This research investigates a novel method for cultivating mycelium-based leather substitutes using a carefully formulated paste consistency substrate. The primary objectives are to enhance nutrient availability, facilitate scalability, and streamline cultivation processes. The study spans a 21-day cultivation period, during which a flower-based medium is employed, eliminating the need for labor-intensive harvesting techniques. Two fungal species, Ganoderma lucidum (rishi) and Pleurotus djamor (pink oyster) are tested to assess their compatibility with the growth method. These species were chosen based on their rapid colonization rates and inherent resilience. The investigation delves into various combinations of crosslinking agents, including glycerol (a plasticizer), commercial tanner, citric acid, and magnesium sulfate. The effects of these agents on tensile strength are compared and qualitative data is analyzed through the use of scanning electron microscopy (SEM) and stereo microscopy. Furthermore, the study explores the fabrication potential of non-woven textiles derived from mycelium, emphasizing their suitability as eco-friendly leather alternatives. Scaled prototypes are highlighted to demonstrate their feasibility. Post-treatment processes, such as dyeing with bio-based dyes and acrylic leather paint, are evaluated for their aesthetic impact. The research contributes a biodegradable material alternative that addresses the environmental challenges of high textile consumption. The findings add to the growing body of sustainable design methods in the realm of leather-like materials in bio-design.

Fungal hyphae associated with tree roots extending into the surrounding substrate are suspected to have to contaminated buried plant material with recent carbon in two examples and to have resulted in erroneously young radiocarbon ages. This problem might be overcome by choosing sampling sites far from trees or by analyzing the lignin component of samples, although the latter is presently difficult.

An isolate of Sclerotinia sclerotiorum (Lib.) de Bary collected from a Canada thistle [Cirsium arvense (L.) Scop. # CIRAR] plant in Montana proved pathogenic on Canada thistle in field trials. In addition to attacking the thistle crown and causing wilting and death of the shoots, S. sclerotiorum also infected the root system. The high percentage of thistle shoot kill (20 to 80%) after treatment, and subsequent reduction in plant thistle density the following year, demonstrated the potential of S. sclerotiorum as a biological control agent for Canada thistle in Montana.

Nine substituted dinitronaline herbicides were studied to determine their effectiveness in controlling common root rot of peas (Pisum sativum L.) caused by Aphanomyces euteiches Drechs. under field conditions. Most of the dinitroaniline herbicide treatments increased plant stand, plant fresh weight, and shelled pea yield due to root rot suppression in each of the three years studied. Weed control was good in all plots and did not contribute to yield differences. Root rot suppression and crop injury were the primary determinants of yields. The greatest yield increases when compared with the weeded control were 82% for 0.56 kg/ha of dinitramine (N4,N4-diethyl-α,α,α-trifluoro-3,5-dinitrotoluene-2,4-diamine) in 1974, 80% for 0.84 kg/ha of fluchloralin [N-(2-chloroethyl)-2,6-dinitro-N-propyl-4-(trifluoromethyl) aniline] in 1975, and 26% for 1.68 kg/ha of pendimethalin [N-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitrobenzenamine] in 1976. The best average yield increases over all years were 54% for the combination of trifluralin (α,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine) and oryzalin (3,5-dinitro-N4,N4-dipropylsulfanilamide) at 0.56 + 0.56 kg/ha, 49% for fluchloralin at 0.84 kg/ha, and 43% for pendimethalin at 0.84 kg/ha. Annual applications of 0.84 kg/ha of trifluralin delayed the rate of pathogen infestation of a field repeatedly planted to peas.

Integration of a fungal pathogen with herbicides may enhance melaleuca control efforts in South Florida. Hyphal inoculum of four Botryosphaeria ribis Gross & Duggar isolates were evaluated in vitro for compatibility with imazapyr, glyphosate, and a surfactant. Imazapyr at 12 to 60 mg ai/ml did not cause significant loss of inoculum viability in all four isolates within 2 h after mixing. After 24 h, inoculum viability of isolate BR-4 remained unchanged at these imazapyr concentrations, but viability of BR-1 through BR-3 was reduced. Glyphosate at the lowest concentration (32 mg ai/ml) significantly reduced inoculum viability of all isolates within 2 h. Initially, the inoculum viability of all isolates remained unaffected by 1, 5, and 10% (v/v) surfactant concentrations. After 24 h, the surfactant reduced inoculum viability of BR-2, BR-3, and BR-4 inconsistently between experiments, while the inoculum viability of BR-1 was reduced significantly at all concentrations. Mixing of the lowest concentrations of imazapyr, glyphosate, and surfactant significantly reduced inoculum viability within 2 h. This corresponded to the results obtained for glyphosate alone. These results show that hyphal inoculum of B. ribis may be mixed with imazapyr and surfactant for field applications, but mixing the fungus with glyphosate may not be as efficacious.

Bipolaris sorghicola (isolate BS1) and an unidentified Bipolaris species (isolate BX1) were isolated from johnsongrass in North Carolina. Inoculum of BX1 was mass produced in solid and liquid cultures, whereas inoculum of BS1 could only be produced in solid cultures. When six formulations of inoculum of BX1 were compared, vegetable oil was the best adjuvant. Isolate BX1 displayed some host specificity in pathogenicity tests. In the greenhouse, isolate BS1 was more virulent on johnsongrass than isolate BX1. In growth chambers, increasing conidium concentration and younger plant ages interacted to increase virulence of BX1, as did interactions between inoculation, johnsongrass density, and low soil fertility. In Raleigh, NC, isolate BX1 caused very little damage in the field, with or without pretreatment with metolachlor. In Greenville, MS, isolate BX1 caused significant (52%) mortality to annual johnsongrass with very little damage to corn or grain sorghum. The biocontrol potential of the two organisms is uncertain.

Laboratory and greenhouse studies examined effects of atrazine, alachlor, and metolachlor on growth and colonization of grain sorghum roots by Macrophomina phaseolina, causal fungus for charcoal rot disease. In laboratory studies, all three herbicides reduced fungal colony diameter and increased production of microsclerotia. Alachlor and metolachlor reduced germination of fungal microsclerotia. Atrazine did not affect microsclerotia germination, but lessened the effects of alachlor and metolachlor on germination when applied in combination. In greenhouse studies, atrazine reduced numbers of M. phaseolina microsclerotia recovered from soil after 8 wk, and this resulted in reduced colonization of roots by this fungus at harvest. Colonization of grain sorghum roots by M. phaseolina was not affected by alachlor or metolachlor. Grain sorghum growth was reduced by atrazine at all intervals and by alachlor and metolachlor at harvest, despite use of seed safened with cyometrinil.

Acifluorfen, alachlor, glufosinate, glyphosate, paraquat, and pendimethalin were evaluated for their effects on mycelial growth and sclerotia/microsclerotia production by Rhizoctonia solani AG-1 IA and IB in culture. All of these herbicides except glufosinate and glyphosate were evaluated for effects on severity of Rhizoctonia foliar blight of soybean in the field. In laboratory studies, all herbicides reduced colony radius of R. solani. Growth reductions for IB were greater than for IA in the presence of pendimethalin, alachlor, and acifluorfen, but glufosinate reduced growth of IA more than IB. Sclerotia production by both isolates was prevented by paraquat, greatly reduced by glufosinate, but markedly less affected by the other herbicides tested. In field studies, all tested herbicides influenced severity of Rhizoctonia foliar blight when disease pressure was low, but only paraquat reduced severity when disease pressure was high.

A complex coacervate formulation was developed for Colletotrichum truncatum 00-003B1 (Ct), a bioherbicidal fungus against scentless chamomile, and tested in the greenhouse. A two-step process was developed to formulate Ct conidia: (1) invert emulsion preparation—emulsify an aqueous suspension of Ct conidia in nonrefined vegetable oil with the aid of a surfactant, and (2) encapsulate the Ct conidia invert emulsion by complex coacervation. Formulation ingredients, including nonrefined vegetable oils, surfactants, proteins, and carbohydrates, and formulation-processing parameters, including mixing speed and the amount of oil added to invert emulsions, were examined for maximum retention of Ct conidia in the formulation. Most formulation ingredients considered and tested in this study were compatible with Ct, with no significant reduction in conidial germination and mycelial growth. The surfactant soya lecithin promoted the greatest retention of Ct conidia (88%) in the invert emulsion, followed by sorbitan monooleate (82%), glycerol monooleate (70%), and sorbitan trioleate (55%). Optimal retention of Ct conidia in the invert emulsion was observed with a water : oil ratio of 1 : 1.8 to 1 : 3.7, and an overhead paddle stirring speed of 300 rpm when preparing the emulsion. Complex coacervate wall ingredients of 1% gelatin and 2% gum arabic were most effective for Ct conidia retention. In greenhouse studies, scentless chamomile disease rating, following a 24-h dew period, was higher on plants sprayed with the Ct conidia complex coacervate formulation than on plants with Ct conidia suspended in 0.1% Tween 80.

Microscopic conformation, growth behaviour and freezing sensitivity of seven strains of Geotrichum candidum, a ripening starter, were studied and compared according to their macroscopic morphotypes. It has been shown that the thallus forming units (TFU)×ml−1/OD600nm ratio as a function of time is an interesting parameter to follow G. candidum sporulation through the growth behaviour. Microscopic conformation, growth behaviour and freezing sensitivity are clearly strain specific and mostly related to their corresponding morphotypes “yeast”, “mould” or “intermediate”. The two “mould” strains that sporulate weakly (UCMA103, UCMA499) showed a low survival rate to freezing stress whereas the “yeast” strains expressed a significant resistance owing to the arthrospore abundance. Interestingly, one strain (UCMA96) which appeared on solid medium in accord with the “mould” morphotype respond similarly to freezing stress.

‘They dream of the acorned swill of the world, the rooting for pigfruit…’ Dylan Thomas, Under Milk Wood.

Carbon and nitrogen isotopes show a marked change in the diet of British pigs between the Neolithic and the Iron Age. The authors neatly deduce that this was due to the loss of the Neolithic wildwood where pigs were wont to root for fungus amongst the rotting trees.

Infectivity of the entomopathogenic fungus Metarhizium anisopliae against workers of the arboreal termite Odontotermes sp. was assayed under laboratory conditions. Test isolates were collected from different sources, including soil from varied locations and insect hosts from the orders Lepidoptera, Coleoptera, Hemiptera and Orthoptera. All the 23 isolates tested and the standard (ARSEF 7413) were pathogenic to the workers of Odontotermes sp. at a concentration of 107 conidia/ml, with mean mortality ranging from 57.5 to 100%. Two of the isolates (Ma2, Ma13) and the standard caused 100% mortality in the termite species. A detailed bioassay was subsequently conducted with the five most promising isolates, namely Ma1, Ma2, Ma13, Ma16 and Ma17, at concentrations ranging from 104 to 107 conidia/ml. The lethal concentrations (LC50) of these isolates ranged from 0.01 to 0.46 × 105 conidia/ml. The average survival time (AST) for the termites treated with the most virulent isolate (Ma2) varied from 4.2 to 5.7 days across the four spore loads, while AST with the standard isolate ranged from 5.3 to 6.3 days. Two of the isolates, Ma2 and Ma13, were found to be significantly more pathogenic to Odontotermes sp. workers than all the others, including the standard.

As wood is prone to fungal degradation, fundamental research is necessary to increase our knowledge aiming at product improvement. Several imaging modalities are capable of visualizing fungi, but the X-ray equipment presented in this article can envisage fungal mycelium in wood nondestructively in three dimensions with submicron resolution. Four types of wood subjected to the action of the white rot fungus Coriolus versicolor (Linnaeus) Quélet (CTB 863 A) were scanned using an X-ray-based approach. Comparison of wood volumes before and after fungal exposure, segmented manually or semiautomatically, showed the presence of the fungal mass on and in the wood samples and therefore demonstrated the usefulness of computed X-ray tomography for mycological and wood research. Further improvements to the experimental setup are necessary to resolve individual hyphae and enhance segmentation.