Revista Mexicana de Ciencias Agrícolas volume 9 number 8 November 12 - December 31, 2018
OI: https://doi.org/10.29312/remexca.v9i8.1368
Article
Susceptibility study of avocado varieties to the attack
of mistletoe in Michoacán
Víctor Manuel Coria Ávalos1
Miguel Ángel Bello González1
H. Jesús Muñoz Flores1§
Moisés Alberto Cortes Cruz2
Luis Felipe Guzmán Rodríguez2
Rosa Gabriela Coria Mora3
1Experimental Field Uruapan-INIFAP. Av. Latinoamericana num. 1101, Col. Revolution, Uruapan, Michoacán, Mexico. ZC. 60150. (coria.victormanuel@inifap.gob.mx; mabellog2@hotmail.com; muñoz.hipolitojesus@inifap.gob.mx). 2Genetic Resources Center-INIFAP. Blvd. of Biodiversity num. 400, Tepatitlán, Jalisco. ZC. 47600. (cortes.moises@inifap.gob.mx; guzman.luis@inifap.gob.mx). 3Faculty of Agrobiology Pdte. Juárez-UMSNH. Paseo Lázaro Cárdenas num. 2290, Col. Emiliano Zapata, Uruapan, Michoacán. ZC. 60170. (coria.mora@hotmail.com).
§Corresponding author: jesusmuflores@yahoo.com.mx.
Abstract
The infestations caused by parasitic mistletoe plants, which attack wild and cultivated perennial plants of Mexico, represent one of the main limiting factors of production and are the cause of high mortality rates in plants. The objective was to study the susceptibility of different avocado materials to attack by mistletoe species and identify the genera and species of mistletoe plants that grow on the diversity of avocado trees in the Michoacán avocado region. A fraction of this region was sampled and botanical material from parasitic plants that were affecting avocado trees was collected. In nursery in ‘Hass’, ‘Fuerte’ and ‘creole’ avocado plants, infestations were induced with seeds of the different mistletoe species collected in avocado trees in situ. Three seeds were placed per plant and by an experimental design of complete blocks at random, with six repetitions; the response was observed during one year, in terms of the rate of germination and development of endophytic tissue of the hemiparasite on the infested plants. There were three genera and four species parasitizing avocado trees (Persea americana Mill. var. drymifolia). The results of the induced colonization of the mistletoe, in Psittacanthus calyculatus, we found a highly significant statistical difference (Pr> F= 0.0024) for the development of endophytic tissue of the parasitic plant on the different avocado materials used. The highest incidence was in ‘creole’ avocado with 83.3% and in ‘Fuerte’ avocado it was 66.7% of infested plants; avocado ‘Hass’ in none of the plants developed the infection.
Keywords: Persea americana Mill., Loranthaceae, parasitic plants.
Reception date: October 2018
Acceptance date: December 2018
Introduction
The infestations and development of the different species of parasitic mistletoe plants, which naturally attack a large number of species of wild and cultivated perennial plants of Mexico, represent one of the main limiting factors of production and are the cause of high rates of mortality in species of cultivated fruit plants (mango, citrus, avocado, guava, apple tree, pear, tejocote, walnut, macadamia, etc.), as well as species of natural forest (pine, oak, spruce, acacia, etc.), ornamental plants (jacaranda, tulip, obelisk, etc.) (Owen, 2004; Vázquez et al., 2006; Agrios 2008; Siegfried et al., 2008; Ishiwu, 2013). Mistletoes, commonly known as graft or mata palo, are aerial plants, hemiparasites of perennial plants, shrubs or trees of a number of gymnosperm and angiosperm species (Bello, 1984; Bello and Gutiérrez, 1985; Rzedowski, 2011).
They are shrubs or sub-shrubs perennial, monoecious or hermaphroditic, with green, yellow, orange or black leaves, simple, whole, sometimes reduced to scales, of variable forms from liguliforms, lanceolate to elliptical or obovate, solitary flowers or arranged in racemose inflorescence, umbela, cimosas, panicles or spikes, actinomorphic with biseriate perianth, of 3 to 6 divisions, green or of striking colors, without differentiation of the calyx and corolla, but sometimes provided with a calculus; the fruit is a fleshy and mucilaginous berry of variable form, with a seed surrounded by an abundant viscid tissue, the seeds to germinate form a specialized adventitious root (haustorio), through which they penetrate through the tissues of branches and stems (cortex) of the host plants to extract water and nutrients, induce the generation of woody tumors that cause severe damage and even death (Sosa and Tressens, 2002).
The viscous tissue that surrounds the seed of these plants, provides a series of adaptive advantages, given that once dispersed, it adheres strongly to branches and bark of the host. Birds are the main dispersing agents of seeds; the viscous tissue that surrounds the seed, allows it to slide through the digestive tract of the bird, often without losing its consistency and viability, to be excreted in different parts of the host plant forming new colonies (Gómez et al., 2011).
This phytosanitary problem represents the second factor of disturbance in the areas of natural forest and commercial plantations (Vázquez et al., 2006). Similar impact of damage has been documented in commercial plantations of many perennial fruit species (López and Sanz, 1992; Edagbo et al., 2013; Zaragoza et al., 2015), as well as in some cases of urban forestry (Arriola et al., 2013). At a global level, parasitic plants and in particular mistletoe have been the subject of multiple studies that have allowed to abound in the knowledge of the species that exist, their distribution, biological cycles and the etiology of the disease; however, to date it has not been possible to generate effective management alternatives to avoid damage to host plants (Vázquez et al., 2006; Cibrián et al., 2007a; Cibrián et al., 2007b).
In the particular case of avocado trees, in other countries there have been documented cases of the presence of mistletoe on this species of plant, without specifying the affected varieties or ecological groups (Ishiwu, 2013), there are also undocumented evidences of the presence and attack by
mistletoe in the producing regions of Michoacán, Mexico, but the species of the hemiparasite associated with the avocado tree are unknown, as well as its distribution and damages, which fully justifies this research, in which the objective of studying the susceptibility of different avocado materials to attack by mistletoe species, and identify the genera and species of mistletoe plants that grow on the diversity of avocado trees that cohabit in the avocado producer region of the state of Michoacán.
Materials and methods
For the study was chosen as sampling universe a highly representative fraction of the different climatic conditions occurring in the central producing region of avocado from Michoacán, which was composed of the municipalities of Tingambato, Ziracuaretiro, Uruapan and Nuevo San Juan Parangaricutiro (Figure 1) which, as a whole, make up a compact area that includes a large part, both of the climatic diversity, as well as wild and cultivated avocado materials that exist in the state. The characteristics of the physical environment that prevail in the work area are described in Table 1.
Figure 1. Location of municipalities sampled for collecting mistletoe parasitizing avocado trees of improved and creole varieties (2017).
During 2015, field trips were made to different places in the region of Uruapan, this with the purpose of sampling ‘Hass’, ‘Fuerte’ avocado trees and wild or semi-domesticated materials of the Mexican ecotype commonly known as ‘creole’ In each of the visited sites, we sought to identify trees parasitized by mistletoe plants; and in the cases in which trees were located with the damage, they were georeferenced with a geopositioning (Garmin-20®). To know the characteristics of the physical environment, according to the description shown in Table 1. Additionally, the surrounding avocado trees were visually inspected within a radius of 20 m around the infested tree.
Table 1. Characteristics of the physical environment in the municipalities that make up the avocado producer region of Uruapan, Michoacán 2017.
Physical characteristics | Municipality | |||
Tingambato | Ziracuaretiro | Uruapan | Nuevo San Juan Parangaricutiro | |
North latitude | 19º25’ and 19o36’ | 19o21’ and 19o31’ | 19o11’ and 19º38’ | 19º17’ and 19º30’ |
West longitude | 101o46’ and 101º57’ | 101º48’ and 102º00’ | 101º563’ and 102º24’ | 102º08’ |
Altitude (m) | 1 600 to 3 000 | 1 200-2 400 | 700 to 3 300 | 1 300 to 3 300 |
Medium temperature | 12 to 22 oC | 16 to 24 oC | 16 to 26 oC | 10 to 22 oC |
Precipitation | 1 000 to 1 500 mm | 700 to 1 100 mm | 800 to 1 500 mm | 800 to 2 000 mm |
Weather | Temperate subhumid and Tempered humid | Temperate sub-humid, Semi-warm humid, Semi-warm sub-humid, warm sub-humid | Temperate sub-humid, tempered humid and semi-warm sub-humid | Temperate wet and semi-warm sub-humid |
Vegetable cover | Pine, oak and bushes | Pine, oak and bushes | Pine, oak and bushes | Pine and oyamel |
Source: INEGI (2009). Municipal geographic information booklet of the United Mexican States. Geostatistical key 16058, 16090, 16102 and 16111.
From each of the trees infested by mistletoe, samples of vegetative material and mature fruits of the hemiparasitic plant were collected, deposited inside perfectly labeled paper bags, for later transfer to the herbarium of the National Institute of Ecology AC (INECOL) located in Patzcuaro, Michoacán, where its taxonomic determination and comparison were carried out to later make the description of the species based on the criteria described by Calderón (1979); Oliva (1983); Bello (1984); Bello and Gutiérrez (1985); Hernández (1991); Acosta et al. (1992); Gómez et al. (2011); Rzedowski and Calderón (2011). The collected specimens are deposited in the herbarium of the Institute of Ecology, AC (INECOL), Patzcuaro, Michoacán.
In the field trips, it was observed that the avocados known as ‘creoles’ (Figure 2a and 2b) and the ‘Fuerte’ variety (Figure 2c) are widely attacked by parasitic mistletoe plants; not so ‘Hass’ avocado trees. To know if this observed situation is the product of chance, or failing that, if the ‘Hass’ avocado is really tolerant of attack; it is proceeded to establish an experiment in the nursery of the Experimental Field Uruapan, for which we used avocado plants ‘Hass’, ‘Fuerte’ and ‘creole’, with an age of 8 months, which were subjected to infestations induced with seeds of the different species of mistletoe collected from avocado trees in situ. For the above, the study carried out by López and Ornelas (2002) was taken as a reference.
Three seeds were placed per plant and by an experimental design of complete blocks at random, with six repetitions; The response was observed during one year, in terms of the rate of germination and development of endophytic tissue of the hemiparasite on the infested plants.
Special care was taken to avoid the supply of nutrition inputs or pesticides that could interfere with the hemiparasitic. For the registered data, an analysis of variance (Anova) was performed using the proc Anova procedure of the statistical package system for Windows version 9.2 (SAS, 2013). The multiple comparison of the means was carried out by the Tukey test (p≥ 0.05), to order the impact of infestation and development of the hemiparasitic plants under treatment.
Figure 2. Trees infested by mistletoe located in places of the avocado producing region of Uruapan, Michoacan 2017. 2a) partial view of a ‘creole’ avocado tree with severe infestation by mistletoe Psittacanthus calyculatus; 2b) plants of P. calyculatus in full flowering; 2c) approach to the foliar area of a ‘Fuerte’ avocado plant infested by mistletoe Struthanthus venetus.
Results and discussion
The taxonomic characterization of the mistletoe plants located in 42 places, in the municipalities of Tingambato, Ziracuaretiro, Uruapan and Nuevo San Juan Parangaricutiro, which are part of the central avocado producing region of Michoacan, allowed to register three genera: Psittacanthus and Struthanthus (Loranthaceae), in addition to Phoradendron (Viscaceae) and four species: Psittancanthus calyculathus, Struthanthus venetus, Struthanthus condensatus and Phoradendron velutinum, which were found parasitizing on avocado trees (Persea americana Mill. var. drymifolia) Mexican horticultural race, commonly known as ‘Creole’ in an altitudinal range that ranged from 1 332 to 2 287 m (Table 2).
Table 2. List of collections made of avocado trees infested by mistletoe. Uruapan Region, Michoacán 2017.
Municipality | Locality | Geographical coordinates | Altitude (m) | Host plant | Mistletoe species | |
North Latitude | West longitude | |||||
Nuevo San Juan Parangaricutiro | Hirambosta | 19 o 54’ 475” | 102 o 27’ 211” | 2 287 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Hirambosta | 19 o 54’ 475” | 102 o 27’ 211” | 2 287 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Huimbam | 19 o 53’ 701” | 102 o 25’ 962” | 2 245 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Huimbam | 19 o 53’ 663” | 102 o 26’ 012” | 2 243 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Hirambosta | 19 o 54’ 439” | 102 o 27’ 208” | 2 240 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Huimbam | 19 o 53’ 628” | 102 o 26’ 723” | 2 225 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Hirambosta | 19 o 53’ 510” | 102 o 27’ 470” | 2 211 | Creole | Phoradendron velutinum |
Nuevo San Juan Parangaricutiro | Hirambosta | 19 o 54’ 445” | 102 o 27’ 211” | 2 210 | Creole | Phoradendron velutinum |
Tingambato | Poblado Tingambato | 19 o 49’ 754” | 101 o 84’ 936” | 1 972 | Creole | Psittacanthus calyculatus |
Tingambato | Poblado Tingambato | 19 o 49’ 741” | 101 o 84’ 936” | 1 972 | Creole | Psittacanthus calyculatus |
Tingambato | Poblado Tingambato | 19 o 49’ 753” | 101 o 84’ 933” | 1 972 | Creole | Psittacanthus calyculatus |
Tingambato | Poblado Tingambato | 19 o 50’ 009” | 101 o 84’ 759” | 1 971 | Creole | Psittacanthus calyculatus |
Tingambato | Centro arqueológico | 19 o 49’ 541” | 101 o 85’ 822” | 1 967 | Creole | Psittacanthus calyculatus |
Tingambato | Llano de la virgen | 19 o 50’ 568” | 101 o 86’ 704” | 1 944 | Creole | Psittacanthus calyculatus |
Tingambato | Centro arqueológico | 19 o 49’ 500” | 101 o 85’ 872” | 1 938 | Creole | Psittacanthus calyculatus |
Tingambato | Centro arqueológico | 19 o 49’ 508” | 101 o 85’ 865” | 1 937 | Creole | Psittacanthus calyculatus |
Tingambato | Llano de la virgen | 19 o 50’ 572” | 101 o 86’ 739” | 1 933 | Creole | Psittacanthus calyculatus |
Tingambato | Centro arqueológico | 19 o 49’ 492” | 101 o 85’ 890” | 1 932 | Creole | Psittacanthus calyculatus |
Tingambato | Llano de la virgen | 19 o 49’ 538” | 101 o 85’ 778” | 1 931 | Creole | Psittacanthus calyculatus |
Tingambato | Centro arqueológico | 19 o 49’ 493” | 101 o 85’ 883” | 1 931 | Creole | Psittacanthus calyculatus |
Tingambato | Llano de la virgen | 19 o 50’ 569” | 101 o 86’ 781” | 1 899 | Creole | Psittacanthus calyculatus |
Ziracuaretiro | Poblado San Ángel | 19 o 46’ 176” | 101 o 88’ 803” | 1 654 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado San Ángel | 19 o 44’ 640” | 101 o 90’ 566” | 1 621 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado San Angel | 19 o 45’ 266” | 101 o 89’ 389” | 1 604 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 550” | 101 o 91’ 151” | 1 332 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 550” | 101 o 91’ 151” | 1 332 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 550” | 101 o 91’ 151” | 1 332 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 550” | 101 o 91’ 151” | 1 332 | Fuerte | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 569” | 101 o 91’ 113” | 1 332 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 464” | 101 o 90’ 626” | 1 332 | Creole | Struthanthus venetus |
Ziracuaretiro | Poblado Ziracuaretiro | 19 o 40’ 901” | 101 o 90’ 277” | 1 332 | Creole | Struthanthus venetus |
Uruapan | Toreo el bajo | 19 o 42’ 701” | 102 o 05’ 635” | 1 655 | Creole | Struthanthus venetus |
Uruapan | Toreo el bajo | 19 o 44’ 624” | 102 o 00’ 542” | 1 650 | Creole | Struthanthus venetus |
Uruapan | Caltzontzin | 19 o 42’ 742” | 102 o 00’ 460” | 1 634 | Creole | Struthanthus venetus |
Uruapan | Caltzontzin | 19 o 42’ 742” | 102 o 00’ 460” | 1 634 | Creole | Struthanthus venetus |
Uruapan | CE Uruapan | 19 o 40’ 722” | 102 o 05’ 22.6” | 1 600 | Creole | Psittacanthus calyculatus |
Uruapan | CE Uruapan | 19 o 40’ 722” | 102 o 05’ 22.6” | 1 600 | Creole | Struthanthus condensatus |
Uruapan | CE. Uruapan | 19 o 40’ 722” | 102 o 05’ 22.6” | 1 600 | Creole | Struthanthus condensatus |
Uruapan | CE. Uruapan | 19 o 40’ 722” | 102 o 05’ 22.6” | 1 600 | Fuerte | Struthanthus condensatus |
Uruapan | CE. Uruapan | 19 o 40’ 722” | 102 o 05’ 2.26” | 1 600 | Creole | Struthanthus condensatus |
Uruapan | Cd. de Uruapan | 19 o 38’ 814 | 102 o 04’ 7.68” | 1 601 | Creole | Psittacanthus calyculatus |
Uruapan | Cd. de Uruapan | 19 o 38’ 905 | 102 o 05’ 4.73” | 1 599 | Creole | Psittacanthus calyculatus |
Although there is documented evidence that avocado is included among the natural mistletoe hosts, mainly of the species Psittacanthus calyculatus (Vázquez et al., 2006; Pérez, 2016), no bibliographic references describe the affected avocado materials. From the results obtained in this investigation, the existence of the Mexican avocado ecotype (Persea americana Mill. var. Drymifolia), infested by mistletoe, which can be observed in backyards of houses, on roadsides and in an isolated way within some commercial avocado orchards ‘Hass’ which is the totally dominant variety in the orchards of the region. Only two localities were located (Ziracuaretiro and CE Uruapan), with presence of ‘Fuerte’ avocado with mistletoe damage (Table 2).
In the case of avocado ‘Hass’ during the field trips no infestations by mistletoe were found in avocado trees of this variety; this even though in several cases they had neighbors and even crossed the branches with ‘creole’ avocado plants infested by mistletoe. This is the first evidence of the absence of the hemiparasite plant known as mistletoe on avocado trees of the ‘Hass’ variety.
In reference to the ‘creole’ avocado, trees were found infested by mistletoe, which correspond to three genera and four species of the family Loranthaceae and Viscaceae. Of the four species reported, Struthanthus venetus has a greater distribution in properties with semi-warm humid, semi-warm subhumid and warm subhumid climates that prevail in the municipalities of Ziracuaretiro and Uruapan (1 332-1 655 mals) S. condensatus, was found in areas with subhumid warm climate of Ziracuaretiro and Uruapan (1 600 masl). Phoradendron velutinum was collected from humid temperate zones of the municipality of Nuevo San Juan Parangaricutiro (2 210-2 287 masl). While Psittacanthus calyculatus was collected in farms with temperate subhumid and semi-warm humid climate of Uruapan and Tingambato (1 599-1 972 masl). When observing the distribution of these hemiparasitic species in the studied region, it can be deduced that their distribution is subject to their climatic and altitudinal preference.
Finally, two cases of ‘Fuerte’ avocado were found with infestations by Struthanthus venetus and S. comdensatus in zones with semi-warm subhumid and warm subhumid climates of the municipalities of Ziracuaretiro and Uruapan at altitudes of 1 332-1 600 m (Table 2).
In the experiment for induced mistletoe colonization, it was found that for the case of the mistletoe species P. calyculatus, at the end of the test, a highly significant statistical difference (Pr> F= 0.0024) was quantified for the development of endophytic tissue of the parasitic plant on the different avocado materials subjected to the test. The highest incidence was registered on "creole" avocado, where 83.3% of the plants developed hemiparasitic haustoria on the host stem, in addition to the vegetative development of the aerial part of the mistletoe (Table 3). The ‘Fuerte’ avocado followed with 66.7% of infested plants; while in the case of avocado ‘Hass’ none of the plants developed the infection. That is, if there was germination of the seed, but could not develop the haustoria that allowed it to adhere to the host, as shown in Figure 3a, 3b, 3c and 3d.
In reference to the case of the mistletoe Struthanthus venetus, a response similar to the previous case was observed, since also at the end of the test a highly significant statistical difference (Pr>F= 0.0202) was presented for the development of endophytic tissue of the parasitic plant on the different avocado materials subjected to the test. The highest incidence was quantified on ‘creole’ avocado, where 66.7% of the plants developed the infection; followed by ‘Fuerte’ avocado with 50% infested plants; while in ‘Hass’ avocado none of the plants developed the infection (Table 3).
Table 3. Mean behavior for infestation induced by mistletoe species on different avocado materials. Uruapan, Michoacán 2017.
Avocado materials | Mistletoe species | ||
Psittacanthus calyculatus | Struthanthus venetus | Phoradendron velutinum | |
“Creole” | 0.8333 a | 0.6667 a | 0 a |
‘Fuerte’ | 0.6667 a | 0.5 ab | 0 a |
‘Hass’ | 0 b | 0 b | 0 a |
Means with the same letter are statistically equal, Tukey (p≥ 0.05).
Figure 3. Development of mistletoe-induced infection in avocado plants. 3a) germination of seeds of Psittacanthus calyculatus on stems of avocado plants ‘Hass’; 3b) development of endophytic tissue of P. calyculatus on avocado plants ‘creole’; 3c) emission of vegetative shoots of P. calyculatus on avocado plants ‘creole’; and 3d) endophytic growth of Struthanthus venetus on ‘Fuerte’ avocado plants.
Finally, the seeds of Phoradendron velutinum during the time the field trial lasted, did not germinate on the ‘Hass’ and ‘Fuerte’ avocado plants, nor did it even replicate the infestation on ‘creole’ avocado plants, even though seeds of P. velutinum were collected precisely from ‘creole’ avocado trees located in the municipality of Nuevo San Juan Parangaricutiro, Michoacán. This could be attributable to the fact that the environmental conditions prevailing in the sites where the ‘creole’ avocado trees were collected with natural infestations in the field, correspond to very specific ecological niches located at approximately 2 200 meters above sea level, where the conditions Environmental factors correspond to a temperate humid climate, with temperatures during the year that range from 10 to 22 °C, which favor the presence of rainfall close to 2 000 mm during the year. This contrasts remarkably with the environmental conditions of the experiment site, which is located at 1 600 meters above sea level, presents a sub-humid temperate climate, with an annual rainfall of 1 400 mm and a temperature ranging from 16 to 26 °C.
Of the mistletoe species Struthanthus condensatus, it was not possible to obtain seed of the trees observed with infestation in the field, since the degree of damage to the trees was quite severe and the owners determined to tear down the trees at a stage when the mistletoe only presented vegetative development.
Conclusions
All ‘Hass’ avocado trees sampled in commercial orchards are free from attack by mistletoe.
Avocados ‘creoles’ can be attacked by mistletoe from one of the species Struthanthus venetus, S. condensatus, Phoradendron velutinum and Psittacanthus calyculatus.
‘Fuerte’ avocado trees were found attacked by Struthanthus venetus and S. condensatus.
In induced infestation on ‘Hass’ avocado nursery plants, germination of seeds of Struthanthus venetus and Psittacanthus calyculatus occurred, but in none of the cases haustorial development by the hemiparasitic plant occurred on the host.
In infestations induced with Struthanthus venetus and Psittacanthus calyculatus on ‘Fuerte’ and ‘creole’ avocado nursery plants, there was germination of seeds and development of the endophytic tissue of the hemiparasitic plant on the host.
The seeds of Phoradendron velutinum did not germinate in any of the avocado materials subjected to the attack.
Cited literature
Acosta, P. R.; Cházaro, M. y Patiño, M. R. 1992. Los muérdagos (Loranthaceae) del estado de TlaxcaIa. Gobierno del Estado de Tlaxcala. Tizatlán, Tlaxcala, México. 89 p.
Agrios, N. G. 2008. Fitopatología. 2ª (Ed.). Ed. Limusa. México, DF. 838 p.
Arriola, P. V. J.; Velasco, B. E.; Hernández, T. T.; González, H. A. y Romero, S. M. E. 2013. Los muérdagos verdaderos del arbolado de la ciudad de México. Rev. Mex. Cien. For. 4(19):34-45.
Bello, G. M. Á. 1984. Estudio de muérdagos (Loranthaceae) en la región Tarasca, Michoacán. Instituto Nacional de Investigaciones Forestales. México, DF. Boletín técnico núm. 102. 62 p.
Bello, G. M. Á. y Gutiérrez, G. M. 1985. Clave para la identificación de la familia Loranthaceae en la porción del Eje Neovolcánico localizado dentro del estado de Michoacán. Ciencia Forestal. 10(54):3-33.
Calderón, R. G. 1979. Loranthaceae. In: Rzedowski, J. y Rzedowski, G. C. de (Eds.). Flora fanerogámica del Valle de México. Ed. CECSA, México, DF. I. 119-124 pp.
Cibrián, T. D.; Vázquez, C. I. y Cibrián, T. J. 2007a. Muérdagos enanos del género Arceuthobium. In: enfermedades forestales en México. Cibrián, T. D.; Alvarado, R. D. y García, D. S. E. (editores). Primera edición. Universidad Autónoma de Chapingo (UACH). 357-395 pp.
Cibrián, T. D.; Koch, D. S. y Vázquez, C. I. 2007b. Muérdago Phoradendron. In: enfermedades forestales en México. Cibrián, T. D.; Alvarado, R. D. y García, D. S. E. (editoes). Primera edición. Universidad Autónoma de Chapingo (UACH). 396-420 pp.
Edagbo, E. D.: Ajiboye, T. O.; Borokini, T. I.; Ighere, D. A.; Alowonle, A. A. and Clement, M. 2013. A study of the conservation status of Citrus sinensis as affected by the African mistletoe, Tapinanthus bangwensis in moor plantation, Ibadan South-west, Nigeria. Inter. J. Current Agric. Sci. 3(1):5-9.
Gómez, S. L.; Sánchez, F. J. y Salazar, O. L. A. 2011. Anatomía de especies mexicanas de los géneros Phoradendron y Psittacanthus, endémicos del Nuevo Mundo. Rev. Mex. Biod. 82(4):1203-1218.
Hernández, C. 1991. Los muérdagos (Loranthaceae) de la región central del estado de Tlaxcala, Jardín Botánico de Tizatlán, núm. 4. Tlaxcala. 38 p.
Ishiwu, C. N.; Obiegbuna, J. E. and Aniagolu, N. M. 2013. Evaluation of chemical properties of mistletoe leaves from three different trees (avocado, African Oil Bean and Kola). Nigerian Food J. 31(2):1-7.
López, De B. L. and Ornelas, J. F. 2002. Host compatibility of the cloud forest mistletoe Psittacanthus schiedeanus (Loranthaceae) in central Veracruz, México. Am. J. Bot. 89(1):95-102.
López, S. J. A. y Sánz, de B. C. 1992. Viscum album L. y sus hospedantes en la Península Ibérica. Bol. San. Veg. Plagas. 18(4):817-825.
Oliva, R. H. 1983. Contribución al conocimiento de la Familia Loranthaceae del centro de Veracruz y zona limítrofe de Puebla. Tesis profesional. Facultad de Biología, Universidad de Veracruz. Xalapa, Veracruz. México. 99 p.
Owen, D. P. 2004. A regional examination of the mistletoe host species inventory. Cunninghamia. 8(3):354-361.
Pérez, I. J. I. 2016. Impacto del muérdago (Psittacanthus calyculatus) en la economía de las familias campesinas en una región del Subtrópico Mexicano. Perspectivas Latinoam. 13(1):141-156.
Rzedowski, J. y Calderón R. G. 2011. Viscaceae. In: flora del Bajío y de regiones adyacentes Fascículo 170. Instituto de Ecología, AC. Centro Regional del Bajío, Pátzcuaro, Michoacán. 59 p.
Siegfried, D. D.; Ndongo, D.; Richard, J. R.; Victor, D.T.; Henri, F.; Georges, S. and Akoa, A. 2008. Parasitism of host trees by the Loranthaceae in the region of Douala (Cameroon). Afr. J. Environ. Sci. Technol. 2(11):371-378.
SAS (Statistical Analysis System). 2013. SAS/STA User’s guide. Release 9.3. SAS, Cary, N.C., USA.
Sosa, M. M. y Tressens, S. G. 2002. Las plantas parásitas. In: Arbo, M. M. y Tressens, S. G. (Eds.). Flora del Iberá. Corrientes, Argentina, Editorial Eudene. 167-178 pp.
Vázquez, C. I.; Villa, R. A. y Madrigal, H. S. 2006. Los muérdagos (Loranthaceae) de Michoacán. INIFAP. CIRPAC. Campo Experimental Uruapan, Michoacán, México. Libro técnico núm. 2. 98 p.
Zaragoza, H. A. Y.; Cetina, A. V. M. y López, L. M. A. 2015. Identificación de daños en el arbolado de tres parques del Distrito Federal. Rev. Mex. Cien. For. 6(32):63-82.