males, and because of this, a male cannot force a female to copulate with him.<a class="footnote-ref" id="fnref:33" href="#fn:33"><sup>33</sup></a> However, there is a lot of male competition.<a class="footnote-ref" id="fnref:34" href="#fn:34"><sup>34</sup></a> There are usually far more males than females on a dung pile,<a class="footnote-ref" id="fnref:35" href="#fn:35"><sup>35</sup></a> which leads to the ability for females to be selective.<a class="footnote-ref" id="fnref:36" href="#fn:36"><sup>36</sup></a> If a female does not want to mate with a male, she begins to shake her body, which either indicates to males that she does not want to mate<a class="footnote-ref" id="fnref:37" href="#fn:37"><sup>37</sup></a> or functions shake the male off of her body.<a class="footnote-ref" id="fnref:38" href="#fn:38"><sup>38</sup></a> </p> <h3>Mate choice</h3> <p>Larger males are more successful at mounting and mating with females, and larger females lay larger clutches of eggs.<a class="footnote-ref" id="fnref:39" href="#fn:39"><sup>39</sup></a> In populations with greater mean body sizes, sexual selection is stronger compared to populations with smaller body sizes.<a class="footnote-ref" id="fnref:40" href="#fn:40"><sup>40</sup></a> Once the male and female move into the grass after she lays her eggs, only about 40% of the pairs actually copulate.<a class="footnote-ref" id="fnref:41" href="#fn:41"><sup>41</sup></a> And when they do, there is evidence to suggest that females get physically injured in the process. The male reproductive organ is spiney, and females are left with scars and have a higher mortality after mating.<a class="footnote-ref" id="fnref:42" href="#fn:42"><sup>42</sup></a> This genital organ is most likely so armored to make it hard for the females to shake the males off; the male has to spin 180 degrees to get his genital organ out of the female.<a class="footnote-ref" id="fnref:43" href="#fn:43"><sup>43</sup></a> If a female does not shake the male off, they copulate. The flies then find another dung site 2–4 days later to repeat the process.<a class="footnote-ref" id="fnref:44" href="#fn:44"><sup>44</sup></a> This results in approximately six generations to progress during each breeding season.<a class="footnote-ref" id="fnref:45" href="#fn:45"><sup>45</sup></a> </p> <h2 id="evolution">Evolution</h2> <h3>Sexual dimorphisms</h3> <p>In the family <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a>, there is clear <a href="/facts/Sexual_dimorphism/nx9wulFy">sexual dimorphism</a>. The male foreleg, for example, differs greatly from a female foreleg, and differs in between <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a> species, as well.<a class="footnote-ref" id="fnref:46" href="#fn:46"><sup>46</sup></a> The <a href="/facts/Morphology_(biology)/Nl3B0myy">Morphology (biology)</a> of the male foreleg evolved to aid the male in mounting the female and staying on her during her characteristic body shaking.<a class="footnote-ref" id="fnref:47" href="#fn:47"><sup>47</sup></a> The male foreleg has evolved to have bristles, indentations, or bumps, which attach to the wing veins and cells on the female's wings.<a class="footnote-ref" id="fnref:48" href="#fn:48"><sup>48</sup></a> In response to this, the female can bend her abdomen to prevent genital contact with the male.<a class="footnote-ref" id="fnref:49" href="#fn:49"><sup>49</sup></a> In some <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a> species without adapted forelegs, the males have adapted an abdomen that bends to make contact with the female genitalia.<a class="footnote-ref" id="fnref:50" href="#fn:50"><sup>50</sup></a> These sexually dimorphic characteristics can be very different between closely related species, so sexually dimorphic characteristics evolve quickly and are involved in speciation in the family <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a>. </p> <h3>Taxonomy</h3> <p>The family <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a> contains more than 320 species and 37 genera, which are globally widespread.<a class="footnote-ref" id="fnref:51" href="#fn:51"><sup>51</sup></a> The sister species <i>S. neocynipsea</i> and <i>S. cynipsea</i> are found on different continents: <i>S. neocynipsea</i> in <a href="/facts/North_America/djNjCQIl">North America</a> and <i>S. cynipsea</i> in Europe primarily.<a class="footnote-ref" id="fnref:52" href="#fn:52"><sup>52</sup></a> <i>Sepsis</i> has more species than other genera of the family <a href="/facts/Sepsidae/7DBkwLBG">Sepsidae</a>.<a class="footnote-ref" id="fnref:53" href="#fn:53"><sup>53</sup></a> Sepsidae is monophyletic, with many different clades, including the Neotropical sepsids, the African clade, and the higher sepsids.<a class="footnote-ref" id="fnref:54" href="#fn:54"><sup>54</sup></a> The sexually dimorphic traits, such as the moveable abdomens, evolved independently multiple times.<a class="footnote-ref" id="fnref:55" href="#fn:55"><sup>55</sup></a> </p> <h3>Sister species</h3> <p><i>Sepsis neocynipsea</i> is only recently diverged from <i>Sepsis cynipsea</i>.<a class="footnote-ref" id="fnref:56" href="#fn:56"><sup>56</sup></a> Even though both species are widespread, overlap geographically, and have similar mitochondrial gene sequences, they have different behaviors and morphologies.<a class="footnote-ref" id="fnref:57" href="#fn:57"><sup>57</sup></a> While <i>S. neocynipsea</i> is most commonly found in North America, it is also present in some of the same geographic locations that <i>S. cynipsea</i> is found in, like the Swiss Alps.<a class="footnote-ref" id="fnref:58" href="#fn:58"><sup>58</sup></a> While <i>S. cynipsea</i> and <i>S. neocynipsea</i> cross-breeding events can produce hybrid offspring, these offspring are typically infertile or have low fertility.<a class="footnote-ref" id="fnref:59" href="#fn:59"><sup>59</sup></a> Pre- and post-zygotic barriers between the species are still forming, so they have recently diverged. In <i>S. cynipsea</i>, female shaking during mating events is more visible than in <i>S. neocynipsea</i>.<a class="footnote-ref" id="fnref:60" href="#fn:60"><sup>60</sup></a> <i>S. cynipsea</i> flies also have higher rates of successful matings per mating attempts than <i>S. neocynipsea</i> do.<a class="footnote-ref" id="fnref:61" href="#fn:61"><sup>61</sup></a> </p> <h3>Genetics</h3> <p>There are high levels of genetic variability between flies, especially related to form. The heritability of these morphological traits ranges between 0.33 and 0.90 for males but is lower for females.<a class="footnote-ref" id="fnref:62" href="#fn:62"><sup>62</sup></a> Male <i>Sepsis cynipsea</i> flies are smaller than females for all traits except for the width of the fore femur.<a class="footnote-ref" id="fnref:63" href="#fn:63"><sup>63</sup></a> Body size and male leg features are selected for, so evolution works on these traits and contributes to sexual dimorphism. </p> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Blanckenhorn, W. (1997). "Altitudinal life history variation in the dung flies Scathophaga stercoraria and Sepsis cynipsea". Oecologia. 109: 342–352. doi:10.1007/s004420050092. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li> <li id="fn:2"><p>Rohner, P. T., Bächli, G. , Pollini Paltrinieri, L. , Duelli, P. , Obrist, M. K., Jochmann, R. and Blanckenhorn, W. U. (2015), Distribution, diversity gradients and Rapoport's elevational rule in the black scavenger flies of the Swiss Alps (Diptera: Sepsidae). Insect Conserv Divers, 8: 367-376. doi:10.1111/icad.12114 <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li> <li id="fn:3"><p>Blanckenhorn, W. (1997). "Altitudinal life history variation in the dung flies Scathophaga stercoraria and Sepsis cynipsea". Oecologia. 109: 342–352. doi:10.1007/s004420050092. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li> <li id="fn:4"><p>Wolf U. Blanckenhorn, David J. Hosken, Oliver Y. Martin, Constanze Reim, Yvonne Teuschl, Paul I. Ward, The costs of copulating in the dung fly Sepsis cynipsea, Behavioral Ecology, Volume 13, Issue 3, May 2002, Pages 353–358, https://doi.org/10.1093/beheco/13.3.353 <a href="https://doi.org/10.1093/beheco/13.3.353" target="_blank">https://doi.org/10.1093/beheco/13.3.353</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li> <li id="fn:5"><p>Blanckenhorn, Morf; Mühlhäuser, Reusch (1999). "Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea". Journal of Evolutionary Biology. 12 (3): 563–576. doi:10.1046/j.1420-9101.1999.00050.x. <a href="https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x" target="_blank">https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></p></li> <li id="fn:6"><p>Blanckenhorn, Morf; Mühlhäuser, Reusch (1999). "Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea". Journal of Evolutionary Biology. 12 (3): 563–576. doi:10.1046/j.1420-9101.1999.00050.x. <a href="https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x" target="_blank">https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></p></li> <li id="fn:7"><p>Blanckenhorn, W. (1997). "Altitudinal life history variation in the dung flies Scathophaga stercoraria and Sepsis cynipsea". Oecologia. 109: 342–352. doi:10.1007/s004420050092. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></p></li> <li id="fn:8"><p>Blanckenhorn, W. (1997). "Altitudinal life history variation in the dung flies Scathophaga stercoraria and Sepsis cynipsea". Oecologia. 109: 342–352. doi:10.1007/s004420050092. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:8" class="footnote-back-ref">↩</a></p></li> <li id="fn:9"><p>Blanckenhorn, Morf; Mühlhäuser, Reusch (1999). "Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea". Journal of Evolutionary Biology. 12 (3): 563–576. doi:10.1046/j.1420-9101.1999.00050.x. <a href="https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x" target="_blank">https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x</a> <a href="#fnref:9" class="footnote-back-ref">↩</a></p></li> <li id="fn:10"><p>Blanckenhorn, Morf; Mühlhäuser, Reusch (1999). "Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea". Journal of Evolutionary Biology. 12 (3): 563–576. doi:10.1046/j.1420-9101.1999.00050.x. <a href="https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x" target="_blank">https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></p></li> <li id="fn:11"><p>Rohner, P. T., Bächli, G. , Pollini Paltrinieri, L. , Duelli, P. , Obrist, M. K., Jochmann, R. and Blanckenhorn, W. U. (2015), Distribution, diversity gradients and Rapoport's elevational rule in the black scavenger flies of the Swiss Alps (Diptera: Sepsidae). Insect Conserv Divers, 8: 367-376. doi:10.1111/icad.12114 <a href="#fnref:11" class="footnote-back-ref">↩</a></p></li> <li id="fn:12"><p>Rohner, P. T., Bächli, G. , Pollini Paltrinieri, L. , Duelli, P. , Obrist, M. K., Jochmann, R. and Blanckenhorn, W. U. (2015), Distribution, diversity gradients and Rapoport's elevational rule in the black scavenger flies of the Swiss Alps (Diptera: Sepsidae). Insect Conserv Divers, 8: 367-376. doi:10.1111/icad.12114 <a href="#fnref:12" class="footnote-back-ref">↩</a></p></li> <li id="fn:13"><p>Rohner, P. T., Bächli, G. , Pollini Paltrinieri, L. , Duelli, P. , Obrist, M. K., Jochmann, R. and Blanckenhorn, W. U. (2015), Distribution, diversity gradients and Rapoport's elevational rule in the black scavenger flies of the Swiss Alps (Diptera: Sepsidae). Insect Conserv Divers, 8: 367-376. doi:10.1111/icad.12114 <a href="#fnref:13" class="footnote-back-ref">↩</a></p></li> <li id="fn:14"><p>Rohner, P. T., Bächli, G. , Pollini Paltrinieri, L. , Duelli, P. , Obrist, M. K., Jochmann, R. and Blanckenhorn, W. U. (2015), Distribution, diversity gradients and Rapoport's elevational rule in the black scavenger flies of the Swiss Alps (Diptera: Sepsidae). Insect Conserv Divers, 8: 367-376. doi:10.1111/icad.12114 <a href="#fnref:14" class="footnote-back-ref">↩</a></p></li> <li id="fn:15"><p>Blanckenhorn, W. U. (1998). Altitudinal differentiation in the diapause response of two species of dung flies. Ecological Entomology 23, 1-8. <a href="/wiki/Diapause" target="_blank">/wiki/Diapause</a> <a href="#fnref:15" class="footnote-back-ref">↩</a></p></li> <li id="fn:16"><p>Blanckenhorn, W. U. (1999). Different growth responses to temperature and resource limitation in three fly species with similar life histories. Evolutionary Ecology 13: 395-409 <a href="#fnref:16" class="footnote-back-ref">↩</a></p></li> <li id="fn:17"><p>Blanckenhorn, W. U. (1999). Different growth responses to temperature and resource limitation in three fly species with similar life histories. Evolutionary Ecology 13: 395-409 <a href="#fnref:17" class="footnote-back-ref">↩</a></p></li> <li id="fn:18"><p>Blanckenhorn, W. U. (1999). Different growth responses to temperature and resource limitation in three fly species with similar life histories. Evolutionary Ecology 13: 395-409 <a href="#fnref:18" class="footnote-back-ref">↩</a></p></li> <li id="fn:19"><p>Blanckenhorn, Morf; Mühlhäuser, Reusch (1999). "Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea". Journal of Evolutionary Biology. 12 (3): 563–576. doi:10.1046/j.1420-9101.1999.00050.x. <a href="https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x" target="_blank">https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x</a> <a href="#fnref:19" class="footnote-back-ref">↩</a></p></li> <li id="fn:20"><p>Blanckenhorn, Morf; Mühlhäuser, Reusch (1999). "Spatiotemporal variation in selection on body size in the dung fly Sepsis cynipsea". Journal of Evolutionary Biology. 12 (3): 563–576. doi:10.1046/j.1420-9101.1999.00050.x. <a href="https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x" target="_blank">https://doi.org/10.1046%2Fj.1420-9101.1999.00050.x</a> <a href="#fnref:20" class="footnote-back-ref">↩</a></p></li> <li id="fn:21"><p>Blanckenhorn, W. U. (1998). Altitudinal differentiation in the diapause response of two species of dung flies. Ecological Entomology 23, 1-8. <a href="/wiki/Diapause" target="_blank">/wiki/Diapause</a> <a href="#fnref:21" class="footnote-back-ref">↩</a></p></li> <li id="fn:22"><p>Rohner, P. T., Bächli, G. , Pollini Paltrinieri, L. , Duelli, P. , Obrist, M. K., Jochmann, R. and Blanckenhorn, W. U. (2015), Distribution, diversity gradients and Rapoport's elevational rule in the black scavenger flies of the Swiss Alps (Diptera: Sepsidae). Insect Conserv Divers, 8: 367-376. doi:10.1111/icad.12114 <a href="#fnref:22" class="footnote-back-ref">↩</a></p></li> <li id="fn:23"><p>Blanckenhorn, W. (1997). "Altitudinal life history variation in the dung flies Scathophaga stercoraria and Sepsis cynipsea". Oecologia. 109: 342–352. doi:10.1007/s004420050092. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:23" class="footnote-back-ref">↩</a></p></li> <li id="fn:24"><p>Teuschl, Y; Blanckenhorn, Wolf U (2007). The reluctant fly: what makes Sepsis cynipsea females willing to copulate? Animal Behaviour, 73(1):85-97. <a href="#fnref:24" class="footnote-back-ref">↩</a></p></li> <li id="fn:25"><p>Parker, G..A. (1972). Reproductive Behaviour of Sepsis Cynipsea (L.) (Diptera: Sepsidae) I. a Preliminary Analysis of the Reproductive Strategy and Its Associated Behaviour Patterns, Behaviour, 41(1-2), 172-205. doi: https://doi.org/10.1163/156853972X00257 <a href="https://doi.org/10.1163/156853972X00257" target="_blank">https://doi.org/10.1163/156853972X00257</a> <a href="#fnref:25" class="footnote-back-ref">↩</a></p></li> <li id="fn:26"><p>Blanckenhorn, W. U., Mühlhäuser, C. , Morf, C. , Reusch, T. and Reuter, M. (2000), Female Choice, Female Reluctance to Mate and Sexual Selection on Body Size in the Dung Fly Sepsis cynipsea. Ethology, 106: 577-593. doi:10.1046/j.1439-0310.2000.00573.x <a href="#fnref:26" class="footnote-back-ref">↩</a></p></li> <li id="fn:27"><p>Blanckenhorn, W. U., Mühlhäuser, C. , Morf, C. , Reusch, T. and Reuter, M. (2000), Female Choice, Female Reluctance to Mate and Sexual Selection on Body Size in the Dung Fly Sepsis cynipsea. Ethology, 106: 577-593. doi:10.1046/j.1439-0310.2000.00573.x <a href="#fnref:27" class="footnote-back-ref">↩</a></p></li> <li id="fn:28"><p>Puniamoorthy, N., Su, K., & Meier, R. (2008). Bending for love: losses and gains of sexual dimorphisms are strictly correlated with changes in the mounting position of sepsid flies (Sepsidae: Diptera). 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