The fruit fly genus Strauzia (Diptera: Tephritidae) is native to North America, and is most widespread and abundant in the Eastern United States / Canada (Norrbom, 1999), though smaller populations have been sporadically observed in the Western US (Hippee et al., 2020; Foote and Blanc, 1963). Strauzia longipennis has been recently recorded in Germany (Bruckner & Korneyev, 2010), and a study three years later showed S. longipennis was in nearly every German province and continues to exist there (Lerche et al., 2013; EPPO 2021). Strauzia is associated with Sunflowers and similar genera, and the most studied member of the group is Strauzia longipennis, which is known as the “sunflower maggot fly” (Westdal and Barrett, 1960). Sunflowers and its close allies are in the tribe Heliantheae, which is a diverse group of flowers that are largely native to North America (Robinson, 1981).
Male Strauzia flies have greatly inflated frontal bristles compared to the females, and are suspected to play some role in female mate choice during courtship (Stoltzfus, 1988). Courtship before mating is started by the male and female approaching face to face, which means the enlarged frontal bristles are right in view for the female. Mating is varied in terms of time, lasting from a few minutes all the way to several hours (Westdal and Barrett, 1960).
After mating, female Strauzia flies stick their ovipositors, the spike-like end of their genitals, into the stems of the sunflowers and inject eggs into the pith of the plant. After about a week, these eggs hatch into larvae, which tunnel up and down the stem for the next month, eating the plant matter it encounters (Westdal and Barrett, 1960). They continue this for about a month, and then get ready to pupate, which is similar to a chrysalis of a butterfly.
For pupation, the place where a species of Strauzia chooses to go represents one axis of differentiation within the group. Different strategies of different species include leaving the stem as a larvae and burying into the soil to pupate, burying into the upper roots to pupate, or just staying as to pupate within the stem of the plant (Stoltzfus, 1988). This behavior is very consistent within a given species, as the flies have evolved for hundreds of thousands of years to get to this point, so this was used as a starting point to differentiate species using the same sunflower species.
On the topic of the sunflowers, the species of Helianthus or related genera that a Strauzia species uses appears to be very specialized. Any given species of Strauzia fly is only associated with one to three species of sunflowers, which leads it to be another axis of differentiation in the life history of the group (Hippee et al., 2020). Additionally, the adults emerge in the summer and disappear in the fall, but the specific time of these events differ between species along the months of May to August (Stoltzfus, 1988). The times at which the larvae decide to pupate also varies during the Fall for each species, and then they wait in their pupa until the next Summer.
Different species have been distinguished based on the coloration of the thorax, the wing patterns, and for females, the tip of their ovipositor. The wing patterns are complicated, however, as they appear to be sexually dimorphic for the majority of Strauzia species, and also differ within species (Axen et al., 2010). Ovipositors are the end of the genitals for the female Strauzia flies, and are specialized so that the stem of the host plant can be pierced exactly right for the eggs to enter.
The original description of Strauzia longipennis is a bit confusing, as two different scientists described it in the same year, 1830, in different languages. The first description of this species was by Wiedemann, a German taxonomist, as Trypeta longipennis; he described many fruit flies as being within a single genus Trypeta. The genus Strauzia itself was coined by Robineau-Desvoidy’s French description of Strauzia inermis in 1830, but his was published slightly later, and thus his name is a junior synonym of Wiedemann’s. However, the genus name made by Robineau-Desvoidy was still valid, and Wiedemann’s longipennis was transferred to Strauzia by Coquillett in 1910.
A few decades later, more species of Strauzia were described as varieties of longipennis by Loew, 1873. These include many of the common species, with him describing Strauzia longipennis var. perfecta, typica, longitudinalis, vittigera, intermedia and arculata. All of these are now arguably valid species except for the errantly described confluens, which has apparently had its type material lost and no matching flies have been found, and has now fallen into obscurity (Hippee et al., 2020).
A surge of research into the taxonomy and species of Strauzia occurred in the 1980’s, with three revisions being made in quick succession. The first was by Edward Lisowski in his 1985 PhD thesis on Strauzia in Illinois, which unfortunately was never published so his proposed species are technically invalid. In it, he raised all varieties of Strauzia longipennis to species level. He also described a species, “Strauzia bushi”, from a small population of males in Indiana, but this fell into obscurity until relatively recently when it was proven to be a distinct species in Hippee et al., 2020. A year later, George Steyskal published his taxonomy of Strauzia in 1986. He raised only some of the varieties of S. longipennis to species level, leaving vittigera and longitudinalis as they were. He also described new species such as verbesinae, gigantei, and the incredibly rare stoltzfusi, which is only known from 2 specimens.
Finally, the most recent taxonomic work was that of Bryan Stoltzfus in 1988. Within it, he effectively combined the work of the two previous authors, accepting the new species of Steyskal while raising all of Loew’s variants of S. longipennis to species level. He also described 3 new species, uvedaliae, rugosum, and noctipennis, differentiated largely from contrasting life cycles of the species. These were relatively controversial moves, and in the work of Foote et al., 1993, these species were not included in the North American handbook of the family Tephritidae because they were “not based strongly enough in morphological differences” to be adequately differentiated from specimens.
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