Five flightless species of Micromus are known from the Hawaiian Archipelago; only one, the rare Micromus usingeri, is reported from the Island of Hawai'i. Herein, we report the natural occurrence of intermediates between this brachypterous species and its near relative, the macropterous Micromus longispinosus. We compare some morphological and life-history characteristics of the two species and the intermediates. Our study shows that: (1) The two closely related species are broadly distributed on Hawai'i, but they appear to be allopatric altitudinally. (2) M. usingeri is associated with a cool, misty, high-altitude environment, M. longispinosus with warmer, rainy conditions at lower elevations. The intermediates occur in both types of situations and generally at intermediate elevations. (3) The macropterous M. longispinosus has large, oblong, flexible, membranous forewings and hind wings. In contrast, the brachypterous M. usingeri has convex, shortened, elytra-like forewings with reticulate venation, and very small, thick, triangular, stub-like hind wings with greatly reduced venation. The wings of intermediate specimens exhibit a broad range of variation between the two species. (4) Several characteristics of wing venation are highly correlated with reduced wing size; others are not. (5) Aside from the wings, adults of M. usingeri and M. longispinosus differ in relatively few morphological features, most notably the antennal and metatibial length, prothoracic length, mesothoracic length and width, and the length of the spine-covered process on the posteroventral margin of the male T9+ectoproct. The intermediate specimens are variable in adult characteristics, but they generally fall between the two species. (6) Egg size and larval characteristics (except the body length of the fully-fed first and third instars) do not differ between the two species. (7) The evolution of the wing variation is discussed.
Our study focuses on a series of biological characteristics that Anomalochrysa hepatica exhibits; herein, we compare these features with those expressed by two other species within the endemic Hawaiian lacewing genus. Some of the characteristics (No. 2-3, below) vary greatly among the three congeners and may be of phylogenetic importance; others (No. 1, below) probably are not. Our study showed the following: (1) Developmental response to temperature. Anomalochrysa hepatica's developmental rates under a range of temperatures parallel those of the congener A. maclachlani, but A. hepatica's thermal threshold is lower. It is possible that both species' developmental responses to temperature are subject to considerable geographic variation and thus are of little phylogenetic significance at the species level. (2) Larval color change. Third instars of A. hepatica undergo a striking color change as they mature. In expressing this trait, A. hepatica resembles its closely related congener, A. maclachlani, but differs from the more distantly related congener, A. frater. This color change may have phylogenetic importance. (3) Reproductive behavior. Courtship and mating in Anomalochrysa comprise a consistent sequence of behavioral elements, some of which differ among the three species. For example, during courtship, A. hepatica produces readily audible clicks that are associated with forward flicking of the forewings; in A. maclachlani, readily audible clicking occurs with simultaneous flicking of the fore- and hind wings; in A. frater wing-flicking is present but we did not perceive audible clicks. Some of the interspecific variation in mating behavior may also involve specific morphological modifications; aspects of both the behavioral and morphological variation may provide useful characters for phylogenetic study. (4) Oviposition and rates of egg survival in the field. Unlike other Chrysopidae, endemic Hawaiian Anomalochrysa, including A. hepatica, typically lay unstalked eggs; however, species vary in their patterns of egg laying. Both A. hepatica and A. maclachlani deposit clustered eggs, whereas A. frater lays eggs singly. In nature, the average rate of hatching per A. hepatica egg mass was ~75%. Several species of introduced predators and a species of trichogrammatid parasitoid attacked these eggs.