Eggplant

The soil-borne fungus infects the root system and enters the vascular bundles, blocking the flow of water within the plant. The plants wilt, first on hot days and often on one side or from the lower leaves, then turn yellow and die despite moist soil. A cross-section of the stem reveals a characteristic brown discolouration of the vascular bundles. The disease intensifies in warmth — the pathogen develops best at high soil temperatures (about 25–30°C), which is why the first symptoms usually appear in midsummer. In the early phase the plants wilt during the hot midday and temporarily recover at night or after watering; over time the wilting becomes permanent. Yellowing progresses from the oldest, lower leaves upwards and is often distinctly one-sided — sometimes only half a leaf or one side of a shoot is affected, on the side along which the blocked vascular bundles run. The plants are stunted (growth is inhibited), and in seedlings fusarium wilt appears as damping-off and toppling of the transplants. Brown discolouration of the vascular bundles is the most reliable diagnostic feature — in fusarium wilt it is usually intense and reaches deep into the stem and the roots. Under moist conditions, especially at the base of the stem or on the cut surface, a delicate pink-salmon or white bloom of fungal sporulation may appear. Fusarium oxysporum occurs in specialised forms (formae speciales), each of which infects only a particular species or genus of plant (e.g. tomato, cucumber, pea, carnation, banana), which helps to distinguish it from pathogens with a wide host range.

A grey-brown, fluffy coating of mycelium on flowers, fruit, leaves and shoots, preceded by watery, rotting spots. It attacks weakened and damaged tissue and develops rapidly in humidity and cool conditions and where air circulation is poor. Common on strawberries, begonias, peonies and roses. The coating is characteristically 'mousy' — fluffy and ashy grey, and when the infected tissue is knocked a visible cloud of spores (conidia) puffs up, which is a diagnostic feature of this disease. Infection usually starts in the weakest tissues: fading petals, wounds, hail marks or pest feeding damage, as well as pollen residue settled on the petals. Small, brown, watery spots appear on the flowers and quickly engulf the whole bloom ('flower blight'); from the infected flower the fungus often grows down into the shoot, causing it to constrict and die back. On soft fruit (strawberry, raspberry, grapes, tomato) a watery, browning rot develops, covered with a thick layer of grey, fluffy felt — the berry softens and 'dissolves'. On seedlings and cuttings Botrytis causes basal stem rot and the sudden collapse of plants. In older, dying mycelium and on plant debris hard, black, irregular lumps form — sclerotia (resting bodies), by which the pathogen overwinters in the soil and in plant debris. The disease also shows up after harvest, as a rapidly advancing storage rot of fruit and vegetables.

Brown to dark-brown spots appear on the leaves with characteristic concentric, zoned rings resembling a "target board", often surrounded by a yellow halo. The spots enlarge and merge, and the leaves dry out and die, starting with the oldest, lower ones. On fruit, tubers and roots, dark, dry, sunken rot spots form, and the infected tissue becomes covered with a dark-olive, velvety coating of spores. The concentric rings within a spot are the most reliable diagnostic feature — they arise from the alternating, day-and-night growth of the mycelium and are best seen against the light. The picture depends on the host and the fungal species: on potato and tomato (Alternaria solani, "early blight") small dark specks on the lower leaves enlarge into oval, zoned necroses; on brassica vegetables (A. brassicae, A. brassicicola) the spots may be surrounded by a broad chlorotic halo and spread onto the seed pods; on carrot (A. dauci) infection begins at the margins of the older leaves, causing blackening and dieback of the foliage that hampers mechanical harvest. Older spots often die and crumble away in the centre, giving the blade a "shot-hole" appearance, and heavy infection leads to yellowing and premature defoliation, which exposes the fruit to sunscald. On stems and leaf stalks elongated, dark, sunken streaks form, and in seedlings the fungus can cause damping-off at the base of the shoot.

A characteristic mosaic appears on the leaves — irregular, interweaving light and dark green or yellow patches and streaks. The leaves are often deformed, wrinkled, curled and smaller, and whole plants become stunted and fruit poorly. The symptoms are most visible on young leaves, and the fruit of cucumber, courgette or tomato may be blotchy and misshapen. The disease affects many vegetables, perennials and ornamental plants. The disease picture depends on the specific virus, the host species and the temperature — the same pathogen produces different symptoms on different plants. A distinguishing feature is that the mosaic is systemic (it affects the whole plant and develops from the youngest leaves) rather than localised like fungal leaf spots — there are no clearly delimited spots with a margin, no mycelial coating and no fruiting bodies. Besides the mosaic, there is vein clearing (a lightening of the tissue along the veins), striping and blister-like bulges of the leaf blade. Severe narrowing and thread-like tomato leaves (the so-called 'shoestring' symptom) is associated mainly with CMV (cucumber mosaic virus), occasionally with tobamoviruses, whereas TMV/ToMV mostly produce mosaic and mottling of the leaves. On the fruit you can observe blotching, concentric rings, wart-like bulges (cucumber) and uneven ripening (tomato), and on the flowers of ornamental plants — colour breaking, i.e. streaks and flecks of discolouration on the petals. In high temperatures (above ~28–30°C) the symptoms may become masked and temporarily disappear, only to return once it cools down — this does not mean the plant has recovered.

A beetle 6–11 mm long with yellow, convex wing cases bearing ten black longitudinal stripes. The larvae are brick-red to orange, hump-backed, with two rows of black dots along the sides; the orange-yellow eggs are laid in clusters on the underside of leaves. Symptoms: larvae and beetles strip the leaves of potato, as well as aubergine, tomato and pepper, down to the veins — under heavy infestation the plant is almost completely eaten. Also characteristic is the orange, black-spotted pronotum (the shield behind the head). The beetles overwinter in the soil at a depth of 10–30 cm and emerge in spring once the surface layer warms to about 14–15°C, usually in May, straight onto the emerging potatoes. A female lays several hundred eggs in total, in clusters of 20–60; after several to a dozen or so days the larvae hatch and pass through four instars (L1–L4). The most voracious and most damaging to the yield are the larvae of the later instars (L3–L4), especially when they feed during tuber initiation and growth. Fully grown larvae move down into the soil and pupate there; under Polish conditions there are usually 1–2 generations per year (up to three in warmer regions). A heavily damaged crop can be seen from afar as patches of stripped plants with remnants of leaf veins and dark larval droppings.

Small (1–3 mm) soft-bodied insects, green, black or pink, feeding in clusters on young shoots and the underside of leaves. They excrete sticky honeydew. The diagnostic feature that distinguishes aphids from other small sucking insects is the pair of siphunculi (tubular projections) at the rear of the abdomen together with a tail-like cauda; a single colony usually holds wingless forms (parthenogenetic females) alongside winged migrants that fly onto new plants in summer. In summer aphids reproduce parthenogenetically and viviparously over many generations, so the population builds up explosively; in autumn many species produce a sexual generation that lays overwintering eggs on the host, and host-alternating species move between a winter host (often a tree or shrub) and a summer host (a herbaceous plant). Feeding symptoms include curling, crinkling and distortion of young leaves, stunted growth, yellowing, and the shedding of buds and fruitlets. Abundant honeydew coats the leaves, and the sooty mould fungus that develops on it forms a black film which limits photosynthesis; the honeydew is fed on by ants, which in return defend the colony against predators. Aphids are also important vectors of plant viruses (mosaics among them), transmitting them from plant to plant even during a brief probing puncture.

Tiny (0.3–0.5 mm) arachnids, hard to spot with the naked eye, feeding on the underside of leaves. Symptoms: fine, pale speckling (feeding punctures); over time the leaves turn grey, yellow and dry out. Under heavy infestation a fine webbing becomes visible. Warm, dry air favours their development — a common problem for houseplants in winter near radiators. Spider mites are not insects but mites of the family Tetranychidae — adults have 8 legs (larvae only 6). The most common in cultivation is the two-spotted spider mite (Tetranychus urticae): yellowish-green females carry two dark spots on the sides of the body, while overwintering females turn orange-red. In orchards the fruit tree red spider mite (Panonychus ulmi) is frequent, whose red eggs overwinter in clusters on the bark of the shoots. Feeding mechanism: the mites puncture the cells of the epidermis and mesophyll on the underside of the leaf and suck out their contents, and the emptied cells fill with air — hence the characteristic, silvery-grey, fine speckling visible from the upper side of the blade (resembling a mosaic discolouration). At high numbers the leaves turn brown, curl and drop prematurely, and the whole plant weakens and loses its growth. Dense webbing spun between the leaves and shoot tips appears only under an advanced attack and is a sign of the risk of the pest spreading to neighbouring plants. The development cycle is very fast in warmth and drought — at a temperature of 25–30°C a single generation can be completed in 1–2 weeks, hence the numerous generations per season and the rapid, exponential build-up of the population. Females lay spherical, transparent eggs on the underside of the leaves. Fertilised females overwinter (in bark crevices, leaf litter and plant debris) or — in the fruit tree red spider mite — the eggs on the bark. Early infestation is easy to miss; diagnosis is helped by shaking a leaf over a white sheet of paper (moving specks become visible) or examining the underside of the leaf with a magnifying glass.

Insects covered in a white, cottony, waxy coating, gathering in leaf axils, at the base of shoots and on the underside of leaf blades. They look like tufts of cotton wool. They suck sap, weaken the plant and excrete sticky honeydew, on which black sooty mould develops. A common pest of houseplants and succulents. Adult females are oval, soft-bodied insects about 2-5 mm long, with a pinkish or grey body hidden under wax, often bearing waxy filaments along the sides and at the tip of the abdomen. Males are tiny, winged and do not feed. In most species eggs are laid in white, cottony ovisacs (cocoons), from which mobile larvae (crawlers) hatch and spread across the plant, carrying the infestation to neighbouring specimens; some mealybugs (e.g. Pseudococcus longispinus), however, are ovoviviparous and give birth to live crawlers without a distinct ovisac. In the warm, dry conditions of homes and glasshouses mealybugs develop all year round, in several overlapping generations - which is why a single treatment is rarely enough. Feeding symptoms are stunted growth, yellowing, deformation and premature leaf drop, and under heavy infestation dieback of shoots; the black sooty mould on the honeydew further reduces photosynthesis and disfigures the plant. A separate form is the root mealybug (Rhizoecus), forming white, waxy clusters on the roots and inside the root ball - the plant weakens and wilts with no visible pest on the above-ground parts. Mealybugs are often attended by ants, which eat the honeydew and protect the colonies from natural enemies.

Very small (1–2 mm), slender, elongated insects with fringed wings, coloured yellow, brown or black; the larvae are pale yellow and wingless. They suck sap from the cells of leaves, petals and buds. Symptoms: silvery to silvery-grey streaks and blotches on the leaves, tiny black specks of excrement, and distortion of young leaves, buds and flowers. They are especially damaging under glass and on houseplants, and some species transmit plant viruses. The silvery sheen appears once the pest has sucked out the contents of the epidermal cells — the empty, air-filled cells reflect light like metallic streaks; they are accompanied by glistening black specks of excrement, which distinguish thrips feeding from that of most other sap-sucking pests. The mouthparts are piercing-sucking and asymmetric (only a single mandible), so the insect first rasps the tissue and then sucks up the exuding sap. On flowers, feeding produces white or brownish discolouration and distortion of the petals — severe on roses, chrysanthemums, orchids and cyclamens. The life cycle is short and, in warm conditions, the generations overlap: the females lay eggs inserted into the plant tissue, the larvae (two instars) feed on the leaves and then drop to the soil or litter, where they pass through the immobile prepupal and pupal stages. Among the most damaging are the western flower thrips (Frankliniella occidentalis) — a key greenhouse pest and vector of tospoviruses (including tomato spotted wilt, TSWV) — and the onion thrips (Thrips tabaci). Only the larvae acquire the viruses, while the adults transmit them, so reducing the larvae also lowers the risk of viral infection.