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Revista de Biología Tropical

On-line version ISSN 0034-7744Print version ISSN 0034-7744

Rev. biol. trop vol.52 n.4 San José Dec. 2004

 

Factors associated with the catastrophic decline of a cloudforest frog fauna in Guatemala

J.R.Mendelson III1, E.D.Brodie,Jr.2, J.H.Malone3, M.E.Acevedo4, M.A.Baker2, N.J. Smatresk3 &J.A.Campbell3

1 Department of Herpetology,Zoo Atlanta,800 Cherokee Ave SE,Atlanta,GA 30315 USA,fax (404)624-5841; jmendelson@zooatlanta.org

2 Department of Biology,Utah State University,Logan,UT 84322-5305 USA,fax (435)797-1575; sapo@biology.usu.edu

3 Department of Biology,The University of Texas at Arlington,Arlington,TX 76019 USA.

4 4a Calle 12-45 Zona 7,Quinta Samayoa,Guatemala City 01007,Guatemala.

Received 20-V-2003. Corrected 24-XI-2003. Accepted 06-I-2004.

Abstract:Comparison of recent and historical surveys of frog populations in cloudforest habitat in Sierra de las Minas,Guatemala,indicated population declines and local extirpation of several species.Pathological exams of diseased tadpoles indicated infection by amphibian chytridiomycosis. The local habitat has been severely altered by recent establishment of large-scale leatherleaf fern production.Analysis of water chemistry at our study site suggested increased nitrogenation associated with the leatherleaf industry.Rev.Biol.Trop.52(4):991-1000. Epub 2005 Jun 24.

Key words:Amphibian decline,chytridiomycosis,Guatemala,Anura,Plectrohyla ,Ptychohyla,leatherleaf fern.

Declines of amphibian populations around the planet in recent years have been documented sufficiently to establish that the phenomenon is real (Lips 1998,1999,Alford and Richards 1999, Houlahan et al.2000)and that "natural" fluctuations in the size of local populations (e.g.,Pechmann et al.1991)are not generally causing temporary,apparent declines. In Mesoamerica and elsewhere,most of the documented declines have been associated with upland (>600 m elevation) populations of frogs that are associated with streams (e.g., Pounds et al.1997,Lips 1998,1999).Beyond simple habitat destruction,many causal agents (e.g .,introduction of alien species,global climate change)have been suspected and investigated at a wide variety of sites (see Collins and Storfer 2003,for review).Despite the real negative influence of some of these causal agents (e.g.,alien species,Kats and Ferrer 2003) the clearest link to amphibian declines (especially in protected regions)is with the fungal disease amphibian chytridiomycosis – perhaps in association with other pathogens (Berger et al.1998,Daszak et al.2003).This disease is caused by the amphibian-specific aquatic fungus,Batrachochytrium dendrobatidis,which was only recently discovered and described (Longcore et al.1999).The pathogen has been clearly implicated in amphibian declines at disjunct sites around the world,and is considered to be an emerging infectious disease (see Daszak et al.2003,for review).The recent documentation of this pathogen around the world (Daszak et al.2003)suggests a recent rapid invasion,which is corroborated by low levels of genetic variation among samples collected worldwide (Morehouse et al.2003); further work on this critical front is warranted. The origin of this fungus and the epidemic is unknown,as is its method of dispersal (Morehouse et al.2003);simply put,the biology of this fungus is virtually unknown.

In Mesoamerica,direct evidence of chytrid-associated declines in amphibians has been documented in Panama (Berger et al.1998), Costa Rica (Lips et al.2003),and Mexico (Lips et al.2004).Indirect evidence of the disease (missing and/or misshapen mouthparts in tadpoles,Fellers et al.2001)has been reported from Guatemala (Campbell and Smith 1992) and Honduras (McCranie and Wilson 2002).

In this paper we report our observations of a severe die-off of tadpoles from a cloudforest site in the Sierra de las Minas of Guatemala,provide the first documented report of chytridiomycosis from that country,and report our long-term observations of declines of frogs from a montane wetland in the same region.We also briefly report on the establishment of commercial leatherleaf fern plantations in the region,and their potential effects on the local environment.

Materials and methods

Diurnal and nocturnal visual surveys for frogs and tadpoles were conducted at Río Cafetal,Baja Verapaz,Guatemala (located in the Sierra de las Minas;see description below). Surveys were conducted on 22 –23 December 2002 (JHM,MEA),24 January 2003 (JRM, EDB,NJS,JAC),and 15 –16 March 2003 (JHM, MEA).We compared the approximate relative abundance of species of stream-associated frogs with historical observations from the site and general region (Campbell 2001). Additional anecdotal observations are reported from a proximate wetland site near the village of Purulhá, Baja Verapaz,Guatemala.Pathological examination was conducted for chytrid fungi on a single tadpole of Ptychohyla hypomykter .Water samples from Río Cafetal were collected on 25 January 2003 and analyzed for evidence of pesticides,herbicides,and semivolatile compounds; these analyses were performed by Chemtech-Ford Analytical Laboratories (Salt Lake City, Utah, USA)in accordance with National Environmental Laboratory Accreditation Program, section 5.13.

Additional samples were analyzed for nutrient chemistry.Samples were filtered (Whatman GF/F 0.7 µm)and acidified to pH-2 in the field. These were analyzed for nitrate-nitrogen (NO3- N)and phosphate-phosphorus (PO4 -P)using ion chromatography (Hedin et al.1995,APHA 1998), total dissolved nitrogen (TDN)and total dissolved phosphorus (TDP)by persulfate oxidation followed by spectroscopic analysis (Valerrama 1981,APHA 1998),and dissolved organic carbon (DOC)by wet persulfate oxidation (Menzel and Vaccaro 1964)by the Aquatic Biogeochemistry Lab at Utah State University.

Study Sites:The Sierra de las Minas is a massive east –west trending range on the Atlantic Versant of Guatemala that separates the humid Polochic Valley from the arid Motagua Valley.Campbell (2001) provided a thorough description of this mountain range,and the specific area in which our study took place. Our surveys took place along the Río Cafetal (Guatemala:Baja Verapaz:3.0 km N of La Unión Barrios,1680 m elevation).The section of the Río Cafetal in which our surveys took place is located in primary cloudforest adjacent to the eastern perimeter of the Biotopo "Mario Dary "preserve.Our surveys took place along a 300 m reach of the stream on the eastern side of highway CA-14,beginning at the highway itself.While our surveys were conducted along a section of stream running through primary cloud forest,the section just upstream (on the other side of the highway)lies adjacent to a massive,recently (since the mid-1980 ’s)established leatherleaf fern (Rumohra adiantiformis ) plantation.Except for a small gallery of remnant vegetation directly along the stream, there is no remaining forest vegetation along that section of the stream (Fig.1).Additional surveys were also conducted at two unnamed streams located within a few km of the Río Cafetal:Stream 1)located 6.1 rd km N of La Unión Barrios on Hwy CA 14 (15 °12 ’42.1 "N; 90 °12 ’ 23.9 "W);Stream 2)located 2 –3 air km NNE of La Unión Barrios (15 °11 ’29.3 "N;90 ° 11 ’ 43.8 "W).Both of these streams run through secondary vegetation in cloudforest at similar elevations to the Río Cafetal study site.

 
The frog fauna of this region was documented by JAC in the 1970s (Campbell 2001) and has been sampled by JAC and associates periodically since that time.Río Cafetal is a primary breeding site for an assemblage of forest-dwelling frogs including four hylid species (Plectrohyla hartwegi, P. pokomchi, P. quecchi,Ptychohyla hypomykter )and one ranid species (Rana maculata ); the centrolenid species Hyalinobatrachium fleischmanni has been seen there sporadically.These species typically deposit eggs in pools (e.g.,splash pools below small waterfalls or between riffle zones)in streams during the dry season (January –May). In part because of the cool water temperatures, metamorphosis of tadpoles may take more than one year.Thus,at any time of the year,different stages of tadpoles of all species may be found in the streams in this area.Additional frogs, most notably several species in the leptodactylid genus Eleutherodactylus,are associated with streams in this area but do not use them to reproduce.The hylid species Hyla bromeliacea and H.minera are also known from the area, but these species deposit eggs in bromeliads and tree cavities.

The wetland extending north from the town of Purulhá (Fig.2)is an open,mostly tree-less marsh dominated by reeds (Fig.2).In the 1970s the hillsides around the marsh were covered in primary cloudforest,and enormous populations of the bufonid Bufo ibarrai,the hylid Hyla bocourti ,and the microhylid Hypopachus barberi bred there (Campbell 2001).

 

Results

On 21 December 2003,tadpoles of Ptychohyla hypomykter (n =12)and Plectrohyla quecchi (n =5)were collected from Stream 1.No malformed mouthparts were observed in subsequent examination of these specimens.A nocturnal survey that night found adults of Plectrohyla quecchi (n =5)and Eleutherodacylus cf.doddi (n =2);males of P. quecchi were vocalizing.

On 22 December 2002,we surveyed a 300 m stretch of Río Cafetal and observed an estimated several thousand tadpoles in the stream.Approximately 60-70%(a conservative estimate)of these tadpoles were either dead or in the process of dying.The dying tadpoles had white-colored tail tips,and the entire body was whitish in those that were dead.Dying tadpoles were observed to swim differently than did the apparently unaffected tadpoles.The discolored portion of the tail did not move when the rest of the tail musculature contracted,causing the tadpole to move irregularly.A random subsample of these tadpoles were all identified as Ptychohyla hypomyketer;it is possible that some individuals of Plectrohyla spp.were also present.No tadpoles of other species were observed.During a nocturnal survey conducted that night,apparently healthy adults of Plectrohyla hartwegi (n =3), Ptychohyla hypomykte r (n =9),and Rana maculata (n =2)were observed.Also observed were unusually long algal mats extending from submerged rocks and streaming in the water current.

On 23 December 2003,tadpoles of Plectrohyla hartwegi (n =2),Plectrohyla quecchi (n =3),and Ptychohyla hypomykter (n = 11)were collected at Stream 2.Mouthparts of tadpoles of all Plectrohyla appeared normal,but 30 %of the Ptychohyla tadpoles had both missing denticle teeth and malformed jaw sheaths.Adults seen at this time included Plectrohyla quecchi (n =4;males calling sporadically), Ptychyohyla hypomykter (n =1), and Rana maculata (n =3).

On 25 January 2003,a diurnal survey of approximately six person-hours on the same 300 m section of the Río Cafetal found only four tadpoles of Ptychohyla hypomykter. Three of these four tadpoles had obviously malformed keratinous jaw sheaths and were missing sections of their keratinous denticle rows. Subsequent pathological analysis of one tadpole provided direct confirmation of infection by the pathogenic fungus B.dendrobatidis;fungi were found in the oral tissues of this tadpole .

A follow-up visit to the Río Cafetal site on 15 –16 March 2003 observed approximately 500 –1000 tadpoles of Ptychohyla hypomykter ; no tadpoles of any other species were observed. Sample collections of tadpoles of Ptychohyla hypomykter were made (n =56,representing Gosner Stages 25 –37)on 16 March 2003. Examination of the mouthparts of these tadpoles revealed that 46 %were missing denticle rows and/or had malformed jaw sheaths.A nocturnal survey on 16 March found adult Ptychohyla hypomykter (n =6)and Plectrohyla hartwegi (n =2),and juvenile Rana maculata (n =2).

Analysis of water samples collected on 25 January 2003 found levels of PCBs, pesticides, herbicides,and semi-volatiles to be below limits established by the United States Environmental Protection Agency for all chemicals tested (Appendix).Nitrogen levels were relatively high for tropical streams,but well below EPA limits for drinking water quality; TDN was 1.22 +0.10 mgN/L and NO3-N was 0.960 +0.002 mgN/L.Phosphorus levels were below the detection limit (0.1 mgP/L for TDP and 0.002 mgP/L for PO4-P)for both analyses. DOC levels averaged 2.22 +0.05 mgC/L.

We (JAC and associates)have opportunistically surveyed the frogs of the marsh near Purulhá at various times between 1975 –2003; these surveys clearly indicate that the three most common species (Bufo ibarrai,Hyla bocourti , and Hypopachus barberi )abruptly disappeared sometime in 1983 –1984.On several visits in the 1990s,teams of herpetologists were also unable to find the historically abundant garter snake Thamnophis fulvus ;this snake frequently preys on frogs and tadpoles.

Discussion

The Sierra de las Minas are certainly experiencing direct habitat alteration and contamination associated with both slash-and-burn and commercial agriculture,and they must be prone to the broader scale environmental influences that affect cloudforests regionally (Foster 2001)and forest ecosystems worldwide (Nosengo 2003).Anurans in this area may well be affected in a synergistic fashion by both local and global effects of environmental and anthropogenic factors.Identifying and demonstrating the cause and direct effects of such synergistic influences is not possible at this time (Collins and Storfer 2003).

While we have observed evident declines in amphibian populations in Guatemala for years (Campbell 1999)and can associate many of these events with rampant deforestation, slash-and-burn agriculture, and pesticides,this is the first confirmed report of amphibian chytridiomycosis in the country.Our results augment recent reports from Mexico (Lips et al.2004)in providing a spatio-temporal link between documented epidemics in lower Central America and North America.But note that indirect evidence of chytrid infection (missing mouthparts in tadpoles;see Fellers et al.2001)was first reported in Guatemala more than a decade ago by Campbell and Smith (1992);at that time it was unknown that missing mouthparts in tadpoles was indicative of the presence of lethal pathogens.

Our anuran surveys at Río Cafetal demonstrate much lower abundance of adults of three anuran species (Plectrohyla hartwegi, Ptychohyla hypomykter,Rana maculata)than was ever observed in the 1970 ’s,and the apparent absence of two species (Plectrohyla pokomchi,P.quecchi ).Our surveys of tadpoles indicate that Ptychohyla hypomykter continues to reproduce there,but that Rana maculata and three species of Plectrohyla (P.hartwegi, P.pokomchi,P.quecchi )do not continue to reproduce there.We have demonstrated that the pathogenic fungus Batrachochytrium dendrobatidis is present at the site,and that it is affecting tadpoles.Because B.dendrobatidis has been identified as a lethal pathogen of anurans (Longcore et al.1999)and it has been directly associated with catastrophic declines of anurans in various regions of the neotropics (e.g.,Berger et al.1998,Lips et al.2003,Ron et al.2003),we posit this pathogen as a direct cause of mortality to anurans at this site.We cannot rule out the possibility that tadpoles may also have been affected by a sudden pulse of contaminants in the stream.Nor can we directly evaluate the potential direct or synergistic effects of the increased nitrogenation of the stream may have had on anuran mortality. Note that our surveys of streams in nearby areas did locate adults of Plectrohyla quecchi, and also tadpoles of Plectrohyla hartwegi .

The timing of our visits coincided with the known breeding and general activities of larval, juvenile,and adult cohorts of all species at our site;such was the case during this same season in the 1970s. However,it should be noted that Plectrohyla quecchi is usually more abundant in smaller tributaries (e.g.Stream 1),often little more than trickles of water.Ptychohyla hypomykter persists at the site,and some tadpoles still occur in the stream.Our discovery of a tadpole of Ptychohyla hypomykter that was

positively infected by B.dendrobatidis indicates that this species does contract amphibian chytridiomycosis.Because Ptychohyla hypomykter appears to persist (though in vacillating numbers)at our site,our observations also suggest that this species may be more tolerant of the pathogen than are other species (e.g .species of Plectrohyla ,whose declines at our site are presumably associated with chytrid infections).While there are no data regarding phylogenetic differences in the susceptibility of frogs to amphibian chytridiomycosis,we note that there is no evidence to suggest that Plectrohyla and Ptychohyla are each others closest relatives (Duellman and Campbell 1992,da Silva 1998). Species of Plectrohyla (and potentially their closest relatives)may be more susceptible to amphibian chytridiomycosis than are species of Ptychohyla.

The large marsh near Purulhá once harbored abundant populations of anurans,and a species of frog-eating garter snake (Thamnophis fulvus )was common (JAC,pers.obs.).As the frogs disappeared in the 1980s,we did not have the opportunity to assess the direct causes of their declines.Channels have been dug throughout this marsh for drainage,and these have clearly modified the local environment.

However,sufficient water remains in some areas to support anuran populations,so it is not clear why these anurans disappeared from this site.In any case,it appears that the disappearance of an anuran prey-base has effected a subsequent decline of a predatory snake (see also Matthews et al.2002).

Vast tracts of cloudforest habitat in the vicinity of the Biotopo "Mario Dary "and the villages of La Unión Barrios and Purulhá, Baja Verapaz,have been recently (beginning in the mid-1980s)cleared and converted into artificially-shaded leatherleaf fern plantations.Fronds of leatherleaf fern are commonly included as part of ornamental cut-flower arrangements;local people at our site indicated that fronds produced in this area are being exported to Europe.Leatherleaf ferns from this region are currently a 12-million dollar export crop (Galinsky 1996).Leatherleaf plantations are typically located on well-drained,fertile soils,with abundant water and mild temperatures (Mo 2001);conditions such as these

that occur at our study site (Campbell 2001). Cultivation of leatherleaf ferns in Costa Rica typically involves application high doses of a wide variety of fungicides,insecticides,and herbicides (Stamps and McColley 1997,see Mo 2001,for review);many of these chemicals are prohibited in Europe and the United States. One predominant fungicide used in cultivation is chlorothalonil (Stamps and McColley 1997, Mo 2001);chlorothalonil is highly toxic to a variety of aquatic animals (Mo 2001). Because leatherleaf is an ornamental plant,rather than an edible plant,importing countries enforce

no maximum allowable limits for chemical residues.In addition,precisely because it is an ornamental plant,specimens with the least damage from insects or fungal pathogens have the greatest value,thus encouraging massive application of pesticides and herbicides (Mo 2001).The primary nutrients required to cultivate leatherleaf ferns are nitrogen (in the form of urea,ammonium,or nitrate)and potassium (Stamps 1995).Stamps specifically emphasized the risks of local environmental contamination associated with leatherleaf fern production:

The high leaching potential of these soils places water resources in leatherleaf fern production areas at risk of contamination unless appropriate management practices are followed …This leachability is a cause for concern, since N [itrogen ]can end up in drinking water supplies where it may become a health hazard (Stamps 1995:2 –3).

We detected relatively high levels of nitrogen in the stream and we suspect that this reflects fertilizer use in the watershed.The long algal mats in the stream are also suggestive of unnaturally high levels of nitrogen in the water; such algal mats were not observed by J.A. Campbell in the 1970s.Information on NO3- N and TDN levels in neotropical streams is limited in the literature.The concentrations we report here are considerably higher than data published for high-elevation tropical streams at the Luquillo Experimental Forest Long Term Ecological Research site in Puerto Rico,where values for NO3-N range from 0.054 –0.066 mg/L and TDN range from 0.190 –0.223 mg/L (McDowell and Asbury 1994).A larger range for NO3-N (0 –0.229 mg/L)was reported from montane tropical streams in the Cordillera Central and the Cordillera de Tilarán of Costa Rica (Pringle et al.1993). The N levels we measured in the Río Cafetal are at least 4X higher than levels reported from similar sites in the neotropics.

While a direct connection between increased nitogenation of stream systems and amphibian chytridiomycosis has not been demonstrated,direct mortality of tadpoles by nitrogen-based fertilizer contamination has been well documented (see Blaustein et al.2003,for review).The symptoms we observed among the dying tadpoles on 22 December 2002 were generally consistent with the effects of nitrogen poisoning documented by Marco et al.(1999).

The water samples we collected and analyzed did not show evidence of contamination by the specific fungicide mentioned above,nor by a broad spectrum of pesticides,herbicides, or other volatile compounds.In light of the exhaustive study by Mo (2001)in Costa Rica, we are forced to conclude that the plantations in Guatemala surely follow similar protocols of heavy applications of a variety of highly toxic chemicals to their crops.We did not detect these chemicals in our analyses,perhaps because they were applied at some unknown time prior to our sampling (i.e.,there was a temporary pulse of contamination that preceded our collecting activities).We note that Mo (2001)was careful to collect water samples from plantation effluents.We did not have sufficient information to organize our sampling in a similar manner.Owners and workers at fern plantations are not willing to discuss their agricultural practices,nor their application regime for agricultural chemicals (pers. obs.,Mo 2001). Pesticide exposure can induce immunosuppression in frogs (Gilbertson et al. 2003),and conceivably could have affected the tadpoles at our site.We do not know what potential effects various agricultural fungicides could possibly have on populations of the pathogenic chytrids in the region.

In any case,our results clearly indicate that yet another assemblage of upland frogs in Mesoamerica has been severely impacted. The pathogenic chtyrid fungus B.dendrobatidis is present at the site,and is affecting tadpoles.As such it appears the declines we have documented have been caused,at least in part,by a local epidemic of amphibian chytridiomycosis.It is possible that local frog populations have also suffered negative effects (direct and/or indirect)from contamination of their natal stream —contamination in the form of increased nitrogenation,and possibly from agricultural chemicals.We cannot predict when,or if,populations at this site will recover from the recent,catastrophic declines. Of the species historically present at our site, Plectrohyla quecchi and Plectrohyla pokomchi have relatively restricted distributions in the highlands of eastern Guatemala;the remaining species have somewhat broader distributions in the uplands of nuclear Central America.We are confident that the recent construction of massive leatherleaf fern plantations in the area has fragmented native habitat and therefore may reduce the likelihood that this area can be recolonized by frogs from other drainages. We also suspect that the local leatherleaf plantations are contaminating the watershed with nitrogen-based fertilizers;our data indirectly suggest that such contamination is related to the local amphibian population declines.

At our study site we have documented habitat destruction,apparent contamination from agricultural chemicals,presence of amphibian chytridiomycosis,a massive amphibian population decline,and the apparently associated decline of a snake species.Amphibian population declines are complex phenomena (Kiesecker et al.2001).The probable synergistic links between the phenomenon we have documented in Guatemala —and indeed influences yet to be identified and considered — remain unclear at our site and globally.

Acknowledgments

We thank Alison Kelly,Karen Lips, Claudette Mo,Robert Puschendorf,and Patricia Burrows for invaluable assistance on this project,and members of the USU Herpetology Group for their insightful critiques and discussions.Allan Pessier (University of Illinois Zoological Pathology Program,Loyola University Medical Center)examined the specimen for Chytrid fungi.Chemical analyses in the Baker lab were conducted by Agnes Chartier. This research was conducted in direct association with The Research Analysis Network for Neotropical Amphibians (RANA),which is supported by the National Science Foundation (DEB-0130273).This research was supported in part by a National Science Foundation grant to J.A.Campbell (DEB-0102383).

Resumen

Una comparación entre un inventario anterior y otro reciente de poblaciones de ranas de bosque nublado en la Sierra de Las Minas de Guatemala demostró disminuciones poblacionales y ausencia localizada de varias especies.El examen patológico de un renacuajo muerto indicó infección por un hongo quítrido propio de los anfibios.El hábitat local ha sido gravemente alterado por el establecimiento reciente de producción a gran escala de helechos ornamentales.El análisis químico del agua en el área de estudio señaló un aumento en nitrogenación asociado al cultivo de helechos.

Palabras clave:declinación de anfibios,quitridiomicosis,Guatemala,Anura,Plectrohyla, Ptychohyla, helechos ornamentales.

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