Structure and Development of the Mature Secondary Haustorium in Alectra vogelii Benth

Anatomical investigations were carried out on the structureand development of the mature secondary haustorium in Alectravogelii growing on Arachis hypogaea or Vigna unguiculata. Followingthe formation of the young secondary haustorium, both the cambiumand pericycle of the host root directly opposite the young secondaryhaustorium are stimulated to divide and form new tissues andorgans including haustorial roots. Further proliferations ofthe host root pericycle and the haustorial cortex give riseto a large, tuberous and complex mature secondary haustoriumwithin which the tissues of the host and parasite remain inintimate contact forming a perfect graft union with a wide zoneof contact. Apart from the haustorial axial xylcm strand whichnormally connects the xylem of the parasite secondary root withthat of the host, direct xylary connections are also establishedbetween the axial xylem of the haustorium and the xylem of thehaustorial roots. The entire surface of the mature secondaryhaustorium of Alectrais covered with these haustorial rootsas was previously observed in its mature primary haustorium. Alectra vogelii Benth, secondary haustorium, haustorium, haustorial roots, root parasite, hemiparasitism, Arachis hypogaea, Vigna unguiculata     

Morphology and Anatomy of the Haustorium of the Root Hemiparasite Olax phyllanthi (Olacaceae), with Special Reference to the Haustorial Interface

Gross morphology and internal structure of haustoria of Olaxphyllanthi are described in parasitism with a range of hosts,including roots of woody and herbaceous dicotyledons and certainmonocotyledons, and occasional instances of autoparasitism andhaustorial formation on monocotyledon rhizomes. Successful penetrationto xylem occurs on virtually all hosts across broad diameters,ages and anatomies of host root, but anatomical impedimentsto haustorial establishment and penetration are recorded forcertain host taxa. Each haustorium is a comparatively simpleand ephemeral structure. Its developing sucker (endophytic regionof the haustorium) spreads laterally around the surface of thehost xylem, yet never completely encircles the host stele. Damageto hosts is minimal and secondary thickening (of hosts) continueson the side of a host root opposite to a haustorium. The haustorialsucker lacks phloem and its interface with host xylem is comprisedalmost entirely (more than 98.7%) of parenchyma. The few terminatingtracheids at an interface lie in very close proximity to oroccasionally directly against exposed xylem vessels, but lumento lumen continuity between tracheary elements of the partnersis not achieved. Three dimensional reconstructions based onserial transverse sectioning indicate that well defined filesof tracheids connect back from an interface to the core of graniferoustracheary elements in the external body of the haustorium, andthence to the xylem of the parent parasite root. The findingsare discussed in relation to existing studies on haustorialanatomy. Root parasite, Olacaceae, haustorial anatomy, host specificity     

The Initiation of the Secondary Haustorium in Alectra vogelii Benth

Anatomical studies were carried out on initiation of the secondaryhaustorium in Alectra vogelii, a root parasite of leguminouscrops in Nigeria. In both the normal and self-haustorium, theformation of the haustorial initial on the parasite root soonafter initial contact between the host and parasite roots isfollowed by the penetration of the host root by the haustorium.Specialized penetrating cells (intrusive cells) at the haustorialfront prise apart and loosen the host root cortical cells, whichlater become digested. Through the same processes, a few ofthese columnar intrusive cells at the haustorial front piercethe endodermis to make contact with the xylem of the host root.Thereafter, a true conductive bridge consisting of short, isodiametric,reticulate vessel elements is established between the parasiteand host roots through the secondary haustorium. No pholem tissuewas observed in the connection. There is a close similaritybetween the mode of initiation of the secondary haustorium ofAlectra vogelii and that previously described for its primaryhaustorium. Alectra vogelii Benth, haustorium, self-haustorium, root parasite, hemiparasitism, Vigna unguiculata, Arachis hypogaea     

Haustorial Structure and Functioning of the Root Hemiparastic Tree Nuytsia floribunda(Labill.) R.Br. and Water Relationships with its Hosts

Observations on the origin and mature structure of the haustoriumof the Western Australian Christmas tree (Nuytsia floribunda)corroborate and extend the findings of earlier workers. We showthat the previously described sclerenchymatous ‘horn’or ‘prong’ formed within the haustorium acts asa sickle-like cutting device which transversely severs the hostroot and then becomes lodged in haustorial collar tissue directlyopposite to that where it originated. The cutting process isdeduced to be rapid and the gland-like fluid filled structurein the haustorium is suggested to generate a hydrostatic forcedriving the device through the host root. The haustorial parenchymacells at the tight junction between the endophytic part of thehaustorium and the cut face of the host root develop balloon-likeoutgrowths which intrude into the lumina of severed xylem vesselsof the host. Experiments feeding 0.05% (w/v) basic fuchsin tofreshly cut ends of host root segments distal to terminally-attachedmature haustoria demonstrate an apoplastic pathway from hostxylem elements fractured at the interface into haustorial parenchyma,and thence through vascular tissue to the haustorium into thetranspiring plant of Nuytsia. Application of labelled water(D₂O) to uncut basal roots of potted plants ofAcacia acuminataparasitized by Nuytsia results in labelling of leafy shootsof parasite and host, indicative of haustorial uptake of waterby Nuytsia from host root xylem in the intact association. Measurementsof xylem water potentials of pot-cultured seedling Nuytsia associatedwith a range of hosts, or of mature trees of Nuytsia and partnerwoody hosts in the native habitat, demonstrate consistentlymore negative potentials in the parasite than host, suggestingthat the parasite may regularly obtain xylem water through itshaustorial apparatus. Copyright 2000 Annals of Botany Company Root hemiparasite, Nuytsia floribunda, Loranthaceae, haustorial structure, host–parasite water relations     

Structure and Development of the Primary Haustorium in Alectra vogelii Benth. (Scrophulariaceae)

Anatomical observations were made on the structure and developmentof the primary haustorium of Alectra vogelii. Its developmentinvolves a mutual aggressive growth of both the host and parasitetissues resulting in the formation of a very large and complextuberous organ. One of the host tissues whose growth is stimulatedby parasite infection is the pericycle whose cells divide repeatedlyand grow around and within the parasite haustorial cortex. Fromvarious points of the proliferating host pericycle, roots becomeinitiated and eventually the entire surface of the haustoriumbecomes covered with these roots. We have referred to them as‘haustorial roots’, a term which we have re-examinedand redefined. True xylary connections are established not onlybetween the parasite and the host root but also between theparasite and these ‘haustorial roots’. The uniquedevelopment of primary haustorium and ‘haustorial roots’in A. vogelii is discussed in relation to the development ofprimary haustoria in other root parasites.     

Ultrastructure of the haustorial interface and apoplastic continuum between host and the root hemiparasiteOlax phyllanthi (Labill.) R. Br. (Olacaceae)

Summary Structural features of haustorial interface parenchyma of the root hemiparasiteOlax phyllanthi are described. Walls contacting host xylem are thickened non-uniformly with polysaccharides, not lignin, and show only a thin protective wall layer when abutting pits in walls of host xylem vessels or tracheids. Lateral walls of interface parenchyma exhibit an expanded middle layer of open fibrillar appearance, sometimes with, but mostly lacking adjoining layers of dense wall material. Free ribosomes and rough endoplasmic reticulum are prominent and occasional wall ingrowths present. Experiments involving transpirational feeding of the apoplast tracers lanthanum nitrate or uranyl acetate to host roots cut below haustorial connections, indicate effective apoplastic transfer from host to parasite root via the haustorium. Deposits of the tracers suggest a major pathway for water flow through host xylem pits, across the thin protective wall layer, and thence into the haustorium via the electronopaque regions of the terminal and lateral walls of the contact parenchyma. Graniferous tracheary elements and walls of parenchyma cells of the body of the haustorium appear to participate in tracer flow as do walls of cortical cells, stele parenchyma and xylem conducting elements of the parasite root, suggesting that both vascular and non-vascular routes are involved in extracytoplasmic transfer of xylem sap from host to parasite. The Casparian strip of the endodermis and the suberin lamella of the exodermis of theOlax root act as barriers to flow within the system.     

Development of Tapinanthus bangwensis (Engler and Krause) Danser and Contact with the Host

Tapinanthus bangwensis forms a single large union with the host.Initially, the haustorium penetrates the host-cortex by thepressure of growth and enzymic action. On contact with the wood,the haustorium induces meristematic activity in the xylem parenchymaand cambium which leads to the dissection of the host wood andpenetration of haustorial branches between the dissected portions.Vascular contact is made by the formation of adjacent conductingcells in the host and parasite tissues.     

Establishment, Structure and Morphology of the Tuber of Balanophora

During germination of the ‘seed’ of Balanophora,endosperm cells at the radicular pole grow out as tubular structuresand anchor the ‘seed’ to the host rootlet. The radiculartier of cells of the embryo elongate as primary haustorial tubesand establish contact with the host root vasculature. A secondaryhaustorium arises from a meristem adjoining the primary haustorium.The remainder of the embryo contributes to the tuber proper. Host parenchyma in the immediate vicinity of the primary haustoriumreverts to meristematic activity. Some of the derivatives matureas perforate tracheary cells. The remainder, retaining meristematicactivity, squeeze themselves between secondary haustorial cellsand together initiate a composite conducting strand, which repeatedlydichotomizes as the tuber grows. The conducting strand of Balanophora is looked upon as the equivalentof combined adventitious root system of parasite and host. Theremaining part of the tuber is equivalent to the shoot. Balanophora, tuber, morphology, host-parasite relations, parasite     

EXPERIMENTAL STUDIES OF HAUSTORIUM INITIATION AND EARLY DEVELOPMENT IN AGALINIS PURPUREA (L.) RAF. (SCROPHULARIACEAE)

In parasitic angiosperms the haustorium, an organ specialized for attachment and penetration of host tissue, functions in the transport of water and nutrients from the host to the parasite. In Agalinis purpurea (L.) Raf. (Scrophulariaceae) these organs are initiated laterally along its roots, opposite a primary xylem pole. Analyses of haustoria distribution and cellular root profiles show that the portion of the root which is most sensitive to haustorial elicitor molecules is the area distal to the zone of elongation and near the root meristem. Sectioned material supports this finding and, further, indicates that the cells which are the first to respond to haustorial elicitors are located in the inner cortex. Haustoria develop rapidly in response to a host root or to isolated chemical elicitors (xenognosins) normally contained in host root exudate. By 6 hr, vacuolation and radial cellular enlargement are observed in the cortex, and a lateral swelling along the root is visible. By 12 hr, cells of the epidermis divide anticlinally to establish a group of densely cytoplasmic cells at the apex of the haustorial swelling. Accompanying these divisions is the differentiation of specialized hair cells which elongate from epidermal cells flanking the presumptive haustorial apex. Next, the internal, radially enlarged cortical cells divide periclinally. Periclinal divisions are subsequently initiated in the pericycle as early as 18 hr post-induction. Cellular division and enlargement continue so that by 24–36 hr a mature pre-contact haustorium is formed. There is a reduction in root elongation concomitant with haustorial initiation. Depending upon the number of haustoria produced, elongation typically returns to the preinduction level within 2 or 3 days.     

Does legume nitrogen fixation underpin host quality for the hemiparasitic plant Rhinanthus minor?

The high quality of leguminous hosts for the parasitic plantRhinanthus minor (in terms of growth and fecundity), comparedwith forbs (non-leguminous dicots) has long been assumed tobe a function of the legume's ability to fix atmospheric nitrogen(N) from the air and the potential for direct transfer of compatibleamino compounds to the parasite. Using associations betweenRhinanthus minor and Vicia faba (Fabaceae) that receive N eitherexclusively via symbiotic associations with rhizobia supplyingorganic N fixed from N₂ or exclusively through the supply ofinorganic nitrate to the substrate, the underlying reasons forthe quality of legumes as hosts for this parasite are unravelled.It is shown that sole dependence of the host, V. faba, on Nfixation results in lower growth of the attached parasite thanwhen the host is grown in a substrate supplied exclusively withinorganic N. In contrast, the host plants themselves achieveda similar biomass irrespective of their N source. The physiologicalbasis for this is investigated in terms of N and abscisic acid(ABA) partitioning, haustorial penetration, and xylem sap aminoacid profiles. It is concluded that legume N fixation does notunderpin the quality of legumes as hosts for Rhinanthus butrather the well-developed haustorium formed by the parasite,coupled with the lack of defensive response of the host tissuesto the invading haustorium and the presence of sufficient nitrogenouscompounds in the xylem sap accessible to the parasite haustoria,would appear to be the primary factors influencing host qualityof the legumes. Key words: ABA, haustorium, legume, nitrogen fixation, nodules, parasitic plant Received 14 November 2007; Revised 7 January 2008 Accepted 8 January 2008     

The haustorium of the root parasite Triphysaria (Scrophulariaceae), with special reference to xylem bridge ultrastructure

Haustoria of Triphysaria pusilla and T. versicolor subsp. faucibarbata from a natural habitat were analyzed by light and electron microscopy. Secretory trichomes (root hairs) participate in securing the haustorium to the surface of the host root. The keel-shaped intrusive part of the secondary haustorium penetrates to the depth of the vascular tissue of the host. Some of the epidermal interface cells differentiate into xylem elements. A significant number of haustoria do not differentiate further, but in most haustoria one to five of the epidermal xylem elements terminate a similar number of xylem strands. The strands mostly consist of vessel members and they connect host xylem or occasionally host parenchyma to the plate xylem adjacent to the stele of the parasite root. Each strand of this xylem bridge is accompanied by highly protoplasmic parenchyma cells with supposed transfer cell function. Increased surface area of the plasmalemma occurs in these cells as it does in interface parenchyma cells. Graniferous tracheary elements are restricted to the haustorium and occur most frequently in the plate xylem. The plate xylem is also accompanied by highly protoplasmic parenchyma cells. Hyphae of mycorrhizal fungi of the host root occasionally penetrate into the distal part of the xylem bridge. We combine structural observations and physiological facts into a hypothesis for translocation of water and nutrients between host and parasite. Some evolutionary aspects related to endogeny/exogeny of haustoria are discussed, and it is argued that the Triphysaria haustorium represents a greatly advanced and/or reduced condition within Scrophulariaceae.     

Interface between haustoria of parasitic members of the Scrophulariaceae and their hosts: A histochemical and immunocytochemical approach

Summary The haustorial structure of three African parasitic members of the family Scrophulariaceae (Buchnera hispida, Rhamphicarpa fistulosa, andStriga hermonthica) has been studied with regard to the interface between haustoria and the invaded host roots. Immunocytochemical observations at the light and electron microscopical level were carried out with monoclonal antibodies against pectin. JIM5, JIM7, and hydroxyproline-rich glycoprotein (HRGP), LM1. Lignins have been visualized by phloroglucinolhydrochloric acid staining. At the margin of the lateral interface (contact area of host root cortex and parasite cells), JIM5- and JIM7-labelled substances accumulate between parasite papillae and the host root surface indicating that pectins are implicated in sealing the parasite to the attacked host organ. The lateral interface is characterized by the presence of compressed, necrotic host cells, whereas the central interface (contact area between host stele and parasite cells) is generally devoid of host cell remnants. Phenolic substances and/or lignins can be found at the site of penetration of the haustorium into the host root. These observations and the fact that HRGPs accumulate at the host side of the interface support the view of, at least, a partial defense reaction in the invaded host root tissues. Within haustoria, HRGPs were restricted to differentiating xylem elements, implying a spatio-temporal regulation of HRGPs in developmental processes.Abbreviations BSA bovine serum albumin - FITC fluorescein isothiocyanate - HRGP hydroxyproline-rich glycoprotein - LM light microscopy - MAb monoclonal antibody - TBSB Tris-buffered saline with bovine serum albumin - TBSB-T Tris-buffered saline with bovine serum albumin and Tween 20 - TEM transmission electron microscopy     

An anatomical study of the haustoria of Rhinanthus minor attached to roots of different hosts

Roots of a range of potential hosts responded differently when Rhinanthus minor attempted to form haustoria. Roots of Fabaceae show the weakest reaction as apart from slight lignification, no reaction was observed at the interface between the endophyte and the cortical tissue of the host root. Grass roots react with strong lignification of all cells within the stele with the exception of a small number of phloem cells whilst the endodermis fully enters the tertiary stage. In the case of Phleum bertolonii the cortical cells also become lignified. The lignification is even observed in the host root tissue in a distance of about 1 mm from the haustorium (both apically and basipetally). In the case of Leucanthemum vulgare, strong suberisation can be observed in the cell walls of the interface between endophyte (tip of the sucker) and host. Plantago lanceolata exhibits the strongest reactions against the haustorial tissues. Cells of the interface between the endophyte and the host cortex are completely destroyed, as well as a few cell layers outside the central xylem cylinder, even in some distance from the haustorium. Thus, host xylem is completely isolated from the haustorium in this case. Extraction of sap from xylem vessels is likely to be drastically impaired in such a situation.     

The Regulation of the Water Potential Gradient in the Host and Parasite Relationship betweenSorghum bicolorandStriga hermonthica

A glasshouse experiment was carried out to investigate the factorscontrolling the abstraction of xylem fluid from its host bythe parasiteStriga hermonthica(Scrophulariaceae).Strigahad amean daily transpiration rate far exceeding that of its hostsorghum (Sorghum bicolor), with infestation byStrigaalso shownto lower the transpiration rate of the host. Stopping the host'stranspiration was shown to decrease the transpiration rate ofthe parasite. Stopping the parasite's transpiration only gavean initial increase in the host's transpiration rate which wasnot sustained. The parasite had a lower water potential thanits host, values being -0.42 MPa and -0.23 MPa, respectively,and an accompanying higher osmotic pressure of 0.68 MPa against0.51 MPa for sorghum. Modifying the water potential gradientby bagging both partners together showed that the differentialin osmotic pressure and water potential was largely maintainedby the parasite's higher rate of transpiration. A favourablewater potential gradient towards the parasite still existedfollowing the cessation of transpiration, this being generatedby the haustorial resistance to hydraulic conductivity whichwas found to be some 1.5–4.5 times greater than that offeredby the parasite shoot. Both the high rate of transpiration andthe increased resistance across the haustoria would appear tobe necessary means to facilitate the diversion of host resourcesto the parasite.Copyright 1997 Annals of Botany Company Striga hermonthica; sorghum; water relations; haustorium; root parasite     

Defense response of resistant host Impatiens balsamina to the parasitic angiosperm Cuscuta japonica

The response of the stem of a resistant host (Impatiens baslamina) to infection by the parasitic flowering plant Cuscuta japonica was studied with light and electron microscopy. The intra- and interfascicular cambial cells in the host stem first reacted to the penetrating upper haustorium by dividing, and the differentiation of the host xylem (vascular) tissues proceeded toward interfascicular areas from vascular bundles. When the host vascular tissue was invaded by the endophyte (haustorial portion in the host stem), the host xylem was displaced, and host vessels became occluded with parenchyma cells, resulting in tyloses. As the parasitism progressed, areas of the host stem penetrated by the endophyte became swollen via secondary growth and cell division in the parenchymatous cortex, pith, and interfascicular areas. During this intrusion by the endophyte, darkly stained necrotic reactions were detected at the interface between the host tissue and the invading endophyte. The results suggested that in the host tissues penetrated by the parasite, the formation of secondary tissue and swellings caused by active cell division of ground tissue and host vessel occlusion by tyloses constitute the host structural defense against the parasite.     

Anatomy of the endophyte of Viscum album L. (Loranthaceae)

Anatomy of the endophyte of Viscum album L. (Loranthaceae). An anatomical investigation into the nature of the host-parasite interaction of V. album and several of its phanerogamic hosts using SEM and light microscopy was conducted. Three kinds of parasite cell (haustorial parenchyma cells, cells resembling transfer cells and haustorial tracheids) were identified at the host-parasite interface. The terms haustorial parenchyma and haustorial tracheid are defined. Haustorial tracheids were seen to have penetrated the walls of host vessel elements and it is suggested that V. album is able to establish on a wide range of hosts because of the anatomically plastic nature of its haustorium. The development of the haustorium depends to a large extent on the nature of the surrounding host tissues. Parasite-induced host abnormalities including hypertrophy, distorted xylem elements, vessel-wall penetration and tylosis-occluded vessels were observed. The macroanatomical features observed are discussed and interpreted by-proposing a new theory for the ontogenesis of the V. album haustorium. Cortical strands with 'chisel' and 'pencil' shaped apices were both found to be present at the same time on one plant and thus were not seasonally separated.     

A Comparative Study of the Haustorial Development of Striga asiatica (L.) Kuntze on Sorghum Cultivars

Ten sorghum cultivars were studied for their mode of Strigaparasitization, and the factors conferring resistance in resistantcultivars most of the Striga haustona failed to penetrate beyondthe endodermis, whereas in susceptible cultivars the haustonapenetrated the endodermis and became established Resistant cultivars showed marked endodermal and pencyclic thickeningand the deposition of silica in their endodermal cells, whichwere lacking in the susceptible cultivars Extra thickening inpencyclic cells as a response to the entrance of haustonum wasobserved in cultivars N-13 and IS-4202 Ten cultivars studied showed differential haustorial reactionsThese reactions included extra thickening in the pericycle inresponse to haustonal infestation, haustonal collapse, tylosts-likeocclusions in the xylem vessels, and the deposition of dark-stainingmaterials in the cortex Although no definite conclusion couldbe drawn regarding the relationship between the degree of mechanicaltissue development and field resistance, there was evidencethat some field-resistant cultivars have strong mechanical tissuesThere could, however, be other factors governing resistanceto Striga in the field Striga asiatica, sorghum, haustorium, anatomy, endodermis, pot test, host resistance mechanism, parasitization, susceptibility     

Water Relations of the Mistletoe Amyema fitzgeraldii and its Host Acacia acuminata

Water relations of the mistletoe Amyema fitzgeraldii and itshost Acacia acuminata were studied near Geraldton, Western Australia.Transpiration rates of host and parasite under unstressed winterconditions varied more than 300–fold between day and nightwhile leaf water potential gradients between the partners remainedwithin the range 0·4–0·6 MPa. Plots of transpirationagainst leaf water potential indicated closely similar fluidphase resistances in host and parasite during daytime but divergentbehaviour at night due to an apparently large increase in resistanceof the haustorial junction between the partners. Data for summerand winter studies across a full range of light intensitiesshowed the parasite to transpire, on average, 1·4 timesfaster and to exhibit noticeably lower water use efficienciesthan its host. Experiments following restorative changes atnight in leaf water potentials of host and parasite on detachedhost branches supplied through their cut ends with water indicatedthat the haustorium offered a major resistance to water uptakeby the parasite. Restoration of leaf water potentials by theparasite lagged markedly behind that of the host, especiallyduring winter, leading to a rapid build up in potential gradientbetween partners. A phase of rapid flow into the parasite thenfollowed, presumably motivated by lowering of the haustorialresistance. Reversal of the potential gradient between hostand parasite was recorded in a night-time study involving abagged (non-transpiring) mistletoe attached to a host branchfrozen at the base to prevent further water uptake. Mechanismsare proposed to account for the apparently highly variable natureof the resistance of the haustorium. Key words: Mistletoe, transpiration, haustorial resistance, Amyema fitzgeraldii, Acacia acuminata     

Epidermal derivatives as xylem elements and transfer cells: a study of the host-parasite interface in two species of Triphysaria (Scrophulariaceae)

Summary Haustoria ofTriphysaria pusilla andT. versicolor subsp.faucibarbata from a natural habitat were analysed by light and electron microscopy. The keel-shaped edge of the secondary haustorium generally splits the epidermis and cortex of the host root parallel to the root axis, and penetrates to the host vascular tissue. Anticlinally elongated epidermal cells of the haustorium constitute most of the host/parasite interface. Some of these epidermal cells are divided by oblique cell walls. Some of their oblique daughter cells as well as some undivided epidermal cells differentiate into xylem elements. Single epidermal cells occasionally intrude into the vascular tissue of the host and individual host cells can be invaded. The surface area of the plasmalemma in parasitic parenchymatous interface cells is increased by the differentiation of wall labyrinths characteristic of transfer cells and by the development of membrane-lined cytoplasmic tubules or flattened sacs which become embedded in the partly lignified interface cell-wall. Mycorrhizal fungal hyphae enter the xylem bridge in some haustoria. Implications of these observations for the function of the haustorium are discussed.     

HowStriga Parasitizes its Host: a TEM and SEM Study

The cellular contact betweenStriga hermonthica andStriga asiaticaand their hosts,Zea mays andSorghum bicolor , was investigatedby light, transmission electron and scanning electron microscopy.The xylem connections between parasites and hosts involve veryspecific, clustered intrusions into the host's water conductingelements, predominantly into the large vessel elements. A singlehaustorial cell can penetrate a host vessel element with morethan one intrusion. All intrusions become covered by an additionalelectron-opaque wall layer. During subsequent differentiation,a dissolution of specific wall parts of the cell intrusionsoccurs so that open, cup- or trunk-like structures result. Thevessel-like host contact can comprise up to five openings withina single intrusion. Concomitantly, the intrusions and the haustorialcells to which they belong lose their protoplasts and transforminto elements which take up water. The walls of the haustorialcells and both wall parts of their appendages become stronglylignified. The water and nutrient absorbing structures insertedinto the host vessel are named ‘oscula’. Withinthe whole haustorial complex of bothStriga species no phloemelements were detected. Translocation of substances from hostto parasite are briefly discussed. Striga hermonthica ; Striga asiatica ; haustorial anatomy; xylem contact; osculum