HYDROMETRINAE, Billberg, 1820
publication ID |
https://doi.org/ 10.5281/zenodo.13245098 |
persistent identifier |
https://treatment.plazi.org/id/32753044-FFC0-FFA0-B033-2CD6FB36F36E |
treatment provided by |
Felipe |
scientific name |
HYDROMETRINAE |
status |
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SUBFAMILY HYDROMETRINAE View in CoL
There are four genera in this subfamily: Bacillometra (South America), Chaetometra , Dolichocephalometra (Marquesas Islands) , and the cosmopolitan Hydrometra . The genus Hydrometra is common and widespread in Southeast Asia.
The body length of Hydrometra ranges from 7 to 18 mm. They are usually brownish, dark greenish or blackish in colour. Species of Hydrometra are quite uniform in general structure, the detailed morphology has been studied by Andersen (1982a) and Polhemus & Polhemus (1995). Some characteristics that are important for species identification are mentioned here.
The elongated head is about 1/3 of the body length; eyes are far away from the anterior margin and divide the head into anteocular (AO) and postocular (PO) parts ( Fig. 2 View Fig ). The length ratio of the AO: PO is sometimes helpful for identification. Antennae are long and semiflagelliform, about half of the body length. The shape of anteclypeus (or clypeus, Figs. 2 View Fig , 12 View Figs ) and its anterior margin vary among different species. It is important for species identification as well as for separation of species groups. Most species have rounded, acute or spine-like anterior, others have broadly rounded to almost straight anterior. The broad anteclypeus with truncate or concave anterior margin type is considered as the most plesiomorphic character state ( Andersen 1977, 1982a) and defines a distinct, widely distributed species group. In the Oriental Region, H ydrometra brevitarsus , gilloglyi , heoki and julieni belong to this group. The gular lobe and maxillary plate ( Figs. 2 View Fig , 26 View Figs , 39 View Figs ) are variable among some species, for example, H. carinata has enlarged maxillary plates.
The thorax is shorter than the head, the distinctive pronotal lobe is covered with punctures and the acetabula usually with acetabular pits. The number of pits differs slightly among species. Some brachypterous females of H. longicapitis bear a long tubercle process on the posterior of the pronotal lobe ( Fig. 4), this unusual polymorphism has not been observed in other species ( Andersen, 1992; Polhemus & Polhemus, 1995). The legs of Hydrometra are long and thread-like, and have 3- segmented tarsi with terminal claws. The modification of legs is mainly through length, with the exception of the species group H. maidli-borneensis - annamana that has a row of hairs on the hind femora of the male.
The wing venation is reduced as compared to most other semiaquatic bugs. In the macropterous (mapt) morph the wings are long, covering most of the abdominal tergites. In the brachypterous (brpt) morph the wings are reduced to narrow straps, which hardly extend onto the surface of the abdomen. In apterous (apt) (or micropterous) morph the wings are either completely covered by the pronotal lobe, or just visible as very tiny pads behind its hind margin. Information on wing morphs is often a valuable hint for recognition of species. In general, Hydrometra species usually occur in two different morphs. Most species have a brachypterous and a macropterous morph. Some species are only known for one morph, an apterous (or micropterous) or a macropterous morph. A few species are only known in brachypterous morph, but the occurrence of macropterous specimens has to be expected. In the key we mention the more common morph first, followed by the less common, e.g., “mapt or brpt”. If one morph occurs rarely, it is put in parenthesis, e.g., “mapt (or brpt)”.
The abdomen ( Figs. 3 View Fig , 4) is relatively long, covered with short and fine pubescence, and some long setae. The mediotergites are narrow, and the width to length ratio is useful in separating some closed related species. Laterotergites (connexiva or paratergites) of some species carry long erected setae ( Figs. 23, 24 View Figs , 33 View Figs , 51 View Figs ). Sternite 7 of the male is modified. Some are transversely concave and dispersed with long setae ( Fig. 40 View Figs ); some with patches of short hairs or with a pair of clustered set of long setae ( Figs. 14, 18 View Figs ), or modified with thorn-like, or spine-like process ( Figs. 29 View Figs , 50 View Figs , 80 View Figs , 88), whilst H. longicapitis has a pair of very distinct fleshy tubercle processes on the anterior of sternite 7 ( Fig. 66 View Figs ). Segment 8 of male is usually not modified, but some species have slight depression or paired cluster of setae ventrolaterally ( Figs. 36 View Figs , 45, 47 View Figs ). The posterodorsal corners are usually rounded, but a few species have distincted outwarded process because of the expanded wing-like structure of the pygophore (S9) ( Fig. 62 View Figs ). The sternite 7 of the female is not modified, but its length and shape, as well as the terminal process of tergite 8 are useful characters for species identification.
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