Mitigating the Mistletoe Menace: History
View Latest Version
Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor:
Gaurav Mudgal
,
Jaspreet Kaur
,
Kartar Chand
,
Manisha Parashar
,
Sanjoy K. Dhar
,
Gajendra B. Singh
,
Mayank A. Gururani

There are nearly 5000 parasitic plant species belonging to 20 families of angiosperms, and many of them cause significant losses in crops used for food and industrial purposes. Alongside the world’s major plant pests, and mistletoes are more pronounced. Striga, Orobanche, and Cuscuta have been reviewed extensively, but attention could be called to mistletoe, which has emerged as a growing global problem and requires better management and control. The mistletoe is a hemiparasitic plant that clings to trees and depletes them of nutrients and materials, and, in many cases, heightened infection can result in tree death. Efficient seed-dispersing mechanisms and/or frugivorous avians, as well as highly diversified haustorial structures, contribute to their enhanced tropism. These pests severely affect tree plantations across the globe. In addition to being a keystone resource of biodiversity and, to a somewhat minimal extent, their medicinal assets, they have also raised serious concerns regarding the commercial fruit and timber farming communities. In spite of the efforts of these and some research communities, conventional mistletoe management approaches have not succeeded in mitigating the mistletoe problem. On the contrary, most of these approaches, such as deliberate fires, herbicide use, pruning, pollarding, plastic wrapping and so on, overlook damages caused to the environment and public health. To counter this, newer approaches followed, exploring hyperparasitism from biological entities that thrive on the mistletoes and testing their worth as mistletoe biocontrol agents (MBCAs). However, no MBCA formulation has yet been translated to the market. Despite some silvicultural trials in small-scale settings, other biotechnological interventions were limited to time-consuming and laborious tree-breeding strategies. Beyond these, transgenic approaches and smart solutions have not yet been explored in the 21st century. In the face of emerging new host records and enhanced tropism, mistletoe seems to be outperforming management initiatives and losing the necessary pace of development and advancement.

  • mistletoe
  • biocontrol
  • transcriptome
  • parasitic plant
  • resistance
  • seed dispersal

1. The Biology of Mistletoe

Mistletoes occur in the order Santalales, occupying the Loranthaceae (approx. 1000 species) and Viscaceae (approx. 550 species)  [1]. Notably, the most notoriously damaging species in the are the honey-suckled (Dendrophthoe spp.), the showy (Helixanthera spp. and Psittacanthus spp.), and the red mistletoes (Tapinanthus spp.), while, among the Viscaceae are the Dwarf (Arceuthobium spp.), the American (Phoradendron spp.), and the European mistletoes (Viscum spp.) [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29]. Mistletoes are characterized as hemiparasitic plants because of their reduced photosynthetic efficiency and the absence of a true rooting feature [30][31]. A false root-like appendage, known as a haustorium, attaches them to their host plants (mostly trees) and draws water and nutrients from them [32][33][34] (Figure 1). Generally, these haustorial connections lack a retranslocation system, meaning that the hemiparasites directly and exclusively associate with the host xylem, but exploitation of the host phloem is never reported [35][36][37]. By transpiring almost nine times as quickly as their hosts, mistletoes suppress their host’s ability to maintain water potential, thus causing early stomatal closure and reduced carbon assimilation [31][38][39][40][41][42]. Hosts find it difficult to maintain their water, carbohydrate, and mineral profiles, especially under drought and soil infertility conditions [43][44][45][46]. In addition, climate change may add to the host detriments since mistletoe may spread to new geographical regions, possibly infecting new hosts and increasing in infectivity[39][43][44]. Mistletoe seeds are dispersed predominantly by fruit-eating birds[47][48]. Some birds have coevolved with mistletoes exhibiting fruiting displays [49]. Mistletoes attract a narrow range of avian dispersers that have anatomical adaptations and dietary preferences specific to mistletoe fruits [33][49][50]. Some Viscaceae mistletoe in the genera Arceuthobium and Korthalsella are equipped with explosive dispersal mechanisms in their seeds [33]. Seed dispersal by these modes has possibly allowed mistletoe to spread to nearby potential host trees, as well as those in islands and continents far off [51][52][53][54]. Seed dispersal on a compatible tree host marks the start of the mistletoe life cycle and parasitism (Figure 2).

Figure 1. Mistletoe parasitism and impacts on a tree host. Specific mistletoe may parasitize its host by exploiting its branch(es) for water and various other resources, thereby limiting its photosynthetic potential, optimal growth, response to various stresses, and fruit or timber production. Gradually, infective spread (by haustorial connections and endophytic expansion) and growing infection instances (ensured by mistletoe seed dispersal) may lead to early senescence of the tree(s). 

Figure 2. A generalized life cycle of a mistletoe parasite on a tree host. Following seed dispersal, a sticky material, viscin, over the seed coat ensures firm attachment to the host branch (in 1) [55][56]. Hypocotyl(s) from the seed then emerges and grows towards the bark (in 2), which eventually, while attaching to the bark (in 3), penetrates through it (in 4) [57]. Once the hypocotyl connects to the host xylem (in 5), it exploits the host for water, minerals, carbohydrates, and secondary metabolites (in 6) [51]. The endophytic system may expand as sinkers (or epicortical roots) along the host cambium, from which sporadically new shoots may emerge (in 7) and facilitate the heightening of infectivity [32].

2. Conventional Control Strategies and Integrated Pest Management Approaches

2.1. Physical Methods

Mistletoe was managed by people in forests and farms using various primitive methods. In the US, western dwarf mistletoe (Arceuthobium campylopodum) predominantly affects Ponderosa and Jeffery pines in forests [58][59]. These mistletoes can reduce life expectancy and result in the poor growth of infected hosts, as well as a loss of their scenic and esthetic value [58][59]. Conventional practices such as pruning and thinning of the affected host parts have proven less helpful [60][61][62][63]. There are many concerns and problematic issues that also have hindered these methods [58][63]. Known practices that have shaped the integrated management regimens for the control of mistletoes have been categorized into direct and indirect approaches [58][64]. Direct methods include the individual removal of infected trees, branches, or mistletoe brooms, or installing buffer strips, and the use of hosts that can resist mistletoe parasitism [58]. These methods could limit mistletoe spread and infection rates to some extent [58]. The potential benefit of removing the infected branches in Scot pines (Pinus sylvestris) aids in evading the inherent competition for water and nutrients within the host plant, which concomitantly results in improved tree health, such as elevated height, biomass growth, and diameter [65]. The downside of the direct methods, however, has been the labor and cost-intensiveness, limiting their application to only local small and high-value areas including parks, city limits, orchards, and nurseries [66][67]. It may be possible to remove large areas of mistletoe-infested trees; however, scheduling this around the growth periods of various hosts would be difficult and time-consuming [68][69]. Additionally, there are many modes of seed dispersal, including birds, winds, and storms, which make these strategies difficult. For example, it is difficult to expect a dwarf mistletoe-free stand within approximately a hundred feet of an infected Ponderosa pine [58][70][71][72]. Reid and Yan [73] highlighted the possibilities of developing aerial, ultra-light, surgical, and/or chemical delivery options. In either case, such approaches may not efficiently eliminate mistletoes from heavily parasitized trees [73]. Surgical methods require time, labor, and financial costs, making them impracticable for small- to large-scale plantations [64]. Owing to expenses, farmers inevitably cannot employ professional services from arborists and tree surgeons who offer tree lopping and pruning options [64]. For them, the only option is to resort to the age-old traditions of pollarding, as in Southeast Australia [64]. This, in addition to mistletoe control, gives them fodder during droughts, shade for livestock, firewood, and fencing [64]. Other physical methods, such as the use of paints and deliberate fires, are viable measures [74]. Fire applications have offered some appreciable control of the mistletoe population in the western USA forests [75][76][77], because of mistletoes’ slow recovery rate compared to host(s) [78][79][80]. However, the use of fire may have limitations in that a weakened host may favor mistletoe regrowth [17][81][82]. Moreover, on holistic grounds, fire applications may raise public and environmental health concerns [83][84]. Indirect methods use irrigation, fertilization, brush and weed control, and regulating human disturbances [58][64][85]. Irrigation profiles of the host may variously impact hemiparasite infectivity. In many cases, the higher water status of the host corroborates with heightened mistletoe infectivity, hinting that intermittent drought regimes would offer some protection for the hosts [58][86][87][88]. Improving the fertility of hosts by the use of nitrogen fertilizers has shown some protection from the mistletoes’ effects, with increments in tree height [89]. Other indirect approaches also aid in improving host vigor and thus can be applied in large settings [58]. Above all, scientific evaluation of the above strategies requires surplus funds and support for research and development communities to devise containment facilities and flexibilities in regulations to work in protected forest areas [64].

2.2. Chemical Methods

Though with only limited prospects, chemical-agent-based approaches to mistletoe control have been more prevalent in various non-European countries such as India, Bangladesh [23][90], Australia [91], and the United States [56]. These methods involve the use of sprays or trunk injections of certain herbicide formulations to selectively control the hemiparasite without negatively impacting the host plant species [91][92][93][94]. In Eastern Australian farm eucalypts, the use of 2,4-D formulations had been investigated long ago in the 1950s and 1960s to control box mistletoes (Ameyema spp.) [94]. Besides their poor control, the trials could not be widely extended or reproduced with equivalent success due to the difficulties in ascertaining the optimum dose as influenced by various factors such as mistletoe host species, its size, the season of injection, the frequency of mistletoe infestation, and others [91][92][93]. Formulations such as 2,4-D, 2,4,5-T, 2,4-MCPB, and dichloroethane have substantially been utilized to destroy Viscum album subsp. abietis on Abies with only insignificant host effects [95]. However, complete resistance to mistletoe is never induced in hosts, as seen in the case of using 2,4-D and glyphosate, wherein mistletoe control only lasts half a year post-treatment [95][96]. A more promising herbicide control measure, according to a large study by Quick [97], involves using an iso-octyl ester of 2,4,5-T, which was later banned for its non-target effects [95]. It was shown that numerous other formulations tested between 1970 and the mid-1990s, such as Nutyrac, Dacamine, Thistrol, MCPA, Goal, D-40, Emulsamine, DPX, Prime, and Weedone, were unreactive to the endophytic system, despite killing mistletoe foliage exclusively, without adverse effects on the host [98]. Similarly, ethephon (Florel, 2-Chloroethyl phosphoric acid), which releases ethylene, a plant growth regulator, has been tested with various dwarf mistletoe–host models in Manitoba, California, Idaho, New Mexico, Oregon, and Minnesota [99][100][101]. With few non-target effects, it results in defoliation in mistletoe, albeit without influencing the haustorial connection, meaning that the complete evasion of infection is still a concern and recurrence cannot be ruled out [102]. A defoliated but active haustorium can persist for over a century [55].
It is still necessary to ensure the prompt delivery and adequate coverage of chemical agents, even if they appear potent enough [95][103][104]. Ground applications can be effective but may not reach the hemiparasites in the tree overstory higher up in the canopies [95]. Helicopter-based aerial delivery approaches, however, are challenged by poor penetration to the lower crowns, as sprays would be hindered by the overstory crowns [105][106]. To continue, chemical control methods pose many difficulties, such as limited technologies for the selective treatment of mistletoe over hosts, chemical damage to hosts, unavoidable reinfestation due to parasite seed germination or spread after chemical application, developing crops with a high tolerance to chemical applications, low penetration, persistence, availability, and so on [102][107]. Again, chemical agents that do not harm the haustorial connections may gradually exhibit resprouting [108]. This will be graver in areas with greater incidences of mistletoe infection and its resprouting-led intensification [108]. Despite the best chemical agents, mistletoe seeds will only be delayed for 2–4 years, so there is only a temporary solution to the problem [95]. Considering these factors, alternative control and management methods are highly sought after.

2.3. Silvicultural Practices

In contrast to the above approaches, silvicultural practices have been more promising [58][68][98]. These work by first clearing mistletoes from infection sites and then reintroducing a fresh lot of plants to the area [109]. Such methods have been implemented for controlling dwarf mistletoes in North America [98][109]. Robinson and colleagues proposed a spatial–statistical model that simulates mistletoe growth and development under many control methods and offers a more preferable option [110].
In small recreational and commercial settings, a silvicultural approach focuses on multiple factors, including ecological disturbances, harvests, prescribed fires, and need analysis and impact assessments [68][109]. They have gained acceptance as a routine strategy for highly devastating mistletoe and have slowed the development of resistant cultivars [95]. Silvicultural practices, however, may not guarantee long-term and consistent efficacies due to the gradual changes in climate and shifts in devastating mistletoes related to their enhanced tropism [109]. In order to scale this approach and ensure its success, newer options are highly desirable. A recent investigation showed an associational resistance to the spread of Viscum album ssp. austriacum in Northern Spain and indicated that mixed plantations of hosts (Scot pine, Pinus sylvestris) with non-host (Maritime pine, P. pinaster) trees greatly reduce mistletoe infestation [111].

3. Mistletoe Control through Biotechnological Interventions and Smart Management

3.1. Mistletoe Biocontrol Agents (MBCAs)

Organisms with specific nutritional requirements that jeopardize their concomitant host(s), have emerged as a biocontrol strategy in most pest management routines [112][113][114]. Integrated pest management practices have become an established part of agriculture, forestry, and horticulture [115]. Such biocontrol agents offer wide acceptability and ease of application due to their straightforward and easy production processes and various biosafety and eco-friendly attributes [116]. In particular, for use as MBCAs against dwarf mistletoes, various fungi, bacteria, and insects have been proposed [117][118][119][120][121].

3.2. Requirements of an Effective MBCA Selection Program

A comprehensive investigation of MBCAs may require expansive sampling and surveys towards generating metadata on biological entities, viz., insects and microbial communities that selectively impose pathogenic symptoms on mistletoes without harming their respective tree hosts. Future research should focus on individual entities and on characterizing the performance of emerging MBCAs against specific mistletoes. There is a need for rigorous research on the synergistic effects of two or more potential species (which could create an MBCA cocktail) for more notorious mistletoe(s), areas complexed with more than one variety, or for those that attack multiple hosts at the same time. Examples of primitive studies of this type exist [122][123]. Insects have equal potential as microbes for use as MBCAs, as many in their larval form feed exclusively on mistletoes [124]. In terms of MBCA potential, mistletoe pathogenicity alone cannot provide a concrete solution. Before selecting MBCAs, a checklist of features that best suit the testing of putative entities should be developed. An ideal checklist should include all the possible critical attributes on which MBCA hyperparasitism can be tested on acid, with a scoring system for their efficacy inherently (as MBCA) and their impact on the mistletoe, its tree host, and other non-host plantations. MBCAs would also require mass production, effective delivery systems, deployment strategies [95], and a consistent monitoring program. Below is a comprehensive checklist of parameters that can be used to test and screen MBCA candidates (Figure 3).
Biology 11 01645 g003 550
Figure 3. Selective traits for testing and screening of potential MBCAs. The infographic depicts a generalized checklist of features desirable for testing and screening of putative MBCAs. A more detailed checklist should include features sought for MBCA formulations of specific organismic entities, viz., microbes, insects, etc. Some features in the above are adapted from known monographs [125][126].

3.3. Challenges with MBCAs

A different perspective considers pathogenic microbes and insects as co-evolving complex relationships with mistletoe hosts [95]. Mistletoe outbreaks are induced or regulated by a variety of factors associated with seasonal and weather variations and their influences on multitrophic communities [95]. This emphasizes the importance of intensive surveying, isolation, and study of the mistletoe–host specificity for each of the biological entities carrying considerable potential as an MBCA. Perhaps many microbes may appear circumstantially sensitive even to minute changes in their growth parameters [127][128]. The culturability and preservation (and conservation) of such organisms is also very important for reproducibility in continued/extended studies and applications. Many of these might be new, yet unexplored, rare, or others nearing extinction regarding strains, varieties, species, and of course their MBCA attributes. Moreover, some of these putative MBCAs may be lost due to environmental calamities and/or seasonal variations, especially for those very specific to the endemic mistletoes (especially their varieties). This must hold for entities that have no alternate host(s) than mistletoes. Examples of this could be the fruitfly genus, Ceratitella, represented by only four species, all of which thrive exclusively on mistletoes [129], or moths such as Zelleria loranthivora (Supplementary Table S1). Potential MBCAs are rare due to the scarcity of hosts that would otherwise enable their ecological expansion on more than one or very few mistletoe species. This seems imperative, especially for those endemic to not-so-vast geographic areas, where MBCA entities might lose some of their importance and worthiness if physical and chemical treatments are practiced in these areas. This will be more serious for entities that are closely related to, dependent on, or paralleled with mistletoe hosts. Mushtaque and Baloch’s study, for example, could not test six of the twelve insect species for MBCA potential [130]. The conservation and production of rare isolates may represent new technical challenges, such as strain- or species-specific media compositions, microbial culturing, and insect-rearing protocols. In addition, selecting MBCAs would pose the challenge of competing with other members of the host–mistletoe microbiome, as has been highlighted recently [131].

3.4. Inducing Host Plant Resistance to Mistletoes and/or Herbicides

Inherent resistance to mistletoes in some trees, such as Chinese pistachio (Pistacia chinensis), crape myrtle (Lagerstroemia), sycamore (Platanus occidentalis), and conifers such as cedars (Cedrus) and redwood (Sequoioideae), has been documented amongst their susceptible genotypes [132]. A call to develop a controlled breeding program catering to the identification of genetic bases for inherent resistance in tree hosts to hemiparasitic mistletoes was made as early as the 1960s [133]. Due to the advent of cost-effective and convenient silviculture solutions, it has received little attention from the scientific community [98]. Understanding the interactions of host–mistletoe compatibility would allow the selection of resistant varieties. Conventional breeding strategies, nevertheless, have developed some stably resistant tree lines [134]. Tree hosts may be evaluated for resistance to herbicides, which may aid in the better application of chemical control approaches following herbicide translocation through such trees to their mistletoe parasite(s). For many tree crops, breeding programs are time-consuming, labor-intensive, require extensive field trials, and have not resulted in herbicide-resistant cultivars [135]. Moreover, the chemical treatment of mistletoes on herbicide-resistant tree hosts might lead to the emergence of herbicide-tolerant mistletoes.

3.5. Hunting for the Genetic Basis to Hosts’ Inherent Resistance to Mistletoes: Background Studies

Because mistletoes have been co-evolving with their tree hosts for nearly 25 million years [136], the emergence of inherent resistance in these hosts cannot be denied [137], especially for the very native and devastating mistletoes [138][139]. A genetically directed effect is also implied by the fact that mistletoes exhibit specificity to their concomitant hosts, as well as variability in host preferences [2][31][85][140][141][142][143][144][145][146][147][148][149][150]. For example, Arceuthobium douglasii does not parasitize Pinus ponderosa [98]; around 70% of dwarf mistletoe species with a principal host also pathogenize other hosts and still with variable levels of symptoms [151]; and A. pusillum fluctuates in terms of infection extent when exposed to Larix laricina, Picea glauca, P. rubens, and Pinus strobes [152]. On the contrary, there are also reported instances where mistletoes, in a heavily infected area, skipped infecting their principal host. A few observations were reviewed previously for Arceuthobium spp. [95] and one for Dendrophthoe falcata more recently [2]. However, studies are yet to present convincing demarcating features of preferred and not-so-preferred host type(s). These reports suggest existing variations in exhibiting resistance within the host population, even though the progeny of these trees have not been tested for resistance (a hotspot for further investigation). It is evident from these findings that few data are available regarding species-specific susceptibilities, which calls for rigorous field examinations such as progeny testing. Grafting techniques with putative resistant tree hosts used the inoculation of grafts and/or out-planting in mistletoe-infected sites [138][153]. Based on these trials, it appears that resistance is genetic rather than environmental. However, the heritability of this genetic regulation could not be documented. Many progeny tests to elucidate the heritability initially met with mixed results, with some escape or non-inheritable events [98][154][155][156]. Positives incidences [138][139][157][158] and later isozyme data from Nowicki’s work (as reviewed in Shamoun and DeWald [95]) more strongly support heritability.

3.6. Mistletoe Community Restructuring, Disturbances, and Biological Interactions

Mistletoe infestations drastically differ at various geographic locations, and as such from urban to forest settings [149][159][160][161][162]. Their prevalence in these areas can be variously influenced by the occurrence of host species [150], host specificity [149][160], the behavior of dispersing agents [47], pollinators [163], habitat disturbances [74][164], herbivory [165], and chemical interactions with the hosts [166][167]. Mistletoes may be differentially prevalent and infective from one to another host and within a population(s) of hosts [168][169]. Generalist mistletoes have a broad host range, while specialists exhibit host preferences [31][149][170][171]. Moreover, community dynamics profoundly impact parasite–host relationships [47][48][143][144][172][173]. Numerous life forms interact directly or indirectly with mistletoe, exhibiting either generalist or specialist behavior in doing so [6][47][48][49][51][52][174][175][176]. Thus, field surveyors must consider influences under various circumstances before taking into account mistletoes’ infectivity, host preferences, and inherent resistance in the hosts within a particular geographical area (especially dense forest settings and commercial tree plantations). Vegetation disturbances such as the incidences of dead trees, grazing, logging, forest fires, and human waste disposal, among many others, may both positively and negatively affect mistletoe prevalence [16][177][178][179][180]. Other than these, mistletoes may differ in their ability to readily establish seedling growth and mature persistently on various hosts [147][181][182]. Mistletoes such as Psittacathus calyculatus, Dendrophthoe falcata, and Phoradendron californicum associate readily with leguminous tree hosts [3][5][183]. Mistletoes’ diversity and evolution may be effectuated by host shifts, followed by host specialization, as well as variations in climate and environment [184]. In addition to these factors, mistletoes’ success as parasites also depends on their complex interactions with herbivores, pollinators, and seed dispersers, such as birds, insects, and bats [6][7][176][185][186][187][188]. Many also believe that the genetic structuring and isolation of mistletoe into populations growing on various hosts within a community is attributed to these avian gene dispersal vectors [7][8][189]. However, based on the notion that most of these agents are insufficiently specialized, some believe that mistletoe speciation is mainly driven by host–parasite interplay [148][174][175][184][190][191][192]. Inconsistencies in mistletoe frequency within host populations are primarily due to seed dispersal mechanisms and disperser behavior. Some mistletoes (such as Arceuthobium spp.) exhibit explosive or ballistic seed dispersal [51]. Bird-dispersed mistletoes generally show a patchy distribution, which is attributable to birds’ eating, roosting, and nesting behaviors [5][20][193][194][195]. Forests with endemic marsupial seed dispersers may hold a similar analogy for effects on mistletoe prevalence and distributions [174][196][197][198]. Many host factors, such as tree diversity [54][147], height, crown width [9][15][173][199][200][201], and bark type [141], as well as the recently studied stand characteristics [202], regulate mistletoes’ colonization and density. These factors may also variously influence seed disperser behaviors. For example, the Sonoran desert mistletoe (Phoradendron californicum) seeds are reported to be less frequently deposited on host tree species Cercidium microphyllum and Acacia constricta [183]. The dense, thorny, and entangling crowns in these trees probably do not facilitate the perching behavior of avian dispersers [183]. Additionally, competition among the host trees may reduce resource availability and negatively impact mistletoe infection and occurrence [46]. Hosts may influence the reproductive phenology of their mistletoe parasites [203]. This could be indirectly orchestrated by host-mediated influences over the pollinator communities with distinct pollinator rewards and those over mistletoes with pollen receipts, as well as avian visitations from distinct taxa on distinct hosts [204][205].

3.7. Transcriptomic/Metabolomic Profiling, Transgenic Trees, and Translational Research Pipeline

The genetic modification of mistletoe hosts to induce resistance, resulting in a new variety, could be a promising strategy for reducing damage [206]. This would require the development of screening programs to characterize the viable sources of host resistance to each of the mistletoes (Figure 4). Such screens can be examined for molecular DNA tags, aiding in expedited marker-assisted selection for mistletoe-resistant hosts. Nonetheless, limited but considerable progress has been made in this direction [95][207][208][209][210]. Metabolomic profiling in other parasitic plants indicated the upregulation of auxin-responsive genes at the host–parasite interface [211][212]. Ichihashi’s group recently carried out both transcriptomic and metabolomic profiling of haustoria in the root hemiparasite Thesium chinense, revealing upregulated transcripts for genes involved in the biosynthesis and signaling of very long-chain fatty acids, auxin, and lateral rhizogenesis [213]. Along similar lines, Wang’s group attempted tissue-specific transcriptomics and whole-genome expression profiling of the shoot, flower, fruit, and seeds of spruce dwarf mistletoe (Arceuthobium sichuanse), revealing 22,641 differentially expressed genes related majorly to photosynthesis, carbohydrate and cell metabolism, transcription, hormone biosynthesis, and their signaling [214]. Recently, Wahid’s work extensively used tools such as suppression subtractive hybridization (SSH) and next-generation sequencing (NGS) to report some 1279 genes in Ziarat junipers (Juniperus excelsa) in Balochistan, which might putatively confer resistance to the dwarf mistletoe Arceuthobium oxycedri [215][216]. Transcriptome profiling of Taxillus nigrans individuals on four different tree hosts revealed many host-specific and common pathways driving this mistletoe’s parasitism [217].
Biology 11 01645 g004 550
Figure 4. Resource-tapping possibilities from genetic pools to strategize transgenic host resistance to mistletoes. The gap in functional genomics studies on mistletoe parasitism has majorly limited the exogenous induction and/or introduction of mistletoe resistance in hosts. This would require, in principle, the characterization of genetic targets in mistletoe and tree hosts that signal and favor easy entry to mistletoes (shown here) and then testing of the conventional gene manipulation and transgenics’ frameworks (see Figure 5). Even putative MBCAs can be screened for genetic elements encoding factors detrimental to mistletoe parasitism and/or its life cycle.
Biology 11 01645 g005 550
Figure 5. Generalized transgenic and translational research pipeline for developing and disseminating stable mistletoe-resistant tree hosts of commercial value(s). Genetic elements (or their homologs) putatively conferring mistletoe resistance may be recovered from relevant repositories such as the NCBI’s GenBank and KEGG, and also may be screened using systems biology and bioinformatics tools, following genomic, transcriptomic, and metabolomic analyses. Some suggestions are depicted in Figure 4. Precisely, such meta-analyses can be performed on various pairs of genetic/expression pools. Once the genetic elements directly encoding the resistance trait or indirectly influencing the parasitism are stipulated, they may be tested on various grounds in small-scale assays and observations, in order to plan the appropriate design of the transgenic framework. In this way, cell and tissue culture models of parasitism involving trees and mistletoes may be indispensable and may generate proof(s) of concept(s). Then, a focused transgenic gene manipulation and characterization stage would involve lab-to-field-scale testing and validation of the successfully developed events. Translational activities would follow commercialization requisites on a case-by-case basis.
Research into transgenics would require a greater understanding of mistletoe’s genetics and molecular basis, as well as the dynamics and kinetics of materials’ flow between the host and its parasite (Figure 4). Alternatively, where the same mistletoe parasitizes multiple hosts, it might be interesting to identify similar genetic and/or molecular elements, their influences, and their interactions within these frameworks. In addition, a comprehensive comparison of meta-analyses arising from infection instances between the same host and different parasite pairs could provide insight into rigidities, flexibilities, crucial events, genetic elements, and/or their encoded influences within these frameworks. These characterizations may lead to the development and testing of transgenic host(s) that are resistant to mistletoe attacks, but also produce fruit and timber in a qualitative and quantitative manner. Technically speaking, genetic engineering is endowed with certain choices of gene knockout and gene silencing options. In addition to site-directed mutagenesis, RNA antisense, small interfering RNA (si-RNA), and the CRISPR-Cas9 approaches, there are time-tested ways to manipulate transcription factors [218][219][220][221][222]. The use of transgenic tree crops for translational research (Figure 5) would revolutionize and open new avenues for commercial fruit and timber businesses worldwide, eliminating the need for the cost-, time-, and labor-intensive management of mistletoe pests, and potentially ending primitive conventional methods that are not eco-friendly. Other than this, transgenic approaches may be combined with chemical control options. This may be realized by developing hosts that can withstand the otherwise mistletoe-intolerable levels of herbicides while delivering them to deter mistletoe hemiparasites. In this arena, it is believed that much of the background work has already been done, as in Oronache and Striga [135][223], and can also be seen in the launch of a transcriptome meta-analysis initiative, the Parasitic Plant Genome Project [224]. There are a variety of reports that offer foundational studies on tree functional genomics [225][226][227][228][229][230]. As highlighted before, biotechnological approaches such as genetic engineering and plant tissue culture [231][232] have been underutilized, which indeed could represent a step away from conventional breeding strategies. There are few examples where tree transformation has been attempted in this regard. This should be seen as a critical requirement for introducing the usefully valued trait into specific fruit and timber tree cultivars [233]. In mitigating the mistletoes, however, such initiatives are yet to see fruitful realization and technology translations.

3.8. Role of Epigenetic Signaling in Mistletoe Parasitism: Moving beyond the Genetic Basis

It is also important for scientists to determine how mistletoe parasitism is epigenetically modulated or influenced. Mistletoes exhibit epigenetic influences in their foliar appearance, mimicking their hosts [234]. It has been previously reported that the unusual behavior of the loranth Dendrophthoe falcata var. falcata, exhibiting two different haustorial types on different fruit tree hosts [2]. Moreover, in areas where more probable and notable hosts were present, only a few uncommon hosts succumbed to infection by D. falcata [2]. Why was this so? It would be imperative to test whether the epicortical roots emerging from D. falcata from one host can attach to a different or the same host in proximity. In a similar manner, some of the other basic questions that are intriguing in this context may be as follows: What signals enable mistletoe seeds to germinate on existing hosts? How do mistletoes expand their host tropism in light of the ever-increasing list of newer hosts? Answers to these questions would offer more useful and efficient strategies to control mistletoes. One such strategy could consider manipulating plant signaling by transgenic and epigenetic interventions, and these may easily be integrated into pest management plans such as silviculture. Both mistletoes (for infection) and their host(s) (for defense) inflict changes in in each other’s physiological and chemical profiles [19][54]. There is still uncertainty as to whether mistletoe–host interactions involve any chemical warning signals analogous to the aposematism seen in other parasites [235]. On the mistletoe’s end, some investigative leads have been gained; for example, the gelatinous seed coat material in Phoradendron spp., viscin, is known to signal host/non-host responses [55][56]. Furthermore, to initiate attachment with the host, the mistletoes require seed germination stimulants (such as ethylene and nucleophilic protein receptor) and a diversity of haustoria-inducing factors (HIFs) [149][236]. HIFs such as xyloglucan endotransgycosylases (XETs), expansins, glucanases, and cell wall hydrolases are expressed in mistletoes [57]. XETs may facilitate haustorial progression into hosts by delinking xyloglucans, which make up the secondary walls in the host vasculature [237][238]. Other HIFs comprise strigolactones, quinones, and flavonoids [149][239][240][241]. Oxidative degradation of host cell wall lignin by the action of peroxidases and H2O2 may also activate HIFs [242]. The defense signals to mistletoes from the host side are analogous to that against herbivores and other biotic stressors [172][243][244][245][246]. These are marked by anatomical variations such as lignification, suberization [247][248][249], and the formation of secondary growth-like wound periderm [168][250], all of which variously oppose progression processes from mistletoes [247]. In addition, hosts respond to mistletoe attack by making inherent changes to their hormone profiles, such as abscisic acid, jasmonic acid, salicylic acid, and indole-6-aminoacid [248]. This may increase levels of potent secondary metabolites such as tannins, terpenes, and phenolic compounds [27][170][243][245][246][251][252]. Furthermore, the infection site may display the accumulation of volatile compounds and ROS, in turn triggering enzyme cascades that signal for apoptosis, culminating in defoliation [27][248][251]. The signaling crosstalk involved during the mistletoe life cycle over a host should therefore be examined for potential candidates that drive the epigenetic control over chemical dynamics. It is also likely that a precise understanding of the epigenetic framework that governs mistletoe–insect interactions may facilitate easier and more effective screening for MBCAs.

3.9. Smart Mistletoe Management: How the 21st Century Can Mitigate the Mistletoe Problem

Herein, it resources do not majorly document any new developments with conventional mistletoe management approaches due to technical glitches or technological paucity. Recently, a group described a novel handheld tool, ‘Mistletoe Eradicator’, which simultaneously provides both mechanical pruning and chemical treatment [253]. The 21st century offers a huge range of possibilities with advancements into big data, automation, artificial intelligence, and platforms such as the Internet of Things (IoTs). Newer technologies such as artificial intelligence, satellite imaging (remote sensing), image recognition, drones, and weather forecasting can be utilized in substantiating smart solutions for mistletoe pest management programs. For example, intelligent drones may permit the aerial screening of forest canopies for mistletoes, as well as for carrying out physical (pruning) and chemical treatments (herbicide spraying, branch injections and so on). To make this possible, detection algorithms would need precision in screening and classifying mistletoes, which might face challenges resulting from the huge diversity of mistletoes, their growth stages, geographical settings, climates, canopy structures, size, density and so on [54][254][255][256][257][258][259]. Moreover, many mistletoe species are known to mimic their hosts in foliar structures [260]. Moser and Campione showed the successful use of Google Earth as a remote sensing tool to detect eastern spruce dwarf mistletoe in the forests of Minnesota [261]. A group from Mexico recently developed a genetic programming-based algorithm that screens mistletoe Phoradendron velutinum using multispectral aerial images collected on a radiation sensor fitted to an unmanned aerial vehicle [262]. This algorithm classifies P. velutinum based on its flowering stage. Before this, several groups had developed other algorithms based on thermal imaging, hyperspectral lines, convolutional neural networks, canopy height, colorimetry, etc. [263][264][265][266][267][268][269]. If developments into these dimensions are studied further, the effective selection of conventional and biotechnological treatment approaches may lead to a productive synchrony with silviculture. Silvicultural decisions such as treatment area and treatment schedule depend on precise knowledge of and attention to the epidemiology of mistletoes and their pathogens, mistletoe population dynamics, and the silvics of the mistletoes’ hosts [95]. In this regard, even automation and artificial intelligence solutions may offer better time-saving, labor-saving, and cost-saving prospects, as well as being amenable to modifications on a case-by-case basis.

Considering the aforementioned promising approaches, and not neglecting the ecological value of the mistletoes (in being a keystone resource for biodiversity), the genetic engineering of hosts to develop, induce, and enhance specific resistance will be greatly rewarding. Even though its benefits include being environmentally safe and with no use of chemical agents, due to the additional labor, costs, complicated management, as well as potential to wipe out the parasite seed banks on hosts, this approach has remained unrealized [135]. Such transgenic trees would satisfy both (i) the conservation of the biodiversity and medicinal value aspects of mistletoes and (ii) aims to foresee a fruit and timber business that is unaffected by mistletoe. Successful examples of the transgenic approach are known in relation to other parasitic weeds, such as Striga, Orobanche, and Cuscuta . In this regard, herein, it was intended to supply blueprints for transgenic and translational research into developing and commercializing stable mistletoe-resistant tree cultivars.

Herein, ecological significance and medicinal value of mistletoes do not be underestimated, both in traditional and modern treatment practices. However, here it was emphasized the development and implementation of more feasible management solutions for highly damaging mistletoes that affect commercial tree plantations. The risks surely outweigh the usefulness of mistletoes in such settings, as others pointed out long ago [124]. Thus, tree decline, combined with mistletoe, cannot be overlooked in itself as a major factor negatively impacting biodiversity and commerce. Hopefully, the biotechnological and smart management approaches discussed here, if operationalized in the future, should serve as a paradigm shift in mistletoe management.

This entry is adapted from the peer-reviewed paper 10.3390/biology11111645

References

  1. Choi, S.-U.; Kim, S.T.; Han, D.G.; Hwang, Y.-H.; Lee, K.Y.; Kim, D.U.; Cho, K.H.; Park, S.Y.; Kim, H.-C.; Kim, S.-B.; et al. Comparative Assessment of Biological Activities of Mistletoes for Cosmetic Applications: Viscum Album Var. Coloratum (Kom.) Ohwi and Loranthus Tanakae Franch. & Sav. J. Cosmet. Sci. 2019, 70, 235–245.
  2. Mudgal, G.; Mudgal, B. Evidence for unusual choice of host and haustoria by Dendrophthoe falcata (Lf) Ettingsh, a leafy mistletoe. Arch. Phytopathol. Plant Prot. 2011, 44, 186–190.
  3. Mudgal, G.; Mudgal, B.; Gururani, M.A.; Jelli, V. Pseudaulacaspis cockerelli (Cooley) hyperparasitizing Dendrophthoe falcata (Lf) Ettingsh. Arch. Phytopathol. Plant Prot. 2011, 44, 282–286.
  4. Singh, S.R.; Piloo, N.; Senjam, P.; Hemanta, L. Need of awareness programme to control the loranthus weed–Helixanthera ligustrina. Agri-India Today 2021, 1, 10–13.
  5. Arce-Acosta, I.; Suzán-Azpiri, H.; García-Rubio, O. Biotic factors associated with the spatial distribution of the mistletoe Psittacanthus calyculatus in a tropical deciduous forest of central Mexico. Bot. Sci. 2016, 94, 89–96.
  6. Fadini, R.F.; Fischer, E.; Castro, S.J.; Araujo, A.C.; Ornelas, J.F.; de Souza, P.R. Bat and bee pollination in Psittacanthus mistletoes, a genus regarded as exclusively hummingbird-pollinated. Ecology 2018, 99, 1239–1241.
  7. Infante, S.D.; Lara, C.; del Coro Arizmendi, M.; Eguiarte, L.E.; Ornelas, J.F. Reproductive ecology and isolation of Psittacanthus calyculatus and P. auriculatus mistletoes (Loranthaceae). PeerJ 2016, 4, e2491.
  8. Pérez-Crespo, M.J.; Lara, C.; Ornelas, J.F. Uncorrelated mistletoe infection patterns and mating success with local host specialization in Psittacanthus calyculatus (Loranthaceae). Evol. Ecol. 2016, 30, 1061–1080.
  9. Teodoro, G.S.; van den Berg, E.; Santos, M.d.C.N.; de Freitas Coelho, F. How does a Psittacanthus robustus Mart. population structure relate to a Vochysia thyrsoidea Pohl. host population? Flora-Morphol. Distrib. Funct. Ecol. Plants 2010, 205, 797–801.
  10. Aliero, B.; Samaila, A. The occurrence of Parasitic mistletoe (Tapinanthus spp) on Parkia biglobosa (Jacq.) Benth (African Locust Bean Tree) in Yauri Local Government Area, Kebbi State. Niger. J. Basic Appl. Sci. 2000, 9, 5–10.
  11. Edagbo, D.E.; Ajiboye, T.O.; Borokini, T.I.; Ighere, D.A.; Alowonle, A.A.; Clement, M. The Influence of African Mistletoe (Tapinanthus bangwensis) on the Conservation Status and Productivity of Irvingia gabonensis in Moor Plantation Area of Ibadan, Nigeria. Int. J. Curr. Res. 2012, 4, 484–487.
  12. Kwon-Ndung, E.; Ismaila, A. Prospects of host resistance in improved and domesticated species of Parkia biglobosa to African mistletoes (Tapinanthus spp.) in Central Nigeria. Electron. J. Environ. Agric. Food Chem. 2009, 8, 382–388.
  13. Ávalos, V.M.C.; Collazo, I.V.; Flores, H.J.M.; Castillo, J.V. Impacto de tierra de diatomeas sobre Arceuthobium globosum Hawksworth & Wiens subsp. grandicaule en Pinus pseudostrobus Lindl. Rev. Mex. Cienc. For. 2010, 1, 39–46.
  14. Gilbert, J.A. The Biology of Dwarf Mistletoes (Arceuthobium spp.) in Manitoba. Master Thesis, University of Manitoba, Winnipeg, MB, Canada, 1984.
  15. Hernández-Benítez, R.; Cano-Santana, Z.; Castellanos-Vargas, I. Incidencia de infestación de Arceuthobium globosum grandicaule (Hawks. y Wiens) en Pinus hartwegii (Lindl.). Cienc. For. En México 2005, 30, 79–86.
  16. Queijeiro-Bolanos, M.E.; Cano-Santana, Z.; Castellanos-Vargas, I. Does disturbance determine the prevalence of dwarf mistletoe (Arceuthobium, Santalales: Viscaceae) in Central Mexico? Rev. Chil. De Hist. Nat. 2013, 86, 181–190.
  17. Shaw, D.C.; Agne, M.C.J.B. Fire and dwarf mistletoe (Viscaceae: Arceuthobium species) in western North America: Contrasting Arceuthobium tsugense and Arceuthobium americanum. Botany 2017, 95, 231–246.
  18. Villier, J.A.d.; Reblin, J.S.; Logan, B.A. Needle properties of host white spruce (Picea glauca Voss) experiencing eastern dwarf mistletoe (Arceuthobium pusillum Peck) infections of differing severity. Botany 2017, 95, 295–305.
  19. Anselmo-Moreira, F.; Teixeira-Costa, L.; Ceccantini, G.; Furlan, C.M. Mistletoe effects on the host tree Tapirira guianensis: Insights from primary and secondary metabolites. Chemoecology 2019, 29, 11–24.
  20. Solís-Gracia, V.; Suzán-Azpiri, H. Análisis de la distribución espacial del muérdago (Phoradendron californicum) en el sur del Desierto Sonorense. Cactáceas Suculentas Mex. 2014, 59, 11–28.
  21. Wiens, D.; Hawksworth, F. New species of Phoradendron (Viscaceae) from Mexico and Guatemala and a synopsis of species in section Pauciflorae. Aliso J. Syst. Evol. Bot. 2002, 21, 33–43.
  22. Ahmad, S.; Mir, N.; Sultan, S. White-berry mistletoe (Viscum album L.): A hemiparasitic plant: Occurrence and ethnobotanical use in Kashmir. J. Pharmacogn. Phytochem. 2018, 7, 1831–1833.
  23. Alam, M. A critical review on the biology and control of Loranthaceae with a particular reference to Bangladesh. Bano Biggyan Patrika 1984, 13, 7–18.
  24. Barbu, C. Impact of mistletoe attack (Viscum album ssp. abietis) on the radial growth of silver fir. A case study in the North of Eastern Carpathians. Ann. For. Res. 2009, 52, 89–96.
  25. Bilgili, E.; Coskuner, K.A.; Öztürk, M. Leaf area–sapwood area relationship in Scots pine (Pinus sylvestris L.) under mistletoe (Viscum album ssp. austriacum) infection. Dendrobiology 2020, 84, 1–11.
  26. Dobbertin, M.; Rigling, A. Pine mistletoe (Viscum album ssp. austriacum) contributes to Scots pine (Pinus sylvestris) mortality in the Rhone valley of Switzerland. For. Pathol. 2006, 36, 309–322.
  27. Mutlu, S.; Osma, E.; Ilhan, V.; Turkoglu, H.I.; Atici, O. Mistletoe (Viscum album) reduces the growth of the Scots pine by accumulating essential nutrient elements in its structure as a trap. Trees 2016, 30, 815–824.
  28. Ozturk, M.; Coskuner, K.A.; Serdar, B.; Atar, F.; Bilgili, E. Impact of white mistletoe (Viscum album ssp. abietis) infection severity on morphology, anatomy and photosynthetic pigment content of the needles of cilicican fir (Abies cilicica). Flora 2022, 294, 152135.
  29. Ozturk, M.; Coskuner, K.A.; Usta, Y.; Serdar, B.; Bilgili, E. The effect of mistletoe (Viscum album) on branch wood and needle anatomy of Scots pine (Pinus sylvestris). IAWA J. 2019, 40, 352–365.
  30. Nickrent, D.L. Parasitic angiosperms: How often and how many? Taxon 2020, 69, 5–27.
  31. Glatzel, G.; Geils, B. Mistletoe ecophysiology: Host–parasite interactions. Botany 2008, 87, 10–15.
  32. Calvin, C.L.; Wilson, C.A. Comparative morphology of epicortical roots in Old and New World Loranthaceae with reference to root types, origin, patterns of longitudinal extension and potential for clonal growth. Flora-Morphol. Distrib. Funct. Ecol. Plants 2006, 201, 51–64.
  33. Barlow, B. MIstletoes in Australia. Available online: http://www.anbg.gov.au/mistletoe/haustoria.html (accessed on 12 January 2020).
  34. Wilson, C.A.; Calvin, C.L. An origin of aerial branch parasitism in the mistletoe family, Loranthaceae. Am. J. Bot. 2006, 93, 787–796.
  35. Smith, S.; Stewart, G.R. Effect of Potassium Levels on the Stomatal Behavior of the Hemi-Parasite Striga hermonthica. Plant Physiol. 1990, 94, 1472–1476.
  36. Lo Gullo, M.A.; Glatzel, G.; Devkota, M.; Raimondo, F.; Trifilò, P.; Richter, H. Mistletoes and mutant albino shoots on woody plants as mineral nutrient traps. Ann. Bot. 2012, 109, 1101–1109.
  37. Karunaichamy, K.S.T.K.; Paliwal, K.; Arp, P.A. Biomass and nutrient dynamics of mistletoe (Dendrophthoe falcata) and neem (Azadirachta indica) seedlings. Curr. Sci. 1999, 76, 840–842.
  38. Schulze, E.D.; Turner, N.; Glatzel, G. Carbon, water and nutrient relations of two mistletoes and their hosts: A hypothesis. Plant Cell Environ. 1984, 7, 293–299.
  39. Zweifel, R.; Bangerter, S.; Rigling, A.; Sterck, F.J. Pine and mistletoes: How to live with a leak in the water flow and storage system? J. Exp. Bot. 2012, 63, 2565–2578.
  40. Urban, J.; Gebauer, R.; Nadezhdina, N.; Čermák, J. Transpiration and stomatal conductance of mistletoe (Loranthus europaeus) and its host plant, downy oak (Quercus pubescens). Biologia 2012, 67, 917–926.
  41. Glatzel, G. Mineral nutrition and water relations of hemiparasitic mistletoes: A question of partitioning. Experiments with Loranthus europaeus on Quercus petraea and Quercus robur. Oecologia 1983, 56, 193–201.
  42. Yang, D.; Goldstein, G.; Wang, M.; Zhang, W.-W.; Wang, A.-Y.; Liu, Y.-Y.; Hao, G.-Y. Microenvironment in the canopy rivals the host tree water status in controlling sap flow of a mistletoe species. Tree Physiol. 2017, 37, 501–510.
  43. Rigling, A.; Eilmann, B.; Koechli, R.; Dobbertin, M. Mistletoe-induced crown degradation in Scots pine in a xeric environment. Tree Physiol. 2010, 30, 845–852.
  44. Dobbertin, M.; Hilker, N.; Rebetez, M.; Zimmermann, N.E.; Wohlgemuth, T.; Rigling, A. The upward shift in altitude of pine mistletoe (Viscum album ssp. austriacum) in Switzerland—The result of climate warming? Int. J. Biometeorol. 2005, 50, 40–47.
  45. Doležal, J.; Lehečková, E.; Sohar, K.; Altman, J. Oak decline induced by mistletoe, competition and climate change: A case study from central Europe. Preslia 2016, 88, 323–346.
  46. Matula, R.; Svátek, M.; Pálková, M.; Volařík, D.; Vrška, T. Mistletoe infection in an oak forest is influenced by competition and host size. PLoS ONE 2015, 10, e0127055.
  47. Aukema, J.E.; Martinez del Rio, C. Mistletoes as parasites and seed-dispersing birds as disease vectors: Current understanding, challenges, and opportunities. In Seed Dispersal and Frugivory: Ecology, Evolution, and Conservation; CABI International: Wallingford, UK, 2002; pp. 99–110.
  48. Aukema, J.E.; Martínez del Rio, C. Where does a fruit-eating bird deposit mistletoe seeds? Seed deposition patterns and an experiment. Ecology 2002, 83, 3489–3496.
  49. Reid, N. Coevolution of mistletoes and frugivorous birds? Aust. J. Ecol. 1991, 16, 457–469.
  50. Green, A.K.; Ward, D.; Griffiths, M.E. Directed dispersal of mistletoe (Plicosepalus acaciae) by Yellow-vented Bulbuls (Pycnonotus xanthopygos). J. Ornithol. 2009, 150, 167–173.
  51. Mathiasen, R.L.; Nickrent, D.L.; Shaw, D.C.; Watson, D.M. Mistletoes: Pathology, systematics, ecology, and management. Plant Dis. 2008, 92, 988–1006.
  52. Watson, D.M. The Relative Contribution of Specialists and Generalists to Mistletoe Dispersal: Insights from a Neotropical Rain Forest. Biotropica 2013, 45, 195–202.
  53. Albert, S.; Rhumeur, A.; Rivière, J.L.; Chauvrat, A.; Sauroy-Toucouère, S.; Martos, F.; Strasberg, D. Rediscovery of the mistletoe Bakerella hoyifolia subsp. bojeri (Loranthaceae) on Reunion Island: Population status assessment for its conservation. Bot. Lett. 2017, 164, 229–236.
  54. Medel, R.; Vergara, E.; Silva, A.; Kalin-Arroyo, M. Effects of vector behavior and host resistance on mistletoe aggregation. Ecology 2004, 85, 120–126.
  55. Gill, L.S.; Hawksworth, F.G. The Mistletoes: A Literature Review; US Department of Agriculture: Washington, DC, USA, 1961.
  56. Berry, A.M.; Lichter, J.M.; Reid, M.S. New Methods for Mistletoe Control. Available online: http://slosson.ucdavis.edu/newsletters/Berry_199129111.pdf (accessed on 29 December 2019).
  57. Ko, S.M.; Kwon, Y.K.; Kim, J.H.; Song, I.-J.; Lee, H.-Y.; Choi, D.-W.; Liu, J.R.; Kim, S.W. Transcriptome analysis of mistletoe (Viscum album) haustorium development. Hortic. Environ. Biotechnol. 2014, 55, 352–361.
  58. Scharpf, R.F.; Smith, R.S.; Vogler, D. Management of Western Dwarf Mistletoe in Ponderosa and Jeffrey Pines in Forest Recreation Areas; Pacific Southwest Research Station, Forest Service; US Department of Agriculture: Washington, DC, USA, 1988; Volume 103, 11p.
  59. Beatty, J.S.; Mathiasen, R.L. Dwarf Mistletoes of Ponderosa Pine; US Department of Agriculture, Forest Service: Washington, DC, USA, 2003.
  60. Pearson, G.; Marsh, R. Timber Growing and Logging Practice in the Southwest and in the Black Hills Region. Available online: https://naldc.nal.usda.gov/download/CAT86200474/PDF (accessed on 22 October 2022).
  61. Knutson, D. Biological and chemical control of dwarf mistletoe. In Proceedings of the Symposium on Dwarf Mistletoe Control through Forest Management, Berkeley, CA, USA, 11–13 April 1978; Gen. Tech. Rep. PSW-31. Scharpf, R.F., Parmeter, J.R., Jr., Eds.; U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: Berkeley, CA, USA, 1978; pp. 151–155.
  62. Milenkovic, M.; Karadzic, D.; Janjic, V.; Mihajlovic, L. Possibilities of mistletoe control. In Proceedings of the Peti Kongres o Korovima, Banja Koviljaca, Serbia, 18–21 June 1996.
  63. Watson, D. Reconnaissance and Recommendations for Mistletoe Management in Macadamia Orchards; Final Report; Hort Innovation: North Sydney, Australia, 2019; pp. 1–30.
  64. Reid, N.; Shamoun, S.F. Contrasting research approaches to managing mistletoes in commercial forests and wooded pastures. Botany 2008, 87, 1–9.
  65. Yan, C.-F.; Gessler, A.; Rigling, A.; Dobbertin, M.; Han, X.-G.; Li, M.-H. Effects of mistletoe removal on growth, N and C reserves, and carbon and oxygen isotope composition in Scots pine hosts. Tree Physiol. 2016, 36, 562–575.
  66. Walldén, B. Misteln vid dess nordgräns: Die Mistel an Ihrer Nordgrenze. Svensk Botanisk Tidskrift 1961, 55, 123.
  67. Weber, H. Untersuchungen zur Entwicklungsweise der Laubholzmistel Viscum album L.(Viscaceae) und über Zuwachsraten während ihrer ersten Stadien. Beiträge Zur Biol. Der Pflanz. 1993, 67, 319–331.
  68. Hoffman, J. Management Guide for Dwarf Mistletoe. Arceuthobium spp. Forest Health Protection and State Forestry Organizations. Available online: https://www.fs.usda.gov/Internet/FSE_DOCUMENTS/stelprdb5187427.pdf (accessed on 22 October 2022).
  69. Zielke, K.; Bancroft, B. Introduction to Silvicultural Systems (Web-Based Workbook). Available online: https://www.for.gov.bc.ca/hfd/pubs/ssintroworkbook/append2.htm (accessed on 20 July 2020).
  70. Parmeter, J.; Scharpf, R.F. Spread of Dwarf Mistletoe from Discrete Seed Sources into Young Stands of Ponderosa and Jeffrey Pines; US Forest Service: Washington, DC, USA; US Department of Agriculture, Pacific Southwest Forest and Range: Vallejo, CA, USA, 1972; Volume 269.
  71. Scharpf, R.F.; Parmeter, J. Seed Production and Dispersal by Dwarf Mistletoe in Overstory Jeffrey Pines in California; US Forest Service: Washington, DC, USA; US Department of Agriculture, Pacific Southwest Forest and Range: Berkeley CA, USA, 1971; Volume 247.
  72. Scharpf, R.F.; Parmeter, J.R., Jr. Spread of Dwarf Mistletoe into Jeffrey Pine Plantation-Trees Infected after 22 Years; U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: Berkeley, CA, USA, 1976; 6p.
  73. Reid, N.; Yan, Z. Mistletoes and Other Phanerogams Parasitic on Eucalypts; CSIRO: Canberra, Australia, 2000; pp. 353–384.
  74. Kelly, P.; Reid, N.; Davies, I. Effects of experimental burning, defoliation, and pruning on survival and vegetative resprouting in mistletoes (Amyema miquelii and Amyema pendula). Int. J. Plant Sci. 1997, 158, 856–861.
  75. Conklin, D.A.; Geils, B.W. Survival and sanitation of dwarf mistletoe-infected ponderosa pine following prescribed underburning. West. J. Appl. For. 2008, 23, 216–222.
  76. Koonce, A.L.; Roth, L.F. The effects of prescribed burning on dwarf mistletoe in ponderosa pine. In Proceedings of the Sixth Conference on Fire and Forest Meteorology, Seattle, WA, USA, 22–24 April 1980; pp. 22–24.
  77. Ritter, S.; Hoffman, C.; Stewart, J.; Zimmerman, T. The influence of prescribed crown fire on lodgepole pine dwarf mistletoe (Arceuthobium americanum) populations 33 years post-fire. For. Pathol. 2018, 48, e12419.
  78. Alexander, M.E.; Hawksworth, F.G. Fire and dwarf mistletoes in North American coniferous forests. J. For. 1976, 74, 446–449.
  79. Kipfmueller, K.F.; Baker, W.L. Fires and dwarf mistletoe in a Rocky Mountain lodgepole pine ecosystem. For. Ecol. Manag. 1998, 108, 77–84.
  80. Manion, P. Tree Diseases Concepts, 2nd ed.; Prentice-Hall: Englewood Cliffs, NJ, USA, 1991.
  81. Knight, D.H. Parasites, lightning, and the vegetation mosaic in wilderness landscapes. In Landscape Heterogeneity and Disturbance; Springer: Berlin/Heidelberg, Germany, 1987; pp. 59–83.
  82. Conklin, D.A.; Armstrong, W.A. Effects of Three Prescribed Fires on Dwarf Mistletoe Infection in Southwestern Ponderosa Pine; US Department of Agriculture, Forest Service, Southwestern Region: Berkeley CA, USA, 2001.
  83. Haikerwal, A.; Reisen, F.; Sim, M.R.; Abramson, M.J.; Meyer, C.P.; Johnston, F.H.; Dennekamp, M. Impact of smoke from prescribed burning: Is it a public health concern? J. Air Waste Manag. Assoc. 2015, 65, 592–598.
  84. Afrin, S.; Garcia-Menendez, F. Potential impacts of prescribed fire smoke on public health and socially vulnerable populations in a Southeastern, U.S. state. Sci. Total Environ. 2021, 794, 148712.
  85. Cirocco, R.M.; Facelli, J.M.; Watling, J.R. High water availability increases the negative impact of a native hemiparasite on its non-native host. J. Exp. Bot. 2015, 67, 1567–1575.
  86. Griebel, A.; Metzen, D.; Pendall, E.; Nolan, R.H.; Clarke, H.; Renchon, A.A.; Boer, M.M. Recovery from Severe Mistletoe Infection After Heat- and Drought-Induced Mistletoe Death. Ecosystems 2022, 25, 1–16.
  87. Griebel, A.; Peters, J.M.R.; Metzen, D.; Maier, C.; Barton, C.V.M.; Speckman, H.N.; Boer, M.M.; Nolan, R.H.; Choat, B.; Pendall, E. Tapping into the physiological responses to mistletoe infection during heat and drought stress. Tree Physiol. 2021, 42, 523–536.
  88. Sidahmed, O.A. Incidence of mistletoe (Loranthus spp.) on citrus and guava trees in the central region of the Sudan. In Proceedings of the VIII African Symposium on Horticultural Crops 143, Wed Medani, Sudan, 20–24 March 1983; pp. 417–420.
  89. Knutson, D.M. The influence of urea fertilization on growth of mistle-toed pine seedlings. In Proceedings of the Second International Congress of plant pathology, Minneapolis, MN, USA, 5–12 September 1973; pp. 5–12.
  90. Kulkarni, H.D.; Srimathi, K. Plant pests of sandal (Santalum album L.). My For. 1988, 24, 29–38.
  91. Minko, G.; Fagg, P.C. Control of some mistletoe species on eucalypts by trunk injection with herbicides. Aust. For. 1989, 52, 94–102.
  92. Brown, A.; Greenham, C. Further investigations in the control of mistletoe by trunk injections. Aust. J. Exp. Agric. 1965, 5, 305–309.
  93. Brown, A. Mistletoe control on a large scale. J. Aust. Inst. Agric. Sci. 1959, 25, 282–286.
  94. Reid, N.; Fittler, J.; Kar, A.; Storey, A.; Cook, T. Effect of Spray Applications of Several Herbicides on the Mortality of Box Mistletoe (Amyema miquelii) and Host Saplings (Eucalyptus blakelyi and E. melliodora). In Ecosystem Management; University of New England: Armidale, Australia, 2008.
  95. Shamoun, S.; DeWald, L. Management strategies for dwarf mistletoes: Biological, chemical, and genetic approaches. In Mistletoes of North American Conifers; Geils, B.W., Tovar, J.C., Moody, B., Eds.; US Department of Agriculture, Forest Service, Rocky Mountain Research Station: Washington, DC, USA, 2002; Volume 98, pp. 75–82.
  96. Watson, W.T.; Martinez-Trinidad, T. Strategies and treatments for leafy mistletoe (Phoradendron tomentosum Engelm ex. Gray) suppression on cedar elm (Ulmus crassifolia Nutt.). Arboric. Urban For. 2006, 32, 265.
  97. Quick, C.R. Experimental Herbicidal Control of Dwarfmistletoe on Some California Conifers; U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station: Berkeley, CA, USA, 1964; Volume 47, 9p.
  98. Hawksworth, F.G.; Wiens, D. Dwarf Mistletoes: Biology, Pathology, and Systematics; Diane Publishing: Washington, DC, USA; Department of Agriculture, Forest Service: Washington, DC, USA, 1996; p. 410.
  99. Livingston, W.; Brenner, M. Ethephon stimulates abscission of eastern dwarf mistletoe aerial shoots on black spruce. Plant Dis. 1983, 67, 909–910.
  100. Livingston, W.H.; Blanchette, R.A.; Brenner, M.L.; Zuzek, K.J. Effective use of ethylene-releasing agents to prevent spread of eastern dwarf mistletoe on black spruce. Can. J. For. Res. 1985, 15, 872–876.
  101. Livingston, W.H.; Brenner, M.L.; Blanchette, R.A. Altered concentrations of abscisic acid, indole-3-acetic acid, and zeatin riboside associated eastern dwarf mistletoe infections on black spruce. In Proceedings of the Biology of Dwarf Mistletoes, Symposium Proceedings, Fort Collins, CO, USA, 8 August 1984; Gen. Tech. Rep. RM-111. Hawksworth, F.G., Scharpf, R.F., Eds.; U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station: Berkeley, CA, USA, 1984; pp. 53–60.
  102. Adams, D.H.; Frankel, S.J.; Lichter, J.M. Considerations when using ethephon for supressing dwarf and leafy mistletoe infestations in ornamental landscapes. J. Arboric. 1993, 19, 351–357.
  103. Watson, D.M.; Cook, M.E.; Fadini, R.R. Towards best-practice management of mistletoes in horticulture. Botany 2020, 98, 489–498.
  104. Winder, R.S.; Shamoun, S.F. Forest pathogens: Friend or foe to biodiversity? Can. J. Plant Pathol. 2006, 28, S221–S227.
  105. Robbins, K.; Johnson, D.W.; Hawksworth, F.G.; Nicholls, T.H. Aerial application of ethephon is ineffective in controlling lodgepole pine dwarf mistletoe. West. J. Appl. For. 1989, 4, 27–28.
  106. Baker, F.; Knowles, K.; Meyer, T.; French, D. Aerial applications of ethylene-releasing chemicals fail to promote abscission of dwarf mistletoe aerial shoots on Jack pine. For. Chron. 1989, 65, 194–195.
  107. Weber, H.C.; Forstreuter, W. Parasitismus von Blutenpflanzen; Wissenschaftliche Buchgesellschaft: Darmstadt, Germany, 1993.
  108. Parks, C.A.; Hoffman, J.T. Control of Western Dwarf Mistletoe with the Plant-Growth Regulator Ethephon; US Department of Agriculture, Forest Service, Pacific Northwest Research Station: Berkeley, CA, USA, 1991; Volume 506.
  109. Muir, J.; Geils, B. Management Strategies for Dwarf Mistletoe: Silviculture; Forest Service: Washington, DC, USA; USDA: Washington, DC, USA, 2002; pp. 83–94.
  110. Robinson, D.C.; Geils, B.W.; Muir, J.A. Spatial statistical model for the spread of dwarf mistletoe within and between stands. In Proceedings of the Second Forest Vegetation Simulator Conference, Fort Collins, CO, USA, 12–14 February 2002; Crookston, N.L., Havis, R.N., Eds.; pp. 178–185.
  111. Van Halder, I.; Castagneyrol, B.; Ordóñez, C.; Bravo, F.; del Río, M.; Perrot, L.; Jactel, H. Tree diversity reduces pine infestation by mistletoe. For. Ecol. Manag. 2019, 449, 117470.
  112. Fernández-Aparicio, M.; Delavault, P.; Timko, M.P. Management of Infection by Parasitic Weeds: A Review. Plants 2020, 9, 1184.
  113. Wyckhuys, K.A.G.; Hughes, A.C.; Buamas, C.; Johnson, A.C.; Vasseur, L.; Reymondin, L.; Deguine, J.P.; Sheil, D. Biological control of an agricultural pest protects tropical forests. Commun. Biol. 2019, 2, 10.
  114. Nzioki, H.S.; Oyosi, F.; Morris, C.E.; Kaya, E.; Pilgeram, A.L.; Baker, C.S.; Sands, D.C. Striga Biocontrol on a Toothpick: A Readily Deployable and Inexpensive Method for Smallholder Farmers. Front. Plant Sci. 2016, 7, 1121.
  115. Bale, J.; Van Lenteren, J.; Bigler, F. Biological control and sustainable food production. Philos. Trans. R. Soc. B Biol. Sci. 2008, 363, 761–776.
  116. Charudattan, R. Biological control of weeds by means of plant pathogens: Significance for integrated weed management in modern agro-ecology. BioControl 2001, 46, 229–260.
  117. Hawksworth, F.G.; Geils, B.W. Biotic Associates; Diane Publishing: Washington, DC, USA; Department of Agriculture, Forest Service: Washington, DC, USA, 1996.
  118. Hawksworth, F.G.; Wicker, E.F.; Scharpf, R.F. Fungal Parasites of Dwarf Mistletoes ; Department of Agriculture, Forest Service: Washington, DC, USA, 1977; p. 14.
  119. Kuijt, J. Distribution of Dwarf Mistletoes and Their Fungus Hyperparasites in Western Canada; Department of Northern Affairs and National Resources: Ottawa, ON, Canada, 1963; Volume 186, pp. 134–148.
  120. Stevens, R.E.; Hawksworth, F.G. Insect-dwarf mistletoe associations: An update. In Proceedings of the Symposium: Biology of Dwarf Mistletoes, Fort Collins, CO, USA, 8 August 1984; pp. 94–101.
  121. Stevens, R.E.; Hawksworth, F.G. Insects and Mites Associated with Dwarf Mistletoes; Research Papers; Rocky Mountain Forest and Range Experiment Station: Fort Collins, CA, USA, 1970; p. 12.
  122. Room, P. The constitution and natural history of the fauna of the mistletoe Tapinanthus bangwensis (Engl. & K. Krause) growing on cocoa in Ghana. J. Anim. Ecol. 1972, 41, 519–535.
  123. Patrick, B.H.; Dugdale, J.S. Mistletoe moths-New Zealand’s loranthaceous mistletoes. In Proceedings of the A Workshop Hosted by Threatened Species Unit, Department of Conservation, Cass, Wellington, New Zealand, 17–20 July 1995; p. 125.
  124. Baloch, G.; Mohyuddin, A. The phytophagous fauna of a mistletoe (Loranthus longiflorus Desr.: Loranthaceae) in West Pakistan. Weed Res. 1969, 9, 62–64.
  125. Mark, W.R.; Hawksworth, F.G.; Oshima, N. Resin disease: A new disease of lodgepole pine dwarf mistletoe. Can. J. For. Res. 1976, 6, 415–424.
  126. Wicker, E.F.; Shaw, C.G. Fungal parasites of dwarf mistletoes. Mycologia 1968, 60, 372–383.
  127. Nguyen, J.; Fernandez, V.; Pontrelli, S.; Sauer, U.; Ackermann, M.; Stocker, R. A distinct growth physiology enhances bacterial growth under rapid nutrient fluctuations. Nat. Commun. 2021, 12, 3662.
  128. Burman, E.; Bengtsson-Palme, J. Microbial Community Interactions Are Sensitive to Small Changes in Temperature. Front. Microbiol. 2021, 12, 1–8.
  129. Hardy, D.E. Studies of fruitflies associated with mistletoe in Australia and Pakistan with notes and decriptions on genera related to Perilampsis Bezzi (Diptera: Tephritidae). Beiträge Zur Entomol. Contrib. Entomol. 1967, 17, 127–149.
  130. Mushtaque, M.; Baloch, G. Possibilities of biological control of mistletoes, Loranthus spp., using oligophagous insects from Pakistan. Entomophaga 1979, 24, 73–81.
  131. Garbelotto, M.; Lowell, N.; Chen, I.Y.; Osmundson, T.W. Evidence for inhibition of a fungal biocontrol agent by a plant microbiome. J. Plant Pathol. 2019, 101, 457–466.
  132. Perry, E. Broadleaf Mistletoe in Landscape Trees; University of California: Berkeley, CA, USA, 1995; p. 14.
  133. Hanover, J.W. Tree improvement for disease resistance in western United States and Canada. In Breeding Pest-Resistant Trees; Elsevier: Amsterdam, The Netherlands, 1966; pp. 53–56.
  134. Rubiales, D. Parasitic plants, wild relatives and the nature of resistance. New Phytol. 2003, 160, 459–461.
  135. Aly, R.; Dubey, N.K. Weed Management for Parasitic Weeds. In Recent Advances in Weed Management; Springer: Berlin/Heidelberg, Germany, 2014; pp. 315–345.
  136. Hawksworth, F.G. Biological factors of dwarf mistletoe in relation to control. In Proceedings of the Symposium on Dwarf Mistletoes Control through Forest Management, Berkeley, CA, USA, 11–13 April 1978; Gen. Tech. Rep. PSW-31. pp. 5–15.
  137. Roth, L.F. Genetic control of dwarf mistletoe. In Proceedings of the Symposium on Dwarf Mistletoes Control through Forest Management, Berkeley, CA, USA, 11–13 April 1978; pp. 69–72.
  138. Scharpf, R.F.; Roth, L.F. Resistance of Ponderosa Pine to Western Dwarf Mistletoe in Central Oregon; Res. Pap. PSW-RP-208; US Department of Agriculture, Pacific Southwest Forest and Range: Albany, CA, USA, 1992; Volume 208, 9p.
  139. Roth, L.F. Resistance of ponderosa pine to dwarf mistletoe. Silvae Genet. 1974, 23, 116–120.
  140. Downey, P.O. An inventory of host species for each aerial mistletoe species (Loranthaceae and Viscaceae) in Australia. Cunninghamia 1998, 5, 685–720.
  141. Arruda, R.; Carvalho, L.N.; Del-Claro, K. Host specificity of a Brazilian mistletoe, Struthanthus aff. polyanthus (Loranthaceae), in Cerrado Tropical Savanna. Flora-Morphol. Distrib. Funct. Ecol. Plants 2006, 201, 127–134.
  142. Atsatt, P. Host-parasite interactions in higher plants. In Physiological Plant Ecology III; Springer: Berlin/Heidelberg, Germany, 1983; Volume 12/C, pp. 519–535.
  143. Dean, W.; Midgley, J.; Stock, W. The distribution of mistletoes in South Africa: Patterns of species richness and host choice. J. Biogeogr. 1994, 21, 503–510.
  144. Downey, P.O.; Gill, A.M.; Banks, J.C. The Influence of Host Attributes on Mistletoe Colonization: An Example from Mulligan’s Flat Nature Reserve, A.C.T. Vic. Nat. 1997, 114, 105–111.
  145. Ghosh, S.K.; Balasundaram, M.; Mohamed, A.M. Studies in Host Parasite Relationship of Phanerogamic Parasites on Teak and Their Possible Control; Kerela Forest Reseach Institute: Kerala, India, 1984; p. 21.
  146. Halbritter, D.A.; Willett, D.S.; Gordon, J.M.; Stelinski, L.L.; Daniels, J.C. Behavioral Evidence for Host Transitions in Plant, Plant Parasite, and Insect Interactions. Environ. Entomol. 2018, 47, 646–653.
  147. Hoffmann, A.J.; Fuentes, E.R.; Cortes, I.; Liberona, F.; Costa, V. Tristerix tetrandrus (Loranthaceae) and its host-plants in the Chilean matorral: Patterns and mechanisms. Oecologia 1986, 69, 202–206.
  148. Norton, D.A.; Carpenter, M.A. Mistletoes as parasites: Host specificity and speciation. Trends Ecol. Evol. 1998, 13, 101–105.
  149. Okubamichael, D.Y.; Griffiths, M.E.; Ward, D. Host specificity in parasitic plants—Perspectives from mistletoes. AoB Plants 2016, 8, plw069.
  150. Rödl, T.; Ward, D. Host recognition in a desert mistletoe: Early stages of development are influenced by substrate and host origin. Funct. Ecol. 2002, 16, 128–134.
  151. Scharpf, R.F. Host resistance to dwarf mistletoe. In Proceedings of the Biology of Dwarf Mistletoes, Symposium Proceedings, Fort Collins, CO, USA, 8 August 1984; Hawksworth, F.G., Scharpf, R.F., Eds.; U.S. Department of Agriculture, Forest Service, Rocky Mountain Forest and Range Experiment Station: Berkeley, CA, USA, 1984; pp. 70–76.
  152. Tainter, F.; French, D. The role of wound periderm in the resistance of eastern larch and jack pine to dwarf mistletoe. Can. J. Bot. 1971, 49, 501–504.
  153. Smith, R.; Wass, E.; Meagher, M. Evidence of resistance to hemlock dwarf mistletoe (Arceuthobium tsugense) in western hemlock (Tsuga heterophylla) clones. Eur. J. For. Pathol. 1993, 23, 163–170.
  154. Roeser, J., Jr. The importance of seed source and the possibilities of forest tree breeding. J. For. 1926, 24, 38–51.
  155. Bates, C.G. Better seeds, better trees. J. For. 1927, 25, 130–144.
  156. Hawksworth, F.G.; Edminster, C.B. Carlos Bates’ Dwarf Mistletoe Resistant Ponderosa Pines: A Postscript after Half a Century; USDA Forest Service, Rocky Mountain Forest and Range Experiment Station: Berkeley, CA, USA, 1981; Volume 412, p. 4.
  157. Roth, L.F. Dwarf mistletoe damage to small ponderosa pines. For. Sci. 1971, 17, 373–380.
  158. Roth, L.F. Juvenile Susceptibility of Ponderosa Pine. Phytopathology 1974, 64, 689–692.
  159. Harrington, T.; Wingfield, M. Diseases and the ecology of indigenous and exotic pines. In Ecology and Biogeography of Pinus; Richardson, D., Ed.; Cambridge University Press: Cambridge, UK, 1998; pp. 1–33.
  160. Okubamichael, D.Y. Host Specificity of the Hemiparasitic Mistletoe, Agelanthus natalitius. Master’s Thesis, University of KwaZulu-Natal, Pietermaritzburg, South Africa, 2009.
  161. Skrypnik, L.; Maslennikov, P.; Feduraev, P.; Pungin, A.; Belov, N. Ecological and Landscape Factors Affecting the Spread of European Mistletoe (Viscum album L.) in Urban Areas (A Case Study of the Kaliningrad City, Russia). Plants 2020, 9, 394.
  162. Zaroug, M.S.; Zahran, E.B.; Abbasher, A.A. Distribution And Host Range of Mistletoe (Tapinanthus globiferus) (A. Rich.) Van Tieghan) Along the Blue Nile Banks in Central Sudan. Int. J. Sci. Technol. Res. 2014, 3, 1–5.
  163. Ladley, J.J.; Kelly, D.; Robertson, A.W. Explosive flowering, nectar production, breeding systems, and pollinators of New Zealand mistletoes (Loranthaceae). N. Z. J. Bot. 1997, 35, 345–360.
  164. Lavorel, S.; Smith, M.S.; Reid, N. Spread of mistletoes (Amyema preissii) in fragmented Australian woodlands: A simulation study. Landsc. Ecol. 1999, 14, 147–160.
  165. Ehleringer, J.; Ullmann, I.; Lange, O.; Farquhar, G.; Cowan, I.; Schulze, E.-D.; Ziegler, H. Mistletoes: A hypothesis concerning morphological and chemical avoidance of herbivory. Oecologia 1986, 70, 234–237.
  166. Yoder, J.I. Parasitic plant responses to host plant signals: A model for subterranean plant–plant interactions. Curr. Opin. Plant Biol. 1999, 2, 65–70.
  167. Tomilov, A.; Tomilova, N.; Shin, D.H.; Jamison, D.; Torres, M.; Reagan, R.; McGray, H.; Horning, T.; Truong, R.; Nava, A. Chemical signalling between plants. In Chemical Ecology: From Gene to Ecosystem; Springer: Dordrecht, The Netherlands, 2006; Volume 16, pp. 55–69.
  168. Yan, Z. Resistance to haustorial development of two mistletoes, Amyema preissii (Miq.) Tieghem and Lysiana exocarpi (Behr.) Tieghem ssp. exocarpi (Loranthaceae), on host and nonhost species. Int. J. Plant Sci. 1993, 154, 386–394.
  169. Lech, P.; Żółciak, A.; Hildebrand, R. Occurrence of European Mistletoe (Viscum album L.) on Forest Trees in Poland and Its Dynamics of Spread in the Period 2008–2018. Forests 2020, 11, 83.
  170. Press, M.C.; Phoenix, G.K. Impacts of parasitic plants on natural communities. New Phytol. 2005, 166, 737–751.
  171. Nickrent, D.; Musselman, L. Introduction to parasitic flowering plants. Plant Health Instr. 2004.
  172. Pennings, S.C.; Callaway, R.M. Parasitic plants: Parallels and contrasts with herbivores. Oecologia 2002, 131, 479–489.
  173. Overton, J.M. Dispersal and infection in mistletoe metapopulations. J. Ecol. 1994, 82, 711–723.
  174. Amico, G.; Aizen, M.A. Mistletoe seed dispersal by a marsupial. Nature 2000, 408, 929–930.
  175. Lira-Noriega, A.; Toro-Núñez, O.; Oaks, J.R.; Mort, M.E. The roles of history and ecology in chloroplast phylogeographic patterns of the bird-dispersed plant parasite Phoradendron californicum (Viscaceae) in the Sonoran Desert. Am. J. Bot. 2015, 102, 149–164.
  176. Pérez-Crespo, M.; Ornelas, J.; Martén-Rodríguez, S.; González-Rodríguez, A.; Lara, C. Reproductive biology and nectar production of the Mexican endemic P. sittacanthus auriculatus (Loranthaceae), a hummingbird-pollinated mistletoe. Plant Biol. 2016, 18, 73–83.
  177. Burgess, V.J.; Kelly, D.; Robertson, A.W.; Ladley, J.J. Positive effects of forest edges on plant reproduction: Literature review and a case study of bee visitation to flowers of Peraxilla tetrapetala (Loranthaceae). N. Z. J. Ecol. 2006, 30, 179–190.
  178. Kelly, D.; Ladley, J.J.; Robertson, A.W.; Crowfoot, L. Flower predation by Zelleria maculata (Lepidoptera) on Peraxilla mistletoes: Effects of latitude and fragmentation, and impact on fruit set. N. Z. J. Ecol. 2008, 32, 186–196.
  179. MacRaild, L.M.; Radford, J.Q.; Bennett, A.F. Non-linear effects of landscape properties on mistletoe parasitism in fragmented agricultural landscapes. Landsc. Ecol. 2010, 25, 395–406.
  180. Bowen, M.E.; McAlpine, C.A.; House, A.P.; Smith, G.C. Agricultural landscape modification increases the abundance of an important food resource: Mistletoes, birds and brigalow. Biol. Conserv. 2009, 142, 122–133.
  181. Reid, N.; Stafford Smith, M.; Yan, Z. Ecology and population biology of mistletoes. In Forest Canopies; Lowman, M.D., Nadkarn, N.M., Eds.; Elsevier: Amsterdam, The Netherlands, 1995; pp. 285–310.
  182. Norton, D.A.; Ladley, J.J. Establishment and early growth of Alepis flavida in relation to Nothofagus solandri branch size. N. Z. J. Bot. 1998, 36, 213–217.
  183. Aukema, J.E.; Del Rio, C.M. Variation in mistletoe seed deposition: Effects of intra-and interspecific host characteristics. Ecography 2002, 25, 139–144.
  184. Baena-Díaz, F.; Ramírez-Barahona, S.; Ornelas, J.F. Hybridization and differential introgression associated with environmental shifts in a mistletoe species complex. Sci. Rep. 2018, 8, 5591.
  185. Azpeitia, F.; Lara, C. Reproductive biology and pollination of the parasitic plant Psittacanthus calyculatus (Loranthaceae) in central México1. J. Torrey Bot. Soc. 2006, 133, 429–438.
  186. Ramírez, M.M.; Ornelas, J.F. Polinización y producción de néctar de Psittacanthus schiedeanus (Loranthaceae) en el centro de Veracruz, México. Boletín De La Soc. Botánica De México 2010, 87, 61–67.
  187. Guerra, T.; Galetto, L.; Silva, W. Nectar secretion dynamic links pollinator behavior to consequences for plant reproductive success in the ornithophilous mistletoe Psittacanthus robustus. Plant Biol. 2014, 16, 956–966.
  188. Belchior, M.M.; Camarota, F.; Antiqueira, P.A.P.; Neves, F.S. A neotropical mistletoe influences herbivory of its host plant by driving changes in the associated insect community. Sci. Nat. 2022, 109, 27.
  189. Ollerton, J.; Stott, A.; Allnutt, E.; Shove, S.; Taylor, C.; Lamborn, E. Pollination niche overlap between a parasitic plant and its host. Oecologia 2007, 151, 473–485.
  190. Kuijt, J. Monograph of Psittacanthus (Loranthaceae). Syst. Bot. Monogr. 2009, 86, 1–362.
  191. Amico, G.C.; Vidal-Russell, R.; Garcia, M.A.; Nickrent, D.L. Evolutionary history of the South American mistletoe Tripodanthus (Loranthaceae) using nuclear and plastid markers. Syst. Bot. 2012, 37, 218–225.
  192. Ornelas, J.F.; Gándara, E.; Vásquez-Aguilar, A.A.; Ramírez-Barahona, S.; Ortiz-Rodriguez, A.E.; González, C.; Saules, M.T.M.; Ruiz-Sanchez, E. A mistletoe tale: Postglacial invasion of Psittacanthus schiedeanus (Loranthaceae) to Mesoamerican cloud forests revealed by molecular data and species distribution modeling. BMC Evol. Biol. 2016, 16, 78.
  193. Reid, N. Dispersal of misteltoes by honeyeaters and flowerpeckers: Components of seed dispersal quality. Ecology 1989, 70, 137–145.
  194. Godschalk, S. Feeding behaviour of avian dispersers of mistletoe fruit in the Loskop Dam Nature Reserve, South Africa. Afr. Zool. 1985, 20, 136–146.
  195. Van Ommeren, R.J.; Whitham, T.G. Changes in interactions between juniper and mistletoe mediated by shared avian frugivores: Parasitism to potential mutualism. Oecologia 2002, 130, 281–288.
  196. García, D.; Rodríguez-Cabal, M.A.; Amico, G.C. Seed dispersal by a frugivorous marsupial shapes the spatial scale of a mistletoe population. J. Ecol. 2009, 97, 217–229.
  197. Rodriguez-Cabal, M.A.; Branch, L.C. Influence of habitat factors on the distribution and abundance of a marsupial seed disperser. J. Mammal. 2011, 92, 1245–1252.
  198. Morales, J.M.; Rivarola, M.D.; Amico, G.; Carlo, T.A. Neighborhood effects on seed dispersal by frugivores: Testing theory with a mistletoe–marsupial system in Patagonia. Ecology 2012, 93, 741–748.
  199. Arriaga, L.; Franco, M.; Sarukhan, J. Identification of natural groups of trees in uneven-aged forests using multivariate methods. J. Ecol. 1988, 76, 1092–1100.
  200. Donohue, K. The spatial demography of mistletoe parasitism on a Yemeni Acacia. Int. J. Plant Sci. 1995, 156, 816–823.
  201. Gairola, S.; Bhatt, A.; Govender, Y.; Baijnath, H.; Procheş, Ş.; Ramdhani, S. Incidence and intensity of tree infestation by the mistletoe Erianthemum dregei (Eckl. & Zeyh.) V. Tieghem in Durban, South Africa. Urban For. Urban Green. 2013, 12, 315–322.
  202. Bilgili, E.; Coskuner, K.A.; Baysal, I.; Ozturk, M.; Usta, Y.; Eroglu, M.; Norton, D. The distribution of pine mistletoe (Viscum album ssp. austriacum) in Scots pine (Pinus sylvestris) forests: From stand to tree level. Scand. J. For. Res. 2020, 35, 20–28.
  203. Teixeira-Costa, L.; Coelho, F.M.; Ceccantini, G.C.T. Comparative phenology of mistletoes shows effect of different host species and temporal niche partitioning. Botany 2017, 95, 271–282.
  204. Yule, K.M.; Bronstein, J.L. Reproductive ecology of a parasitic plant differs by host species: Vector interactions and the maintenance of host races. Oecologia 2018, 186, 471–482.
  205. Cuadra-Valdés, J.; Vizentin-Bugoni, J.; Fontúrbel, F.E. An exotic magnet plant alters pollinator abundance and behavior: A field test with a native mistletoe. Biol. Invasions 2021, 23, 2515–2525.
  206. Cubero, J.; Hernández, L. Breeding faba bean (Vicia faba L.) for resistance to Orobanche crenata Forsk. Options Méditerranéennes 1991, 10, 51–57.
  207. Ringnes, D.; Stover, P.; Scharpf, R. Dwarf mistletoe resistance in ponderosa pine: Selection and testing protocols. In Proceedings of the Congresos y Jornadas-Junta de Andalucia (Espana), Cordoba, Spain, 16–18 April 1996; pp. 690–696.
  208. Haussmann, B.; Hess, D.; Reddy, B.; Mukuru, S.; Seetharama, N.; Kayentao, M.; Welz, H.; Geiger, H. QTL for Striga resistance in sorghum populations derived from IS 9830 and N 13. In Proceedings of the Breeding for Striga Resistance in Cereals: Proceedings of a Workshop, IITA, Ibadan, Nigeria, 18–20 August 1999; pp. 18–20.
  209. Mohamed, A.; Rich, P.; Housley, T.; Ejeta, G. In vitro techniques for studying mechanisms of Striga resistance in sorghum. In Proceedings of the 7th International Parasitic Weed Symposium, Nantes, France, 3–8 June 2001; pp. 96–100.
  210. Omanya, G.O.; Haussmann, B.I.G.; Hess, D.E.; Reddy, B.V.S.; Kayentao, M.; Welz, H.G.; Geiger, H.H. Utility of indirect and direct selection traits for improving Striga resistance in two sorghum recombinant inbred populations. Field Crops Res. 2004, 89, 237–252.
  211. Zhang, X.; Liu, B.; Guo, Q.; Song, L.; Chen, L.; Wang, C. Construction of a haustorium development associated SSH library in Thesium chinense and analysis of specific ESTs included by Imperata cylindrica. Biochem. Syst. Ecol. 2016, 64, 46–52.
  212. Ranjan, A.; Ichihashi, Y.; Farhi, M.; Zumstein, K.; Townsley, B.; David-Schwartz, R.; Sinha, N.R. De novo assembly and characterization of the transcriptome of the parasitic weed dodder identifies genes associated with plant parasitism. Plant Physiol. 2014, 166, 1186–1199.
  213. Ichihashi, Y.; Kusano, M.; Kobayashi, M.; Suetsugu, K.; Yoshida, S.; Wakatake, T.; Kumaishi, K.; Shibata, A.; Saito, K.; Shirasu, K.J.P.; et al. Transcriptomic and metabolomic reprogramming from roots to haustoria in the parasitic plant, Thesium chinense. Plant Cell Physiol. 2018, 59, 729–738.
  214. Wang, Y.; Li, X.; Zhou, W.; Li, T.; Tian, C.J.B.g. De novo assembly and transcriptome characterization of spruce dwarf mistletoe Arceuthobium sichuanense uncovers gene expression profiling associated with plant development. BMC Genom. 2016, 17, 1–14.
  215. Abdul Wahid, H. Identification of Dwarf Mistletoe Resistant Genes in Ziarat Junipers (Juniperus excelsa M. Bieb). Ph.D. Thesis, University of Baluchistan, Quetta, Pakistan, 2019.
  216. Abdul Wahid, H.; Barozai, M.Y.K.; Din, M. Identification and characterization of dwarf mistletoe responding genes in Ziarat juniper tree (Juniperus excelsa M. Bieb) through suppression subtractive hybridization and deep sequencing. Trees 2019, 33, 1027–1039.
  217. Kuang, J.; Wang, Y.; Mao, K.; Milne, R.; Wang, M.; Miao, N. Transcriptome Profiling of a Common Mistletoe Species Parasitizing Four Typical Host Species in Urban Southwest China. Genes 2022, 13, 1173.
  218. Dan, M.W.; Filiz, G. Plant Genome Editing and its Applications in Cereals. In Genetic Engineering; Farrukh, J., Ed.; IntechOpen: Rijeka, Croatia, 2016; p. 4.
  219. Mandal, K.; Boro, P.; Chattopadhyay, S. Micro-RNA based gene regulation: A potential way for crop improvements. Plant Gene 2021, 27, 100312.
  220. Yu, H.; Li, J. Breeding future crops to feed the world through de novo domestication. Nat. Commun. 2022, 13, 1171.
  221. Van Esse, H.P.; Reuber, T.L.; van der Does, D. Genetic modification to improve disease resistance in crops. New Phytol. 2020, 225, 70–86.
  222. Zaidi, S.S.-e.-A.; Mahas, A.; Vanderschuren, H.; Mahfouz, M.M. Engineering crops of the future: CRISPR approaches to develop climate-resilient and disease-resistant plants. Genome Biol. 2020, 21, 289.
  223. Clarke, C.R.; Timko, M.P.; Yoder, J.I.; Axtell, M.J.; Westwood, J.H. Molecular Dialog Between Parasitic Plants and Their Hosts. Annu. Rev. Phytopathol. 2019, 57, 279–299.
  224. Westwood, J.H.; de Pamphilis, C.W.; Das, M.; Fernández-Aparicio, M.; Honaas, L.A.; Timko, M.P.; Wafula, E.K.; Wickett, N.J.; Yoder, J.I. The Parasitic Plant Genome Project: New Tools for Understanding the Biology of Orobanche and Striga. Weed Sci. 2017, 60, 295–306.
  225. Neale, D.B.; Kremer, A. Forest tree genomics: Growing resources and applications. Nat. Rev. Genet. 2011, 12, 111.
  226. Muleo, R.; Morgante, M.; Velasco, R.; Cavallini, A.; Perrotta, G.; Baldoni, L. Olive tree genomic. In Olive Germplasm–The Olive Cultivation, Table Olive and Olive Oil Industry in Italy, 1st ed.; Muzzalupo, I., Ed.; Intechopen: Rijeka, Croatia, 2012; pp. 133–148.
  227. Diningrat, D.; Widiyanto, S.; Pancoro, A.; Shim, D.; Panchangam, B.; Zembower, N.; Carlson, J.E. Transcriptome of teak (Tectona grandis, Lf) in vegetative to generative stages development. J. Plant Sci. 2015, 10, 1.
  228. Schnell, R.J.; Priyadarshan, P. Genomics of Tree Crops; Springer Science & Business Media; Springer: New York, NY, USA, 2012.
  229. Gmitter, F.G.; Chen, C.; Machado, M.A.; De Souza, A.A.; Ollitrault, P.; Froehlicher, Y.; Shimizu, T. Citrus genomics. Tree Genet. Genomes 2012, 8, 611–626.
  230. Arias, R.S.; Borrone, J.W.; Tondo, C.L.; Kuhn, D.N.; Irish, B.M.; Schnell, R.J. Genomics of tropical fruit tree crops. In Genomics of Tree Crops; Springer: Berlin/Heidelberg, Germany, 2012; pp. 209–239.
  231. Deeks, S.J.; Shamoun, S.F.; Punja, Z.K. In vitro germination and development of western hemlock dwarf mistletoe. Plant Cell Tissue Organ Cult. 2001, 66, 97–105.
  232. Marler, M.; Pedersen, D.; Mitchell-Olds, T.; Callaway, R. A polymerase chain reaction method for detecting dwarf mistletoe infection in Douglas-fir and western larch. Can. J. For. Res. 1999, 29, 1317–1321.
  233. Petri, C.; Burgos, L. Transformation of fruit trees. Useful breeding tool or continued future prospect? Transgenic Res. 2005, 14, 15–26.
  234. Atsatt, P.R. On the evolution of leaf resemblance between mistletoes and their hosts. In Proceedings of the 2nd Symposium on Parasitic Weeds, Raleigh, NC, USA, 16–19 July 1979.
  235. Lev-Yadun, S. Does chemical aposematic (warning) signaling occur between host plants and their potential parasitic plants? Plant Signal. Behav. 2013, 8, e24907.
  236. Yoshida, S.; Cui, S.; Ichihashi, Y.; Shirasu, K. The Haustorium, a Specialized Invasive Organ in Parasitic Plants. Annu. Rev. Plant Biol. 2016, 67, 643–667.
  237. Chang, M.; Lynn, D.G. The haustorium and the chemistry of host recognition in parasitic angiosperms. J. Chem. Ecol. 1986, 12, 561–579.
  238. Sallé, G.L. Germination and Establishment of Viscum album. In The Biology of Mistletoes; Calder, D., Bernhardt, P., Eds.; Academic Press: London, UK, 1983.
  239. Bandaranayake, P.C.G.; Yoder, J.I. Haustorium Initiation and Early Development. In Parasitic Orobanchaceae: Parasitic Mechanisms and Control Strategies; Joel, D.M., Gressel, J., Musselman, L.J., Eds.; Springer: Berlin Heidelberg, Germany, 2013; pp. 61–74.
  240. Saucet, S.B.; Shirasu, K. Molecular Parasitic Plant-Host Interactions. PLoS Pathog. 2016, 12, e1005978.
  241. Kokla, A.; Melnyk, C.W. Developing a thief: Haustoria formation in parasitic plants. Dev. Biol. 2018, 442, 53–59.
  242. Keyes, W.J.; Palmer, A.G.; Erbil, W.K.; Taylor, J.V.; Apkarian, R.P.; Weeks, E.R.; Lynn, D.G. Semagenesis and the parasitic angiosperm Striga asiatica. Plant J. Cell Mol. Biol. 2007, 51, 707–716.
  243. Klutsch, J.G.; Erbilgin, N. Dwarf mistletoe infection in jack pine alters growth-defense relationships. Tree Physiol. 2018, 38, 1538–1547.
  244. Smith, J.L.; De Moraes, C.M.; Mescher, M.C. Jasmonate- and salicylate-mediated plant defense responses to insect herbivores, pathogens and parasitic plants. Pest Manag. Sci. 2009, 65, 497–503.
  245. Runyon, J.B.; Mescher, M.C.; De Moraes, C.M. Plant defenses against parasitic plants show similarities to those induced by herbivores and pathogens. Plant Signal. Behavior. 2010, 5, 929–931.
  246. Cuevas-Reyes, P.; Pérez-López, G.; Maldonado-López, Y.; González-Rodríguez, A. Effects of herbivory and mistletoe infection by Psittacanthus calyculatus on nutritional quality and chemical defense of Quercus deserticola along Mexican forest fragments. Plant Ecol. 2017, 218, 687–697.
  247. Teixeira-Costa, L.; Ceccantini, G. Embolism increase and anatomical modifications caused by a parasitic plant: Phoradendron crassifolium (Santalaceae) on Tapirira guianensis (Anacardiaceae). IAWA J. 2015, 36, 138–151.
  248. Hu, B.; Sakakibara, H.; Takebayashi, Y.; Peters, F.S.; Schumacher, J.; Eiblmeier, M.; Arab, L.; Kreuzwieser, J.; Polle, A.; Rennenberg, H. Mistletoe infestation mediates alteration of the phytohormone profile and anti-oxidative metabolism in bark and wood of its host Pinus sylvestris. Tree Physiol. 2017, 37, 676–691.
  249. War, A.R.; Paulraj, M.G.; Ahmad, T.; Buhroo, A.A.; Hussain, B.; Ignacimuthu, S.; Sharma, H.C. Mechanisms of plant defense against insect herbivores. Plant Signal. Behav. 2012, 7, 1306–1320.
  250. Sallé, G.L.; Armillotta, A.; Frochot, H. Mechanisms of resistance of four cultivars of poplar against Viscum album L. In Proceedings of the 3rd International Symposium of Parasitic Weeds, Aleppo, Syria, 7–10 May 1984; Parker, C., Musselman, L.J., Polhill, R.M., Wilson, A.K., Eds.;
  251. Lázaro-González, A.; Hódar, J.A.; Zamora, R. Mistletoe Versus Host Pine: Does Increased Parasite Load Alter the Host Chemical Profile? J. Chem. Ecol. 2019, 45, 95–105.
  252. Ferrenberg, S. Dwarf Mistletoe Infection Interacts with Tree Growth Rate to Produce Opposing Direct and Indirect Effects on Resin Duct Defenses in Lodgepole Pine. Forests 2020, 11, 222.
  253. Bhat, K.A.; Akhtar, S.; Dar, N.A.; Bhat, M.I.; Bhat, F.A.; Rizwan, R.; Horielov, O.; Krasylenko, Y. Mistletoe Eradicator—A Novel Tool for Simultaneous Mechanical and Chemical Control of Mistletoe. J. Vis. Exp. 2022, 181, e63455.
  254. Schrader-Patton, C.; Grulke, N.; Bienz, C. Assessment of Ponderosa Pine Vigor Using Four-Band Aerial Imagery in South Central Oregon: Crown Objects to Landscapes. Forests 2021, 12, 612.
  255. Barbedo, J. A Review on the Use of Unmanned Aerial Vehicles and Imaging Sensors for Monitoring and Assessing Plant Stresses. Drones 2019, 3, 40.
  256. Duarte, A.; Borralho, N.; Cabral, P.; Caetano, M. Recent Advances in Forest Insect Pests and Diseases Monitoring Using UAV-Based Data: A Systematic Review. Forests 2022, 13, 911.
  257. Thapa, S. Detection and Mapping of Incidence of Viscum album in Pinus sylvestris Forest of Southern French Alpe Using Satellite and Airborne Optical Imagery. Master’s Thesis, University of Twente, Enskode, The Netherlands, 2013.
  258. Barbosa, J.; Sebastián-González, E.; Asner, G.; Knapp, D.; Anderson, C.; Martin, R.; Dirzo, R. Hemiparasite-host plant interactions in a fragmented landscape assessed via imaging spectroscopy and LiDAR. Ecol. Appl. 2016, 26, 55–66.
  259. Lawley, V.; Lewis, M.; Clarke, K.; Ostendorf, B. Site-based and remote sensing methods for monitoring indicators of vegetation condition: An Australian review. Ecol. Indic. 2016, 60, 1273–1283.
  260. Barlow, B.A.; Wiens, D. Host-Parasite Resemblance in Australian Mistletoes: The Case for Cryptic Mimicry. Evolution 1977, 31, 69–84.
  261. Windmuller-Campione, M.A.; Moser, R.L. Remote and Seasonal Field Detection of Eastern Spruce Dwarf Mistletoe in Northern Minnesota; Minnesota Forestry Research Notes; Department of Forest Resources, University of Minnesota: St. Paul, MN, USA, 2022; Volume 315.
  262. Mejia-Zuluaga, P.A.; Dozal, L.; Valdiviezo-N., J.C. Genetic Programming Approach for the Detection of Mistletoe Based on UAV Multispectral Imagery in the Conservation Area of Mexico City. Remote Sens. 2022, 14, 801.
  263. Pernar, R.; Bajic, M.; Ancic, M.; Seletkovic, A.; Idzojtic, M. Detection of mistletoe in digital colour infrared images of infested fir trees. Period. Biol. 2007, 109, 67–75.
  264. Sabrina, F.; Sohail, S.; Thakur, S.; Azad, S.; Wasimi, S. Use of deep learning approach on UAV imagery to detect mistletoe infestation. In Proceedings of the 2020 IEEE Region 10 Symposium (TENSYMP), Dhaka, Bangladesh, 5–7 June 2020; pp. 556–559.
  265. Ančić, M.; Pernar, R.; Bajić, M.; Seletković, A.; Kolić, J. Detecting mistletoe infestation on Silver fir using hyperspectral images. Iforest-Biogeosci. For. 2014, 7, 85.
  266. Maes, W.H.; Huete, A.R.; Avino, M.; Boer, M.M.; Dehaan, R.; Pendall, E.; Griebel, A.; Steppe, K. Can UAV-based infrared thermography be used to study plant-parasite interactions between mistletoe and eucalypt trees? Remote Sens. 2018, 10, 2062.
  267. Xiong, D.; Huang, H.; Wang, Z.; Li, Z.; Tian, C. Assessment of dwarf mistletoe (Arceuthobium sichuanense) infection in spruce trees by using hyperspectral data. For. Pathol. 2021, 51, e12669.
  268. Miraki, M.; Sohrabi, H.; Fatehi, P.; Kneubuehler, M. Detection of mistletoe infected trees using UAV high spatial resolution images. J. Plant Dis. Prot. 2021, 128, 1679–1689.
  269. León-Bañuelos, L.A.; Endara-Agramont, A.R.; Gómez-Demetrio, W.; Martínez-García, C.G.; Gabino Nava-Bernal, E. Identification of Arceuthobium globosum using unmanned aerial vehicle images in a high mountain forest of central Mexico. J. For. Res. 2020, 31, 1759–1771.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
This entry is offline, you can click here to edit this entry!
ScholarVision Creations
Feedback