Literature DB >> 21594022

The mycetophagidae (coleoptera) of the maritime provinces of Canada.

Christopher G Majka1.   

Abstract

The Mycetophagidae (hairy fungus beetles) of the Maritime Provinces of Canada are surveyed. Seven species in the genera Mycetophagus, Litargus, and Typhaea are found in the region. Six new provincial records are reported including Mycetophagus punctatus and Mycetophagus flexuosus, whichare newly recorded in the Maritime Provinces. The distribution of all species is mapped, colour habitus photographs of all species are figured, and an identification key to species is provided. The discussion notes that four of the species found in the region are apparently rare, possibly due to the history of forest management practices in the region; a situation similar to that of a significant proportion of other saproxylic beetles found in the Maritime Provinces.

Entities:  

Keywords:  Canada; Coleoptera; Litargus; Mycetophagidae; Mycetophaginae; Mycetophagus; Typhaea; aritime Provinces; biodiversity; fungus beetles; rare species

Year:  2010        PMID: 21594022      PMCID: PMC3088403          DOI: 10.3897/zookeys.64.553

Source DB:  PubMed          Journal:  Zookeys        ISSN: 1313-2970            Impact factor:   1.546


Introduction

The Mycetophagidae (hairy fungus beetles) are a family of relatively small, fungus-eating beetles. Only five genera and 26 species are known in North America, 15 of which have been recorded in Canada (Bousquet 1991; Young 2002). Parsons (1975) provided the most recent species-level taxonomic revision of the family. Only two species, Mycetophagus quadriguttatus Müller and Typhaea stercorea (Linnaeus), have previously PageBreakbeen recorded from the Maritime Provinces of Canada (New Brunswick, Nova Scotia, and Prince Edward Island) (Bousquet 1991). Species of Mycetophagus are commonly found in the decaying fruiting bodies of mushrooms and fleshy polypores, particularly those that have begun to dehydrate (Young 2002). Typhaea stercorea (Linnaeus), an adventive Palaearctic species, is associated with a large variety of moldy substances and is found both outdoors in natural environments, and indoors in association with a variety of stored products (Campbell et al. 1989). The biology of Litargus species is poorly known, however, there are records of a number of species associated with fungi, under bark, and in decaying logs (Schwarz 1876; Cline and Leschen 2005; Ulyshen and Hanula 2010). The present study reports the results of an investigation into the biodiversity of this family in the Maritime Provinces.

Methods and conventions

Acronyms (largely following Evenhuis 2010) of collections referred to in the text are: ACNS Agriculture and Agri-Food Canada, Kentville, Nova Scotia, Canada ACPE Agriculture and Agri-Food Canada, Charlottetown, Prince Edward Island, Canada CBU Cape Breton University, Sydney, Nova Scotia, Canada CGMC Christopher G. Majka Collection, Halifax, Nova Scotia, Canada CNC Canadian National Collection of Insects, Arachnids, and Nematodes, Ottawa, Ontario, Canada DHWC David H. Webster Collection, Kentville, Nova Scotia, Canada JCC Joyce Cook Collection (now at the New Brunswick Museum, Saint John, New Brunswick, Canada) JOC Jeffrey Ogden Collection, Truro, Nova Scotia, Canada KIC Kent Island Collection, Bowdoin College, Brunswick, Maine, USA NSAC Nova Scotia Agricultural College, Bible Hill, Nova Scotia, Canada NSMC Nova Scotia Museum, Halifax, Nova Scotia, Canada NSNR Nova Scotia Department of Natural Resources Insectary, Shubenacadie, Nova Scotia, Canada RMC Richard Migneault Collection, Edmundson, New Brunswick, Canada Abbreviations: FIT , flight intercept trap.

Identification

An identification key to species [adapted from Young (2002) and Parsons (1975)] found in the Maritime Provinces is provided below. For more detail, elytral patterns, illustrations of antennae, and general species descriptions refer to Parsons (1975).PageBreak

B. Key to species of Mycetophagus Hellwig*

* Note: elytral markings on Mycetophagus species are variable.

Results

In the course of this survey 175 specimens of Mycetophagidae were examined – 8 from New Brunswick, 149 from Nova Scotia, and 18 from Prince Edward Island. Included were specimens of seven species in three genera. Mycetophagus flexuosus Say is newly recorded in the Maritime Provinces from New Brunswick; Mycetophagus punctatus Say is newly recorded in the Maritime Provinces from Nova Scotia; Mycetophagus serrulatus Casey is newly recorded in New Brunswick; Mycetophagus pluripunctatus LeConte is newly recorded in New Brunswick; Mycetophagus quadriguttatus Müller is newly recorded in Nova Scotia; and Litargus tetraspilotus LeConte is newly recorded in Prince Edward Island – a total of five new provincial records, two of which are newly recorded PageBreakin the region. Four species are known from New Brunswick, six from Nova Scotia, and two from Prince Edward Island (Table 1).
Table 1.

Mycetophagidae fauna of the Maritime Provinces of Canada

NBNSPEDistribution in NE North America
Mycetophaginae
Mycetophagus Hellwig
subgenus Mycetophagus Hellwig
Mycetophagus flexuosus Say1MA, ME, NB, NH, NY, ON, QC, VT
Mycetophagus punctatus Say1CT, MA, ME, NH, NS, NY, ON, QC, VT
Mycetophagus serrulatus Casey11NB, NH, NS, NY, ON, QC, VT
subgenus Ilendus Casey
Mycetophagus pluripunctatus LeConte11MA, ME, NB, NH, NS, NY, ON, QC, VT
subgenus Parilendus Casey
Mycetophagus quadriguttatus Müller *11MA, ME, NB, NH, NS, NY, ON, QC, VT
Typhaea stercorea (Linnaeus) †111MA, ME, NB, NH, NS, NY, ON, PE, QC, RI, VT
Litargus tetraspilotus LeConte11MA, ME, NH, NS, NY, ON, PE, QC, RI, VT
totals462

Notes: * Holarctic species; † adventive Palaearctic species; NB New Brunswick; PE Prince Edward Island; NS Nova Scotia.

Distribution in northeastern North America: for the purposes of this treatment, northeastern North America is taken to consist of the following jurisdictions: CT Connecticut; LB Labrador; MA Massachusetts; ME Maine; NB New Brunswick; NF insular Newfoundland; NH New Hampshire; NS Nova Scotia; NY New York; ON Ontario; PE Prince Edward Island; PM Saint-Pierre et Miquelon; QC Québec; RI Rhode Island; and VT Vermont.

Mycetophagidae fauna of the Maritime Provinces of Canada Notes: * Holarctic species; † adventive Palaearctic species; NB New Brunswick; PE Prince Edward Island; NS Nova Scotia. Distribution in northeastern North America: for the purposes of this treatment, northeastern North America is taken to consist of the following jurisdictions: CT Connecticut; LB Labrador; MA Massachusetts; ME Maine; NB New Brunswick; NF insular Newfoundland; NH New Hampshire; NS Nova Scotia; NY New York; ON Ontario; PE Prince Edward Island; PM Saint-Pierre et Miquelon; QC Québec; RI Rhode Island; and VT Vermont. Distribution of Litargus tetraspilotus, Mycetophagus pluripunctatus, Mycetophagus punctatus, Mycetophagus quadriguttatus, Mycetophagus serrulatus, and Mycetophagus flexuosus in the Maritime Provinces of Canada. Distribution of Typhaea stercorea in the Maritime Provinces of Canada. Dorsal habitus photograph of Mycetophagus punctatus. Length: 4.6–6.3 mm. Photo credit: Guy A. Hanley.

Say, 1826

Distribution.

NEW BRUNSWICK: Madawaska County: Edmundston, 47°22.285'N; 68°14.663'W, 14 August 2010, R. Migneault, in polypore on dead aspen log (1, RMC); Edmundston, 47°22.285'N; 68°14.663'W, 22 August 2010, R. Migneault, in polypore on dead aspen log (1, RMC).

Notes.

Mycetophagus flexuosus is newly recorded in the Maritime Provinces from New Brunswick (Fig. 1). Cline and Leshen (2005) recorded it from oyster mushroom (Pleurotus ostreatus) Fries; Weiss (1920) recorded it from turkey-tail polypore (Tramates versicolor (Fr.) Pil.); and Minch (1952) and Pielou and Pielou (1968) recorded it from birch polypore (Piptoporus betulinus) (Fr.) Kar.
Figure 1.

Distribution of Litargus tetraspilotus, Mycetophagus pluripunctatus, Mycetophagus punctatus, Mycetophagus quadriguttatus, Mycetophagus serrulatus, and Mycetophagus flexuosus in the Maritime Provinces of Canada.

Dorsal habitus photograph of Mycetophagus flexuosus. Length: 3.0–4.6 mm. Photo credit: Tom Murray. Say, 1826 NOVA SCOTIA: Halifax Co.: Soldier Lake, 7 June 2005, J. Ogden, spruce beetle trap (1, NSNR); Hants Co.: Smileys Park, 6 July 2005, J. Ogden, spruce beetle trap (1, NSNR). Mycetophagus punctatus Say is newly recorded in the Maritime Provinces from Nova Scotia. Both specimens were collected in the central mainland of Nova Scotia (Fig. 1). The species is common under loose bark and on fungi (Downie and Arnett 1996); specifically it has been found on a dead black oak (Quercus velutina Lamb.) in Virginia (Robinson 1918); on rooting polypore (Polyporus radicatus Schw.) in Iowa (Weiss 1924); on oyster mushroom (Pleurotus ostreatus) (Cline and Leshen 2005); and on birch polypore (Piptoporus betulinus) growing on gray birch (Betula populifolia Marshall) in New York (Minch 1952). Casey, 1900 NEW BRUNSWICK: Charlotte Co.: Grand Manan archipelago, Kent Island, 23 July 2012, M. Steck, balsam fir forest, sweeping (1, KIC). NOVA SCOTIA: Annapolis Co.: Durland Lake, 21 June 2003, P. Dollin, hemlock/balsam fir/black spruce forest (120+ years), bracket fungi on white birch (1, NSMC). Mycetophagus serrulatus Casey is newly recorded in New Brunswick. The species was reported from Nova Scotia by Dollin et al. (2008) (Fig. 1). Both specimens were found in coniferous forests, one on a polypore fungus growing on a white birch (Betula papyrifera Marshall). Cline and Leshen (2005) recorded it from oyster mushroom (Pleurotus ostreatus).PageBreak Dorsal habitus photograph of Mycetophagus serrulatus. Length: 1.3–3.6 mm. Photo credit: Christopher G. Majka. LeConte, 1856 NEW BRUNSWICK: Madawaska County: Edmundston, 47°22.285'N; 68°14.663'W, 22 August 2010, R. Migneault, in polypore on dead aspen log (1, RMC). NOVA SCOTIA: Antigonish Co.: Cape George Point, 23 June1993, M. LeBlanc, funnel trap (1, NSMC); Colchester Co.: Kemptown, 1 June 1995, 28 June 1995, C. Corkum, young deciduous forest, FIT (2, NSMC); Upper Bass River, 18 May 1995, C. Corkum, old deciduous forest, FIT (1, NSMC); Upper Bass River, 3 June 1995, C. Corkum, old deciduous forest, FIT (1, NSMC); Cumberland Co.: East Leicester, 2 June 1995, C. Corkum, old deciduous forest, FIT (1, NSMC); East Leicester, 14 June 1995, C. Corkum, old deciduous forest, FIT (1, NSMC); East Leicester, 15 June 1995, C. Corkum, old deciduous forest, FIT (1, NSMC); Fox River, PageBreak17 May 1995, C. Corkum, young deciduous forest, FIT (1, NSMC); Fox River, 3 June 1995, C. Corkum, young deciduous forest, FIT (1, NSMC); Harrington River, 13 July 1995, C. Corkum, young deciduous forest, FIT (1, NSMC); Wentworth, 21 May-5 July 1965, B. Wright, sugar maple forest, window trap (1, NSMC); Halifax Co.: Halifax, 1 December 1986, B. Wright (1, NSMC); Soldier Lake, 30 July 2004, D. MacDonald, spruce beetle trap (1, NSNR); Lunenburg Co.: Card Lake, 2-15 June, 1997, D.J. Bishop, red spruce/hemlock forest (old growth), FIT (1, NSMC); Yarmouth Co.: Wellington, 23-29 August 1992, J. & F. Cook, mixed forest (1, JCC). Mycetophagus pluripunctatus LeConte is newly recorded in New Brunswick. The species was reported from Nova Scotia by Bishop et al. (2009) and appears to be distributed throughout much of the mainland of Nova Scotia (Fig. 1). In Nova Scotia, it was collected almost exclusively with flight intercept traps in deciduous forests. Pielou and Pielou (1968) reported it on birch polypore (Piptoporus betulinus), Cline and Leshen (2005) recorded it from oyster mushroom (Pleurotus ostreatus), and Leschen (1988) recorded it from Spongipellis unicolor (Schw.) growing on a fallen white oak (Quercus alba L.) in Arkansas. Schwartz (1876) said it was “abundant in fungus” in Michigan.PageBreak Dorsal habitus photograph of Mycetophagus pluripunctatus. Length 3.2–4.7 mm. Photo credit: Nicholas Gompel. Müller, 1821 NOVA SCOTIA: Annapolis Co.: Paradise, 11 June 2005, K. Webster, spruce beetle trap (1, NSNR); Colchester Co.: Balmoral Mills, 19 June 1974, B. Wright, grist mill (1, NSMC); Kings Co.: Kentville, 10 August 2005, D.H. Webster, compost heap, moldy corncobs (1, DHWC). Mycetophagus quadriguttatus Müller is newly recorded in Nova Scotia (Fig. 1). The species was reported from New Brunswick by Bousquet (1991), however, I have not been able to locate a voucher specimen for this record; it is not present in the CNC nor was it reported from New Brunswick by Campbell et al. (1989). Pending confirmation its status in New Brunswick should be regarded as provisional. In Nova Scotia, one specimen was collected in a grist mill and another in a compost heap. Campbell et al. (1989) reported the species in waste feed, sacked grain, grain elevators, warehouses, flour mills, old flour barrels, fungi at the base of old hay stacks, fungi on trees, a vegetable store, and a corn shop. Although Hatch (1962) thought it was probably an introduced species, other investigators (Parsons 1975; Bousquet 1991; Downie and Arnett 1996) have classified it as a native Holarctic species. Mycetophagus quadriguttatus is widely distributed in Europe having been reported throughout the continent except for Corsica, Crete, Cyprus, Estonia, Ireland, Norway, Portugal, and Sicily (Nikitsky 2010), and is also found across North Africa, in the eastern Palaearctic, Asia, and Australia (Nikitsky 2010). Dorsal habitus photograph of Mycetophagus quadriguttatus. Length 3.3–4.0 mm. Photo credit: Christopher G. Majka. (Linnaeus, 1758) Eighty-two specimens (NB=6, NS=66, PE=12) were examined. The earliest records from each province are: NEW BRUNSWICK: Northumberland Co.: Tabusintac, 13 June 1939, 26 July 1939, W.J. Brown (2, CNC). NOVA SCOTIA: Colchester Co.: Truro, 4 March 1919, collector not recorded (8, NSAC). PRINCE EDWARD ISLAND: Prince Co.: Central Bedeque, 29 July 1954, F.M. Cannon (1, ACPE). Typhaea stercorea (Linnaeus) was reported from New Brunswick, Nova Scotia, and Prince Edward Island by Bousquet (1991). The species is widely distributed throughout the Maritime Provinces, including Cape Breton Island (Fig. 2). A majority of specimens were collected outdoors in native habitats. It is an adventive Palaearctic beetle found both outdoors and in association with various stored products. Typhaea stercorea has been found in corn fields (on decaying kernels of exposed ears), warehouses, stores, flour mills, mangers, railway boxcars, dwellings, and granaries in stored grain and seeds, tobacco, peanuts, cacao, corn, millet, wheat, apricots, and moldy grape skins, as well as in nests of swans and moorhens (Campbell et al. 1989). In Nova Scotia it was reported in large numbers in dairy barns (Campbell et al. 1989).
Figure 2.

Distribution of Typhaea stercorea in the Maritime Provinces of Canada.

The dates of earliest detection are given above: New Brunswick (1939), Nova Scotia (1919), and Prince Edward Island (1954). Typhaea stercorea is widespread in Europe, having been recorded in every country and region in the continent (Nikitsky 2010)PageBreak, and is also virtually cosmopolitan globally, being found in every region of the world except (doubtfully) South and Central America (Nikitsky 2010). Dorsal habitus photograph of Typhaea stercorea. Length: 2.2–3.2 mm. Photo credit: Tim Moyer. LeConte, 1856 NOVA SCOTIA: Cape Breton Co.: East Bay, 9 September 2003, C.W. D’Orsay (1, CBU); Colchester Co.: Bible Hill, 8 July 2004, K.R. Aikens, pasture, sweep (1, CBU); Bible Hill, 14 June 2005, S.M. Townsend, sweep (3, CBU); Debert, 9 June 1994, J. Ogden (1, NSNR); Masstown, 7 September 2002, C.G. Majka, marshy swamp (1, CGMC); Shubenacadie, 26 August 1997, J. Ogden (1, NSNR); Digby Co.: Brier Island, Pond Cove, 9 August 2004, J. Ogden & K. Goodwin, knapweed, sweep (3, JOC); Brier Island, Pond Cove, 10 August 2004, J. Ogden & K. Goodwin, sweep (1, JOC); Brier Island, Westport, 9 August 2004, J. Ogden & K. Goodwin, grassland, sweep (2, JOC); Halifax Co.: Big Indian Lake, 16 July 2003, P. Dollin, Picea rubens forest (80-120 years), in rotting mushroom (1, NSMC); Point Pleasant Park, 15 August 2000, 7 September 2000, C.G. Majka, mixed forest (2, CGMC); Point Pleasant Park, 9 September 2000, 2 June 2002, 23 July 2002, C.G. Majka, coniferous forest (3,PageBreak CGMC); Point Pleasant Park, 12 May 2001, 10 June 2001, 25 May 2002, C.G. Majka, coniferous forest, on Picea rubens (6, CGMC); Point Pleasant Park, 19 May 2001, 29 May 2001, C.G. Majka, coniferous forest, on Pinus strobus (4, CGMC); 29 July 2001, 18 August 2001, Point Pleasant Park, C.G. Majka, mixed forest (2, CGMC); PageBreakPoint Pleasant Park, 9 May 2002, C.G. Majka, coniferous forest, on Abies balsamea (1, CGMC); Point Pleasant Park, 9 June 2002, C.G. Majka, mixed forest, on Aralia hispida (1, CGMC); Point Pleasant Park, 7 July 2002, C.G. Majka, seashore (1, CGMC); Point Pleasant Park, 14 September 2002, C.G. Majka, marsh, on herbaceous vegetation (1, CGMC); Point Pleasant Park, 30 June 2004, C.G. Majka, coniferous forest, on Pinus sylvestris (2, CGMC); West Dover, 7 September 2003, C.G. Majka, coastal barrens, heaths (1, CGMC); Kings Co.: Aldershot, 5 August 1949, 2 August 1949, 10 August 1949, 20 August 1949, 16 May 1950, H.T. Stultz (5, ACNS); Greenwich, 29 May 1958, H.T. Stultz (1, ACNS); Kingston, 30 June 2002, C.G. Majka, sandy pine barren (1, CGMC); Queens Co.: Eight Mile Lake, 11 August 2003, P. Dollin, PageBreakPicea rubens forest (40-80 years), in vegetation, sweep (1, NSMC); Little Ponhook Lake, 1 August 1993, B. Wright, in oak apple galls (3, NSMC); Ponhook Lake nr. Greenfield, 13 July 1993, J. Cook, ultraviolet light trap (2, JCC); Shelburne Co.: Clyde River Road, 16 July 1992, S. & J. Peck, forest, car net (1, JCC); Forbes Point, 9 July 2007, R. Gorham, grass/alders (4, CGMC); Victoria Co.: Cape Breton Highlands: Kelly Rd, 24 June 2005, J. Ogden, malaise trap (1, NSNR); Yarmouth Co.: Moses Lake, 8 km N of Argyle, 17-22 July 1993, J. & T. Cook, mixed forest, FIT (1, JCC). PRINCE EDWARD ISLAND: Queens Co.: Cavendish, 19 July 2001, C.G. Majka, coastal vegetation (1, CGMC); Princeton-Wharburton Road, 19 August 2002, C.G. Majka, old field (3, CGMC); St. Patricks, 18 August 2002, C.G. Majka, old field (1, CGMC); St. Patricks, 29 June 2003, C.G. Majka, mixed forest (1, CGMC). Litargus tetraspilotus LeConte is newly recorded from Prince Edward Island. Klimaszewski and Majka (2007) first reported this species in Nova Scotia. There are PageBreakmany records from the southern mainland of Nova Scotia, Cape Breton Island, and Prince Edward Island (Fig. 1). Records from New Brunswick and the northern mainland of Nova Scotia are lacking, but it is probable that it is found throughout the region. In the Maritime Provinces Litargus tetraspilotus has been collected in many habitats including coniferous, deciduous, and mixed forests, seashores, coastal barrens, grasslands, marshy areas, a sandy pine barren, and an old field ecosystem. Specimens have been collected on the foliage of white pine (Pinus strobus L.), jack pine (Pinus sylvestris L.), red spruce (Picea rubens Sarg.), balsam fir (Abies balsamea (L.) Mill.), on deciduous, and herbaceous vegetation, on bristly sarsaparilla (Aralia hispida Vent.), and in a rotting mushroom. Klimaszewski and Majka (2007) reported Litargus tetraspilotus as an inquline inhabitant of oak apple galls on red oak (Quercus rubra L.) induced by Andricus (Callirhytis) sp. (Cynipidae) wasps. Rauf et al. (1985) found it on jack pine, Tucker (1919) found it on American mistletoe (Phoradendron flavescens (Pursh) Nutt., and Ulyschen and Hanula (2010) reared it from decomposing loblolly pine (Pinus taeda L.) logs in South Carolina. Dorsal habitus photograph of Litargus tetraspilotus. Length: 1.8–2.0 mm. Photo credit: Christopher G. Majka.

Discussion

Typhaea stercorea and Litargus tetraspilotus are abundant and widely distributed in the Maritime Provinces. Mycetophagus pluripunctatus appears to be uncommon but widely distributed on the mainland of Nova Scotia. The other four species of mycetophagids – Mycetophagus punctatus, Mycetophagus flexuosus, Mycetophagus serrulatus, and Mycetophagus quadriguttatus – are all represented by a handful of specimens or less. They would all appear to qualify asPageBreak “apparently rare” saproxylic beetles as defined by Majka (2007b) (i.e., representing < 0.005% of specimens examined from the region). In investigating 283 species of saproxylic beetles from 18 families, Majka (2007b) found that 33% of these fell into this category of apparently rare species. Similarly in examining the Endomychidae and Erotylidae of the Maritime Provinces, two other families of beetles closely associated with fungi, Majka (2007b) found that 40% of the 15 species found in the region are apparently rare. Majka (2007a, b) suggested that this large proportion might be ascribable to the history of forest management practices in the region. These apparently rare species of Mycetophagus, three of which are closely associated with saproxylic fungi, may belong to this same suite of insects for similar reasons. In general, mycetophagids have received rather little attention by researchers in North America, and the bionomics of many species have not been carefully investigated. Certainly this is true in the Maritime Provinces and additional fieldwork in the region is required to ascertain more about their distribution, abundance, bionomics, and ecological role in the habitats that they inhabit.
1Epipleural fold of elytra concave; Litargus ErichsonLitargus tetraspilotus (Fig. 9)
Epipleural fold of elytra horizontal and flat2
2Eyes transverse, sinuate anteriorlyMycetophagus Hellwig
Eyes more rounded, not sinuate anteriorly; Typhaea CurtisTyphaea stercorea (Fig. 8)
1Antennae gradually widening towards apex with the last 3, 4, or 5 antennomeres before the apical one more or less serrate and slightly asymmetrical; subgenus Mycetophagus (s. str.)2
Antennae with a 4- or 5-segmented club, strongly to feebly differentiated from preceding antennomeres; antennomeres bilaterally symmetrical4
2(1)Apical antennomere longer than 2 preceding combined; length 4.6–6.3 mmMycetophagus punctatus (Fig. 3)
Apical antennomere shorter than or as long as 2 preceding combined; length 3.6 mm or less3
3(2)Pale elytral markings reaching or crossing suture from basal 1/5 to 1/2 of elytraMycetophagus flexuosus (Fig. 4)
Pale elytral markings not attaining sutureMycetophagus serrulatus (Fig. 5)
4(1)Antennae with a 5-segmented club; subgenus Ilendus Casey; length 3.2–4.7 mmMycetophagus pluripunctatus (Fig. 6)
Antennae with a 4-segmented club; subgenus Parilendus Casey; length 3.3–4.0 mmMycetophagus quadriguttatus (Fig. 7)
  1 in total

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  1 in total
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