Atkinson & Peck:Bark and Ambrosia Beetles of South Florida313 ANNOTATED CHECKLIST OF THE BARK AND AMBROSIA BEETLES (COLEOPTERA: PLATYPODIDAE AND SCOLYTIDAE) OF TROPICAL SOUTHERN FLORIDA THOMAS H. ATKINSON1,3 AND STEWART B. PECK2 1 Entomology and Nematology Department, University of Florida Gainesville, FL USA 32611 2 Department of Biology, Carleton University Ottawa, Ontario, Canada K1S 5B6 ABSTRACT The fauna of Scolytidae and Platypodidae is reviewed for tropical southern Florida (Collier, Broward, Dade, and Monroe Counties). The family Platypodidae is repre- sented by 3 species, all in the genus Platypus. The family Scolytidae includes 83 spe- cies in 37 genera in the region. This total includes 20 species considered immigrants to the area. Three species previously reported from the region, Cryptocarenus spatu- latus Wood, Xyleborus xylographus (Say), and Araptus politus (Blandford), probably do not occur there. Feeding habits, mating systems, hosts, and distributions are sum- marized for all species included. Key Words: Taxonomy, distributions, ecology, hosts, introduced species RESUMEN Se revisa la fauna de las familias Scolytidae y Platypodidae de la region tropical del sur de Florida (condados de Collier, Broward, Dade y Monroe). La familia Platypo- didae está representada por 3 especies, todas en el genero Platypus. La familia Scoly- tidae esta representada por 83 especies en 37 generos. Este total incluye 20 especies las cuales se consideran inmigrantes al area. Tres especies previamente reportadas de la region, Cryptopcarenus spatulatus Wood, Xyleborus xylographus (Say) y Araptus politus (Blandford), probablemente no existen allí. Habitos alimenticios, sistemas de apareamiento y distribuciones se resumen para todas las especies incluidas. Bark and ambrosia beetles (Coleoptera: Scolytidae and Platypodidae) constitute a diverse group of beetles that bore in a variety of woody tissues and are well repre- sented in most temperate and tropical forests. Best known are species of Dendrocto- nus, Ips, and Scolytus that are primary pests of conifers in high-latitude forests, although most of these are atypical of the group as a whole. All species breed in live, stressed, or newly-killed host material. Adults excavate a system of galleries within which eggs are laid and immature development occurs. The greater part of the life cy- cle takes place within host tissues, except for dispersal between hosts. A fascinating range of patterns of host plant utilization (tissues consumed, relationships with fun- gal symbionts, and host specificity) and mating behaviors exists within this basic life 3 Current address: Dow Elanco, 13355 Noel Rd., Suite 1045 Dallas, TX 75240-6604 This article is from Florida Entomologist Online, Vol. 77, No. 3 (1994). FEO is available from the Florida Center for Library Automation gopher (sally.fcla.ufl.edu) and is identical to Florida Entomologist (An International Journal for the Americas). FEO is prepared by E. O. Painter Printing Co., P.O. Box 877, DeLeon Springs, FL. 32130. 314 Florida Entomologist 77(3) September, 1994 history paradigm. Most species leave a persistent physical record of their life history and activities in the woody tissues of their hosts that can be interpreted by a student of the group. As a consequence, one can easily tabulate several important biological parameters for a large proportion of the species in an area, including those that have not been studied in detail. The taxonomy of the group is well-known (Wood 1982, Wood & Bright 1993) for the United States as a whole, but there is little information available from southern Flor- ida, largely due to its remoteness. Some collecting was done near the turn of the cen- tury by E. A. Schwarz and A.D. Hopkins. S. L. Wood collected there in the 1950’s. Besides ourselves, more recent collectors of note include D.E. Bright, M. A. Deyrup, R. H. Turnbow, E. G. Riley and R. A. Anderson. Bright’s (1985) checklist of the Caribbean highlighted the paucity of available information from that region. No student of the group has ever collected extensively on any of the Greater Antilles. The physical, historical, and floristic geography of southern Florida has been re- viewed by Peck (1989). The area is geologically recent and has a subtropical climate. It has had direct and continuous land contact with temperate areas, but has never had any land connections with any tropical areas that would serve as source areas for its current biota. Most of the Neotropical flora of southern Florida has apparently dis- persed there by wind, water, or birds from the Bahamas and Greater Antilles (Tom- linson 1980). This checklist represents a convergence of 2 separate projects, a faunal study of the entire group for the southeastern United States by the first author and a biogeo- graphic study of the insect fauna of tropical southern Florida by the second author (Peck 1989). The purpose of this paper is to document the scolytid and platypodid fauna of tropical southern Florida for a subsequent ecological and biogeographical analysis. METHODS The second author has collected extensively in the region and accumulated large numbers of specimens of bark and ambrosia beetles as part of a large scale project on the biogeography of the insect fauna of tropical southern Florida (Peck 1989). Sam- pling was done with flight intercept traps that were left in place over extended periods for 5 years in areas of natural vegetation on the Keys and mainland (sites described in Peck 1989). Over 2,500 specimens of Scolytidae and Platypodidae were collected. Most specimens and representatives of all species collected by the second author were deposited in the Canadian National Collection, the Canadian Museum of Nature, and the S.B. Peck collection (all in Ottawa, Ontario). Some representative specimens were deposited in the Florida State Collection of Arthropods, Gainesville, Florida. The first author has been involved in a faunal study of the Scolytidae and Platy- podidae of the southeastern United States for several years. A total of 1,250 speci- mens (other than those collected by the second author) were examined from southern Florida, as well as an additional 3,000 specimens of the same species from other parts of the United States, Canada, the Caribbean, and Latin America. Scolytidae and Platypodidae were examined by the first author from the following collections (abbre- viations used are from Arnett & Samuelson (1986)): Archbold Biological Station, Lake Placid, Florida (ABSC); Canadian Museum of Nature Collection, Ottawa, Ontario (CMNC); E. G. Riley private collection, College Station, Texas (EGRC), Department of Forestry and Environmental Science, State University of New York, Syracuse, New York (DFEC), Florida State Collection of Arthropods, Gainesville, Florida (FSCA), Henry and Ann Howden collection, Ottawa, Ontario, (CHAH), Museum of Compara- Atkinson & Peck:Bark and Ambrosia Beetles of South Florida315 tive Zoology, Cambridge, Massachusetts (MCZC), R.H. Turnbow private collection, Ft. Rucker, Alabama (RHTC), S.L. Wood private collection, Provo, Utah (SLWC); T.H. At- kinson private collection, Riverside, California (THAC), University of Georgia at Ath- ens Georgia (UGCA), and U. S.. National Museum of Natural History, Washington, D.C. (USNM). In addition to data taken from museum specimens, the relevant literature on the Scolytidae and Platypodidae was critically reviewed by the first author for specific dis- tribution records in southern Florida, as well as host records and distribution records for the entire ranges of the species included. ADVENTIVE SPECIES Exactly what constitutes an adventive species and unambiguous criteria by which one might judge particular cases are matters of considerable debate (Frank & McCoy 1990, 1992, Whitehead & Wheeler 1990). Whitehead & Wheeler (1990) argued that as a general criterion one should consider species to be adventive if newly reported (or detected) in the United States. They recognized that southern Florida had not been well-collected historically and that new records for Antillean species did not necessar- ily imply that these species were non-native. Frank & McCoy followed this criterion literally in their recent list of new immigrants into Florida (1992) (i.e., new record means new arrival), although they also acknowledged the lack of complete historical information on the insect fauna of tropical southern Florida. Part of the problem is semantic (Frank & McCoy 1990). Many terms have been used inconsistently in the literature to indicate natural occurrence, occurrence through human intervention (accidental or not), and various types of restricted dis- tributions. Frank & McCoy (1990) restricted the term “introduced” to mean species deliberately brought into a new area. They used the term “immigrant” to refer to spe- cies that have arrived and become established without intentional human activities. Their definition is deficient in an important sense in that it does not distinguish be- tween the accidental establishment of species through human agency and the move- ment and establishment of species into historically new areas by natural means of dispersal, passive or active. To further complicate matters, there is no reason to sup- pose that the process of accumulation of the biota of southern Florida through “natu- ral means” has come to a stop. This distinction is not trivial for southern Florida. Given that southern peninsular Florida (including the Keys) has only become emergent in Wisconsonian and recent geological periods (Tomlinson 1980, Peck 1989) and has never had any land connec- tions to the Greater Antilles, virtually any species with an Antillean or Neotropical distribution currently found in Florida is immigrant by this definition. Nonetheless, most of these occur there naturally and should be considered native. These would not be considered “indigenous” as defined by Frank & McCoy (1990). The same would also be true of any Neartic or Holarctic species occurring naturally in the Florida penin- sula as well, although it has been available for colonization by terrestrial organisms since the mid-late Tertiary and Pleistocene. Some Nearctic and Holartic species have only recently been reported from the peninsula (e.g., Deyrup & Atkinson 1987, Atkin- son et al. 1991), yet no one would think to call these “immigrants”. To avoid confusion, we consistently use the terms “adventive” and “immigrant” to refer to species that do not naturally occur in southern Florida. None of the adventive species known from the area have been deliberately introduced in the sense of Frank & McCoy (1990). We use the term “native” to refer to any species which we believe oc- curs naturally in southern Florida whether “indigenous” (sensu Frank & McCoy 1990) 316 Florida Entomologist 77(3) September, 1994 or “immigrant” in the sense of having dispersed to Florida as part of a natural dis- persal process not mediated by deliberate or accidental human activity. There is no evidence that any Neotropical species of Scolytidae or Platypodidae has been introduced, intentionally or accidentally, into Florida in modern times. Such an event might have occurred more than 150 years ago and passed unnoticed (i.e., be- fore the publication dates of works treating the area). Neotropical adventives may be recognized by any combination of the following criteria: (1) the main part of the spe- cies’ historical distribution does not include the Caribbean; (2) strict association with a non-native host plant; (3) clear association with disturbed habitats and / or absence from natural communities; and (4) documented invasion and / or subsequent spread. Several species that originated in the Old World tropics have become established in this century in the United States and have shown an historical pattern of distribution consistent with spread from a single point, even when the original invasion and colo- nization passed unremarked. Examples include Xylosandrus germanus (Blandford) (Bright 1968, Chapin & Oliver 1986, Staines 1984, Weber & MacPherson 1982), X. compactus (Eichhoff) (Dixon & Woodruff 1982, Ngoan et al. 1976), X. crassiusculus (Motschulsky) (Anderson 1974, Chapin & Oliver 1986, Deyrup & Atkinson 1987, Ko- vach & Gorsuch 1985, Atkinson et al. 1991), and Xyleborus atratus (Eichhoff) (Atkin- son et al. 1990, 1991). In all of these cases, either the historical pattern of spread can be documented from collection records (Xylosandrus spp.) or else a “novel species” known from another continent is detected over a wide area almost simultaneously (Xyleborus atratus). We maintain that any species that is currently found in southern Florida and in the Bahamas and / or the Greater Antilles should be considered native (although al- most certainly immigrant) unless there is evidence to the contrary. There are 24 spe- cies in our area that have this distribution pattern. By the same token, any Neotropical species whose modern range includes the Gulf Coast of the southeastern United States and Texas and is continuously distributed into Mexico and Central America should also be considered native (12 species, some of which are also widely distributed in the eastern United States and / or the Caribbean). By our restricted criteria, we consider 20 species of Scolytidae found in southern Florida to be immigrants, mostly from Africa or Asia. Frank & McCoy (1992), by a me- chanical application of the rule of “recent record means new immigrant ”, listed 3 other species as immigrants (Pseudothysanoes securigerus (Blackman), Theoborus solitariceps Schedl, and Trischidias exigua Wood) that we consider natives. Wood (1977, 1982) listed an additional 14 Neotropical species as immigrants with distribu- tions that fit one of the 2 patterns described above. Cryptocarenus heveae (Hagedorn), C. seriatus (Eggers), Xyleborus volvulus (F.), Xylosandrus zimmermanni (Hopkins), and Corthylus spinifer Schwarz have ranges that include the Antilles and South Flor- ida. Hypothenemus eruditus Westwood, H. seriatus (Eichhoff), Xyleborus affinis Eich- hoff, and X. ferrugineus (F.) are continuously distributed along the Gulf Coast into Mexico and Central America. In contrast, other Neotropical species with similar dis- tributions were treated as native. Dendrosinus bourreriae Schwarz, Chaetophloeus insularis (Blackman), Pycnarthrum hispidum (Ferrari), Scolytodes schwarzi (Hop- kins), and Ambrosiodmus lecontei Hopkins are found in the Antilles and South Flor- ida. Cnesinus strigicollis LeConte is continuously distributed along the Gulf Coast through Texas and into Mexico. In neither publication were the criteria explained by which this conclusion was reached. All of these putative “Neotropical exotics” are host generalists (polyphagous) and many reproduce by inbred polygyny. As noted by Wood (1977), this is true of many species recently established in North America, but it does not constitute a priori evidence that a particular species is non-native. Atkinson & Peck:Bark and Ambrosia Beetles of South Florida317 EXCLUDED SPECIES Three species previously reported from southern Florida, Cryptocarenus spatula- tus Wood, Xyleborus xylographus (Say), and Araptus politus (Blandford), probably do not occur there. Cryptocarenus spatulatus and Araptus politus were intercepted com- ing into Miami from Latin America (Wood 1982), but no specimens of either species have ever been collected from local populations. Araptus politus is a host specialist and breeds in seeds of Mucuna spp. (Leguminosae) which are not known to occur in Florida. Xyleborus xylographus was cited by Bright (1968) and Wood (1982) from Key West (presumably from the same specimen(s) in the Canadian National Collection). This species breeds in oaks and no other authentic specimens have ever been found in peninsular Florida despite extensive collecting by the first author in northern Florida. The only species of oak that occurs in southern Florida is Quercus virginiana L., found only in Dade County near Miami and on Key Largo (Long & Lakela 1971, Tomlinson 1980). The “Key West” material most likely represents an error in labelling or an in- terception. ORGANIZATION OF CHECKLIST The sequence of subfamilies and tribes follows Wood & Bright (1992). Species are arranged alphabetically within genera, and genera alphabetically within tribes. Ab- breviations for feeding habits (host tissues consumed), degree of host specificity, and mating system are listed in parenthesis for each species. Host information and overall distribution patterns are also included. Abbreviations are used to indicate: (1) Feed- ing Habits: ph, phloem feeding (= true bark beetles) (phloeophagy); xm, feeding on ec- tosymbiotic fungi (=ambrosia beetles) (xylomycetophagy); xy, direct feeding on sapwood (xylophagy); my, pith of twigs and branches (myelophagy); sp, seeds (sper- matophagy); myc, non-ambrosial fungi (mycophagy); (2) Host Specificity: mo, re- stricted to hosts of a single species or genus (monophagy); ol, restricted to hosts of a single family (or to a very limited number of hosts) (oligophagy); po, not host specific (polyphagy); (3) Mating Systems: mg, monogyny; hpg, harem polygyny (including big- amy); ipg, inbred polygyny (mating terminology follows Kirkendall 1983). A question mark (?) after any abbreviation indicates an absence of data. Collection localities are listed by county for the four southern Florida counties in the following sequence: Collier, Broward, Dade and Monroe. Each locality is followed by a parenthetical reference to the collection(s) in which specimens are deposited (ab- breviations listed in Methods) or a literature reference. Complete collection data are not included because of space limitations, but are available from the authors. Speci- mens were examined by the first author for all localities for which a collection is des- ignated. ANNOTATED CHECKLIST OF THE PLATYPODIDAE AND SCOLYTIDAE OF SOUTHERN FLORIDA Family Platypodidae Platypus compositus Say. (xm, po, mg). Found in large trunks and stumps of most hardwoods within its range, also bald cypress, Taxodium distichum (L.) Rich.. Widely distributed in the Neotropics, apparently adventive to Africa. Southeastern U.S. from 318 Florida Entomologist 77(3) September, 1994 Texas eastward. Collier: Royal Palm Hammock St. Park (USNM); Dade: Paradise Key (USNM); Monroe: Big Pine Key (CMNC); Sugarloaf Key (CMNC). Platypus flavicornis (F.). (xm, mo, mg). Found in trunks and stumps of all species of Pinus (Pinaceae) within its range. Southeastern U.S., from eastern Texas. Dade: Homestead (FSCA); Opa-locka (FSCA). Platypus parallelus (F.). (xm, po, mg). Breeds in large diameter host material of virtually any woody plant within its range. It has also been reported from palm trunks. Widely distributed in the Neotropics. In the U.S. found only in southern Flor- ida and southern Texas. Broward: Fort Lauderdale(FSCA); Collier: Collier Semi- nole St. Park (FSCA); Marco Island (FSCA); 8 mi SE Naples, (USNM); Dade: Everglades Natl. Park, Royal Palm Hammock (CMNC); Homestead (FSCA); 6 mi N Homestead, (USNM); Miami (FSCA); Miami Beach (FSCA); Perrine (FSCA); West Mi- ami (FSCA); Monroe: Big Pine Key (EGRC); Big Torch Key (CMNC); Cape Sable (FSCA); John Pennekamp St. Park (ABSC); Key Largo (USNM, RHTC); Key West (FSCA); No Name Key (EGRC); Plantation Key (FSCA); Stock Island (FSCA, USNM). Family Scolytidae Subfamily Hylesininae Tribe Hylastini Hylastes salebrosus Eichhoff. (ph, mo, mg). Found in roots, stumps, or branches in contact with the soil of most Pines within its range. Southeastern U.S., from Texas eastward. Dade: “Biscayne Bay” (Wood 1982). Hylastes tenuis Eichhoff. (ph, mo, mg). Found in roots, stumps or branches in con- tact with the soil of most Pines within its range. Southeastern U.S., from Texas east- ward, also known from Hispaniola. Southwestern U.S. to central Mexico in montane regions. Monroe: Key West (USNM). Tribe Tomicini Dendroctonus terebrans (Olivier). (ph, mo, mg). Found in stumps, large roots, and the lower portion of large pines. Southeastern U.S. from eastern Texas to Atlantic sea- board. Broward: Fort Lauderdale (Wood 1982); Dade: Kendall (FSCA); Opa-locka (FSCA). Tribe Bothrosternini Cnesinus strigicollis LeConte. (my, po, mg). Very polyphagous, breeding in twigs of a wide variety of plant species. Southeastern U.S. from eastern Texas to lower Atlan- tic seaboard. In Mexico along Gulf Coast to Yucatan Peninsula. Dade: Elliot Key (ABSC); Miami (FSCA); Deering Estate (CMNC); Matheson Hammock (CMNC); Monroe: Key Largo (UGCA, CMNC, Wood 1982); N. Key Largo (ABSC); Plantation Key (FSCA, ABSC). Pagiocerus frontalis (F.) (sp, mo, mg). Breeds in fleshy seeds of several genera of Lauraceae, notably Persea. Widely distributed in lowland Neotropical areas. In U.S. found along lower Gulf Coast and lower Atlantic seaboard to North Carolina. It has not been collected in the Keys but native and exotic species of Persea (avocado) do oc- cur there (Long & Lakela 1971, Tomlinson 1980). Collier: Monroe Sta. (ABSC); Dade: Chekika St. Rec. Area, 50 km SW Miami (CMNC); Miami, Deering Estate (CMNC). Atkinson & Peck:Bark and Ambrosia Beetles of South Florida319 Tribe Phloeotribini Phloeotribus texanus Schaeffer. (ph, mo, mg). Breeds in branches of Celtis spp (Ul- maceae). Southeastern U.S. from Texas eastward; lowland regions of Mexico. Collier: Collier Seminole St. Park (ABSC); Dade: “Biscayne” (Wood 1982). Tribe Phloeosinini Dendrosinus bourreriae Schwarz (xy, po, mg). Reported from branches of several unrelated families of tropical hardwoods. Known only from southern Florida and Greater Antilles. This species has not been collected from the mainland although some of its reported hosts are found in tropical hardwood hammocks there (Long & Lakela 1971, Tomlinson 1980). Monroe: Key Largo (FSCA); Stock Island (FSCA). Phloeosinus taxodii taxodii Blackman. (ph, mo, mg). Breeds in branches of bald cy- press, Taxodium distichum (Taxodiaceae). Southeastern U.S. from eastern Texas. A different subspecies, P. taxodii taxodiicolens Wood, is found throughout Mexico in Montezuma cypress, Taxodium mucronatum Ten. Collier: Naples, 8 mi SE (USNM). Tribe Hypoborini Chaetophloeus insularis (Blackman). (ph, mo, mg). Breeds in branches of native and exotic Manilkara spp. (Sapotacae). Southern Florida and Greater Antilles. This species has not been collected from the mainland although its native host, Manilkara bahamensis (Baker) Lam. & Meeuse, is found in there and an exotic host, M. zapota (L.) Royen is grown widely in southern Florida (Long & Lakela 1971, Tomlinson 1980). Monroe: Big Pine Key, Cactus Hammock (CMNC); Big Torch Key (CMNC); Cudjoe Key (CMNC); Fat Deer Key (CMNC); Key West (Wood 1982); Lower Mate- cumbe Key (Wood 1982); No Name Key (CMNC); Sugarloaf Key (CMNC, Wood 1982). Subfamily Scolytinae Tribe Scolytini Cnemonyx ficus (Schwarz). (ph, mo?, mg). The type series was reportedly collected from Ficus (Moraceae), probably due to an error in identification. The true host is the manchineel tree, Hippomane mancinella L. (Euphorbiaceae) (Atkinson 1993). This species breeds in larger branches (> 3 cm diameter) and trunks of its host tree. The host occurs throughout the Keys and on the mainland near Cape Sable, although it is not abundant (Long & Lakela 1971, Tomlinson 1980). Southern Florida, Bahamas, Virgin Islands. Monroe: Big Pine Key (CMNC, THAC); Key West (MCZC, Wood 1982). Cnemonyx vagabundus Wood. (ph, mo?, mg). The type series was reportedly col- lected from Piscidia piscipula (Leguminosae), probably due to an error in identifica- tion. The true host is the manchineel tree, Hippomane mancinella L. (Euphorbiaceae) (Atkinson 1993). This species breeds in smaller branches (< 3 cm diameter) and trunks of its host tree. Southern Florida, Puerto Rico and Panama. Monroe: Big Pine Key (CMNC, THAC); Key West (Wood 1982). Tribe Ctenophorini Pycnarthrum hispidum (Ferrari). (ph, mo, mg). Branches of native and exotic figs (Ficus spp.) (Moraceae). Widely distributed in lowland Neotropical areas. In the U.S. 320 Florida Entomologist 77(3) September, 1994 known only from southern Florida and southern Texas. Broward: 1 mi N Andytown, (RHTC); Dade: “Biscayne” (MCZC); Coconut Grove (MCZC); Homestead (SLWC); Mi- ami (FSCA); Monroe: Key Largo (UGCA); Plantation Key (FSCA); Stock Isl. (FSCA); Sugarloaf Key (SLWC). Scolytodes schwarzi (Hopkins). (ph, mo, hpg). Breeds in shaded-out branches of living Ficus spp. (Moraceae). Based on personal experience (THA), this species does not breed in cut branches. Southern Florida, Greater Antilles, lowland regions of Mex- ico. Broward: 1 mi N Andytown (RHTC); Collier: Corkscrew Swamp Sanctuary (ABSC); Dade: “Biscayne” (MCZC); Deering Estate Park (CMNC); Matheson Ham- mock (ABSC); Miami (Wood 1982); Monroe: Big Pine Key (CMNC); Everglades Natl. Park (Wood 1982); Key Largo (ABSC, Wood 1982); Plantation Key (Wood 1982); Sug- arloaf Key (SLWC). Tribe Micracini Micracis swainei Blackman. (xy, po, hpg). Reported from branches of a variety of hardwood species. It is commonly found in willow (Salix) in Florida. Southeastern U.S. from eastern Texas, lowland regions of Mexico and Central America. Dade: 6 mi N. Homestead (USNM). Micracisella nanula (LeConte). (my, po, mg). Breeds in twigs of a variety of trees, shrubs, and vines. Southeastern U.S. from Texas eastward. A closely related species, M. opacithorax Schedl (possibly conspecific) is found in southern Texas and the Gulf Coast of Mexico. Dade: “Biscayne” (DFEC, MCZC); Homestead (Wood 1982); Miami (Wood 1982); Monroe: Big Pine Key (ABSC, Wood 1982); Key Largo (Wood 1982); Key Vaca, Marathon (Wood 1982); Key West (Wood 1982, Blackman 1928); Missouri Key (Wood 1982); N. Key Largo (ABSC); Sugarloaf Key (CMNC, Wood 1982). Pseudothysanoes securigerus (Blackman). (?,?,?). Nothing is known about the hosts or feeding habits of this species. Species of Pseudothysanoes may be either phloem or sap-wood borers. All studied species are bigynous. Southern Florida, Hispaniola. Dade: Everglades Natl. Park, Long Pine Key (CMNC); Monroe: Big Pine Key (CMNC); No Name Key (CMNC). Thysanoes fimbricornis LeConte. (xy, po, hp). Breeds in branches of a variety of hardwood species. Southeastern U.S. from eastern Texas. Found in lowland areas of eastern and southeastern Mexico. Dade: “Biscayne” (Blackman 1928). Tribe Ipini Ips avulsus (Eichhoff). (ph, mo, hp). Breeds in branches and crowns of all pines within its range. Southeastern U.S. from eastern Texas. Dade: “Biscayne” (MCZC); Miami (MCZC). Ips calligraphus (Germar). (ph, mo, hp). Breeds in trunks and large branches of all pines within its range. Eastern U.S. and southeastern Canada, Montane regions of the southwestern U.S., Mexico, Guatemala and Honduras. Cuba and Hispaniola. Dade: Everglades Natl. Park, Paradise Key (Hopping 1965b); Monroe: Key Largo (Hopping 1965b); Key West (Hopping 1965b). Ips grandicollis (Eichhoff). (ph, mo, hpg). Breeds in branches and trunks of all pines within its range. Eastern U.S. and southeastern Canada, Montane regions of the southwestern U.S., Mexico, Guatemala and Honduras. Cuba and Hispaniola. Dade: Biscayne (MCZC); Everglades Natl. Park, Long Pine Key (CMNC); Everglades Natl. Park, Paradise Key (Hopping 1965a); Homestead (Hopping 1965a); Monroe: Big Pine Key (CMNC). Atkinson & Peck:Bark and Ambrosia Beetles of South Florida321 Tribe Dryocoetini Coccotrypes advena (Blandford). (sp, po, ipg). Breeds in seeds of a variety of plants. Widely distributed in Old World tropics, adventive in New World. Dade: Coral Gables (FSCA). This species was intercepted in imported seeds and may not actually be es- tablished in Florida. Coccotrypes carpophagus (Hornung). (sp, ol, ipg). Breeds in seeds of palms, espe- cially Sabal palmetto (Walt.) Lodd. ex Schultes and Washingtonia robusta Wendl. Widely distributed in Old World tropics, adventive in New World. Dade: Coconut Grove (Wood 1982); Deering Estate Park (CMNC); Everglades Natl. Park, Royal Palm Hammock (CMNC); Homestead (ABSC); Matheson Hammock (CMNC); Monroe: Big Pine Key (CMNC); Big Torch Key (CMNC); Cudjoe Key (CMNC); Fat Deer Key (CMNC); Grassy Key (ABSC); Key Largo (CMNC); Key Vaca, Marathon (CMNC, MCZC); No Name Key (CMNC); Plantation Key (ABSC); Sugarloaf Key (CMNC). Coccotrypes cyperi (Beeson). (sp-ph, po, ipg). Extremely polyphagous. Breeds in phloem and seeds of many hosts. Widely distributed in Old World tropics, adventive in New World. Dade: Deering Estate Park (CMNC); Homestead (ABSC); Miami (FSCA); Monroe: Big Pine Key (CMNC); Fat Deer Key (CMNC). Coccotrypes dactyliperda (F.). (sp, ol, ipg). Breeds in seeds of palms, especially Phoenix spp. Widely distributed in Old World tropics, adventive in New World. Mon- roe: Sugarloaf Key (CMNC). Coccotrypes distinctus (Motschulsky). (sp, ol, ipg). Breeds in seeds of palms, espe- cially Phoenix spp., Sabal palmetto, and Washingtonia robusta. Widely distributed in Old World tropics, adventive in New World. Collier: Collier Seminole St. Park (ABSC); Dade: Chekika State Rec. Area (CMNC); Coconut Grove (Wood 1982); Deer- ing Estate Park (CMNC); Everglades Natl. Park, Long Pine Key (CMNC); Fairchild Tropical Gardens (FSCA); Homestead (ABSC); Matheson Hammock (CMNC); Miami (FSCA); Miami Beach (Wood 1982); Old Cutler Hammock (CMNC); Monroe: Planta- tion Key (ABSC); Stock Isl. (ABSC, CHAH, CMNC). Coccotrypes rhizophorae (Hopkins). (sp, ol, ipg). Hosts: (Rhizophoraceae) Breeds in expanding prop roots and propagules of its host, Rhizophora mangle L. All other spe- cies of Coccotrypes found in the New World are believed to be immigrants from Africa or Asia. C. rhizophorae is a special case and possible exception because it may have immigrated to the New World without human aid or intervention. Coccotrypes rhizo- phorae is also known from southeastern Asia in Rhizophora spp. Given that this bee- tle breeds in the fruits and developing seedlings of red mangrove which are capable of floating long distances in salt water, it is entirely plausible that this insect was dis- persed to the New World by infested host propagules, just as its host presumably dis- persed to the New World by ocean currents (Tomlinson 1980). Collier: Everglades City (USNM); Dade: Homestead (Wood 1982); Miami (MCZC, THAC); Miami, Deer- ing Estate (CMNC); Monroe: Key Largo (ABSC, USNM); Key West (Wood 1982). Coccotrypes robustus Eichhoff (sp, ?, ipg). Reported from seeds of Euterpe sp. (Pal- mae). No host records from Florida. This species is known only from southern Florida and the Greater Antilles. It is presumably of Old World origin as are all other species in this genus. Dade: Deering Estate Park (CMNC); Monroe: Big Pine Key (CMNC); Big Torch Key (CMNC); Cudjoe Key (CMNC); Fat Deer Key (CMNC); Key Vaca (CMNC); No Name Key (CMNC); Sugarloaf Key (THAC). Coccotrypes vulgaris (Eggers). (sp, po, ipg). Breeds in seeds of many hosts. Widely distributed in Old World tropics, immigrant in New World. Dade: Everglades Natl. Park, Long Pine Key (CMNC). Dendrocranulus carbonarius (Hopkins). (my, ol?, mo?). All species of Dendrocran- ulus with known habits breed in the stems of cucurbit vines. Presumably D. carbon- 322 Florida Entomologist 77(3) September, 1994 arius does so as well. The original host record from Annona is almost certainly due to an error in labelling. Found in southern Florida and Caribbean Islands. This species has not been collected in Florida since its original description. Dade: “Biscayne Bay” (Wood 1982). Tribe Crypturgini Crypturgus alutaceus Schwarz. (ph, mo, mg). Breeds in phloem of dead or dying pines (Pinaceae). Southeastern U.S. from eastern Texas to Atlantic seaboard. Collier: Collier Seminole St. Park (Wood 1982); Monroe: Big Pine Key (Wood 1982). Tribe Xyleborini Ambrosiodmus devexulus (Wood). (xm, po, ipg). In wide variety of hosts. Dade: Homestead (Wood 1982). Ambrosiodmus lecontei Hopkins. (xm, po, ipg). Wide variety of hosts. Usually found in branches or other small diameter material. Peninsular Florida and Carib- bean. Dade: “Biscayne” (MCZC); Everglades Natl. Park, Long Pine Key (CMNC); Ev- erglades Natl. Park, Royal Palm Hammock (CMNC); Homestead (FSCA, Wood 1982); Miami (FSCA, Wood 1982); North Miami (FSCA); Monroe: Key Largo (CMNC, Wood 1982); Key Vaca (CMNC); Key West (Wood 1982); No Name Key (CMNC); Sugarloaf Key (CMNC). Ambrosiodmus obliquus (LeConte). (xm, po, ipg). Wide variety of hosts. Widely dis- tributed in lowland Neotropical areas. Southeastern U.S. Dade: Everglades Natl. Park, Long Pine Key (CMNC); Everglades Natl. Park, Royal Palm Hammock (CMNC); Homestead (Bright 1968); Monroe: Cudjoe Key (CMNC); No Name Key (CMNC); Sugarloaf Key (CMNC). Dryocoetoides sp. (xm, po?, ipg). Hosts unknown. A single specimen was collected in a flight-intercept trap. It may represent an undescribed species because it does not agree with any species of this genus previously reported from the Caribbean or Me- soamerica and is not of any species found in the USNM or SLWC. Monroe: Big Torch Key (CMNC). Premnobius cavipennis Eichhoff. (xm, po, ipg). Breeds in trunks of a wide variety of hosts. Native to Africa, widely distributed in lowland Neotropical areas. In the U.S., found in southern Florida only. Collier: Collier Semenole St. Park (Bright 1968); Dade: Chekika State Rec. Area (CMNC); Everglades Natl. Park, Long Pine Key (CMNC); Everglades Natl. Park, Royal Palm Hammock (CMNC); Homestead (Bright 1968); Miami (Wood 1982); Monroe: Big Pine Key (CMNC); Flamingo Camp, Ever- glades (ABSC); Key Largo (CMNC); No Name Key (CMNC); Sugarloaf Key (CMNC). Theoborus solitariceps Schedl. (xm, po, ipg). Found in branches of a wide variety of hosts. Widely distributed in lowland Neotropical areas including the Caribbean. Known only from a single collection in Florida. Dade: Deering Estate Park (CMNC). Xyleborinus gracilis (Eichhoff). (xm, po, ipg). Breeds in a wide variety of hosts. Lowland Neotropical areas. In U.S. known from Florida, Louisiana and North Caro- lina (Bright 1987). Dade: Biscayne Bay (Wood 1982); Everglades Natl. Park, Long Pine Key (CMNC). Xyleborinus saxeseni (Ratzeburg). (xm, po, ipg). Breeds in virtually any woody plant within its range, including conifers. Eurasian species, immigrant in the New World. Dade: Deering Estate Park (CMNC); Everglades Natl. Park, Long Pine Key (CMNC).