Shasta daisy

The first symptom is a sudden wilting and drying of leaves on individual branches or on one side of the crown, while the rest of the plant appears healthy. A cross-section of an infected shoot reveals a brownish or greenish discolouration of the wood — the vascular bundles clogged by the fungus, which can no longer conduct water. The disease progresses over successive years, affecting an ever-larger part of the crown and leading to the gradual death of the plant. Maples (especially Japanese maple), catalpa and many other trees, shrubs and perennials are particularly susceptible. The disease takes two forms: an 'acute' form, in which a branch or the whole plant dies rapidly within a few weeks, and a 'chronic' form — a slow decline spread over several seasons, with smaller, paler leaves, marginal scorching of the blades (resembling sunburn) and premature autumn colouring on infected shoots. The sectoral, one-sided distribution of symptoms is the hallmark of Verticillium wilt above all on woody plants — the part of the crown supplied by the clogged vessels dies off. The discolouration of the wood is best seen just under the bark as longitudinal streaks, and in cross-section as an interrupted ring; in maples it is often olive-green. Symptoms intensify in heat and during drought, when the demand for water exceeds the capacity of the damaged bundles. On herbaceous plants (dahlia, aster, chrysanthemum, tomato, potato, strawberry) one observes wilting and yellowing of the lower leaves, stunting and one-sided (half-blade) yellowing of the leaf — on these species, however, the symptom picture alone is unreliable for differentiation, because one-sided yellowing may also be caused by Fusarium wilt. The vascular discolouration by itself is not conclusive — a definitive diagnosis requires laboratory isolation of the pathogen.

Numerous small, round spots appear on the leaves with a lighter, greyish centre and a darker, brown margin. Within the spots tiny black dots are visible – pycnidia, the fruiting bodies of the fungus, which distinguishes this disease from other leaf spots. The infection progresses from the lower, oldest leaves upwards; with heavy infection the spots merge, the leaves yellow, dry out and drop prematurely, weakening the plant. Affected plants include tomato, currant, phlox and many perennials. The spots are usually 2–5 mm across; the decisive identifying sign is the dark pycnidia at their centre – best seen through a hand lens, and in high humidity exuding whitish 'tendrils' of spores. Leaves densely peppered with spots look as if dusted. The disease is favoured by warm (about 20–25°C), humid weather and water lingering on the leaves for a long time (rain, dew, overhead watering). On tomato the infection is confined almost exclusively to the leaves and leaf stalks – the fruit usually stays healthy – but the loss of the photosynthetic apparatus leads to smaller fruit and exposes it to sunscald.

The disease develops in overly wet, poorly aerated substrate and attacks the roots and the base of the stem. The roots turn brown, rot and lose their bark, which slips off easily, and a dark, watery rot appears at the stem base. The above-ground part wilts, yellows and dies back despite moist soil – a characteristic symptom, because the damaged roots no longer take up water. Especially at risk are houseplants, succulents and cacti (from overwatering), and in the ground conifers, rhododendrons, ericaceous plants and strawberries on waterlogged sites. The process begins inconspicuously at the root hairs and root tips, which darken and disappear, after which the rot advances towards the framework roots and the root collar. Healthy, pale, active roots waste away — what remains is a dark, rusty-brown or blackish, watery mass, and the outer layer of the root bark slips off like a glove, exposing the discoloured central cylinder. In trees and shrubs, infection of the collar and the base of the trunk (stem-base rot) shows as a dark, often streaking patch, sometimes with oozing, and the bark there is moist and sunken; in conifers and rhododendrons, browning and dieback are seen from the bottom or from the centre of the crown while the soil is still moist. Characteristic is the nested (patchy) occurrence of symptoms in the bed — where water and the pathogen accumulate locally. It is worth distinguishing the two causal oomycete genera: Pythium mainly attacks seedlings and fine roots, causing damping-off and root rot in cool, wet substrate, whereas Phytophthora also attacks older, woody plants, framework roots and the collar, more strongly in warmer, water-saturated soil. Key for diagnosis is the contradiction of the symptoms: the plant wilts and looks 'dry', although the substrate is wet — this results from the destruction of the roots, not from a shortage of water.

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.

Slugs and shelled snails that feed at night and after rain. Symptoms: irregular holes in the leaves and young seedlings eaten off completely, silvery slime trails on leaves and soil. The greatest damage occurs in damp, shaded spots — particularly on lettuce, strawberries and hostas. The most damaging in gardens are the slugs (which lack an external shell): the Spanish slug (Arion vulgaris, formerly described as A. lusitanicus) and the grey field slug (Deroceras reticulatum). The leopard slug (Limax maximus) can be morphologically similar to them, but it feeds mainly on decaying organic matter and fungi and may even prey on other slugs, so it is of little importance as a pest of living plants. Shelled forms — grove snails (Cepaea) or the protected Roman snail (Helix pomatia) — usually cause less damage. The body is soft, elongated and permanently covered in slime; on the head there are two pairs of retractable tentacles — the longer upper pair bears the eyes, the shorter lower pair serves a tactile and olfactory function. Slugs and snails are hermaphrodites: they lay spherical, transparent or pearly eggs in clusters, hidden in damp soil, under stones and in leaf litter. A single Spanish slug can lay several hundred eggs; both eggs and young slugs overwinter, and feeding lasts from spring to late autumn, intensifying on warm, damp nights. The damage has smooth edges and often appears in the middle of the leaf blade, not only from the margin; seedlings and transplants are sometimes eaten down to bare soil, and on strawberries and ripening vegetables the slugs gnaw hollows into the fruit. The decisive diagnostic sign is the dried, silvery glistening slime trail — no insect leaves one.