Research Article
Research Article
The blowflies of the Madeira Archipelago: species diversity, distribution and identification (Diptera, Calliphoridaes. l.)
expand article infoCatarina Prado e Castro, Krzysztof Szpila§, Ana Isabel Martínez-Sánchez|, Carla Rego, Isamberto Silva#, Artur R.M. Serrano¤, Mário Boieiro
‡ University of Coimbra, Coimbra, Portugal
§ Copernicus University, Torun, Poland
| University of Alicante, Aalicante, Spain
¶ University of Azores, Azores, Portugal
# Madeira Nature Park, Madeira, Portugal
¤ Universidade de Lisboa, Lisboa, Portugal
Open Access


Knowledge on the taxonomic diversity and distribution of blowflies from the Madeira Archipelago is updated. New and interesting findings are reported for poorly studied islands and islets of this archipelago, together with a brief analysis of the diversity of Macaronesian Calliphoridaes. l. Seven blowfly species were collected during this study, including the first records of Calliphora vicina Robineau-Desvoidy, 1830, Chrysomya albiceps (Wiedemann, 1819), Lucilia sericata (Meigen, 1826), Pollenia rudis (Fabricius, 1794) and Stomorhina lunata (Fabricius, 1805) from Porto Santo, and of C. vicina, L. sericata and S. lunata from Desertas Islands. The presence of Calliphora loewi Enderlein, 1903 in Madeira Laurisilva forest is discussed and its first instar larva is redescribed, revealing important differences in relation to its original description. An identification key to the adult Madeiran blowflies is provided for the first time.


Calliphora loewi , island diversity, key, larval description, Laurisilva, Macaronesia


Blowflies in the broad sense (Diptera: Calliphoridae, Mesembrinellidae, Rhiniidae) (Kutty et al. 2010, Marinho et al. 2016) are conspicuous flies that can be found in both synanthropic and natural ecosystems. Some species exhibit beautiful metallic colours, ranging from green to violet, while others have a more cryptic colouration. Nevertheless, due to their moderate size and frequent association with domestic and human-disturbed environments, blowflies are usually familiar to people.

There are 115 blowfly species in Europe (Rognes and Baz 2007, Rognes 2013), 12 of these being Rhiniidae, once a subfamily of Calliphoridaes. l. but recently raised to the rank of family (Kutty et al. 2010). Recent molecular studies also point to a similar status for the Polleniinae, but this taxon is still treated as a subfamily of Calliphoridaes. str. (e.g., Kutty et al. 2010, Singh and Wells 2013, Marinho et al. 2016, Zhang et al. 2016). Adult blowflies have a wide variety of life habits: some species feed on pollen and nectar, playing a role in pollination (Rognes 1998, Pérez-Bañon et al. 2007), while most are usually associated with faeces, animal corpses and other decaying organic matter (Norris 1965, Heath 1982, Rognes 1998). A considerable number of species are parasites or predators of earthworms (Bellardia Robineau-Desvoidy, 1863, Onesia Robineau-Desvoidy, 1830 and Pollenia Robineau-Desvoidy, 1830 species), snails (Angioneura Brauer & Bergenstamm, 1893, Eurychaeta Brauer & Bergenstamm, 1891 and Melinda Robineau-Desvoidy, 1830 species), or parasites of bird nestlings (Protocalliphora Hough, 1899 and Trypocalliphora Peus, 1960 species) (Rognes 1998). Many blowfly species play a key ecological role as natural agents of decomposition (Erzinçlioglu 1985) and are also important in human and veterinary medicine as transmitters of pathogens and as agents of myiasis (Zumpt 1965, Greenberg 1971, Erzinçlioglu 1985, Rognes 1998). In the Rhiniidae, however, the immature morphology and life cycles are unknown for almost all species, though a predatory/parasitic behaviour in nests of social insects and on orthopteran egg-masses has been either suggested or confirmed (Peris 1952, Rognes 1998, Bharti and Bharti 2016).

The catalogue of Iberian Diptera (Carles-Tolrá 2002), which also includes information on the Canarian, Azorean and Madeiran islands, is a landmark in the study of these insects by providing valuable information on the taxonomic diversity of Diptera at both the national and regional level. Furthermore, the comparison of checklists and associated scientific literature presented in the catalogue clearly highlights disparities in knowledge on many families between the different regions. For example, the poor knowledge of the Portuguese fauna, with only 19 blowfly species recorded (13 Calliphoridae and 6 Rhiniidae) contrasts with the amount of information available for Spain, where 48 blowfly species (41 Calliphoridae and 7 Rhiniidae) are known to occur (Martínez-Sánchez et al. 2002). New findings of blowflies have been reported for continental Portugal (Prado e Castro and García 2009, Prado e Castro et al. 2010) and Spain (Carles-Tolrá 2007) in the last decade, but no significant changes were recorded for the fauna of the Madeira Archipelago. In Portugal, including the Azores and Madeira archipelagos, there is still scarce information on the taxonomic diversity of blowflies due to a lack of national experts and severe limitations in funding for biodiversity inventorying and monitoring programmes targeting invertebrates.

The checklist of Madeiran terrestrial biodiversity (Borges et al. 2008) reports nine species, and recently, C. loewi was found for the first time in the archipelago (Prado e Castro et al. 2016). Earlier studies on blowflies from the Madeira Archipelago are scarce and all species records are restricted to the main island (Báez and Santos-Pinto 1975, Rognes 1987, Báez 1990). Herein, an updated checklist is provided of the Calliphoridae and Rhiniidae of the Madeira Archipelago, including new data on the distribution and abundance of seven species. The presence of Calliphora loewi Enderlein in Madeira Laurisilva is discussed and its first instar larva is redescribed, showing significant differences in relation to the original description. Finally, a key is provided to enable the identification of adults of all species so far reported from the archipelago.

Material and methods

Study area

The Madeira Archipelago is located in the North Atlantic, nearly 600 km from the African coast (Morocco), between latitudes 32°24' and 33°07'N and longitudes 16°16' and 17°16'W. The archipelago consists of three groups of volcanic islands and islets, namely Madeira, Porto Santo and Desertas. Madeira is the largest (~ 740 km2) and highest (1862 m) island and also presents the highest diversity of habitat types, including the largest surviving area of Laurisilva forest in Macaronesia. Laurisilva is a relict laurel forest native to the Macaronesian archipelagos of Azores, Canaries and Madeira, which during the Tertiary covered a considerable area of the western Mediterranean Basin (Aguiar et al. 2004). Madeira Island has a considerable number of laurel forest fragments in pristine condition (Neves et al. 1996), which led Madeiran Laurisilva to be classified as a UNESCO World Natural Heritage site (IUCN 1999). Furthermore, mostly due to the unique biodiversity associated with Laurisilva, the Madeira Archipelago was included in one of the most important global biodiversity hotspots, the Mediterranean hotspot (Médail and Quézel 1999, Myers et al. 2000). Porto Santo and Desertas have drier environmental conditions than Madeira. On these islands, the dominant plant cover is of herbaceous communities with some thermophilous shrub species, but there are also a considerable number of areas lacking vegetation and affected by soil erosion.

Protected areas cover a large fraction of the archipelago, aiming to maintain and protect its native biodiversity from a number of human-related threats (Martin et al. 2008, Silva et al. 2008; see also Nevertheless, despite the recognized vulnerability of several endemic terrestrial arthropod species (Martin et al. 2008, Crespo et al. 2014), very few conservation actions specifically targeting this animal group have been carried out.

Sampling and laboratory work

A sampling programme encompassing different habitat types in all islands of Madeira Archipelago was carried out during the springs and summers of 2011 and 2012 (Table 1). At each site, a combination of sampling techniques (direct sampling, pitfall trapping, vegetation sweeping) were applied to provide an inventory of species of several groups of terrestrial arthropods. Detailed information on the sampling methodology was provided by Serrano et al. (2014). The samples were sorted in the Entomology Laboratory of the Faculty of Sciences, University of Lisbon, Portugal, where adult blowfly specimens were identified to species level using Olympus SZX7 stereomicroscopes and several taxonomic resources (González-Mora and Peris 1988, González-Mora 1989, Peris and González-Mora 1991, Szpila 2012). Pollenia rudis specimens were identified, using specific literature (Rognes 1987, 1992), with a Leica M80 at the laboratory of the Department of Environmental Sciences and Natural Resources, University of Alicante, Spain. All identified adult specimens are deposited in the entomological collection of the Department of Animal Biology, University of Lisbon, Portugal.

Table 1.

Information on sampling dates and localities (site name, habitat type, and geographic coordinates) in the Madeira Archipelago.

Island group Site name Habitat type Latitude (N) Longitude (W) Dates
Madeira Abobreiras Heathland 32°43'13" 16°51'37" 30/V-13/VI/2011
Achadas da Cruz Eucalyptus plantation 32°50'42" 17°12'25" 26/V-9/VI/2011
Bica da Cana Pinus plantation 32°44'47" 17°03'25" 26/VI-9/VII/20110
Calheta 1 Heathland 32°45'28" 17°08'48" 27/V-10/VI/20110
Calheta 2 Eucalyptus plantation 32°45'06" 17°09'14" 27/V-10/VI/20110
Dunas da Piedade Dune system 32°44'49" 16°39'27" 2-16/V/20110
Funduras Laurisilva 32°44'58" 16°47'30" 31/V-14/VI/20110
Galhano 1 Laurisilva 32°48'07" 17°09'57" 4-18/VII/20120
Galhano 3 Laurisilva 32°47'48" 17°10'30" 5-19/VII/20120
Ilhéu do Farol Coastal vegetation 32°43'43" 16°39'27" 18/V-1/VI/20110
Loreto Pinus plantation 32°46'41" 17°12'36" 24/VI-9/VII/20110
Miradouro das Voltas 1 Laurisilva 32°48'28" 16°57'00" 2-16/VI/20110
Miradouro das Voltas 2 Laurisilva 32°48'15" 16°56'48" 2-16/VI/20110
Miradouro das Voltas Ps Pseudotsuga plantation 32°48'43" 16°57'04" 2-16/VI/20110
Miradouro das Voltas Seq Sequoia plantation 32°48'24" 16°56'47" 2-16/VI/20110
Montado dos Pessegueiros 2 Laurisilva 32°47'40" 17°05'12" 3-17/VII/20120
Montado dos Pessegueiros 3 Laurisilva 32°47'44" 17°05'07" 3-17/VII/20120
Pico das Pedras L Laurisilva 32°46'08" 16°54'42" 31/V-14/VI/20110
Pico das Pedras Ps Pseudotsuga plantation 32°46'33" 16°53'48" 31/V-14/VI/20110
Ponta de S. Lourenço E Coastal vegetation 32°44'56" 16°41'30" 3-17/V/20110
Parque eólico Semi-natural meadow 32°44'45" 16°43'29" 2-16/V/20110
Ponta de S. Lourenço W Coastal vegetation 32°44'50" 16°41'55" 3-17/V/20110
Portela Eucalyptus plantation 32°44'45" 16°49'23" 3-17/VI/20110
Porto Moniz Eucalyptus plantation 32°50'46" 17°10'37" 24/V-7/VI/20110
Prazeres Pinus plantation 32°45'58" 17°11'33" 24/VI-9/VII/20110
Ribeira da Cruz Laurisilva 32°49'34" 17°12'35" 26/V-9/VI/20110
Santana Pinus plantation 32°48'09" 16°51'57" 25/VI-10/VII/20110
Desertas Bugio N Coastal vegetation 32°24'52" 16°28'40" 27/IV-19/V/2011
Bugio S Coastal vegetation 32°24'38" 16°28'23" 27/IV-19/V/2011
Castanheira N Coastal vegetation 32°33'52" 16°32'12" 26/IV-10/V/20110
Castanheira S Coastal vegetation 32°33'11" 16°31'47" 26/IV-10/V/20110
Eira Coastal vegetation 32°30'50" 16°30'10" 27/IV-11/V/20110
Doca Coastal vegetation 32°31'03" 16°30'41" 26/IV-10/V/20110
Ilhéu Chão N Coastal vegetation 32°35'10" 16°32'43" 28/IV-18/V/20110
Ilhéu Chão S Coastal vegetation 32°34'52" 16°32'25" 28/IV-18/V/20110
Porto Santo Fonte da Areia Dune system 33°04'54" 16°21'18" 21/VI-5/VII/20110
Ilhéu da Cal N Coastal vegetation 33°0'41" 16°23'07" 22/VI-6/VII/20110
Ilhéu da Cal S Coastal vegetation 33°00'7" 16°23'01" 22/VI-6/VII/20110
Ilhéu do Farol N Coastal vegetation 33°03'19" 16°17'04" 20/VI-4/VII/20110
Ilhéu do Farol S Coastal vegetation 33°03'13" 16°16'43" 20/VI-4/VII/20110
Ilhéu do Ferro Coastal vegetation 33°02'16" 16°24'28" 21/VI-5/VII/20110
Pico Ana Ferreira Pinus plantation 33°02'36" 16°22'24" 21/IV-5/V/20110
Pico Branco Cup Cupressus plantation 33°05'40" 16°17'55" 23/IV-7/V/20110
Pico Branco mead Semi-natural meadow 33°05'29" 16°18'23" 23/IV-7/V/20110
Pico do Castelo Pinus plantation 33°04'51" 16°19'55" 22/IV-6/V/20110
Pico do Facho Cup Cupressus plantation 33°05'02" 16°19'17" 22/IV-6/V/20110
Pico do Facho Pin Pinus plantation 33°04'58" 16°19'28" 22/IV-6/V/20110
Pico Juliana Cupressus plantation 33°05'33" 16°19'20" 23/IV-7/V/20110

The unexpected finding of larviposition by Calliphora loewi in Madeira Laurisilva (Prado e Castro et al. 2016) allowed for a detailed study of its first instar larval morphology. A revision of the first instar larval morphology of forensically important European Calliphorinae species was recently published by Szpila et al. (2014); for a few species, including C. loewi, the authors were unable to access original material and had to base their conclusions on information from the literature (Erzinçlioglu 1985). The study of the first instar larva of C. loewi was carried out in Poland (Chair of Ecology and Biogeography Laboratory, Faculty of Biology and Environmental Protection, Nicolaus Copernicus University, Toruń) after extraction from dissected, gravid females. Abdomens of females were detached from the rest of the body and boiled in a 5% KOH solution for 5 minutes. Each abdomen was dissected by slicing the membrane between the tergites and sternites, enabling intact first instars to be pulled out of the female oviduct. The larvae were slide-mounted in Hoyer’s medium for study under a light microscope. A Nikon 8400 digital camera, mounted on a Nikon Eclipse E200 microscope, was used for documentation of larval morphology. The larval specimens are housed in the entomological collection of the Chair of Ecology and Biogeography, Nicolaus Copernicus University, Toruń, Poland.

The classification and the taxonomic terminology used in the key follow Rognes (1991), while the terminology used in the description of the first instar larva morphology follows Szpila et al. (2014) and Grzywacz et al. (2014).


The blowfly species of the Madeira Archipelago

Four-hundred and seventy (470) specimens of six Calliphoridae and one Rhiniidae species were collected during this study. The occurrence of blowfly species is reported for the first time from Porto Santo and Desertas. Detailed information associated with the specimens collected in the Madeira Archipelago (sampling date, location, geographic coordinates, habitat-type and number and sex of specimens) is presented under “Material examined” and in Table 1. An updated list of blowfly species from the Madeira Archipelago is presented in Table 2, while the spatial distribution of new species records is shown in Figure 1.

Figure 1. 

Blowfly records collected during the present study in the islands and islets of the Madeira Archipelago. Species records are plotted on a simplified representation of the archipelago to ease understanding.

Table 2.

Updated list of the Calliphoridae and Rhiniidae of the Madeira Archipelago. New records are indicated by a full black circle. M – Madeira Island, PS – Porto Santo Island and surrounding islets, D – Desertas islands (Ilhéu Chão, Deserta Grande and Bugio).

Species M PS D
Calliphora loewi Enderlein, 1903 X
Calliphora vicina Robineau-Desvoidy, 1830 X
Calliphora vomitoria (Linnaeus, 1758) X
Chrysomya albiceps (Wiedemann, 1819) X
Chrysomya megacephala (Fabricius, 1794) X
Lucilia sericata (Meigen, 1826) X
Pollenia angustigena Wainwright, 1940 X
Pollenia pediculata Macquart, 1834 X
Pollenia rudis (Fabricius, 1794) X
Stomorhina lunata (Fabricius, 1805) X

Calliphora loewi Enderlein, 1903

Figs 2J, 3A

Material examined

Madeira: Galhano 3 (20 females); Montado dos Pessegueiros 2 (1 female); Montado dos Pessegueiros 3 (3 females).


Calliphora loewi is a carrion-breeder present in the Holarctic and in a small part of the Oriental Region (Schumann 1986, Verves 2005). It is found in forests of northern and central Europe (Smith 1986, Byrd and Castner 2010), being common in alpine regions. In North America it is found in Alaska, Canada and in the northern continental United States (Rognes 1991, Tantawi et al. in press). Throughout its range, this species is generally not found in urban and disturbed areas (Byrd and Castner 2010). Although widespread, C. loewi is rarely recorded, and usually in low abundance, in carcasses of large vertebrates, demonstrating a preference for small animal remains (Szpila et al. 2014). In Madeira, C. loewi is restricted to a few native forest areas at high altitude (1000–1300 m) (Fig. 1). This species was recently collected for the first time in Madeira (Prado e Castro et al. 2016).

Figure 2. 

Diagnostically important characters of Madeiran blowflies (Diptera, Calliphoridaes. l.): A Chrysomya albiceps, basal part of wing, dorsal surface, showing haired stem vein B Stomorhina lunata, basal part of wing, dorsal surface, showing haired stem vein C Calliphora vicina, basal part of wing, dorsal surface, showing bare stem vein D Calliphora vomitoria, thorax, upper and lower calypters E Lucilia sericata, thorax, upper and lower calypters F Stomorhina lunata, female, head, lateral view G Chrysomya albiceps, female, head, lateral view H Chrysomya megacephala, female, head, lateral view I Calliphora vicina, female, head, lateral view J Calliphora loewi, female, head, lateral view K Calliphora vomitoria, female, head, lateral view L Lucilia sericata, female, head, lateral view M Pollenia rudis, female, head, lateral view N Pollenia rudis, thorax, upper and lower calypters O Pollenia pediculata, basal part of wing, ventral surface, showing haired node of subcostal and humeral veins P Pollenia rudis, basal part of wing, ventral surface, showing bare node of subcostal and humeral veins Q Pollenia angustigena, mid tibia R Pollenia rudis, mid tibia. Abbreviations: ad, anterodorsal seta; ant spir, anterior spiracle; eh, eye height; gen dil, genal dilation; gdh, genal dilation height; lfm, lower facial margin; low cal, lower calypter; p pl, parafacial plate; psg, postgena; sc-h n, node subcosta-humeral vein.

Figure 3. 

Habitus in antero-lateral view of Madeiran blowflies: A Calliphora loewi B Calliphora vicina C Calliphora vomitoria D Chrysomya albiceps E Chrysomya megacephala F Lucilia sericata G Pollenia rudis H Stomorhina lunata.

Figure 4. 

First instar larva of Calliphora loewi from Madeira: A Habitus in lateral view B Cephaloskeleton in lateral view C Anterior part of cephaloskeleton in lateral view. Abbreviations: a1-a7, abdominal segments; ad, anal division; db, dorsal bridge; dc, dorsal cornua; is, intermediate sclerite; lb, labrum; mh, mouthhook; pb, parastomal bar; pc, pseudocephalon; t1-t3, thoracic segments.

Calliphora vicina Robineau-Desvoidy, 1830

Figs 2I, 3B

Material examined

Madeira: Abobreiras (1 female); Achadas da Cruz (1 male); Calheta 1 (1 female); Calheta 2 (1 female); Ponta de São Lourenço E (1 male); Ilhéu do Farol (1 male); Funduras (1 female); Galhano 1 (1 female); Miradouro das Voltas 1 (1 female); Miradouro das Voltas 2 (1 female); Miradouro das Voltas Ps (1 female); Miradouro das Voltas Seq (2 females); Montado dos Pessegueiros 2 (1 female, 1 male); Montado dos Pessegueiros 3 (1 female, 2 males); Pico das Pedras L (1 female); Pico das Pedras Ps (2 females); Portela (1 female); Porto Moniz (2 females); Ribeira da Cruz (1 female); Santana (1 female); PORTO SANTO: Ilhéu da Cal S (1 female, 1 male); Fonte da Areia (1 female, 1 male); Pico Ana Ferreira (7 females, 1 male); Pico do Facho Cup (1 female); Pico Juliana (1 female); DESERTAS: Bugio N (12 females, 5 males); Bugio S (7 females, 1 male); Ilhéu Chão N (1 female, 1 male).


Calliphora vicina is a cosmopolitan species, widely distributed all over the world and closely connected with human activity (Zumpt 1965, Greenberg 1971, González-Mora 1989, Martínez-Sánchez et al. 2002), being commonly found in urban areas (Erzinçlioglu 1985, Rognes 1998, Szpila et al. 2014). The adults are attracted to faeces, meat and fruits, while the larvae are mainly necrophagous, usually developing in carrion (Zumpt 1965, Greenberg 1971). This species is widespread in a variety of habitat types in the Madeira Archipelago (Table 1).

Calliphora vomitoria (Linnaeus, 1758)

Figs 2K, 3C

Material examined

Madeira: Bica da Cana (1 female).


This common carrion-breeder is distributed throughout the Holarctic Region and is also present in the Oriental and Australasian regions (Erzinçlioglu 1985). It is more rural in its distribution than C. vicina (Smith 1986), frequenting natural and cultivated forests and showing a preference for more shaded habitats (Szpila et al. 2014). Calliphora vomitoria was found only in Madeira, in a pine plantation with low human disturbance.

Chrysomya albiceps (Wiedemann, 1819)

Figs 2G, 3D

Material examined

Porto Santo: Ilhéu do Farol S (1 female).


Chrysomya albiceps can be found from the southern Palaearctic Region (southern Europe, Arabia, India) through to Africa (Zumpt 1965) and the Americas, where since its introduction it has rapidly expanded north (Guimarães et al. 1978, Baumgartner and Greenberg 1984). In Europe it is very abundant in the Iberian Peninsula (Martínez-Sánchez et al. 2002, Prado e Castro et al. 2012) and is expanding towards central Europe, having reached France, Switzerland and Austria (Grassberger et al. 2003), the Ukraine (Verves 2004) and Poland, from where its current northernmost records are known (Szpila et al. 2008, Michalski and Szpila in press). Our record from Ilhéu do Farol is the first for Porto Santo. Chrysomya albiceps normally breeds in carrion; newly-hatched first instar larvae feed on exudations of decomposing flesh, but the second and third larval stages are facultative predators, feeding also on the larvae of other blowfly species (Zumpt 1965).

Chrysomya megacephala (Fabricius, 1794)

Figs 2H, 3E


Madeira: Funchal (Báez 1990).


Chrysomya megacephala is widely distributed over the Oriental and Australasian regions, also occurring in many neighbouring parts of the Palaearctic Region (Zumpt 1965). It was introduced in South America (Guimarães et al. 1978), probably from southern Africa (Baumgartner and Greenberg 1984), and into the United States (Greenberg 1988). In Europe it is known from Spain (Martínez-Sánchez et al. 2001), Portugal (Prado e Castro and García 2009), Malta (Ebejer 2007) and from the archipelagos of Madeira (Báez 1990) and the Canaries (Báez et al. 1981). Chrysomya megacephala is normally a faeces and carrion breeder (Zumpt 1965), considered a dangerous dipteran vector of pathogens (Wells 1991) and a major pest of fish products (Wall et al. 2001).

Lucilia sericata (Meigen, 1826)

Figs 2L, 3F

Material examined

Madeira: Dunas da Piedade (1 male); Ilhéu do Farol (1 female); Porto Santo: Ilhéu da Cal S (1 male); Ilhéu do Farol N (1 female, 5 males); Ilhéu do Farol S (2 females); Ilhéu do Ferro (1 female); Desertas: Bugio N (130 females, 30 males); Bugio S (116 females, 34 males); Castanheira N (13 females, 5 males); Castanheira S (3 females); Doca (10 females, 5 males); Eira (1 female); Ilhéu Chão N (1 female); Ilhéu Chão S (1 female).


A very common fly in temperate areas of the Holarctic Region (Zumpt 1965). It is practically cosmopolitan, widespread throughout the major zoogeographical regions (Smith 1986, Rognes 1991), and is directly connected to human activity (Martínez-Sánchez et al. 2002). Lucilia sericata was found in all island groups of the Madeira Archipelago where it was occasionally recorded in high abundance. The adults are attracted mainly to carrion or open wounds (usually with necrotic tissues) (Zumpt 1965).

Pollenia angustigena Wainwright, 1940


Madeira: Madeira (Rognes 1987).


This species is cited from most countries of Europe and from the Nearctic Region (Rognes 1991). In Europe, P. angustigena can be found from the southern parts of Norway and Finland to Italy and the Iberian Peninsula (Martínez-Sánchez et al. 2002). In the Iberian Peninsula the species seems to be restricted to high altitudes (from 300 m to above 1200 m) (Martínez-Sánchez et al. 1998). No specimens were caught in this study but the species was previously cited from Madeira (Rognes 1987, Martínez-Sánchez and Rognes 2008). Adults of this fly are active mostly from March to October with peaks in early spring in the northern parts of its range (Rognes 1991). As the rest of Pollenia spp., it is a predator on earthworm species (Rognes 1987). The egg and first instar larva of this species were described by Grzywacz et al. (2012) and Szpila (2003), respectively, and their morphology is significantly different compared to that of necrophagous blowflies.

Pollenia pediculata Macquart, 1834


Madeira: Madeira (Rognes 1987).


This species is distributed throughout most zoogeographical regions, being widespread in Europe. Pollenia pediculata was first cited from Madeira by Rognes (1987), but no specimens were obtained in the present study. The adults are active mainly in summer (Martínez-Sánchez et al. 2001). The larvae are predators on earthworms, including the lumbricid Eisenia rosea (Savigny) (Rognes 1987). The early immature stages were described by Szpila (2003) and Grzywacz et al. (2012).

Pollenia rudis (Fabricius, 1794)

Figs 2M, 3G

Material examined

Madeira: Parque eólico (2 females); Ponta de São Lourenço W (1 female); Porto Santo: Pico Branco Cup (6 females); Pico Branco mead (4 females); Pico do Castelo (4 females).


This is the most common species in the genus, being widespread in the Palaearctic, Nearctic and Oriental regions. In Porto Santo it was found in different habitat types (Table 1). Pollenia rudis uses earthworms as larval hosts and is active all year round, particularly during spring (Rognes 1987, Martínez-Sánchez et al. 1998). The immature stages were described by Yahnke and George (1972), Szpila (2003) and Grzywacz et al. (2012).

Stomorhina lunata (Fabricius, 1805)

Figs 2F, 3H

Material examined

Madeira: Bica da Cana (2 females); Loreto (3 females); Prazeres (1 female); Parque eólico (1 female); Ponta de São Lourenço W (1 female); Porto Santo: Ilhéu da Cal N (4 females); Ilhéu da Cal S (2 females); Ilhéu do Ferro (1 female); Fonte da Areia (7 females); Pico do Facho Pin (1 female); Desertas: Castanheira N (1 female).


Stomorhina lunata is distributed almost worldwide, being absent only from the Neotropical and Australasian regions (Rognes 2013). It is common in Europe including all of the Mediterranean area, and is widely distributed throughout the Iberian Peninsula (González-Mora and Peris 1988). It is known as a predator on egg-masses of the locust Schistocerca gregaria (Forskål, 1775) (Rognes 1998) and a parasite in nests of ants (Bharti and Bharti 2016). Adults are commonly found on flowers (González-Mora and Peris 1988).

Key to the adult blowflies of the Madeira Archipelago

1 Stem-vein with a row of weak setulae on dorsal surface (Fig. 2A, B) 2
Stem-vein bare on dorsal surface (Fig. 2C) 4
2 Lower facial margin strongly protruded (Fig. 2F); arista bare on ventral side (Fig. 2F); abdomen with a yellow pattern on black background Stomorhina lunata
Lower facial margin not protruded (Fig. 2G, H); arista always with hairs dorsally and ventrally (Fig. 2G, H); abdomen lustrous, bluish or green, with dark transverse strips on posterior margins of segments 3
3 Anterior spiracle light-coloured, white-yellowish (Fig. 2G) Chrysomya albiceps
Anterior spiracle dark, brownish (Fig. 2H) Chrysomya megacephala
4 Lower calypter black or at least darkly infuscate, with numerous long hairs on dorsal surface (Fig. 2D) 5
Lower calypter white-yellowish and bare on dorsal surface (Fig. 2E, N) 7
5 Facial ridge, lower facial margin and anterior part of genal dilation yellowish-red (Fig. 2I); anterior spiracle (Fig. 2I) and basicosta light-coloured, brownish Calliphora vicina
Facial ridge, lower facial margin and anterior part of genal dilation black (Fig. 2J, K); anterior spiracle and basicosta black (Fig. 2J, K) 6
6 Hairs on posterior part of genal dilation and postgena black (Fig. 2J) Calliphora loewi
Hairs on posterior part of genal dilation and postgena orange (Fig. 2K) Calliphora vomitoria
7 Parafacial plates narrow and bare, with white dusting (Figs 2L, 3F); height of genal dilation distinctly shorter than half of eye height (Fig. 2L); body lustrous green (Fig. 3F) Lucilia sericata
Parafacial plates broad and densely haired, with brown-yellowish dusting (Fig. 2M); height of genal dilation distinctly longer than half of eye height (Fig. 2M); body dark, abdomen with grey tessellated pattern 8
8 Node at junction of humeral crossvein and subcostal vein with a bundle of several light-coloured hairs (Fig. 2O) Pollenia pediculata
Node at junction of humeral crossvein and subcostal vein bare (Fig. 2N, P) 9
9 Mid tibia with one anterodorsal seta (Fig. 2Q) Pollenia angustigena
Mid tibia with two or three anterodorsal setae (Fig. 2R) Pollenia rudis

Redescription of the first instar larva of Calliphora loewi

Calliphora loewi Enderlein, 1903

Material examined

Madeira: Galhano 3 (15 first instar larvae). The first instar larvae (Fig. 4A) were obtained from 13 gravid females collected in Galhano (Prado e Castro et al. 2016).


The first instar larvae of C. loewi from Madeira possess the general habitus characteristic of most Calyptratae, being divided into a bilobed pseudocephalon (pc), three thoracic segments (t1–t3), seven abdominal segments (a1–a7), and an anal division (ad) that carries the posterior spiracles.


Body length: 1.4–5.1 mm. Pseudocephalon. Antennal complex with small antennal dome situated on basal ring, antennal dome slightly longer than height of basal ring; maxillary palpus located on anterior surface of pseudocephalic lobe and readily visible under a light microscope as a flat disc clearly distinguished from the surrounding cuticular surface; oral ridges present from lateral margins of functional mouth opening to ventral and lateral surfaces of pseudocephalon; functional mouth opening with two lateral tufts of numerous cirri. Cephaloskeleton. As in other necrophagous blowflies; consisting of unpaired labrum (lb), paired mouthhooks (mh), unpaired and H-shaped intermediate sclerite (is) and basal sclerite with parastomal bars (pb), vertical plates (vp) and ventral and dorsal cornua (vc, dc) (Figs 4B, C); each mouthhook an L-shaped bar, with tip equipped with 6 strong, pointed teeth directed ventrally, teeth arranged in one row with one tooth situated in front of row (well visible in ventral view); basal part of mouthhook also strongly sclerotized and equipped with a lateral arm (Figs 4B, C); labrum with readily differentiated sharp and curved apical part, ventral incision separating apical and basal parts of labrum indistinct (Fig. 4C); epistomal sclerite [“posterior expansion of labrum” in Szpila et al. (2014)] flat in lateral view (Fig. 4C); parastomal bars (pb) long and slender; intermediate sclerite (is) and crossbeam of intermediate sclerite broad; vertical plate (vp) as broad as width of ventral cornua (Fig. 4B); dorsal cornua slightly longer than ventral cornua (Fig. 4B); dorsal bridge present (Fig. 4B). Thoracic segments Anterior spinose band on first thoracic segment broad (Fig. 4A), with spines arranged in 5–7 rows dorsally and 12–14 rows ventrally; anterior spinose bands of second and third thoracic segments with homogenous conical, slightly flattened spines, tip of spines slightly curved. Abdominal segments. Anterior spinose bands complete on segments a1–a5, narrowly interrupted dorsally on segment a6; segment a7 with anterior spinose band on ventral and ventro-lateral surfaces and with several spines on lateral surface; posterior spinose band on segment a1 reduced to two small groups of spines situated ventro-laterally, on a2 posterior spines only on ventral and ventro-lateral surfaces, segment a3 with narrow posterior spinose band interrupted dorsally, segments a4–a7 with complete posterior spinose band. Anal division. Anal pads rounded and slightly protruding, anal tuft with several spines dorsally; circle of hair-like spines around spiracular field complete; anterior spinose band developed only on ventral and ventro-lateral surfaces.

Comparison with original description

The comparison of first instar larval specimens from Madeira with the original description (Erzinçlioğlu 1985) points to several discrepancies. Erzinçlioğlu (1985) described the anterior spinose band on a5 of Calliphora loewi as interrupted dorsally. Szpila et al. (2014) used this character for separation of C. loewi larvae from those of C. vicina and Cynomya mortuorum (Linnaeus, 1761), where the anterior spinose band on a5 is complete. However, the first instar larvae of C. loewi from Madeira also possess a complete anterior spinose band on a5. This character seems to be variable and cannot be treated as reliable. Serious discrepancies between the material from Madeira and the British larvae studied by Erzinçlioğlu (1985) were also found in the morphology of the labrum in the cephaloskeleton. Larvae from Madeira possess a massive labrum with broad basal part and well differentiated apical part. Additionally, the apical part of the labrum is noticeably curved downward. The cephaloskeleton of C. loewi larvae in the schematic illustration provided by Erzinçlioğlu (1985, fig. 28) possesses an elongated labrum (labelled as “median tooth”), without clear differentiation between an apical part and a basal part. Unfortunately, at this stage it is not possible to state that these differences between Madeira specimens and the original description result from interpopulation variation or inaccuracy of observation, as the larval material analyzed for the original description is unavailable (Szpila et al. 2013). Future studies on the variation of C. loewi larval morphology across the species distribution range will help to clarify this issue.


The effective conservation of insect diversity is, to some extent, hindered by the lack of knowledge of species taxonomy as well as by poor data on species distribution, abundance and sensitivity to habitat change (e.g., Cardoso et al. 2011, New 2012). Consequently, major efforts have been made during the last decade to overcome these obstacles, leading to the production of updated catalogues of species and the identification of conservation priorities for many countries and regions in the world (e.g., Martín et al. 2008, Verdú and Galante 2009, Van Swaay et al. 2010).

This recent survey of the calliphorid diversity on the islands and islets of the Madeira Archipelago allowed the collection of valuable information concerning species taxonomy, distribution and ecology, including the first report of blowfly species from Porto Santo and Desertas islands (Table 2). The number of Calliphoridaes. l. species known from the Madeira Archipelago is presently ten, but there is a considerable difference in calliphorid species richness between islands: Madeira (10 spp.), Porto Santo (5 spp.) and Desertas (3 spp.). The lower number of blowfly species recorded from Porto Santo and Desertas is not only due to geographic and ecological determinants (e.g. lower surface area, lower habitat diversity), but also a result of undersampling. Our blowfly survey was the first carried out in Porto Santo and Desertas. These islands have traditionally been disregarded by taxonomic experts, who have focused their sampling efforts exclusively on the main island when visiting the archipelago. Consequently, the present knowledge of Madeiran biodiversity is biased and efforts should be addressed to develop inventory programmes exploring the taxonomic biodiversity of also Porto Santo and Desertas.

This study presents evidence that the species found in the Madeira Archipelago use different habitats: C. vicina was the most widespread blowfly, occurring in a variety of habitat types (natural, semi-natural and forest plantations) and ranging from thermophilous coastal areas to native forest patches in valleys and mountainous areas. Three other species (L. sericata, P. rudis, S. lunata) were more common in coastal areas and inland forest plantations, while the two remaining Calliphora species (C. loewi and C. vomitoria) were restricted to a few forest locations at higher altitudes. A similar pattern of calliphorid species distribution was found in the Canaries, where C. vicina was considered an “extreme habitat generalist”, L. sericata seemed to be restricted to open habitats at low altitudes and C. splendens Macquart, 1839 and C. vomitoria were rare and confined to forest habitats (Hanski 1977).

The finding of Calliphora loewi in the Madeira Archipelago was surprising, since in Europe the species is known to occur mainly in forest ecosystems at much higher latitudes (Smith 1986, Byrd and Castner 2010) and is absent from the Azores and the Canary Islands (Arechavaleta et al. 2010, Borges et al. 2010). It is presumed that the Madeiran populations of C. loewi are relictual due to their isolation from the nearest mainland populations and considering the historical biogeography of Laurisilva, a laurel forest type once distributed throughout the western Mediterranean and which is now restricted to Macaronesia (Neves et al. 1996). Furthermore, the finding that the Madeiran populations of C. loewi are strictly associated with pristine Laurisilva patches at high altitudes also seems to support their relictual origin: the two Laurisilva patches where C. loewi was found, Montado dos Pessegueiros and Galhano, are well preserved, have minimal human disturbance, and show similar plant compositions (Neves et al. 1996). Like C. loewi, the Canarian endemic C. splendens is also restricted to native forest areas at higher altitudes (above 400 m) being absent from disturbed, low altitude areas where introduced calliphorids dominate (Hanski 1977, Báez 1988).

The number of calliphorid species so far recorded for the Madeira Archipelago remains low, but it is similar to numbers reported from the Azores (nine species) and Canary Islands (ten species) (Báez and Oromí 2010, Martínez-Sánchez 2010). The low species richness of these oceanic archipelagos is in part due to the difficulties faced in overcoming the ecological barrier posed by the ocean, even for insects with a good flight capacity such as blowflies. Moreover, according to Hanski (1977), the most likely explanation for the impoverished calliphorid faunas of Madeira and the Canaries is the intense interspecific competition due to low carrion density and diversity in these isolated ecosystems, which severely constrains species richness and abundance of the carrion breeding species.

During the last decades we have witnessed a significant increase in the number of blowfly introductions in oceanic archipelagos worldwide due to human-assisted dispersal (Hanski 1977, Báez et al. 1981, Báez 1990, Peck et al. 1998, Jensen et al. 2013). The dramatic increase in the frequency of transport of human commodities to islands (Pombo et al. 2010) is a serious challenge for local authorities that have to deal with the consequences of undesired introductions of pathogens, agricultural and forest pests, and disease vectors such as calliphorid species of veterinary or medical importance (Heath and Bishop 2006). The checklists of Calliphoridaes. l. of the Madeira, Azores and Canaries archipelagos show that, as a result of human activities, introduced species are well represented, with six species being common to the three archipelagos and widespread in each of them (Martínez-Sánchez and Rognes 2008, Báez and Oromí 2010, Martínez-Sánchez 2010). For example, the introduction of Chrysomya megacephala in Tenerife was followed by its expansion within this island and to other Canary Islands (Gran Canaria, Fuerteventura and Lanzarote), andit was later found also in Madeira (Báez et al. 1981, Báez 1990). The increase in blowfly species introductions has led to the increased homogenization of the faunas of the Macaronesian islands, but its consequences for native biodiversity remain unstudied (Hanski 1977). Thus, efforts should be made to implement monitoring programmes to evaluate the conservation status of native blowfly species in Macaronesia, particularly the Canarian endemic Calliphora splendens and the recently discovered C. loewi, and assess their vulnerability to introduced species.


The authors wish to thank Madeira Nature Park for logistic support and permission for the collection of specimens in Madeira archipelago. This study was financed by Portuguese National Funds, through FCT – Fundação para a Ciência e a Tecnologia, within the projects PTDC/BIABEC/99138/2008, UID/BIA/00329/2013 and also by FCT/MEC through national funds and the co-funding by the FEDER, within the PT2020 Partnership Agreement, and COMPETE 2020, within the project UID/BIA/04004/2013. We are also grateful to Carlos Aguiar and Fernando Pereira for help during fieldwork, to Inês Trindade for checking the English text and to the reviewers and journal editor for the careful revision and improvement of the manuscript. KS was supported by a project of the Polish National Science Centre (2012/07/B/NZ8/00158), while CR and MB were supported by FCT grants (SFRH/BPD/91357/2012 and SFRH/BPD/86215/2012, respectively).


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